Skip to Content
Merck
All Photos(5)

Key Documents

335150

Sigma-Aldrich

Phenylsilane

97%

Synonym(s):

Monophenylsilane

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5SiH3
CAS Number:
Molecular Weight:
108.21
Beilstein:
2935169
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.510 (lit.)

bp

120 °C (lit.)

density

0.877 g/mL at 25 °C (lit.)

SMILES string

[SiH3]c1ccccc1

InChI

1S/C6H8Si/c7-6-4-2-1-3-5-6/h1-5H,7H3

InChI key

PARWUHTVGZSQPD-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Phenylsilane (PhSiH3) may be used as a reducing agent for the partial reduction of phosphine oxide groups in poly(4,4′-diphenylphenylphosphine oxide) (PAPO) to phosphine. It can also undergo photopolymerization with methyl methacrylate(MMA) to form poly(MMA) containing SiH groups. PhSiH3 may be used as a silicon source to synthesize crystalline Si nanowires via Au-nanocrystal-seeded supercritical fluid-liquid-solid (SFLS) synthesis.

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

4.3 - Hazardous materials which set free flammable gases upon contact with water

WGK

WGK 1

Flash Point(F)

46.4 °F - closed cup

Flash Point(C)

8 °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

Synthesis of poly (arylene phosphine oxide) by nickel-catalysed coupling polymerization.
Ghassemi H
Polymer, 38(12), 3139-3143 (1997)
Chayanon Ngambenjawong et al.
Bioconjugate chemistry, 27(12), 2854-2862 (2016-10-26)
Peptide cyclization is a strategy used to improve stability and activity of peptides. The most commonly used cyclization method is disulfide bridge formation of cysteine-containing peptides, as is typically found in nature. Over the years, an increasing number of alternative
William S Kish et al.
Journal of chromatography. A, 1500, 105-120 (2017-04-24)
This work presents the selection and characterization of erythropoietin (EPO)-binding cyclic peptide ligands. The sequences were selected by screening a focused library of cyclic depsipeptides cyclo[(N
Grace Flynn et al.
Nano letters, 16(1), 374-380 (2015-12-18)
Herein, we report the formation of multisegment Si-Ge axial heterostructure nanowires in a wet chemical synthetic approach. These nanowires are grown by the liquid injection of the respective silicon and germanium precursors into the vapor phase of an organic solvent
The Role of Precursor?Decomposition Kinetics in Silicon?Nanowire Synthesis in Organic Solvents.
Lee DC
Angewandte Chemie (International Edition in English), 44(23), 3573-3577 (2005)

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