http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S55167266-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6db78e3c1e9bf1b878d149a4db7c019d
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-075
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-00
filingDate 1979-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_21d9530a596d3c91c7cedb36f4fec5fe
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publicationDate 1980-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S55167266-A
titleOfInvention Recovery of alpha-l-aspartyl-l-phenylalanine lower alkyl ester
abstract PURPOSE: To recover the titled compound useful as a low-caloric sweetening agent, by adding a basic substance to an aqueous solution containing at least 3-benzyl-6- carboxymethyl-2,5-diketopiperazine as an impurity, and by crystallizing the titled compound. n CONSTITUTION: A basic substance, e.g. NaOH, is added to an aqueous solution of an α-L-aspartyl-L-phenylalanine lower alkyl ester(α-APE) containing at least 3-benzyl-6-carboxymethyl-2,5-diketopiperazine (DKP) as an impurity to crystallize and recover the isolated α-APE. Preferably, the pH of the aqueous solution is kept at 4.5W8 after the addition of the basic substance at a relatively high temperature, and the crystals are deposited most efficiently by cooling the mixture immediately after the addition. n EFFECT: DKP which cannot be effectively removed by the conventional recrystallization method can be readily eliminated. n COPYRIGHT: (C)1980,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5621137-A
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priorityDate 1979-06-15-04:00^^<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: 27.