CAS 16339-07-4
:1-Methyl-4-nitrosopiperazine
Description:
1-Methyl-4-nitrosopiperazine is a chemical compound characterized by its piperazine structure, which includes a nitroso group and a methyl substituent. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its state at room temperature. It is known for its potential use in various chemical syntheses and research applications, particularly in the field of medicinal chemistry. The presence of the nitroso group can impart unique reactivity, making it a subject of interest in studies related to nitrosation reactions and the formation of nitrosamines. Additionally, 1-Methyl-4-nitrosopiperazine may exhibit biological activity, which warrants careful handling due to potential health risks associated with nitroso compounds. As with many nitrogen-containing heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and electrophilic additions. Proper safety measures should be observed when working with this compound, as it may pose hazards typical of nitroso compounds, including toxicity and potential carcinogenicity.
Formula:C5H11N3O
InChI:InChI=1S/C5H11N3O/c1-7-2-4-8(6-9)5-3-7/h2-5H2,1H3
InChI key:InChIKey=CEAIOKFZXJMDAS-UHFFFAOYSA-N
SMILES:N(=O)N1CCN(C)CC1
Synonyms:- 1-Nitroso-4-methylpiperazine
- Brn 0117135
- Ccris 1151
- Methylnitrosopiperidine
- Methylpiperazinenitrosamine
- N'-Methyl-N-nitrosopiperazine
- N-Methyl-npz
- N-Methylnitrosopiperazine
- N-Nitroso-N'-methylpiperazin
- N-Nitroso-N'-methylpiperazin [German]
- N-Nitroso-N'-methylpiperazine
- N-Nitrosomethylpiperazine
- Nsc 523886
- Piperazine, 1-methyl-4-nitroso-
- 1-Methyl-4-nitrosopiperazine
- 1-Methyl-4-nitrosopiperazine
- See more synonyms
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Found 16 products.
Ref: 3W-CS-T-81242
10mgTo inquire1-Methyl-4-nitrosopiperazine (MNP) Solution (1 mL ) (1-Methyl-4-nitrosopiperazine)
CAS:Diagnostic or lab reagents on a backing, prepared diagnostic or lab reagents whether or not on a backing, whether or not in the form of kits, nesoiFormula:C5H11N3OColor and Shape:Colorless LiquidMolecular weight:129.09021Piperazine, 1-methyl-4-nitroso-
CAS:Formula:C5H11N3OPurity:95%Color and Shape:LiquidMolecular weight:129.1603N-Nitroso Chlorcyclizine EP Impurity A-15N (N-Nitroso Cyclizine EP Impurity A-15N, N-Nitroso Cyclizine USP Related Compound A-15N)
CAS:Formula:C5H11N215NOMolecular weight:130.16N-Nitroso Chlorcyclizine EP Impurity A (N-Nitroso Cyclizine EP Impurity A, N-Nitroso Cyclizine USP Related Compound A)
CAS:Formula:C5H11N3OMolecular weight:129.16N-Nitroso-N'-methylpiperazine
CAS:Controlled ProductFormula:C5H11N3OColor and Shape:Colourless To Light YellowMolecular weight:129.161-Methyl-4-nitrosopiperazine
CAS:Formula:C5H11N3OPurity:>95.0%(GC)Color and Shape:Colorless to Yellow to Yellow green clear liquidMolecular weight:129.16N-Nitroso Chlorcyclizine EP Impurity A-d11 (N-Nitroso Cyclizine EP Impurity A-d11, N-Nitroso Cyclizine USP Related Compound A-d11)
CAS:Formula:C5D11N3OMolecular weight:140.23N-Methyl-N’-nitrosopiperazine
CAS:Controlled Product<p>Stability Light Sensitive<br>Applications N-Methyl-N’-nitrosopiperazine was used as a reagent in the organic synthesis of several compounds including that of (4-methoxyphenoxy)acetic and (3,4,5-trimethoxyphenoxy)acetic acid amides and hydrazides which display antimicrobial and anthelmintic properties and may act as potential neurotropic and cardiovascular agents. N-Methyl-N’-nitrosopiperazine also diplayed strong nasal carcinogenity and genotoxicity toward nasal cells.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Valenta, V., et al.: Collect. Czech. Chem. C., 52, 3013 (1987); Klein, R., et al.: Carcinogenesis, 20, 1629 (1999);<br></p>Formula:C5H11N3OColor and Shape:Colourless To Light YellowMolecular weight:129.16N-Methyl-N’-nitrosopiperazine (100mg/L in Methanol)
CAS:Formula:C5H11N3OColor and Shape:Single SolutionMolecular weight:129.16N-Methyl-N’-nitrosopiperazine
CAS:<p>N-Methyl-N’-nitrosopiperazine is a chemical that has been shown to produce genotoxic effects in mammalian cells. It was found to be carcinogenic in rats, but not in mice. This chemical induces mutations by reacting with nucleic acids and producing covalent DNA adducts. The uptake of N-methyl-N’-nitrosopiperazine into the body occurs through inhalation, ingestion, or skin contact. It can also be detected using analytical methods such as high performance liquid chromatography (HPLC) and gas chromatography/mass spectrometry (GC/MS).</p>Formula:C5H11N3OPurity:Min. 95 Area-%Color and Shape:Clear LiquidMolecular weight:129.16 g/molN-Methyl-N’-nitrosopiperazine-15N3
CAS:Controlled ProductFormula:C5H1115N3OColor and Shape:NeatMolecular weight:132.141N-Methyl-N’-nitrosopiperazine-15N
CAS:Controlled ProductFormula:C5H1115NN2OColor and Shape:NeatMolecular weight:130.154










