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外観
白色/無色～うすい黄色粉末～塊～透明液体
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用途
ビタミンK3用原料、Β‐ナフトエ酸原料 (化学工業日報社)
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説明
2-Methylnaphthalene is a polycyclic aromatic hydrocarbon (PAH), consisting of two-fused aromatic rings with a methyl group attached on one of the rings at the number two carbon.
2-Methylnaphthalene is a natural component of crude oil and coal, and is found in pyrolysis and combustion products such as cigarette and wood smoke, emissions from combustion engines, asphalt, coal tar residues, and used oils (ATSDR, 1995; HSDB, 2002; Warshawsky, 2001).
In the United States, 2-methylnaphthalene is used for making detergents, dyes, solvents, as well as vitamin K. 2-methylnapthalene is also used to make some pesticides, or as an additional ingredient in some pesticides. 2- methylnaphthalene is released into the environment when wood or fossil fuels are burned or when there are spills of products containing fossil fuels. 2-methylnaphthalene can evaporate or break down quickly in soils exposed to air or containing certain microorganisms, but it could stay a year or more under other conditions in certain sediments or soils.
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化学的特性
1-Methylnaphthalene and 2-methylnaphthalene are naphthalenerelated compounds. 1-Methylnaphthalene is a clear liquid and 2- methylnaphthalene is a solid. Insoluble inwater; soluble in alcohol and ether. Combustible. both can be smelled in air and in water at very low concentrations. The taste and odor of 2-methylnaphthalene have not been described. Its presence can be detected at a concentration of 10 ppb in air and 10 ppb in water.
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使用
2-methylnaphthalene are used to make other chemicals such as dyes, insecticides, Organic synthesis and resins. Pure 2-methylnaphthalene is a component used in the manufacture of vitamin K and the insecticide carbaryl (1-naphthyl-N-methylcarbamate) (HSDB, 2002).
Methylnaphthalene (CASRN 1321-94-4) refers to a mixture of approximately two-thirds 2-methylnaphthalene and one-third 1-methylnaphthalene (CASRN 90-12-0). Methylnaphthalene is manufactured from coal tar through the extraction of heteroaromatics and phenols. Distillation of methylnaphthalene removes 1-methylnaphthalene, leaving 2-methylnaphthalene. Mixtures containing 2-methylnaphthalene are used in the formulation of alkyl-naphthalenesulfonates (used for detergents and textile wetting agents), chlorinated naphthalenes, and hydronaphthalenes (used as solvents).
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調製方法
Alkylnaphthalenes are formed as pyrolysis products in cigarette
smoke. Some have been identified in commercial
carbon paper. They are also the major components of the
C10–C13 alkylnaphthalene concentrate fraction, which distills
at 400–500F. A C11–C12 petroleum mixture of reformates
that contained about 23% alkylnaphthalenes caused
skin and eye effects. The toxicity of the alkylnaphthalenes
to marine species is greater than that of the alkylbenzenes
(85). The toxicity and the bioaccumulation increase
with molecular weight. Nocardia cultures, isolated from
soil, preferentially oxidized alkylnaphthalenes when methylated
in the two positions. Methylnaphthalene can
occur as the 1- or 2-, the alpha or the beta isomer.
1-Naphthalene, a flammable solid, has also been identified
in the wastewater of coking operations, and in textile
processing plants. Methylnaphthalene is used as a component
in slow-release insecticides and in mole repellents.
Workplace exposures to 18–32 mg/m3 for 2-methylnaphthalene
have been reported.
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定義
ChEBI: A methylnaphthalene carrying a methyl substituent at position 2.
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一般的な説明
White crystalline solid.
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空気と水の反応
Insoluble in water.
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反応プロフィール
2-Methylnaphthalene is incompatible with strong oxidizing agents. 2-Methylnaphthalene is also incompatible with peroxides and oxygen.
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危険性
Lower respiratory tract irritant and lungdamage. Questionable carcinogen.
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火災危険
2-Methylnaphthalene is combustible.
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発がん性
The carcinogenic potential of
1- and 2-methyl was investigated in B6C3F1 mice. Female
and male mice were given methylnaphthalene in their diets
for 81 weeks. The results indicated that 1-methyl was a
possible weak carcinogen in the lung of male but not female
mice whereas 2-methyl did not possess unequivocal
carcinogenic potential in these mice.
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環境運命予測
Biological. 2-Naphthoic acid was reported as the biooxidation product of 2-methylnaphthalene
by Nocardia sp. in soil using n-hexadecane as the substrate (Keck et al., 1989). Dutta et al. (1998)
investigated the degradation of 2-methylnaphthalene using a bacterial strain of Sphingomonas
paucimobilis grown on phenanthrene. Degradation products identified using GC-MS were 4-
methylsalicylate, 2-methylnaphthoate, and 1-hydroxy-2-methylnaphthoate.
Estimated half-lives of 2-methylnaphthalene (0.6 μg/L) from an experimental marine mesocosm
during the spring (8–16 °C), summer (20–22 °C), and winter (3–7 °C) were 11, 1.0, and 13
d, respectively (Wakeham et al., 1983).
Photolytic. Fukuda et al. (1988) studied the photodegradation of 2-methylnaphthalene and other
alkylated naphthalenes in distilled water and artificial seawater using a high-pressure mercury
lamp. Based upon an experimentally rate constant of 0.042/h, the photolytic half-life of 2-
methylnaphthalene in water is 16.4 h.
Phousongphouang and Arey (2002) investigated gas-phase reaction of naphthalene with OH
radicals in a 7-L Teflon chamber at 25 °C and 740 mmHg containing 5% humidity. The rate
constant for this reaction was 4.86 x 10-11 cm3/molecule?sec.
Chemical/Physical. An aqueous solution containing chlorine dioxide in the dark for 3.5 d at
room temperature oxidized 2-methylnaphthalene into the following: 1-chloro-2-methylnaphthalene,
3-chloro-2-methylnaphthalene, 1,3-dichloro-2-methylnaphthalene, 3-hydroxymethylnaphthalene,
2-naphthaldehyde, 2-naphthoic acid, and 2-methyl-1,4-naphthoquinone (Taymaz et al.,
1979).
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純化方法
Fractionally crystallise repeatedly from its melt, then fractionally distil under reduced pressure. It has been crystallised from *benzene and dried under vacuum in an Abderhalden pistol. It can be purified via its picrate (m 114-115o) or better via the 1,3,5-trinitrobenzene complex as for 1-methylnaphthalene (above). [Beilstein 5 IV 1693.]
