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108006

Sigma-Aldrich

Benzyl alcohol

ReagentPlus®, ≥99%

Synonym(s):

Benzenemethanol

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About This Item

Linear Formula:
C6H5CH2OH
CAS Number:
Molecular Weight:
108.14
Beilstein:
878307
EC Number:
MDL number:
UNSPSC Code:
12352104
eCl@ss:
39023110
PubChem Substance ID:
NACRES:
NA.21

vapor density

3.7 (vs air)

Quality Level

vapor pressure

13.3 mmHg ( 100 °C)
3.75 mmHg ( 77 °C)

product line

ReagentPlus®

Assay

≥99%

form

liquid

autoignition temp.

817 °F

expl. lim.

0.34-6.3 %

refractive index

n20/D 1.539 (lit.)

bp

203-205 °C (lit.)

mp

−16-−13 °C (lit.)

solubility

water: soluble 33 g/L at 20 °C

density

1.045 g/mL at 25 °C (lit.)

SMILES string

OCc1ccccc1

InChI

1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2

InChI key

WVDDGKGOMKODPV-UHFFFAOYSA-N

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General description

Benzyl alcohol, an aromatic alcohol, is widely used in cosmetics and hair dyes. It undergoes oxidation in the absence of solvent catalyzed by Pd catalysts supported on TiO2 functionalized with various amounts of 3-aminopropyltriethoxysilane (APTES).

Application

Benzyl alcohol may be used in the preparation of benzoic acid, via oxidation.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

213.8 °F - DIN 51758

Flash Point(C)

101 °C - DIN 51758


Certificates of Analysis (COA)

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Surface functionalized TiO2 supported Pd catalysts for solvent-free selective oxidation of benzyl alcohol.
Weerachawanasak P, et al.
Catalysis Today, 250, 218-225 (2015)
I H Blank et al.
The Journal of investigative dermatology, 85(6), 522-526 (1985-12-01)
Although it is known that benzene may be absorbed from inhaled air, the amount that may enter the system by percutaneous absorption is less well established. We have measured the penetration of benzene through human abdominal skin in vitro from
Meenakshisundaram Sankar et al.
ACS nano, 6(8), 6600-6613 (2012-07-10)
We report a convenient excess anion modification and post-reduction step to the impregnation method which permits the reproducible preparation of supported bimetallic AuPd nanoparticles having a tight particle size distribution comparable to that found for sol-immobilization materials but without the
Luis E Santos-Figueroa et al.
Chemical Society reviews, 42(8), 3489-3613 (2013-02-13)
This review focuses on examples reported in the years 2010-2011 dealing with the design of chromogenic and fluorogenic chemosensors or reagents for anions.
Eagleson M.
Concise Encyclopedia Chemistry, 122-122 (1994)

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