Keywords

• N-desmethylxanomeline
• 131986-96-4
• Xanomeline Impurity

Quick Details

• ProName: N-Desmethylxanomeline
• CasNo: 131986-96-4
• Molecular Formula: C13H21N3OS
• Appearance: off-white powder
• 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

I. Product Overview
Xanomeline Impurity Reference Standard is a high-purity reference material designed for pharmaceutical R&D, drug quality control, and laboratory research. Its precise chemical composition and rigorous quality control ensure reliable analytical results, facilitating compliance with international regulatory standards.

II. Technical Specifications

III. Compliance & Certification

• Standards Compliance: GMP/GLP, ISO, ASTM, and other international quality control standards.
• Pharmacopoeial References: Supports procurement of USP, EP, BP, JP, and other pharmacopoeial standards.
• Traceability Documents: Each batch includes Certificate of Analysis (COA), MSDS, and structural confirmation spectra (NMR, IR, UV, etc.).

IV. Applications

1. Drug Submission: For impurity profiling and consistency evaluation to meet regulatory requirements.
2. Instrument Calibration: As a quantitative benchmark for HPLC, MS, and other analytical instruments.
3. Scientific Research: Studying drug stability, metabolic pathways, and impurity toxicity.

V. Product Advantages

• High Purity Assurance: Rigorous quality control processes ensure experimental reproducibility.
• Rapid Response: 20,000+ in-stock items, same-day shipping, and support for urgent orders.
• Customization Services: Offering impurity synthesis, purification, and custom development of novel drug impurities.

VI. Packaging & Stability

• Packaging: Sealed vials/amber bottles with labels (including CAS number, batch number, expiration date).
• Stability: Long-term monitoring data shows a shelf life ≥2 years under low-temperature storage.