GB673611A - Stabilization of nuclear chlorostyrenes by 2,6-dinitrophenols - Google Patents

Stabilization of nuclear chlorostyrenes by 2,6-dinitrophenols

Info

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
Application number
GB2211450A
Inventor
Stevens S Drake
John L Lang
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.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
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 Dow Chemical Co filed Critical Dow Chemical Co
Priority to GB2211450A priority Critical patent/GB673611A/en
Publication of GB673611A publication Critical patent/GB673611A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/38Separation; Purification; Stabilisation; Use of additives
    • C07C17/42Use 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.
GB2211450A 1950-09-07 1950-09-07 Stabilization of nuclear chlorostyrenes by 2,6-dinitrophenols Expired GB673611A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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

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