Olanzapine Impurity 41 CAS 610-17-3
| CAS No. | 610-17-3 |
| Molecular Formula | C8H10N2O2 |
| Molecular Weight | 166.18 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Chemical Structure
Description
Compared with other compounds in its class, the molecular weight of 166.18 g/mol gives Olanzapine Impurity 41 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
Olanzapine Impurity 41 (CAS 610-17-3) is a certified pharmaceutical impurity reference standard with the molecular formula C8H10N2O2 and a molecular weight of 166.18 g/mol.
The molecular framework of Olanzapine Impurity 41 (C8H10N2O2) is characterized by an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).
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.
CATO manufactures Olanzapine Impurity 41 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.
Physical & Chemical Properties
| Molecular Formula | C8H10N2O2 |
| Molecular Weight | 166.18 g/mol |
| Appearance | Off-white to pale yellow crystalline powder. (faint amine-like odor) |
| Purity | >95% |
| Storage | Store at 2-8°C, protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 5.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1957 |
| Nitrogen Atoms | 2 |
Related Olanzapine Standards
- Olanzapine Impurity 62 (CAS 17842-18-1)
- Olanzapine Impurity 30 (CAS 55525-92-3)
- Olanzapine Impurity 31 (CAS CATO-C4X-117831)
- Olanzapine Impurity 40 (CAS 1493-27-2)
- Olanzapine Impurity 7 (CAS 138564-58-6)
- Olanzapine Impurity 24 (CAS 24878-25-9)
- Olanzapine Impurity 29 (CAS 134801-02-8)
- Olanzapine Impurity 29 (CAS 52833-34-8)
Recommended Standards
- Amoxicillin Impurity 97 (CAS 53958-19-3)
- Ramosetron Impurity 15 (CAS 26751-24-6)
- Amoxicillin Impurity 74 (CAS 54397-23-8)
- Pazopanib Impurity 29 (CAS 20191-74-6)
- Felbinac Impurity 3 (CAS 26140-60-3)
- Apalutamide Impurity 118 (CAS CATO-C4X-2749118)
- Norfloxacin Impurity 19 (CAS 74011-42-0)
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- Palmitoyl Tripeptide-1 TFA salt (CAS 2803375-47-3)
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