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Postion:Product Catalog >Analytical Chemistry>Standard>Pharmaceutical Impurity Reference Standards>Timolol Impurity
Timolol Impurity
  • Timolol Impurity
  • Timolol Impurity
  • Timolol Impurity
  • Timolol Impurity
  • Timolol Impurity

Timolol Impurity NEW

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

Product Details

Product Name: Timolol Impurity Min. Order: 10mg
Purity: 99%+ HPLC Supply Ability: 1000
Release date: 2025/07/31
Molecular formula: C13H23N5O4S

Timolol Impurity

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


  • Product Number: T023017

  • English Name: Timolol Impurity 17

  • English Alias: (S)-N-(tert-butyl)-N-(2-hydroxy-3-((4-morpholino-1,2,5-thiadiazol-3-yl)oxy)propyl)nitrous amide

  • CAS Number: None

  • Molecular Formula: C₁₃H₂₃N₅O₄S

  • Molecular Weight: 345.42

  • As a nitroso impurity of timolol, the research advantages of this compound lie in:

  • Analyzing the by-product formation mechanism of nitrosation reactions during timolol synthesis or storage to optimize processes for controlling nitroso impurity generation;

  • Serving as a reference standard containing nitroso, hydroxyl, thiadiazole, and morpholine structures to provide a standard substance for detecting impurities with complex structures in drugs, assisting in evaluating drug safety (nitroso compounds may have potential carcinogenicity);

  • Helping study the impact of multi-functional group structures on drug stability and toxicological properties to provide a scientific basis for formulating impurity control strategies.


  • Drug Development: Used as an impurity reference standard to identify and quantify Impurity 17 in timolol preparations, evaluating the purity of APIs and formulations;

  • Quality Control: Acting as a standard substance to validate the sensitivity of detection methods (e.g., HPLC or LC-MS), ensuring nitroso impurity content meets ICH guideline requirements during production;

  • Toxicological Research: Assisting in evaluating the potential genotoxicity of nitroso impurities to provide data support for drug safety evaluation.


  • Timolol is a β-blocker commonly used in the treatment of glaucoma, hypertension, and angina. Due to the potential carcinogenic risk of nitroso compounds (such as N-nitrosamines), drug regulatory authorities worldwide have put forward strict control requirements for nitroso impurities in drugs. Timolol Impurity 17, as an impurity containing a nitroso structure, may be generated during timolol synthesis, storage, or metabolism, making research on it a key link in drug quality control and safety assessment.
  • Current research focuses on:

  • Synthesis Methods: Developing high-purity synthesis processes for Timolol Impurity 17, solving the synthesis and purification challenges of multi-functional group compounds to meet the needs of toxicological research and quality control;

  • Detection Technologies: Establishing trace detection methods for nitroso impurities (detection limits reach ppb level) using ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) and other technologies;

  • Toxicological Evaluation: Studying the potential mutagenicity and carcinogenicity of this impurity through in vitro Ames tests and animal models;

  • Process Control: Analyzing the inducements (such as raw material residues, reaction conditions) of nitrosation reactions to optimize the synthesis route or storage conditions to reduce the generation of nitroso impurities.

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




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