JPS6116888A - 感熱記録体 - Google Patents
感熱記録体Info
- Publication number
- JPS6116888A JPS6116888A JP59137565A JP13756584A JPS6116888A JP S6116888 A JPS6116888 A JP S6116888A JP 59137565 A JP59137565 A JP 59137565A JP 13756584 A JP13756584 A JP 13756584A JP S6116888 A JPS6116888 A JP S6116888A
- Authority
- JP
- Japan
- Prior art keywords
- group
- sensitive recording
- coloration
- dye
- heat
- 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.)
- Granted
Links
- 239000000981 basic dye Substances 0.000 claims abstract description 12
- 239000000975 dye Substances 0.000 claims abstract description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 5
- 238000006243 chemical reaction Methods 0.000 claims abstract description 4
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims abstract description 3
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 3
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims abstract description 3
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims abstract description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
- 239000000126 substance Substances 0.000 claims description 13
- 239000003086 colorant Substances 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 9
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- -1 propinyl group Chemical group 0.000 abstract description 5
- 230000000694 effects Effects 0.000 abstract description 4
- 239000003814 drug Substances 0.000 abstract 3
- 229940079593 drug Drugs 0.000 abstract 3
- 230000006866 deterioration Effects 0.000 abstract 1
- 230000002349 favourable effect Effects 0.000 abstract 1
- 239000007788 liquid Substances 0.000 description 14
- 230000035945 sensitivity Effects 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 230000000052 comparative effect Effects 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
- 150000003951 lactams Chemical class 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920000609 methyl cellulose Polymers 0.000 description 3
- 239000001923 methylcellulose Substances 0.000 description 3
- 235000010981 methylcellulose Nutrition 0.000 description 3
- DLRJIFUOBPOJNS-UHFFFAOYSA-N phenetole Chemical compound CCOC1=CC=CC=C1 DLRJIFUOBPOJNS-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 229940037312 stearamide Drugs 0.000 description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-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
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 description 2
- MOZDKDIOPSPTBH-UHFFFAOYSA-N Benzyl parahydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OCC1=CC=CC=C1 MOZDKDIOPSPTBH-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 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
- JJXVDRYFBGDXOU-UHFFFAOYSA-N dimethyl 4-hydroxybenzene-1,2-dicarboxylate Chemical compound COC(=O)C1=CC=C(O)C=C1C(=O)OC JJXVDRYFBGDXOU-UHFFFAOYSA-N 0.000 description 2
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- OKJFKPFBSPZTAH-UHFFFAOYSA-N (2,4-dihydroxyphenyl)-(4-hydroxyphenyl)methanone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1O OKJFKPFBSPZTAH-UHFFFAOYSA-N 0.000 description 1
- FTEYESKEGOVPNV-UHFFFAOYSA-N (2-chlorophenyl) 4-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OC1=CC=CC=C1Cl FTEYESKEGOVPNV-UHFFFAOYSA-N 0.000 description 1
- SXJSETSRWNDWPP-UHFFFAOYSA-N (2-hydroxy-4-phenylmethoxyphenyl)-phenylmethanone Chemical compound C=1C=C(C(=O)C=2C=CC=CC=2)C(O)=CC=1OCC1=CC=CC=C1 SXJSETSRWNDWPP-UHFFFAOYSA-N 0.000 description 1
- YNUJSCOOTDIWRJ-UHFFFAOYSA-N (4-chlorophenyl)methyl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=C(Cl)C=C1 YNUJSCOOTDIWRJ-UHFFFAOYSA-N 0.000 description 1
- RELJKYBOPGHDNL-UHFFFAOYSA-N (4-methoxyphenyl)methyl 4-hydroxybenzoate Chemical compound C1=CC(OC)=CC=C1COC(=O)C1=CC=C(O)C=C1 RELJKYBOPGHDNL-UHFFFAOYSA-N 0.000 description 1
- JDRZXRVFQKESQC-UHFFFAOYSA-N 1-(cyclohexen-1-yl)-4-(2-phenoxyethoxy)benzene Chemical compound C=1C=CC=CC=1OCCOC(C=C1)=CC=C1C1=CCCCC1 JDRZXRVFQKESQC-UHFFFAOYSA-N 0.000 description 1
- RVQDDTWSMXKJGF-UHFFFAOYSA-N 1-[4-(2-phenoxyethoxy)phenyl]ethanone Chemical compound C1=CC(C(=O)C)=CC=C1OCCOC1=CC=CC=C1 RVQDDTWSMXKJGF-UHFFFAOYSA-N 0.000 description 1
- CSKNJHKEOHTSQR-UHFFFAOYSA-N 1-[4-(2-phenoxyethoxy)phenyl]propan-1-one Chemical compound C1=CC(C(=O)CC)=CC=C1OCCOC1=CC=CC=C1 CSKNJHKEOHTSQR-UHFFFAOYSA-N 0.000 description 1
- PCKIUSGYJAJSQD-UHFFFAOYSA-N 1-[4-[2-(2-methylphenoxy)ethoxy]phenyl]ethanone Chemical compound C1=CC(C(=O)C)=CC=C1OCCOC1=CC=CC=C1C PCKIUSGYJAJSQD-UHFFFAOYSA-N 0.000 description 1
- PPYPHIFNOWLDFY-UHFFFAOYSA-N 1-[4-[2-(4-tert-butylphenoxy)ethoxy]phenyl]ethanone Chemical compound C1=CC(C(=O)C)=CC=C1OCCOC1=CC=C(C(C)(C)C)C=C1 PPYPHIFNOWLDFY-UHFFFAOYSA-N 0.000 description 1
- OJRKKJZDTZSQJN-UHFFFAOYSA-N 1-chloro-2-(2-phenoxyethoxy)benzene Chemical compound ClC1=CC=CC=C1OCCOC1=CC=CC=C1 OJRKKJZDTZSQJN-UHFFFAOYSA-N 0.000 description 1
- QNTIAELGXLIPQZ-UHFFFAOYSA-N 1-chloro-2-[2-(2-methylphenoxy)ethoxy]benzene Chemical compound CC1=CC=CC=C1OCCOC1=CC=CC=C1Cl QNTIAELGXLIPQZ-UHFFFAOYSA-N 0.000 description 1
- MVNCLLLTDLUUGF-UHFFFAOYSA-N 1-chloro-2-[2-(3-methylphenoxy)ethoxy]benzene Chemical compound CC1=CC=CC(OCCOC=2C(=CC=CC=2)Cl)=C1 MVNCLLLTDLUUGF-UHFFFAOYSA-N 0.000 description 1
- LNUXOECUNLSQMA-UHFFFAOYSA-N 1-chloro-2-[2-(4-methylphenoxy)ethoxy]benzene Chemical compound C1=CC(C)=CC=C1OCCOC1=CC=CC=C1Cl LNUXOECUNLSQMA-UHFFFAOYSA-N 0.000 description 1
- BDCNTSHIADXFPV-UHFFFAOYSA-N 1-chloro-4-(2-phenoxyethoxy)benzene Chemical compound C1=CC(Cl)=CC=C1OCCOC1=CC=CC=C1 BDCNTSHIADXFPV-UHFFFAOYSA-N 0.000 description 1
- XAIXUHMMSHEMNA-UHFFFAOYSA-N 1-chloro-4-[2-(2-methylphenoxy)ethoxy]benzene Chemical compound CC1=CC=CC=C1OCCOC1=CC=C(Cl)C=C1 XAIXUHMMSHEMNA-UHFFFAOYSA-N 0.000 description 1
- XARVAXOPQJFBFD-UHFFFAOYSA-N 1-chloro-4-[2-(3-methylphenoxy)ethoxy]benzene Chemical compound CC1=CC=CC(OCCOC=2C=CC(Cl)=CC=2)=C1 XARVAXOPQJFBFD-UHFFFAOYSA-N 0.000 description 1
- OLGQCBSIFHJRAI-UHFFFAOYSA-N 1-chloro-4-[2-(4-methylphenoxy)ethoxy]benzene Chemical compound C1=CC(C)=CC=C1OCCOC1=CC=C(Cl)C=C1 OLGQCBSIFHJRAI-UHFFFAOYSA-N 0.000 description 1
- DPCREAWSBWEYJE-UHFFFAOYSA-N 1-methoxy-2-[2-(4-methylphenoxy)ethoxy]benzene Chemical compound COC1=CC=CC=C1OCCOC1=CC=C(C)C=C1 DPCREAWSBWEYJE-UHFFFAOYSA-N 0.000 description 1
- MGHXNMHBEQYYKO-UHFFFAOYSA-N 1-methoxy-3-[2-(4-methylphenoxy)ethoxy]benzene Chemical compound COC1=CC=CC(OCCOC=2C=CC(C)=CC=2)=C1 MGHXNMHBEQYYKO-UHFFFAOYSA-N 0.000 description 1
- IYQIAVRZWFMVGZ-UHFFFAOYSA-N 1-methoxy-4-(2-phenoxyethoxy)benzene Chemical compound C1=CC(OC)=CC=C1OCCOC1=CC=CC=C1 IYQIAVRZWFMVGZ-UHFFFAOYSA-N 0.000 description 1
- YMCGPYYJJZFVBL-UHFFFAOYSA-N 1-methoxy-4-(4-phenoxybutoxy)benzene Chemical compound C1=CC(OC)=CC=C1OCCCCOC1=CC=CC=C1 YMCGPYYJJZFVBL-UHFFFAOYSA-N 0.000 description 1
- QHLJMDDGQALHRZ-UHFFFAOYSA-N 1-methoxy-4-[2-(2-methylphenoxy)ethoxy]benzene Chemical compound C1=CC(OC)=CC=C1OCCOC1=CC=CC=C1C QHLJMDDGQALHRZ-UHFFFAOYSA-N 0.000 description 1
- WWHWOXMOOULLJQ-UHFFFAOYSA-N 1-methoxy-4-[2-(3-methylphenoxy)ethoxy]benzene Chemical compound C1=CC(OC)=CC=C1OCCOC1=CC=CC(C)=C1 WWHWOXMOOULLJQ-UHFFFAOYSA-N 0.000 description 1
- DIRNDCKKTNISNE-UHFFFAOYSA-N 1-methoxy-4-[2-(4-methylphenoxy)ethoxy]benzene Chemical compound C1=CC(OC)=CC=C1OCCOC1=CC=C(C)C=C1 DIRNDCKKTNISNE-UHFFFAOYSA-N 0.000 description 1
- ISZIUYSZSKGNLP-UHFFFAOYSA-N 1-methyl-4-(2-phenoxyethylsulfanyl)benzene Chemical compound C1=CC(C)=CC=C1SCCOC1=CC=CC=C1 ISZIUYSZSKGNLP-UHFFFAOYSA-N 0.000 description 1
- DIVALLOEQCJUOV-UHFFFAOYSA-N 1-methyl-4-(4-phenoxybutylsulfanyl)benzene Chemical compound C1=CC(C)=CC=C1SCCCCOC1=CC=CC=C1 DIVALLOEQCJUOV-UHFFFAOYSA-N 0.000 description 1
- NOGLRDHYCIPRRN-UHFFFAOYSA-N 1-methyl-4-[2-(4-nitrophenoxy)ethoxy]benzene Chemical compound C1=CC(C)=CC=C1OCCOC1=CC=C([N+]([O-])=O)C=C1 NOGLRDHYCIPRRN-UHFFFAOYSA-N 0.000 description 1
- HRBVDXVFAYYMJV-UHFFFAOYSA-N 1-nitro-4-(2-phenoxyethoxy)benzene Chemical compound C1=CC([N+](=O)[O-])=CC=C1OCCOC1=CC=CC=C1 HRBVDXVFAYYMJV-UHFFFAOYSA-N 0.000 description 1
- DTLBEHALPJZWKK-UHFFFAOYSA-N 1-tert-butyl-4-[2-(4-chlorophenoxy)ethoxy]benzene Chemical compound C1=CC(C(C)(C)C)=CC=C1OCCOC1=CC=C(Cl)C=C1 DTLBEHALPJZWKK-UHFFFAOYSA-N 0.000 description 1
- NRLNVIUFIUYGKI-UHFFFAOYSA-N 1-tert-butyl-4-[2-(4-methoxyphenoxy)ethoxy]benzene Chemical compound C1=CC(OC)=CC=C1OCCOC1=CC=C(C(C)(C)C)C=C1 NRLNVIUFIUYGKI-UHFFFAOYSA-N 0.000 description 1
- XWVWJFSDIXLKBL-UHFFFAOYSA-N 1-tert-butyl-4-[2-(4-methylphenyl)sulfanylethoxy]benzene Chemical compound CC1=CC=C(SCCOC2=CC=C(C=C2)C(C)(C)C)C=C1 XWVWJFSDIXLKBL-UHFFFAOYSA-N 0.000 description 1
- ALLSOOQIDPLIER-UHFFFAOYSA-N 2,3,4-trichlorobenzoic acid Chemical compound OC(=O)C1=CC=C(Cl)C(Cl)=C1Cl ALLSOOQIDPLIER-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
- VVGKSTMFQLTJSB-UHFFFAOYSA-N 2-(1-phenylethoxy)benzoic acid Chemical compound C=1C=CC=CC=1C(C)OC1=CC=CC=C1C(O)=O VVGKSTMFQLTJSB-UHFFFAOYSA-N 0.000 description 1
- DZZPJWJPJJNWHM-UHFFFAOYSA-N 2-hydroxy-3-(1-phenylethyl)benzoic acid Chemical compound C=1C=CC(C(O)=O)=C(O)C=1C(C)C1=CC=CC=C1 DZZPJWJPJJNWHM-UHFFFAOYSA-N 0.000 description 1
- YBXZFYBYIPONRP-UHFFFAOYSA-N 2-hydroxy-3-phenyl-5-(2-phenylpropan-2-yl)benzoic acid Chemical compound C=1C(C(O)=O)=C(O)C(C=2C=CC=CC=2)=CC=1C(C)(C)C1=CC=CC=C1 YBXZFYBYIPONRP-UHFFFAOYSA-N 0.000 description 1
- XGAYQDWZIPRBPF-UHFFFAOYSA-N 2-hydroxy-3-propan-2-ylbenzoic acid Chemical compound CC(C)C1=CC=CC(C(O)=O)=C1O XGAYQDWZIPRBPF-UHFFFAOYSA-N 0.000 description 1
- PVOSMOVHDHSYCE-UHFFFAOYSA-N 2-phenylethyl 4-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OCCC1=CC=CC=C1 PVOSMOVHDHSYCE-UHFFFAOYSA-N 0.000 description 1
- IKEHOXWJQXIQAG-UHFFFAOYSA-N 2-tert-butyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C(C)(C)C)=C1 IKEHOXWJQXIQAG-UHFFFAOYSA-N 0.000 description 1
- MPKIZIGHGVKHDY-UHFFFAOYSA-N 2-tert-butyl-5-methylbenzene-1,4-diol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1O MPKIZIGHGVKHDY-UHFFFAOYSA-N 0.000 description 1
- ZDFKSZDMHJHQHS-UHFFFAOYSA-N 2-tert-butylbenzoic acid Chemical compound CC(C)(C)C1=CC=CC=C1C(O)=O ZDFKSZDMHJHQHS-UHFFFAOYSA-N 0.000 description 1
- ZKUWHPNJONEJEE-UHFFFAOYSA-N 3-[4-(dimethylamino)phenyl]-3-(2-methyl-1h-indol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2C3=CC=CC=C3NC=2C)C2=CC=CC=C2C(=O)O1 ZKUWHPNJONEJEE-UHFFFAOYSA-N 0.000 description 1
- YUVVASYGZFERRP-UHFFFAOYSA-N 3-benzyl-2-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=CC(CC=2C=CC=CC=2)=C1O YUVVASYGZFERRP-UHFFFAOYSA-N 0.000 description 1
- JCGRUCSGOUFSCY-UHFFFAOYSA-N 3-chloro-2-hydroxy-5-(1-phenylethyl)benzoic acid Chemical compound C=1C(Cl)=C(O)C(C(O)=O)=CC=1C(C)C1=CC=CC=C1 JCGRUCSGOUFSCY-UHFFFAOYSA-N 0.000 description 1
- HINSTNAJIHVPOM-UHFFFAOYSA-N 3-cyclohexyl-4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(C2CCCCC2)=C1 HINSTNAJIHVPOM-UHFFFAOYSA-N 0.000 description 1
- MFLGDXPSNXUOMQ-UHFFFAOYSA-N 3-phenylpropyl 4-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OCCCC1=CC=CC=C1 MFLGDXPSNXUOMQ-UHFFFAOYSA-N 0.000 description 1
- ZAAMQANODYDRDF-UHFFFAOYSA-N 3-tert-butyl-2-hydroxybenzoic acid Chemical compound CC(C)(C)C1=CC=CC(C(O)=O)=C1O ZAAMQANODYDRDF-UHFFFAOYSA-N 0.000 description 1
- TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 1
- GJGRFUMBXZMRIB-UHFFFAOYSA-N 4-(2-phenoxyethoxy)benzonitrile Chemical compound C1=CC(C#N)=CC=C1OCCOC1=CC=CC=C1 GJGRFUMBXZMRIB-UHFFFAOYSA-N 0.000 description 1
- DJKSRHOTQCDOPE-UHFFFAOYSA-N 4-[2-(2-methylphenoxy)ethoxy]benzonitrile Chemical compound CC1=CC=CC=C1OCCOC1=CC=C(C#N)C=C1 DJKSRHOTQCDOPE-UHFFFAOYSA-N 0.000 description 1
- UAHCOVMEVGXMNA-UHFFFAOYSA-N 4-[2-(3-methylphenoxy)ethoxy]benzonitrile Chemical compound CC1=CC=CC(OCCOC=2C=CC(=CC=2)C#N)=C1 UAHCOVMEVGXMNA-UHFFFAOYSA-N 0.000 description 1
- IHHQSJQLPIKEJX-UHFFFAOYSA-N 4-[2-(4-methylphenoxy)ethoxy]benzonitrile Chemical compound C1=CC(C)=CC=C1OCCOC1=CC=C(C#N)C=C1 IHHQSJQLPIKEJX-UHFFFAOYSA-N 0.000 description 1
- OMNHTTWQSSUZHO-UHFFFAOYSA-N 4-hydroxy-3,5-dimethylbenzoic acid Chemical compound CC1=CC(C(O)=O)=CC(C)=C1O OMNHTTWQSSUZHO-UHFFFAOYSA-N 0.000 description 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- VUPFPYYWAFXPEE-UHFFFAOYSA-N 6-(dimethylamino)-3,3-bis(2-phenyl-1h-indol-3-yl)-2-benzofuran-1-one Chemical compound C=1C(N(C)C)=CC=C2C=1C(=O)OC2(C=1C2=CC=CC=C2NC=1C=1C=CC=CC=1)C(C1=CC=CC=C1N1)=C1C1=CC=CC=C1 VUPFPYYWAFXPEE-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Chemical class 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Chemical class 0.000 description 1
- 229920000084 Gum arabic Chemical class 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
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- 239000002270 dispersing agent Substances 0.000 description 1
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- 239000002612 dispersion medium Substances 0.000 description 1
- OJLOUXPPKZRTHK-UHFFFAOYSA-N dodecan-1-ol;sodium Chemical compound [Na].CCCCCCCCCCCCO OJLOUXPPKZRTHK-UHFFFAOYSA-N 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
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- 150000002148 esters Chemical class 0.000 description 1
- 229960001617 ethyl hydroxybenzoate Drugs 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 229920000159 gelatin Chemical class 0.000 description 1
- 239000008273 gelatin Chemical class 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
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- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- DEOIIOVUIGWUNZ-UHFFFAOYSA-N methyl 4-(2-phenoxyethoxy)benzoate Chemical compound C1=CC(C(=O)OC)=CC=C1OCCOC1=CC=CC=C1 DEOIIOVUIGWUNZ-UHFFFAOYSA-N 0.000 description 1
- ZSYJMXLJNPEAGP-UHFFFAOYSA-N methyl n-cyanocarbamate Chemical compound COC(=O)NC#N ZSYJMXLJNPEAGP-UHFFFAOYSA-N 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000010680 novolac-type phenolic resin Substances 0.000 description 1
- GYCKQBWUSACYIF-UHFFFAOYSA-N o-hydroxybenzoic acid ethyl ester Natural products CCOC(=O)C1=CC=CC=C1O GYCKQBWUSACYIF-UHFFFAOYSA-N 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- QVCFKJHETLCZHN-UHFFFAOYSA-N pentan-2-yl 2-hydroxybenzoate Chemical compound CCCC(C)OC(=O)C1=CC=CC=C1O QVCFKJHETLCZHN-UHFFFAOYSA-N 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Chemical class 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000001454 recorded image Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000008542 thermal sensitivity Effects 0.000 description 1
- 239000001016 thiazine dye Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Heat Sensitive Colour Forming Recording (AREA)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59137565A JPS6116888A (ja) | 1984-07-02 | 1984-07-02 | 感熱記録体 |
| KR1019840005538A KR910007066B1 (ko) | 1983-09-08 | 1984-08-07 | 감열(感熱)기록체 |
| US06/642,816 US4531140A (en) | 1983-09-08 | 1984-08-21 | Heat-sensitive recording material |
| AU32428/84A AU578908B2 (en) | 1983-09-08 | 1984-08-27 | Heat-sensitive recording material |
| EP84110708A EP0141170B1 (en) | 1983-09-08 | 1984-09-07 | Heat-sensitive recording material |
| DE8484110708T DE3463630D1 (en) | 1983-09-08 | 1984-09-07 | Heat-sensitive recording material |
| US07/209,196 USRE36321E (en) | 1983-09-08 | 1988-06-20 | Heat-sensitive recording material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59137565A JPS6116888A (ja) | 1984-07-02 | 1984-07-02 | 感熱記録体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6116888A true JPS6116888A (ja) | 1986-01-24 |
| JPH0339475B2 JPH0339475B2 (enrdf_load_stackoverflow) | 1991-06-13 |
Family
ID=15201688
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59137565A Granted JPS6116888A (ja) | 1983-09-08 | 1984-07-02 | 感熱記録体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6116888A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6158789A (ja) * | 1984-08-31 | 1986-03-26 | Fuji Photo Film Co Ltd | 感熱記録材料 |
| JPS61176544A (ja) * | 1985-01-30 | 1986-08-08 | Fuji Photo Film Co Ltd | 芳香族エ−テル |
| JPH03173678A (ja) * | 1989-11-30 | 1991-07-26 | Kanzaki Paper Mfg Co Ltd | 感熱記録体 |
-
1984
- 1984-07-02 JP JP59137565A patent/JPS6116888A/ja active Granted
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6158789A (ja) * | 1984-08-31 | 1986-03-26 | Fuji Photo Film Co Ltd | 感熱記録材料 |
| JPS61176544A (ja) * | 1985-01-30 | 1986-08-08 | Fuji Photo Film Co Ltd | 芳香族エ−テル |
| JPH03173678A (ja) * | 1989-11-30 | 1991-07-26 | Kanzaki Paper Mfg Co Ltd | 感熱記録体 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0339475B2 (enrdf_load_stackoverflow) | 1991-06-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |