
CAS 5632-47-3: 1-nitrosopiperazine
Formula:C4H9N3O
InChI:InChI=1S/C4H9N3O/c8-6-7-3-1-5-2-4-7/h5H,1-4H2
InChI key:InChIKey=CVTIZMOISGMZRJ-UHFFFAOYSA-N
SMILES:N(=O)N1CCNCC1
Synonyms:- N-Mononitrosopiperazine
- N-Nitrosopiperazine
- NSC 50269
- NSC 525340
- Piperazine, 1-Nitroso-
- 1-Nitrosopiperazine
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Found 4 products.
N-Nitrosopiperazine
CAS:N-Nitrosopiperazine is a nitrosating agent that forms N-nitrosamines in the body. It is used to produce anthelmintic drugs, such as albendazole and mebendazole. It is also used to activate aromatic amines. Piperazine reacts with electrophilic nucleophiles by nucleophilic attack at the alpha carbon of the piperazine ring to form substituted piperazines. The reaction proceeds via a S1 mechanism and the rate of formation is proportional to the concentration of substrate and inversely proportional to pH. N-Nitrosopiperazine has been shown to be present in human urine samples, with a formation rate that increases significantly when exposed to acidic conditions. This drug was found to have immunotoxic effects, including induction of chronic oral toxicity, autoimmune diseases, and cancer in rats.Formula:C4H9N3OPurity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:115.13 g/molN-Nitrosopiperazine
CAS:Stability Light Sensitive Applications A carcinogenic nitrosocompound. References Wong, H., et al.: Carcinogenesis, 24, 291Formula:C4H9N3OColor and Shape:Light YellowMolecular weight:115.13N-Nitroso Piperazine Solution (1 mL ) (1-nitrosopiperazine)
CAS:Compounds containing a pyrimidine ring, whether or not hydrogenated, or piperazine ring in the structure, nesoiFormula:C4H9N3OColor and Shape:Colorless LiquidMolecular weight:115.07456