http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5713999-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B48-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B67-20
filingDate 1996-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e10073801db4a51b2323185ddf72e2d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4b81b37fc4ee88d74697bfc7c2f0c417
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publicationDate 1998-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5713999-A
titleOfInvention Incorporation of pigment derivatives in quinacridone processes
abstract This invention relates to a process for the preparation of quinacridone pigments by n (a) heating, at a temperature of about 80° C. to about 145° C., a reaction mixture containing n (i) 2,5-dianilinoterephthalic acid, a 2,5-dianilino-3,6-dihydroterephthalic acid ester, and/or a derivative thereof, n (ii) about 3 to about 15 parts by weight, per part of component (a)(i), of a dehydrating agent, and n (iii) about 0.1 to about 15 percent by weight, based on component (a)(i), of one or more non-quinacridone pigments, n with the proviso that if component (a)(i) is a 2,5-dianilino-3,6-dihydroterephthalic acid ester or a derivative thereof, reaction step (a) additionally comprises an oxidation step; n (b) drowning the reaction mixture from step (a) by adding said reaction mixture to about 3 to about 15 parts by weight, per part of component (a)(i), of a liquid in which the quinacridone pigment is substantially insoluble; n (c) isolating the quinacridone pigment; n (d) optionally, conditioning the quinacridone pigment; and n (e) optionally, blending the resultant pigment with one or more quinacridone derivatives.
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priorityDate 1996-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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