JPH0461785B2 - - Google Patents
Info
- Publication number
- JPH0461785B2 JPH0461785B2 JP58172726A JP17272683A JPH0461785B2 JP H0461785 B2 JPH0461785 B2 JP H0461785B2 JP 58172726 A JP58172726 A JP 58172726A JP 17272683 A JP17272683 A JP 17272683A JP H0461785 B2 JPH0461785 B2 JP H0461785B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- ester
- transfer
- layer
- sheet
- 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
- 239000000945 filler Substances 0.000 claims description 14
- 238000010521 absorption reaction Methods 0.000 claims description 13
- 239000002985 plastic film Substances 0.000 claims description 7
- 229920006255 plastic film Polymers 0.000 claims description 7
- 239000000975 dye Substances 0.000 description 26
- 229920005989 resin Polymers 0.000 description 15
- 239000011347 resin Substances 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- 125000000217 alkyl group Chemical group 0.000 description 13
- -1 polyethylene Polymers 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 150000002148 esters Chemical class 0.000 description 10
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 9
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 8
- 238000000576 coating method Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 6
- 229910052736 halogen Inorganic materials 0.000 description 6
- 150000002367 halogens Chemical class 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 125000002947 alkylene group Chemical group 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000010419 fine particle Substances 0.000 description 5
- FWQHNLCNFPYBCA-UHFFFAOYSA-N fluoran Chemical compound C12=CC=CC=C2OC2=CC=CC=C2C11OC(=O)C2=CC=CC=C21 FWQHNLCNFPYBCA-UHFFFAOYSA-N 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 125000001033 ether group Chemical group 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
- 229960004889 salicylic acid Drugs 0.000 description 4
- 238000007651 thermal printing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-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
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- FWSWFCIRSUDUOM-UHFFFAOYSA-N (2-chlorophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1Cl FWSWFCIRSUDUOM-UHFFFAOYSA-N 0.000 description 2
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-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
- 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 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
- DBOSBRHMHBENLP-UHFFFAOYSA-N 4-tert-Butylphenyl Salicylate Chemical compound C1=CC(C(C)(C)C)=CC=C1OC(=O)C1=CC=CC=C1O DBOSBRHMHBENLP-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
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 2
- 125000004423 acyloxy group Chemical group 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 125000002102 aryl alkyloxo group Chemical group 0.000 description 2
- 125000004104 aryloxy group Chemical group 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
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 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
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- 229910001862 magnesium hydroxide Inorganic materials 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
- 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
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000003825 pressing Methods 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
- 239000005060 rubber Substances 0.000 description 2
- CQRYARSYNCAZFO-UHFFFAOYSA-N salicyl alcohol Chemical compound OCC1=CC=CC=C1O CQRYARSYNCAZFO-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent 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
- UNNUESFABWIRHI-UHFFFAOYSA-N (2,4-dichlorophenyl) benzoate Chemical compound ClC1=CC(Cl)=CC=C1OC(=O)C1=CC=CC=C1 UNNUESFABWIRHI-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
- RRTHUXNSBDKADU-UHFFFAOYSA-N (2,6-dichloro-4-methylphenyl) benzoate Chemical compound ClC1=CC(C)=CC(Cl)=C1OC(=O)C1=CC=CC=C1 RRTHUXNSBDKADU-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
- 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
- TVFLZSCYOACNAS-UHFFFAOYSA-N (3-hydroxyphenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC(OC(=O)C=2C(=CC=CC=2)O)=C1 TVFLZSCYOACNAS-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
- 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 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
- 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
- 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
- PMRMHHUTWZPFIY-UHFFFAOYSA-N (4-methoxyphenyl) benzoate Chemical compound C1=CC(OC)=CC=C1OC(=O)C1=CC=CC=C1 PMRMHHUTWZPFIY-UHFFFAOYSA-N 0.000 description 1
- MJLXQKNXJKYSOA-UHFFFAOYSA-N (4-methylphenyl) 2-nitrobenzoate Chemical compound C1=CC(C)=CC=C1OC(=O)C1=CC=CC=C1[N+]([O-])=O MJLXQKNXJKYSOA-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
- GFLGTOLWFQLOPT-UHFFFAOYSA-N (4-naphthalen-1-ylphenyl) benzoate Chemical compound C=1C=C(C=2C3=CC=CC=C3C=CC=2)C=CC=1OC(=O)C1=CC=CC=C1 GFLGTOLWFQLOPT-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
- OWZCLYMEMJOKAC-UHFFFAOYSA-N (4-tert-butylphenyl) benzoate Chemical compound C1=CC(C(C)(C)C)=CC=C1OC(=O)C1=CC=CC=C1 OWZCLYMEMJOKAC-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
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- OYIZIUPDFGVXNG-UHFFFAOYSA-N n-decylpropanamide Chemical compound CCCCCCCCCCNC(=O)CC OYIZIUPDFGVXNG-UHFFFAOYSA-N 0.000 description 1
- OABSGFGMOISEKF-UHFFFAOYSA-N n-docosyl-2-methylbenzamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCNC(=O)C1=CC=CC=C1C OABSGFGMOISEKF-UHFFFAOYSA-N 0.000 description 1
- MJIPWYIXBOTFRC-UHFFFAOYSA-N n-docosyl-2-phenylacetamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCNC(=O)CC1=CC=CC=C1 MJIPWYIXBOTFRC-UHFFFAOYSA-N 0.000 description 1
- GKIGWMCWSLVNNQ-UHFFFAOYSA-N n-docosylbenzamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCNC(=O)C1=CC=CC=C1 GKIGWMCWSLVNNQ-UHFFFAOYSA-N 0.000 description 1
- MDYPFOFSXHBHFE-UHFFFAOYSA-N n-dodecylacetamide Chemical compound CCCCCCCCCCCCNC(C)=O MDYPFOFSXHBHFE-UHFFFAOYSA-N 0.000 description 1
- URMJLBKGJTXVGC-UHFFFAOYSA-N n-dodecylpropanamide Chemical compound CCCCCCCCCCCCNC(=O)CC URMJLBKGJTXVGC-UHFFFAOYSA-N 0.000 description 1
- FEQGPEABBFYLNO-UHFFFAOYSA-N n-ethyldodecanamide Chemical compound CCCCCCCCCCCC(=O)NCC FEQGPEABBFYLNO-UHFFFAOYSA-N 0.000 description 1
- VLYFHHYLZLDEIU-UHFFFAOYSA-N n-ethyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCC VLYFHHYLZLDEIU-UHFFFAOYSA-N 0.000 description 1
- BKGFGPAWUGWQAB-UHFFFAOYSA-N n-ethylpentadecanamide Chemical compound CCCCCCCCCCCCCCC(=O)NCC BKGFGPAWUGWQAB-UHFFFAOYSA-N 0.000 description 1
- HODFTZHFCOHHMM-UHFFFAOYSA-N n-ethyltetradecanamide Chemical compound CCCCCCCCCCCCCC(=O)NCC HODFTZHFCOHHMM-UHFFFAOYSA-N 0.000 description 1
- KNIHPOVOZDEDNP-UHFFFAOYSA-N n-ethyltridecanamide Chemical compound CCCCCCCCCCCCC(=O)NCC KNIHPOVOZDEDNP-UHFFFAOYSA-N 0.000 description 1
- QFZHIMKZKRGXQF-UHFFFAOYSA-N n-ethylundecanamide Chemical compound CCCCCCCCCCC(=O)NCC QFZHIMKZKRGXQF-UHFFFAOYSA-N 0.000 description 1
- IHQFBJFDYNPKBQ-UHFFFAOYSA-N n-hexadecyl-2,4-dimethylbenzamide Chemical compound CCCCCCCCCCCCCCCCNC(=O)C1=CC=C(C)C=C1C IHQFBJFDYNPKBQ-UHFFFAOYSA-N 0.000 description 1
- FZKOWDKRBSXWTK-UHFFFAOYSA-N n-methyldocosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)NC FZKOWDKRBSXWTK-UHFFFAOYSA-N 0.000 description 1
- APWSJINSLHHRPD-UHFFFAOYSA-N n-methyldodecanamide Chemical compound CCCCCCCCCCCC(=O)NC APWSJINSLHHRPD-UHFFFAOYSA-N 0.000 description 1
- STEVSDAHHBNTQD-UHFFFAOYSA-N n-methylhexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)NC STEVSDAHHBNTQD-UHFFFAOYSA-N 0.000 description 1
- JJOVCQBPDCSFDT-UHFFFAOYSA-N n-methylnonadecanamide Chemical compound CCCCCCCCCCCCCCCCCCC(=O)NC JJOVCQBPDCSFDT-UHFFFAOYSA-N 0.000 description 1
- HNUFCQUTJXHEPI-UHFFFAOYSA-N n-methyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC HNUFCQUTJXHEPI-UHFFFAOYSA-N 0.000 description 1
- YMGFGHQHTDLOJF-UHFFFAOYSA-N n-methylpentadecanamide Chemical compound CCCCCCCCCCCCCCC(=O)NC YMGFGHQHTDLOJF-UHFFFAOYSA-N 0.000 description 1
- 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
- HWEOYOXBRATLKT-UHFFFAOYSA-N n-octadecylbenzamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)C1=CC=CC=C1 HWEOYOXBRATLKT-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
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 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
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 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
- 239000003208 petroleum Substances 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
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 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 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
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000007639 printing Methods 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
- 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
- 150000003839 salts Chemical class 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000007787 solid 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
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/42—Intermediate, backcoat, or covering layers
-
- 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
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/42—Intermediate, backcoat, or covering layers
- B41M5/426—Intermediate, backcoat, or covering layers characterised by inorganic compounds, e.g. metals, metal salts, metal complexes
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Color Printing (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58172726A JPS6063193A (ja) | 1983-09-19 | 1983-09-19 | 感熱転写媒体 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58172726A JPS6063193A (ja) | 1983-09-19 | 1983-09-19 | 感熱転写媒体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6063193A JPS6063193A (ja) | 1985-04-11 |
| JPH0461785B2 true JPH0461785B2 (en]) | 1992-10-02 |
Family
ID=15947186
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58172726A Granted JPS6063193A (ja) | 1983-09-19 | 1983-09-19 | 感熱転写媒体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6063193A (en]) |
-
1983
- 1983-09-19 JP JP58172726A patent/JPS6063193A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6063193A (ja) | 1985-04-11 |
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