Keywords

• ERA7295N7W
• SCHEMBL21886407
• 3-[4-(Hexyloxy)-1,2,5-thiadiazol-3-yl]-1-methylpyridinium

Quick Details

• ProName: Era7295N7W
• CasNo: 759425-28-0
• Molecular Formula: C14H20N3OS+
• Appearance: White solid
• Application: Pharmaceutical research
• DeliveryTime: prompt delivery
• PackAge: Screw bottle,foil bags,Reagent bottles
• Port: shenzhen/hongkong
• ProductionCapacity: 5000 Metric Ton/Year
• Purity: 95%+
• Storage: cool and dry
• Transportation: DHL,FedEx,UPS,EMS,TNT;
• LimitNum: 1 Kilogram
• Moisture Content: 0.1%
• Impurity: 0.1%

Superiority

We supply over 20000 types of spot impurity reference materials, with sufficient supply and same day delivery to meet customers' urgent needs for replenishment at any time. The company has its own research and development center and laboratory, and the team members have over ten years of experience in developing drug impurity reference standards. Our website www.molcoo.com covers over 98% of cutting-edge generic drug projects, with complete structural formulas that greatly save customers time in impurity structure analysis and inference. All products undergo strict quality control testing and provide relevant information such as COA, H-NMR, C-NMR, MS/GC-MS, HPLC/GC purity, QNMR quantification, TGA thermogravimetric analysis, IR infrared, UV ultraviolet, two-dimensional (COSY, NOESY, HMBC, HMQC), etc. These structural confirmation spectra ensure quality and reliability. Our products have a wide range of categories, fast delivery time, good quality, and low prices, which can quickly solve various customer needs such as replenishment and consistency evaluation.

Details

In the journey of pharmaceutical R&D and quality control, impurity research is the cornerstone of ensuring drug safety and efficacy. Xanomeline Impurity Standards act as your "precision ruler," delivering excellence and expertise to support accurate analysis of every drug sample.

Key Advantages:

1. High Purity, Strong Traceability
   Rigorous adherence to international standards ensures ≥95% purity, with full structural confirmation and traceability to authoritative databases.
2. Broad Structural Coverage
   Includes critical process-related impurities, degradation products, and analogs of xanomeline, addressing synthesis optimization, stability studies, and more.
3. Professional Services, End-to-End Support
   Customized impurity preparation, method validation, and regulatory compliance assistance to streamline approval processes.

Applications:

• Drug Development: Accelerate NDA submissions and mitigate impurity risks.
• Quality Control: Establish robust internal standards and enhance product competitiveness.
• Research: Support mechanism studies and drive academic innovation.

Choose Xanomeline Impurity Standards for:
? Scientific Rigor: Certificates of Analysis (COA), HPLC/NMR spectra included with every batch.
? Efficiency & Reliability: Reduce testing timelines and R&D costs.
? Regulatory Compliance: Aligned with ICH, FDA, NMPA, and other global guidelines.

No more ambiguity in impurity research—
Unlock clarity in drug quality today!