JP2010285617A5 - - Google Patents

Info

Publication number

JP2010285617A5

JP2010285617A5 JP2010127511A JP2010127511A JP2010285617A5 JP 2010285617 A5 JP2010285617 A5 JP 2010285617A5 JP 2010127511 A JP2010127511 A JP 2010127511A JP 2010127511 A JP2010127511 A JP 2010127511A JP 2010285617 A5 JP2010285617 A5 JP 2010285617A5

Authority

JP

Japan

Prior art keywords

wax

ink composition

polar

composition according

polar wax

Prior art date

2010-06-03

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.)

Pending

Links

• Espacenet
• Global Dossier
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• 239000001993 wax Substances 0.000 claims 11
• 239000002253 acid Substances 0.000 claims 3
• 230000002378 acidificating effect Effects 0.000 claims 2
• 239000003963 antioxidant agent Substances 0.000 claims 2
• 230000003078 antioxidant effect Effects 0.000 claims 2
• 239000003086 colorant Substances 0.000 claims 2
• 150000002193 fatty amides Chemical class 0.000 claims 2
• 239000000992 solvent dye Substances 0.000 claims 2
• OXDXXMDEEFOVHR-CLFAGFIQSA-N (z)-n-[2-[[(z)-octadec-9-enoyl]amino]ethyl]octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCCNC(=O)CCCCCCC\C=C/CCCCCCCC OXDXXMDEEFOVHR-CLFAGFIQSA-N 0.000 claims 1
• QPQKUYVSJWQSDY-UHFFFAOYSA-N 4-phenyldiazenylaniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=CC=C1 QPQKUYVSJWQSDY-UHFFFAOYSA-N 0.000 claims 1
• 235000013869 carnauba wax Nutrition 0.000 claims 1
• 239000004203 carnauba wax Substances 0.000 claims 1
• 239000003795 chemical substances by application Substances 0.000 claims 1
• 230000008018 melting Effects 0.000 claims 1
• 238000002844 melting Methods 0.000 claims 1
• DJWFNQUDPJTSAD-UHFFFAOYSA-N n-octadecyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CCCCCCCCCCCCCCCCC DJWFNQUDPJTSAD-UHFFFAOYSA-N 0.000 claims 1
• 238000007127 saponification reaction Methods 0.000 claims 1
• 239000002904 solvent Substances 0.000 claims 1
• 0 CC(C)(C)C(C=C(CCC(*CC(C*C(CCc(cc1C(C=C)=*C)cc(C(C)(C)*)c1O)=O)(COC(CCc(cc1C(*)(*)*)cc(C(C)(*)*)c1N)O)COC(CCc(cc1C(C)(*)*)cc2c1OICC2(C)C)=O)=O)CC1C(C)(*)CI)=C1O Chemical compound CC(C)(C)C(C=C(CCC(*CC(C*C(CCc(cc1C(C=C)=*C)cc(C(C)(C)*)c1O)=O)(COC(CCc(cc1C(*)(*)*)cc(C(C)(*)*)c1N)O)COC(CCc(cc1C(C)(*)*)cc2c1OICC2(C)C)=O)=O)CC1C(C)(*)CI)=C1O 0.000 description 1