JPH025193B2 - - Google Patents
Info
- Publication number
- JPH025193B2 JPH025193B2 JP57145181A JP14518182A JPH025193B2 JP H025193 B2 JPH025193 B2 JP H025193B2 JP 57145181 A JP57145181 A JP 57145181A JP 14518182 A JP14518182 A JP 14518182A JP H025193 B2 JPH025193 B2 JP H025193B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- ester
- transfer
- sheet
- image
- Prior art date
- 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.)
- Expired - Lifetime
Links
- 239000000975 dye Substances 0.000 description 23
- 125000000217 alkyl group Chemical group 0.000 description 13
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 8
- -1 o-chloroanilino Chemical group 0.000 description 8
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 7
- 238000003490 calendering Methods 0.000 description 6
- 239000000945 filler Substances 0.000 description 6
- 229910052736 halogen Inorganic materials 0.000 description 6
- 150000002367 halogens Chemical class 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 6
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 238000004040 coloring Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 230000008542 thermal sensitivity Effects 0.000 description 5
- 239000005711 Benzoic acid Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 125000003710 aryl alkyl group Chemical group 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 235000010233 benzoic acid Nutrition 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 4
- 238000007651 thermal printing Methods 0.000 description 4
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 3
- WYCMXEZEGOOMSO-UHFFFAOYSA-N (3-methylphenyl) 2-hydroxybenzoate Chemical compound CC1=CC=CC(OC(=O)C=2C(=CC=CC=2)O)=C1 WYCMXEZEGOOMSO-UHFFFAOYSA-N 0.000 description 3
- QFOHBWFCKVYLES-UHFFFAOYSA-N Butylparaben Chemical compound CCCCOC(=O)C1=CC=C(O)C=C1 QFOHBWFCKVYLES-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- FWQHNLCNFPYBCA-UHFFFAOYSA-N fluoran Chemical compound C12=CC=CC=C2OC2=CC=CC=C2C11OC(=O)C2=CC=CC=C21 FWQHNLCNFPYBCA-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- 229920006255 plastic film Polymers 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 229960004889 salicylic acid Drugs 0.000 description 3
- PMRMHHUTWZPFIY-UHFFFAOYSA-N (4-methoxyphenyl) benzoate Chemical compound C1=CC(OC)=CC=C1OC(=O)C1=CC=CC=C1 PMRMHHUTWZPFIY-UHFFFAOYSA-N 0.000 description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- SULYEHHGGXARJS-UHFFFAOYSA-N 2',4'-dihydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1O SULYEHHGGXARJS-UHFFFAOYSA-N 0.000 description 2
- NKTOLZVEWDHZMU-UHFFFAOYSA-N 2,5-xylenol Chemical compound CC1=CC=C(C)C(O)=C1 NKTOLZVEWDHZMU-UHFFFAOYSA-N 0.000 description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 2
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 description 2
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 2
- ZSBDGXGICLIJGD-UHFFFAOYSA-N 4-phenoxyphenol Chemical compound C1=CC(O)=CC=C1OC1=CC=CC=C1 ZSBDGXGICLIJGD-UHFFFAOYSA-N 0.000 description 2
- KBPUBCVJHFXPOC-UHFFFAOYSA-N Ethyl 3,4-dihydroxybenzoate Natural products CCOC(=O)C1=CC=C(O)C(O)=C1 KBPUBCVJHFXPOC-UHFFFAOYSA-N 0.000 description 2
- JZJYYCFYGXPUMF-QXMHVHEDSA-N Oleoyl ethylamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCC JZJYYCFYGXPUMF-QXMHVHEDSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 125000004423 acyloxy group Chemical group 0.000 description 2
- 125000004104 aryloxy group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- MJIPWYIXBOTFRC-UHFFFAOYSA-N n-docosyl-2-phenylacetamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCNC(=O)CC1=CC=CC=C1 MJIPWYIXBOTFRC-UHFFFAOYSA-N 0.000 description 2
- HWEOYOXBRATLKT-UHFFFAOYSA-N n-octadecylbenzamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)C1=CC=CC=C1 HWEOYOXBRATLKT-UHFFFAOYSA-N 0.000 description 2
- 125000002560 nitrile group Chemical group 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- LPNBBFKOUUSUDB-UHFFFAOYSA-N p-toluic acid Chemical compound CC1=CC=C(C(O)=O)C=C1 LPNBBFKOUUSUDB-UHFFFAOYSA-N 0.000 description 2
- LIDDQKAMUXHIQD-UHFFFAOYSA-N phenyl 2-benzoyloxybenzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 LIDDQKAMUXHIQD-UHFFFAOYSA-N 0.000 description 2
- GJLNWLVPAHNBQN-UHFFFAOYSA-N phenyl 4-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OC1=CC=CC=C1 GJLNWLVPAHNBQN-UHFFFAOYSA-N 0.000 description 2
- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical class C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- CQRYARSYNCAZFO-UHFFFAOYSA-N salicyl alcohol Chemical compound OCC1=CC=CC=C1O CQRYARSYNCAZFO-UHFFFAOYSA-N 0.000 description 2
- WVYADZUPLLSGPU-UHFFFAOYSA-N salsalate Chemical compound OC(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1O WVYADZUPLLSGPU-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- CHIJIQHKEIBUPB-UHFFFAOYSA-N (2,3-dichlorophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC(Cl)=C1Cl CHIJIQHKEIBUPB-UHFFFAOYSA-N 0.000 description 1
- VZWVHUUGXIFDKA-UHFFFAOYSA-N (2,4,6-tribromophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=C(Br)C=C(Br)C=C1Br VZWVHUUGXIFDKA-UHFFFAOYSA-N 0.000 description 1
- SFPHCLSJMWGJBT-UHFFFAOYSA-N (2,4,6-trichlorophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=C(Cl)C=C(Cl)C=C1Cl SFPHCLSJMWGJBT-UHFFFAOYSA-N 0.000 description 1
- RHEZJKZNYHZXMR-UHFFFAOYSA-N (2,4,6-trichlorophenyl) benzoate Chemical compound ClC1=CC(Cl)=CC(Cl)=C1OC(=O)C1=CC=CC=C1 RHEZJKZNYHZXMR-UHFFFAOYSA-N 0.000 description 1
- YMWXQUBFDGEVNI-UHFFFAOYSA-N (2,4-dibromophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(Br)C=C1Br YMWXQUBFDGEVNI-UHFFFAOYSA-N 0.000 description 1
- WHWSHWZIJIZSIG-UHFFFAOYSA-N (2,4-dibromophenyl) benzoate Chemical compound BrC1=CC(Br)=CC=C1OC(=O)C1=CC=CC=C1 WHWSHWZIJIZSIG-UHFFFAOYSA-N 0.000 description 1
- YBFZUTPPMWWFLT-UHFFFAOYSA-N (2,4-dimethylphenyl) 2-hydroxybenzoate Chemical compound CC1=CC(C)=CC=C1OC(=O)C1=CC=CC=C1O YBFZUTPPMWWFLT-UHFFFAOYSA-N 0.000 description 1
- WKNSZPXEBNSBOM-UHFFFAOYSA-N (2,6-dibromophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=C(Br)C=CC=C1Br WKNSZPXEBNSBOM-UHFFFAOYSA-N 0.000 description 1
- HKBDCEKFCUXJCV-UHFFFAOYSA-N (2,6-dichlorophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=C(Cl)C=CC=C1Cl HKBDCEKFCUXJCV-UHFFFAOYSA-N 0.000 description 1
- VPGDZNFUPPCJOB-UHFFFAOYSA-N (2-acetyloxyphenyl) benzoate Chemical compound CC(=O)OC1=CC=CC=C1OC(=O)C1=CC=CC=C1 VPGDZNFUPPCJOB-UHFFFAOYSA-N 0.000 description 1
- CBLBPSNUGAXWGH-UHFFFAOYSA-N (2-benzoyl-5-methylphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC(C)=CC=C1C(=O)C1=CC=CC=C1 CBLBPSNUGAXWGH-UHFFFAOYSA-N 0.000 description 1
- LVTPRIAGCBEGPW-UHFFFAOYSA-N (2-benzoyloxyphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1OC(=O)C1=CC=CC=C1 LVTPRIAGCBEGPW-UHFFFAOYSA-N 0.000 description 1
- IWMGPWMKJSTOAA-UHFFFAOYSA-N (2-bromophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1Br IWMGPWMKJSTOAA-UHFFFAOYSA-N 0.000 description 1
- FWSWFCIRSUDUOM-UHFFFAOYSA-N (2-chlorophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1Cl FWSWFCIRSUDUOM-UHFFFAOYSA-N 0.000 description 1
- WIRVGPKLACEVRA-UHFFFAOYSA-N (2-ethoxyphenyl) 2-hydroxybenzoate Chemical compound CCOC1=CC=CC=C1OC(=O)C1=CC=CC=C1O WIRVGPKLACEVRA-UHFFFAOYSA-N 0.000 description 1
- RFIRCRFSWDHEBP-UHFFFAOYSA-N (2-methoxy-4-methylphenyl) 4-hydroxybenzoate Chemical compound COC1=CC(C)=CC=C1OC(=O)C1=CC=C(O)C=C1 RFIRCRFSWDHEBP-UHFFFAOYSA-N 0.000 description 1
- APMWEQQELZTXTL-UHFFFAOYSA-N (2-methoxyphenyl) 2-hydroxybenzoate Chemical compound COC1=CC=CC=C1OC(=O)C1=CC=CC=C1O APMWEQQELZTXTL-UHFFFAOYSA-N 0.000 description 1
- GWILBJJMTLPFGX-UHFFFAOYSA-N (2-methoxyphenyl) 3,5-dichloro-2-hydroxybenzoate Chemical compound COC1=CC=CC=C1OC(=O)C1=CC(Cl)=CC(Cl)=C1O GWILBJJMTLPFGX-UHFFFAOYSA-N 0.000 description 1
- YHCOQZVGVFISLR-UHFFFAOYSA-N (2-methoxyphenyl) 4-hydroxybenzoate Chemical compound COC1=CC=CC=C1OC(=O)C1=CC=C(O)C=C1 YHCOQZVGVFISLR-UHFFFAOYSA-N 0.000 description 1
- ALYKUDRBSKNACP-UHFFFAOYSA-N (3-bromophenyl) benzoate Chemical compound BrC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 ALYKUDRBSKNACP-UHFFFAOYSA-N 0.000 description 1
- BCUFQMVZYDFSIG-UHFFFAOYSA-N (3-iodophenyl) benzoate Chemical compound IC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 BCUFQMVZYDFSIG-UHFFFAOYSA-N 0.000 description 1
- QKOXLEURWZTLAY-UHFFFAOYSA-N (3-methoxyphenyl) 2-hydroxybenzoate Chemical compound COC1=CC=CC(OC(=O)C=2C(=CC=CC=2)O)=C1 QKOXLEURWZTLAY-UHFFFAOYSA-N 0.000 description 1
- YHPFQXCLANCCKD-UHFFFAOYSA-N (3-methylphenyl) 5-chloro-2-hydroxybenzoate Chemical compound CC1=CC=CC(OC(=O)C=2C(=CC=C(Cl)C=2)O)=C1 YHPFQXCLANCCKD-UHFFFAOYSA-N 0.000 description 1
- JWLQSDXEKWFFBU-UHFFFAOYSA-N (3-nitrophenyl) benzoate Chemical compound [O-][N+](=O)C1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 JWLQSDXEKWFFBU-UHFFFAOYSA-N 0.000 description 1
- DLLWMHSSGQYZPE-UHFFFAOYSA-N (4-benzoylphenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(C(=O)C=2C=CC=CC=2)C=C1 DLLWMHSSGQYZPE-UHFFFAOYSA-N 0.000 description 1
- MCDYTRXHCNELKZ-UHFFFAOYSA-N (4-benzoylphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C=C1)=CC=C1C(=O)C1=CC=CC=C1 MCDYTRXHCNELKZ-UHFFFAOYSA-N 0.000 description 1
- XSGIPGFJYOYADV-UHFFFAOYSA-N (4-benzylphenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC(C=C1)=CC=C1CC1=CC=CC=C1 XSGIPGFJYOYADV-UHFFFAOYSA-N 0.000 description 1
- QMMQPXSGXXDYHG-UHFFFAOYSA-N (4-benzylphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C=C1)=CC=C1CC1=CC=CC=C1 QMMQPXSGXXDYHG-UHFFFAOYSA-N 0.000 description 1
- INUXCUFFKPBMKK-UHFFFAOYSA-N (4-bromophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(Br)C=C1 INUXCUFFKPBMKK-UHFFFAOYSA-N 0.000 description 1
- SUEYSYGFYRKFKO-UHFFFAOYSA-N (4-chloro-2-methylphenyl) benzoate Chemical compound CC1=CC(Cl)=CC=C1OC(=O)C1=CC=CC=C1 SUEYSYGFYRKFKO-UHFFFAOYSA-N 0.000 description 1
- CDBOTLBWQJJKQJ-UHFFFAOYSA-N (4-chloro-3-methylphenyl) 2-hydroxybenzoate Chemical compound C1=C(Cl)C(C)=CC(OC(=O)C=2C(=CC=CC=2)O)=C1 CDBOTLBWQJJKQJ-UHFFFAOYSA-N 0.000 description 1
- TUYYMOBSJNEIKN-UHFFFAOYSA-N (4-chlorophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(Cl)C=C1 TUYYMOBSJNEIKN-UHFFFAOYSA-N 0.000 description 1
- BXXPTNJQVHYLIK-UHFFFAOYSA-N (4-chlorophenyl) 4-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OC1=CC=C(Cl)C=C1 BXXPTNJQVHYLIK-UHFFFAOYSA-N 0.000 description 1
- CHMPIVCGVXDTTL-UHFFFAOYSA-N (4-ethoxycarbonylphenyl) 4-methoxybenzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1OC(=O)C1=CC=C(OC)C=C1 CHMPIVCGVXDTTL-UHFFFAOYSA-N 0.000 description 1
- HXUSROHSMQXTIY-UHFFFAOYSA-N (4-ethoxycarbonylphenyl) 4-methylbenzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1OC(=O)C1=CC=C(C)C=C1 HXUSROHSMQXTIY-UHFFFAOYSA-N 0.000 description 1
- UFNKAYBBJKLRIW-UHFFFAOYSA-N (4-hydroxyphenyl) 2-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1OC(=O)C1=CC=CC=C1O UFNKAYBBJKLRIW-UHFFFAOYSA-N 0.000 description 1
- KVFFCZXWUPJFFQ-UHFFFAOYSA-N (4-methoxyphenyl) 4-methoxybenzoate Chemical compound C1=CC(OC)=CC=C1OC(=O)C1=CC=C(OC)C=C1 KVFFCZXWUPJFFQ-UHFFFAOYSA-N 0.000 description 1
- VXCLPVZGTDMDND-UHFFFAOYSA-N (4-methylphenyl) 4-nitrobenzoate Chemical compound C1=CC(C)=CC=C1OC(=O)C1=CC=C([N+]([O-])=O)C=C1 VXCLPVZGTDMDND-UHFFFAOYSA-N 0.000 description 1
- LLRZUDIHEZXFGV-UHFFFAOYSA-N (4-methylphenyl) benzoate Chemical compound C1=CC(C)=CC=C1OC(=O)C1=CC=CC=C1 LLRZUDIHEZXFGV-UHFFFAOYSA-N 0.000 description 1
- NORUOMLCLAGATK-UHFFFAOYSA-N (4-prop-1-enylphenyl) 2-hydroxybenzoate Chemical compound C1=CC(C=CC)=CC=C1OC(=O)C1=CC=CC=C1O NORUOMLCLAGATK-UHFFFAOYSA-N 0.000 description 1
- KPVUCQCHICRYHH-UHFFFAOYSA-N (4-propan-2-ylphenyl) benzoate Chemical compound C1=CC(C(C)C)=CC=C1OC(=O)C1=CC=CC=C1 KPVUCQCHICRYHH-UHFFFAOYSA-N 0.000 description 1
- NJNFUPWMCKHLRE-KHPPLWFESA-N (z)-n-methyloctadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NC NJNFUPWMCKHLRE-KHPPLWFESA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 1
- WXTMDXOMEHJXQO-UHFFFAOYSA-N 2,5-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC(O)=CC=C1O WXTMDXOMEHJXQO-UHFFFAOYSA-N 0.000 description 1
- VXHYVVAUHMGCEX-UHFFFAOYSA-N 2-(2-hydroxyphenoxy)phenol Chemical compound OC1=CC=CC=C1OC1=CC=CC=C1O VXHYVVAUHMGCEX-UHFFFAOYSA-N 0.000 description 1
- QSOVSKMNRYAVJR-UHFFFAOYSA-N 2-benzoyloxybenzoic acid Chemical class OC(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1 QSOVSKMNRYAVJR-UHFFFAOYSA-N 0.000 description 1
- XBQRPFBBTWXIFI-UHFFFAOYSA-N 2-chloro-4-[2-(3-chloro-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C=1C=C(O)C(Cl)=CC=1C(C)(C)C1=CC=C(O)C(Cl)=C1 XBQRPFBBTWXIFI-UHFFFAOYSA-N 0.000 description 1
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- QUBGMQIUQXZHBL-UHFFFAOYSA-N n-methyltetradecanamide Chemical compound CCCCCCCCCCCCCC(=O)NC QUBGMQIUQXZHBL-UHFFFAOYSA-N 0.000 description 1
- PKDVDHHRICWWGY-UHFFFAOYSA-N n-methyltridecanamide Chemical compound CCCCCCCCCCCCC(=O)NC PKDVDHHRICWWGY-UHFFFAOYSA-N 0.000 description 1
- MUZVJRFZJAXVBM-UHFFFAOYSA-N n-methylundecanamide Chemical compound CCCCCCCCCCC(=O)NC MUZVJRFZJAXVBM-UHFFFAOYSA-N 0.000 description 1
- PMNNKCGDKSIBLA-UHFFFAOYSA-N n-octadecyl-2-phenylacetamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CC1=CC=CC=C1 PMNNKCGDKSIBLA-UHFFFAOYSA-N 0.000 description 1
- UOJWCKBTLPPNFI-UHFFFAOYSA-N n-octadecylcyclohexanecarboxamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)C1CCCCC1 UOJWCKBTLPPNFI-UHFFFAOYSA-N 0.000 description 1
- DJWFNQUDPJTSAD-UHFFFAOYSA-N n-octadecyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CCCCCCCCCCCCCCCCC DJWFNQUDPJTSAD-UHFFFAOYSA-N 0.000 description 1
- JHHXEQAVFNLSQT-UHFFFAOYSA-N n-pentadecylacetamide Chemical compound CCCCCCCCCCCCCCCNC(C)=O JHHXEQAVFNLSQT-UHFFFAOYSA-N 0.000 description 1
- UAXSNGWZTKJBRN-UHFFFAOYSA-N n-pentadecylpropanamide Chemical compound CCCCCCCCCCCCCCCNC(=O)CC UAXSNGWZTKJBRN-UHFFFAOYSA-N 0.000 description 1
- FLWVQJFJIXHMAY-UHFFFAOYSA-N n-propyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCC FLWVQJFJIXHMAY-UHFFFAOYSA-N 0.000 description 1
- JFFBOCCNFSWIPM-UHFFFAOYSA-N n-tetradecylacetamide Chemical compound CCCCCCCCCCCCCCNC(C)=O JFFBOCCNFSWIPM-UHFFFAOYSA-N 0.000 description 1
- BEZPEVVJBRYCOZ-UHFFFAOYSA-N n-tetradecylpropanamide Chemical compound CCCCCCCCCCCCCCNC(=O)CC BEZPEVVJBRYCOZ-UHFFFAOYSA-N 0.000 description 1
- GMXKHKFLSPARRX-UHFFFAOYSA-N n-tridecylacetamide Chemical compound CCCCCCCCCCCCCNC(C)=O GMXKHKFLSPARRX-UHFFFAOYSA-N 0.000 description 1
- VLJHXDQQQCBDLX-UHFFFAOYSA-N n-tridecylpropanamide Chemical compound CCCCCCCCCCCCCNC(=O)CC VLJHXDQQQCBDLX-UHFFFAOYSA-N 0.000 description 1
- GJLSRNILTWBICQ-UHFFFAOYSA-N n-undecylacetamide Chemical compound CCCCCCCCCCCNC(C)=O GJLSRNILTWBICQ-UHFFFAOYSA-N 0.000 description 1
- MKSYQMZLSQHYLU-UHFFFAOYSA-N n-undecylpropanamide Chemical compound CCCCCCCCCCCNC(=O)CC MKSYQMZLSQHYLU-UHFFFAOYSA-N 0.000 description 1
- CVRCFLFEGNKMEC-UHFFFAOYSA-N naphthalen-1-yl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC2=CC=CC=C12 CVRCFLFEGNKMEC-UHFFFAOYSA-N 0.000 description 1
- ZBJVLWIYKOAYQH-UHFFFAOYSA-N naphthalen-2-yl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(C=CC=C2)C2=C1 ZBJVLWIYKOAYQH-UHFFFAOYSA-N 0.000 description 1
- GHLZUHZBBNDWHW-UHFFFAOYSA-N nonanamide Chemical compound CCCCCCCCC(N)=O GHLZUHZBBNDWHW-UHFFFAOYSA-N 0.000 description 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- RARSHUDCJQSEFJ-UHFFFAOYSA-N p-Hydroxypropiophenone Chemical compound CCC(=O)C1=CC=C(O)C=C1 RARSHUDCJQSEFJ-UHFFFAOYSA-N 0.000 description 1
- KLAKIAVEMQMVBT-UHFFFAOYSA-N p-hydroxy-phenacyl alcohol Natural products OCC(=O)C1=CC=C(O)C=C1 KLAKIAVEMQMVBT-UHFFFAOYSA-N 0.000 description 1
- ALDPCROMRXIHET-UHFFFAOYSA-N phenacyl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OCC(=O)C1=CC=CC=C1 ALDPCROMRXIHET-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- PHLUHHLZOWJCEW-UHFFFAOYSA-N phenyl 3,4-dihydroxybenzoate Chemical compound C1=C(O)C(O)=CC=C1C(=O)OC1=CC=CC=C1 PHLUHHLZOWJCEW-UHFFFAOYSA-N 0.000 description 1
- CZEPEQHOBBKCSQ-UHFFFAOYSA-N phenyl 4-acetyloxybenzoate Chemical compound C1=CC(OC(=O)C)=CC=C1C(=O)OC1=CC=CC=C1 CZEPEQHOBBKCSQ-UHFFFAOYSA-N 0.000 description 1
- TXPWNLLOFXHCPZ-UHFFFAOYSA-N phenyl 4-benzoyloxybenzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C=C1)=CC=C1C(=O)OC1=CC=CC=C1 TXPWNLLOFXHCPZ-UHFFFAOYSA-N 0.000 description 1
- BNZYBNYNPXKWCM-UHFFFAOYSA-N phenyl 4-methoxybenzoate Chemical compound C1=CC(OC)=CC=C1C(=O)OC1=CC=CC=C1 BNZYBNYNPXKWCM-UHFFFAOYSA-N 0.000 description 1
- WOHDXQQIBRMRFA-UHFFFAOYSA-N phenyl 4-methylbenzoate Chemical compound C1=CC(C)=CC=C1C(=O)OC1=CC=CC=C1 WOHDXQQIBRMRFA-UHFFFAOYSA-N 0.000 description 1
- NVGUCNZOTBWESS-UHFFFAOYSA-N phenyl 4-phenoxybenzoate Chemical compound C=1C=C(OC=2C=CC=CC=2)C=CC=1C(=O)OC1=CC=CC=C1 NVGUCNZOTBWESS-UHFFFAOYSA-N 0.000 description 1
- PSBAIJVSCTZDDB-UHFFFAOYSA-N phenyl acetylsalicylate Chemical compound CC(=O)OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 PSBAIJVSCTZDDB-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- CHGCLEZHDRWBLZ-UHFFFAOYSA-N propyl 4-benzoyloxybenzoate Chemical compound C1=CC(C(=O)OCCC)=CC=C1OC(=O)C1=CC=CC=C1 CHGCLEZHDRWBLZ-UHFFFAOYSA-N 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- GDESWOTWNNGOMW-UHFFFAOYSA-N resorcinol monobenzoate Chemical compound OC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 GDESWOTWNNGOMW-UHFFFAOYSA-N 0.000 description 1
- 229960000953 salsalate Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- ZAYKUYSGARCXKQ-UHFFFAOYSA-N tetracosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC(N)=O ZAYKUYSGARCXKQ-UHFFFAOYSA-N 0.000 description 1
- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical compound OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 description 1
- 229940103494 thiosalicylic acid Drugs 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/38235—Contact thermal transfer or sublimation processes characterised by transferable colour-forming materials
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Description
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Claims (1)
- ïŒ ãã€ã³ææãäž»æåãšãã転åå±€ãæãã転
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城ãšããæç±è»¢ååªäœã
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57145181A JPS5935984A (ja) | 1982-08-20 | 1982-08-20 | æç±è»¢ååªäœ |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57145181A JPS5935984A (ja) | 1982-08-20 | 1982-08-20 | æç±è»¢ååªäœ |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5935984A JPS5935984A (ja) | 1984-02-27 |
| JPH025193B2 true JPH025193B2 (ja) | 1990-01-31 |
Family
ID=15379295
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57145181A Granted JPS5935984A (ja) | 1982-08-20 | 1982-08-20 | æç±è»¢ååªäœ |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5935984A (ja) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60110488A (ja) * | 1983-11-21 | 1985-06-15 | Toshiba Corp | ç±è»¢åèšé²çšçŽåã³ãããçšããç±è»¢åèšé²è£ 眮 |
| JPH0725223B2 (ja) * | 1984-07-19 | 1995-03-22 | 倧æ¥æ¬å°å·æ ªåŒäŒç€Ÿ | 被ç±è»¢åã·âã |
| JPH0714665B2 (ja) * | 1985-06-10 | 1995-02-22 | 倧æ¥æ¬å°å·æ ªåŒäŒç€Ÿ | 被ç±è»¢åã·âã |
| JP2977404B2 (ja) * | 1993-02-24 | 1999-11-15 | å å€ã«ãŒãã³ã€ã³ãæ ªåŒäŒç€Ÿ | æå§æç±å€éè€åçŽ |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS553919A (en) * | 1978-06-22 | 1980-01-12 | Nippon Telegr & Teleph Corp <Ntt> | Thermal recording medium |
| JPS5542824A (en) * | 1978-09-20 | 1980-03-26 | Mitsubishi Electric Corp | Thermo transfer copying medium of inked pattern |
| JPS5712693A (en) * | 1980-06-27 | 1982-01-22 | Mitsubishi Paper Mills Ltd | Thermo-sensitive recording body for simultaneous copying |
-
1982
- 1982-08-20 JP JP57145181A patent/JPS5935984A/ja active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS553919A (en) * | 1978-06-22 | 1980-01-12 | Nippon Telegr & Teleph Corp <Ntt> | Thermal recording medium |
| JPS5542824A (en) * | 1978-09-20 | 1980-03-26 | Mitsubishi Electric Corp | Thermo transfer copying medium of inked pattern |
| JPS5712693A (en) * | 1980-06-27 | 1982-01-22 | Mitsubishi Paper Mills Ltd | Thermo-sensitive recording body for simultaneous copying |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5935984A (ja) | 1984-02-27 |
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