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About This Item
Empirical Formula (Hill Notation):
C11H10
CAS Number:
Molecular Weight:
142.20
EC Number:
202-078-3
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
906859
MDL number:
grade
analytical standard
packaging
ampule of 1000 mg
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
environmental
format
neat
storage temp.
room temp
SMILES string
Cc1ccc2ccccc2c1
InChI
1S/C11H10/c1-9-6-7-10-4-2-3-5-11(10)8-9/h2-8H,1H3
InChI key
QIMMUPPBPVKWKM-UHFFFAOYSA-N
Gene Information
human ... CYP1A2(1544)
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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Kazutoshi Shindo et al.
Bioscience, biotechnology, and biochemistry, 75(3), 505-510 (2011-03-11)
We performed combinational bioconversion of substituted naphthalenes with PhnA1A2A3A4 (an aromatic dihydroxylating dioxygenase from marine bacterium Cycloclasticus sp. strain A5) and prenyltransferase NphB (geranyltransferase from Streptomyces sp. strain CL190) or SCO7190 (dimethylallyltransferase from Streptomyces coelicolor A3(2)) to produce prenyl naphthalen-ols.
Radosław Swiercz et al.
International journal of occupational medicine and environmental health, 23(4), 385-389 (2011-02-11)
The aim of the study was to evaluate the toxicokinetics of 2-methylnaphtalene (2-MN) during and after inhalation exposure. Male Wistar rats were exposed to 2-MN vapours at nominal concentrations of 200 or 400 mg/m3 in the dynamic inhalation chamber for
Raymond J DiDonato et al.
PloS one, 5(11), e14072-e14072 (2010-12-03)
Anaerobic polycyclic hydrocarbon (PAH) degradation coupled to sulfate reduction may be an important mechanism for in situ remediation of contaminated sediments. Steps involved in the anaerobic degradation of 2-methylnaphthalene have been described in the sulfate reducing strains NaphS3, NaphS6 and

