GB1014043A - Isocyanate compositions - Google Patents

Isocyanate compositions

Info

Publication number
GB1014043A
GB1014043A GB2601763A GB2601763A GB1014043A GB 1014043 A GB1014043 A GB 1014043A GB 2601763 A GB2601763 A GB 2601763A GB 2601763 A GB2601763 A GB 2601763A GB 1014043 A GB1014043 A GB 1014043A
Authority
GB
United Kingdom
Prior art keywords
phosphite
bis
hydroxyphenyl
tris
butyl
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
GB2601763A
Inventor
Derek Williams
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 GB2601763A priority Critical patent/GB1014043A/en
Publication of GB1014043A publication Critical patent/GB1014043A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C265/00Derivatives of isocyanic acid
    • C07C265/14Derivatives of isocyanic acid containing at least two isocyanate groups bound to the same carbon skeleton

Abstract

Isocyanates are stabilized by incorporating a mixture of a triaryl phosphite and a phenolic antioxidant. The triaryl phosphite is a compound of a formula (RO)3P, wherein R is an aryl radical which may be substituted in an aromatic nucleus. Examples specified are triphenyl phosphite, tricresyl phosphite, tris-(-p nonylphenyl)phosphite, tri - beta - naphthyl phosphite, tris - (p - chlorophenyl) - phosphite and tris - (p - nitrophenyl) phosphite. The phenolic antioxidant is a phenol having antioxidant properties and in particular an orthosubstituted phenol and phenols carrying substituents, especially alkyl and aralkoxy substituents, in each of the positions orthoto the phenolic hydroxyl group, and bis-phenols corresponding with the following formulae <FORM:1014043/C2/1> ; <FORM:1014043/C2/2> wherein A is an alkylene or alkylidene radical or a sulphur atom, R1 is an alkyl or an alkoxy group and R2, R3 and R4 are hydrogen atoms or alkyl groups and may be the same or different. Specified examples are 2-(a -methylcyclohexyl)-4 : 6 - dimethylphenol, 2 : 6 - di - t - butyl - 4 - methylphenol, bis - (2 - (a - methylcyclohexyl-5-methyl - 2 - hydroxyphenyl) - methane, bis-(3-t-butyl - 5 - methyl - 2 - hydroxyphenyl) - ethane, bis - (3 - t - butyl - 5 - methyl - 2 - hydroxyphenyl) sulphide and styrenated phenol. Also suitable are polyhydric phenols which may be substituted in the aromatic nucleus, such as propyl gallate, 4-t-butylcatechol and hydroquinone. Specification 866,396 is referred to.
GB2601763A 1963-07-01 1963-07-01 Isocyanate compositions Expired GB1014043A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2601763A GB1014043A (en) 1963-07-01 1963-07-01 Isocyanate compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2601763A GB1014043A (en) 1963-07-01 1963-07-01 Isocyanate compositions

Publications (1)

Publication Number Publication Date
GB1014043A true GB1014043A (en) 1965-12-22

Family

ID=10237049

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2601763A Expired GB1014043A (en) 1963-07-01 1963-07-01 Isocyanate compositions

Country Status (1)

Country Link
GB (1) GB1014043A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0445602A2 (en) * 1990-03-06 1991-09-11 BASF Aktiengesellschaft Process for the preparation of mixtures of diphenylmethane-diisocyanates and polyphenylmethylene-polyisocyanates with a reduced iodic colorimetric measure
EP0531803A2 (en) * 1991-09-09 1993-03-17 Sumitomo Bayer Urethane Co., Ltd. Method for preventing coloration of aromatic isocyanate compounds

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0445602A2 (en) * 1990-03-06 1991-09-11 BASF Aktiengesellschaft Process for the preparation of mixtures of diphenylmethane-diisocyanates and polyphenylmethylene-polyisocyanates with a reduced iodic colorimetric measure
EP0445602A3 (en) * 1990-03-06 1992-04-15 Basf Aktiengesellschaft Process for the preparation of mixtures of diphenylmethane-diisocyanates and polyphenylmethylene-polyisocyanates with a reduced iodic colorimetric measure
EP0531803A2 (en) * 1991-09-09 1993-03-17 Sumitomo Bayer Urethane Co., Ltd. Method for preventing coloration of aromatic isocyanate compounds
EP0531803A3 (en) * 1991-09-09 1993-05-19 Sumitomo Bayer Urethane Co., Ltd. Method for preventing coloration of aromatic isocyanate compounds
US5258548A (en) * 1991-09-09 1993-11-02 Sumitomo Bayer Urethane Co., Ltd. Method for preventing coloration of aromatic isocyanate compounds

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