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Merck
CN

188212

3-Methylbenzyl alcohol

98%

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About This Item

Linear Formula:
CH3C6H4CH2OH
CAS Number:
Molecular Weight:
122.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-595-3
MDL number:
Assay:
98%
Form:
liquid
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InChI key

JJCKHVUTVOPLBV-UHFFFAOYSA-N

InChI

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

SMILES string

Cc1cccc(CO)c1

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.)

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

WGK 3

flash_point_f

222.8 °F - closed cup

flash_point_c

106.00 °C - closed cup

ppe

Eyeshields, Gloves


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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
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
Anu Vaidyanathan et al.
Journal of toxicology and environmental health. Part A, 66(12), 1133-1143 (2003-06-07)
Xylene is used as a solvent in paints, cleaning agents, and gasoline. Exposure occurs primarily by inhalation. The volatility and lipophilicity of the xylenes make the lung and nasal mucosa the primary target organs. m-Xylene (m-XYL) has been shown to

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