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Sigma-Aldrich

Trioctylphosphine

97%

Synonym(s):

TOP, P(Oct)3

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About This Item

Linear Formula:
[CH3(CH2)7]3P
CAS Number:
Molecular Weight:
370.64
Beilstein/REAXYS Number:
1776995
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

form

liquid

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand

refractive index

n20/D 1.468 (lit.)

bp

284-291 °C/50 mmHg (lit.)

density

0.831 g/mL at 25 °C (lit.)

functional group

phosphine

SMILES string

CCCCCCCCP(CCCCCCCC)CCCCCCCC

InChI

1S/C24H51P/c1-4-7-10-13-16-19-22-25(23-20-17-14-11-8-5-2)24-21-18-15-12-9-6-3/h4-24H2,1-3H3

InChI key

RMZAYIKUYWXQPB-UHFFFAOYSA-N

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General description

Trioctylphosphine serves as a phosphorus source and used in the synthesis of metal nanoparticles.

Application

Trioctylphosphine can be used for the conversion of metal nanocrystals, bulk powders, foils, wires, thin films to metal phosphides. It can also act as a solvent and stabilizer for synthesizing cadmium sulfide nanorods from cadmium acetate and sulfur.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

WGK 2

flash_point_f

296.6 °F - closed cup

flash_point_c

147 °C - closed cup


Certificates of Analysis (COA)

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Trioctylphosphine as both solvent and stabilizer to synthesize CdS nanorods.
Chen S, et al.
Nanoscale Research Letters, 4(10), 1159-1159 (2009)
Jaehoon Lim et al.
Nature materials, 17(1), 42-49 (2017-11-29)
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Trioctylphosphine: a general phosphorus source for the low-temperature conversion of metals into metal phosphides.
Henkes AE & Schaak RE.
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