N-Nitroso-1-(2-methoxyphenyl)-piperazine
≥95%
- Product Code: 121477
CAS:
2219339-64-5
| Molecular Weight: | 221.26 g./mol | Molecular Formula: | C₁₁H₁₅N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
Used primarily in research settings, this compound is studied for its potential role in understanding nitrosamine chemistry and its implications in carcinogenesis. It serves as a model compound in toxicology to investigate the formation, stability, and reactivity of N-nitroso derivatives, which are often associated with carcinogenic properties. Researchers utilize it to explore metabolic pathways and the mechanisms by which nitrosamines induce DNA damage. Additionally, it may be employed in the development of analytical methods for detecting and quantifying nitrosamines in various matrices, such as food, pharmaceuticals, and environmental samples. Its structural features also make it a candidate for studying structure-activity relationships in the context of mutagenicity and toxicity.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Yellow Oil |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿12,600.00 |
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| 0.100 | 10-20 days | ฿34,200.00 |
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N-Nitroso-1-(2-methoxyphenyl)-piperazine
Used primarily in research settings, this compound is studied for its potential role in understanding nitrosamine chemistry and its implications in carcinogenesis. It serves as a model compound in toxicology to investigate the formation, stability, and reactivity of N-nitroso derivatives, which are often associated with carcinogenic properties. Researchers utilize it to explore metabolic pathways and the mechanisms by which nitrosamines induce DNA damage. Additionally, it may be employed in the development of analytical methods for detecting and quantifying nitrosamines in various matrices, such as food, pharmaceuticals, and environmental samples. Its structural features also make it a candidate for studying structure-activity relationships in the context of mutagenicity and toxicity.
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