http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-122020013212-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e2122663e9899d2eb18bcaa811431c85
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D319-12
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-11
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-12
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filingDate 2010-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e0a6499f9f21946039179097cff94ee9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b93a1d2577f78433c95194e6a4069aba
publicationDate 2021-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-122020013212-B1
titleOfInvention METHODS FOR THE FORMATION OF LACTILATE USING DILACTIDS
abstract the present invention involves a new synthetic route for the formation of lactylates. the method comprises reacting a dilactide with a compound comprising a hydroxy group. this reaction is preferably carried out in the presence of a cation or other source of alkalinity. preferred compounds comprising a hydroxy group include any fatty acid and fatty acid alcohol (particularly c1-c26 fatty acid chains). preferred cations include group i and ii metal cations, with sodium, calcium and potassium cations being particularly preferred. the reactions of the invention proceed much more quickly than the reactions of the prior art lactylate synthesis, and can be used to form 1-, 2-, 3-, 4- and 5-lactylates.
priorityDate 2010-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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