GRADE & PURITY ≥99%

Synonyms

1,1',1''-Methylidynetris[benzene] | Benzene,1',1''-methylidynetris- | Triphenylmethyl radical | A828866 | Benzhydrylbenzene | benzhydryl-benzene | Q424277 | CHEBI:76212 | triphenyl methane | UNII-8O4UTW9E17 | DTXSID3060164 | CCRIS 5194 | SY012825 | AI3-02

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

1, 1', 1''-Methylidynetris[benzene] | Benzene, 1', 1''-methylidynetris- | Triphenylmethyl radical | A828866 | Benzhydrylbenzene | benzhydryl-benzene | Q424277 | CHEBI:76212 | triphenyl methane | UNII-8O4UTW9E17 | DTXSID3060164 | CCRIS 5194 | SY012825 | AI3-02

Specifications & Purity

≥99%

Storage

Room temperature

Shipped In

Normal

Purity

≥99%

Names and Identifiers

• Pubchem Sid: 488181151
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181151
• Canonical Smiles: C1=CC=C(C=C1)C(C2=CC=CC=C2)C3=CC=CC=C3
• IUPAC Name: benzhydrylbenzene
• InChIKey: AAAQKTZKLRYKHR-UHFFFAOYSA-N
• 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
• Isomeric SMILES: C1=CC=C(C=C1)C(C2=CC=CC=C2)C3=CC=CC=C3
• WGK Germany: 3
• PubChem CID: 10614
• Molecular Weight: 244.33
• Beilstein: 1909753
• Reaxy-Rn: 1909753

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Triphenyl compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Triphenyl compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Triphenyl compounds
• Alternative Parents: Benzene and substituted derivatives Aromatic hydrocarbons Unsaturated hydrocarbons
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Triphenyl compound - Monocyclic benzene moiety - Aromatic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety.
• External Descriptors: triarylmethane

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Solubility in Toluene very faint turbidity
• Boil Point(°C): 358-359 °C/754 mmHg
• Melt Point(°C): 92-95°C
• Molecular Weight: 244.300 g/mol
• XLogP3: 5.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 244.125 Da
• Monoisotopic Mass: 244.125 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 196.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Fan Yang, Zhihui Liu, Xiaodong Liu, Andong Feng, Bing Zhang, Wang Yang, Yongfeng Li.  (2020)  Cobalt single atoms anchored on nitrogen-doped porous carbon as an efficient catalyst for oxidation of silanes.  GREEN CHEMISTRY,  23  (2): (1026-1035).  [PMID:] [10.1039/D0GC03498C]

2. Ganshang Si, Yanchun Wang, Xu Liu, Changwei Sun, Junfang Miao, Zhengang Li.  (2024)  Detection of powder samples based on UV Raman-fluorescence spectroscopy.  OPTICS COMMUNICATIONS,      [PMID:] [10.1016/j.optcom.2024.130950]

3. Qiang Chen, Pengzhu Gai, Wang Feng, Jin Zhang, Yuqin Lu, Fang Xu, Huidong Qian, Kang Huang, Zhi Xu.  (2026)  Partially branched poly (aryl piperidinium) anion exchange membranes with excellent efficiency for neutral aqueous organic redox flow batteries.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2026.125329]