| Identification | More | [Name]
Trioctylphosphine oxide | [CAS]
78-50-2 | [Synonyms]
CYANEX 921
TOPO
TRI-N-OCTYLPHOSPHINE OXIDE
TRI-N-OCTYLPHOSPHINOXIDE
TRIOCTYLPHOSPHINE OXIDE
hostarexpx324
trioctyl-phosphineoxid
TRIOCTYLPHOSPHINE OXIDE, TECH., 90%
TRIOCTYLPHOSPHINE OXIDE, REAGENTPLUS, 99%
TRIOCTYLPHOSPHINE OXIDE REAGENTPLUS(TM&
TRIOCTYLPHOSPHINE OXIDE (CYANEX 921) CYTEC QUALITY
TRIOCTYLPHOSPHINE OXIDE, FOR EXTRACTION ANALYSIS
Tri-N-OctylphosphineOxideGr
Tri-n-octylphosphineoxide,98%
Trioctylphosphineoxide,99%TOPO
Trioctylphosphineoxide,min.90%TOPO
Phosphine oxide, trioctyl-
HISHICOLIN PO-8
Tri-n-octylphosphine oxide: (Trioctylphophine oxide)
TOPO(R) | [EINECS(EC#)]
201-121-3 | [Molecular Formula]
C24H51OP | [MDL Number]
MFCD00002083 | [Molecular Weight]
386.63 | [MOL File]
78-50-2.mol |
| Chemical Properties | Back Directory | [Appearance]
white crystalline powder | [Melting point ]
50-52 °C(lit.)
| [Boiling point ]
201-202 °C2 mm Hg(lit.)
| [density ]
0,88 g/cm3 | [vapor pressure ]
0.004Pa at 50℃ | [Fp ]
>230 °F
| [storage temp. ]
Store below +30°C. | [solubility ]
<1g/l | [form ]
Crystalline Powder, Crystals or Flakes | [color ]
White to slightly yellow | [Stability:]
Stable. Incompatible with strong oxidizing agents. | [Water Solubility ]
Insoluble | [BRN ]
1796648 | [CAS DataBase Reference]
78-50-2(CAS DataBase Reference) | [EPA Substance Registry System]
78-50-2(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R38:Irritating to the skin.
R41:Risk of serious damage to eyes. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/39:Wear suitable protective clothing and eye/face protection .
S39:Wear eye/face protection . | [RIDADR ]
3261 | [WGK Germany ]
2
| [RTECS ]
SZ1662500
| [Autoignition Temperature]
270 °C | [TSCA ]
Yes | [PackingGroup ]
II | [HS Code ]
29310095 | [HS Code ]
32019090 | [Hazardous Substances Data]
78-50-2(Hazardous Substances Data) | [Toxicity]
LD50 orally in Rabbit: > 10000 mg/kg LD50 dermal Rat 2830 mg/kg |
| Hazard Information | Back Directory | [Chemical Properties]
white crystalline powder | [Uses]
Catalyst in:
- Preparation of tetradentate planar-chiral hydroxy-substituted ferrocenecarboxaldimine Schiff base ligands
- Reactions of allyl esters with hydrosilanes
- Asymmetric cyanosilylation of aldehydes
- Preparation of chlorothiol formates from thiols and phosgene
| [Uses]
Tri-n-octylphosphine oxide is a solvent used in the extraction of metals, especially uranium, zirconium and hafnium. It is also used as an auxiliary reagent in the solvent extraction of metals. It is also used to extract hydrogen bonding organic compounds. Further, it is useful as a capping ligand for the production of quantum dots, such as those consisting of cadmium selenide. | [Uses]
Trioctylphosphine oxide (TOPO) is most commonly used as the solvent due to its high boiling point and chemical stability, and its ability to prevent particle aggregation via coordination to the NP surface. trioctylphosphine oxide is a frequently used surfactant, starts to decompose at around 425°C.
The industrial applications of trioctylphosphine oxide, make use of its complexing powers with metals and with hydrogen donor organic compounds. Commercial uses as a solvent extraction reagent are in the recovery of uranium from wet process phosphoric acid and in the recovery of byproduct acetic acid and furfural generated during sulphite wood pulping.
TOPO is a widely used chemical compound in nanocrystal synthesis, for the removal of heavy metals, and the removal of toxins in waste water. TOPO is often used as a ligand stabilizer for colloids in traditional thermal decomposition synthetic techniques.
trioctylphosphine oxide became a nearly irreplaceable solvent (mp 51-52°C) for high-temperature preparation of various type of nanocomposites. TOPO has a very high boiling point (411°C) which is an important prerequisite for the homogeneous nucleation and good crystallinity of the nanoparticles.
| [General Description]
| [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.] |
|
|