GB816888A - Improvements in or relating to polyfunctional surface-active agents - Google Patents

Improvements in or relating to polyfunctional surface-active agents

Info

Publication number
GB816888A
GB816888A GB609257A GB609257A GB816888A GB 816888 A GB816888 A GB 816888A GB 609257 A GB609257 A GB 609257A GB 609257 A GB609257 A GB 609257A GB 816888 A GB816888 A GB 816888A
Authority
GB
United Kingdom
Prior art keywords
chloride
groups
tertiary amine
protein
halogenated acid
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
GB609257A
Inventor
Jean Bolle
Pierre Ragon
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.)
INNOVATIONS CHIMIQUES SINNOVA
Original Assignee
INNOVATIONS CHIMIQUES SINNOVA
Filing date
Publication date
Application filed by INNOVATIONS CHIMIQUES SINNOVA filed Critical INNOVATIONS CHIMIQUES SINNOVA
Publication of GB816888A publication Critical patent/GB816888A/en
Expired legal-status Critical Current

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  • Peptides Or Proteins (AREA)

Abstract

A protein product, useful as a surface-active agent, comprising quaternary ammonium groups and salifiable carboxyl groups, is produced by reacting a degraded protein with a halogenated acid chloride and condensing the reaction product with a tertiary amine. The degraded protein containing liberated SH groups may first be condensed through a Schotten-Baumann process with strongly reactive halogenated acid chlorides to form thioester groups, and then the halogen still available in the degraded protein reacted with a tertiary amine to obtain a quaternary ammonium compound. The protein degradation product may be obtained from vegetable proteins, e.g. gliadine, animal proteins, e.g. fibrin or gelatin, or fish proteins. Halogenated acid chlorides specified are chloroacetyl chloride, a -chloropropionyl-, a -chlorobutyryl-, a -chlorolauryl and a -chlorophenylacetyl-chloride, di- and tri-chloroacetyl chloride, chloroacetylamidobenzoyl- and chloromethylbenzoyl-chloride, and a -b -dichloropropionyl chloride. The tertiary amine may be a straight-chain tertiary amine, e.g. octyldimethyl-, lauryldimethyl-, lauryldiethyl-, or myristyldimethyl-amine, or branched-chain tertiary amines, e.g. ethylhexyl dimethyl-, t-octyldimethyl-, or t-dodecyldimethylamine, hydroaromatic or arylaliphatic amines, e.g. dodecyldimethylaniline or dodecyldimethyl benzylamine, and tertiary amines containing other functional groups, e.g. dimethylaminoethanol esters or diamines of amides.
GB609257A 1957-02-22 Improvements in or relating to polyfunctional surface-active agents Expired GB816888A (en)

Publications (1)

Publication Number Publication Date
GB816888A true GB816888A (en) 1959-07-22

Family

ID=1628509

Family Applications (1)

Application Number Title Priority Date Filing Date
GB609257A Expired GB816888A (en) 1957-02-22 Improvements in or relating to polyfunctional surface-active agents

Country Status (1)

Country Link
GB (1) GB816888A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2603402C2 (en) * 2013-06-17 2016-11-27 Институт Одлевництва Composition of ceramic layer for making moulds and other articles

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2603402C2 (en) * 2013-06-17 2016-11-27 Институт Одлевництва Composition of ceramic layer for making moulds and other articles

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