Abstract: The present invention relates to a process for preparing a beta-phase metal phthalocyanine pigments in which(a) a crude metal phthalocyanine having an average particle size of about 10 to about 200 .mu.M is dry milled until the average particle size is reduced to about 0.01 to about 0.5 .mu.m;(b) the milled metal phthalocyanine is finished by thoroughly mixing said metal phthalocyanine with at least about 4 parts by weight, relative to the metal phthalocyanine, of a finishing solvent containing a mixture of(i) about 5 to 100 percent by weight, based on the total amount of finishing solvent, of a monocarboxylic acid monoester, dicarboxylic acid diester, diol diester, lactone, or cyclic carbonate, or a mixture thereof, and(ii) 0 to about 95 percent by weight, based on the total amount of finishing solvent, of water;(c) the ester used in step (b) is hydrolyzed; and(d) the beta-phase metal phthalocyanine pigment is collected.

Abstract: A process for the production of a .beta.-form copper phthalocyanine having a particle size of 0.005 to 0.2 .mu.m and an aspect ratio of 1 to 3, which comprises the following steps:a. dry-milling a crude copper phthalocyanine in a milling apparatus until the resultant dry-milled product has an .alpha.-crystal content of more than 45% by weight,wet-milling the resultant dry-milled product in the presence of a water-soluble inorganic salt and at least one organic liquid selected from the group consisting of water-soluble alkylene glycols having 2 to 3 carbon atoms and polyoxyalkylene glycols, wherein the inorganic salt is used in an amount that is 2 to 10 times, by weight, as large as that of the dry-milled copper phthalocyanine, and wherein the organic liquid is used in an amount that is 0.1 to 2 times, by weight, as large as that of the dry-milled copper phthalocyanine, andc. removing the inorganic salt and the organic liquid from the resultant wet-milled product.

Abstract: Compounds of the formula: ##STR1## wherein one X is COOR, CH.sub.2 COOR, CH(COOR).sub.2, CONHR, CH.sub.2 CONHR, or CNremaining X's are H, F, CH.sub.3, OH, COOR, CH.sub.2 COOR, CH(COOR).sub.2, CONHR, CH.sub.2 CONHR, or CN;Y is ##STR2## R is H, alkyl of 1-5 carbon atoms, or benzyl; R.sub.1 is CH.sub.2 OR.sub.3, COOR, or CONHR;R.sub.2 is H, OR.sub.3, or BR;R.sub.3 is H, COR.sub.4, or tetrahydropyranyl;R.sub.4 is alkyl of 1-5 carbon atoms or benzyl;R.sub.5 is H or COR.sub.4 ;represents a single or double bond;represents .alpha.-position, .beta.-position, or a mixture of .alpha.- and .beta.-positions; and--- represents .alpha.-position;and methods for preparing the same.