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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
form:
liquid
Assay:
98%

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[1].

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

222.8 °F - closed cup

Flash Point(C)

106.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
Gas phase hydrogenation/hydrogenolysis of isophthaldehyde over Ni/SiO2.
Keane MA.
Bull. Soc. Chim. Belg., 104(2), 63-67 (1995)
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
Production of ligninolytic enzymes of the white rot fungus Panus tigrinus.
Leontievsky AA, et al.
Journal of Biotechnology, 32(3), 299-307 (1994)
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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