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Postion:Product Catalog >Xanomeline Impurity 5
Xanomeline Impurity 5
  • Xanomeline Impurity 5
  • Xanomeline Impurity 5
  • Xanomeline Impurity 5
  • Xanomeline Impurity 5
  • Xanomeline Impurity 5

Xanomeline Impurity 5 NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-08-21

Product Details

Product Name: Xanomeline Impurity 5 Min. Order: 10mg
Purity: 99%+ HPLC Supply Ability: 1000
Release date: 2025/08/21
Molecular formula: C13H20N4O2S

Xanomeline Impurity 5

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

Product Information

  • Product Number: X002005

  • English Name: Xanomeline Impurity 5

  • English Alias: 3-(hexyloxy)-4-(1-nitroso-1,2,5,6-tetrahydropyridin-3-yl)-1,2,5-thiadiazole

  • CAS Number: None

  • Molecular Formula: C₁₃H₂₀N₄O₂S

  • Molecular Weight: 296.39

Advantages

As Impurity 5 of Xanomeline, this compound has the following advantages:


  • Well-defined with distinct polyheterocyclic features: Contains 1,2,5-thiadiazole ring (3-hexyloxy, 4-tetrahydropyridinyl substituted) and 1-nitroso-1,2,5,6-tetrahydropyridine ring. Unlike xanomeline (muscarinic acetylcholine receptor agonist with non-nitroso tetrahydropyridine), its nitroso polarity, thiadiazole sulfur properties, and hexyloxy hydrophobicity create significant differences, enabling precise differentiation via HPLC/GC as a specific marker;

  • High stability and traceability: Rigid thiadiazole/tetrahydropyridine structures and stability of ether bonds ensure stability under dark, low-temperature conditions. As a byproduct from tetrahydropyridine ring nitrosation during storage/degradation of xanomeline, it directly reflects tertiary amine oxidation activity and nitrite exposure risk, improving process tracing accuracy;

  • High detection sensitivity: Thiadiazole-tetrahydropyridine conjugation shows strong UV absorption (240-270nm), combined with m/z 297 [M+H]⁺ enabling ppb-level analysis via LC-MS, compatible with muscarinic agonist nitroso impurity systems.

Applications

  • Pharmaceutical quality control: Used as an impurity reference standard to quantify Xanomeline Impurity 5 in APIs, ensuring compliance with limits for potentially harmful impurities;

  • Stability studies: Monitoring impurity levels under varying conditions (pH, light) to assess nitrosation trends and support safety assurance over shelf life;

  • Synthesis assessment: Evaluating purity of tetrahydropyridine-containing intermediates in xanomeline synthesis to reduce nitrosation risk at the source.

Background Description

Xanomeline is a muscarinic acetylcholine receptor agonist containing 1,2,5-thiadiazole and tetrahydropyridine rings. Its tetrahydropyridine tertiary amine (-N-) may undergo nitrosation upon exposure to nitrous acid (e.g., from nitrate conversion) during production or storage, forming 1-nitroso-1,2,5,6-tetrahydropyridine derivatives like Xanomeline Impurity 5. Due to potential toxicity of nitroso compounds, their residues impact xanomeline safety, requiring strict detection and control.

Research Status

Current research focuses on:


  • Analytical method validation: Developing HPLC assays with C18 columns for separation, achieving 0.1 ppb detection limits;

  • Nitrosation mechanism: Studying impurity formation kinetics under varying nitrite concentration and pH to clarify tetrahydropyridine tertiary amine-to-nitroso conversion pathways;

  • Control strategies: Exploring nitrosation inhibitors (e.g., vitamin C) to keep impurity levels below safety limits;

  • Toxicity evaluation: Conducting in vitro cell studies to assess potential toxicity and support limit setting



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

Company Profile Introduction

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