Manufacture of organic pigments

[6. A process as claimed in claim 3, in

• which the condensation is carried out at a pH of from 1.5 to 3.5.] 7. A process as [claimed] set forth in claim 2, in which the surfactants used are the alkali metal salts of sulfonic acids derived from alkylbenzenes where alkyl is of 3 to 15 carbon atoms, alkylnaphthalenes where alkyl is of 3 to 15 carbon atoms or alkylphenols where alkyl is of 3 to 15 carbon atoms or of condensation products of phenolsulfonic acids
• with formaldehyde and urea. 8. A process as [claimed] set forth in claim 2, in which the surfactants used are adducts obtained by the reaction of propylene oxide with ethylene glycol, propylene glycol or ethylenediamine, followed by reaction of the products with ethylene oxide.
• . A process as [claimed] set forth in claim 3, in which the surfactants used are adducts obtained by the reaction of propylene oxide with ethylene glycol, propylene glycol or ethylenediamine, followed
• by reaction of the products with ethylene oxide. 10. A process as [claimed] set forth in claim 1 wherein the reactant (B)
• is barbituric acid. 11. A process for the manufacture of an easily dispersed colorant of the formula ##STR23## wherein:
• ##STR24## is a radical of barbituric acid, N-methylbarbituric acid, N,N'-dimethylbarbituric acid, N,N'-diphenylbarbituric acid, 2-thiobarbituric acid or 2-iminobarbituric acid;
• and
• the o-phenylene radical is unsubstituted or substituted by chlorine, bromine, alkyl of 1 to 4 carbon atoms, phenyl, alkylcarbonylamino where alkyl is of 1 to 3 carbon atoms, benzoylamino, phenoxy, methoxy or ethoxy, the number of substituents being not more than 2;
• which process comprises:
• condensing (A) a compound of the formula ##STR25## wherein R' and R" each is hydrogen, alkyl of 1 to 4 cabon atoms, hydroxyalkyl of 2 or 3 carbon atoms, phenylalkyl of 7 or 8 carbon atoms or phenyl, with (B) barbituric acid, N-methylbarbituric acid, N,N'-dimethylbarbituric acid, N,N'-diphenylbarbituric acid, 2-thiobarbituric acid or 2-iminobarbituric acid, in the molar ratio of (A):(B) of 1:2, in water and in the presence of an acid selected from the group consisting of aliphatic carboxylic acids, aromatic carboxylic acids, aliphatic sulfonic acids, aromatic sulfonic acids, mineral acids and mixtures thereof, at a pH of from [1 to 6] 1.5 to 3.5 and at a temperature from 20.degree. to 150.degree. C. 12. A process as [claimed] set forth in claim 11, in which the condensation is carried out in the presence of an aliphatic carboxylic
• acid. 13. A process as [claimed] set forth in claim 11, in which the condensation is carried out in the presence of formic acid
• [at a pH of from 1.5 to 3.5]. 14. A process as [claimed] set forth in claim 11, in which the condensation is carried out in the presence of surfactants which may be alkali metal salts of sulfonic acids derived from alkylbenzenes where alkyl is of 3 to 15 carbon atoms, alkylnaphthalenes where alkyl is of 3 to 15 carbon atoms or alkylphenols where alkyl is of 3 to 15 carbon atoms or of condensation products of phenolsulfonic acid with formaldehyde and urea, or adducts obtained by reaction of propylene oxide with ethylene glycol, propylene glycol or ethylenediamine, followed by reaction of ethylene oxide with the products.
• 5. A process as [claimed] set forth in claim 12, in which the condensation is carried out in an aqueous aliphatic carboxylic acid solution which contains from 5 to 40% by weight, based on the
• solution, of carboxylic acid. 16. A process as [claimed] set forth in claim 12, in which the condensation is carried out in an aqueous aliphatic carboxylic acid solution which contains from 10 to 20%
• by weight, based on the solution, of carboxylic acid. 17. A process as [claimed] set forth in claim 11 wherein the reactant (B) is barbituric acid.