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Tributylphosphine

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Tributylphosphine Basic information

Product Name:
Tributylphosphine
Synonyms:
  • TRI-N-BUTYLPHOSPHINE (10 WT% IN HEXANE)
  • TRIBUTYL PHOSPHINE (TBP)
  • Tri-n-butylphosphine,99%
  • Tri-n-butylphosphine,99%(10wt%inhexane)
  • Tri-n-butylphosphine,min.93%
  • cytop 340
  • tributylphosphine solution
  • PBU3
CAS:
998-40-3
MF:
C12H27P
MW:
202.32
EINECS:
213-651-2
Product Categories:
  • Catalysis and Inorganic Chemistry
  • Chemical Synthesis
  • Ligand
  • organophosphorus ligand
  • organophosphine ligand
  • Phosphine Compounds
  • Tertiary Phosphines
  • Mitsunobu Reaction
  • Phosphine Ligands
  • Phosphines (Mitsunobu Reaction)
  • Synthetic Organic Chemistry
  • Achiral Phosphine
  • Alkyl Phosphine
  • 998-40-3
  • bc0001
Mol File:
998-40-3.mol
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Tributylphosphine Chemical Properties

Melting point:
-65 °C
Boiling point:
150 °C50 mm Hg(lit.)
Density 
0.81 g/mL at 25 °C(lit.)
vapor density 
9 (vs air)
vapor pressure 
1.9Pa at 20℃
refractive index 
n20/D 1.462(lit.)
Flash point:
99 °F
storage temp. 
2-8°C
form 
liquid
Specific Gravity
0.820 (20/4℃)
color 
Clear colorless to pale yellow
Water Solubility 
insoluble
Sensitive 
Moisture Sensitive/Air Sensitive
BRN 
1738261
Stability:
Stable, but pyrophoric - spontaneously inflammable in air. Incompatible with oxidizing agents. Moisture sensitive.
InChIKey
TUQOTMZNTHZOKS-UHFFFAOYSA-N
CAS DataBase Reference
998-40-3(CAS DataBase Reference)
NIST Chemistry Reference
Phosphine, tributyl-(998-40-3)
EPA Substance Registry System
Phosphine, tributyl- (998-40-3)
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Safety Information

Hazard Codes 
Xi,F,C,T
Risk Statements 
36/38-34-21/22-17-11-37-36/37/38-61
Safety Statements 
41-36/37/39-26-16-45-43-17-5-53
RIDADR 
UN 3254 4.2/PG 1
WGK Germany 
3
RTECS 
SZ3270000
10-13-23
Autoignition Temperature
392 °F
TSCA 
Yes
HazardClass 
4.2
PackingGroup 
I
HS Code 
29319090

MSDS

  • Language:English Provider:TBUP
  • Language:English Provider:SigmaAldrich
  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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Tributylphosphine Usage And Synthesis

Chemical Properties

Clear liquid

Uses

1,4-addition catalyst; used with disulfides for the thioetherification of alcohols; acylation catalyst; used to prepare active esters.

Uses

suzuki reaction

Uses

Tributylphosphine is usually used as catalyst for Domino reactions of activated conjugated dienes with β,γ-unsaturated-α-ketoesters, [3+2]-Cycloadditions,Umpolung addition reactions,Reductive carbonylation, Allylation reactions.

Synthesis Reference(s)

Tetrahedron Letters, 25, p. 2493, 1984 DOI: 10.1016/S0040-4039(01)81213-2

General Description

Tributylphosphane is a colorless to yellowish liquid with a strong garlic-like odor. Tributylphosphane is insoluble in water. Tributylphosphane is liable to heat and ignite spontaneously in air. If involved in a fire phosphine gas, a highly flammable and toxic gas, will evolve. Tributylphosphane is irritating to mucous membranes.

Air & Water Reactions

Highly flammable. May ignite on contact with air or moist air. Insoluble in water.

Reactivity Profile

Organophosphates, such as Tributylphosphane, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

Health Hazard

Fire will produce irritating, corrosive and/or toxic gases. Inhalation of decomposition products may cause severe injury or death. Contact with substance may cause severe burns to skin and eyes. Runoff from fire control may cause pollution.

Fire Hazard

Flammable/combustible material. May ignite on contact with moist air or moisture. May burn rapidly with flare-burning effect. Some react vigorously or explosively on contact with water. Some may decompose explosively when heated or involved in a fire. May re-ignite after fire is extinguished. Runoff may create fire or explosion hazard. Containers may explode when heated.

Purification Methods

Fractionally distil it under reduced pressure in an inert atmosphere (N2) through an 8inch gauze-packed column (b 110-111o/10mm) and redistil it in a vacuum, then seal it in thin glass ampoules. It is easily oxidised by air to tri-n-butylphosphine oxide, b 293-296o/745mm. It has a characteristic odour, it is soluble in EtOH, Et2O, and *C6H6 but is insoluble in H2O and less easily oxidised by air than the lower molecular weight phosphines. It forms complexes, e.g. with CS2 (1:1) m 65.5o (from EtOH). [Davies & Jones J Chem Soc 33 1929, Chernick & Skinner J Chem Soc 1401 1956, Beilstein 4 IV 3436.]

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