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HomeProduct name listBenzyltriphenylphosphonium chloride

Benzyltriphenylphosphonium chloride

Synonym(s):Benzyltriphenylphosphonium chloride;BTPPC;NSC 116712;Triphenyl(phenylmethyl)phosphonium chloride;Triphenylbenzylphosphonium chloride

  • CAS NO.:1100-88-5
  • Empirical Formula: C25H22ClP
  • Molecular Weight: 388.87
  • MDL number: MFCD00011913
  • EINECS: 214-154-3
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-12-18 14:08:57
Benzyltriphenylphosphonium chloride Structural

What is Benzyltriphenylphosphonium chloride?

Chemical properties

Benzyltriphenylphosphonium Chloride is a white to off white powder, It is highly soluble in water and polarizable solvents. It is a quaternary phosphonium salt mainly used in organic synthesis as a wittig reagent and as a phase transfer catalyst in the production of fluoroelastomers and printing inks.

The Uses of Benzyltriphenylphosphonium chloride

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.

What are the applications of 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

Not classified

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.]

Properties of Benzyltriphenylphosphonium chloride

Melting point: ≥300 °C (lit.)
Density  1.18 g/cm3 (20℃)
vapor pressure  0.1 hPa
Flash point: 300°C
storage temp.  Store at <= 20°C.
form  Crystalline Powder
color  White to almost white
Water Solubility  SOLUBLE
Sensitive  Hygroscopic
BRN  3599868
Stability: Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference 1100-88-5(CAS DataBase Reference)
EPA Substance Registry System Phosphonium, triphenyl(phenylmethyl)-, chloride (1100-88-5)

Safety information for Benzyltriphenylphosphonium chloride

Signal word Danger
Pictogram(s)
ghs
Corrosion
Corrosives
GHS05
ghs
Skull and Crossbones
Acute Toxicity
GHS06
ghs
Health Hazard
GHS08
ghs
Environment
GHS09
GHS Hazard Statements H318:Serious eye damage/eye irritation
H335:Specific target organ toxicity, single exposure;Respiratory tract irritation
H372:Specific target organ toxicity, repeated exposure
H410:Hazardous to the aquatic environment, long-term hazard
Precautionary Statement Codes P260:Do not breathe dust/fume/gas/mist/vapours/spray.
P273:Avoid release to the environment.
P280:Wear protective gloves/protective clothing/eye protection/face protection.
P314:Get medical advice/attention if you feel unwell.
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Computed Descriptors for Benzyltriphenylphosphonium chloride

InChIKey USFRYJRPHFMVBZ-UHFFFAOYSA-M

Benzyltriphenylphosphonium chloride manufacturer

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A.B.ENTERPRISES

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