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2304-30-5

2304-30-5 Structure

2304-30-5 Structure
IdentificationMore
[Name]

Tetrabutylphosphonium chloride
[CAS]

2304-30-5
[Synonyms]

TETRABUTYLPHOSPHONIUM CHLORIDE
TETRA-N-BUTYLPHOSPHONIUM CHLORIDE
Phosphonium,tetrabutyl-,chloride
tetrabutyl-phosphoniuchloride
HISHICOLIN PX-4C
TETRA-N-BUTYLPHOSPHONIUM CHLORIDE: 80% IN WATER
Tetrabutylphosphonium Chloride (80% in Water)
[EINECS(EC#)]

218-964-8
[Molecular Formula]

C16H36ClP
[MDL Number]

MFCD00011854
[Molecular Weight]

294.88
[MOL File]

2304-30-5.mol
Questions And AnswerBack Directory
[Preparation]

190.9 mL of P(C4H7)3 (154.7 g, 0.764 mol) was added to a flask equipped with a stirrer and a reflux condenser. The flask contained 100 mL of dried and degassed diethyl ether. 96.5 mL of butyl chloride (84.938 g, 0.918 mol) was added, and the solution was stirred under reflux for 2 weeks. This produced a very small amount of crystalline white product. To accelerate the reaction, the diethyl ether was stripped by distillation, and the reaction was continued under reflux for 1.5 days, during which the size of the product layer increased. The mixture was cooled to room temperature, forming a solid product layer, and 50 mL of diethyl ether (for storage) was added on top. The diethyl ether was then decanted, and the product was dissolved in 100 mL of acetone. After adding 1200 mL of diethyl ether, the product precipitated. The precipitate was filtered, washed with 3 × 150 mL of diethyl ether, and dried under vacuum to give a white powder of Tetrabutylphosphonium chloride (161.8 g, 0.680 mol, 89%).

Chemical PropertiesBack Directory
[Melting point ]

62-66 °C (dec.) (lit.)
[Boiling point ]

344.8℃[at 101 325 Pa]
[density ]

0.978[at 20℃]
[vapor pressure ]

0.018Pa at 25℃
[refractive index ]

1.5
[Fp ]

4°C (39°F)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

liquid
[color ]

colorless to pale-yellow
[Specific Gravity]

0.91
[Hydrolytic Sensitivity]

4: no reaction with water under neutral conditions
[BRN ]

4019186
[Stability:]

Hygroscopic
[InChI]

1S/C16H36P.ClH/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H/q+1;/p-1
[InChIKey]

IBWGNZVCJVLSHB-UHFFFAOYSA-M
[SMILES]

[Cl-].CCCC[P+](CCCC)(CCCC)CCCC
[LogP]

-0.44 at 23℃
[CAS DataBase Reference]

2304-30-5(CAS DataBase Reference)
[EPA Substance Registry System]

2304-30-5(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Skull and Crossbones (GHS06)
GHS05,GHS06
[Signal word ]

Danger
[Hazard statements ]

H302-H310+H330-H314
[Precautionary statements ]

P260-P280-P301+P312-P303+P361+P353-P304+P340+P310-P305+P351+P338
[Hazard Codes ]

T
[Risk Statements ]

R22:Harmful if swallowed.
R24:Toxic in contact with skin.
R34:Causes burns.
[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) .
[RIDADR ]

UN 2928 6.1/PG 2
[WGK Germany ]

3
[RTECS ]

TA2419000
[F ]

3-10
[TSCA ]

No
[HS Code ]

2931.90.9051
[REACH Registrations]

Active
[HazardClass ]

6.1(a)
[PackingGroup ]

II
[Storage Class]

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

Acute Tox. 1 Inhalation
Acute Tox. 3 Dermal
Acute Tox. 4 Oral
Aquatic Chronic 2
Eye Dam. 1
Skin Corr. 1C
Skin Sens. 1B
Hazard InformationBack Directory
[Uses]

Tetrabutylphosphonium Chloride functions as inhibitor of bovine serum amine oxidase.
[Application]

Tetrabutylphosphonium chloride is a green organic compound with a wide range of uses in catalysis, flame retardancy, solubility, ionic liquids and electroplating.
(1) As a catalyst for organic synthesis, it can be used to prepare alkyl bromides, 2-amino-4H-chromium derivatives, and methyl ester compounds.
(2) As a flame retardant additive for vinyl resins and chloroprene rubber, it is used to reduce the flammability and smoke emissions of these materials.
(3) As an ionic liquid, it provides a phosphorus source for microwave-driven synthesis of nickel phosphide nanoparticles, which are then used for efficient hydrogen evolution reactions.
(4) As an electroplating agent for various metals (such as copper, nickel, zinc, tin, lead, silver, gold, platinum, palladium and their alloys) to enhance the corrosion resistance and mechanical properties of metal coatings.
[General Description]

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
Spectrum DetailBack Directory
[Spectrum Detail]

Tetrabutylphosphonium chloride(2304-30-5)MS
Tetrabutylphosphonium chloride(2304-30-5)1HNMR
Tetrabutylphosphonium chloride(2304-30-5)13CNMR
Tetrabutylphosphonium chloride(2304-30-5)IR1
Tetrabutylphosphonium chloride(2304-30-5)Raman
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

2304-30-5(sigmaaldrich)
[TCI AMERICA]

Tetrabutylphosphonium Chloride  (80% in Water)(2304-30-5)
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