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Postion:Product Catalog >N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide
N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide
  • N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide
  • N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide
  • N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide
  • N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide
  • N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide

N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-06-20

Product Details

Product Name: N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide CAS No.: 27646-81-7
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/06/20
Molecular formula: C5H12N2O2

N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide;27646-81-7

=Article illustration

WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com

Product Information

  • Product Code:B201378

  • English Name:N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide

  • English Alias:N-(1-hydroxy-2-methylpropan-2-yl)-N-methylnitrous amide

  • CAS No.:27646-81-7

  • Molecular Formula:C?H??N?O?

  • Molecular Weight:132.16

Advantages

  • High-Purity Reference Standard:Confirmed by HPLC (≥99.0%), NMR (1H, 13C), HRMS, and elemental analysis, suitable for nitroso compound impurity analysis and quality control.

  • Stability Assurance:Stable for 36 months at -20℃ under light-protected, sealed storage; degradation rate <0.3% in methanol-water mixture within 6 months.

Applications

  • Quality Control Testing:Used for UPLC-MS/MS detection of this nitroso impurity in related API and formulations, controlling content to meet ICH Q3A standards (single impurity limit ≤0.1%).

  • Process Optimization Research:Monitors nitroso impurity formation during target compound synthesis, reducing generation by >40% by adjusting reaction system pH (e.g., neutral to weakly alkaline) and temperature (≤25℃).

  • Method Validation:Serves as a standard for developing nitroso impurity detection methods, verifying UPLC resolution (≥3.0) and LOD (0.01 ng/mL).

Background Description

Nitroso compounds, as potential genotoxic impurities (GTIs), are commonly found in the synthesis of amine-containing drugs, possibly originating from side reactions between amines and nitrosating agents. The nitrosamide group in this compound has potential carcinogenicity, and its hydroxyl and tert-butyl structures may affect drug metabolic stability and interaction with biological macromolecules. Strict control of genotoxic impurities in pharmaceuticals makes research on this impurity crucial for ensuring drug safety.

Research Status

  • Detection Technology:UPLC-MS/MS with C18 column (1.7μm) and 0.1% formic acid-acetonitrile gradient elution achieves separation within 5 minutes, with LOD of 0.002 ng/mL for trace analysis of genotoxic impurities.

  • Formation Mechanism:Formed by reaction of N-methyl-2-methyl-2-propanamine with nitrite under acidic conditions (e.g., pH <3); optimizing nitrosating agent dosage and post-reaction processing inhibits formation.

  • Safety Evaluation:In vitro Ames test shows potential mutagenicity, and in vivo mouse model tests demonstrate DNA adduct formation in gastric mucosa at a 10 mg/kg dose. Accelerated stability testing is ongoing to systematically study degradation characteristics and mutagenic risks under high temperature and humidity conditions.

NOTE!

We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS.
This product is intended for laboratory use only!

WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com


NEW IN STOCK!

The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery! 







Company Profile Introduction

1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability. 2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs. 3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects. 4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes. 5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.

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