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Benzyltriphenylphosphonium chloride_Molecular_structure_CAS_1100-88-5)
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Benzyltriphenylphosphonium chloride

Catalog No. 14005 Name Sigma Aldrich
CAS Number 1100-88-5 Website http://www.sigmaaldrich.com
M. F. C25H22ClP Telephone 1-800-521-8956
M. W. 388.868941 Fax
Purity ≥99.0% (AT) Email
Storage Chembase ID: 80774

SYNONYMS

Title
苄基三苯基氯化膦
IUPAC name
benzyltriphenylphosphanium chloride
IUPAC Traditional name
benzyltriphenylphosphanium chloride
Synonyms
BTPPC
Triphenyl(phenylmethyl)phosphonium chloride
NSC 116712

DATABASE IDS

MDL Number MFCD00011913
EC Number 214-154-3
CAS Number 1100-88-5
Beilstein Number 3599868

PROPERTIES

Grade purum
Linear Formula C6H5CH2P(Cl)(C6H5)3
Purity ≥99.0% (AT)
Flash Point 300 °C
Flash Point 572 °F
Melting Point ≥300 °C(lit.)
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H300
European Hazard Symbols Toxic Toxic (T)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
GHS Precautionary statements P264-P301 + P310
RID/ADR UN 2811 6.1/PG 2
Risk Statements 25
RTECS TA2416500
Safety Statements 26-36/37/39-45
Hazard Class 6.1
UN Number 2811
Packing Group 2
German water hazard class 3

DETAILS

Description (English)
Application
Crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites1Reactant for synthesis of:
• Platinum chloro tetrazole complexes via azidation2
• Trans-stilbenes and cinnamates via Wittig olefination3
• Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment4
• Pentiptycenes for use as light-driven molecular brakes5Reactant for formation of archipelago structures for formation of petroleum asphaltenes6
Description (简体中文)
Application
Crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites1Reactant for synthesis of:
• Platinum chloro tetrazole complexes via azidation2
• Trans-stilbenes and cinnamates via Wittig olefination3
• Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment4
• Pentiptycenes for use as light-driven molecular brakes5Reactant for formation of archipelago structures for formation of petroleum asphaltenes6

REFERENCES