GB926853A - Process for the manufacture of colourless or only slightly coloured addition products of alkylene oxides - Google Patents

Process for the manufacture of colourless or only slightly coloured addition products of alkylene oxides

Info

Publication number
GB926853A
GB926853A GB1870159A GB1870159A GB926853A GB 926853 A GB926853 A GB 926853A GB 1870159 A GB1870159 A GB 1870159A GB 1870159 A GB1870159 A GB 1870159A GB 926853 A GB926853 A GB 926853A
Authority
GB
United Kingdom
Prior art keywords
hydrazine hydrate
acid
hypophosphoric
ethylene oxide
acids
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
GB1870159A
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst 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 Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB926853A publication Critical patent/GB926853A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • C11C3/003Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fatty acids with alcohols
    • 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
    • C08G65/26Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Anti-Oxidant Or Stabilizer Compositions (AREA)

Abstract

In the reaction of alkylene oxides with organic compounds containing a reactive hydrogen, e.g. an acid, amine, alcohol or phenol, up to 2% of an oxidation inhibitor or reducing agent is present in order to prevent or reduce undesired colouration. The reducing agent is colourless or has only a slight colour, and in the form of the oxidation product thereof, or in the form of an alkylene oxide addition product thereof has no or only a slight colour and does not form an insoluble precipitation. Specified are hydrazine hydrate, hydroxylamine, phosphorous and hypophosphoric acids, the salts of the compounds, the esters of the acids, or a mixture of two or more of these compounds, and hydroxylamine chlorohydrate, thiourea and sodium hyposulphite. Examples describe the reaction of (1) ethylene oxide (30 mols.) with stearic acid in the presence of hydrazine hydrate and hypophosphoric acid; (5) ethylene oxide (10 mols.) with stearylamine in the presence of hydrazine hydrate; (7) and (8) ethylene oxide (20 mols.) with oleylamine and coconut oil amine respectively in the presence of hydrazine hydrate; and also the preparation of polyethylene, polypropylene and polybutylene glycols.ALSO:In the reaction of alkylene oxides with organic compounds containing a reactive hydrogen e.g. an acid, amine, alcohol or phenol, up to 2% of an oxidation inhibitor or reducing agent is present in order to prevent or reduce undesired colouration. The reducing agent is colourless or has only a slight colour, and in the form of the oxidation product thereof, or in the form of an alkylene oxide addition product thereof, has no or only a slight colour and does not form an insoluble precipitate, and hydrazine hydrate, hydroxylamine, phosphorous and hypophosphoric acids, the salts of the compounds, the esters of the acids, or a mixture of two or more of these compounds, and hydroxylamine chlorohydrate thiourea, and sodium hyposulphite are specified. Examples describe the reaction of ethylene oxide with (1) stearic acid in the presence of hydrazine hydrate and/or hypophosphoric acid (2),(3) and (4) triethanolamine in the presence of hydroxylamine chlorohydrate, hydrazine hydrate, thiourea and sodium hyposulphite (5) and (6) stearylamine in the presence of hydrazine hydrate (7) oleylamine and hydrazine hydrate (8) coconut oil amine and hydrazine hydrate (10) diethylene glycol with hypophosphoric acid; a - and b -butylene oxides with 1.3 butylene glycol in the presence of hypophosphoric acid and hydrazine hydrate; ethylene oxide with (13) tributyl phenol with hypophosphoric acid and (14) oleic acid with hypophosphoric acid and (16) oleyl alcohol with sodium hypophosphite; and (15) propylene oxide with coconut oil fatty acids with sodium hypophosphite.
GB1870159A 1958-05-30 1959-06-01 Process for the manufacture of colourless or only slightly coloured addition products of alkylene oxides Expired GB926853A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF25852A DE1090433B (en) 1958-05-30 1958-05-30 Process for the production of colorless or only slightly colored addition products of alkylene oxides with organic compounds which contain at least one mobile hydrogen atom

Publications (1)

Publication Number Publication Date
GB926853A true GB926853A (en) 1963-05-22

Family

ID=7091785

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1870159A Expired GB926853A (en) 1958-05-30 1959-06-01 Process for the manufacture of colourless or only slightly coloured addition products of alkylene oxides

Country Status (3)

Country Link
CH (1) CH428231A (en)
DE (1) DE1090433B (en)
GB (1) GB926853A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2153373A (en) * 1984-01-30 1985-08-21 Procter & Gamble Process for minimizing color formation during base catalyzed ethoxylation of 2- hydroxyethylamines
EP1510536A1 (en) * 2003-08-21 2005-03-02 Basf Aktiengesellschaft Method for producing polyether alcohols

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2441547A (en) * 1944-11-08 1948-05-11 Ind Patents Corp Hydroxylamine stabilized fatty materials
DE927032C (en) * 1952-04-05 1955-04-28 Hoechst Ag Process for the production of light, odorless condensation products

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2153373A (en) * 1984-01-30 1985-08-21 Procter & Gamble Process for minimizing color formation during base catalyzed ethoxylation of 2- hydroxyethylamines
EP1510536A1 (en) * 2003-08-21 2005-03-02 Basf Aktiengesellschaft Method for producing polyether alcohols

Also Published As

Publication number Publication date
DE1090433B (en) 1960-10-06
CH428231A (en) 1967-01-15

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