T

Triphenylmethane

IUPAC: benzhydrylbenzene

C19H16 Organic Compounds CAS 519-73-3
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Quick Reference
Formula / NotationC19H16
CAS Number519-73-3
Molecular Weight244.3
AppearanceSolid; [Merck Index] Light yellow solid; [Aldrich MSDS] Light brown powder; [Alfa Aesar MSDS]
Also Known Asbenzhydrylbenzene; 519-73-3; Tritane; Benzene, 1,1',1''-methylidynetris-; 8O4UTW9E17; NSC-4049; CHEBI:76212; RefChem:6332; 208-275-0; Benzhydrylbenzene
CategoryOrganic Compounds

What is Triphenylmethane?

Triphenylmethane is a triarylmethane in which the three aryl groups are phenyl. It forms the basic skeleton of several synthetic dyes. It has a role as a xenobiotic and an environmental contaminant.

Formula & Notation

C19H16

IUPAC Name: benzhydrylbenzene

Other Names / Synonyms: benzhydrylbenzene; 519-73-3; Tritane; Benzene, 1,1',1''-methylidynetris-; 8O4UTW9E17; NSC-4049; CHEBI:76212; RefChem:6332; 208-275-0; Benzhydrylbenzene

Properties & Characteristics

Appearance: Solid; [Merck Index] Light yellow solid; [Aldrich MSDS] Light brown powder; [Alfa Aesar MSDS]. Molecular formula: C19H16. Molecular weight: 244.3 g/mol. LogP: 5.3.

Physical Data

PropertyValue
Molecular Weight244.3
AppearanceSolid; [Merck Index] Light yellow solid; [Aldrich MSDS] Light brown powder; [Alfa Aesar MSDS]

Uses & Applications

Used as an industrial feedstock, solvent, pharmaceutical intermediate, flavoring agent, or chemical building block.

Safety Information

Flammable or irritant. Many organic compounds are flammable liquids or vapours. Keep away from ignition sources. Consult SDS for specific hazard data.

Always consult the SDS/MSDS before handling any chemical. This information is for educational purposes only.

Key Facts

Term Triphenylmethane
Formula C19H16
CAS Number 519-73-3
Molecular Weight 244.3
Synonyms benzhydrylbenzene; 519-73-3; Tritane; Benzene, 1,1',1''-methylidynetris-; 8O4UTW9E17; NSC-4049; CHEBI:76212; RefChem:6332; 208-275-0; Benzhydrylbenzene

Frequently Asked Questions

Triphenylmethane is a triarylmethane in which the three aryl groups are phenyl. It forms the basic skeleton of several synthetic dyes. It has a role as a xenobiotic and an environmental contaminant.

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Editorial standards: Chemical data is sourced from peer-reviewed literature, CAS Registry, NIST WebBook, and PubChem. Safety information reflects guidance from OSHA, ECHA, and IAEA. For educational purposes only — always consult official SDS documentation and qualified professionals before handling chemicals.