ChemicalBook--->CAS DataBase List--->1100-88-5

1100-88-5

1100-88-5 Structure

1100-88-5 Structure
IdentificationMore
[Name]

Benzyltriphenylphosphonium chloride
[CAS]

1100-88-5
[Synonyms]

AURORA KA-1173
BENZYLIDENE(TRIPHENYL)PHOSPHORANE
(phenylmethyl)triphenyl-phosphoniuchloride
(phenylmethyl)triphenylphosphoniumchloride
Benzyltriphenylchlorophosphine
benzyltriphenylphosphonidechloride
benzyltriphenyl-phosphoniuchloride
Phosphonium,triphenyl(phenylmethyl)-,chloride
triphenyl(phenylmethyl)-phosphoniuchloride
triphenyl(phenylmethyl)phosphoniumchloride
Triphenyl(phenylmethyl)-phosphoniumchloride
BPP
Benzyltriphenylphosphoniumchloride,99%
BTPPCl: Benzyltriphenylphosphonium Chloride
Benzyltriphenylphosphonium chloride
BENZYL TRIPHENYL PHOSPHONIUM CHLORIDE(BTTPC)
Phosphonium, benzyltriphenyl, chloride
Triphenylbenzylidenephosphorane
benzyltriphenilphosphonium chloride
[EINECS(EC#)]

214-154-3
[Molecular Formula]

C25H22ClP
[MDL Number]

MFCD02177525
[Molecular Weight]

388.87
[MOL File]

1100-88-5.mol
Chemical PropertiesBack Directory
[Appearance]

white powder
[Melting point ]

≥300 °C (lit.)
[density ]

1.18 g/cm3 (20℃)
[vapor pressure ]

0.1 hPa
[Fp ]

300°C
[storage temp. ]

Store at <= 20°C.
[form ]

Crystalline Powder
[color ]

White to almost white
[Stability:]

Stable. Incompatible with strong oxidizing agents.
[Water Solubility ]

SOLUBLE
[Sensitive ]

Hygroscopic
[BRN ]

3599868
[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
[InChIKey]

USFRYJRPHFMVBZ-UHFFFAOYSA-M
[SMILES]

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

-0.7 at 20℃
[CAS DataBase Reference]

1100-88-5(CAS DataBase Reference)
[Storage Precautions]

Light sensitive;Moisture sensitive
[EPA Substance Registry System]

1100-88-5(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Skull and Crossbones (GHS06)Health Hazard (GHS08)Environment (GHS09)
GHS05,GHS06,GHS08,GHS09
[Signal word ]

Danger
[Hazard statements ]

H300+H330-H318-H335-H372-H410
[Precautionary statements ]

P260-P273-P280-P304+P340+P310-P305+P351+P338-P314
[Hazard Codes ]

T,Xi
[Risk Statements ]

R25:Toxic if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
R24/25:Toxic in contact with skin and if swallowed .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36:Wear suitable protective clothing .
[RIDADR ]

UN 2811 6.1/PG 2
[WGK Germany ]

3
[RTECS ]

TA2416500
[TSCA ]

Yes
[REACH Registrations]

Active
[HazardClass ]

6.1
[PackingGroup ]

II
[HS Code ]

29310095
[Storage Class]

6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
[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
[Toxicity]

LD50 orally in Rabbit: 43 mg/kg
Raw materials And Preparation ProductsBack Directory
[Raw materials]

3-Cyanopyridine
[Preparation Products]

Sulindac-->Flunarizine EP Impurity D-->(Z)-Cinnarizine
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Benzyltriphenylphosphonium chloride(1100-88-5).msds
Hazard InformationBack Directory
[Chemical Properties]

white powder
[Uses]

Benzyltriphenylphosphonium Chloride was used as a reagent in the organic synthesis of several compounds including that of stabilised phosphonium ylides containing saturated oxygen heterocycles. Also used in the synthesis of novel substituted cis-stilbene derivatives which display antimicrobial activity.
[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
[Flammability and Explosibility]

Notclassified
[reaction suitability]

reaction type: C-C Bond Formation
[Purification Methods]

Wash it with Et2O and crystallise it from EtOH (six-sided plates). It is hygroscopic and forms crystals with one molecule of H2O. [Michaelis & Soden Justus Liebigs Ann Chem 229 320 1885, Kr.hnke Chem Ber 83 291 1950, Beilstein 16 IV 994.]
Spectrum DetailBack Directory
[Spectrum Detail]

Benzyltriphenylphosphonium chloride(1100-88-5)MS
Benzyltriphenylphosphonium chloride(1100-88-5)1HNMR
Benzyltriphenylphosphonium chloride(1100-88-5)13CNMR
Benzyltriphenylphosphonium chloride(1100-88-5)IR1
Benzyltriphenylphosphonium chloride(1100-88-5)IR2
Benzyltriphenylphosphonium chloride(1100-88-5)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Benzyltriphenylphosphonium chloride, 99%(1100-88-5)
[Alfa Aesar]

Benzyltriphenylphosphonium chloride, 99%(1100-88-5)
[Sigma Aldrich]

1100-88-5(sigmaaldrich)
[TCI AMERICA]

Benzyltriphenylphosphonium Chloride,>98.0%(T)(1100-88-5)
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