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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
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General Description |
Visit our Sensor Applications portal to learn more. |
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Flammability and Explosibility |
Nonflammable |
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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
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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
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C24 H51 BrClP
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78-50-2
cyanex-921
| Conditions | Yield |
|---|---|
|
With
water;
In
toluene;
at 20 ℃;
for 1h;
|
92.6%
|
-
-
111-87-5
octanol
-
-
7539-86-8
dioctylphosphinyl chloride
-
-
78-50-2
cyanex-921
| Conditions | Yield |
|---|---|
|
In
chloroform;
at 50 ℃;
for 2h;
|
95.1%
|
78-50-2 Upstream products
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17049-49-9
octylmagnesium bromide
-
111-85-3
n-chlorooctane
-
3011-82-3
oxyde de dioctyl phosphine
-
1779-48-2
phenylphosphinic acid
78-50-2 Downstream products
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134285-08-8
4-trioctylphosphinimino-3-phenylfuroxane
-
307-34-6
Perfluorooctane
-
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
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106446-20-2
3-(4-chlorophenyl)-4-trioctylphosphiniminofurazan