序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
41 Multicolor heat-sensitive recording material JP816187 1987-01-19 JP2530442B2 1996-09-04 OOHASHI MIHO; KURISU TOKUO
42 Reversible recording material JP722687 1987-01-14 JPH0829621B2 1996-03-27 MARUYAMA KATSUJI; KUBO TAKASHI
43 JPH0566430B2 - JP11354786 1986-05-20 JPH0566430B2 1993-09-21 TSUTSUMI HARUKI; YAMAGUCHI TAKAMINE; HIRAYAMA NOBUHIRO; AKAHORI HIROYUKI; ASANO MAKOTO
44 Stable type indoaniline-based leuco coloring matter JP5882389 1989-03-11 JPH02238059A 1990-09-20 KUBO YOSHIHARU; YOSHIDA KATSUHEI
NEW MATERIAL:A compound expressed by formula I (R 1 is H or halogen; R 2 and R 3 are lower alkyl; X is H or lower alkyl). EXAMPLE: A compound expressed by formula II. USE: A recording material. PREPARATION: An indoaniline-based compound expressed by formula III is reacted with sodium dithionite, etc., and the resultant compound is then reduced. COPYRIGHT: (C)1990,JPO&Japio
45 New leuco dye JP6489388 1988-03-17 JPH01236279A 1989-09-21 HIGETA SHIGERU; GOTO HIROSHI; SHIOJIMA ISAO
PURPOSE:To obtain a new leuco dye having a strong absorption band in a near-infrared region unlike leuco dyes so far used in conventional thermal and pressure-sensitive recording media, by using a compound of a specified structural formula. CONSTITUTION:This leuco dye is represented by formula I, wherein R1-R8 are each lower alkyl; R9 and R10 are each H, -CN or -COR11 (except for the case where both of them are H at the same time); and R11 is phenyl, halogenated phenyl, naphthyl, lower alkyl or alkoxy. It can be obtained as white or light-colored crystals by reacting 1,1,5,5-tetrakis-(p- dialkylaminophenyl)-2,4-pentadien-1-ol perchlorate of formula II (wherein R1-R8 are each lower alkyl) with a compound of formula III (wherein R9 and R10 are the same as in formula I) in an organic solvent at 0-80 deg.C, and purifying the reaction product.
46 Multi-color heat sensitive recording material JP816187 1987-01-19 JPS63176177A 1988-07-20 OHASHI MIHO; KURISU TOKUO
PURPOSE:To provide a multi-color thermal recording material having excellent decoloring performance in low temperature coloring layer and excellent color separation performance, in a multi-color thermal recording material composed of at least one decoloring agent, two kinds or more dyes and one kind or more developer, by incorporating two kinds or more leuco dyes having excellent decoloring performance in the low temperature coloring layer. CONSTITUTION:Preferably, combination of leuco dye is composed of green, magenta yellow, cyan, magenta, etc., and combination of green and magenta is especially preferable. Any leuco dye being conventionally employed in this type of thermal material can be employed freely, for example leuco compound of triphenyl methane series, fluoran series, phenothiazine series, auramine series, spiropilane series, indolinophthalid series dye is employed. In order to obtain a two color thermally recording material, liquid containing dispersed or dissolved coloring dye, developer, decoloring agent, binder, etc., is applied onto a supporting material such as paper, synthetic paper, plastic film, etc., then it is dried, and said process is repeated.
47 Reversible recording material JP722687 1987-01-14 JPS63173684A 1988-07-18 MARUYAMA KATSUJI; KUBO TAKASHI
PURPOSE:To enable a fixing in a color-forming state, by a method wherein a recording layer containing a fluorane leuco dye shown by a specific general formula and an ascorbic acid 6-0-acyl derivative is formed on a substrate. CONSTITUTION:A coating liquid is prepared by dissolving or dispersing a mixed material of a fluorane leuco dye shown by formula I (R1, R2 represent respectively hydrogen, a 3-18 C alkyl, aralkyl, aryl, substd. aryl, and cycloalkyl, and R3 represents alkyl, halogen, alkyl aralkyl, and aryl-substd. amino), an ascorbic acid-6-0-acyl derivative, and a binder in a solvent such as an acetone. This coating liquid is applied on a substrate, such as a paper, plastic, and synthetic paper, and dried; in this manner, a reversible recording material is produced.
48 Thioindigo dye and production thereof JP917586 1986-01-20 JPS62167360A 1987-07-23 WAKEMOTO HIROBUMI; ISHIHARA SHOICHI; MATSUO YOSHIHIRO; MORIMOTO KAZUHISA
NEW MATERIAL:The compound of formula I (R 1 is a substituent group having asymmetric carbon atom; R 2 is substituent group having asymmetric carbon atom, alkyl, alkoxy, aryl or aryloxy; R 3 and R 4 are 1W3C alkyl, 1W3C alkoxy, halogen, nitro, amino, 1W3C alkylamino or dialkylamino; m and n are 0W3). EXAMPLE: 5-(S-2-methylbutyl)-5'-(4-pentylphenyl)thioindigo. USE: A material for liquid crystal display or optical recording. PREPARATION: The objective compound can be synthesized according to the reaction formula from an optically active benzene derivative of formula II having a substituent group containing asymmetric carbon atom. COPYRIGHT: (C)1987,JPO&Japio
49 Kannetsukirokushiito JP410375 1974-12-24 JPS5174643A 1976-06-28 YAMATO NOBORU; HASEGAWA KO; NISHIKUBO TOSHIBUMI; SUZUKI MAMORU; YAMAGUCHI MINORU
50 LEUCO COLORANTS AS BLUING AGENTS IN LAUNDRY CARE COMPOSITIONS EP17804361.8 2017-11-01 EP3535367A1 2019-09-11 MIRACLE, Gregory, Scot; DITULLIO, Daniel, Dale; VALENTI, Dominick, Joseph; DEY, Sanjeev, Kumar; QIN, Haihu
51 THERMOCHROMIC COMPOSITIONS FROM TRISUBSTITUTED PYRIDINE LEUCO DYES EP12772640.4 2012-09-26 EP2760940A1 2014-08-06 KRUTAK, James, J.; HENARY, Maged; OWEN, Timothy, J.
A thermochromic leuco dye composition contains a leuco dye moiety including one or more tri-aryl substituted pyridines, a UVA developer moiety including at least one UVA developer selected from the group consisting of salicylic acid and derivatives thereof, and biphenyls and derivatives thereof, and a carrier selected from the group consisting of a fatty ester, fatty alcohol, fatty amide, and combinations thereof.
52 PIGMENT EP02802750.6 2002-10-15 EP1442083B1 2005-05-18 BREIVIK, Harald; AANESEN, Berit, Annie; KULAS, Elin
This invention relates to a new pigment in feed for salmonids, a new feed comprising this pigment and use of this pigment. The pigment comprises a diester of predominantly (3R,3'R)-astaxanthin, cantaxanthin or other carotenoids that can be used for pigmentation of salmonids prepared with an omega-3 fatty acid and/or a shortchain corboxylic acid. By this invention a pigment for feed to salmonids that is more or as stable as, and biologically more effective than free astaxanthin and previously known diesters of astaxanthin and commercially available astaxanthin and cantaxanthin products, is provided. The said diesters are also useful for enhancing the growth of farmed fish, as a growth-enhancing agent in feed for farmed fish, as an appetizer in feed for fish as well as for increasing the utilization of the feed for farmed fish, and foroptimising health and well-being of farmed fish.
53 PIGMENT EP02802750.6 2002-10-15 EP1442083A1 2004-08-04 BREIVIK, Harald; AANESEN, Berit, Annie; KUL S, Elin
This invention relates to a new pigment in feed for salmonids, a new feed comprising this pigment and use of this pigment. The pigment comprises a diester of predominantly (3R,3'R)-astaxanthin, cantaxanthin or other carotenoids that can be used for pigmentation of salmonids prepared with an omega-3 fatty acid and/or a shortchain corboxylic acid. By this invention a pigment for feed to salmonids that is more or as stable as, and biologically more effective than free astaxanthin and previously known diesters of astaxanthin and commercially available astaxanthin and cantaxanthin products, is provided. The said diesters are also useful for enhancing the growth of farmed fish, as a growth-enhancing agent in feed for farmed fish, as an appetizer in feed for fish as well as for increasing the utilization of the feed for farmed fish, and foroptimising health and well-being of farmed fish.
54 안료 KR1019970004219 1997-02-13 KR100433640B1 2005-06-16 터크,브리안; 스터링,존앤드류; 파르노치,캐롤진; 맥가이로베르트브루스
본 발명은 11.82, 7.71 및 3.32 x 10 -10 m의 "d" 간격에 상응하는 3개의 주요 X-선 회절선을 갖는 X-선 회절 패턴을 나타내는 결정 형태의 색지수 안료 옐로우 12의 신규 다형체를 제공한다.
55 근 IR 영역을 흡수하는 염료 KR1019910007740 1991-05-14 KR1019910020122A 1991-12-19 조제프켈레멘; 한스알테르마트
내용 없음
56 개찰기(改札機) KR2019810001751 1981-03-12 KR2019820001097Y1 1982-05-22 권혁성
내용 없음.
57 IMAGING MEDIA PCT/US2018/064356 2018-12-06 WO2020117255A1 2020-06-11 TOLES, Christopher; BHATT, Jayprakash C.; CUMBIE, Michael W.

The present disclosure is drawn to imaging media. In one example, an imaging medium includes a substrate and a color-forming layer on the substrate. The color-forming layer includes a pattern of color-forming regions. Individual color-forming regions include multiple adjacently-applied leuco dyes in a colorless state. The leuco dyes are developable to generate color upon contact with developer compound. The imaging medium is devoid of developer compound.

58 LEUCO COLORANTS AS BLUING AGENTS IN LAUNDRY CARE COMPOSITIONS PCT/US2017/059425 2017-11-01 WO2018085312A1 2018-05-11 MIRACLE, Gregory, Scot; DITULLIO, Daniel, Dale

A laundry care composition including: (a) at least one laundry care ingredient and (b) a leuco composition. The laundry care composition after 30 days of storage at 25 °C provides a whiteness benefit to cotton upon washing that is greater than the initial whiteness benefit. Methods of treating textiles with such laundry care compositions.

59 LEUCO COLORANTS AS BLUING AGENTS IN LAUNDRY CARE COMPOSITIONS PCT/US2017/059423 2017-11-01 WO2018085310A1 2018-05-11 MIRACLE, Gregory, Scot; DITULLIO, Daniel, Dale; VALENTI, Dominick, Joseph; DEY, Sanjeev, Kumar; QIN, Haihu

A laundry care composition including: (a) at least one laundry care ingredient and (b) a leuco composition. The laundry care composition has a ΔHA of at least 10. Methods of treating textiles with such laundry care compositions.

60 THERMOCHROMIC COMPOSITIONS FROM TRISUBSTITUTED PYRIDINE LEUCO DYES PCT/US2012/057366 2012-09-26 WO2013049229A1 2013-04-04 KRUTAK, James, J.; HENARY, Maged; OWEN, Timothy, J.

A thermochromic leuco dye composition contains a leuco dye moiety including one or more tri-aryl substituted pyridines, a UVA developer moiety including at least one UVA developer selected from the group consisting of salicylic acid and derivatives thereof, and biphenyls and derivatives thereof, and a carrier selected from the group consisting of a fatty ester, fatty alcohol, fatty amide, and combinations thereof.

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