GB950384A - Alkylbenzyldiethylenetriamine acetic acids - Google Patents

Alkylbenzyldiethylenetriamine acetic acids

Info

Publication number
GB950384A
GB950384A GB15193/62A GB1519362A GB950384A GB 950384 A GB950384 A GB 950384A GB 15193/62 A GB15193/62 A GB 15193/62A GB 1519362 A GB1519362 A GB 1519362A GB 950384 A GB950384 A GB 950384A
Authority
GB
United Kingdom
Prior art keywords
ammonium
alkyl
acid
compounds
potassium
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
GB15193/62A
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.)
Novartis AG
Original Assignee
JR Geigy 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 JR Geigy AG filed Critical JR Geigy AG
Publication of GB950384A publication Critical patent/GB950384A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • C23F11/14Nitrogen-containing compounds
    • C23F11/144Aminocarboxylic acids
    • 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
    • A61K47/183Amino acids, e.g. glycine, EDTA or aspartame
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/17Amines; Quaternary ammonium compounds
    • C08K5/175Amines; Quaternary ammonium compounds containing COOH-groups; Esters or salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • C11D1/10Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D9/00Compositions of detergents based essentially on soap
    • C11D9/04Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
    • C11D9/045Compositions of detergents based essentially on soap containing compounding ingredients other than soaps containing substances which prevent the deterioration of soaps, e.g. light or heat stabilisers or antioxidants
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D9/00Compositions of detergents based essentially on soap
    • C11D9/04Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
    • C11D9/22Organic compounds, e.g. vitamins
    • C11D9/30Organic compounds, e.g. vitamins containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/26Amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/046Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/06Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Biochemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Compounds of formula (I), wherein R is C6-24 alkyl, M is H, alkali metal or ammonium (optionally alkyl- or hydroxyalkyl-substituted), m and q are each 1, 2, 3 or 4 and n is 0, 1, 2 or 3, such that (q + m + n) = 5 <FORM:0950384/C1/1> may be employed in the foam separation of e.g. radioactive strontium. The preferred compounds (I) are N-dodecylbenzyldiethylenetriamine mono-, di-, tri- and tetra-acetic acids; mention is made of the free acids, their hydrochlorides and the sodium, potassium, ammonium, triethanolamine, t - octylamine and dodecylamine salts, with particular reference to the di-acid. In Example 4, details are given of the use of the disodium salt of dodecylbenzyldiethylenetriaminetriacetic acid in the foam separation of radio-active strontium in strontium chloride.ALSO:The invention comprises compounds of formula (I) wherein R is C6-24 alkyl; M is H, alkali metal or ammonium which may be alkyl-or hydroxyalkyl-substituted; m and q are each 1, 2, 3 or 4 and n is 0, 1, 2, or 3, such that (q+m+ n)=5. <FORM:0950384/C2/1> <FORM:0950384/C2/2> Such compounds are produced by reacting amines of formula (II), wherein n1 is 1, 2, 3 or 4 such that (q+n1)=5, with 1-4 moles of a compound introducing the -CH2CO2H group; where the latter is introduced in a modified form, the acid group is liberated and optionally reacted with alkali or ammonium ions. The preferred compounds (I) are N-dodecylbenzyl-diethylenetriamine mono-, di-, tri- and tetraacetic acids; in examples, the parent triamine is reacted with sodium or potassium chloroacetate and the di-acid, in particular, may be isolated as the free acid, its hydrochloride, or the sodium, potassium, ammonium, triethanolamine, t-octylamine or dodecylamine salts. Reagents which may in general be used to introduce the acetic acid group are: monochloro- and monobromo-acetic acids, their salts, esters, amides and nitriles, formaldehyde cyanohydrin or mixtures of alkali a hydrogen cyanide with formaldehyde. U.S.A. Specification 2,952,635 is referred to.ALSO:Compounds of formula (I), wherein R is C6-2 4 alkyl, M is H, alkali metal or ammonium (optionally alkyl- or hydroxyalkyl-substituted), m and q are each 1, 2, 3 or 4 and n is 0, 1, 2 or 3, such that (q+m+n)=5, <FORM:0950384/C3/1> may be employed as additives to rubber and other plastic materials. The preferred compounds (I) are N-dodecylbenzyldiethylenetriamine mono-, di-, tri- and tetra-acetic acids, mention is made of the free acids, their hydrochlorides and the sodium, potassium, ammonium, triethanolamine, t-octylamine and dodecylamine salts, with particular reference to the di-acid.ALSO:Compounds of formula (I), wherein R is C6-24 alkyl, M is H, alkali metal or ammonium (optionally alkyl- or hydroxyalkyl-substituted), m and q are each 1, 2, 3 or 4 and n is 0, 1, 2 or 3, such that (q+m+n) = 5, <FORM:0950384/C3/1> may be employed as wetting and foaming agents, as pigment dispersing agents, and for prevention of rancidity in soaps (solid or aqueous solutions). The preferred compounds (I) are N - dodecylbenzyldiethylenetriamine mono-, di-, tri- and tetra-acetic acids, mention is made of the free acids, their hydrochlorides and the sodium, potassium, ammonium, triethanolamine, t-octylamine and dodecylamine salts, with particular reference to the di-acid.ALSO:Compounds of formula (I) wherein R is C6-24 alkyl, M is H, alkali metal or ammonium (optionally alkyl- or hydroxyalkyl-substituted), m and q are each 1, 2, 3 or 4 and n is 0, 1, 2 or 3, such that (q + m + n) = 5, <FORM:0950384/A5-A6/1> (I) may be employed as stabilizers/corrosion inhibitors in lubricating oils or in oleaginous-aqueous systems such as emulsions of dilute acetic acid and vegetable oils (e.g. olive and cottonseed oils), as detoxification agents for living organisms when contaminated (at least externally) with polyvalent radioactive metal ions and metals and other toxic metal ions and metals, as antienzyme agents for prevention of deterioration in living materials comprising calcium, e.g. for the prevention of dental caries in mammals and as stabilizers for aqueous oleaginous emulsions. The preferred compounds (I) are N-dodecylbenzyldiethylenetriamine mono-, di-, tri- and tetra-acetic acids, mention is made of the free acids, their hydrochlorides and the sodium, potassium, ammonium, triethanolamine, t-octylamine and dodecylamine salts, with particular reference to the di-acid.ALSO:Compounds of formula (I), wherein R is C6-24 alkyl, M is H, alkali metal or ammonium (optionally alkyl- or hydroxyalkylsubstituted), m and q are each 1, 2, 3 or 4 and n is 0, 1, 2, or 3, such that (q + m + n) = 5, <FORM:0950384/D1-D2/1> may be employed as antistatic agents for the prevention of dust gathering on fabrics e.g. silk or nylon. The preferred compounds (I) are N-dodecylbenzyldiethylenetriamine mono-, di-, tri- and tetra-acetic acids, mention is made of the free acids, their hydrochlorides and the sodium, potassium, ammonium, triethanolamine, t-octylamine and dodecylamine salts, with particular reference to the di-acid.ALSO:As stabilizers for oil-water emulsions, e.g. emulsions of olive oil and cottonseed oil in dilute acetic acid, are employed the surface active, chelating agents of formula: <FORM:0950384/A1-A3/1> wherein R is C6-24 alkyl, M is H, alkali metal or amonium (optionally alkyl- or hydroxyalkylsubstituted), m and q are each 1, 2, 3 or 4 and n is O, 1, 2 or 3, such that (q + m + n) = 5, may be employed. The preferred compounds (1) are N-dodecyl-benzyldiethylenstriamine mono-, di, tri- and tetra-acetic acids, mention is made of the free acids, their hylrochlorides and the sodium, potassium, amonium, triethanolamine, t-octylamine and dodecylamine salts, with particular reference to the di-acid.
GB15193/62A 1961-04-28 1962-04-19 Alkylbenzyldiethylenetriamine acetic acids Expired GB950384A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10619061A 1961-04-28 1961-04-28

Publications (1)

Publication Number Publication Date
GB950384A true GB950384A (en) 1964-02-26

Family

ID=22310013

Family Applications (1)

Application Number Title Priority Date Filing Date
GB15193/62A Expired GB950384A (en) 1961-04-28 1962-04-19 Alkylbenzyldiethylenetriamine acetic acids

Country Status (4)

Country Link
BE (1) BE630552A (en)
CA (1) CA718041A (en)
CH (1) CH424798A (en)
GB (1) GB950384A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110008634A1 (en) * 2008-08-11 2011-01-13 Autonetworks Technologies, Ltd. Rust inhibitor and surface treatment metal material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110008634A1 (en) * 2008-08-11 2011-01-13 Autonetworks Technologies, Ltd. Rust inhibitor and surface treatment metal material

Also Published As

Publication number Publication date
CA718041A (en) 1965-09-14
BE630552A (en)
CH424798A (en) 1966-11-30

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