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WO2015001391A1 - Compositions comprenant du triamide d'acide (thio)phosphorique et d'autres composés, présentant un effet amélioré d'inhibition de l'uréase - Google Patents

Compositions comprenant du triamide d'acide (thio)phosphorique et d'autres composés, présentant un effet amélioré d'inhibition de l'uréase Download PDF

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Publication number
WO2015001391A1
WO2015001391A1 PCT/IB2013/055484 IB2013055484W WO2015001391A1 WO 2015001391 A1 WO2015001391 A1 WO 2015001391A1 IB 2013055484 W IB2013055484 W IB 2013055484W WO 2015001391 A1 WO2015001391 A1 WO 2015001391A1
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WIPO (PCT)
Prior art keywords
composition according
anyone
group
alkyl
groups
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/IB2013/055484
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English (en)
Inventor
Karl-Heinrich Schneider
Claudia Klodwig
Gregor Pasda
Alexander Wissemeier
Daniella LOHE
Achim Reddig
Christian Carlos MIYAGAWA
Wolfram Zerulla
Steffen Tschirschwitz
Ralf-Thomas Rahn
Ansgar Gereon Altenhoff
Stephan Hüffer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF China Co Ltd
BASF SE
Original Assignee
BASF China Co Ltd
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Application filed by BASF China Co Ltd, BASF SE filed Critical BASF China Co Ltd
Priority to PCT/IB2013/055484 priority Critical patent/WO2015001391A1/fr
Priority to US14/902,181 priority patent/US10150712B2/en
Priority to PCT/IB2014/062667 priority patent/WO2015001457A2/fr
Priority to JP2016522940A priority patent/JP6576917B2/ja
Priority to MX2015017715A priority patent/MX2015017715A/es
Priority to EP14819297.4A priority patent/EP3016921B1/fr
Priority to CN201480048545.8A priority patent/CN105517977B/zh
Priority to BR112015032664-1A priority patent/BR112015032664B1/pt
Priority to PL14819297T priority patent/PL3016921T3/pl
Priority to NZ715778A priority patent/NZ715778B2/en
Priority to RU2016103491A priority patent/RU2656416C2/ru
Priority to ES14819297T priority patent/ES2741280T3/es
Priority to RU2018119775A priority patent/RU2018119775A/ru
Priority to AU2014285758A priority patent/AU2014285758B2/en
Priority to CA2916529A priority patent/CA2916529C/fr
Priority to TR2019/10755T priority patent/TR201910755T4/tr
Priority to UAA201600784A priority patent/UA116147C2/uk
Priority to ARP140102486A priority patent/AR097136A1/es
Priority to UY0001035645A priority patent/UY35645A/es
Publication of WO2015001391A1 publication Critical patent/WO2015001391A1/fr
Priority to SA516370350A priority patent/SA516370350B1/ar
Anticipated expiration legal-status Critical
Priority to ZA2016/00606A priority patent/ZA201600606B/en
Priority to US16/197,665 priority patent/US20190084898A1/en
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C05—FERTILISERS; MANUFACTURE THEREOF
    • C05C—NITROGENOUS FERTILISERS
    • C05C9/00—Fertilisers containing urea or urea compounds
    • C05C9/005—Post-treatment
    • C—CHEMISTRY; METALLURGY
    • C05—FERTILISERS; MANUFACTURE THEREOF
    • C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
    • C05G3/90—Mixtures of one or more fertilisers with additives not having a specially fertilising activity for affecting the nitrification of ammonium compounds or urea in the soil

Definitions

  • compositions with improved urease-inhibiting effect comprising (thio)phosphoric acid triamide and further compounds
  • This invention essentially relates to compositions with improved urease-inhibiting effect comprising (thio)phosphoric acid triamide and further compounds and the use of such compositions as additive or coating material for nitrogen-containing fertilizers.
  • Urea itself, however, is a form of nitrogen which is absorbed very little if at all, being hydrolyzed relatively rapidly by the enzyme urease, which is present ubiquitously in the soil, to form ammonia and carbon dioxide. In this process, in certain circumstances, gaseous ammonia is emitted to the atmosphere, and is then no longer available in the soil for the plants, thereby lowering the efficiency of fertilization.
  • N-alkylthiophosphoric acid triamides such as N-(n-butyl)thiophosphoric acid triamide (NBPT) and N-(n-propyl)thiophosphoric acid triamide (NPPT) can be used.
  • NBPT N-(n-butyl)thiophosphoric acid triamide
  • NPPT N-(n-propyl)thiophosphoric acid triamide
  • the urease inhibitor may be incorporated in the urea by, for example, dissolving it into the melt prior to urea granulation or prilling. A process of this kind is described in U.S. Pat. No. 5,352,265, for example. A further option is to apply the urease inhibitor to the urea granules or prills, in the form of a solution, for example. Corresponding processes for application, and suitable solvents, are described in US 2010/218575 A1 , for example.
  • amines selected from me- thyldiethanolamine, tetrahydroxypropylethylenediamine, trimethylaminoethylethanolamine, N,N,N',N'-tetramethyl-1 ,6-hexanediamine, N,N',N"-tris(dimethylaminopropyl)hexahydrotriazine, and 2,2'-dimorpholinyldiethyl ether, are described in US 201 1/0154874 A1.
  • the storage life of the urease inhibitor is limited. The higher the temperature, the shorter the storage life. If, for example, urea is stored under tropical conditions, a major part of the urease inhibitor has undergone decomposition, generally, after about four weeks of storage. If the ure- ase inhibitor is introduced into the urea melt, the decomposition is less. For the commercialization of the urea stabilized with the urease inhibitor, however, it is often vital to apply the urease inhibitor to urea and to store the treated fertilizer until the time of its spreading to the soil.
  • One of the objects of the present invention was to provide a composition containing (thio)phosphoric acid triamide which
  • composition (Q1 ) which comprises:
  • X is oxygen or sulfur
  • R 1 is a Ci to C20 alkyl, C3 to C20 cycloalkyl, Ce to C20 aryl, or dialkylaminocarbonyl group;
  • R 2 is H, or R 1 and R 2 together with the nitrogen atom linking them define a 5- or 6-membered saturated or unsaturated heterocyclic radical, which optionally comprises 1 or 2 further heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur,
  • wt.% stands for "percent by weight” based on the total weight of the composition (Q1 ),
  • R 11 is aryl or alkylaryl
  • R 12 is H or alkyl
  • R 13 is H or alkyl. Accordingly, a further composition (Q2) was found which comprises:
  • X is oxygen or sulfur
  • R 1 is a Ci to C20 alkyl, C3 to C20 cycloalkyl, Ce to C20 aryl, or dialkylaminocarbonyl group;
  • R 2 is H, or
  • R 1 and R 2 together with the nitrogen atom linking them define a 5- or 6-membered satu- rated or unsaturated heterocyclic radical, which optionally comprises 1 or 2 further heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur,
  • (C2) an amine containing not more than one amino group and at least three alkoxy- or hydroxy-substituted C2 to C12 alkyl groups R 21 , wherein at least one of the groups R 21 is different to the other groups R 21 , and
  • (C3) an amine containing not more than one amino group and at least two alkoxy- or hy- droxy-substituted C2 to C12 alkyl groups R 22 , wherein at least one of the groups R 22 bears the alkoxy or hydroxy substituent at a secondary or tertiary carbon atom and wherein at least one of the groups R 22 is different to the other group(s) R 22 , and
  • (C5) a saturated or unsaturated heterocyclic amine which contains at least one oxygen atom as ring atom and which does not contain a further alkoxy group.
  • composition (Q3) which comprises: (A) a mixture comprising at least one (thio)phosphoric acid triamide according to the general formula (I)
  • X is oxygen or sulfur
  • R 1 is a Ci to C20 alkyl, C3 to C20 cycloalkyl, Ce to C20 aryl, or dialkylaminocarbonyl group;
  • R 2 is H , or
  • R 1 and R 2 together with the nitrogen atom linking them define a 5- or 6-membered saturated or unsaturated heterocyclic radical, which optionally comprises 1 or 2 further heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur,
  • R 31 CO is an acyl radical having 1 to 22 carbon atoms
  • R 32 is hydrogen or alkyl
  • R 33 is hydrogen or alkyl, or
  • R 32 and R 33 together with the nitrogen atom linking them define a 5- or 6-membered saturated or unsaturated heterocyclic radical, which optionally comprises 1 or 2 further heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur.
  • a process for treating the soil comprising applying the compositions of the invention into the soil in-furrow and/or as side dress and/or as broadcast was found.
  • compositions of the invention as additive or coating material for nitrogen-containing fertilizers has been found.
  • At least one is to be understood as 1 , 2, 3 or more.
  • a mixture comprising at least one amine refers for example to a mixture comprising 1 , 2, 3 or more amines.
  • soil is to be understood as a natural body comprised of living (e.g. microorganisms (such as bacteria and fungi), animals and plants) and non-living matter (e.g. minerals and organic matter (e.g. organic compounds in varying degrees of decomposition), liquid, and gases) that occurs on the land surface, and is characterized by soil horizons that are distinguishable from the initial material as a result of various physical, chemical, biological, and anthropogenic processes. From an agricultural point of view, soils are predominantly regarded as the anchor and primary nutrient base for plants (plant habitat).
  • fertilizer is to be understood as chemical compounds applied to promote plant and fruit growth.
  • Fertilizers are typically applied either through the soil (for uptake by plant roots) or by foliar feeding (for uptake through leaves).
  • the term "fertilizer” can be subdivided into two major categories: a) organic fertilizers (composed of decayed plant/animal matter) and b) inor- ganic fertilizers (composed of chemicals and minerals).
  • Organic fertilizers include manure, slurry, worm castings, peat, seaweed, sewage, and guano. Green manure crops are also regularly grown to add nutrients (especially nitrogen) to the soil.
  • Manufactured organic fertilizers include compost, blood meal, bone meal and seaweed extracts. Further examples are enzymatically digested proteins, fish meal, and feather meal.
  • inorganic fertilizers are usually manufactured through chemical processes (such as the Haber-Bosch process), also using naturally occurring deposits, while chemically altering them (e.g. concentrated triple superphosphate).
  • Naturally occurring inorganic fertilizers include Chilean sodium nitrate, mine rock phosphate, and limestone.
  • Manure is organic matter used as organic fertilizer in agriculture. Depending on its structure, manure can be divided into liquid manure, semi-liquid manure, stable or solid manure and straw manure. Depending on its origin, manure can be divided into manure derived from animals or plants. Common forms of animal manure include feces, urine, farm slurry (liquid manure) or farmyard manure (FYM) whereas FYM also contains a certain amount of plant material (typically straw), which may have been used as bedding for animals. Animals from which manure can be used comprise horses, cattle, pigs, sheep, chickens, turkeys, rabbits, and guano from seabirds and bats.
  • plant manure when used as fertilizer highly depends on the origin (type of animals). Plant manures may derive from any kind of plant whereas the plant may also be grown explicitly for the purpose of plowing them in (e.g. leguminous plants), thus improving the structure and fertility of the soil. Furthermore, plant matter used as manure may include the contents of the rumens of slaughtered ruminants, spent hops (left over from brewing beer) or seaweed.
  • compositions of the invention are referred to as the compositions (Q1 ), (Q2), and (Q3) in the following.
  • the composition (Q1) comprises (A) and (B) - latter in an amount of more than 10wt.% based on the total weight of (Q1) - and optionally further components as described below.
  • the composition (Q2) comprises (A) and (C) and optionally further components as de- scribed below.
  • the composition (Q3) comprises (A) and (D) and optionally further components as described below.
  • compositions (Q1), (Q2), and (Q3) comprises - as one of their essential components -
  • X is oxygen or sulfur
  • R 1 is a Ci to C20 alkyl, C3 to C20 cycloalkyl, Ce to C20 aryl, or dialkylaminocarbonyl group;
  • R 2 is H, or
  • R 1 and R 2 together with the nitrogen atom linking them define a 5- or 6-membered saturated or unsaturated heterocyclic radical, which optionally comprises 1 or 2 further heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur.
  • X in the general formula (I) of (A) is preferably sulfur.
  • R 1 in the general formula (I) of (A) is preferably Ci-C2o-alkyl, more preferably Ci-Cio-alkyl, most preferably C2-C7 alkyl, for example C3-C4 alkyl.
  • alkyl groups are methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert- butyl, pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, 2-methylpentyl, heptyl, octyl, 2-ethylhexyl, isooctyl, nonyl, isononyl, decyl and isodecyl.
  • Examples of cycloalkyl groups are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cyclooctyl, examples of aryl groups are phenyl or naph- thyl.
  • Examples of heterocyclic radicals R1 R2N- are piperazinyl, morpholinyl, pyrrolyl, pyrazolyl, triazolyl, oxazolyl, thiazolyl or imidazolyl groups.
  • (A) comprises N-n-butylthiophosphoric acid triamide (NBPT) and/or N-n-propylthiophosphoric acid triamide (NPPT), preferably NBPT and NPPT.
  • NBPT N-n-butylthiophosphoric acid triamide
  • NPPT N-n-propylthiophosphoric acid triamide
  • (A) comprises at least two different (thio)phosphoric acid triamides having structures of the general formula (I) and wherein said at least two different (thio)phosphoric acid triamides differ in at least one of radicals R 1 or R 2 , and preferably, one of said at least two different (thio)phosphoric acid triamides is N-n-butylthiophosphoric acid tri- amide (NBPT), and more preferably, the other of said at least two different (thio)phosphoric acid triamides is selected from the group consisting of N-cyclohexyl-, N-pentyl-, N-isobutyl- and N-n- propylphosphoric acid triamide and -thiophosphoric acid triamide.
  • NBPT N-n-butylthiophosphoric acid tri- amide
  • mixtures (A) which comprise NBPT in amounts of from 40 to 95 wt.%, most preferably from 60 to 85% wt.%, particularly preferably from 72 to 80 wt.%, in each case based on the total weight of (A).
  • the mixture (A) can be contained in varying amounts in the composition (Q1 ), (Q2), or (Q3).
  • the amount of (A) is not more than 85 wt.% (wt.% stands for "percent by weight"), more preferably not more than 60 wt.%, most preferably not more than 45 wt.%, most particularly preferably not more than 35 wt.%, particularly not more than 30 wt.%, for example not more than 27 wt.%, based on the total weight of the composition (Q1 ), (Q2), or (Q3).
  • the amount of (A) is at least 1 wt.%, more preferably at least 4 wt.%, most preferably at least 10 wt.%, most particularly preferably at least 15 wt.%, particularly at least 20 wt.%, for example at least 23 wt.%, based on the total weight of the composition (Q1 ), (Q2), or (Q3).
  • the composition (Q1) comprises - as one of its essential compo- nents -
  • R 11 is aryl or alkylaryl
  • R 12 is H or alkyl
  • R 13 is H or alkyl.
  • compositions (Q2) and (Q3) can further optionally comprise
  • R 11 is aryl or alkylaryl
  • R 12 is H or alkyl
  • R 13 is H or alkyl.
  • the aromatic alcohol (B) is preferably used as solvent in the composition (Q1 ). If present, the aromatic alcohol (B) is preferably used as solvent in the compositions (Q2), or (Q3).
  • R 12 in the general formula (I I) of (B) is C1-C40 alkyl, preferably Ci to C20 alkyl, more preferably Ci to C10 alkyl, most preferably Ci to C 5 alkyl.
  • R 13 in the general formula (I I) of (B) is C1-C40 alkyl, preferably Ci to C20 alkyl, more preferably Ci to C10 alkyl, most preferably Ci to C 5 alkyl.
  • R 12 in the general formula (I I) of (B) is H.
  • R 13 in the general formula (I I) of (B) is H.
  • R 13 in the general formula (I I) of (B) is H.
  • R 11 in the general formula (I I) of (B) is aryl.
  • R 11 in the general formula (I I) of (B) is phenyl, naphthyl, pyridyl, or pyrrolyl, pyra- zolyl, triazolyl, oxazolyl, thiazolyl or imidazolyl.
  • R 11 in the general formula (I I) of (B) is phenyl.
  • (B) is benzyl alcohol.
  • the aromatic alcohol (B) can be contained in any amounts greater than 10 wt.% in the composition (Q1 ) based on the total weight of the composition (Q1 ).
  • the amount of (B) is not more than 99 wt.% (wt.% stands for "percent by weight"), more preferably not more than 93 wt.%, most preferably not more than 87 wt.%, most particularly preferably not more than 80 wt.%, particularly not more than 75 wt.%, for example not more than 70 wt.%, based on the total weight of the composition (Q1).
  • the amount of (B) is at least 13 wt.%, more preferably at least 20 wt.%, most preferably at least 35 wt.%, most particularly preferably at least 45 wt.%, particularly at least 55 wt.%, for example at least 60 wt.%, based on the total weight of the composition (Q1 ).
  • the amount of (B) is preferably not more than 78 wt.%, more preferably not more than 67 wt.%, most preferably not more than 61 wt.%, most particularly preferably not more than 56 wt.%, particularly not more than 53 wt.%, for example not more than 50 wt.%, based on the total weight of the composition (Q1).
  • the amount of (B) is at least 16 wt.%, more preferably at least 21 wt.%, most preferably at least 26 wt.%, most particularly preferably at least 30 wt.%, particularly at least 37 wt.%, for example at least 40 wt.%, based on the total weight of the composition (Q1).
  • the aromatic alcohol (B) can generally be contained in varying amounts in the composition (Q2) or (Q3).
  • the amount of (B) is preferably not more than 95 wt.% (wt.% stands for "percent by weight"), more preferably not more than 80 wt.%, most preferably not more than 70 wt.%, most particularly preferably not more than 60 wt.%, particularly not more than 55 wt.%, for example not more than 50 wt.%, based on the total weight of the composition (Q2) or (Q3).
  • the amount of (B) is preferably at least 6 wt.%, more preferably at least 13 wt.%, most preferably at least 21 wt.%, most particularly preferably at least 30 wt.%, particularly at least 35 wt.%, for example at least 40 wt.%, based on the total weight of the composition (Q2), or (Q3).
  • composition (Q2) comprises - as one of its essential components - and the compositions (Q1 ) and (Q3) can further comprise - as one of its optional components -
  • (C2) an amine containing not more than one amino group and at least three alkoxy- or hydroxy-substituted C2 to C12 alkyl groups R 21 , wherein at least one of the groups R 21 is different to the other groups R 21 , and
  • (C3) an amine containing not more than one amino group and at least two alkoxy- or hydroxy-substituted C2 to C12 alkyl groups R 22 , wherein at least one of the groups R 22 bears the alkoxy or hydroxy substituent at a secondary or tertiary carbon atom and wherein at least one of the groups R 22 is different to the other group(s) R 22 , and
  • (C5) a saturated or unsaturated heterocyclic amine which contains at least one oxygen atom as ring atom and which does not contain a further alkoxy group.
  • the amine(s) (C) can be contained in varying amounts in the composition (Q2).
  • the amount of (C) is not more than 90 wt.% (wt.% stands for "percent by weight”), more preferably not more than 65 wt.%, most preferably not more than 48 wt.%, most particularly preferably not more than 37 wt.%, particularly not more than 30 wt.%, for example not more than 24 wt.%, based on the total weight of the composition (Q2).
  • the amount of (C) is at least 1 wt.%, more preferably at least 3 wt.%, most preferably at least 6 wt.%, most particularly preferably at least 9 wt.%, particularly at least 14 wt.%, for example at least 18 wt.%, based on the total weight of the composition (Q2).
  • the amine(s) (C) can generally be contained in varying amounts in the composition (Q1 ) or (Q3).
  • the amount of (C) is preferably not more than 90 wt.% (wt.% stands for "percent by weight”), more preferably not more than 65 wt.%, most preferably not more than 48 wt.%, most particularly preferably not more than 37 wt.%, particularly not more than 30 wt.%, for example not more than 24 wt.%, based on the total weight of the composition (Q1 ) or (Q3).
  • the amount of (C) is preferably at least 1 wt.%, more preferably at least 3 wt.%, most preferably at least 6 wt.%, most particularly preferably at least 9 wt.%, particularly at least 14 wt.%, for example at least 18 wt.%, based on the total weight of the composition (Q1 ) or (Q3).
  • (C) is
  • (C1 ) can be any polymeric polyamine, and is preferably a polyalkyleneimine or poly- vinylamine, more preferably a polyalkyleneimine, most preferably a polyethyleneimine, polypro- pyleneimine, or polybutyleneimine, particularly a polyethyleneimine.
  • (C1 ) is preferably any polymeric polyamine comprising ethylene- imine (— CH2CH2NH— ) as monomeric units, including homopolymers and any copolymers of ethyleneimine, and is preferably a homopolymer of ethyleneimine.
  • Copolymers can be alternating, periodic, statistical or block copolymers.
  • (C1 ) can be of any polymer structure, for example a linear polymer, a ring polymer, a cross-linked polymer, a branched polymer, a star polymer, a comb polymer, a brush polymer, a dendronized polymer, or a dendrimer etc.
  • (C1 ) is an essentially linear polymer, and is preferably a linear polymer.
  • Polyethyleneimines which may be used are polyethyleneimine homopolymers which may be present in uncrosslinked or crosslinked form.
  • the polyethyleneimine homopolymers can be prepared by known processes, as described, for example, in Rompps (Chemie Lexikon, 8th edition, 1992, pages 3532-3533), or in Ullmanns Enzyklopadie der Technischen Chemie, 4th edition, 1974, vol. 8, pages 212-213. and the literature stated there. They have a molecular weight in the range from about 200 to 1 000 000 g/mol.
  • Corresponding commercial products are for example available under the name Lupasol® from BASF SE.
  • the polyethyleneimine (C1) is preferably a poly- ethylenimine having a degree of branching in the range of from 0.1 to 0.95 (also referred to as "highly branched polyethyleneimine”), and more preferably a polyethylenimine having a degree of branching in the range of from 0.25 to 0.90, more preferably a polyethylenimine having a de- gree of branching in the range of from 0.30 to 0.80, und most preferably a polyethylenimine having a degree of branching in the range of 0.50 to 0.80.
  • Highly branched polyethyleneimines are characterized by its high degree of branching, which can be determined for example via 13 C-NM spectroscopy, preferably in D2O, and is defined as follows:
  • the polymeric polyamine (C1 ) can have different weight average molecular weights.
  • the weight average molecular weight of (C1) is preferably at least 200, more preferably at least 400, most preferably at least 550, particularly at least 650, for example at least 750.
  • the weight average molecular weight of (C1) is preferably not more than 10,000, more preferably not more than 4,000, most preferably not more than 1 ,900, particularly not more than 1 ,500, for example not more than 1 ,350.
  • the weight average molecular weight can be determined by standard gel permeation chromatography (GPC) known to the person skilled in the art.
  • (C2) an amine containing not more than one amino group and at least three alkoxy- or hy- droxy-substituted C2 to C12 alkyl groups R 21 , wherein at least one of the groups R 21 is different to the other groups R 21 .
  • a number of groups R 21 within (C2) is at least 3, preferably 3 to 5, more preferably 3 to 4, and most preferably 3.
  • the number of carbon atoms in each group R 21 within (C2) is 2 to 12, preferably 2 to 9, more preferably 2 to 7, most preferably 2 to 5, particularly preferably 2 to 4, particularly 2 to 3, for example 3, wherein said number of carbon atoms does not include carbon atoms in any alkoxy groups or any other substituents of R 21 .
  • the groups R 21 within (C2) are alkoxy- or hydroxy-substituted, preferably hydroxy-substituted.
  • At least one of the groups R 21 is different to the other groups R 21 , preferably one of the groups R 21 is different to the other groups R 2 .
  • - is an amine containing not more than one amino group and at least three hydroxy-substituted C ⁇ to Ce - or preferably C2 to C 5 - alkyl groups R 21 , wherein at least one of the groups R 21 is different to the other groups R 21 ,
  • - is preferably an amine containing not more than one amino group and at least three hydroxy- substituted C2 to C3 alkyl groups R 21 , wherein at least one of the groups R 21 is different to the other groups R 21 ,
  • - is more preferably an amine containing not more than one amino group and three hydroxy- substituted C2 to C3 alkyl groups R 21 which are covalently bound to the amino group, wherein one of the groups R 21 is different to the other groups R 21 , and
  • - is for example an amine selected from the group consisting of Bis(hydroxyethyl)- isopropanolamine (DEIPA), and 1 ,1 '-((2-Hydroxyethyl)imino)dipropan-2-ol.
  • DEIPA Bis(hydroxyethyl)- isopropanolamine
  • 1 ,1 '-((2-Hydroxyethyl)imino)dipropan-2-ol is for example an amine selected from the group consisting of Bis(hydroxyethyl)- isopropanolamine (DEIPA), and 1 ,1 '-((2-Hydroxyethyl)imino)dipropan-2-ol.
  • (C2) is an amine N(R 21 )3 wherein
  • R 21 is a an alkoxy- or hydroxy-substituted - preferably a hydroxyl-substituted - C2 to C12 - pref- erably a C2 to C7, more preferably a C2 to C3 - alkyl group and wherein one of the groups R 21 is different to the other group R 21 .
  • (C2) is an amine N(R 21 )3 wherein
  • R 21 is a an alkoxy- or hydroxy-substituted - preferably a hydroxyl-substituted - C2 to C12 - pref- erably a C2 to C7, more preferably a C2 to C3 - alkyl group and wherein one of the groups R 21 is different to the other group R 21 and wherein at least one of the groups R 21 bears the alkoxy or hydroxy substituent at a secondary or tertiary carbon atom.
  • (C3) an amine containing not more than one amino group and at least two alkoxy- or hydroxy- substituted C2 to C12 alkyl groups R 22 , wherein at least one of the groups R 22 bears the alkoxy or hydroxy substituent at a secondary or tertiary carbon atom and wherein at least one of the groups R 22 is different to the other group(s) R 22 .
  • a number of groups R 22 within (C3) is at least 2, preferably 2 to 5, more preferably 2 to 4, and most preferably 2 to 3, for example 2.
  • the number of carbon atoms in each group R 22 within (C3) is 2 to 12, preferably 2 to 9, more preferably 2 to 7, most preferably 2 to 5, particularly preferably 2 to 4, particularly 2 to 3, for ex- ample 3, wherein said number of carbon atoms does not include carbon atoms in any alkoxy groups or any other substituents of R 22 .
  • the groups R 22 within (C3) are alkoxy- or hydroxy-substituted, preferably hydroxy-substituted.
  • For one amine (C3) among the at least two groups R 22 , at least one of the groups R 22 is different to the other group(s) R 22 , preferably one of the groups R 22 is different to the other group(s) R 22 .
  • At least one of the groups R 22 bears the alkoxy or hydroxy substituent at a secondary or tertiary carbon atom, particularly at a secondary carbon atom.
  • - is an amine containing not more than one amino group and at least two hydroxy-substituted C ⁇ to C7 alkyl groups R 22 , wherein at least one of the groups R 22 bears the hydroxy substitu- ent at a secondary or tertiary carbon atom and wherein at least one of the groups R 22 is different to the other group(s) R 22 ,
  • - is more preferably an amine containing not more than one amino group and at least two hydroxy-substituted C2 to C4 alkyl groups R 22 , wherein at least one of the groups R 22 bears the hydroxy substituent at a secondary carbon atom and wherein at least one of the groups R 22 is different to the other group(s) R 22 ,
  • - is most preferably an amine containing not more than one amino group and two hydroxy- substituted C2 to C3 alkyl groups R 22 which are covalently bound to the amino group of the amine (C3), wherein at least one of the groups R 22 bears the hydroxy substituent at a secondary carbon atom and wherein one of the groups R 22 is different to the other group R 22 , - is for example an amine selected from the group consisting of 1-((2-hydroxyethyl)amino)- propan-2-ol, and N-Methyl-N-hydroxyethyl-isopropanolamine.
  • (C3) is an amine R 24 N(R 22 )2 wherein
  • R 24 is H or a Ci to C12- preferably a Ci to C 7 , more preferably a Ci to C3 - alkyl group and R 22 is an alkoxy- or hydroxy-substituted - preferably a hydroxyl-substituted - C2 to C12 - preferably a C2 to C 7 , more preferably a C2 to C3 - alkyl group and wherein at least one of the groups R 22 bears the hydroxy substituent at a secondary carbon atom and wherein one of the groups R 22 is different to the other group R 22 .
  • (C) is
  • (C4) an amine containing at least one saturated or unsaturated Ce to C40 alkyl group R 23 .
  • the number of carbon atoms in each group R 23 within (C4) is 8 to 40, preferably 8 to 32, more preferably 8 to 24, most preferably 8 to 19, particularly preferably 8 to 16.
  • the group R 23 within (C4) is saturated or unsaturated, preferably unsaturated.
  • (C4) contains at least one alkoxy or hydroxy group, more preferably at least one alkoxy and at least one hydroxy groups, most preferably at least two alkoxy and at least one hydroxyl group, particularly at least four alkoxy and at least one hy- droxyl group.
  • (C4) is an amine selected from the group consisting of: ethoxylated (2) cocoalkyl- amine, ethoxylated (5) cocoalkylamine, ethoxylated (15) cocoalkylamine, ethoxylated (2) oleylamine, lauryl-dimethylamine, oleyl-dimethylamine, and 2-propylheptylamine ethoxylate (5 EO), 2-propylheptylamine ethoxylate (10 EO), and 2-propylheptylamine ethoxylate (20 EO).
  • heterocyclic amine stands for a heterocyclic compound in which at least one ring atom of the heterocyclic ring is a nitrogen atom.
  • the heterocyclic amine (C5) is saturated or unsaturated, preferably saturated.
  • the heterocyclic amine (C5) contains preferably a 5-, 6- or 7-membered heterocyclic ring, more preferably a 5- or 6-membered ring, most preferably a 6-membered ring.
  • the heterocyclic amine (C5) contains at least one, more preferably 1 to 3, most preferably 1 to 2, particularly one oxygen atom(s) as ring atom(s) of the heterocyclic ring.
  • the heterocyclic amine (C5) is preferably a morpholine or morpholine derivative, more preferably N-alkyl morpholine, most preferably N-methyl, N-ethyl, N-propyl, or N-butyl morpholine, for example N-methyl morpholine.
  • the composition (Q3) comprises - as one of its essential components - and the compositions (Q1 ) and (Q2) can further comprise - as one of its optional components -
  • R 3 CO is an acyl radical having 1 to 22 carbon atoms
  • R 32 is H or alkyl
  • R33 is H or alkyl, or
  • R 32 and R 33 together with the nitrogen atom linking them define a 5- or 6-membered saturated or unsaturated heterocyclic radical, which optionally comprises 1 or 2 further heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur.
  • the amide(s) (D) can be contained in varying amounts in the composition (Q3).
  • the amount of (D) is not more than 90 wt.% (wt.% stands for "percent by weight”), more preferably not more than 65 wt.%, most preferably not more than 45 wt.%, most particularly preferably not more than 30 wt.%, particularly not more than 22 wt.%, for example not more than 16 wt.%, based on the total weight of the composition (Q3).
  • the amount of (D) is at least 1 wt.%, more preferably at least 3 wt.%, most preferably at least 6 wt.%, most particularly preferably at least 9 wt.%, particularly at least 12 wt.%, for example at least 15 wt.%, based on the total weight of the composition (Q3).
  • the amide (D) can generally be contained in varying amounts in the composition (Q1 ) or (Q2).
  • the amount of (D) is preferably not more than 90 wt.% (wt.% stands for "percent by weight”), more preferably not more than 65 wt.%, most preferably not more than 45 wt.%, most particularly preferably not more than 30 wt.%, particularly not more than 22 wt.%, for example not more than 16 wt.%, based on the total weight of the composition (Q1 ) or (Q2).
  • the amount of (D) is preferably at least 1 wt.%, more preferably at least 3 wt.%, most preferably at least 6 wt.%, most particularly preferably at least 9 wt.%, particularly at least 12 wt.%, for example at least 15 wt.%, based on the total weight of the composition (Q1 ) or (Q2).
  • (III) of (D) 32 is H or alkyl, preferably H or Ci to C40 alkyl, more prefera- bly H or Ci to C20 alkyl, most preferably H or Ci to C10 alkyl, particularly preferably H or Ci to C4 alkyl, most particularly preferably Ci to C 4 alkyl, particularly Ci to C 2 alkyl, for example methyl.
  • R 33 is H or alkyl, preferably H or Ci to C40 alkyl, more preferably H or Ci to C20 alkyl, most preferably H or Ci to C10 alkyl, particularly preferably H or Ci to C 4 alkyl, most particularly preferably Ci to C 4 alkyl, particularly Ci to C 2 alkyl, for example methyl.
  • R 32 is H or Ci to C 4 alkyl
  • R 33 is H or Ci to C 4 alkyl
  • R 32 is Ci to C 4 alkyl
  • R 33 is Ci to C 4 alkyl
  • R 33 is Ci to C2 alkyl.
  • R 31 CO is a hydroxysubstituted acyl radical having 1 to 22 carbon atoms, and more preferably, R 31 CO is a hydroxysubstituted acyl radical having 1 to 22 carbon atoms, and R 32 is alkyl, and R 33 is alkyl, and most preferably, R 31 CO is a hydroxysubstituted acyl radical having 1 to 7 carbon atoms, and R 32 is Ci to C 4 alkyl, and R 33 is Ci to C 4 alkyl.
  • the amide (D) is a ⁇ , ⁇ -dialkyl amide based on lactic acid, citric acid, tartaric acid, ricinoleic acid, 12-hydroxy stearic acid, or their mixtures, preferably a ⁇ , ⁇ -dialkyl amide based on lactic acid, citric acid, tartaric acid, or their mixtures, most preferably a ⁇ , ⁇ -dimethyl amide based on lactic acid, citric acid, tartaric acid, particularly a lactic acid N,N-dimethylamide.
  • R 3 CO in the general formula (III) of (D) R 3 CO is an acyl radical having 6 to 12 carbon atoms, more preferably, R 31 CO is an acyl radical having 8 to 10 carbon atoms.
  • R 31 CO in the general formula (III) of (D) R 31 CO does not contain a hydroxy group, and more preferably, R 31 CO does not contain a hydroxy group and is an acyl radical having 6 to 12 carbon atoms, and most preferably, R 31 CO does not contain a hydroxy group and is an acyl radical having 8 to 10 carbon atoms.
  • the amide (D) is selected from the group consisting of ⁇ , ⁇ -dimethyloctanamide, N,N-dimethylnonanamide, and N,N-dimethyldecanamide.
  • R 31 CO is an acyl radical having 1 to 3 carbon atoms, more preferably, R 31 CO is an acyl radical having 1 to 2 carbon atoms.
  • R 32 and R 33 together with the nitrogen atom linking them define a 5- or 6-membered saturated or unsaturated heterocyclic radical which optionally comprises 1 or 2 further heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, and more preferably, R 32 and R 33 together with the nitrogen atom linking them define a 6-membered saturated or unsaturated heterocyclic radical which optionally comprises one further heteroatom selected from the group consisting of nitrogen, oxygen, and sulfur, most preferably R 32 and R 33 together with the nitrogen atom linking them define a 6-membered saturated heterocyclic radical which comprises one further oxygen heteroatom, particularly R 32 and R 33 together with the nitrogen atom linking them define a mor- pholinyl radical.
  • the amide (D) is N-acetylmorpholine or N-formylmorpholine.
  • R 32 and R 33 together with the nitrogen atom linking them define a 5-membered saturated or unsaturated heterocyclic radical which optionally comprises 1 or 2 further heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, and more preferably, R 32 and R 33 together with the nitrogen atom linking them define a 5-membered saturated heterocyclic radical which optionally comprises one further nitrogen heteroatoms, most preferably R 32 and R 33 together with the nitrogen atom linking them define a 5-membered saturated heterocyclic radical which comprises one further nitrogen heteroatom which is covalently bound to the carbon atom of the car- bonyl group of R 31 CO, particularly R 32 and R 33 together with the nitrogen atom linking them define a imidazolidinonyl radical.
  • the amide (D) is 1 ,3-Dimethyl-2-imidazolidinone (also referred to as dimethylethylenurea).
  • R 32 is an acyloxy substituted alkyl group, more preferably, R 31 CO is an acyl radical having 1 to 4 carbon atoms, and R 32 is an acyloxy substituted alkyl group, most preferably, R 31 CO is an acyl radical having 1 to 4 carbon atoms, R 32 is an acyloxy substituted alkyl group and R 33 is Ci to C4 alkyl.
  • the amide (D) is N-[2-(acetyloxy)ethyl]-N-methyl acetamide.
  • the composition (Q1), (Q2), or (Q3) can further optionally comprise
  • (E) an alcohol comprising at least two hydroxy groups which are not dissociable in the aqueous medium.
  • the alcohol (E) is different from the components (A), (B), (C) and (D).
  • “Not dissociable” means that the pK a value (logarithmic measure of the acid dissociation constant) for the reaction alcohol (D) ⁇ deprotonated alcohol (D) + H + of the hydroxy group in the neutral aqueous phase is more than 9.9, more preferably more than 1 1 , most preferably more than 12, particularly preferably more than 13, for example more than 14 as measured in de-ionized water at 25°C and atmospheric pressure.
  • propane- 1 ,2-diol alpha-propylene glycol
  • the alcohol (E) is preferably used as solvent in the compositions (Q1 ), (Q2), or (Q3).
  • the alcohol (E) is a diol, triol, tetraol, pentaol, hexaol, heptaol, octaol, nonaol, decaol, or a polyol. More preferably, (E) is a diol, triol, tetraol, pentaol, or hexaol. Most preferably, (E) is a diol.
  • (E) is ethanediol (ethylene glycol), propanediol (propylene glycol), or butanediol (butylene glycol).
  • (E) is propanediol (propylene glycol).
  • (E) is propane-1 ,2-diol (alpha-propylene glycol).
  • the alcohol (E) is preferably an alcohol having 2 to 50 carbon atoms, more preferably an alcohol having 2 to 20 carbon atoms, most preferably an alcohol having 2 to 1 1 carbon atoms, particularly preferably an alcohol having 2 to 7 carbon atoms, in particular an alcohol having 2 to 4 carbon atoms, for example an alcohol having 3 carbon atoms.
  • the alcohol (E) can be contained in varying amounts in the composition (Q1), (Q2), or (Q3).
  • the amount of (E) is preferably not more than 99 wt.% (wt.% stands for "percent by weight"), more preferably not more than 93 wt.%, most preferably not more than 87 wt.%, most particularly preferably not more than 80 wt.%, particularly not more than 75 wt.%, for ex- ample not more than 70 wt.%, based on the total weight of the composition (Q1), (Q2), or (Q3).
  • the amount of (E) is at least 13 wt.%, more preferably at least 20 wt.%, most preferably at least 35 wt.%, most particularly preferably at least 45 wt.%, particularly at least 55 wt.%, for example at least 60 wt.%, based on the total weight of the composition (Q1 ), (Q2), or (Q3).
  • the amount of (E) is preferably not more than 78 wt.%, more preferably not more than 67 wt.%, most preferably not more than 61 wt.%, most particularly preferably not more than 56 wt.%, particularly not more than 53 wt.%, for example not more than 50 wt.%, based on the total weight of the composition (Q1), (Q2), or (Q3).
  • the amount of (E) is at least 16 wt.%, more preferably at least 21 wt.%, most preferably at least 26 wt.%, most particularly preferably at least 30 wt.%, particularly at least 37 wt.%, for example at least 40 wt.%, based on the total weight of the composition (Q1 ), (Q2), or (Q3).
  • composition (Q1), (Q2), or (Q3) can further optionally comprise (F) a nitrogen-containing fertilizer.
  • the nitrogen-containing fertilizer (F) is different from the components (A), (B), (C) and (D).
  • the nitrogen-containing fertilizer (F) preferably comprises manure, ammonium sulfate, ammoni- um nitrate, ammonium chloride, cyanamide, dicyandiamide (DCD), calcium nitrate, or urea- containing fertilizer (F1 ), more preferably comprises urea-containing fertilizer (F1 ), most preferably comprises urea, for example is urea.
  • the urea-containing fertilizer (F1 ) is defined as a fertilizer comprising at least one component selected from the group consisting of urea, urea ammonium nitrate (UAN), isobutylidene diurea (IBDU), crotonylidene diurea (CDU) and urea formaldehyde (UF), urea-acetaldehyde, and urea- glyoxal condensates.
  • the urea has a purity of at least 90%, and may for example be in crystalline, granulated, compacted, prilled or ground form.
  • the fertilizer (F) can be contained in varying amounts in the composition (Q1 ), (Q2), or (Q3).
  • the amount of (F) is preferably not more than 99.99 wt.% (wt.% stands for "percent by weight"), more preferably not more than 99.9 wt.%, most preferably not more than 99.5 wt.%), most particularly preferably not more than 99 wt.%o , particularly not more than 98 wt.%, for example not more than 97 wt.%, based on the total weight of the composition (Q1 ), (Q2), or (Q3).
  • the amount of (F) is preferably at least 96 wt.%, more preferably at least 93 wt.%, most preferably at least 90 wt.%, most particularly preferably at least 82 wt.%, particularly at least 70 wt.%, for example at least 50 wt.%, based on the total weight of the com- position (Q1), (Q2), or (Q3).
  • compositions (Q1), (Q2), or (Q3) - such as stability, storage life, or stability when applied to or coated on nitrogen-containing fertilizers (F) such as urea - may depend on the pH of the corresponding composition.
  • the composition (Q1 ), (Q2), or (Q3) can have any pH value.
  • the pH value of the composition (Q1 ), (Q2), or (Q3) is preferably not more than 14, more preferably not more than 13, most preferably not more than 12, particularly preferably not more than 1 1.6, particularly most preferably not more than 11 .3, particularly not more than 11 , for example not more than 10.7.
  • the pH value of the composition (Q1 ), (Q2), or (Q3) is preferably at least 6, more preferably at least 7, most preferably at least 7.5, particularly prefer- ably at least 8.0, particularly most preferably at least 8.2, particularly at least 8.5, for example at least 8.7.
  • the pH value of the composition (Q1 ), (Q2), or (Q3) is preferably in the range of from 6 to 14, more preferably from 7 to 13, most preferably from 7.5 to 12, particularly preferably from 8 to 1 1.6, particularly most preferably from 8.2 to 11 .3, particularly from 8.5 to 1 1 , for example from 8.7 to 10.7.
  • the composition (Q1 ), (Q2), or (Q3) can further optionally contain at least one pH adjusting agent (G).
  • the pH adjusting agent (G) is different from the components (A), (B), (C) and (D).
  • the pH adjusting agent (G) is a compound which is added to the composition (Q1 ), (Q2), or (Q3) to have its pH value adjusted to the required value.
  • the composition (Q1 ), (Q2), or (Q3) contains at least one pH adjusting agent (G).
  • Preferred pH adjusting agents are inorganic acids, carboxylic acids, amine bases, alkali hydroxides, ammonium hydroxides, including tetraalkylammonium hydroxides.
  • the pH adjusting agent (G) is nitric acid, sulfuric acid, ammonia, sodium hydroxide, or potassium hydroxide.
  • the pH adjusting agent (G) is potassium hydroxide.
  • the pH adjusting agent (G) can be contained in varying amounts in the composition (Q1 ), (Q2), or (Q3). If present, the amount of (G) is preferably not more than 10 wt.%, more preferably not more than 2 wt.%, most preferably not more than 0.5 wt.%, particularly not more than 0.1 wt.%, for example not more than 0.05 wt.%, based on the total weight of the corresponding composition (Q1 ), (Q2), or (Q3).
  • the amount of (G) is preferably at least 0.0005 wt.%, more preferably at least 0.005 wt.%, most preferably at least 0.025 wt.%, particularly at least 0.1 wt.%, for example at least 0.4 wt.%, based on the total weight of the corre- sponding composition (Q1 ), (Q2), or (Q3).
  • composition (Q1), (Q2), or (Q3) can further optionally contain the compound (K) selected from the group consisting of (K1) an amine selected from the group consisting of methyldiethanolamine, tetrahydroxypro- pylethylenediamine, trimethylaminoethylethanolamine, N,N,N',N'-tetramethyl-1 ,6- hexanediamine, N,N',N"-tris(dimethylaminopropyl)hexahydrotriazine, and 2,2'- dimorpholinyldiethyl ether,
  • (K2) an amine containing not more than one amino group and at least three alkoxy- or hydroxy- substituted C2 to C12 alkyl groups R 41 , wherein all groups R 41 within said amine are identical, and
  • (K3) an amine containing not more than one amino group and at least two alkoxy- or hydroxy- substituted C2 to C12 alkyl groups R 42 , wherein at least one of the groups R 42 bears the alkoxy or hydroxy substituent at a secondary or tertiary carbon atom and wherein all groups R 42 with said amine are identical.
  • (K2) or (K3) are preferably triethanolamine, tripropanolamine, diisopropanolamine, triisopro- panolamine, diethanolamine, methyldiethanolamine, or methyldipropanolamine. If present, the compound (K) can generally be contained in varying amounts in the composition (Q1 ), (Q2), or (Q3).
  • the amount of (K) is preferably not more than 40 wt.% (wt.% stands for "percent by weight”), more preferably not more than 30 wt.%, most preferably not more than 25 wt.%, most particularly preferably not more than 20 wt.%, particularly not more than 18 wt.%, for example not more than 15 wt.%, based on the total weight of the composition (Q1 ), (Q2), or (Q3).).
  • the amount of (K) is preferably at least 1 wt.%, more preferably at least 3 wt.%, most preferably at least 5 wt.%, most particularly preferably at least 8 wt.%, particularly at least 1 1 wt.%, for example at least 14 wt.%, based on the total weight of the composition (Q1), (Q2), or (Q3).
  • composition (Q1), (Q2), or (Q3) can further optionally contain components (H) which are selected from the group consisting of auxiliaries, solvents, solid carriers, surfactants, adjuvants, thickeners, bactericides, anti-freezing agents, anti-foaming agents, colorants, tackifiers, binders, preservatives, antioxidants, and odorants.
  • the component (H) is different from the components (A), (B), (C) and (D).
  • Suitable auxiliaries are solvents, liquid carriers, solid carriers or fillers, surfactants, dispersants, emulsifiers, wetters, adjuvants, solubilizers, penetration enhancers, protective colloids, adhesion agents, thickeners, humectants, repellents, attractants, feeding stimulants, compatibilizers, bactericides, anti-freezing agents, anti-foaming agents, colorants, tackifiers and binders.
  • Suitable solvents and liquid carriers are water and organic solvents, such as mineral oil fractions of medium to high boiling point, e.g. kerosene, diesel oil; oils of vegetable or animal origin; aliphatic, cyclic and aromatic hydrocarbons, e. g. toluene, paraffin, tetrahydronaphthalene, al- kylated naphthalenes; alcohols, e.g. ethanol, propanol, butanol, cyclohexanol; glycols; DMSO; ketones, e.g. cyclohexanone; esters, e.g.
  • mineral oil fractions of medium to high boiling point e.g. kerosene, diesel oil
  • oils of vegetable or animal origin oils of vegetable or animal origin
  • aliphatic, cyclic and aromatic hydrocarbons e. g. toluene, paraffin, tetrahydronaphthalene, al- kylated naphthal
  • lactates carbonates, fatty acid esters, gamma- butyrolactone; fatty acids; phosphonates; amines; amides, e.g. N-methylpyrrolidone, fatty acid dimethylamides; and mixtures thereof.
  • Suitable solid carriers or fillers are mineral earths, e.g. silicates, silica gels, talc, kaolins, limestone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium oxide; polysaccharides, e.g. cellulose, starch; fertilizers, e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas; products of vegetable origin, e.g. cereal meal, tree bark meal, wood meal, nutshell meal, and mixtures thereof.
  • Suitable surfactants are surface-active compounds, such as anionic, cationic, nonionic and amphoteric surfactants, block polymers, polyelectrolytes, and mixtures thereof. Such surfactants can be used as emusifier, dispersant, solubilizer, wetter, penetration enhancer, protective colloid, or adjuvant. Examples of surfactants are listed in McCutcheon's, Vol.1 : Emulsifiers & De- tergents, McCutcheon's Directories, Glen Rock, USA, 2008 (International Ed. or North American Ed.).
  • Suitable anionic surfactants are alkali, alkaline earth or ammonium salts of sulfonates, sulfates, phosphates, carboxylates, and mixtures thereof.
  • sulfonates are alkylarylsulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignine sulfonates, sulfonates of fatty acids and oils, sulfonates of ethoxylated alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of condensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenes and alkylnaphthalenes, sulfosuccinates or sulfosuccinamates.
  • Examples of sulfates are sulfates of fatty acids and oils, of ethoxylated alkylphenols, of alcohols, of ethoxylated alcohols, or of fatty acid esters.
  • Examples of phosphates are phosphate esters.
  • Examples of carboxylates are alkyl carboxylates, and carboxylated alcohol or alkylphenol ethoxylates.
  • Suitable nonionic surfactants are alkoxylates, N-subsituted fatty acid amides, amine oxides, esters, sugar-based surfactants, polymeric surfactants, and mixtures thereof.
  • alkoxylates are compounds such as alcohols, alkylphenols, amines, amides, arylphenols, fatty acids or fatty acid esters which have been alkoxylated with 1 to 50 equivalents.
  • Ethylene oxide and/or propylene oxide may be employed for the alkoxylation, preferably ethylene oxide.
  • N-subsititued fatty acid amides are fatty acid glucamides or fatty acid alkanolamides.
  • esters are fatty acid esters, glycerol esters or monoglycerides.
  • sugar- based surfactants are sorbitans, ethoxylated sorbitans, sucrose and glucose esters or al- kylpolyglucosides.
  • polymeric surfactants are home- or copolymers of vinylpyrroli- done, vinylalcohols, or vinylacetate.
  • Suitable cationic surfactants are quaternary surfactants, for example quaternary ammonium compounds with one or two hydrophobic groups, or salts of long-chain primary amines.
  • Suitable amphoteric surfactants are alkylbetains and imidazolines.
  • Suitable block polymers are block polymers of the A-B or A-B-A type comprising blocks of polyethylene oxide and polypropylene oxide, or of the A-B-C type comprising alkanol, polyethylene oxide and polypropylene oxide.
  • Suitable polyelectrolytes are polyacids or polybases. Examples of polyacids are alkali salts of polyacrylic acid or polyacid comb polymers. Examples of polybases are polyvinylamines or pol- yethyleneamines.
  • Suitable adjuvants are compounds, which have a neglectable or even no pesticidal activity themselves, and which improve the biological performance of the compound I on the target.
  • examples are surfactants, mineral or vegetable oils, and other auxilaries. Further examples are listed by Knowles, Adjuvants and additives, Agrow Reports DS256, T&F Informa UK, 2006, chapter 5.
  • Suitable thickeners are polysaccharides (e.g. xanthan gum, carboxymethylcellulose), anorganic clays (organically modified or unmodified), polycarboxylates, and silicates.
  • Suitable bactericides are bronopol and isothiazolinone derivatives such as alkylisothiazolinones and benzisothiazolinones.
  • Suitable anti-freezing agents are ethylene glycol, propylene glycol, urea and glycerin.
  • Suitable anti-foaming agents are silicones, long chain alcohols, and salts of fatty acids.
  • Suitable colorants are pigments of low water solubility and water- soluble dyes. Examples are
  • inorganic colorants such as iron oxide, titan oxide, iron hexacyanoferrate,
  • metal-complex dyes such as chromium-complex dyes, for example Orasol Yellow 141 ,
  • organic colorants such as alizarin-, azo- and phthalocyanine colorants.
  • Preferred colorants are metal-complex dyes, more preferably chromium-complex dyes, for example Orasol Yellow 141.
  • Suitable tackifiers or binders are polyvinylpyrrolidones, polyvinylacetates, polyvinyl alcohols, polyacrylates, biological or synthetic waxes, and cellulose ethers.
  • Suitable preservatives include e.g. sodium benzoate, benzoic acid, sorbic acid, and derivatives thereof.
  • Suitable antioxidants include sulfites, ascorbic acid, tocopherol, tocopherol acetate, tocotrienol, melatonin, carotene, beta-carotene, ubiquinol, and derivatives thereof. Tocophercol acetate is preferred as antioxidant.
  • Suitable odorants include perfume materials which are for example mentioned in US 7 182 537, including allo-ocimene, Allyl cyclohexanepropionate, Allyl heptanoate, trans-Anethole, Benzyl butyrate, Camphene, Cadinene, Carvacrol, cis-3-Hexenyl tiglate, Citronellol, Citronellyl acetate, Citronellyl nitrile, Citronellyl propionate, Cyclohexylethyl acetate, Decyl Aldehyde (Capralde- hyde), Dihydromyrcenol, Dihydromyrcenyl acetate, 3,7-Dimethyl-1-octanol, Diphenyloxide, Fen- chyl Acetate (1 ,3,3-Trimethyl-2-norbornanyl acetate), Geranyl acetate, Geranyl formate, Gera- nyl n
  • compositions (Q1), (Q2), or (Q3) such as parts of a kit or parts of a binary or ternary mixture may be mixed by the user himself in a spray tank and further auxiliaries may be added, if appropriate.
  • the component (H) can be contained in varying amounts in the composition (Q1 ), (Q2), or (Q3). If present, the amount of (H) is preferably not more than 10 wt.%, more preferably not more than 4 wt.%, most preferably not more than 2 wt.%, particularly not more than 1 wt.%, for example not more than 0.5 wt.%, based on the total weight of the corresponding composition (Q1 ), (Q2), or (Q3).
  • the amount of (H) is preferably at least 0.0005 wt.%, more preferably at least 0.005 wt.%, most preferably at least 0.025 wt.%, particularly at least 0.1 wt.%, for example at least 0.4 wt.%, based on the total weight of the corresponding composition (Q1 ), (Q2), or (Q3).
  • the weight ratio of the mixture (A) to the aromatic alcohol (B) - in case of (Q2) or (Q3) only as far as (B) is present - is preferably between 50:1 and 1 :50, more preferably between 10:1 and 1 :10, most preferably between 5:1 and 1 :5, particularly preferably between 3:1 and 1 :3, particularly most preferably between 2:1 and 1 :2, particularly between 1 :1 and 1 :2, for example between 1 :1.5 to 1 :1.8.
  • the weight ratio of the mixture (A) to the amine (C) - in case of (Q1 ) or (Q3) only as far as (C) is present - is preferably between 100:1 and 1 :20, more preferably between 40:1 and 1 :8, most preferably between 30:1 and 1 :6, particularly preferably between 20:1 and 1 :5, particularly most preferably between 10:1 and 1 :2, particularly between 5:1 and 1 :1.2, for example between 2:1 to 1 :1.
  • the weight ratio of the mixture (A) to the amide (D) - in case of (Q1 ) or (Q2) only as far as (D) is present - is preferably between 50:1 and 1 :50, more preferably between 10:1 and 1 :10, most preferably between 5:1 and 1 :5, particularly preferably between 3:1 and 1 :3, particularly most preferably between 2.5:1 and 1 :2, particularly between 2:1 and 1 :1 , for example between 1.8:1 to 1.2:1.
  • compositions (Q1 ), (Q2), or (Q3) were found.
  • said process comprises: applying the compositions (Q1 ), (Q2), or (Q3) by spraying it onto the soil. More preferably, said process are conducted in a way wherein the compositions (Q1 ), (Q2), or (Q3) are - either at the same time (i.e. simultaneously) or with a time difference (i.e. separately) - applied together with at least one nitrogen-containing fertilizer (F) into the soil in-furrow and/or as side-dress and/or as broadcast.
  • the compositions (Q1 ), (Q2), or (Q3) can be used as additive or as coating material for nitrogen-containing fertilizers (F), particularly for urea-containing fertilizer (F1 ), for example for urea.
  • compositions (Q1 ), (Q2), or (Q3) are used as coating material for nitrogen-containing fertilizers (F), particularly for urea-containing fertilizer (F1 ), for example for urea.
  • the nitrogen-containing fertilizer (F) cam be in crystalline, granulated, compacted, prilled or ground form, and is preferably in granulated from.
  • compositions (Q1 ), (Q2), or (Q3) can be applied to or on nitrogen-containing fertilizers (F) by either mixing the (Q1 ), (Q2), or (Q3), in either liquid or solid form, with the nitrogen-containing fertilizer (F), or incorporating them into (F) by granulation, compacting or prilling, by addition to a corresponding fertilizer mixture or to a mash or melt.
  • the compositions (Q1 ), (Q2), or (Q3) are applied to the surface of existing granules, compacts or prills of the nitrogen-containing fertilizer (F) - particularly of the urea-containing fertilizer (F1) - by means of spraying, powder application or impregnating, for example.
  • compositions (Q1 ), (Q2), or (Q3) are used in the context of fertilization with nitrogen-containing fertilizer (F), particularly with urea-containing fertilizer (F1 ). Application takes place preferably to an agriculturally or horticulturally exploited plot.
  • compositions (Q1 ), (Q2), or (Q3) In parallel with the improvement of the utilization of nitrogen in the urea-containing, mineral and organic fertilizers, the use of the compositions (Q1 ), (Q2), or (Q3) has the effect that there is an Increase - in some cases considerably - in the yields or production of biomass of crop plants.
  • compositions (Q1), (Q2), or (Q3) may be added to organic fertilizers, such as liquid manure, for example, during the actual storage of such fertilizers, in order thus to prevent nitrogen nutri- ent losses, by virtue of decelerated conversion of the individual forms of nitrogen into gaseous nitrogen compounds, which are therefore volatile, and in order as a result, at the same time, to contribute to a lowering of the ammonia load in animal stables.
  • compositions (Q1 ), (Q2), (Q3) are incorporated, by melting, for example, into the nitrogen-containing fertilizer (F), or else are applied to the fertilizer surface or applied separately from the spreading of the fertilizer, in the form, for example, of a (suspension) concentrate, a solution or a formulation.
  • ad100 the percent by weight of this component is 100% minus the sum of the weight percentages (in percent by weight) of all other components comprised in the composition
  • Coat. coated on urea (all the data in the rows below the "coated row” are experimental data after the composition has been coated on urea)
  • DEI Bis(hydroxyethyl)-isopropanolamine (DEI PA)
  • dev. deviation, as an indicator for the stability after coated on urea, calculated as difference between the NxPT content in the heat stability test and the content in the cold stability test - both after coated on urea -, indicated as percent
  • LFG polyethyleneimine with a weight average molecular weight of 800 g/mol as measured by GPC (dry substance, at pH 4.5)
  • LGA polyethyleneimine with a weight average molecular weight of 1300 g/mol as measured by GPC (dry substance, at pH 4.5)
  • LPN N,N',N"-tris(dimethylaminopropyl)hexahydrotriazine
  • LT technical mixture (with a 84.27% concentration of NxPT based on the total amount of the technical mixture) containing 23.7% NPPT and 76.3% NBPT, based on the total amount of NxPT within the technical mixture
  • HCM Mixture of N,N-Dimethyloctanamide (50-65%) and N,N-Dimethyldecanamide (37 -50%)
  • MDA Methyldiethanolamine
  • NB/c Content (percent by weight) of NBPT in cold stability test (2 weeks at 5°C)
  • NP/c Content (percent by weight) of NPPT in cold stability test (2 weeks at 5°C)
  • Nx/c Content (Percent by weight) of NxPT in cold stability test (2 weeks at 5°C)
  • NB/h Content (Percent by weight) of NBPT in heat stability test (2 weeks at 54°C)
  • NP/h Content (Percent by weight) of NPPT in heat stability test (2 weeks at 54°C)
  • Nx/h Content (Percent by weight) of NxPT in heat stability test (2 weeks at 54°C)
  • NB/a Content (Percent by weight) of NBPT in cold stability test (2 weeks at 5°C) after coated on urea
  • NP/a Content (Percent by weight) of NPPT in cold stability test (2 weeks at 5°C) after coated on urea
  • Nx/a Content (Percent by weight) of NxPT in cold stability test (2 weeks at 5°C) after coated on urea
  • NB/b Percent by weight of NBPT in heat stability test (4 weeks at 40°C and 50% air humidity) after coated on urea
  • NP/b Percent by weight of NPPT in heat stability test (4 weeks at 40°C and 50% air humidity) after coated on urea
  • Nx/b Percent by weight of NxPT in heat stability test (4 weeks at 40°C and 50% air humidity) after coated on urea
  • NxPT Mixture (A) comprising NBPT and NPPT (the content of NxPT is the sum of the content of NBPT and NPPT)
  • NyPT Mixture (A) comprising NBPT and/or NPPT
  • NMM N-methyl-morpholine
  • NMP N-methyl-pyrrolidinone
  • PEI polyethyleneimine
  • stabi. storage stability of NxPT, calculated as difference between the NxPT content in the heat stability test and the content in the cold stability test, indicated as percent
  • TPA tocopherol acetate
  • compositions as listed in Table 1 are preferred embodiments of the present invention.
  • (C1 ) is a polymeric polyamine
  • (C2) is an amine containing not more than one amino group and at least three alkoxy- or hydroxy-substituted C2 to C12 alkyl groups R 21 , wherein at least one of the groups R 21 is different to the other groups R 21 ;
  • (C3) is an amine containing not more than one amino group and at least two alkoxy- or hydroxy- substituted C2 to C12 alkyl groups R 22 , wherein at least one of the groups R 22 bears the alkoxy or hydroxy substituent at a secondary or tertiary carbon atom and wherein at least one of the groups R 22 is different to the other group(s) R 22 ;
  • (C4) is an amine containing at least one saturated or unsaturated Ce to C40 alkyl group R 23
  • (C5) is a saturated or unsaturated heterocyclic amine which contains at least one oxygen atom as ring atom and which does not contain a further alkoxy group.
  • R 31 CO is a hydroxysubstituted acyl radical having 1 to 22 carbon atoms
  • R 32 is H or Ci to C 4 alkyl
  • R 33 is H or Ci to C 4 alkyl.
  • R 31 CO is a is an acyl radical having 1 to 22 carbon atoms which do not contain a hydroxyl group
  • R 32 is H or Ci to C 4 alkyl
  • R 33 is H or Ci to C 4 alkyl.
  • R 31 CO is an acyl radical having 1 to 22 carbon atoms
  • R 32 and R 33 together with the nitrogen atom linking them define a 6-membered saturated heterocyclic radical which comprises one further oxygen heteroatom.
  • (D4) is an amide according to the general formula (III)
  • R 31 CO is an acyl radical having 1 to 22 carbon atoms
  • R 32 and R 33 together with the nitrogen atom linking them define a 5-membered saturated heterocyclic radical which comprises one further nitrogen heteroa- tom.
  • R 31 CO is an acyl radical having 1 to 22 carbon atoms
  • R 32 is an acyloxy substituted alkyl group
  • R 33 is H or alkyl.
  • the advantages of the invention are that the enhancement of the stability of the (thio)phosphoric acid triamide(s) - particularly when applied to or coated on nitrogen-containing fertilizers such as urea - and a relatively long storage life - particularly before being applied to or coated on nitrogen-containing fertilizers - was achieved with the compositions (Q1 ), (Q2), (Q3). Moreover, the compositions (Q1 ), (Q2), (Q3) do not adversely affect the urease-inhibiting effect and/or activity of the (thio)phosphoric acid triamide. Last, but not least, the compositions (Q1 ), (Q2), (Q3) can be easily and safely packaged, transported and shipped, even in large quantities, and can be easily and safely handled and applied for soil treatment, even in large quantities
  • the technical mixture LT (25% pure NxPT) was mixed with 50.08% benzyl alcohole and 10% LFG,10% DML and 0.25% colo. The mixture was stirred until complete dissolution of the solid and analyzed for NxPT content (by HPLC), viscosity, dissolution (2%) in water and pH.
  • the mixture of each example (e.g. Ex.#310092) was stored in closed bottles for 14 days at 54°C (referred to as heat stability test in the following) and then analyzed for the content of NxPT.
  • the mixture of each example (e.g. Ex.#310092) was also stored in closed bottles for 14 days at 5°C (referred to as cold stability test in the following) and then analyzed for the content of NxPT.
  • the storage stability in % was calculated as difference between the content in the heat stability test and the content in the cold stability test.
  • the coated urea sample of 300 g was stored in a petri dish for 4 weeks at 50% humidity in a climate chamber.
  • the sample was homogenized and analyzed for the content of NBPT, NPPT, NxPT (by HPLC)
  • NxPT measured by HPLC measurement
  • Viscosity was measured at the undiluted formulation with a cone-plate rheometer A 2000ex (TA Instruments) at shear rate of 100s "1 and 20°C.
  • the pH value was measured at 2% concentration in CIPAC water D. All examples of the inventions are liquid, clear compositions which are either colourless or yellow.
  • Table 2 Examples of the compositions of the invention and of comparative compositions, and data on their viscosity, pH value, storage stability and stability after coated on urea Table 2 - part 1 of 1 1
  • NMP (at least in amounts as applied in Ex# 310043) is toxicologically objectionable.

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Soil Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

L'invention porte sur une composition comprenant : (A) un mélange comprenant au moins un triamide d'acide (thio)phosphorique de formule générale (I) : R1R2N–P(X)(NH2)2, dans laquelle X est un atome d'oxygène ou de soufre ; R1 est un alkyle en C1 à C20, un cycloaklyle en C3 à C20, un aryle en C6 à C20, ou un groupe dialkylaminocarbonyle ; R2 est un atome d'hydrogène, ou R1 et R2 définissent ensemble, avec l'atome d'azote qui les relie, un radical hétérocylique saturé ou insaturé à 5 ou 6 membres, lequel comprend éventuellement 2 autres hétéroatomes choisis dans le groupe constitué de l'azote, de l'oxygène et du soufre, et (C) au moins une amine choisie dans le groupe constitué de (C1) une polyamine polymère et (C2) une amine ne contenant pas plus d'un groupe amino et au moins trois groupes alkyle R21 en C2 à C12 à substitution alkoxy ou hydroxy, l'un au moins des groupes R21 étant différent des autres groupes R21, (C3) une amine ne contenant pas plus d'un groupe amino et au moins deux groupes alkyle R22 en C2 à C12 à substitution alkoxy ou hydroxy, l'un au moins des groupes R22 portant le substituant alkoxy ou hydroxy au niveau d'un atome de carbone secondaire ou tertiaire et l'un au moins des groupes R22 étant différent du ou des autres groupes R22, (C4) une amine contenant au moins un groupe alkyle R23 saturé ou insaturé en C8 à C40, et (C5) une amine hétérocyclique saturée ou insaturée contenant au moins un atome d'oxygène comme atome de cycle et qui ne contient pas d'autre groupe alkoxy.
PCT/IB2013/055484 2013-07-04 2013-07-04 Compositions comprenant du triamide d'acide (thio)phosphorique et d'autres composés, présentant un effet amélioré d'inhibition de l'uréase Ceased WO2015001391A1 (fr)

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PCT/IB2013/055484 WO2015001391A1 (fr) 2013-07-04 2013-07-04 Compositions comprenant du triamide d'acide (thio)phosphorique et d'autres composés, présentant un effet amélioré d'inhibition de l'uréase
RU2018119775A RU2018119775A (ru) 2013-07-04 2014-06-27 Композиции с улучшенным ингибирующим уреазу действием, содержащие триамид (тио)фосфорной кислоты и другие соединения
ES14819297T ES2741280T3 (es) 2013-07-04 2014-06-27 Composiciones con efecto mejorado de inhibición de ureasa que comprenden triamida de ácido (tio)fosfórico y compuestos adicionales
JP2016522940A JP6576917B2 (ja) 2013-07-04 2014-06-27 （チオ）リン酸トリアミド及びさらなる化合物を含む、改善されたウレアーゼ阻害効果を有する組成物
MX2015017715A MX2015017715A (es) 2013-07-04 2014-06-27 Composiciones con efecto inhibidor de ureasa mejorado que comprende triamida de acido (tio)fosforico y compuestos adicionales.
EP14819297.4A EP3016921B1 (fr) 2013-07-04 2014-06-27 Compositions présentant un effet d'inhibition de l'uréase amélioré comprenant du triamide d'acide (thio)phosphorique et autres composés
CN201480048545.8A CN105517977B (zh) 2013-07-04 2014-06-27 包含(硫代)磷酸三酰胺和其它化合物的具有改进脲酶抑制效应的组合物
PCT/IB2014/062667 WO2015001457A2 (fr) 2013-07-04 2014-06-27 Compositions présentant un effet d'inhibition de l'uréase amélioré comprenant du triamide d'acide (thio)phosphorique et autres composés
PL14819297T PL3016921T3 (pl) 2013-07-04 2014-06-27 Kompozycje o poprawionym działaniu hamującym ureazę zawierające triamid kwasu (tio)fosforowego i dodatkowe związki
NZ715778A NZ715778B2 (en) 2013-07-04 2014-06-27 Compositions with improved urease-inhibiting effect comprising (thio)phosphoric acid triamide and further compounds
RU2016103491A RU2656416C2 (ru) 2013-07-04 2014-06-27 Композиции с улучшенным ингибирующим уреазу действием, содержащие триамид (тио)фосфорной кислоты и другие соединения
US14/902,181 US10150712B2 (en) 2013-07-04 2014-06-27 Compositions with improved urease-inhibiting effect comprising (thio)phosphoric acid triamide and further compounds
BR112015032664-1A BR112015032664B1 (pt) 2013-07-04 2014-06-27 Composições com efeito aprimorado de inibição da urease compreendendo triamida de ácido (tio)fosfórico e compostos adicionais
AU2014285758A AU2014285758B2 (en) 2013-07-04 2014-06-27 Compositions with improved urease-inhibiting effect comprising (thio)phosphoric acid triamide and further compounds
CA2916529A CA2916529C (fr) 2013-07-04 2014-06-27 Compositions presentant un effet d'inhibition de l'urease ameliore comprenant du triamide d'acide (thio)phosphorique et autres composes
TR2019/10755T TR201910755T4 (tr) 2013-07-04 2014-06-27 (Tiyo)fosforik asit triamit ve ilave bileşikler içeren geliştirilmiş üreaz inhibe edici etkiye sahip olan bileşimler.
UAA201600784A UA116147C2 (uk) 2013-07-04 2014-06-27 Композиції з покращеною інгібувальною уреазу дією, що містять триамід (тіо)фосфорної кислоти й інші сполуки
ARP140102486A AR097136A1 (es) 2013-07-04 2014-07-03 Composiciones con efecto inhibidor de la ureasa mejorado que comprenden triamida del ácido (tio)fosfórico y otros compuestos
UY0001035645A UY35645A (es) 2013-07-04 2014-07-04 Composiciones con efecto inhibidor de la ureasa mejorado que comprenden triamida del ácido (tio)fosfórico y otros compuestos
SA516370350A SA516370350B1 (ar) 2013-07-04 2016-01-04 تركيبات ذات تأثير تثبيط-إنزيم يورياز محسن تشتمل على تراي أميد حمض (ثيو)فوسفوريك ومركبات إضافية
ZA2016/00606A ZA201600606B (en) 2013-07-04 2016-01-28 Compositions with improved urease-inhibiting effect comprising (thio)phosphoric acid triamide and further compounds
US16/197,665 US20190084898A1 (en) 2013-07-04 2018-11-21 Compositions with improved urease-inhibiting effect comprising (thio)phosphoric acid triamide and further compounds

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US14/902,181 Continuation US10150712B2 (en) 2013-07-04 2014-06-27 Compositions with improved urease-inhibiting effect comprising (thio)phosphoric acid triamide and further compounds

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WO2016103168A1 (fr) * 2014-12-23 2016-06-30 Basf Se Compositions présentant un effet d'inhibition de l'uréase amélioré comprenant du triamide d'acide (thio)phosphorique et autres composés tels que amines et colorants
WO2016186526A1 (fr) * 2015-05-20 2016-11-24 Ballance Agri-Nutrients Limited Composition d'engrais
WO2017100507A1 (fr) * 2015-12-11 2017-06-15 Koch Agromonic Services, Llc Compositions fertilisantes contenant un inhibiteur d'uréase résistant aux acides
US9834487B2 (en) 2015-07-13 2017-12-05 Koch Agronomic Services, Llc Highly concentrated phosphoric or thiophosphoric triamide formulation
KR20180002064A (ko) * 2016-06-28 2018-01-05 (주)엠포러스 사용자 및 환경 정보 기반의 음량 최적화 장치 및 방법
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US10954256B2 (en) 2015-10-01 2021-03-23 Basf Se Process for recovering a mixture comprising a (thio)phosphoric acid derivative
US20210101846A1 (en) * 2019-10-04 2021-04-08 Milliken & Company Horticulture Additive
US20220098125A1 (en) * 2018-11-20 2022-03-31 Sabic Global Technologies B.V. Coated fertilizer containing urease inhibitor
US11999662B2 (en) 2017-05-17 2024-06-04 SABIC Agri-Nutrients Company Anti-caking fertilizer compositions
US12281052B2 (en) 2018-12-11 2025-04-22 SABIC Agri-Nutrients Company Acidified NP, PK, NPK fertilizer granules for fertigation

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Cited By (19)

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RU2759183C1 (ru) * 2014-12-23 2021-11-10 Басф Се Композиции с улучшенным эффектом ингибирования уреазы, которые содержат триамид (тио)фосфорной кислоты и дополнительные соединения, такие как амины и красители
WO2016103168A1 (fr) * 2014-12-23 2016-06-30 Basf Se Compositions présentant un effet d'inhibition de l'uréase amélioré comprenant du triamide d'acide (thio)phosphorique et autres composés tels que amines et colorants
US10577290B2 (en) 2014-12-23 2020-03-03 Basf Se Compositions with improved urease-inhibiting effect comprising (thio)phosphoric acid triamide and further compounds such as amines and colorants
AU2015370455B2 (en) * 2014-12-23 2020-03-26 Basf Se Compositions with improved urease-inhibiting effect comprising (thio) phosphoric acid triamide and further compounds such as amines and colorants
US11384033B2 (en) 2014-12-23 2022-07-12 Basf Se Compositions with improved urease-inhibiting effect comprising (thio)phosphoric acid triamide and further compounds such as amines and colorants
WO2016186526A1 (fr) * 2015-05-20 2016-11-24 Ballance Agri-Nutrients Limited Composition d'engrais
US9834487B2 (en) 2015-07-13 2017-12-05 Koch Agronomic Services, Llc Highly concentrated phosphoric or thiophosphoric triamide formulation
US10487019B2 (en) 2015-07-13 2019-11-26 Koch Agronomic Services, Llc Highly concentrated phosphoric or thiophosphoric triamide formulation
EP3356375B1 (fr) * 2015-10-01 2023-01-04 Basf Se Procédé de récupération d'un mélange comprenant un dérivé d'acide (thio)phosphorique
US10954256B2 (en) 2015-10-01 2021-03-23 Basf Se Process for recovering a mixture comprising a (thio)phosphoric acid derivative
WO2017100507A1 (fr) * 2015-12-11 2017-06-15 Koch Agromonic Services, Llc Compositions fertilisantes contenant un inhibiteur d'uréase résistant aux acides
KR20180002064A (ko) * 2016-06-28 2018-01-05 (주)엠포러스 사용자 및 환경 정보 기반의 음량 최적화 장치 및 방법
WO2018116046A1 (fr) * 2016-12-22 2018-06-28 Basf Se Mélange d'inhibiteurs d'uréase de type triamide d'acide (thio)phosphorique substitué par aryle avec des engrais à base d'urée contenant du phosphore
US11999662B2 (en) 2017-05-17 2024-06-04 SABIC Agri-Nutrients Company Anti-caking fertilizer compositions
US20220098125A1 (en) * 2018-11-20 2022-03-31 Sabic Global Technologies B.V. Coated fertilizer containing urease inhibitor
US12110258B2 (en) * 2018-11-20 2024-10-08 SABIC Agri-Nutrients Company Coated fertilizer containing urease inhibitor
US12281052B2 (en) 2018-12-11 2025-04-22 SABIC Agri-Nutrients Company Acidified NP, PK, NPK fertilizer granules for fertigation
US20210101846A1 (en) * 2019-10-04 2021-04-08 Milliken & Company Horticulture Additive
US11891346B2 (en) * 2019-10-04 2024-02-06 Milliken & Company Horticulture additive

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