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Postion:Product Catalog >N-Nitroso Terbutaline
N-Nitroso Terbutaline
  • N-Nitroso Terbutaline
  • N-Nitroso Terbutaline
  • N-Nitroso Terbutaline
  • N-Nitroso Terbutaline
  • N-Nitroso Terbutaline

N-Nitroso Terbutaline NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-31

Product Details

Product Name: N-Nitroso Terbutaline Min. Order: 10mg
Purity: 99%+ HPLC Supply Ability: 1000
Release date: 2025/07/31
Molecular formula: C12H18N2O4

N-Nitroso Terbutaline;C12H18N2O4  

=Article illustration

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

Product Information

  • Product Code:N031232

  • English Name:N-Nitroso Terbutaline

  • English Alias:N-(tert-butyl)-N-(2-(3,5-dihydroxyphenyl)-2-hydroxyethyl)nitrous amide

  • CAS No.:Not provided

  • Molecular Formula:C??H??N?O?

  • Molecular Weight:254.28

Advantages

  • High-Purity Reference Standard:Confirmed by HPLC (≥99.0%), NMR (1H, 13C), HRMS, and elemental analysis, suitable for Terbutaline nitroso 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 N-nitroso impurities in Terbutaline API and formulations, controlling content to meet ICH Q3A standards (single impurity limit ≤0.1%).

  • Process Optimization Research:Monitors nitroso impurity formation during Terbutaline synthesis, reducing generation by >40% by adjusting reaction system pH (e.g., neutral to weakly alkaline) and temperature (≤30℃).

  • 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

Terbutaline, a selective β?-adrenergic receptor agonist, is used for treating bronchial asthma, chronic bronchitis, and other respiratory diseases by relaxing bronchial smooth muscle. N-Nitroso Terbutaline, a potential genotoxic impurity (GTI), may originate from side reactions between amine compounds and nitrosating agents during production. Nitroso compounds have potential carcinogenicity, and their nitrosamide groups and hydroxyphenyl groups may enhance interaction with DNA, making control of this impurity critical for 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 7 minutes, with LOD of 0.002 ng/mL for trace analysis of genotoxic impurities.

  • Formation Mechanism:Formed by reaction of Terbutaline's secondary amine group with nitrite under acidic conditions (e.g., pH <4); optimizing nitrosating agent residue control 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 lung tissue at a 5 mg/kg dose. Accelerated stability and forced degradation tests are ongoing to systematically study degradation pathways and mutagenic risks under light, heat, and oxidation 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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