| Weight | 114.148 g/mol |
|---|---|
| Formula | C5H10N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
1-Nitrosopiperidine (100-75-4)
nitrosopiperidine · N-nitrosopiperidine · N-nitrosopentamethyleneimine
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- Effect of ascorbic acid and green tea on endogenous formation of N-nitrosodimethylamine and N-nitrosopiperidine in humans. (Mutation Research, 1999)
- Cytochrome P450 2A-catalyzed metabolic activation of structurally similar carcinogenic nitrosamines: N'-nitrosonornicotine enantiomers, N-nitrosopiperidine, and N-nitrosopyrrolidine. (Chemical Research in Toxicology, 2005)
- Formation of N-nitrosopiperidine from piperidine and sodium nitrite in the stomach and the isolated intestinal loop of the rat. (Nature, 1971)
- Stereoselectivity in the Reactions of Nitrosopiperidine Carbanions. Steric vs. Stereoelectronic Control (Canadian Journal of Chemistry, 1975)
- Comparative Studies With Different Doses of N-Nitrosomorpholine, N-Nitrosopiperidine, N-Nitrosomethylurea, and Dimethylnitrosamine in Syrian Golden Hamsters (Journal of the National Cancer Institute, 1973)
- Carcinogenic effect of nitrosopyrrolidine, nitrosopiperidine and nitrosohexamethyleneimine in Fischer rats (Cancer Letters, 1981)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - nitrosopiperidine
- N-nitrosopiperidine
- N-nitrosopentamethyleneimine
-
SMILESC1CCN(CC1)N=O
-
InChIKeyUWSDONTXWQOZFN-UHFFFAOYSA-N
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