Skip to Content
Merck
All Photos(1)

Documents

265020

Sigma-Aldrich

Dimethylphenylphosphine

99%

Synonym(s):

Me2PPh, Phenyldimethylphosphine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(CH3)2PC6H5
CAS Number:
672-66-2
Molecular Weight:
138.15
Beilstein:
742064
EC Number:
211-595-3
MDL number:
MFCD00008509
UNSPSC Code:
12352002
PubChem Substance ID:
24856050
NACRES:
NA.22

vapor pressure

11 mmHg ( 68 °C)

Quality Level

200

Assay

99%

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 1.563 (lit.)

bp

74-75 °C/12 mmHg (lit.)

density

0.971 g/mL at 25 °C (lit.)

functional group

phosphine

SMILES string

CP(C)c1ccccc1

InChI

1S/C8H11P/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3

InChI key

HASCQPSFPAKVEK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

accessory

Product No.
Description
Pricing

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226 - H315 - H319 - H335

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

120.2 °F - closed cup

Flash Point(C)

49 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 3

1 of 3

Dicyclohexylphenylphosphine 95%

Sigma-Aldrich

288284

Dicyclohexylphenylphosphine

3-(Acryloyloxy)-2-hydroxypropyl methacrylate

Sigma-Aldrich

454982

3-(Acryloyloxy)-2-hydroxypropyl methacrylate

Bis(3,5-dimethylphenyl)phosphine

Sigma-Aldrich

695157

Bis(3,5-dimethylphenyl)phosphine

Xiao Yang et al.
Colloids and surfaces. B, Biointerfaces, 160, 136-143 (2017-09-19)
Hydroxyapatite-based implant is widely used in the fields of artificial teeth and bones. However, the problem of microbial communities on hydroxyapatite surfaces remain a great challenge. In order to inhibit bacterial adhesion and activity in a long term, a salivary
Fan Zhang et al.
Journal of the American Chemical Society, 140(42), 13854-13868 (2018-10-03)
Inorganic oxides play a crucial role in the activation of atomically dispersed metal oxides for catalytic olefin transformations, but the inefficient activation processes remain poorly understood. Activation of methyltrioxorhenium (MTO) for propene metathesis via its deposition on the surface of
Omed Al-Jaf et al.
Soft matter, 13(10), 2075-2084 (2017-02-22)
The nanomechanical properties of zwitterionic poly(cysteine methacrylate) (PCysMA) brushes grown from planar surfaces by atom transfer radical polymerisation have been characterised by friction force microscopy (FFM). FFM provides quantitative insights into polymer structure-property relationships and in particular illuminates the dependence
Yangyang Han et al.
Mikrochimica acta, 186(6), 331-331 (2019-05-08)
Polyhedral oligomeric silsesquioxane (POSS) was used to modify spherical silica to fabricate core-shell POSS@SiO2 microspheres. The material was characterized by Fourier transform infrared experiments, scanning electron microscopy, thermogravimetric analysis and elemental analysis. The material was also used as a stationary phase
Ruting Xiao et al.
Journal of chromatography. A, 1617, 460807-460807 (2020-01-01)
Click chemistry has attracted increasing attention for the synthesis of novel stationary phases. Considering the advantage of click chemistry, a strategy based on thiol-Michael addition was developed for the preparation of a new stationary phase herein, and a phenyl vinyl
View All Related Papers

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