推荐产品
等级
certified reference material
Agency
BCR®
制造商/商品名称
JRC
技术
HPLC: suitable
gas chromatography (GC): suitable
mp
65-73 °C
应用
cleaning products
cosmetics
environmental
food and beverages
personal care
pharmaceutical (small molecule)
包装形式
neat
储存温度
2-8°C
SMILES字符串
[O-][N+](=O)c1ccc2ccccc2c1
InChI
1S/C10H7NO2/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7H
InChI key
ZJYJZEAJZXVAMF-UHFFFAOYSA-N
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分析说明
For more information please see:
BCR307
BCR307
法律信息
BCR is a registered trademark of European Commission
警示用语:
Danger
危险声明
危险分类
Aquatic Chronic 2 - Carc. 1B - Flam. Sol. 2
储存分类代码
4.1B - Flammable solid hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
危险化学品
1-nitronaphthalene.
IARC monographs on the evaluation of carcinogenic risks to humans, 46, 303-312 (1989-01-01)
Analytical and bioanalytical chemistry, 381(2), 520-525 (2004-12-31)
The polarographic behaviour of 2-nitronaphthalene was investigated by DC tast polarography (DCTP) and differential pulse polarography (DPP), both at a dropping mercury electrode, and differential pulse voltammetry and adsorptive stripping voltammetry, both at a hanging mercury drop electrode. Optimum conditions
all-trans-retinol modulation of nitronaphthalene-induced lung and liver injury in male Sprague-Dawley rats.
Proceedings of the Western Pharmacology Society, 38, 29-31 (1995-01-01)
Mutation research, 445(1), 113-125 (1999-10-16)
2-Nitronaphthalene (2NN) has been identified as a mutagenic atmospheric reaction product of naphthalene in the Ames bacterial reversion assay. Recent experiments have shown this nitroarene to be genotoxic in a human lymphoblastoid cell line (MCL-5) transfected with plasmids encoding epoxide
Mutation research, 301(1), 7-12 (1993-01-01)
Salmonella typhimurium YG1024 is a derivative of S. typhimurium TA98 with a high level of N-hydroxyarylamine O-acetyltransferase (OAT) activity. We have demonstrated that this strain is highly sensitive to the mutagenic actions of N-hydroxyarylamines derived from aromatic amines and nitroarenes.
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