Weight | 244.337 g/mol |
---|---|
Formula | C19H16 |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 3 |
Rotatable Bonds | 3 |
TRIPHENYLMETHANE (519-73-3)
Score:
#1988 in Physics
,
#4855 in Biology
,
#6206 in Chemistry
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- THE PHOTOCHEMISTRY AND PHOTOPHYSICS OF TRIPHENYLMETHANE DYES IN SOLID AND LIQUID MEDIA (Chemical Reviews, 1993)
- TiO2-mediated photocatalytic degradation of a triphenylmethane dye (gentian violet), in aqueous suspensions (Dyes and Pigments, 2003)
- Aptamers Switch on Fluorescence of Triphenylmethane Dyes (Journal of the American Chemical Society, 2003)
- A review of the genotoxicity of food, drug and cosmetic colours and other azo, triphenylmethane and xanthene dyes (Mutation Research\/reviews in Genetic Toxicology, 1982)
- Biodegradation of triphenylmethane dyes (Enzyme and Microbial Technology, 1998)
- Synthesis and characterization of g-C3N4/Ag3VO4 composites with significantly enhanced visible-light photocatalytic activity for triphenylmethane dye degradation (Applied Catalysis B-environmental, 2014)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(C2=CC=CC=C2)C3=CC=CC=C3
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InChIKeyAAAQKTZKLRYKHR-UHFFFAOYSA-N
- Pubchem - TRIPHENYLMETHANE
- Wikipedia - triphenylmethane
Triphenylmethane, or triphenyl methane, is the hydrocarbon with the formula (C6H5)3CH. This colorless solid is soluble in nonpolar organic solvents and not in water. Triphenylmethane is the basic skeleton of many synthetic dyes called triarylmethane dyes, many of them are pH indicators, and some display fluorescence.
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