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Merck

B32807

Sigma-Aldrich

Benzyltriphenylphosphonium chloride

99%

Sinónimos:

BTPPC, NSC 116712, Triphenyl(phenylmethyl)phosphonium chloride

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About This Item

Fórmula lineal:
C6H5CH2P(Cl)(C6H5)3
Número de CAS:
Peso molecular:
388.87
Beilstein/REAXYS Number:
3599868
EC Number:
MDL number:
UNSPSC Code:
12352107
PubChem Substance ID:
NACRES:
NA.22

assay

99%

form

powder

reaction suitability

reaction type: C-C Bond Formation

mp

≥300 °C (lit.)

SMILES string

[Cl-].C(c1ccccc1)[P+](c2ccccc2)(c3ccccc3)c4ccccc4

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

InChI key

USFRYJRPHFMVBZ-UHFFFAOYSA-M

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Application

Benzyltriphenylphosphonium chloride can be used as a reactant for the synthesis of:
  • Platinum chloro-tetrazole complexes via azidation.
  • Trans-stilbenes and cinnamates via Wittig olefination.
  • Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment.
  • Pentiptycenes for use as light-driven molecular brakes.
  • Archipelago structures for formation of petroleum asphaltenes.


It is also used as a crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites.
Crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites

Reactant for synthesis of:
  • Platinum chloro tetrazole complexes via azidation
  • Trans-stilbenes and cinnamates via Wittig olefination
  • Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment
  • Pentiptycenes for use as light-driven molecular brakes

Reactant for formation of archipelago structures for formation of petroleum asphaltenes

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - STOT RE 1 - STOT SE 3

target_organs

Lungs,nasal cavity, Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

572.0 °F - closed cup

flash_point_c

300 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

Pentiptycene?Derived Light?Driven Molecular Brakes: Substituent Effects of the Brake Component.
Sun W T, et al.
Chemistry?A European Journal , 16(38), 11594-11604 (2010)
Orally active achiral N-hydroxyformamide inhibitors of ADAM-TS4 (aggrecanase-1) and ADAM-TS5 (aggrecanase-2) for the treatment of osteoarthritis.
De Savi , et al.
Bioorganic & Medicinal Chemistry Letters, 21(11), 3301-3306 (2011)
Synthesis and tyrosinase inhibition activity of trans-stilbene derivatives.
Ismail T, et al.
Bioorganic Chemistry, 64, 97-102 (2016)
A new route to N (1)-5R-tetrazole complexes via azidation to nitriles coordinated to Pt (II) and Pt (IV).
Popova E A, et al.
Inorgorganica Chimica Acta, 375(1), 242-247 (2011)
Formation of archipelago structures during thermal cracking implicates a chemical mechanism for the formation of petroleum asphaltenes.
Alshareef A H, et al.
Energy and Fuels, 25(5), 2130-2136 (2011)

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