http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-201431965-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_59a9fce1101cb36f49b4e59e6569ef1f
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G77-26
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L83-08
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02B1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08L83-07
filingDate 2013-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dec9d1c78e274f6fee2abfcc62f799e1
publicationDate 2014-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-201431965-A
titleOfInvention Contact lens material, method of manufacturing contact lens, and contact lens manufactured thereby
abstract The present invention provides a contact lens material comprising: a first oxane alkane having a number average molecular weight of about 1,000 to 10,000 and having a crosslinking function, and is represented by the formula (I): □ in the formula (I) Wherein R1, R2 and R3 are each independently a C1-C4 alkyl group, and R4 is a C1-C6 alkenyl group, a C1-C6 alkylene group or a C1-C6 alkylene group having an ether functional group, and R5 is O or NH. R6 is a C1-C6 alkenyl group, a C1-C6 alkylene group or a C1-C6 alkylene group containing an ether functional group, and R7 is hydrogen, a C1-C6 alkylene group or a C1-C6 alkylene group having an ether functional group. , R 8 is a residue having a reactive functional group of a hydroxyl group, an acid group, an epoxy group or an acid anhydride functional group; a second alkoxy alkane giant is selected as a macrosiloxane represented by the formula (II) And a group consisting of a macrosiloxane represented by the formula (III): □ □ at least one hydrophilic monomer; and a starter.
priorityDate 2013-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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