http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2102183-B1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5b85d2c18cffe2787c0d94e12d6f61ea
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D319-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-12
filingDate 2007-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0a260d8c5cf892ce99c929a2ce3a4c6
publicationDate 2012-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2102183-B1
titleOfInvention Production of cyclic diesters of alpha-hydroxyacids
abstract The raw material used in m ost process for the production of cyclic diesters of alpha - hydroxiacids, such as Lactide and Glycolide, is a 10% solution of Hydroxyacid. During the evacuation of the solution and condensation reaction water, the organic molecules may be damaged. The prese nt process is caracterized by the use of reactants that bring as little water as possible to the reactor. In particular, for the production of Lactide, the main reactant may be anhydrous Calcium Lactate, that will react at about room temperature, for insta nce, with Sulfuric Anhydride, to give a solid mixture of Lactide, Calcium Sulfate Dihydrate and Calcium Sulfate Hemihydrate. Partial dehydration of the Dihydrate under mild temperature is followed by distillation of the Lactide out of the remaining powder of Calcium Sulfate Hemihydrate, and desublimation of the Lactide. Purification of the Lactide is done in situ in the desublimator.
priorityDate 2006-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 19.