http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006047110-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_225bd5721d711494d3b6ae0baa985cc6 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H13-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-08 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08B31-00 |
filingDate | 2005-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_40c49f288898da4a8d790a86d8ddaf72 |
publicationDate | 2006-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-2006047110-A1 |
titleOfInvention | Synthesis of alkoxylated sucrose esters |
abstract | A process for the preparation of an alkoxylated sucrose ester including the steps of: forming an initial reaction mixture of a sucrose ester and from about 0.01% to about 5% of a catalyst; and forming an initial reaction product by reacting the initial reaction mixture with an epoxide for a period of time in the range of from about 30 minutes to about 6 hours and at a temperature in the range of from about 80° C. to about 120° C.; wherein the epoxide and the sucrose ester are selected such that a mole ratio of epoxide groups to sucrose hydroxyls is from about 1 to about 100. Useful catalysts include sodium metals, potassium metals, sodium/potassium alloys, and mixtures thereof |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9284518-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010160621-A1 |
priorityDate | 2004-08-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 69.