442430
1-Methylnaphthalene
analytical standard
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About This Item
Linear Formula:
C10H7CH3
CAS Number:
Molecular Weight:
142.20
EC Number:
201-966-8
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
506793
MDL number:
grade
analytical standard
autoignition temp.
984 °F
packaging
ampule of 500 mg
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
refractive index
n20/D 1.615 (lit.)
bp
240-243 °C (lit.)
mp
−22 °C (lit.)
density
1.001 g/mL at 25 °C (lit.)
application(s)
environmental
format
neat
storage temp.
room temp
SMILES string
Cc1cccc2ccccc12
InChI
1S/C11H10/c1-9-5-4-7-10-6-2-3-8-11(9)10/h2-8H,1H3
InChI key
QPUYECUOLPXSFR-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
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Asp. Tox. 1
Storage Class
10 - Combustible liquids
flash_point_f
179.6 °F - closed cup
flash_point_c
82 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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K G Kropp et al.
Biodegradation, 7(3), 203-221 (1996-06-01)
Dimethylbenzothiophenes are among the sulfur heterocycles in petroleum that are known to be degraded by microbial activity. Six of the 15 possible isomers of dimethylbenzothiophene were synthesized and used in bio-transformation studies with three Pseudomonas isolates that oxidize a variety
Adeola L N'Guessan et al.
Environmental science & technology, 38(5), 1554-1560 (2004-03-30)
The majority of polycyclic aromatic hydrocarbons (PAHs) released to the environment come from anthropogenic sources involving the incomplete combustion of organic compounds. Several techniques are available for the degradation of PAHs. Among the abiotic/biotic processes used to degrade PAHs, an
C E Cerniglia et al.
Applied and environmental microbiology, 47(1), 111-118 (1984-01-01)
Cunninghamella elegans metabolized 1- and 2-methylnaphthalene primarily at the methyl group to form 1- and 2-hydroxymethylnaphthalene, respectively. Other compounds isolated and identified were 1- and 2-naphthoic acids, 5-hydroxy-1-naphthoic acid, 5-hydroxy-2-naphthoic acid, 6-hydroxy-2-naphthoic acid, and phenolic derivatives of 1- and 2-methylnaphthalene.