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等级
analytical standard
自燃温度
984 °F
包装
ampule of 500 mg
技术
HPLC: suitable
gas chromatography (GC): suitable
折射率
n20/D 1.615 (lit.)
沸点
240-243 °C (lit.)
mp
−22 °C (lit.)
密度
1.001 g/mL at 25 °C (lit.)
应用
environmental
包装形式
neat
储存温度
room temp
SMILES字符串
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
基因信息
human ... CYP1A2(1544)
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应用
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Chronic 2 - Asp. Tox. 1
储存分类代码
10 - Combustible liquids
WGK
WGK 2
闪点(°F)
179.6 °F - closed cup
闪点(°C)
82 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
U Kulka et al.
Mutation research, 208(3-4), 155-158 (1988-07-01)
Chromosome analyses were carried out in human lymphocytes treated in vitro with 1- and 2-methylnaphthalene (1-MN, 2-MN) in the presence and absence of the mammalian metabolic activation system, S9 mix. Without S9 mix there was no indication of induction of
Mykola Seredych et al.
Langmuir : the ACS journal of surfaces and colloids, 26(1), 227-233 (2009-12-30)
Two synthetic, polymer-derived carbons were modified with urea to incorporate nitrogen surface functional groups. Then they were investigated as adsorbents of dibenzothiophene (DBT) and 4, 6-dimethyldibenzothiophene (DMDBT) from simulated diesel fuel under dynamic conditions with the total concentration of sulfur
Dominik Heger et al.
The journal of physical chemistry. A, 115(41), 11412-11422 (2011-09-03)
A combined experimental-computational approach was used to study the self-organization and microenvironment of 1-methylnaphthalene (1MN) deposited on the surface of artificial snow grains from vapors at 238 K. The specific surface area of this snow (1.1 × 10(4) cm(2) g(-1))
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.
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
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