http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004094497-A1

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filingDate 2004-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52065b4d6b2524eef2d3414f42807f6e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8eb31d6d899e3da56dbdfbccc2cb1f7f
publicationDate 2004-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2004094497-A1
titleOfInvention Crosslinking composition
abstract This invention relates to a crosslinking composition comprising a compound having the structure of Formula I: A’-NRA-RD where A’ is a moiety derived from the group consisting of linear or cyclic ureas, cyanuric acid, substituted cyanuric acids, linear or cyclic amides, glycolurils, hydantoins, linear or cyclic carbamates and mixtures thereof, or a moiety comprising the structure: Where RA is RD, hydrogen, an alkyl of 1 to 20 carbon atoms, or taken together with A’ forms a cyclic compound; RD is-CHRC ORB, wherein RBis hydrogen, alkyl, aryl, aralkyl or an alkaryl having from 1 to about 24 carbon atoms and RC is an alkyl, halogenated alkyl, aryl, aralkyl, halogenated aralkyl, alkoxyalkyl or an alkaryl having from 1 to about 24 carbon atoms; A is a moiety derived from the group consisting of linear or cyclic ureas, cyanuric acid, substituted cyanuric acids, linear or cyclic amides, glycolurils, hydanoins, linear or cyclic carbamates and mixtures thereof; B is a residue of a poly(alkylaldehyde) with n aldehyde groups; n is an integer of 2 to about 8; Ra is Rd, hydrogen, an alkyl of 1 to about 20 carbon atoms, or taken together with A forms a cyclic compound; where Rd is CHRCORbor where Rb is hydrogen, alkyl, aryl, aralkyl or an alkaryl having from 1 to about 24 carbon atoms and RC is an alkyl, halogenated alkyl, aryl, aralkyl, halogenated aralkyl, alkoxyalkyl or an alkaryl having from 1 to about 24 carbon atoms; and where the alkyl or aryl groups in each radical may optionally have heteroatoms in their structure. This invention also relates to a process for producing the crosslinking composition by reacting an amino compound containing amino groups; a mono(alkylaldehyde) and/or a poly(alkylaldehyde), and an alcohol; where said amino compound is selected from the group consisting of: linear or cyclic ureas, cyanuric acid, substituted cyanuric acids, linear or cyclic amides, glycolurils, hydantoins, linear or cyclic carbamates and mixtures thereof.
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priorityDate 2003-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523358
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID141097068
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID232013703
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559464
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129249196
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6560
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394128
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID702
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135861049
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID62705
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6561
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448469429
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226426547
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127427273
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID25457
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21896498
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128023837
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID89549914
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID31289
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419842142
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10006
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127427561
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415721314
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226551332
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135747202
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416290180
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID89549916
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID90363356
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID996
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7371
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID31234
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1030
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450273274
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11596
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID90191729
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419589325
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393245
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7532
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419576745
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID521998
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54390233
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129752010
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69034
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67989503
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID453
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67989504

Total number of triples: 336.