JP2015120898A5 - - Google Patents

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Publication number

JP2015120898A5

JP2015120898A5 JP2014238949A JP2014238949A JP2015120898A5 JP 2015120898 A5 JP2015120898 A5 JP 2015120898A5 JP 2014238949 A JP2014238949 A JP 2014238949A JP 2014238949 A JP2014238949 A JP 2014238949A JP 2015120898 A5 JP2015120898 A5 JP 2015120898A5

Authority

JP

Japan

Prior art keywords

compound

group

urea

phase change

branched alkyl

Prior art date

2014-11-26

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
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• 150000001875 compounds Chemical class 0.000 claims 12
• 239000004202 carbamide Substances 0.000 claims 9
• 238000000034 method Methods 0.000 claims 8
• -1 n-amyl Chemical group 0.000 claims 8
• 239000012071 phase Substances 0.000 claims 7
• 125000000217 alkyl group Chemical group 0.000 claims 6
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 2
• 239000003086 colorant Substances 0.000 claims 2
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
• 238000010438 heat treatment Methods 0.000 claims 2
• 238000007641 inkjet printing Methods 0.000 claims 2
• 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 claims 2
• 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([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
• 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
• 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 claims 2
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
• 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
• 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
• 238000007599 discharging Methods 0.000 claims 1
• 238000011067 equilibration Methods 0.000 claims 1
• 238000002844 melting Methods 0.000 claims 1
• 230000008018 melting Effects 0.000 claims 1
• 239000007787 solid Substances 0.000 claims 1
• 239000007790 solid phase Substances 0.000 claims 1
• 239000000758 substrate Substances 0.000 claims 1
• 0 *NC(N*NC(N*=C)=O)=O Chemical compound *NC(N*NC(N*=C)=O)=O 0.000 description 1