http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6114221-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-00
filingDate 1984-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aeaa37e7afb1ba493a49e37c6496ad1f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3fbd6a85e952b5c2dec957bbfb675d96
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b553773c41719cbe1be29399cbcf5777
publicationDate 1986-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6114221-A
titleOfInvention Production of thermoplastic polyurethane of excellent mold resistance
abstract PURPOSE: To produce the titled polyurethane, by reacting a specified polyester- diol with an organic diisocyanate at a predetermined ratio and chain-extending the prepolymer. n CONSTITUTION: A hydroxyl group-terminated polyesterdiol (of an MW of 800W 1,500) is obtained by reacting 3-methyl-1,5-pentanediol with a dicarboxylic acid (e.g., adipic, succinic or sebacic acid). Said polyesterdiol is reacted with an organic diisocyanate (e.g., 4,4'-diphenylmethane diisocyanate) in an amount satisfying the relationship (wherein M is the average MW of the polyester-diol and R is a molar ratio of the organic diisocyanate to the polyester-diol) at a temperature ≤about 120°C, and the obtained isocyanate-terminated prepolymer is reacted with a chain extender (e.g., 1,4-butanediol) at about 50W160°C. n COPYRIGHT: (C)1986,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63202613-A
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priorityDate 1984-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 32.