http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-102012206183-B4

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_79b5f9d76648dfc226a261cfb970de9c
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09D11-34
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09D11-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B41J2-015
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09D11-34
filingDate 2012-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e62a9a7d6e956390bd048ba9ddce3d0a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bdfd81b62649087af9e182cca89d4751
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d1f4fb3877a62116ebd93c7c411ec6ab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11cf897a3a207a14c5e27067c6720b85
publicationDate 2018-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-102012206183-B4
titleOfInvention Hot melt ink composition, their use in ink jet printing processes and printing processes
abstract A hot melt ink comprising one or more oxazoline compounds and / or one or more oxazoline derivatives, the ink composition further comprising: an optional colorant; at least one crystalline phase transformation agent, at least one amorphous binder; optionally one or more additives; wherein the at least one amorphous binder, the at least one phase change agent, and / or the optional additive or additives of said hot melt ink composition comprises one or more substituted oxazoline compounds and / or one or more substituted oxazoline derivatives wherein the one or more oxazoline compounds and / or substituted oxazoline derivatives are one or more compounds according to the following general formulas: wherein R 1 is an alkylene group, arylene group, arylalkylene group, alkylarylene group, and R 2 is an alkyl group, aryl group, alkylaryl group, aromatic group, a hydrogen, - (C = O) - (CH 2 ) n CH 3 , where n is zero or an integer in the range of 1 to 50, or wherein R y = H, OH, OCH 3 , Cl, Br, F, I, NH (COCH 3 ), CH 3 , CH 2 CH 3 , isopropyl, t-butyl, CO 2 CH 3 , CO 2 H, an alkyl group Is 1 to 66 carbons, or an alkoxy group of 1 to 8 carbons, or - (C = O) -NH-R z wherein R z is either a linear alkyl group of formula - (CH 2) n CH 3, wherein n is either zero or an integer in the range of 1 to 36, or wherein R z is an alkylaryl group of 6 to 20 carbon atoms; wherein R 4 is an alkyl group, aryl group, alkylaryl group, or an aromatic group; R 5 is an alkyl group, aryl group, alkylaryl group, aromatic group, a hydrogen, - (C = O) - (CH 2 ) n CH 3 , wherein n is zero or an integer in the range of 1 to 50, or wherein R y = H, OH, OCH 3 , Cl, Br, F, I, NH (COCH 3 ), CH 3 , CH 2 CH 3 , isopropyl, t -butyl, CO 2 CH 3 , CO 2 H, an alkyl group with 1 to 66 carbons, or an alkoxy group of 1 to 8 carbons, or - (C = O) -NH-R z where R z is either a linear alkyl group of the formula - (CH 2 ) n CH 3 where n is zero or an integer of 1 to 36, or wherein R z is an alkylaryl group of 6 to 20 carbon atoms; R 6 is an alkylene group, arylene group, arylalkylene group, alkylarylene group, wherein n is an integer ranging from 6 to 36, a branched alkylene group of the general formula C 36 H 64 + n , where n is defined as an integer in the range from 0 to 8, or wherein m is an integer of 1 to 100, wherein R 7 is an alkyl group, aryl group, or an aromatic group; and R 8 is an alkylene group, arylene group, arylalkylene group, alkylarylene group, wherein n is an integer ranging from 6 to 36, a branched alkylene group of the general formula C 34 H 60 + n , in which n is an integer in the range from 0 to 8, or or wherein R 9 is an alkyl group, aryl group, alkylaryl group, or aromatic group; R 10 , R 11 , R 12 and R 13 is the same or different and is an alkyl group, aryl group, alkylaryl group, alkoxy group, or aromatic group, a hydroxyalkyl of 1 to 60 carbons, an alkyl ester of 1 to 60 carbons, or an aryl ester wherein at least one of R 9 , R 10 , R 11 , R 12 and R 13 is an aromatic group; or Mixtures thereof.
priorityDate 2011-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID105034
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415761015
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18503
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426080535
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416022856
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414860678
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID585129
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413959477
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423390498
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID85760
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415730097
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424479044
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22825
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419587169
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12736
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413959593
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9322
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457815268
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID468036613
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414352241
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426078868
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413957613
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415730120

Total number of triples: 302.