GB673611A - Stabilization of nuclear chlorostyrenes by 2,6-dinitrophenols - Google Patents
Stabilization of nuclear chlorostyrenes by 2,6-dinitrophenolsInfo
- Publication number
- GB673611A GB673611A GB2211450A GB2211450A GB673611A GB 673611 A GB673611 A GB 673611A GB 2211450 A GB2211450 A GB 2211450A GB 2211450 A GB2211450 A GB 2211450A GB 673611 A GB673611 A GB 673611A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chlorostyrenes
- dinitrophenol
- chlorostyrene
- per cent
- dinitrophenols
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/38—Separation; Purification; Stabilisation; Use of additives
- C07C17/42—Use of additives, e.g. for stabilisation
Abstract
A process for the stabilization against polymerization of nuclear chlorostyrenes containing not more than two chlorine atoms per molecule comprises dissolving in the chlorostyrene an inhibitor consisting of a 2,6-dinitrophenol <FORM:0673611/IV (b)/1> where R is hydrogen or an alkyl or cycloalkyl group containing not more than 6 carbon atoms. The chlorostyrenes may be pure individual compounds or mixtures, e.g. such as are produced by pyrolysis of mono-ethylated mono-and di-chlorobenzenes, by the dehydration of nuclearly chlorinated phenyl ethyl alcohols, and by the dechlorination of nuclearly chlorinated chlorethyl benzenes. Radicals represented by R mentioned are methyl, ethyl, propyl, butyl and cyclohexyl. Amounts of the inhibitor between 0.05 and 5 per cent by weight on the weight of chlorostyrene are mentioned. Examples show compositions of (1) mixed 2-, 3-, and 4-chlorostyrenes with 1 per cent of 2,6-dinitrophenol; (2) mixed 2-and 4-chlorostyrenes with 1 per cent of various 2,6-dinitrophenols; (3) pure 4-chlorostyrene and 2,6-dinitrophenol; (4) 2,5-dichlorostyrene and 2,6-dinitrophenol. The viscosity of the mixtures before and after heating to 100 DEG or 130 DEG C. is shown, and for comparison the results using other inhibitors under the same conditions is given.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2211450A GB673611A (en) | 1950-09-07 | 1950-09-07 | Stabilization of nuclear chlorostyrenes by 2,6-dinitrophenols |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2211450A GB673611A (en) | 1950-09-07 | 1950-09-07 | Stabilization of nuclear chlorostyrenes by 2,6-dinitrophenols |
Publications (1)
Publication Number | Publication Date |
---|---|
GB673611A true GB673611A (en) | 1952-06-11 |
Family
ID=10174120
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2211450A Expired GB673611A (en) | 1950-09-07 | 1950-09-07 | Stabilization of nuclear chlorostyrenes by 2,6-dinitrophenols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB673611A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1076668B (en) * | 1956-05-26 | 1960-03-03 | Distillers Co Yeast Ltd | Process for the preparation of 2-chlorobutadiene-1, 3 |
DE1092005B (en) * | 1958-03-27 | 1960-11-03 | Basf Ag | Stabilization of ethylenically unsaturated, polymerizable, monomeric compounds against polymerization |
-
1950
- 1950-09-07 GB GB2211450A patent/GB673611A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1076668B (en) * | 1956-05-26 | 1960-03-03 | Distillers Co Yeast Ltd | Process for the preparation of 2-chlorobutadiene-1, 3 |
DE1092005B (en) * | 1958-03-27 | 1960-11-03 | Basf Ag | Stabilization of ethylenically unsaturated, polymerizable, monomeric compounds against polymerization |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB988633A (en) | Self-extinguishing alkenyl aromatic polymeric compositions | |
GB874006A (en) | Flame retardant polyolefine mixtures | |
GB673611A (en) | Stabilization of nuclear chlorostyrenes by 2,6-dinitrophenols | |
GB972153A (en) | Process for production of acetylene by regenerative thermal decomposition of hydrocarbons | |
GB927739A (en) | Tetracycline compounds and preparation thereof | |
GB910033A (en) | A process for the production of synthetic polypropylene filamentary materials | |
ES278066A1 (en) | Method of preparation of a compound corresponding to the formula (Machine-translation by Google Translate, not legally binding) | |
GB882037A (en) | Stabilized polyolefins | |
GB1000194A (en) | Aziridine compounds and method of preparing same | |
GB889090A (en) | Stabilised olefine polymers | |
GB938845A (en) | Production of acetylene and ethylene by incomplete combustion of hydrocarbons | |
ES271457A1 (en) | Procedure for obtaining polymer compositions (Machine-translation by Google Translate, not legally binding) | |
GB892775A (en) | New phosphorus nitrilo compounds | |
GB875151A (en) | Improvements in antiozonants for rubber | |
GB885612A (en) | Improvements in or relating to trialkyl aluminium compounds and their preparation | |
GB919068A (en) | Protective chemicals and method | |
GB957230A (en) | Tricyclic compounds and their manufacture | |
ES303532A1 (en) | A procedure for the stabilization of poliolephins. (Machine-translation by Google Translate, not legally binding) | |
GB1045036A (en) | New 1ª-methyl-í¸-5ª-androsten-17ª-ols and process for their manufacture | |
GB1096496A (en) | Improvements relating to the stabilization of halogenated hydrocarbons | |
GB838732A (en) | Polymer compositions | |
ES261724A1 (en) | 1-[3-(5-nitro-2-furyl)-2-propen-1-ylideneamino]-2-imidazolidinethione | |
GB997632A (en) | New pyrimidines and process for their manufacture | |
GB544890A (en) | Halogenated organic compounds and compositions containing the same | |
ES239621A1 (en) | Procedure for the preparation of detergents (Machine-translation by Google Translate, not legally binding) |