http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4476253-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G18-10
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-65
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-32
filingDate 1984-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1984-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fb9b7b2548880b1e0fc3d8390eeb162c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b0fb0ba116a8233cd625ab0e303bda1f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77263a29ab94e48b6fbf5dc30845d886
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publicationDate 1984-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4476253-A
titleOfInvention Process for the preparation of polyurethane elastomers using diols of the anhydro-tetritol series
abstract Polyurethane elastomers are made by reacting organic polyisocyanates with compounds having at least two groups containing isocyanate-reactive hydrogen atoms and a molecular weight of from 400 to 10,000 and a 1,4-monoanhydro-tetritol in accordance with techniques known to those in the art. Known chain-lengthening agents, auxiliaries and additives may be included in the reaction mixture. The reaction mixtures employed in the process of the present invention have a longer pot life than prior art reaction mixtures. The elastomers produced by this process are shrink stable.
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priorityDate 1983-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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