Benzyltriphenylphosphonium chloride - ≥99% , CAS No.1100-88-5

CAS: 1100-88-5 Cat. No.: B109283 Peso molecular: 388.87 Beilstein Registry Number: 3599868 Número EC: 214-154-3

GRADE & PURITY ≥99%

Synonyms

Phosphonium, triphenyl(phenylmethyl)-, chloride | USFRYJRPHFMVBZ-UHFFFAOYSA-M | TRIPHENYL(PHENYLMETHYL)PHOSPHONIUM CHLORIDE | benzyl (triphenyl)phosphonium chloride | MFCD00011913 | benzyltriphenyl phosphonium chloride | Phosphonium, triphenyl(phenylmethy

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Specifications

Sinónimos

Phosphonium, triphenyl(phenylmethyl)-, chloride | USFRYJRPHFMVBZ-UHFFFAOYSA-M | TRIPHENYL(PHENYLMETHYL)PHOSPHONIUM CHLORIDE | benzyl (triphenyl)phosphonium chloride | MFCD00011913 | benzyltriphenyl phosphonium chloride | Phosphonium, triphenyl(phenylmethy

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature, Argon charged

Enviado en

Normal

Pureza

≥99%

Nombres e identificadores

• Sonrisas canónicas: C1=CC=C(C=C1)C[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[Cl-]
• IUPAC Name: benzyl(triphenyl)phosphanium;chloride
• InChIKey: USFRYJRPHFMVBZ-UHFFFAOYSA-M
• INCHI: 1S/C25H22P.ClH/c1-5-13-22(14-6-1)21-26(23-15-7-2-8-16-23,24-17-9-3-10-18-24)25-19-11-4-12-20-25;/h1-20H,21H2;1H/q+1;/p-1
• Isómeros SMILES: C1=CC=C(C=C1)C[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[Cl-]
• WGK Alemania: 3
• RTECS: TA2416500
• Número ONU: 2811
• Peso molecular: 388.87
• Beilstein: 3599868
• Reaxy-Rn: 3599868
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3599868&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Phenylphosphines and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylphosphines and derivatives
• Alternative Parents: Organopnictogen compounds Organophosphorus compounds Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Triphenylphosphine - Phenylphosphine - Organopnictogen compound - Hydrocarbon derivative - Organic chloride salt - Organic salt - Organophosphorus compound - Aromatic homomonocyclic compound
• Descripción: 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

Propiedades químicas y físicas

• Solubilidad: Soluble in water and alcohol. Insoluble in acetone
• Sensibilidad: Moisture sensitive;Light sensitive
• Punto de inflamación (°F): 572 °F
• Punto de inflamación (°C): 300 °C
• Punto de fusión (°C): 300°C
• Peso molecular: 388.900 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 388.115 Da
• Monoisotopic Mass: 388.115 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 27
• Formal Charge: 0
• Complexity: 347.000
• 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

Referencias

1. Shengda Wang, Shenghui Lou, Penghui Fan, Li Ma, Jie Liu, Tao Tang.  (2023)  A novel aromatic imine-containing DOPO-based reactive flame retardant towards enhanced flame-retardant and mechanical properties of epoxy resin.  POLYMER DEGRADATION AND STABILITY,      [PMID:] [10.1016/j.polymdegradstab.2023.110364]

2. Wannan Chen, Shuqin Zheng, Fengxiang Zhou, Yangkun Huang, Mei Tu, Lingxiang Jiang.  (2023)  Endoskeletal coacervates with mobile-immobile duality for long-term utility.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.142165]

3. Fu Wang, Kangkang Wang, Qiyu Zhao, Zuobin Tang, Binbin Su, Jiaren Du, Hu Liu, Huidong Xie.  (2025)  Triple-mode Luminescence and Versatile Applications of 0D Manganese-based Hybrid Halides.  Advanced Optical Materials,      [PMID:] [10.1002/adom.202403234]

4. Yan Zhang, Xiaowei Chen, Wei Li, Baoyi Wang, Qian Zhang, Zhuo Zhao, Yafei Wang, Ying Guan, Yongjun Zhang.  (2025)  Construction of Stretchable, Tough and Damped Eutectogel Resistant to −100 °C using 2-Methyl-1,3-Propanediol Based Deep Eutectic Solvent.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202511554]

5. Xuetao Yan, Lifei Chen, Yuze Ren, Kaixuan Cui, Tianliang Li, Lixing Lin, Zeyu Li, Haicheng Song, Yingying Chen, Zhenzhen Li, Lingyan Feng.  (2026)  Explainable Machine Learning for Solvents-Driven G-quartet Circularly Polarized Luminescence Material in Multilevel Anti-counterfeiting.  Advanced Optical Materials,      [PMID:] [10.1002/adom.71180]