GB950384A - Alkylbenzyldiethylenetriamine acetic acids - Google Patents
Alkylbenzyldiethylenetriamine acetic acidsInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23F—NON-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
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting 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
- C23F11/14—Nitrogen-containing compounds
- C23F11/144—Aminocarboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
- A61K47/183—Amino acids, e.g. glycine, EDTA or aspartame
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/175—Amines; Quaternary ammonium compounds containing COOH-groups; Esters or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/10—Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/045—Compositions 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
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/30—Organic compounds, e.g. vitamins containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/26—Amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/046—Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/06—Macromolecular 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.
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)
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 |
-
0
- CA CA718041A patent/CA718041A/en not_active Expired
- BE BE630552D patent/BE630552A/xx unknown
-
1962
- 1962-04-18 CH CH473762A patent/CH424798A/en unknown
- 1962-04-19 GB GB15193/62A patent/GB950384A/en not_active Expired
Cited By (1)
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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