Lovastatin Impurity N1 CAS 106909-04-0
| CAS No. | 106909-04-0 |
| Molecular Formula | C23H34O6 |
| Molecular Weight | 406.51 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 406.51 g/mol gives Lovastatin Impurity N1 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
Lovastatin Impurity N1 (CAS 106909-04-0) is a certified pharmaceutical impurity reference standard with the molecular formula C23H34O6 and a molecular weight of 406.51 g/mol.
The molecular framework of Lovastatin Impurity N1 (C23H34O6) is characterized by a flavonoid core, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional 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 Lovastatin Impurity N1 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 | C23H34O6 |
| Molecular Weight | 406.51 g/mol |
| Appearance | Off-white to pale yellow crystalline powder |
| Purity | 97%+ |
| Storage | Store at room temperature, protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in methanol, acetonitrile, DMSO, water (slightly soluble) |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 7.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1987 |
Related Lovastatin Standards
- Lovastatin EP Impurity E (CAS 77517-29-4)
- Lovastatin-d3 (CAS 1002345-93-8)
- Lovastatin Anhydro Acid Sodium Salt (CAS 188067-71-2)
- Lovastatin Impurity 10 (CAS CATO-C4X-168410)
- Lovastatin EP Impurity F (CAS 1048973-04-1)
- Lovastatin Impurity 26 (CAS CATO-C4X-168426)
- Lovastatin EP Impurity A (CAS 73573-88-3)
- Lovastatin EP Impurity B (CAS 75225-51-3)
Recommended Standards
- Imrecoxib Impurity 16-d7 (CAS 896729-08-1 (unlabelled))
- 5β-PREGNAN-3α, 17, 21-TRIOL-11, 20-DIONE 21-ACETATE (CAS 17736-20-8)
- Ceftaroline Fosamil Impurity 22 (CAS CATO-C4X-148322)
- Panduratin A (CAS 89837-52-5)
- Leuprorelin EP Impurity J Acetate (CAS CATO-C4X-182228)
- Remdesivir Impurity 27 (CAS CATO-C4X-210027)
- Safinamide Impurity 37 (CAS 1000370-27-3)
- 2-((4-Amino-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)thio)-N-(3-chlorophenyl)acetamide (CAS 898622-11-2)
- (1R,2S)-2-aminocycloheptan-1-ol (CAS 932-57-0)
- Empagliflozin impurity 228 (CAS CATO-C4X-1065228)
- (1S,3S)-3-methoxycyclopentan-1-amine (CAS 1821430-33-4)
- 6-Bromo-4-chloro-5,7-dimethylpyrrolo[2,1-f][1,2,4]triazine (CAS 1780024-55-6)
- (R)-2-Amino-3-(4-isopropylphenyl)propanoic acid (CAS 755724-85-7)
- Semaglutide Impurity 158 (x TFA Salt) (CAS CATO-C4X-2226158)
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