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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-65748
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-527
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-6578
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6578
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6574
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-527
filingDate 1995-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1996-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6416dd5ea374aac0159c4c618758cc3
publicationDate 1996-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5565600-A
titleOfInvention Alkyl-aromatic diphosphites
abstract Novel alkyl-aromatic diphosphites having antioxidant and flame-retarding abilities and corresponding to the formula: <IMAGE> can be prepared by reacting a 2,2'-bridged bisphenol corresponding to the formula: <IMAGE> with pentaerythritol dichlorophosphite at 20-150 DEG C. in the presence of a basic catalyst; R and R' in the formulas representing hydrocarbyl groups, R'' being a divalent bridging group, and n being 0 or 1. These diphosphites have good hydrolytic stability per se and can be made even more resistant to hydrolysis by stabilizing them with at least 0.5% by weight of an acid scavenger, preferably before they are recovered from their synthesis reaction mixtures.
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priorityDate 1991-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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