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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B43-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B62-0064
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B62-006
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B43-44
filingDate 1995-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d3d0065cd79f16213229825bfea2cf10
publicationDate 1997-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-19527438-A1
titleOfInvention Process for the preparation of reactive azo dyes
abstract Prepn. of reactive amino-azo 1-naphthol sulphonic cid cpds. (I) of formula (A; X = a fibre-reactive heterocyclic gp.) comprises (a) hydrolysing maleamido-azo dyes (II) of formula (A:X = -CO-CH=CH-COOH); and (b) reacting with a reactive component X-Hal, without isolating the intermediate; m = 0 or 1; A = the radical of a diazo component; Hal = halogen, esp. Cl or F. (I) are useful for dyeing and printing natural or synthetic substrates contg. OH or amide gps., e.g. silk, leather, wool, synthetic polyamide fibres and esp. cellulosic fibres, e.g. linen, staple rayon, regenerated cellulose and partic. cotton. The process eliminates isolation of the intermediate amine after removing the protective acyl gp., which used to ensure selective coupling.
priorityDate 1995-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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