GB1014043A - Isocyanate compositions - Google Patents
Isocyanate compositionsInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C265/00—Derivatives of isocyanic acid
- C07C265/14—Derivatives 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.
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)
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 |
-
1963
- 1963-07-01 GB GB2601763A patent/GB1014043A/en not_active Expired
Cited By (5)
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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