Triphenylmethane - CAS 519-73-3

Name: Triphenylmethane
Brand: BOC Sciences
Rating: 5 (1 reviews)

Technical Data

IUPAC Name:	benzhydrylbenzene
Description:	Triphenylmethane (CAS# 519-73-3) is a triarylmethane compound used as the backbone of synthetic dyes. Triphenylmethane has also been shown to inhibit 3-methylcholanthrene-induced neoplastic transformation of 10T1/2 cells.
Molecular Weight:	244.33
Molecular Formula:	C19H16
Canonical SMILES:	C1=CC=C(C=C1)C(C2=CC=CC=C2)C3=CC=CC=C3
InChI:	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
Boiling Point:	358-359 °C
Melting Point:	90-94 °C
Purity:	> 98 %
Density:	1.014 g/cm³
Appearance:	Off-white to brown solid
Storage:	2-8 °C
MDL:	MFCD00004763
LogP:	4.86680

GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]; H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]; H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statement:	P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
Signal Word:	Warning

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PMID	Publication Date	Title	Journal
28927721	20180201	Agonistic effects of diverse xenobiotics on the constitutive androstane receptor as detected in a recombinant yeast-cell assay	Toxicology in vitro : an international journal published in association with BIBRA
27373978	20161001	Down-Regulation of SOX2 Underlies the Inhibitory Effects of the Triphenylmethane Gentian Violet on Melanoma Cell Self-Renewal and Survival	The Journal of investigative dermatology
26177467	20151201	Redox-modulating agents target NOX2-dependent IKKε oncogenic kinase expression and proliferation in human breast cancer cell lines	Redox biology
26289545	20151101	Effect of chronic exposure to two components of Tritan copolyester on Daphnia magna, Moina macrocopa, and Oryzias latipes, and potential mechanisms of endocrine disruption using H295R cells	Ecotoxicology (London, England)
25477506	20150116	The quinone methide aurin is a heat shock response inducer that causes proteotoxic stress and Noxa-dependent apoptosis in malignant melanoma cells	The Journal of biological chemistry

Complexity:	196
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	244.12520051
Formal Charge:	0
Heavy Atom Count:	19
Hydrogen Bond Acceptor Count:	0
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	244.12520051
Rotatable Bond Count:	3
Topological Polar Surface Area:	0
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	5.3