http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2003238-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G59-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C235-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G59-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C235-02
filingDate 1970-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8fd7c35b1e22c7afc7804a9865ac59d8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3b53a858c5ee9ddc58439c40bc43ec3
publicationDate 1971-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2003238-A1
titleOfInvention Hydroxypivalic acid amide
abstract Hydroxypivalic acid aminde (I) is prepared by reacting neopentylglycol monohydroxypivalate (II) with excess NH3 in a closed vessel at 100-200 degrees C to form (I) and neopentylglycol (III) and separating the two products. (I) promotes reaction of epoxide cpds. with cpds. containing basic NH- or NH2 groups (amine hardening of epoxy resins). Hardening times of polyepoxides with polyamides or amidoamines are reduced by 25-40% by addition of 0.1-7 (0.5-4) % (I). (I) is also useful as intermediate for pharmaceuticals and plastics. (III) is useful as diol component of polyesters.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0266690-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0266690-A2
priorityDate 1970-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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