MX173707B - Proceso para hacer carboxilados de alquil etoxi - Google Patents

Proceso para hacer carboxilados de alquil etoxi

Info

Publication number
MX173707B
MX173707B MX020818A MX2081890A MX173707B MX 173707 B MX173707 B MX 173707B MX 020818 A MX020818 A MX 020818A MX 2081890 A MX2081890 A MX 2081890A MX 173707 B MX173707 B MX 173707B
Authority
MX
Mexico
Prior art keywords
alkaline earth
chloroacetic acid
earth metal
metal salt
alkali metal
Prior art date
Application number
MX020818A
Other languages
English (en)
Inventor
Thomas Anthony Cripe
Original Assignee
Procter & Gamble
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 Procter & Gamble filed Critical Procter & Gamble
Publication of MX173707B publication Critical patent/MX173707B/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/125Saturated compounds having only one carboxyl group and containing ether groups, groups, groups, or groups
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/86Polyethers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/367Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of functional groups containing oxygen only in singly bound form
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32Polymers modified by chemical after-treatment
    • C08G65/329Polymers modified by chemical after-treatment with organic compounds
    • C08G65/337Polymers modified by chemical after-treatment with organic compounds containing other elements
    • 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
    • C11D1/06Ether- or thioether carboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Birds (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Wood Science & Technology (AREA)
  • Detergent Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

Abstract

La presente invención se refiere a un proceso para preparar un surfactante de carboxilado de alquil etoxi de la fórmula: RO(CH2CH2O)xCH2COO-M+ donde R es un grupo alquilo de C8 a C18, x es un número cuyo promedio va de 1 hasta 15 y M es un catión de metal alcalino o de metal alcalinoterreo caracterizado porque dicho proceso comprende hacer reaccionar; a) un alcohol graso etoxilado de la fórmula RO(CH2CH2O)xH, donde R es un grupo alquilo de C8 a C18 y x es un número cuyo promedio va de 1 a 15, b) una base impedida de la fórmula RO-M+, donde RO- es un alcóxido secundario o terciario, R es un grupo alquilo no lineal de C4 a C12 con por lo menos un punto de ramificación dentro de los 3 átomos de carbono del átomo de oxígeno y M es un catión de metal alcalinoo de metal alcalinoterreo; y c) ácido cloroacetico anhidro, a una relación molar de la base impedida con el ácido cloroacetico anhidro de 2:1, o una sal de metal alcalino o una sal de metal alcalinoterreo del a´cido cloroacetico anhidro, a una relación molar de la base impedida con la sal de metal alcalino o de metal alcalinoterreo de ácido cloroacetico de 1:1, donde la relación molar del alcohol graso etoxilado con el ácido cloroacetico anhidro o la sal de metal alcalino o alcalinoterreo del mismo es de 1:0.7 a 1:1.25, la temperatura es desde 20 hasta 140 grados C y la presión es desde 1 hasta 760 mm Hg.
MX020818A 1989-05-22 1990-05-22 Proceso para hacer carboxilados de alquil etoxi MX173707B (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US35496889A 1989-05-22 1989-05-22

Publications (1)

Publication Number Publication Date
MX173707B true MX173707B (es) 1994-03-23

Family

ID=23395671

Family Applications (1)

Application Number Title Priority Date Filing Date
MX020818A MX173707B (es) 1989-05-22 1990-05-22 Proceso para hacer carboxilados de alquil etoxi

Country Status (15)

Country Link
EP (1) EP0399751A3 (es)
JP (1) JPH0347147A (es)
KR (1) KR900017981A (es)
CN (1) CN1030700C (es)
AR (1) AR244656A1 (es)
AU (1) AU620713B2 (es)
BR (1) BR9002407A (es)
CA (1) CA2012171A1 (es)
FI (1) FI902494A0 (es)
MA (1) MA21849A1 (es)
MX (1) MX173707B (es)
MY (1) MY105621A (es)
NZ (1) NZ233746A (es)
PT (1) PT94098A (es)
TR (1) TR25183A (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3855344B2 (ja) * 1997-02-19 2006-12-06 日本油脂株式会社 ポリオキシアルキレンカルボン酸の製造方法
DE19740954C1 (de) * 1997-09-17 1998-12-24 Henkel Kgaa Verfahren zur Herstellung von hellfarbigen Ethercarbonsäuren
CN1086185C (zh) * 1999-11-15 2002-06-12 广州绿色化学品研究中心 醇醚羧酸二价金属盐的制备方法
EP2146949B1 (de) * 2007-05-05 2017-03-01 Basf Se Ionische flüssigkeiten mit polyethercarboxylaten als anionen, deren herstellung und verwendung
AU2010279232A1 (en) 2009-08-07 2012-03-08 Basf Se Lubricant composition comprising alkylethercarboxylic acid
US8802606B2 (en) 2010-08-06 2014-08-12 Basf Se Lubricant composition having improved antiwear properties
CN102276428B (zh) * 2010-06-10 2015-11-25 克施乐化学工厂两合公司 制备醇乙氧基化物的方法及产品
JP5255103B2 (ja) * 2010-09-03 2013-08-07 花王株式会社 洗浄剤組成物

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1920137A (en) * 1932-09-28 1933-07-25 Resinous Prod & Chemical Co Alkoxyacetic acids
GB456517A (en) * 1935-04-05 1936-11-05 Ig Farbenindustrie Ag Improvements in the manufacture and production of washing, wetting, emulsifying, softening and like agents
DE3248463A1 (de) * 1982-12-29 1984-07-12 Haarmann & Reimer Gmbh, 3450 Holzminden Alkoxyessigsaeuren, ein verfahren zu ihrer herstellung und ihre verwendung

Also Published As

Publication number Publication date
NZ233746A (en) 1992-05-26
EP0399751A2 (en) 1990-11-28
AU620713B2 (en) 1992-02-20
MY105621A (en) 1994-11-30
JPH0347147A (ja) 1991-02-28
TR25183A (tr) 1992-11-01
CA2012171A1 (en) 1990-11-22
CN1047493A (zh) 1990-12-05
AU5574990A (en) 1990-11-22
KR900017981A (ko) 1990-12-20
CN1030700C (zh) 1996-01-17
AR244656A1 (es) 1993-11-30
EP0399751A3 (en) 1991-11-13
MA21849A1 (fr) 1990-12-31
BR9002407A (pt) 1991-08-06
PT94098A (pt) 1991-01-08
FI902494A0 (fi) 1990-05-21

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