101303
Triphenylmethane
99%
Synonym(s):
1,1′,1′′-Methylidynetris[benzene], Tritane
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About This Item
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Quality Level
Assay
99%
form
solid
bp
358-359 °C/754 mmHg (lit.)
mp
92-94 °C (lit.)
density
1.014 g/mL at 25 °C (lit.)
functional group
phenyl
SMILES string
c1ccc(cc1)C(c2ccccc2)c3ccccc3
InChI
1S/C19H16/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,19H
InChI key
AAAQKTZKLRYKHR-UHFFFAOYSA-N
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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A collaborative study was conducted to evaluate the AOAC First Action 2012.25 LC-MS/MS analytical method for the determination of residues of three triphenylmethane dyes (malachite green, crystal violet, and brilliant green) and their metabolites (leucomalachite green and leucocrystal violet) in
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The characterization of a spore laccase from Bacillus vallismortis fmb-103, isolated from textile industry disposal sites, is described. The activity was 6.5 U/g of dry spore with ABTS as the substrate. The enzyme was quite stable at high temperature. It
Journal of the American Chemical Society, 134(36), 14650-14653 (2012-09-01)
We have increased organic field-effect transistor (OFET) NH(3) response using tris(pentafluorophenyl)borane (TPFB) as a receptor. OFETs with this additive could detect concentrations of 450 ppb v/v, with a limit of detection of 350 ppb, the highest sensitivity reported to date
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