JP2005518966A - 顕色剤の混合物 - Google Patents
顕色剤の混合物 Download PDFInfo
- Publication number
- JP2005518966A JP2005518966A JP2003572772A JP2003572772A JP2005518966A JP 2005518966 A JP2005518966 A JP 2005518966A JP 2003572772 A JP2003572772 A JP 2003572772A JP 2003572772 A JP2003572772 A JP 2003572772A JP 2005518966 A JP2005518966 A JP 2005518966A
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- bis
- anilinofluorane
- urea
- toluenesulfonyl
- 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.)
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- 150000001875 compounds Chemical class 0.000 claims abstract description 24
- 239000000463 material Substances 0.000 claims abstract description 24
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 10
- 125000004442 acylamino group Chemical group 0.000 claims abstract description 4
- 125000003118 aryl group Chemical group 0.000 claims abstract description 4
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 4
- 150000002367 halogens Chemical class 0.000 claims abstract description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
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- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
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- YASWBJXTHOXPGK-UHFFFAOYSA-N n-(4-hydroxyphenyl)octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC1=CC=C(O)C=C1 YASWBJXTHOXPGK-UHFFFAOYSA-N 0.000 description 1
- JHOKTNSTUVKGJC-UHFFFAOYSA-N n-(hydroxymethyl)octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCO JHOKTNSTUVKGJC-UHFFFAOYSA-N 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
- BTUGJXBGEVREOK-UHFFFAOYSA-N n-[3-[(4-methylphenyl)sulfonylcarbamoylamino]phenyl]acetamide Chemical compound CC(=O)NC1=CC=CC(NC(=O)NS(=O)(=O)C=2C=CC(C)=CC=2)=C1 BTUGJXBGEVREOK-UHFFFAOYSA-N 0.000 description 1
- BXQLAGQBGJFQBE-UHFFFAOYSA-N n-[4-(benzenesulfonylcarbamoylamino)phenyl]-2,2-dimethylpropanamide Chemical compound C1=CC(NC(=O)C(C)(C)C)=CC=C1NC(=O)NS(=O)(=O)C1=CC=CC=C1 BXQLAGQBGJFQBE-UHFFFAOYSA-N 0.000 description 1
- AECNRQZQYOMGOJ-UHFFFAOYSA-N n-[4-[(4-chlorophenyl)sulfonylcarbamoylamino]phenyl]-2,2-dimethylpropanamide Chemical compound C1=CC(NC(=O)C(C)(C)C)=CC=C1NC(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 AECNRQZQYOMGOJ-UHFFFAOYSA-N 0.000 description 1
- WKHIPVQKWXFTOR-UHFFFAOYSA-N n-[4-[(4-chlorophenyl)sulfonylcarbamoylamino]phenyl]sulfonylacetamide Chemical compound C1=CC(S(=O)(=O)NC(=O)C)=CC=C1NC(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 WKHIPVQKWXFTOR-UHFFFAOYSA-N 0.000 description 1
- YOJDGOVLHJCEGR-UHFFFAOYSA-N n-ethoxy-3-[(4-methylphenyl)sulfonylcarbamoylamino]benzamide Chemical compound CCONC(=O)C1=CC=CC(NC(=O)NS(=O)(=O)C=2C=CC(C)=CC=2)=C1 YOJDGOVLHJCEGR-UHFFFAOYSA-N 0.000 description 1
- MGNPLIACIXIYJE-UHFFFAOYSA-N n-fluoroaniline Chemical compound FNC1=CC=CC=C1 MGNPLIACIXIYJE-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- XAUGWFWQVYXATQ-UHFFFAOYSA-N n-phenylbenzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC1=CC=CC=C1 XAUGWFWQVYXATQ-UHFFFAOYSA-N 0.000 description 1
- 101150032584 oxy-4 gene Proteins 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl 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])[H] 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
- QHDYIMWKSCJTIM-UHFFFAOYSA-N phenyl 1-hydroxynaphthalene-2-carboxylate Chemical compound C1=CC2=CC=CC=C2C(O)=C1C(=O)OC1=CC=CC=C1 QHDYIMWKSCJTIM-UHFFFAOYSA-N 0.000 description 1
- 125000005506 phthalide group Chemical group 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 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
- 238000001953 recrystallisation Methods 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 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
- 150000004961 triphenylmethanes Chemical class 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 125000002256 xylenyl group Chemical group C1(C(C=CC=C1)C)(C)* 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- JFTNAXDYYMQUHC-UHFFFAOYSA-L zinc;4-nitrobenzoate Chemical compound [Zn+2].[O-]C(=O)C1=CC=C([N+]([O-])=O)C=C1.[O-]C(=O)C1=CC=C([N+]([O-])=O)C=C1 JFTNAXDYYMQUHC-UHFFFAOYSA-L 0.000 description 1
- JDLYKQWJXAQNNS-UHFFFAOYSA-L zinc;dibenzoate Chemical compound [Zn+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 JDLYKQWJXAQNNS-UHFFFAOYSA-L 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
- B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
- B41M5/132—Chemical colour-forming components; Additives or binders therefor
- B41M5/155—Colour-developing components, e.g. acidic compounds; Additives or binders therefor; Layers containing such colour-developing components, additives or binders
-
- 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
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
- B41M5/333—Colour developing components therefor, e.g. acidic compounds
- B41M5/3333—Non-macromolecular compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02405172 | 2002-03-06 | ||
| PCT/EP2003/001897 WO2003074284A1 (en) | 2002-03-06 | 2003-02-25 | Mixture of colour developers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005518966A true JP2005518966A (ja) | 2005-06-30 |
| JP2005518966A5 JP2005518966A5 (enExample) | 2006-03-30 |
Family
ID=27771977
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003572772A Withdrawn JP2005518966A (ja) | 2002-03-06 | 2003-02-25 | 顕色剤の混合物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20050255998A1 (enExample) |
| EP (1) | EP1480836A1 (enExample) |
| JP (1) | JP2005518966A (enExample) |
| AU (1) | AU2003212273A1 (enExample) |
| MY (1) | MY151831A (enExample) |
| WO (1) | WO2003074284A1 (enExample) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPWO2013154006A1 (ja) * | 2012-04-12 | 2015-12-17 | 長瀬産業株式会社 | 感熱記録材料 |
| WO2017111032A1 (ja) * | 2015-12-25 | 2017-06-29 | 日本化薬株式会社 | 感熱記録材料 |
| JP2018144392A (ja) * | 2017-03-07 | 2018-09-20 | 三光株式会社 | 感熱記録材料 |
| JP2019043005A (ja) * | 2017-08-31 | 2019-03-22 | 三光株式会社 | 感熱記録材料 |
| JP2019084758A (ja) * | 2017-11-07 | 2019-06-06 | 日本化薬株式会社 | 感熱記録材料 |
| JP2020520833A (ja) * | 2017-05-24 | 2020-07-16 | パピエルファブリーク・アウグスト・ケーラー・エスエー | 非フェノール系顕色剤および感熱記録材料 |
| JP2022033031A (ja) * | 2020-08-11 | 2022-02-25 | 三光株式会社 | 感熱記録材料、フェニレンジアミン尿素誘導体、及び、感熱記録層 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070015092A1 (en) * | 2005-07-13 | 2007-01-18 | Gore Makarand P | Color forming compositions |
| US9457115B2 (en) * | 2013-05-31 | 2016-10-04 | Avent, Inc. | Recyclable indicator tape for sterilization |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9827569D0 (en) | 1998-12-16 | 1999-02-10 | Ciba Geigy Ag | Heat sensitive recording material |
| MY141478A (en) * | 2002-06-04 | 2010-04-30 | Ciba Sc Holding Ag | Heat sensitive recording material |
-
2003
- 2003-02-25 US US10/506,137 patent/US20050255998A1/en not_active Abandoned
- 2003-02-25 MY MYPI20030641 patent/MY151831A/en unknown
- 2003-02-25 JP JP2003572772A patent/JP2005518966A/ja not_active Withdrawn
- 2003-02-25 WO PCT/EP2003/001897 patent/WO2003074284A1/en not_active Ceased
- 2003-02-25 EP EP03708136A patent/EP1480836A1/en not_active Withdrawn
- 2003-02-25 AU AU2003212273A patent/AU2003212273A1/en not_active Abandoned
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPWO2013154006A1 (ja) * | 2012-04-12 | 2015-12-17 | 長瀬産業株式会社 | 感熱記録材料 |
| WO2017111032A1 (ja) * | 2015-12-25 | 2017-06-29 | 日本化薬株式会社 | 感熱記録材料 |
| KR20180097579A (ko) * | 2015-12-25 | 2018-08-31 | 닛뽄 가야쿠 가부시키가이샤 | 감열 기록 재료 |
| JPWO2017111032A1 (ja) * | 2015-12-25 | 2018-10-18 | 日本化薬株式会社 | 感熱記録材料 |
| US10780724B2 (en) | 2015-12-25 | 2020-09-22 | Nippon Kayaku Kabushiki Kaisha | Heat-sensitive recording material |
| KR102493552B1 (ko) | 2015-12-25 | 2023-01-30 | 닛뽄 가야쿠 가부시키가이샤 | 감열 기록 재료 |
| JP2018144392A (ja) * | 2017-03-07 | 2018-09-20 | 三光株式会社 | 感熱記録材料 |
| JP7046984B2 (ja) | 2017-05-24 | 2022-04-04 | パピエルファブリーク・アウグスト・ケーラー・エスエー | 非フェノール系顕色剤および感熱記録材料 |
| JP2020520833A (ja) * | 2017-05-24 | 2020-07-16 | パピエルファブリーク・アウグスト・ケーラー・エスエー | 非フェノール系顕色剤および感熱記録材料 |
| JP2019043005A (ja) * | 2017-08-31 | 2019-03-22 | 三光株式会社 | 感熱記録材料 |
| JP2019084758A (ja) * | 2017-11-07 | 2019-06-06 | 日本化薬株式会社 | 感熱記録材料 |
| JP2022033031A (ja) * | 2020-08-11 | 2022-02-25 | 三光株式会社 | 感熱記録材料、フェニレンジアミン尿素誘導体、及び、感熱記録層 |
| JP7373214B2 (ja) | 2020-08-11 | 2023-11-02 | 三光株式会社 | 感熱記録材料、フェニレンジアミン尿素誘導体、及び、感熱記録層 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2003074284A1 (en) | 2003-09-12 |
| US20050255998A1 (en) | 2005-11-17 |
| MY151831A (en) | 2014-07-14 |
| EP1480836A1 (en) | 2004-12-01 |
| AU2003212273A1 (en) | 2003-09-16 |
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Legal Events
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| A621 | Written request for application examination |
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