GB537744A - Manufacture of thiazolinyl sulphide derivatives and their use as vulcanisation accelerators - Google Patents

Manufacture of thiazolinyl sulphide derivatives and their use as vulcanisation accelerators

Info

Publication number
GB537744A
GB537744A GB17340A GB17340A GB537744A GB 537744 A GB537744 A GB 537744A GB 17340 A GB17340 A GB 17340A GB 17340 A GB17340 A GB 17340A GB 537744 A GB537744 A GB 537744A
Authority
GB
United Kingdom
Prior art keywords
give
thiazolinylsulphide
vulcanization accelerators
mercaptothiazoline
formaldehyde
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
GB17340A
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB17340A priority Critical patent/GB537744A/en
Publication of GB537744A publication Critical patent/GB537744A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/08—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D277/12—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/16—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0025—Crosslinking or vulcanising agents; including accelerators

Abstract

537,744. Thiazolinylsulphide derivatives ; vulcanization accelerators. BAIRD, W., FOWKES, F. S., NETTLESHIP, G. E., and IMPERIAL CHEMICAL INDUSTRIES, Ltd. Jan. 3, 1940, No.' 173. [Class 2 (iii)] [Also in Group V] Products stated to be useful as vulcanization accelerators are prepared by combining 2- mercaptothiazoline, formaldehyde and a primary or secondary amine containing not more than 12 carbon atoms. A hydroxy, methoxy or ethoxy group may be present in the amine. In examples, 2-mercaptothiazoline and formaldehyde are reacted with aniline to give anilinomethylthiazolinyl sulphide, with cyclohexylamine to give cyclohexylaminomethyl-2- thiazolinylsulphide, with p-n-butylaniline to give p-n-butylanilinomethyl-2-thiazolinylsulphide, with monoethanolamine to give #- hydroxyethylaminomethyl - 2 - thiazolinylsulphide and with hexamethyleneimine to give hexamethyleneiminomethyl - 2 - thiazolinesulphide. In further examples, the products are used as vulcanization accelerators in mixtures of smoked rubber sheet, zinc oxide, channel black (or blanc fixe), stearic acid and sulphur. Specification 287,001, [Class 2 (iii)], is referred to.
GB17340A 1940-01-03 1940-01-03 Manufacture of thiazolinyl sulphide derivatives and their use as vulcanisation accelerators Expired GB537744A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB17340A GB537744A (en) 1940-01-03 1940-01-03 Manufacture of thiazolinyl sulphide derivatives and their use as vulcanisation accelerators

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB17340A GB537744A (en) 1940-01-03 1940-01-03 Manufacture of thiazolinyl sulphide derivatives and their use as vulcanisation accelerators

Publications (1)

Publication Number Publication Date
GB537744A true GB537744A (en) 1941-07-04

Family

ID=9699695

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17340A Expired GB537744A (en) 1940-01-03 1940-01-03 Manufacture of thiazolinyl sulphide derivatives and their use as vulcanisation accelerators

Country Status (1)

Country Link
GB (1) GB537744A (en)

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