GB996245A - Substituted phenyl esters of benzene carboxylic acids, process for their production and polymer compositions containing them - Google Patents
Substituted phenyl esters of benzene carboxylic acids, process for their production and polymer compositions containing themInfo
- Publication number
- GB996245A GB996245A GB72962A GB72962A GB996245A GB 996245 A GB996245 A GB 996245A GB 72962 A GB72962 A GB 72962A GB 72962 A GB72962 A GB 72962A GB 996245 A GB996245 A GB 996245A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carbon atoms
- alkyl
- alkoxy
- styrene
- halogen
- 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
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/12—Esters; Ether-esters of cyclic polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention comprises compounds of formula <FORM:0996245/C2/1> wherein n is 1 or 2, R1, R2 and R3 are alkyl groups having a total of 3-23 carbon atoms, R4 is halogen, alkyl or alkoxy, x is 0-4 and the carboxyl groups are on non-adjacent carbon atoms. These compounds are made by reacting together the appropriate terephthalic, isophthalic or trimeric acid or their acid halides with a p-t-alkylphenol (or with an isomeric mixture of alkylphenols containing predominantly this isomer). A number of examples are provided in which the unsubstituted carboxylic acid chlorides are reacted with various phenols in presence of Mg, triethylamine or pyridine, and optionally benzene.ALSO:Polymers are stabilized against the effects of ultra-light by incorporating a compound of formula <FORM:0996245/C3/1> wherein n is 1 or 2, R1, R2 and R3 are alkyl groups having a total of 3-23 carbon atoms, R4 is halogen, alkyl or alkoxy, x is 0-4 and the carboxyl groups are on non-adjacent carbon atoms. The polymers may be derived from monomers having ethylenic unsaturation, or they may be cellulose derivatives (see Division B5), polyesters, epoxy resins, polyurethanes, phenolic resins, aminoplasts, polyamides, polyethers or polymeric aldehydes. Examples describe the stabilization of natural rubber film and chlorinated rubber, polyethylene, polypropylene, polystyrene, styrene-butadiene, styrene-acrylonitrile, ethylene-maleic anhydride, vinyl methyl ether-maleic anhydride, styrene-methyl methacrylate, poly(ethyl methacrylate), polyvinyl chloride, polyvinylidene chloride, vinyl chloride-vinylidene chloride; polymeric formaldehyde resin; and 1,5-pentanediol/sebacic acid/4,41-dicarboxydiphenylsulphone polyester.ALSO:Cotton, linen, regenerated cellulose, kapok, hemp, twines, wood-pulp, paper, cardboard and pressed board are stabilized against the effects of ultra-violet light by incorporating a compound of formula <FORM:0996245/D1-D2/1> wherein n is 1 or 2, R1, R2 and R3 are alkyl groups having a total of 3-23 carbon atoms, R4 is halogen, alkyl or alkoxy, x is 0-4 and the carboxyl groups are on or adjacent carbon atoms. In Example 3, a piece of filter paper is dipped in a 0.45% chloroform solution of [4 (1, 1, 3, 3-tetramethylbutyl) phenyl] 4-t-butylphenyl isophthalate and dried.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US8128061A | 1961-01-09 | 1961-01-09 | |
| US8127961A | 1961-01-09 | 1961-01-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB996245A true GB996245A (en) | 1965-06-23 |
Family
ID=26765423
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB72962A Expired GB996245A (en) | 1961-01-09 | 1962-01-08 | Substituted phenyl esters of benzene carboxylic acids, process for their production and polymer compositions containing them |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB996245A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0230741A2 (en) * | 1986-01-18 | 1987-08-05 | Technochemie GmbH - Verfahrenstechnik | Curable resins |
-
1962
- 1962-01-08 GB GB72962A patent/GB996245A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0230741A2 (en) * | 1986-01-18 | 1987-08-05 | Technochemie GmbH - Verfahrenstechnik | Curable resins |
| EP0230741A3 (en) * | 1986-01-18 | 1988-11-02 | Technochemie Gmbh | Curable resins |
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