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188212

Sigma-Aldrich

3-Methylbenzyl alcohol

98%

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About This Item

Linear Formula:
CH3C6H4CH2OH
CAS Number:
Molecular Weight:
122.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.534 (lit.)

bp

215 °C/740 mmHg (lit.)

density

1.015 g/mL at 25 °C (lit.)

SMILES string

Cc1cccc(CO)c1

InChI

1S/C8H10O/c1-7-3-2-4-8(5-7)6-9/h2-5,9H,6H2,1H3

InChI key

JJCKHVUTVOPLBV-UHFFFAOYSA-N

General description

3-Methylbenzyl alcohol participates in gas phase hydrogenation of methanolic solutions of isophthaldehyde over a Ni/SiO2 catalyst.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

222.8 °F - closed cup

flash_point_c

106.00 °C - closed cup

ppe

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’.

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Gas phase hydrogenation/hydrogenolysis of isophthaldehyde over Ni/SiO2.
Keane MA.
Bull. Soc. Chim. Belg., 104(2), 63-67 (1995)
S Fraile et al.
Journal of bacteriology, 183(19), 5571-5579 (2001-09-07)
We have isolated a recombinant phage antibody (Phab) that binds a distinct epitope of the subclass of the sigma(54)-dependent prokaryotic enhancer-binding proteins that respond directly to aromatic effectors, e.g., those that activate biodegradative operons of Pseudomonas spp. The DNA segments
Production of ligninolytic enzymes of the white rot fungus Panus tigrinus.
Leontievsky AA, et al.
Journal of Biotechnology, 32(3), 299-307 (1994)
Chun Chau Sze et al.
Journal of bacteriology, 184(3), 760-770 (2002-01-16)
Pseudomonas-derived regulators DmpR and XylR are structurally and mechanistically related sigma(54)-dependent activators that control transcription of genes involved in catabolism of aromatic compounds. The binding of distinct sets of aromatic effectors to these regulatory proteins results in release of a
K M Engström
Scandinavian journal of work, environment & health, 10(2), 75-81 (1984-04-01)
Gas chromatographic methods have been developed for the urinalysis of metabolic products of ethylbenzene. "Minor" metabolites were emphasized in this process. The methods were worked out so that simultaneous determination of several compounds could be achieved with one method. On

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