FR2648674A1 - PROCESS FOR INHIBITING GERMINATION OF POTATOES - Google Patents
PROCESS FOR INHIBITING GERMINATION OF POTATOES Download PDFInfo
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- FR2648674A1 FR2648674A1 FR9008301A FR9008301A FR2648674A1 FR 2648674 A1 FR2648674 A1 FR 2648674A1 FR 9008301 A FR9008301 A FR 9008301A FR 9008301 A FR9008301 A FR 9008301A FR 2648674 A1 FR2648674 A1 FR 2648674A1
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- Prior art keywords
- carbetamide
- potatoes
- germination
- amount
- inhibiting
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- 244000061456 Solanum tuberosum Species 0.000 title claims abstract description 29
- 235000002595 Solanum tuberosum Nutrition 0.000 title claims abstract description 29
- 230000035784 germination Effects 0.000 title claims abstract description 27
- 235000012015 potatoes Nutrition 0.000 title claims abstract description 25
- 238000000034 method Methods 0.000 title claims description 17
- 230000002401 inhibitory effect Effects 0.000 title claims description 5
- 230000008569 process Effects 0.000 title description 4
- 239000005490 Carbetamide Substances 0.000 claims abstract description 49
- AMRQXHFXNZFDCH-SECBINFHSA-N [(2r)-1-(ethylamino)-1-oxopropan-2-yl] n-phenylcarbamate Chemical compound CCNC(=O)[C@@H](C)OC(=O)NC1=CC=CC=C1 AMRQXHFXNZFDCH-SECBINFHSA-N 0.000 claims abstract description 49
- 238000003860 storage Methods 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 239000006185 dispersion Substances 0.000 claims description 6
- 238000005507 spraying Methods 0.000 claims description 3
- 239000007900 aqueous suspension Substances 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 238000011282 treatment Methods 0.000 description 10
- 230000005764 inhibitory process Effects 0.000 description 9
- 239000000843 powder Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000003112 inhibitor Substances 0.000 description 5
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 239000000417 fungicide Substances 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000010410 dusting Methods 0.000 description 3
- 239000002917 insecticide Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 3
- 230000004580 weight loss Effects 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 244000061176 Nicotiana tabacum Species 0.000 description 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 230000000622 irritating effect Effects 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- PWHWWMHNXSWQLD-SCSAIBSYSA-N (2r)-n-ethyl-2-hydroxypropanamide Chemical compound CCNC(=O)[C@@H](C)O PWHWWMHNXSWQLD-SCSAIBSYSA-N 0.000 description 1
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 1
- MQAISPIJGUNNSJ-UHFFFAOYSA-N 2-[(3-amino-3-oxopropyl)amino]ethylsulfanylphosphonic acid Chemical compound NC(=O)CCNCCSP(O)(O)=O MQAISPIJGUNNSJ-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000005795 Imazalil Substances 0.000 description 1
- 239000005867 Iprodione Substances 0.000 description 1
- 244000081841 Malus domestica Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 230000028446 budding cell bud growth Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 230000007665 chronic toxicity Effects 0.000 description 1
- 231100000160 chronic toxicity Toxicity 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000012864 cross contamination Methods 0.000 description 1
- 150000003997 cyclic ketones Chemical class 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 229940075894 denatured ethanol Drugs 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229960002125 enilconazole Drugs 0.000 description 1
- IIVSHOZBTQJMPI-UHFFFAOYSA-N ethylcarbamoyl N-ethylcarbamate Chemical compound CCNC(=O)OC(=O)NCC IIVSHOZBTQJMPI-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 230000000442 meristematic effect Effects 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- -1 nonylphenyl Chemical group 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/20—N-Aryl derivatives thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23B—PRESERVATION OF FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES; CHEMICAL RIPENING OF FRUIT OR VEGETABLES
- A23B2/00—Preservation of foods or foodstuffs, in general
- A23B2/70—Preservation of foods or foodstuffs, in general by treatment with chemicals
- A23B2/725—Preservation of foods or foodstuffs, in general by treatment with chemicals in the form of liquids or solids
- A23B2/729—Organic compounds; Microorganisms; Enzymes
- A23B2/742—Organic compounds containing oxygen
- A23B2/75—Organic compounds containing oxygen with doubly-bound oxygen
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23B—PRESERVATION OF FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES; CHEMICAL RIPENING OF FRUIT OR VEGETABLES
- A23B2/00—Preservation of foods or foodstuffs, in general
- A23B2/70—Preservation of foods or foodstuffs, in general by treatment with chemicals
- A23B2/725—Preservation of foods or foodstuffs, in general by treatment with chemicals in the form of liquids or solids
- A23B2/729—Organic compounds; Microorganisms; Enzymes
- A23B2/762—Organic compounds containing nitrogen
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23B—PRESERVATION OF FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES; CHEMICAL RIPENING OF FRUIT OR VEGETABLES
- A23B7/00—Preservation of fruit or vegetables; Chemical ripening of fruit or vegetables
- A23B7/14—Preserving or ripening with chemicals not covered by group A23B7/08 or A23B7/10
- A23B7/153—Preserving or ripening with chemicals not covered by group A23B7/08 or A23B7/10 in the form of liquids or solids
- A23B7/154—Organic compounds; Microorganisms; Enzymes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23B—PRESERVATION OF FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES; CHEMICAL RIPENING OF FRUIT OR VEGETABLES
- A23B7/00—Preservation of fruit or vegetables; Chemical ripening of fruit or vegetables
- A23B7/16—Coating with a protective layer; Compositions or apparatus therefor
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Microbiology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines Containing Plant Substances (AREA)
- Supports For Plants (AREA)
- Storage Of Harvested Produce (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Abstract
La présente invention concerne l'utilisation de carbétamide pour inhiber la germination des pommes de terre, par exemple pendant l'entreposage.The present invention relates to the use of carbetamide to inhibit the germination of potatoes, for example during storage.
Description
La présente invention a pour objet la limita-The object of the present invention is the limitation
tion et l'inhibition de la germination des pommes de terre et, plus précisément, l'inhibition chimique de cette tion and inhibition of the germination of potatoes and, more specifically, the chemical inhibition of this
germination par application de carbétamide. germination by application of carbetamide.
Le carbétamide est le composé de formule: Carbetamide is the compound of formula:
C6H5-NH-COO-CH(CH3)-CO-NH-C2H5C6H5-NH-COO-CH (CH3) -CO-NH-C2H5
Il est par ailleurs connu sous le nom de It is also known as
phénylcarbamate de D-N-éthyl-lactamide ou de N-phényl-l- D-N-ethyl-lactamide or N-phenyl-1- phenylcarbamate
(éthylcarbamoyl)éthylcarbamate (isomère D). (ethylcarbamoyl) ethylcarbamate (D isomer).
0 Les pommes de terre (Solanum tuberosum) peuvent être soumises à des périodes prolongées d'entreposage entre la récolte et la consommation. Pendant ces périodes, la culture récoltée tend à germer. Cette germination a pour résultat un certain pourrissement, qu'il est souhaitable d'éviter. On connaît un certain nombre d'agents chimiques 0 Potatoes (Solanum tuberosum) may be subjected to extended storage periods between harvest and consumption. During these periods, the harvested crop tends to germinate. This germination results in a certain rotting, which it is desirable to avoid. A number of chemical agents are known
qui inhibent cette germination (par exemple le chlorpropha- which inhibit this germination (e.g. chlorpropha-
me, le prophame, le tecnazène>, mais tous ces agents présentent divers inconvénients. Il a été trouvé à présent que le carbétamide est un inhibiteur efficace de la germination, qui réduit en outre la perte d'humidité et maintient la turgescence et possède plusieurs avantages par me, prophame, tecnazène>, but all these agents have various drawbacks. Carbetamide has now been found to be an effective inhibitor of germination, which further reduces moisture loss and maintains turgor and has several advantages by
rapport aux substances actuellement utilisées. in relation to the substances currently used.
Outre l'inhibition de la germination pendant l'entreposage, il a été trouvé également que le carbétamide peut être utilisé pour retarder la germination de ces pommes de terre avant plantation, une libération ayant lieu In addition to inhibiting germination during storage, it has also been found that carbetamide can be used to delay the germination of these potatoes before planting, with release taking place
une fois la plantation effectuée.after planting.
Inhibition de la germination signifie une réduction du nombre de germes par tubercule et/ou une réduction de la longueur moyenne des germes. En conséquence, la présente invention propose un procédé pour inhiber la germination des pommes de terre qui consiste à appliquer à ces pommes de terre une quantité de carbétamide suffisante pour inhiber la germination de Inhibition of germination means a reduction in the number of sprouts per tuber and / or a reduction in the average length of the sprouts. Consequently, the present invention provides a method for inhibiting the germination of potatoes which consists in applying to these potatoes a quantity of carbetamide sufficient to inhibit the germination of
ces pommes de terre.these potatoes.
Le carbétamide peut être appliqué, par exemple, avant ou pendant l'entreposage pour inhiber la germination des pommes de terre entreposées. Lè carbétamide est de préférence appliqué au moment de, ou après, la période usuelle de conservation, après arrachage de la culture et avant entreposage. De préférence, les tubercules ne doivent pas être lavés avant traitement (bien qu'un lavage dans de l'eau à des températures soigneusement ajustées soit réalisable). 24 Le carbétamide est un herbicide sélectif connu qui a été largement utilisé dans la culture du fourrage, des crucifères potagères ou cultivées pour leurs graines, des légumes et pour d'autres cultures très diverses. Il est également utilisé pour lutter contre les mauvaises herbes Carbetamide can be applied, for example, before or during storage to inhibit the germination of stored potatoes. Carbetamide is preferably applied at the time of, or after, the usual storage period, after lifting the crop and before storage. Preferably, the tubers should not be washed before treatment (although washing in water at carefully adjusted temperatures is achievable). 24 Carbetamide is a known selective herbicide which has been widely used in the cultivation of fodder, cruciferous vegetables or cultivated for their seeds, vegetables and other very diverse crops. It is also used to control weeds
dans les jachères, les vergers, les vignes et les pépiniè- in fallows, orchards, vineyards and nurseries
res. Le carbétamide présente également une activité régulatrice de croissance des plantes et peut être utilisé comme un inhibiteur efficace des gourmands chez les plants de tabac o il bloque ou inhibe la croissance des bourgeons res. Carbetamide also has plant growth regulating activity and can be used as an effective greedy inhibitor in tobacco plants where it blocks or inhibits bud growth
axillaires par modification de l'activité méristématique. axillary by modification of meristematic activity.
Cependant, le mode d'action de la présente invention est différent, la totalité de la germination étant inhibée dans une culture déjà récoltée tandis que, chez le tabac, l'action principale est l'inhibition sélective de la croissance de bourgeons particuliers (c'est-a-dire non However, the mode of action of the present invention is different, all germination being inhibited in an already harvested crop while, in tobacco, the main action is the selective inhibition of the growth of particular buds (c is to say no
terminaux) chez la plante en cours de croissance. terminals) in the growing plant.
Le procédé de la présente invention pour le traitement des pommes de terre peut utiliser n'importe laquelle des compositions connues de carbétamide. Des compositions convenables pour l'utilisation dans le procédé de la présente invention comprennent du carbétamide en association avec un diluant ou support. Ces compositions peuvent être préparées sous forme, par exemple, de poudres mouillables, de poudres pour poudrage, de solutions, de concentrés émulsionnables, d'émulsions, de concentrés de suspensions et d'aérosols, et comprennent généralement 1 à % en poids de substance active; les autres ingrédients qui peuvent être présents comprennent des surfactants et d'autres adjuvants acceptables tels que des absorbants, des liants, des agents de pénétration, des stabilisants et d'autres matières actives, par exemple des fongicides et des insecticides. Le terme "support" désigne une matière organique ou inorganique, naturelle ou synthétique, à 24 laquelle le carbétamide est mélange afin de faciliter son application, son transport, sa manipulation ou son adhérence à la pomme de terre. Le support peut être solide The process of the present invention for the treatment of potatoes can use any of the known compositions of carbetamide. Compositions suitable for use in the process of the present invention include carbetamide in combination with a diluent or carrier. These compositions can be prepared in the form, for example, of wettable powders, dusting powders, solutions, emulsifiable concentrates, emulsions, suspension concentrates and aerosols, and generally comprise 1 to% by weight of substance active; other ingredients which may be present include surfactants and other acceptable adjuvants such as absorbents, binders, penetrating agents, stabilizers and other active ingredients, for example fungicides and insecticides. The term "support" denotes an organic or inorganic, natural or synthetic material, to which the carbetamide is mixed in order to facilitate its application, its transport, its handling or its adhesion to the potato. Support can be solid
(par exemple une argile ou un silicate naturel ou synthéti- (for example a natural or synthetic clay or silicate
que) ou fluide (par exemple l'eau ou des solvants organi- ) or fluid (e.g. water or organic solvents
ques, comprenant des cétones telles que l'acétone, l'acétophénone, et des cétones cycliques telles que la cyclohexanone; le diméthylformamide; des alcanols inférieurs tels que le méthanol ou l'éthanol dénaturé; des hydrocarbures chlorés, tels que le chlorure de méthylène; des solvants aromatiques, tels que le toluène et le xylène; et des fractions de pétrole). Les supports solides préférés sont solubles dans l'eau et de qualité alimentaire comme par exemple l'alcool polyvinylique (APV) ques, comprising ketones such as acetone, acetophenone, and cyclic ketones such as cyclohexanone; dimethylformamide; lower alkanols such as methanol or denatured ethanol; chlorinated hydrocarbons, such as methylene chloride; aromatic solvents, such as toluene and xylene; and petroleum fractions). The preferred solid supports are soluble in water and of food grade such as for example polyvinyl alcohol (PVA)
et des produits à base de sucre.and sugar products.
Le surfactant peut être un agent émulsionnant, dispersant ou mouillant et peut être ionique ou non ionique. Des émulsionnants convenables comprennent les The surfactant can be an emulsifying, dispersing or wetting agent and can be ionic or non-ionic. Suitable emulsifiers include
matières cationiques, anioniques, non ioniques ou zwit- cationic, anionic, nonionic or zwit-
terioniques couramment utilisées telles que, par exemple, commonly used terionics such as, for example,
les sels d'acides polyacryliques, d'acides lignosulfoni- the salts of polyacrylic acids, of lignosulfonic acids
ques, et les produits de condensation de l'oxyde d'éthylène ques, and the condensation products of ethylene oxide
avec des alcools, des acides et des amines gras. with fatty alcohols, acids and amines.
D'autres adjuvants qui peuvent être incorporés à la composition pour une application simultanée sont des fongicides et des insecticides. Des exemples de fongicides qui peuvent être appliqués avec le carbétamide sont Other adjuvants which can be incorporated into the composition for simultaneous application are fungicides and insecticides. Examples of fungicides that can be applied with carbetamide are
l'imazalil et l'iprodione.imazalil and iprodione.
Il est préféré d'appliquer le carbétamide sous forme d'une dispersion dans ou sur des milieux liquides ou solides, classiquement à des concentrations de 0,01% à 80%, It is preferred to apply the carbetamide in the form of a dispersion in or on liquid or solid media, conventionally at concentrations of 0.01% to 80%,
par exemple de 0,5% à 50% en poids. for example from 0.5% to 50% by weight.
Le carbétamide est soluble dans l'eau dans la proportion d'environ 3,5 g/litre. Dans des milieux 2t liquides, le carbetamide est donc appliqué de préférence sous forme d'une dispersion émulsionnee dans de l'eau par émulsionnement d'une solution concentrée dans un solvant convenable. Le carbétamide peut également être appliqué sous forme d'une suspension aqueuse formée à partir d'une poudre mouillable. Les solvants, l'agent actif et les surfactants sont préparés sous forme de concentrés émulsionnables qui sont ensuite dilués avec de l'eau, avant Carbetamide is soluble in water in the proportion of about 3.5 g / liter. In 2t liquid media, the carbetamide is therefore preferably applied in the form of an emulsified dispersion in water by emulsification of a concentrated solution in a suitable solvent. Carbetamide can also be applied as an aqueous suspension formed from a wettable powder. The solvents, the active agent and the surfactants are prepared in the form of emulsifiable concentrates which are then diluted with water, before
application, à la concentration appropriée. Des composi- application, at the appropriate concentration. Compounds
tions concentrées liquides sont préférées pour la prépara- Concentrated liquids are preferred for preparation.
tion de dispersions destinées à être appliquées par pulvérisation. Cependant, ces concentrés peuvent être tion of dispersions intended to be applied by spraying. However, these concentrates can be
modifiés pour l'application de dispersions par l'inter- modified for the application of dispersions via the
médiaire d'aérosols, de nébulisats ou de brouillards. Ces medium of aerosols, nebulisates or mists. These
techniques de modification sont bien connues. modification techniques are well known.
Les formulations liquides de carbétamide peuvent être appliquées par des procédés manuels tels que la pulvérisation manuelle, l'utilisation de réservoirs d'arrosage, le trempage, etc., mais, dans des opérations à grande échelle, un appareil classique (par exemple un appareillage monté sur des tables a rouleaux) peut être utilisé. Les liquides peuvent également être distribués par Liquid carbetamide formulations can be applied by manual methods such as manual spraying, use of spray tanks, soaking, etc., but, in large-scale operations, a conventional apparatus (e.g., apparatus mounted on roller tables) can be used. Liquids can also be dispensed by
des nébuliseurs.nebulizers.
Le carbétamide peut également être appliqué sous forme solide, c'est-àdire par l'intermédiaire de poudres mouillables, de poudres pour poudrage ou de granules. Ces poudres ou granules sont appliqués par poudrage ou dispersion des matières solides, en les quantités requises, sur la culture entreposée à traiter, par exemple au moyen d'appareils de dispersion de granules de poudre. Les poudres mouillables ou les granules sont Carbetamide can also be applied in solid form, that is to say by means of wettable powders, powders for dusting or granules. These powders or granules are applied by dusting or dispersing the solid materials, in the required quantities, on the stored culture to be treated, for example by means of dispersing powder granules. Wettable powders or granules are
préférés pour l'application d'agents solides. preferred for the application of solid agents.
Les compositions concentrées, à l'état liquide, solide ou semi-solide, sont diluées avant application pour garantir une répartition uniforme. Le degré de dilution requis dépend du mode d'application. Lorsque le carbétamide est pulvérisé sous forme liquide par l'intermédiaire d'une dispersion ou suspension aqueuse, la concentration d'ingrédient actif peut être comprise dans l'intervalle de The concentrated compositions, in the liquid, solid or semi-solid state, are diluted before application to guarantee a uniform distribution. The degree of dilution required depends on the mode of application. When carbetamide is sprayed in liquid form via an aqueous dispersion or suspension, the concentration of active ingredient may be in the range of
0,01 à 80%, par exemple de 4,5 à 50% en poids. 0.01 to 80%, for example 4.5 to 50% by weight.
Des poudres mouillables comprenant environ 65% en poids de carbétamide sont préférees, tout comme des solutions de carbétamide comprenant 100 à 300 g/l de carbétamide. Des compositions solides sont utilisées pour Wettable powders comprising about 65% by weight of carbetamide are preferred, as are solutions of carbetamide comprising 100 to 300 g / l of carbetamide. Solid compositions are used for
administrer une concentration d'ingrédient actif approxima- administer an approximate active ingredient concentration
tivement identique à celle des compositions liquides. identical to that of liquid compositions.
De la manière précitee, le carbétamide est compatible avec d'autres substances actives, telles que des fongicides et des insecticides, et il peut donc être appliqué aux cultures entreposées en association avec ces substances actives. Cette application peut être effectuée As mentioned above, carbetamide is compatible with other active substances, such as fungicides and insecticides, and it can therefore be applied to crops stored in association with these active substances. This app can be done
de manière distincte, séquentielle ou simultanée. separately, sequentially or simultaneously.
La quantité de carbétamide appliquée va généralement de 17 a 200 g de i.a. (ingrédient actif)/tonne The amount of carbetamide applied generally ranges from 17 to 200 g of i.a. (active ingredient) / tonne
de pommes de terre.potatoes.
Dans l'inhibition temporaire de la germination des pommes de terre à semences après plantation, une quantité de 17 à 50 g de i.a./tonne est de préférence In the temporary inhibition of germination of seed potatoes after planting, an amount of 17 to 50 g of a.i./tonne is preferably
utilisée. Il est considéré que le carbétamide est soumis à- used. Carbetamide is considered to be subject to-
une dégradation dans le sol: plus la quantité de car- degradation in the soil: the higher the amount of
bétamide utilisée est forte, plus le retard de germination betamide used is strong, the longer the delay in germination
est important.is important.
Dans l'inhibition de la germination des pommes de terre entreposées, une quantité de 17 à 200 g de i.a./tonne est avantageusement utilisée, de préférence de In the inhibition of the germination of stored potatoes, an amount of 17 to 200 g of a.i./tonne is advantageously used, preferably
à 70 g de i.a./tonne.70 g a.i./tonne.
En général, plus la température est basse, plus la quantité de carbétamide requise pour inhiber la 0 germination est faible. La quantité de carbétamide requise peut varier également suivant la variété de pomme de terre, certaines variétés étant plus susceptibles de germer In general, the lower the temperature, the lower the amount of carbetamide required to inhibit germination. The amount of carbetamide required may also vary depending on the variety of potato, some varieties being more likely to germinate
que d'autres.that others.
A titre d'exemple, les compositions suivantes peuvent être utilisées dans le procédé conforme à la By way of example, the following compositions can be used in the process according to
présente invention.present invention.
Poudres mouillables (pourcentage en poids) carbétamide 70 50 nonylphénol oxyethyl-17 (agent mouillant) 2 2 polycarboxylate (agent dispersant) 2 2 silice (support) 26 25 carbonate de calcium (support) 0 21 Concentré émulsionnable carbétamide 300 g acetophénone (support) 180 g nonylphényl oxyéthyl-7 (agent mouillant) 200 g cyclohexanone (support) qs pour 1000 cm3 Le carbétamide possède une DL50 aiguë chez le rat égale a 11 000 mg/kg de poids corporel de l'animal et est pratiquement dépourvu de toxicité chronique. Des applications topiques au niveau de l'oeil du lapin (5 mg) et de la peau du lapin (crème a 5%) démontrent également Wettable powders (percentage by weight) carbetamide 70 50 nonylphenol oxyethyl-17 (wetting agent) 2 2 polycarboxylate (dispersing agent) 2 2 silica (support) 26 25 calcium carbonate (support) 0 21 Emulsifiable carbetamide concentrate 300 g acetophenone (support) 180 g nonylphenyl oxyethyl-7 (wetting agent) 200 g cyclohexanone (support) qs per 1000 cm3 Carbetamide has an acute LD50 in rats equal to 11000 mg / kg of body weight of the animal and is practically devoid of chronic toxicity . Topical applications in the rabbit eye (5 mg) and rabbit skin (5% cream) also demonstrate
l'absence d'effets irritants.the absence of irritant effects.
Ainsi, le carbétamide est moins toxique ou irritant pour les espèces de mammifères que les inhibiteurs de germination utilisés antérieurement et est d'une utilisation plus sûre pour un ouvrier inexpérimenté. En outre, en l'absence de toxicité notable, les résidus Thus, carbetamide is less toxic or irritating to mammalian species than the germination inhibitors previously used and is safer to use for an inexperienced worker. In addition, in the absence of significant toxicity, the residues
présents sur les tubercules présentent un danger notable- present on the tubers present a significant danger-
ment inférieur pour la santé et l'environnement des inferior to the health and environment of
préparateurs et des consommateurs finals. preparers and end consumers.
Le carbétamide provoque également une plus faible altération des tubercules traités, ce qui rend ces Carbetamide also causes less deterioration of the treated tubers, making these
derniers plus acceptables pour la consommation. latter more acceptable for consumption.
En outre, le carbétamide est beaucoup moins volatil que les inhibiteurs de germination actuellement utilisés. Ceci permet donc une sélectivité de traitement et évite une contamination croisée, la zone d'efficacité d'un traitement ne s'étendant pas. En conséquence, il n'existe aucun besoin de séparation des tubercules traités des tubercules non traités ou d'autres cultures entreposées, ou bien d'utilisation de modes opératoires complexes de séparation au cours du traitement, comme cela est requis avec les inhibiteurs actuellement utilisés. La très faible In addition, carbetamide is much less volatile than the germination inhibitors currently used. This therefore allows treatment selectivity and avoids cross contamination, the zone of effectiveness of a treatment not extending. As a result, there is no need to separate treated tubers from untreated tubers or other stored crops, or use complex separation procedures during processing, as required with the inhibitors currently in use. . The very weak
volatilité évite également un quelconque risque d'exposi- volatility also avoids any risk of exposure
tion à des vapeurs pour les ouvriers des entrepôts de steamers for warehouse workers
pommes de terre.potatoes.
Le traitement conforme à la présente invention Treatment according to the present invention
a également pour résultat des pertes de poids non supé- also results in weight loss not greater than
rieures à celles des traitements classiques. lower than those of conventional treatments.
L'exemple suivant illustre l'utilisation de The following example illustrates the use of
carbétamide conformément à la présente invention. carbetamide according to the present invention.
EXEMPLEEXAMPLE
Quatre variétés de pomme de terre ont été traitées avec différentes quantités d'une poudre mouillable Four varieties of potato were treated with different amounts of a wettable powder
contenant 65% en poids/poids de carbétamide. Le degré. containing 65% w / w carbetamide. Degree.
d'inhibition de la germination a été déterminé, par comparaison avec des pommes de terre non traitées, au bout de trois mois d'entreposage. Les résultats étaient les suivants: inhibition of germination was determined, by comparison with untreated potatoes, after three months of storage. The results were as follows:
Variété de pcome Taux d'application de la Inhibition (pour- Variety of pcome Inhibition application rate (for-
de terre caposition (g/tonne) centage) au bout de 3 mois 5 mois Squire 50 69 99 of land caposition (g / ton) centering) after 3 months 5 months Squire 50 69 99
96 9996 99
99 9999 99
300 99 99300 99 99
Romano 50 * 75Romano 50 * 75
100 * 93100 * 93
* 96* 96
300 * 97300 * 97
Desiree 50 71 98Desiree 50 71 98
/Z 100 97 98/ Z 100 97 98
99 9999 99
300 100 99300 100 99
Cara 50 88 87 0loo 98 98Cara 50 88 87 0loo 98 98
150 100 99150 100 99
300 100 99300 100 99
* Variété à germination tardive Dans des expériences comparatives, un essai similaire a été mis en oeuvre, sauf que le traitement a été effectué avec du BYGRAN S (une composition du commerce à base de tecnazène) à un taux de 1300 g/tonne. Les résultats étaient les suivants: Variété de pomme Inhibition (pourcentage) de terre au bout de 3 mois 5 mois Squire 78 92 Romano * 75 Desiree 93 83 Cara 85 82 Les pertes de poids des pommes de terre soumises aux différents traitements ont été également é. valuées et comparees à celles résultant d'un traitement classique et à celles des témoins non traités. Les valeurs moyennes pour toutes les variétés de pommes de terre testées sont les suivantes: Traitement Perte de poids (%) au bout de 3 mois 5 mois Aucun (témoin) 1,8 3,3 Carbétamide 50 g/tonne 1,4 2,8 g/tonne 1,5 2,8 " 150 g/tonne 1,3 ' 2, 2 " 300 g/tonne 1,5 2,3 Bygran S 1300 g/tonne 1,9 3,5 l1 * Variety with late germination In comparative experiments, a similar test was carried out, except that the treatment was carried out with BYGRAN S (a commercial composition based on tecnazene) at a rate of 1300 g / ton. The results were as follows: Apple variety Inhibition (percentage) of earth after 3 months 5 months Squire 78 92 Romano * 75 Desiree 93 83 Cara 85 82 The weight losses of the potatoes subjected to the various treatments were also measured. . evaluated and compared with those resulting from conventional treatment and those of untreated controls. The average values for all the varieties of potatoes tested are as follows: Treatment Weight loss (%) after 3 months 5 months None (control) 1.8 3.3 Carbetamide 50 g / ton 1.4 2, 8 g / ton 1.5 2.8 "150 g / ton 1.3 '2.2" 2 g 300 g / ton 1.5 2.3 Bygran S 1300 g / ton 1.9 3.5 l1
Claims (10)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB898914748A GB8914748D0 (en) | 1989-06-27 | 1989-06-27 | New method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| FR2648674A1 true FR2648674A1 (en) | 1990-12-28 |
Family
ID=10659135
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR9008301A Withdrawn FR2648674A1 (en) | 1989-06-27 | 1990-06-26 | PROCESS FOR INHIBITING GERMINATION OF POTATOES |
Country Status (23)
| Country | Link |
|---|---|
| CN (1) | CN1048784A (en) |
| AT (1) | AT393933B (en) |
| AU (1) | AU622813B2 (en) |
| BE (1) | BE1003881A5 (en) |
| CA (1) | CA2019518A1 (en) |
| CH (1) | CH680826A5 (en) |
| DD (1) | DD295970A5 (en) |
| DE (1) | DE4020499A1 (en) |
| DK (1) | DK154890A (en) |
| ES (1) | ES2032242B1 (en) |
| FR (1) | FR2648674A1 (en) |
| GB (1) | GB8914748D0 (en) |
| GR (1) | GR1000652B (en) |
| HU (1) | HUT59801A (en) |
| IE (1) | IE902201A1 (en) |
| IT (1) | IT1249013B (en) |
| LU (1) | LU87755A1 (en) |
| NL (1) | NL9001454A (en) |
| PL (1) | PL285789A1 (en) |
| PT (1) | PT94500A (en) |
| RU (1) | RU1833138C (en) |
| YU (1) | YU124390A (en) |
| ZA (1) | ZA904825B (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104397149B (en) * | 2014-11-11 | 2017-03-15 | 新疆林科院经济林研究所 | A kind of method of employing Sorbus sibirica extracting solution inhibition of potato sprouting |
| CN105123905A (en) * | 2015-09-15 | 2015-12-09 | 齐鲁工业大学 | Method for inhibiting potato sprouting |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1346425A (en) * | 1962-11-07 | 1963-12-20 | Vondelingen Plaat Bv | Potato preservation process |
| GB959204A (en) * | 1959-11-17 | 1964-05-27 | Rhone Poulenc Sa | New carbamic esters, processes for their preparation and herbicidal compositions containing them |
| US4095971A (en) * | 1977-03-08 | 1978-06-20 | Rhodia, Inc. | Tobacco sucker control |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR95866E (en) * | 1968-05-10 | 1971-11-12 | Inst Francais Du Petrole | New compound food containing algae of the spirulina type. |
| EP0104902A3 (en) * | 1982-09-24 | 1986-01-22 | Wheatley Chemical Company Limited | Protection agent for fruits and vegetable tubers |
| DE3713198A1 (en) * | 1987-04-18 | 1988-10-27 | Boehringer Ingelheim Kg | Germinating agents for potatoes |
-
1989
- 1989-06-27 GB GB898914748A patent/GB8914748D0/en active Pending
-
1990
- 1990-06-18 IE IE220190A patent/IE902201A1/en unknown
- 1990-06-21 ZA ZA904825A patent/ZA904825B/en unknown
- 1990-06-21 CA CA002019518A patent/CA2019518A1/en not_active Abandoned
- 1990-06-25 PL PL28578990A patent/PL285789A1/en unknown
- 1990-06-25 AT AT0135390A patent/AT393933B/en not_active IP Right Cessation
- 1990-06-25 AU AU57761/90A patent/AU622813B2/en not_active Ceased
- 1990-06-25 NL NL9001454A patent/NL9001454A/en not_active Application Discontinuation
- 1990-06-25 GR GR900100486A patent/GR1000652B/en unknown
- 1990-06-26 PT PT94500A patent/PT94500A/en not_active Application Discontinuation
- 1990-06-26 YU YU124390A patent/YU124390A/en unknown
- 1990-06-26 RU SU904830320A patent/RU1833138C/en active
- 1990-06-26 DK DK154890A patent/DK154890A/en not_active IP Right Cessation
- 1990-06-26 FR FR9008301A patent/FR2648674A1/en not_active Withdrawn
- 1990-06-26 ES ES9001762A patent/ES2032242B1/en not_active Expired - Lifetime
- 1990-06-26 CN CN90106662A patent/CN1048784A/en active Pending
- 1990-06-27 BE BE9000658A patent/BE1003881A5/en not_active IP Right Cessation
- 1990-06-27 CH CH2147/90A patent/CH680826A5/fr not_active IP Right Cessation
- 1990-06-27 IT IT02079390A patent/IT1249013B/en active IP Right Grant
- 1990-06-27 DE DE4020499A patent/DE4020499A1/en not_active Withdrawn
- 1990-06-27 LU LU87755A patent/LU87755A1/en unknown
- 1990-06-27 HU HU904012A patent/HUT59801A/en unknown
- 1990-06-27 DD DD90342158A patent/DD295970A5/en not_active IP Right Cessation
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB959204A (en) * | 1959-11-17 | 1964-05-27 | Rhone Poulenc Sa | New carbamic esters, processes for their preparation and herbicidal compositions containing them |
| FR1346425A (en) * | 1962-11-07 | 1963-12-20 | Vondelingen Plaat Bv | Potato preservation process |
| US4095971A (en) * | 1977-03-08 | 1978-06-20 | Rhodia, Inc. | Tobacco sucker control |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2019518A1 (en) | 1990-12-27 |
| GR900100486A (en) | 1991-11-15 |
| ZA904825B (en) | 1991-04-24 |
| IT9020793A0 (en) | 1990-06-27 |
| ES2032242B1 (en) | 1993-12-16 |
| GR1000652B (en) | 1992-09-25 |
| IE902201A1 (en) | 1991-01-02 |
| YU124390A (en) | 1992-12-21 |
| IT1249013B (en) | 1995-02-11 |
| AU622813B2 (en) | 1992-04-16 |
| CH680826A5 (en) | 1992-11-30 |
| BE1003881A5 (en) | 1992-07-07 |
| IE902201L (en) | 1990-12-27 |
| NL9001454A (en) | 1991-01-16 |
| RU1833138C (en) | 1993-08-07 |
| ATA135390A (en) | 1991-07-15 |
| HUT59801A (en) | 1992-07-28 |
| LU87755A1 (en) | 1991-02-18 |
| DK154890A (en) | 1990-12-28 |
| DD295970A5 (en) | 1991-11-21 |
| DK154890D0 (en) | 1990-06-26 |
| PL285789A1 (en) | 1991-03-11 |
| PT94500A (en) | 1991-02-08 |
| GB8914748D0 (en) | 1989-08-16 |
| IT9020793A1 (en) | 1991-12-27 |
| CN1048784A (en) | 1991-01-30 |
| HU904012D0 (en) | 1990-12-28 |
| ES2032242A1 (en) | 1993-01-16 |
| AU5776190A (en) | 1991-01-03 |
| DE4020499A1 (en) | 1991-01-03 |
| AT393933B (en) | 1992-01-10 |
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