子分类：
- C09B69/001： .{包含通过桥连接到染料骨架上的鎓基团的染料}
- C09B69/007： .{含膦酸或次膦酸基团或其衍生物的染料}
- C09B69/008： .{含取代基的染料,取代基中包含硅原子}
- C09B69/02： .染料的盐,例如酸性染料与碱性染料的盐(关于染料的Na、K或NH4+盐或关于氯化物、硫酸盐或氯锌酸盐,见有关的染料组)
- C09B69/08： .含有一种易分裂的水增溶基的染料{含有经桥连接到染料分子的鎓基团的染料被视为阳离子染料,并按单独的染料分类入如C09B 44/02至C09B 44/08;C09B69/001-C09B69/005 }
- C09B69/10： .聚合的染料;染料与单体或高分子化合物的反应产物{(染料的环氧烷加成产物入C09B 69/00;用聚合的染料染色入D06P 1/0056)}
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 141 | WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE | US15605616 | 2017-05-25 | US20180100861A1 | 2018-04-12 | Tracy Matray; Hesham Sherif |
| Compounds useful as fluorescent or colored dyes are disclosed. The compounds have the following structure (I): including stereoisomers, salts and tautomers thereof, wherein R1a, R1b, R2a, R2b, R2c, R2d, R2e, R2f, R2g, R2h, R2i, R2j, R2k, R2l, R2m, R2n, R2o, R2p, R2q, R2r and R2s are as defined herein. Methods associated with preparation and use of such compounds are also provided. | ||||||
| 142 | Fluorogenic pH sensitive dyes and their method of use | US14455550 | 2014-08-08 | US09910051B2 | 2018-03-06 | Daniel Beacham; Jeffrey Dzubay; Kyle Gee; Vladimir Martin; Aleksey Rukavishnikov |
| A new class of pH sensitive fluorescent dyes and assays relating thereto are described. The dyes and assays are particularly suited for biological applications including phagocytosis and monitoring intracellular processes. The pH sensitive fluorescent dyes of the present invention include compounds of Formula I: wherein the variables are described throughout the application. | ||||||
| 143 | FLUORESCENT WATER-SOLVATED CONJUGATED POLYMERS | US15642216 | 2017-07-05 | US20180009990A1 | 2018-01-11 | Glenn P. Bartholomew; Yongchao Liang; Brent S. Gaylord |
| Water solvated polymeric dyes and polymeric tandem dyes are provided. The polymeric dyes include a water solvated light harvesting multichromophore having a conjugated segment of aryl or heteroaryl co-monomers linked via covalent bonds, vinylene groups or ethynylene groups. The polymeric tandem dyes further include a signaling chromophore covalently linked to the multichromophore in energy-receiving proximity therewith. Also provided are labeled specific binding members that include the subject polymeric dyes. Methods of evaluating a sample for the presence of a target analyte and methods of labeling a target molecule in which the subject polymeric dyes find use are also provided. Systems and kits for practicing the subject methods are also provided. | ||||||
| 144 | BENZOPYRYLIUM COMPOUNDS | US15493208 | 2017-04-21 | US20180002340A1 | 2018-01-04 | Greg Hermanson; Peter T. Czerney; Surbhi Desai; Matthias S. Wenzel; Frank G. Lehmann; Marie Christine Nlend |
| Compounds used as labels with properties comparable to known fluorescent compounds. The compounds are conjugated to proteins and nucleic acids for biological imaging and analysis. Synthesis of the compounds, formation and use of the conjugated compounds, and specific non-limiting examples of each are provided. | ||||||
| 145 | Whitening agents for cellulosic substrates | US15283456 | 2016-10-03 | US09777250B2 | 2017-10-03 | Sanjeev K. Dey; Gregory Scot Miracle |
| The present application relates to novel whitening agents for cellulosic substrates. The whitening agents are comprised of at least two constituents: at least one chromophore constituent and at least one polymeric constituent. Suitable chromophore components generally fluoresce blue, red, violet, or purple color when exposed to light, or they may absorb light to reflect these same shades. This disclosure also relates to laundry care compositions including but not limited to liquid and/or powder laundry detergent formulations and rinse added fabric softening (RAFS) compositions that comprise such whitening agents. | ||||||
| 146 | Bis-Azo Colorants For Use As Bluing Agents | US15363022 | 2016-11-29 | US20170218202A1 | 2017-08-03 | Sanjeev K. Dey; Eduardo Torres; Gregory S. Miracle; Daniel D. Ditullio, JR. |
| This invention relates to bis-azo colorants for use as bluing agents, laundry care compositions comprising bis-azo colorants that may serve as bluing agents, processes for making such bluing agents and laundry care compositions and methods of using the same. The bluing agents are generally comprised of at least two components: at least one chromophore component and at least one polymeric component. These bluing agents are advantageous in providing a whitening effect to fabrics, while not building up over time and causing undesirable blue discoloration to the treated fabrics. | ||||||
| 147 | Detergent composition comprising bluing agent and clay soil removal / anti-redeposition agent | US13313340 | 2011-12-07 | US09708573B2 | 2017-07-18 | Patrick Christopher Stenger; Gregory Scot Miracle; Andrew Philip Moon; Brian Joseph Loughnane; Sivaramakrishnan Muthukrishnan |
| A laundry detergent composition having: (a) detersive surfactant; (b) bluing agent, and (c) a clay and soil removal/anti-redeposition agent; and (d) optionally, one or more additional laundry detergent ingredients. | ||||||
| 148 | Water soluble fluorescent or colored dyes and methods for their use | US15112395 | 2015-01-16 | US09689877B2 | 2017-06-27 | Tracy Matray; Hesham Sherif |
| Compounds useful as fluorescent or colored dyes are disclosed. The compounds have the following structure (I): Formula (I), including stereoisomers, salts and tautomers thereof, wherein R1a, R1b, R2a, R2b, R2c, R2d, R2e, R2f, R2g, R2h, R2i, R2j, R2k, R2l, R2m, R2n, R2o, R2p, R2q, R2r and R2s are as defined herein. Methods associated with preparation and use of such compounds are also provided. | ||||||
| 149 | PHOTOSTABLE FLUORESCENT POLYMERIC TANDEM DYES INCLUDING LUMINESCENT METAL COMPLEXES | US15371064 | 2016-12-06 | US20170174892A1 | 2017-06-22 | Robert J. Radford; Douglas B. Sherman; Jody Martin; James Ghadiali |
| Photostable polymeric tandem dyes are provided. The photostable polymeric tandem dyes include a water soluble light harvesting multichromophore and a luminescent metal complex covalently linked to the multichromophore and in energy-receiving proximity therewith. Also provided are labelled specific binding members that include the subject dyes. Methods of evaluating a sample for the presence of a target analyte and methods of labelling a target molecule in which the subject polymeric tandem dyes find use are also provided. Systems and kits for practicing the subject methods are also provided. | ||||||
| 150 | BENZOPYRYLIUM COMPOUNDS | US14411447 | 2013-08-20 | US20170152267A9 | 2017-06-01 | Greg Hermanson; Peter T. Czerney; Surbhi Desai; Matthias S. Wenzel; Frank G. Lehmann; Marie Christine Nlend |
| Compounds used as labels with properties comparable to known fluorescent compounds. The compounds are conjugated to proteins and nucleic acids for biological imaging and analysis. Synthesis of the compounds, formation and use of the conjugated compounds, and specific non-limiting examples of each are provided. | ||||||
| 151 | Laundry Care Compositions Containing Dyes | US15421621 | 2017-02-01 | US20170137629A1 | 2017-05-18 | Eduardo Torres; Gregory Scot Miracle |
| Laundry care compositions comprising thiophene azo carboxylate fabric shading dyes and methods of treating a textile comprising such laundry care compositions. | ||||||
| 152 | Novel Whitening Agents for Cellulosic Substrates | US15283464 | 2016-10-03 | US20170101537A1 | 2017-04-13 | Dominick J. Valenti; Eduardo Torres; Sanjeev K. Dey; Gregory Scot Miracle |
| The present application relates to novel whitening agents for cellulosic substrates. The whitening agents are comprised of at least two constituents: at least one chromophore constituent and at least one polymeric constituent. Suitable chromophore components generally fluoresce blue, red, violet, or purple color when exposed to light, or they may absorb light to reflect these same shades. This disclosure also relates to laundry care compositions including but not limited to liquid and/or powder laundry detergent formulations and rinse added fabric softening (RAFS) compositions that comprise such whitening agents. | ||||||
| 153 | MULTIMERIC PROTECTED FLUORESCENT REAGENTS | US15015602 | 2016-02-04 | US20160237279A1 | 2016-08-18 | Frank ZHENG; Jeremiah HANES; Gene SHEN; Louis BROGLEY; Stephen YUE; Yuri LAPIN; John LYLE; Honey OSUNA; Andrei FEDOROV; Lubomir SEBO |
| Multimeric protected fluorescent reagents and their methods of synthesis are provided. The reagents are useful in various fluorescence-based analytical methods, including the analysis of highly multiplexed optical reactions in large numbers at high densities, such as single molecule real time nucleic acid sequencing reactions. The reagents contain fluorescent dye elements, that allow the compounds to be detected with high sensitivity at desirable wavelengths, binding elements, that allow the compounds to be recognized specifically by target biomolecules, and protective shield elements, that decrease undesirable contacts between the fluorescent dye elements and the bound target biomolecules and that therefore decrease photodamage of the bound target biomolecules by the fluorescent dye elements. The reagents also contain coupling elements connect monomeric compounds into multimeric forms, thereby increasing brightness. | ||||||
| 154 | CYANINE COMPOUNDS | US15042495 | 2016-02-12 | US20160168383A1 | 2016-06-16 | Greg Hermanson; Peter T. Czerney; Surbhi Desai; Matthias S. Wenzel; Boguslawa R. Dworecki; Frank G. Lehmann |
| Compounds used as labels with properties comparable to known fluorescent compounds. The compounds can be conjugated to proteins and nucleic acids for biological imaging and analysis. Synthesis of the compounds, formation and use of the conjugated compounds, and specific non-limiting examples of each are provided. | ||||||
| 155 | Azo compound, pigment dispersant containing the azo compound, pigment composition, pigment dispersion and toner | US14370873 | 2013-02-27 | US09298118B2 | 2016-03-29 | Masashi Kawamura; Yasuaki Murai; Waka Hasegawa; Yuki Hasegawa; Takayuki Toyoda; Taiki Watanabe; Masanori Seki; Chiaki Nishiura; Ayano Mashida; Masashi Hirose |
| An object of the present invention is to provide an azo compound capable of improving the dispersibility of an azo pigment in a non-water-soluble solvent. The object of the present invention is achieved with an azo compound wherein a coloring matter moiety having a diketone azo structure and a polymer are bonded to each other. | ||||||
| 156 | Laundry care composition comprising carboxylate dye | US14489500 | 2014-09-18 | US09267098B2 | 2016-02-23 | Gregory Scot Miracle |
| The present invention relates to laundry care compositions comprising thiophene azo carboxylate dyes. | ||||||
| 157 | FLUORESCENT COMPOUNDS | US14733764 | 2015-06-08 | US20160033520A1 | 2016-02-04 | Fei Mao; Wai-Yee Leung; Ching-Ying Cheung; Hye Eun Hoover |
| The present invention relates to fluorescent dyes in general. The present invention provides a wide range of fluorescent dyes and kits containing the same, which are applicable for labeling a variety of biomolecules, cells and microorganisms. The present invention also provides various methods of using the fluorescent dyes for research and development, forensic identification, environmental studies, diagnosis, prognosis, and/or treatment of disease conditions. | ||||||
| 158 | Laundry care composition comprising carboxylate dye | US14489504 | 2014-09-18 | US09234163B2 | 2016-01-12 | Gregory Scot Miracle |
| The present invention relates to laundry care compositions comprising mono-azo carboxylate dyes. | ||||||
| 159 | Thiophene azo carboxylate dyes and laundry care compositions containing the same | US13479340 | 2012-05-24 | US09163146B2 | 2015-10-20 | Eduardo Torres; John D. Bruhnke; Sanjeev K. Dey; Gregory S. Miracle |
| This application relates to thiophene azo carboxylate dyes for use as hueing agents, laundry care compositions comprising such dyes that may serve as hueing agents, processes for making such dyes and laundry care compositions and methods of using the same. The aforementioned dyes contain a formally charged moiety and are generally comprised of at least two components: at least one chromophore component and at least one polymeric component. Suitable chromophore components generally fluoresce blue, red, violet, or purple color when exposed to ultraviolet light, or they may absorb light to reflect these same shades. Such dyes are advantageous in providing a hueing effect, for example, a whitening effect to fabrics, while not building up over time and causing undesirable blue discoloration to the treated fabrics. Such dyes are also generally stable to bleaching agents used in laundry care compositions. | ||||||
| 160 | METHOD FOR PRODUCING CONTRAST AGENT | US14534111 | 2014-11-05 | US20150126749A1 | 2015-05-07 | Tatsuki Fukui; Atsushi Takahashi; Daisuke Sasaguri; Fumiko Tomatsu |
| A method for producing a contrast agent includes the reaction step of allowing a cyanine dye containing a naphthyl group and a carboxyl or carboxylate group to react with a polyethylene glycol containing an amino group in an organic solvent to form a conjugate, and the purification step of purifying the conjugate using an organic solvent. | ||||||
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