188212
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 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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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
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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