112631
2-甲氧基-4-硝基苯胺
98%
别名:
4-硝基邻茴香胺
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关于此项目
线性分子式:
CH3OC6H3(NO2)NH2
化学文摘社编号:
分子量:
168.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-588-6
Beilstein/REAXYS Number:
879619
MDL number:
Assay:
98%
产品名称
2-甲氧基-4-硝基苯胺, 98%
InChI key
GVBHRNIWBGTNQA-UHFFFAOYSA-N
InChI
1S/C7H8N2O3/c1-12-7-4-5(9(10)11)2-3-6(7)8/h2-4H,8H2,1H3
SMILES string
COc1cc(ccc1N)[N+]([O-])=O
assay
98%
mp
140-142 °C (lit.)
Quality Level
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Application
2-甲氧基-4-硝基苯胺作为光度试剂，用于测定乙炔雌醇（ETE），乙炔雌醇是一种半合成的雌激素，广泛用于口服避孕药。
Biochem/physiol Actions
在 Harlan Sprague Dawley 大鼠和 B6C3F（1）/N 小鼠中，2-甲氧基-4-硝基苯胺（MNA）通过苯环的羟基化作用代谢生成 6-羟基 MNA。
General description
2-甲氧基-4-硝基苯胺由于分子量小，因此是 CYP1A2 的重要诱导剂。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
危险化学品
此项目有
Use of nitroanilines for spectrophotometric determination of ethinylestradiol in pharmaceutical formulations.
Leonardo SG, et al.
Analytical Methods : Advancing Methods and Applications, 3(5), 1198-1201 (2011)
James M Mathews et al.
Xenobiotica; the fate of foreign compounds in biological systems, 42(12), 1213-1224 (2012-06-26)
The disposition of 2-Methoxy-4-nitroaniline (MNA) was investigated in male and female Harlan Sprague Dawley rats and B6C3F(1)/N mice following oral, intravenous, and dermal exposure to [(14)C]MNA at 2, 15, or 150 mg/kg. Clearance of MNA was investigated in male and
M Degawa et al.
Cancer letters, 96(1), 95-98 (1995-09-04)
Male F344 rats were treated with a chemical (aniline, nitrobenzene, 2-methoxy-p-phenylenediamine, 2-methoxy-4-nitroaniline or 2-methoxy-4-nitroazobenzene) produced by the azo-reduction and/or N-oxidation of 2-methoxy-4-amino-azo-benzene, a selective inducer of cytochrome P450IA2 (CYP1A2), and their effects on the induction of CYP1A enzymes in the
Rachel P Frawley et al.
Toxicology, 441, 152474-152474 (2020-05-08)
2-Methoxy-4-nitroaniline (MNA), an intermediate in the synthesis of azo dyes used in textiles and paints, is structurally similar to carcinogenic anilines. Human exposure occurs primarily in the occupational setting through handling of dye dust, and through use and disposal of
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