Merck
All Photos(5)

T84409

Sigma-Aldrich

Triphenylphosphine

ReagentPlus®, 99%

Synonym(s):
Phosphorustriphenyl
Linear Formula:
(C6H5)3P
CAS Number:
Molecular Weight:
262.29
Beilstein:
610776
EC Number:
MDL number:
PubChem Substance ID:

vapor density

9 (vs air)

Quality Level

vapor pressure

5 mmHg ( 20 °C)

product line

ReagentPlus®

Assay

99%

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
reaction type: Cross Couplings

bp

377 °C (lit.)

mp

79-81 °C (lit.)

functional group

phosphine

SMILES string

c1ccc(cc1)P(c2ccccc2)c3ccccc3

InChI

1S/C18H15P/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

InChI key

RIOQSEWOXXDEQQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

1 of 4

This Item
8.082709309208902
Triphenylphosphine ReagentPlus®, 99%

Sigma-Aldrich

T84409

Triphenylphosphine

Triphenylphosphine for synthesis

Sigma-Aldrich

8.08270

Triphenylphosphine

Triphenylphosphine ≥95.0% (GC)

Sigma-Aldrich

93092

Triphenylphosphine

Triphenylphosphine oxide analytical standard

Supelco

08902

Triphenylphosphine oxide

assay

99%

assay

≥99.0% (GC)

assay

≥95.0% (GC)

assay

≥98.5% (HPLC)

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
reaction type: Cross Couplings

reaction suitability

-

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

reaction suitability

-

bp

377 °C (lit.)

bp

377 °C/1013 hPa

bp

377 °C (lit.)

bp

-

mp

79-81 °C (lit.)

mp

78.5-81.5 °C

mp

77-84 °C, 79-81 °C (lit.)

mp

150-157 °C (lit.)

functional group

phosphine

functional group

-

functional group

phosphine

functional group

-

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

100

General description

Rhodium and triphenylphosphine catalyst system has been used for the hydroformylation of soybean, safflower and linseed oils and their methyl esters. Polymer supported triphenylphosphine has been reported to efficiently catalyze the γ-addition of pronucleophiles to alkynoate. Triphenylphosphine reacts with hydrated ruthenium trichloride in methanol to afford [RuCl2(PPh3)4], [RuCl2(PPh3)3] and [RuCl3(PPh3)2CH3OH]. It participates in the Heck reaction of 4-bromoanisole and ethyl acrylate in ionic liquids.

Application

Triphenylphosphine was used in the synthesis of mono-6-amino-deoxy-6-cyclodextrin. It was also employed as catalyst during the synthesis of C-aryl furanosides.

Legal Information

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1B - STOT RE 1 Inhalation

Storage Class Code

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flash Point(F)

356.0 °F - closed cup

Flash Point(C)

180 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service