质量水平
方案
99%
沸点
262 °C (lit.)
mp
106-110 °C (lit.)
SMILES字符串
Cc1ccc2cc(C)ccc2c1
InChI
1S/C12H12/c1-9-3-5-12-8-10(2)4-6-11(12)7-9/h3-8H,1-2H3
InChI key
YGYNBBAUIYTWBF-UHFFFAOYSA-N
基因信息
human ... CYP1A2(1544)
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一般描述
2,6-二甲基萘是一种存在于水体中的多环芳烃，可通过火焰离子化气相色谱进行测定。
应用
2,6-二甲基萘在分子内同位素效应实验中可作为底物用于比较CYP2E1和CYP2A6中的底物动力学。
警示用语：
Warning
危险声明
预防措施声明
危险分类
Aquatic Acute 1 - Aquatic Chronic 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Effect of Aroclor 1254 on the biological fate of 2,6-dimethylnaphthalene in coho salmon (Oncorhynchus kisutch).
T K Collier et al.
Bulletin of environmental contamination and toxicology, 34(1), 114-120 (1985-01-01)
Dietary accumulation of dimethylnaphthalene by the grass shrimp Palaemonetes pugio under stable and fluctuating temperatures.
T M Dillon
Bulletin of environmental contamination and toxicology, 28(2), 149-153 (1982-02-01)
N Miyachi et al.
Applied and environmental microbiology, 59(5), 1504-1506 (1993-05-01)
Three bacterial strains, identified as Alcaligenes sp. strain D-59 and Pseudomonas sp. strains D-87 and D-186, capable of growing on 2,6-dimethylnaphthalene (2,6-DMN) as the sole source of carbon and energy were isolated from soil samples. 2,6-Naphthalene dicarboxylic acid was formed
M M Krahn et al.
Journal of chromatography, 236(2), 441-452 (1982-02-19)
An automated extractor-concentrator was used to extract metabolites of naphthalene, 2,6-dimethylnaphthalene, and benzo[a]pyrene from serum, bile and liver homogenate of rainbow trout (Salmo gairdneri). The extracts were analyzed by reversed-phase high-performance liquid chromatography (HPLC) with fluorescence detection. Recoveries of naphthalene
J V Schnell et al.
Xenobiotica; the fate of foreign compounds in biological systems, 10(3), 229-234 (1980-03-01)
1. Benzo[a]pyrene, 2,6-dimethylnaphthalene, and naphthalene were used as substrates for a coho salmon (Oncorhynchus kisutch) liver microsomal preparation. 2. The apparent Michaelis constants (Km) were as follows: benzo[a]pyrene, 2.1 microM; 2,6-dimethylnaphthalene, 15.3 microM; and naphthalene, 300 microM. 3. The results
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