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GB698636A - Improvements in the manufacture of condensation products - Google Patents

Improvements in the manufacture of condensation products

Info

Publication number
GB698636A
GB698636A GB1269/51A GB126951A GB698636A GB 698636 A GB698636 A GB 698636A GB 1269/51 A GB1269/51 A GB 1269/51A GB 126951 A GB126951 A GB 126951A GB 698636 A GB698636 A GB 698636A
Authority
GB
United Kingdom
Prior art keywords
acid
group
reacted
amino
dodecyl
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.)
Expired
Application number
GB1269/51A
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 SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
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.)
Filing date
Publication date
Application filed by BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB698636A publication Critical patent/GB698636A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/16Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
    • A61K47/18Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/45Derivatives containing from 2 to 10 oxyalkylene groups

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Birds (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Dermatology (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

Abstract

Condensation products, apparently amino-esters and amino-ethers, are prepared by heating a polyglycol ether product of the formula A.(OC2H4)n.B (in which A is an aliphatic hydrocarbon chain with at least four carbon atoms, B is -OH, -ONa, -OK, or the radical of an inorganic acid, and n is an integer) with an aromatic acid or phenol or a functional derivative thereof containing in its molecule as a substituent at least one amino group or a nitro group, and converting any nitro groups present in the product into amino groups. The polyglycolether chain may be interrupted by a divalent group or sulphur, and the amino group of the aromatic acid or phenol may be protected, e.g. by a benzal group. The products are soluble and may be made more so by introduction of sulphuric acid radicals or polyglycol ether radicals or by peralkylation. They form difficultly soluble products with tannin, synthetic or natural tanning agents, phosphotungstic acid, phosphomolybdic acid, phosphotungstomolybdic acid, or silicolungstic acid. They have disinfecting, preserving, pesticidal, antiseptic, foaming, wetting, and dispersing properties. In examples: (1) dodecyl nonaglycol ether is reacted in toluene with phosphorus tribromide to give dodecyl nonaglycol bromide, which is reacted with the potassium salt of para-aminobenzoic acid; (2) cetyl decaglycol bromide is reacted with sodium p-benzolaminophenate, the benzal group being split off; (3) dodecyl nonaglycol ether is reacted with sodium in benzene and then with p-nitrobenzoyl chloride, followed by hydrogenation.
GB1269/51A 1950-01-26 1951-01-17 Improvements in the manufacture of condensation products Expired GB698636A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE698636X 1950-01-26

Publications (1)

Publication Number Publication Date
GB698636A true GB698636A (en) 1953-10-21

Family

ID=6608212

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1269/51A Expired GB698636A (en) 1950-01-26 1951-01-17 Improvements in the manufacture of condensation products

Country Status (1)

Country Link
GB (1) GB698636A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE974320C (en) * 1954-05-14 1960-11-24 Ciba Geigy Process for the preparation of a p-amino-benzoic acid-polyglycol ester which can be used as a local anesthetic
EP0675939A4 (en) * 1993-10-28 1996-03-20 Chevron Chem Co Fuel compositions containing poly(oxyalkylene) aromatic ethers.

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE974320C (en) * 1954-05-14 1960-11-24 Ciba Geigy Process for the preparation of a p-amino-benzoic acid-polyglycol ester which can be used as a local anesthetic
EP0675939A4 (en) * 1993-10-28 1996-03-20 Chevron Chem Co Fuel compositions containing poly(oxyalkylene) aromatic ethers.

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