Methyltriphenylphosphonium chloride - ≥97% , CAS No.1031-15-8

CAS: 1031-15-8 Cat. No.: M102707 Molecular Weight: 312.77 EC Number: 418-400-2

GRADE & PURITY ≥97%

Synonyms

methyltriphenylphosphanium chloride | Methyltriphenylphosphonium chloride | methyl(triphenyl)phosphanium;chloride | SCHEMBL114803 | METHYLTRIPHENYLPHOSPHONIUM CHLORIDE;PHOSPHONIUM, METHYLTRIPHENYL-, CHLORIDE | DTXSID70432258 | Methyl triphenyl phosphonium

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyms

methyltriphenylphosphanium chloride | Methyltriphenylphosphonium chloride | methyl(triphenyl)phosphanium;chloride | SCHEMBL114803 | METHYLTRIPHENYLPHOSPHONIUM CHLORIDE;PHOSPHONIUM, METHYLTRIPHENYL-, CHLORIDE | DTXSID70432258 | Methyl triphenyl phosphonium

Specifications & Purity

≥97%

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 504765032
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504765032
• Canonical Smiles: C[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Cl-]
• IUPAC Name: methyl(triphenyl)phosphanium;chloride
• InChIKey: QRPRIOOKPZSVFN-UHFFFAOYSA-M
• INCHI: 1S/C19H18P.ClH/c1-20(17-11-5-2-6-12-17,18-13-7-3-8-14-18)19-15-9-4-10-16-19;/h2-16H,1H3;1H/q+1;/p-1
• Isomeric SMILES: C[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Cl-]
• WGK Germany: 2
• UN Number: 3077
• Molecular Weight: 312.77
• Reaxy-Rn: 4168881
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4168881&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Phenylphosphines and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Phenylphosphines and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylphosphines and derivatives
• Alternative Parents: Organophosphorus compounds Organic chloride salts Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Triphenylphosphine - Phenylphosphine - Hydrocarbon derivative - Organic chloride salt - Organic salt - Organophosphorus compound - Organic cation - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as phenylphosphines and derivatives. These are compounds containing a phenylphosphine, which consists of phosphine substituent bound to a phenyl group.
• External Descriptors: Not available

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: Soluble in water
• Sensitivity: Hygroscopic
• Melt Point(°C): 221°C
• Molecular Weight: 312.800 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 312.083 Da
• Monoisotopic Mass: 312.083 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 235.000
• 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: 2

XLogP3

References

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2. Gaokuo Du, Huanrong Li, Zixuan Li, Xinchi Ye, Yige Wang.  (2024)  Luminescence Boosting after adding Quaternary ammonium/Phosphine Cations to Europium (III) Laponite Clay.  APPLIED CLAY SCIENCE,      [PMID:] [10.1016/j.clay.2024.107584]

3. Pan Deng, Lin Chen, Zi-Jie Cao, Yue Li, Guan-Qi Zheng, Yu-Zhong Wang, Xiu-Li Wang.  (2025)  Bioinspired Dual-Stimulus-Responsive Macromolecular Engineering Enables Chemically Recyclable, High-Performance and Fire-Retardant Plastic.  MACROMOLECULES,      [PMID:] [10.1021/acs.macromol.5c00753]

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