Trioctylphosphine oxide

CAS No.: 78-50-2

product details:

Purity: 99%

Contact us

Trioctylphosphine oxide GMP Manufacturer Global Trade 78-50-2 with Fast Delivery

  • Molecular Formula: C24H51OP
  • Molecular Weight: 386.642
  • Appearance/Colour: white crystalline powder 
  • Vapor Pressure: 1.61E-06mmHg at 25°C 
  • Melting Point: 50-55°C 
  • Refractive Index: 1.447 
  • Boiling Point: 408.842 °C at 760 mmHg 
  • Flash Point: 259.779 °C 
  • PSA: 26.88000 
  • Density: 0.861 g/cm3 
  • LogP: 9.43100 

Trioctylphosphine oxide(Cas 78-50-2) Usage

General Description

Visit our Sensor Applications portal to learn more.

Flammability and Explosibility

Nonflammable

Purification Methods

Mason, McCarty and Peppard [J Inorg Nuclear Chem 24 967 1962] stirred a 0.1M solution in *benzene with an equal volume of 6M HCl at 40o in a sealed flask for 48hours, then washed the *benzene solution successively with water (twice), 5% aqueous Na2CO3 (three times) and water (six times). The *benzene and water were then evaporated under reduced pressure at room temperature. Zingaro and White [J Inorg Nucl Chem 12 315 1960] treated a pet ether solution with aqueous KMnO4 (to oxidise any phosphinous acids to phosphinic acids), then with sodium oxalate, H2SO4 and HCl (to remove any manganese compounds). The pet ether solution was slurried with activated alumina (to remove phosphinic acids), filtered, evaporated and the residue was recrystallised from pet ether or cyclohexane at -20o. It can also be recrystallised from EtOH. [Beilstein 4 IV 3466.]

InChI:InChI=1/C24H51OP/c1-4-7-10-13-16-19-22-26(25,23-20-17-14-11-8-5-2)24-21-18-15-12-9-6-3/h4-24H2,1-3H3

78-50-2 Relevant articles

Photolytic C-O Bond Cleavage with Quantum Dots

Enright, Michael J.,Gilbert-Bass, Kito,Sarsito, Harrison,Cossairt, Brandi M.

, p. 2677 - 2682 (2019/04/25)

Quantum dots are used as photoredox cata...

Single-stage synthesis of alkyl-H-phosphinic acids from elemental phosphorus and alkyl bromides

Gusarova, Nina K.,Sutyrina, Anastasiya O.,Kuimov, Vladimir A.,Malysheva, Svetlana F.,Belogorlova, Natalia A.,Volkov, Pavel A.,Trofimov, Boris A.

, p. 328 - 330 (2019/06/13)

Elemental phosphorus (red or white) reac...

A trioctylphosphine phosphine oxide compound and its preparation method

-

Paragraph 0064; 0065, (2018/01/13)

The invention aims to provide a trioctyl...

Function of substituents in coordination behaviour, thermolysis and ligand crossover reactions of phosphine oxides

Pavankumar,Goud, E. Veerashekhar,Selvakumar,Kumar, S. K. Ashok,Sivaramakrishna, Akella,Vijayakrishna, Kari,Rao, C. V. S. Brahmananda,Sabharwal,Jha, Prakash C.

, p. 4727 - 4736 (2015/03/03)

Some selected aminophosphine oxides (AmP...

78-50-2 Process route

C<sub>24</sub>H<sub>51</sub>BrClP

C24 H51 BrClP

cyanex-921
78-50-2

cyanex-921

Conditions
Conditions Yield
With water; In toluene; at 20 ℃; for 1h;
92.6%
octanol
111-87-5

octanol

dioctylphosphinyl chloride
7539-86-8

dioctylphosphinyl chloride

cyanex-921
78-50-2

cyanex-921

Conditions
Conditions Yield
In chloroform; at 50 ℃; for 2h;
95.1%

78-50-2 Upstream products

  • 17049-49-9
    17049-49-9

    octylmagnesium bromide

  • 111-85-3
    111-85-3

    n-chlorooctane

  • 3011-82-3
    3011-82-3

    oxyde de dioctyl phosphine

  • 1779-48-2
    1779-48-2

    phenylphosphinic acid

78-50-2 Downstream products

  • 134285-08-8
    134285-08-8

    4-trioctylphosphinimino-3-phenylfuroxane

  • 307-34-6
    307-34-6

    Perfluorooctane

  • 58431-38-2
    58431-38-2

    1-(Bis-heptadecafluorooctyl-phosphinoyl)-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-octane

  • 106446-20-2
    106446-20-2

    3-(4-chlorophenyl)-4-trioctylphosphiniminofurazan

*Product Name
CasNo
Purity
Quantity
Company name
*Email
*Other Description
*Verification code:
Submit
Purchase Posted Successfully, our staff will contact you within 24 hours.