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 oxidesInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/003—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fatty acids with alcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular 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.
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)
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)
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 |
-
1958
- 1958-05-30 DE DEF25852A patent/DE1090433B/en active Pending
-
1959
- 1959-05-28 CH CH7366459A patent/CH428231A/en unknown
- 1959-06-01 GB GB1870159A patent/GB926853A/en not_active Expired
Cited By (2)
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 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB926853A (en) | Process for the manufacture of colourless or only slightly coloured addition products of alkylene oxides | |
ES409235A1 (en) | Pigment formulation | |
GB1028458A (en) | Cutting fluid | |
ES304789A1 (en) | Procedure for the preparation of an antistatic agent, for poliolephins. (Machine-translation by Google Translate, not legally binding) | |
ES439148A1 (en) | Liquid preparation of fatty acid/alkanolamine condensates | |
GB1074495A (en) | Novel gonane derivatives and processes for their preparation | |
GB940952A (en) | Process for preparing textile fibres | |
GB987925A (en) | Pharmaceutical compositions comprising a propanol derivative | |
GB642950A (en) | Process for the preparation of alkanolamines | |
FR1519503A (en) | Method for preparing variety of hydrated iron oxide | |
GB1132040A (en) | Complex salts of alkyl phenols and alkyl phenol sulphides | |
GB857068A (en) | Motor fuel compositions | |
GB1360553A (en) | Chemical compounds suitable for use as x-ray contrast agents | |
GB978304A (en) | Improvements in and relating to shaped articles of polymethylene terephthalates | |
GB1263343A (en) | Delta<2>-CEPHEM-4-CARBOXYLIC ACID ESTERS | |
GB993255A (en) | Process for the production of dibenzoazepine derivatives | |
ES364711A1 (en) | Procedure for the preparation of new derivatives of sulfanilamide. (Machine-translation by Google Translate, not legally binding) | |
GB1038721A (en) | Biologically active anthrones-lithium rheinanthrones | |
GB912131A (en) | Substituted glycolic acid esters of 1,4-bis-(hydroxy alkyl)-piperazines and process of preparing same | |
GB980854A (en) | 5-acyloxyuracils | |
GB937598A (en) | Process for the production of reserpic acid diesters | |
GB911488A (en) | Improvements in or relating to photographic materials | |
GB1074274A (en) | A process for the production of bis-(2-hydroxyethyl) terephthalates | |
ES340049A1 (en) | Procedure for the production of derivatives of sulfonilic urea. (Machine-translation by Google Translate, not legally binding) | |
GB2002808A (en) | Particulate additive for detergent compositions |