554-70-1

  • Product Name:Triethylphosphine
  • Molecular Formula:C6H15P
  • Purity:99%
  • Molecular Weight:118.159
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Product Details;

CasNo: 554-70-1

Molecular Formula: C6H15P

Appearance: clear liquid

factory and supplier 554-70-1 Triethylphosphine in stock

  • Molecular Formula:C6H15P
  • Molecular Weight:118.159
  • Appearance/Colour:clear liquid 
  • Vapor Pressure:14.1mmHg at 25°C 
  • Melting Point:-3oC 
  • Refractive Index:1.456 
  • Boiling Point:126.516 °C at 760 mmHg 
  • Flash Point:27.202 °C 
  • PSA:13.59000 
  • Density:0.88g/mLat 20°C 
  • LogP:2.52800 

Triethylphosphine(Cas 554-70-1) Usage

Safety Profile

Highly flammable liquid. Reactswith oxygen at low temperatures to form an explosiveproduct. When heated to decomposition it emits toxicfumes of POx.

Purification Methods

All operations should be carried out in an efficient fume cupboard because it is flammable, toxic and has a foul odour. Purify the phosphine by fractional distillation at atmospheric pressure in a stream of dry N2, as it is oxidised by air to the oxide. In 300% excess of CS2 it forms Et3PCS2 (m 118-120o crystallising from MeOH) which decomposes in CCl4 to give Et3PS as a white solid m 94o when recrystallised from EtOH. [Sorettas & Isbell J Org Chem 27 273 1962, Henderson & Streuli J Am Chem Soc 82 5791 1960, pK: Henderson & Streuli J Am Chem Soc 82 5791 1960, see also trimethylphosphine.] Store it in sealed vials under N2. Alternatively, dissolve it in Et2O and shake it with a solution of AgI and KI to form the insoluble complex. Filter off the complex, dry it over P2O5 and the Et3P is regenerated by heating the complex in a tube attached to a vacuum system. [Hewitt & Holliday J Chem Soc 530 1953, Schettas & Isbell J Org Chem 27 2573 1962, Kosolapoff Organophosphorus Compounds, Wiley p 31 1950, Beilstein 4 IV 3431.]

InChI:InChI=1/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H3

554-70-1 Relevant articles

Phosphine-substituted and phosphido-bridged metal clusters in homogeneous catalysis I. Synthesis and reactivity of (η5-C5H5)NiM3(μ-H)3(CO)(9-n)Ln (M = Ru, Os, n = 1,2: L = PPh3, PPh2H, PCy3, PEt3) and M3(CO)(12-n)Ln (M = Ru, N = 1-3: L = PPh3,

Castiglioni, Mario,Giordano, Roberto,Sappa, Enrico

, p. 97 - 110 (1988)

The complexes (η5-C5H5)NiM3(μ-H)3(CO)(9-...

Bis(pertrifluoromethylcatecholato)silane: Extreme Lewis Acidity Broadens the Catalytic Portfolio of Silicon

Thorwart, Thadd?us,Roth, Daniel,Greb, Lutz

supporting information, p. 10422 - 10427 (2021/05/27)

Given its earth abundance, silicon is id...

The Trityl-Cation Mediated Phosphine Oxides Reduction

Landais, Yannick,Laye, Claire,Lusseau, Jonathan,Robert, Frédéric

supporting information, p. 3035 - 3043 (2021/05/10)

Reduction of phosphine oxides into the c...

Reversing Lewis acidity from bismuth to antimony

Balasubramaniam, Selvakumar,Jemmis, Eluvathingal D.,Kumar, Sandeep,Sharma, Deepti,Venugopal, Ajay

supporting information, p. 8889 - 8892 (2021/09/10)

Investigations on the boundaries between...

Method for producing alkyl phosphine

-

Paragraph 0044-0059, (2020/11/23)

The invention provides a method for prod...

554-70-1 Process route

triethylbenzyl phosphonium chloride
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triethylbenzyl phosphonium chloride

benzyl chloride
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benzyl chloride

triethylphosphine
554-70-1

triethylphosphine

Conditions
Conditions Yield
at 340 ℃;
ethanol
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ethanol

sodium ethanolate
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sodium ethanolate

triethyl-phenethyl-phosphonium; bromide

triethyl-phenethyl-phosphonium; bromide

styrene
100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6

styrene

triethylphosphine oxide
597-50-2

triethylphosphine oxide

1-butylbenzene
104-51-8

1-butylbenzene

triethylphosphine
554-70-1

triethylphosphine

Conditions
Conditions Yield
beim anschliessenden Erhitzen unter Stickstoff;

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