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Brilliant green

About: Brilliant green is a research topic. Over the lifetime, 627 publications have been published within this topic receiving 12495 citations.


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Journal ArticleDOI
TL;DR: In this article, the authors explored the adsorptive characteristics of Brilliant Green dye from aqueous solution onto NaOH treated saw dust of Indian Eucalyptus wood, a timber industry waste.

223 citations

Journal ArticleDOI
TL;DR: It was found that substitution of phenyl or thiophene rings at 6 and 6' positions of the benzothiophene-1,1-dioxide groups is effective to increase the fluorescence quantum yields of the closed-ring isomers over 0.7 and absorption coefficients over 4 × 10(4) M(-1) cm(-1).
Abstract: Photoswitchable or photoactivatable fluorescent dyes are potentially applicable to ultrahigh density optical memory media as well as super-resolution fluorescence imaging when the dyes are highly fluorescent and have large absorption coefficients. Here, we report on highly fluorescent photochromic dyes, which are initially nonluminous in solution under irradiation with visible light but activated to emit green or red fluorescence upon irradiation with ultraviolet (UV) light. The dyes 5a–9a are sulfone derivatives of 1,2-bis(2-ethyl-6-phenyl(or thienyl)-1-benzothiophen-3-yl)perfluorocyclopentene. It was found that substitution of phenyl or thiophene rings at 6 and 6′ positions of the benzothiophene-1,1-dioxide groups is effective to increase the fluorescence quantum yields of the closed-ring isomers over 0.7 and absorption coefficients over 4 × 104 M–1 cm–1. The phenyl-substituted derivatives 5a–7a undergo photocyclization reactions to produce yellow closed-ring isomers 5b–7b, which emit brilliant green fl...

189 citations

Book
29 Mar 2010
TL;DR: In this article, the authors discuss the use of COELENTERAZINE and its application in the field of cancer treatment, and propose a method to use it in the treatment of cancer.
Abstract: PREFACE. ABOUT THE AUTHOR. ACID FUCHSIN. ACRIDINE HOMODIMER. ACRIDINE ORANGE. ALCIAN BLUE 8GX. ALIZARIN. ALIZARIN RED S. ALLURA RED. AMARANTH. 9-AMINO-6-CHLORO-2-METHOXYACRIDINE (ACMA). ANILINE BLUE (METHYL BLUE). AURAMINE O. AZURE A. AZURE B. BAPTA. BAPTA AM. BASIC FUCHSIN. BISMARK BROWN Y. BLUE TETRAZOLIUM (BT). BOBO 1. BOBO 3. BODIPY FL C5-CERAMIDE. BRILLIANT BLUE FCF. BRILLIANT CRESYL BLUE. BRILLIANT GREEN. BSPT. BTC. BTC AM. CALCEIN. CALCEIN AM. CALCEIN BLUE. CALCEIN BLUE AM. CALCIUM GREEN 1. CALCIUM GREEN 2. CALCIUM GREEN 5N. CARMINE. COELENTERAZINE. COELENTERAZINE cp. COELENTERAZINE f. COELENTERAZINE h. COELENTERAZINE hcp. COELENTERAZINE n. CONGO RED. CoroNa GREEN. CoroNa GREEN AM. CoroNa RED. CRESYL VIOLET ACETATE. CRYSTAL VIOLET. CYANOTOLYL TETRAZOLIUM CHLORIDE (CTC). DAF FM. DANSYL CADAVERINE. DAPI. DARROW RED. DASPEI. DASPMI. Di-2-ANEPEQ. Di-4-ANEPPS. Di-8-ANEPPS. DiBAC4(3). DiBAC4(5). DiD. DIHYDROETHIDIUM. DIHYDRORHODAMINE 6G. DIHYDRORHODAMINE 123. DiI. DiIC1(5). DiOC2(3). DiOC5(3). DiOC6(3). DiOC7(3). DiSBAC2(3). DiSC3(5). EOSIN B. EOSIN Y. ERYTHROSIN. ETHIDIUM BROMIDE. ETHIDIUM HOMODIMER-1 (EthD-1). ETHIDIUM HOMODIMER-2 (EthD-2). ETHIDIUM MONOAZIDE (EMA). ETHYL EOSIN. FAST GREEN FCF. FLUO 3. FLUO 3 AM. FLUO 4. FLUO 4 AM. FLUOZIN 1. FLUOZIN 2. FLUOZIN 3. FM 4-64. FURA 2. FURA 2 AM. FURA 2FF. GIEMSA STAIN. HEMATOXYLIN. HEXIDIUM IODIDE. HOECHST 33258. HOECHST 33342. HOECHST 34580. INDIGO CARMINE. INDO 1. INDO 1 AM. IODONITRO TETRAZOLIUM (INT). JANUS GREEN B. JC 1. JC 9. JOJO 1. JO-PRO 1. LIGHT GREEN SF YELLOWISH. LOLO 1. LUCIFER YELLOW CH. LUCIFER YELLOW VS. LUCIGENIN. MAG-FURA 2 (FURAPTRA). MAG-FURA 2 AM. MAG-INDO 1. MAG-INDO 1 AM. MAGNESIUM GREEN. MALACHITE GREEN. MALACHITE GREEN OXALATE SALT. MEQ. METHYLENE BLUE. METHYLENE BLUE TRIHYDRATE. METHYLENE VIOLET (METHYLENE VIOLET BERNTHSEN). METHYL GREEN. METHYL ORANGE (ORANGE III). METHYLTHIAZOLETETRAZOLIUM (MTT). METHYL VIOLET 2B (METHYL VIOLET). MONOBROMOBIMANE (mBBr). MQAE. NBD C6-CERAMIDE. NBD METHYLHYDRAZINE. NEOTETRAZOLIUM (NT). NEUTRAL RED. NEWPORT GREEN DCF. NEWPORT GREEN PDX. NIGROSIN. NILE BLUE A. NITRO BLUE TETRAZOLIUM (NBT). NONYL-ACRIDINE ORANGE (NAO). NUCLEAR YELLOW. OIL RED O. ORANGE II (TROPAEOLIN OOO). ORANGE G. ORCEIN. OXONOL V. OXONOL VI. PARAROSANILINE HYDROCHLORIDE. PBFI. PBFI AM. PHEN GREEN SK. PHLOXINE B. PONCEAU SX. POPO 1. POPO 3. PO-PRO 1. PO-PRO 3. PROPIDIUM IODIDE. PYRONIN B. PYRONIN Y. QSY 7 CARBOXYLIC ACID, SUCCINIMIDYL ESTER. QSY 9 CARBOXYLIC ACID, SUCCINIMIDYL ESTER. QSY 21 CARBOXYLIC ACID, SUCCINIMIDYL ESTER. QUIN 2. QUIN 2 AM. REDOXSENSOR RED CC-1. RESAZURIN SODIUM SALT. RH 237. RH 414. RH 421. RH 795. RHODAMINE 6G. RHODAMINE 123. RHODZIN 3. ROSE BENGAL. SAFRANIN O. SBFI. SBFI AM. SPQ. STAINS-ALL. STILBENE ISOTHIOCYANATE SULFONIC ACID (SITS). SUDAN BLACK B. SUDAN III. SUDAN IV. SUNSET YELLOW FCF. TARTRAZINE. TETRANITRO BLUE TETRAZOLIUM (TNBT). TETRAZOLIUM VIOLET (TV). THIONIN. TMRE. TMRM. TOLUIDINE BLUE O. TO-PRO 1. TO-PRO 3. TO-PRO 5. TOTO 1. TOTO 3. TRIPHENYL TETRAZOLIUM CHLORIDE (TTC). TSQ. XTT. YO-PRO 1. YO-PRO 3. YOYO 1. YOYO 3. ZINQUIN. ZINQUIN ESTER. APPENDIX A INDEX OF CAS REGISTRY NUMBERS. APPENDIX B INDEX OF BIOLOGICAL DYES/STAINS (CERTIFIED BYBIOLOGICAL STAIN COMMISSION). APPENDIX C INDEX OF FD&C DYES (APPROVED BY FOOD & DRUGADMINISTRATION). APPENDIX D INDEX OF METAL INDICATORS. APPENDIX E INDEX OF NUCLEIC ACID STAINS. APPENDIX F INDEX OF ORGANELLE PROBES. APPENDIX G INDEX OF pH INDICATORS.

181 citations

Journal ArticleDOI
TL;DR: In this paper, the effect of experimental factors such as pH (2-10), particle size (58-150μm), adsorbent dose (0.3-1.5), contact time (5-1500min), initial dye concentration (20-100mg/L), and temperature (25-65°C) on the adsorption of Brilliant Green (BG) dye was investigated.

178 citations

Journal ArticleDOI
TL;DR: A Citrobacter sp.
Abstract: A Citrobacter sp., isolated from soil at an effluent treatment plant of a textile and dyeing industry, decolorized several recalcitrant dyes except Bromophenol Blue. More than 90% of Crystal Violet and Methyl Red at 100 μM were reduced within 1 h. Gentian Violet, Malachite Green and Brilliant Green lost over 80% of their colors in the same condition, but the percentage decolorization of Basic Fuchsin and Congo Red were less than the others, 66 and 26%, respectively. Decolorization of Congo Red was mainly due to adsorption to cells. Color removal was optimal at pH 7–9 and 35–40 °C. Decolorization of dyes was also observed with extracellular culture filtrate, indicating the color removal by enzymatic biodegradation.

171 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202332
202277
202131
202040
201950
201829