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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C14C3-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C14C3-18
filingDate 1994-09-20^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1995-05-23^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6d96568ae3c7648bb696e000ecd3688
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_397d052b4a6078bbe349653c726450f9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2484ca2cb06797ce0c74d0d47a515362
publicationDate 1995-05-23^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5417723-A
titleOfInvention Use of ester urethanes for retanning
abstract The present invention relates to a process for retanning chrome-tanned leather comprising applying to leather a reaction product of n (a) at least one glycerol monoester of a saturated C 12-18 monocarboxylic acid, n (b) at least one diisocyanate selected from the group consisting of toluene diisocyanate, hexamethylene diisocyanate, and isophorone diisocyanate, and n (c) dimethylolpropionic acid, n wherein n (i) the components (a), (b) and (c) are so selected that the molar ratio of the isocyanate groups of component (b) to the sum of the hydroxyl groups of components (a) plus (c) is about 0.5 to about 1.05 and n (ii) the molar ratio of compound (c) to compound (a) is about 0.7 to about 1.5 and wherein n (iii) the carboxyl groups originating from compound (c) are at least partly neutralized.
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priorityDate 1993-03-25^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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