Branched chain dodecyl isomeric mixtures of 2-(5-dodecyl-2-hydroxy phenyl) benzotriazole as stabilizers for heat and light sensitive materials

Claim 2

A normally liquid composition for stabilizing heat and light sensitive materials consisting essentially of a mixture of branched-chain dodecyl isomers of 2-(5'-dodecyl-2'-hydroxyphenyl) benzotriazole said mixture having a melting point below 0°C.

Claim 3

The composition according to claim 1 which is substantially free of n-dodecyl isomer and wherein the predominant proportion of the dodecyl isomers contains a preponderance of carbon atoms in the alkyl carbon backbone connected to the hydroxyphenyl group.

Claim 4

The composition according to claim 2 wherein the mixture of branched chain dodecyl isomers contains at least 70% by weight of dodecyl isomers having at least 7 carbon atoms in the alkyl carbon backbone connected to the hydroxyphenyl group, with respect to the total isomeric mixture.

Claim 5

The composition of claim 2 wherein the isomeric mixture contains at least 4 isomers.

Claim 6

The composition of claim 4 wherein the isomeric mixture contains 6 to 12 isomers.

Claim 7

The composition of claim 2 wherein the composition has a melting point below 0°C and a boiling range between 190° and 260°C at 0.02-0.05 mm Hg pressure.

Claim 8

A process for the preparation of the composition of claim 1 which comprises: a. Coupling a 2-nitrophenyl diazonium salt with a normally liquid mixture of branched chain dodecyl isomers of 4-dodecyl phenol in the presence of glacial acetic acid and an alkali metal salt of a carboxylic acid at a pH between about 3 and about 5.5 at below 15°C to form the corresponding branched chain dodecyl isomeric mixture of 2-(2'-nitro-phenylazo)-4-dodecylphenols; and b. Cyclizing said branched chain isomeric mixture of said 2-(2'-nitrophenylazo)-4-dodecylphenols to the corresponding branched chain dodecyl isomeric mixture of triazoles in a solution with a zinc catalyst in the presence of a mineral acid to form the corresponding normally liquid mixture of claim 1 as the product of the process.

Claim 9

The process of claim 7 wherein the isomeric mixture of 4-dodecyl phenols contains a predominant proportion of dodecyl isomers having a preponderance of carbon atoms in the alkyl carbon backbone connected to the hydroxyphenyl group.

Claim 10

The process of claim 7 wherein the isomeric mixture of 4-dodecylphenols contains at least 4 isomeric forms.

Claim 11

The process of claim 7 wherein the product of step (b) is contacted with between about 5 and about 30 mole percent of an organic anhydride selected from the group of alkyl anhydride having from 4 to 8 carbon atoms, phthalic anhydride and succinic anhydride and distilling the resulting liquid under vacuum, 0.01 to 0.15 mm Hg pressure, to separate a distillate fraction boiling between about 180° and about 250°C and recovering the corresponding normally liquid mixture of branched chain dodecyl isomers of 2-(5'-dodecyl-2'-hydroxyphenyl)benzotriazole.

Claim 12

The process of claim 10 wherein the organic anhydride is acetic anhydride.

Claim 13

The process of claim 10 wherein the normally liquid distilled mixture is contacted with oxygen and redistilled under 0.02 mm to 0.06 mm Hg pressure to separate a distillate fraction boiling between about 180° and about 230°C and recovering the corresponding normally liquid mixture of branched chain dodecyl isomers of 2-(5'-dodecyl-2'-hydroxyphenyl)benzotriazole.

Claim 14

The process of claim 12 wherein the normally liquid distilled mixture is contacted with air at a temperature between about 50° and about 150°C.