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Supelco

2-Methylnaphthalene

analytical standard

Synonym(s):

β-Methylnaphthalene

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About This Item

Empirical Formula (Hill Notation):
C11H10
CAS Number:
91-57-6
Molecular Weight:
142.20
Beilstein:
906859
EC Number:
202-078-3
MDL number:
MFCD00004118
UNSPSC Code:
41116107
PubChem Substance ID:
329756957
NACRES:
NA.24

grade

analytical standard

Quality Level

100

Assay

≥98.0% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

neat

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

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General description

2-Methylnaphthalene belongs to the class of polycyclic aromatic hydrocarbons (PAHs), found to be a major environmental contaminant. It can occur in high concentrations in a variety of commercial products including coal tar, crude oil, etc.

Application

2-Methylnaphthalene may be used to identify the analyte from thermal degradation of bituminous/anthracite coals, tyres, and cellulose samples using gas chromatography-mass spectrometry (GC-MS) technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF3786
BCBS8736
BCBS8736V
SZBC047XV
SZB7178XV

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Phenanthrene 98%

Sigma-Aldrich

P11409

Phenanthrene

Michael Safinowski et al.
FEMS microbiology letters, 240(1), 99-104 (2004-10-27)
The upper pathway of anaerobic degradation of 2-methylnaphthalene was studied with a sulphate-reducing enrichment culture, which is able to grow with naphthalene or 2-methylnaphthalene as sole carbon source and electron donor. Anaerobic degradation of 2-methylnaphthalene is initiated by an addition
Eva Annweiler et al.
Applied and environmental microbiology, 68(2), 852-858 (2002-02-02)
Anaerobic degradation of naphthalene, 2-methylnaphthalene, and tetralin (1,2,3,4-tetrahydronaphthalene) was investigated with a sulfate-reducing enrichment culture obtained from a contaminated aquifer. Degradation studies with tetralin revealed 5,6,7,8-tetrahydro-2-naphthoic acid as a major metabolite indicating activation by addition of a C(1) unit to
Young-Bum Kim et al.
Applied biochemistry and biotechnology, 159(1), 1-10 (2009-02-14)
Amphiphilic polyurethane (APU) nano-particle enhanced the mobilization of 2-methylnaphthalene (2-MNPT) in soil. Significant increase in the solubility of 2-MNPT was achieved. The molar solubilization ratio was 0.4 (mole 2-MNPT/mole APU). Simple precipitation of APU particle by 2 N CaCl(2) recovered
Gro Harlaug Olsen et al.
Marine environmental research, 72(4), 179-187 (2011-09-13)
Reliable risk assessment approaches for Arctic environments are requested to manage potential impacts associated with increased activities in Arctic regions. We performed toxicity tests on Arctic and temperate species exposed to the narcotic acting oil component, 2-methyl naphthalene. The experimental
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
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