推荐产品
化驗
97%
形狀
liquid
折射率
n20/D 1.522 (lit.)
bp
184-189 °C (lit.)
密度
0.939 g/mL at 25 °C (lit.)
SMILES 字串
CNCc1ccccc1
InChI
1S/C8H11N/c1-9-7-8-5-3-2-4-6-8/h2-6,9H,7H2,1H3
InChI 密鑰
RIWRFSMVIUAEBX-UHFFFAOYSA-N
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訊號詞
Danger
危險聲明
危險分類
Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 1
閃點(°F)
167.0 °F - closed cup
閃點(°C)
75 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Proceedings of the National Academy of Sciences of the United States of America, 78(3), 1878-1881 (1981-03-01)
Previous studies in Linxian, an area of China with a high incidence of esophageal carcinoma, showed that fungal infections are common in the esophageal epithelium of patients with either premalignant changes or early esophageal carcinoma. Fungi of the genus Candida
Journal of the National Cancer Institute, 72(2), 419-425 (1984-02-01)
Nine-week-old zinc-sufficient (100 mg zinc/kg feed) and zinc-deficient (7 mg zinc/kg feed) noninbred male Sprague-Dawley rats were given free access 5 days a week to deionized drinking water containing low (0.05%) or high (0.25%) quantities of benzylmethylamine (BMA) and concurrently
British journal of pharmacology, 90(2), 335-345 (1987-02-01)
In an effort to explore the contribution of the metabolites of pargyline towards the in vivo inhibition of monoamine oxidase (MAO), the effects of pargyline and its major metabolites on the production and metabolism of a number of biogenic amines
Journal of chromatography, 307(1), 145-153 (1984-04-13)
The separation of racemic benoxaprofen into the two benoxaprofen enantiomers by preparative high-performance liquid chromatography and the application of the activated enantiomers as derivatization reagents for the simultaneous stereoselective determination of chiral amines in biological material is described. Activated (+)-
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 26(6), 511-516 (1988-06-01)
Thioproline, which is readily nitrosated to form nitrosothioproline, is expected to act as a nitrite scavenger. The effect of thioproline as an inhibitor of the carcinogenesis induced by N-nitroso-N-benzylmethylamine precursors was examined. Two groups of male F-344 rats were given
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