Xanomeline Impurity 7 CAS CATO-C4X-33017
| CAS No. | CATO-C4X-33017 |
| Molecular Formula | C7H5N3OS |
| Molecular Weight | 179.20 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Chemical Structure
Description
CATO manufactures Xanomeline Impurity 7 under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.
As a process- or degradation-related impurity, Xanomeline Impurity 7 (CAS CATO-C4X-33017, C7H5N3OS) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.
The molecular framework of Xanomeline Impurity 7 (C7H5N3OS) is characterized by an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.
This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.
Physical & Chemical Properties
| Molecular Formula | C7H5N3OS |
| Molecular Weight | 179.20 g/mol |
| Purity | >95% |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 7.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| Nitrogen Atoms | 3 |
| Sulfur Atoms | 1 |
Related Xanomeline Standards
- Xanomeline Impurity 17 (CAS 2644093-98-9)
- Xanomeline impurity 48 (CAS CATO-C4X-330148)
- Xanomeline Impurity 15 (CAS CATO-C4X-330115)
- Xanomeline Impurity 19 (CAS 131987-61-6)
- Xanomeline Impurity 8 (CAS 131987-88-7)
- Xanomeline impurity 49 (CAS 141136-36-9)
- Xanomeline impurity 41 (CAS CATO-C4X-330141)
- Xanomeline impurity 59 (CAS CATO-C4X-330159)
Recommended Standards
- Hexamethylphosphoramide (CAS 680-31-9)
- N-Nitroso Lansoprazole EP Impurity E (CAS CATO-C4X-111356)
- 2-(4-Fluorophenyl)thiazole (CAS 1005196-13-3)
- Butafosfan (CAS 17316-67-5)
- Trimebutine EP Impurity E (CAS 84333-59-5)
- Difluprednate Impurity 5 (CAS 1270039-29-6)
- Sodium Valproate Impurity 41 (CAS CATO-C4X-116641)
- N-(2-{[4-(Benzyloxy)phenyl]methanesulfonyl}-1-phenylethyl)-N-hydroxyformamide (CAS 1253527-86-4)
- 6-tert-Butyl-2-({[3-(trifluoromethyl)phenyl]methyl}sulfanyl)-3,4-dihydropyrimidin-4-one (CAS 478259-92-6)
- Nilotinib Impurity 15 (CAS 917391-28-7)
- (5-Ethyl-5-methyltetrahydrofuran-2-yl)methanamine (CAS 1849237-72-4)
- 2-(2-Carboxycyclopropaneamido)benzoic acid (CAS 1024114-61-1)
- 6-Bromo-5-fluoro-1H-indazole (CAS 1286734-85-7)
- Tirzepatide Impurity 58 (CAS CATO-C4X-324058)
Why CATO?
- ISO 17034 accredited reference material producer (CNAS + ANAB dual accreditation)
- 130,000+ catalog items in stock, COA supplied with every batch
- Worldwide shipping with full export documentation (HS code guidance available)
- Technical support: +86 18665070610 / Nicole.chen@cato-chem.com