16339-21-2 Usage
Description
4-Methyl-4-(methylnitrosoamino)-2-pentanone is a chemical compound characterized by its potential mutagenic and carcinogenic properties. It is recognized for its ability to induce DNA damage and mutations, making it a significant subject of study in research and testing environments. 4-Methyl-4-(methylnitrosoamino)-2-pentanone serves as a model for understanding the effects of nitrosamines, which are known environmental toxins and potent carcinogens.
Uses
Used in Research and Testing:
4-Methyl-4-(methylnitrosoamino)-2-pentanone is used as a model compound in research and testing for studying the effects of nitrosamines. Its application is crucial for understanding the mechanisms by which these environmental toxins and potent carcinogens induce DNA damage and mutations.
Used in Environmental Toxicology Studies:
In the field of environmental toxicology, 4-Methyl-4-(methylnitrosoamino)-2-pentanone is utilized to investigate the impact of nitrosamines on biological systems. This helps in the development of strategies aimed at minimizing exposure to these hazardous substances and mitigating their harmful effects on human health.
Used in Cancer Research:
4-Methyl-4-(methylnitrosoamino)-2-pentanone is also employed in cancer research to explore its mutagenic properties and its role in the induction of cancer. Understanding its mechanisms of action can contribute to the advancement of cancer prevention and treatment approaches.
Used in Regulatory Compliance and Safety Assessments:
4-Methyl-4-(methylnitrosoamino)-2-pentanone is utilized in regulatory compliance and safety assessments to evaluate the potential risks associated with exposure to nitrosamines in various consumer products and industrial processes. It aids in the establishment of safety standards and guidelines to protect public health.
Check Digit Verification of cas no
The CAS Registry Mumber 16339-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,3 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16339-21:
(7*1)+(6*6)+(5*3)+(4*3)+(3*9)+(2*2)+(1*1)=102
102 % 10 = 2
So 16339-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2O2/c1-6(10)5-7(2,3)9(4)8-11/h5H2,1-4H3
16339-21-2Relevant articles and documents
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Berenbom,Fones
, p. 1629 (1949)
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PROCESS FOR THE CYCLOPROPANATION OF OLEFINS USING N-METHYL-N-NITROSO COMPOUNDS
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Page/Page column 11-12, (2017/04/11)
A process of converting a carbon-carbon double bond on a substrate into a cyclopropane ring, which method comprises the step of treating the substrate with a N-alkyl-N-nitroso compound, a transition metal catalyst and an aqueous base, wherein the N-alkyl-N-nitroso compound is formed by reacting an alkyl amine with an alkali metal nitrite in the presence of a mono-basic or di-basic acid, or a mixture thereof, and wherein the N-alkyl-N-nitroso compound is not distilled before it is mixed with the substrate, catalyst and base.
A METHOD FOR THE PREPARATION OF DIAZOALKANES
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Page/Page column 14; 15, (2013/08/15)
The present invention relates to a method of forming diazoalkanes. One aspect of the present invention provides a method for the production of a N-alkyl-N-nitroso compound from a starting material, comprising the use of a tribasic acid to acidify an amine. A second aspect of the present invention provides a method for the production of a diazoalkane, comprising reacting a N-alkyl-N-nitroso compound with a base and a phase transfer catalyst, wherein no organic solvent is used,
