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93050

Triphenylmethane

Name: Triphenylmethane
Brand: SIAL

purum, ≥97.0% (HPLC)

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About This Item

Linear Formula:

(C₆H₅)₃CH

CAS Number:

519-73-3

Molecular Weight:

244.33

EC Number:

208-275-0

UNSPSC Code:

12352100

PubChem Substance ID:

24889780

Beilstein/REAXYS Number:

1909753

MDL number:

MFCD00004763

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grade

purum

assay

≥97.0% (HPLC)

bp

358-359 °C/754 mmHg (lit.)

mp

92-94 °C

solubility

dioxane: 0.1 g/mL, clear

density

1.014 g/mL at 25 °C (lit.)

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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Removal of triphenylmethane dyes by bacterial consortium.

Jihane Cheriaa et al.

TheScientificWorldJournal, 2012, 512454-512454 (2012-05-25)

A new consortium of four bacterial isolates (Agrobacterium radiobacter; Bacillus spp.; Sphingomonas paucimobilis, and Aeromonas hydrophila)-(CM-4) was used to degrade and to decolorize triphenylmethane dyes. All bacteria were isolated from activated sludge extracted from a wastewater treatment station of a

Phytoremediation of triphenylmethane dyes by overexpressing a Citrobacter sp. triphenylmethane reductase in transgenic Arabidopsis.

Xiao-Yan Fu et al.

Applied microbiology and biotechnology, 97(4), 1799-1806 (2012-05-11)

Triphenylmethane dyes are extensively utilized in textile industries, medicinal products, biological stains, and food processing industries, etc. They are generally considered as xenobiotic compounds, which are very recalcitrant to biodegradation. The widespread persistence of such compounds has generated concerns with

Decolorizing activity of malachite green and its mechanisms involved in dye biodegradation by Achromobacter xylosoxidans MG1.

Ji'ai Wang et al.

Journal of molecular microbiology and biotechnology, 20(4), 220-227 (2011-08-26)

An Achromobacter xylosoxidans MG1 strainisolated from the effluent treatment plant of a textile and dyeing factory from Yunnan Province in China was found capable of decolorizing the malachite green dye at a high efficacy. Strain MG1 reduced 86% malachite green

Site-directed mutagenesis provides insights into the selective binding of trityl derivatives to Plasmodium falciparum dUTPase.

Eliseo Recio et al.

European journal of medicinal chemistry, 46(8), 3309-3314 (2011-05-24)

We have previously identified a series of triphenylmethane derivatives of deoxyuridine with antimalarial activity in vitro which selectively inhibit Plasmodium falciparum deoxyuridine triphosphate nucleotidohydrolase (PfdUTPase) compared to the human enzyme. The crystal structure of PfdUTPase in complex with one of these

IncP-1β plasmids of Comamonas sp. and Delftia sp. strains isolated from a wastewater treatment plant mediate resistance to and decolorization of the triphenylmethane dye crystal violet.

Yvonne Stolze et al.

Microbiology (Reading, England), 158(Pt 8), 2060-2072 (2012-06-02)

The application of toxic triphenylmethane dyes such as crystal violet (CV) in various industrial processes leads to large amounts of dye-contaminated sludges that need to be detoxified. Specific bacteria residing in wastewater treatment plants (WWTPs) are able to degrade triphenylmethane

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Global Trade Item Number

SKU	GTIN
261513-100G	04061836831950
261513-25G	04061826107515

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