http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-0161597-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-86
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-86
filingDate 1995-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0bb56b5f24da3bce529aa8323d9bf1b7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9fe23f9f981bf412b39d941b759a0993
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed4a0ad6a4a6013d907c62c73a5971e2
publicationDate 1999-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-0161597-B1
titleOfInvention Method for preparing acetylsalicylic acid DL-lysine salt
abstract In the present invention, acetylsalicylic acid is dissolved in 94% to 96%, in particular 95% ethanol, treated with activated carbon, aseptically treated, then sterilized and then slowly added aseptic powdery DL-lysine or its monohydrate while stirring under cooling. Thereby crystallizing the acetylsalicylic acid DL-lysine salt, and the crystallized DL-lysine salt is filtered under vacuum, washed with a solvent, and dried under vacuum. According to the method of the present invention, since no external water is added during the reaction, it is possible to recover the entire amount of the high-purity ethanol used after the reaction is completed without changing the purity, and it is economical, and crystallization of DL-lysine salt of acetylsalicylic acid is greatly precipitated. This provides the advantage of easy recovery of the crystals.
priorityDate 1995-07-07-04:00^^<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.