JP2014136802A5 - - Google Patents

Info

Publication number

JP2014136802A5

JP2014136802A5 JP2014002923A JP2014002923A JP2014136802A5 JP 2014136802 A5 JP2014136802 A5 JP 2014136802A5 JP 2014002923 A JP2014002923 A JP 2014002923A JP 2014002923 A JP2014002923 A JP 2014002923A JP 2014136802 A5 JP2014136802 A5 JP 2014136802A5

Authority

JP

Japan

Prior art keywords

ink composition

composition according

group

butyl

substituted

Prior art date

2014-01-10

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Granted

Links

• Espacenet
• Global Dossier
• Discuss

• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 7
• 229920005862 polyol Polymers 0.000 claims 7
• 150000003077 polyols Chemical class 0.000 claims 7
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 3
• DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims 2
• 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims 2
• 125000001931 aliphatic group Chemical group 0.000 claims 2
• 125000000217 alkyl group Chemical group 0.000 claims 2
• 125000003118 aryl group Chemical group 0.000 claims 2
• 239000003086 colorant Substances 0.000 claims 2
• 150000001875 compounds Chemical class 0.000 claims 2
• 125000000753 cycloalkyl group Chemical group 0.000 claims 2
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
• 125000002877 alkyl aryl group Chemical group 0.000 claims 1
• -1 diester compound Chemical class 0.000 claims 1
• VSSBWJOYPQVXKX-UHFFFAOYSA-N dioctadecyl benzene-1,4-dicarboxylate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCCCCCCCCCCCC)C=C1 VSSBWJOYPQVXKX-UHFFFAOYSA-N 0.000 claims 1
• 229910052736 halogen Chemical group 0.000 claims 1
• 150000002367 halogens Chemical group 0.000 claims 1
• 229920001223 polyethylene glycol Polymers 0.000 claims 1
• 125000001424 substituent group Chemical group 0.000 claims 1
• 238000006467 substitution reaction Methods 0.000 claims 1
• 150000005846 sugar alcohols Chemical class 0.000 claims 1
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1