Lovastatin Impurity 17 CAS CATO-C4X-168417
| CAS No. | CATO-C4X-168417 |
| Molecular Formula | C10H22 |
| Molecular Weight | N/A |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Chemical Structure
Description
The occurrence of Lovastatin Impurity 17 is closely related to an organic framework in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
CATO supplies Lovastatin Impurity 17 (CAS CATO-C4X-168417), a pharmacopoeial impurity reference standard (molecular formula C10H22C5H12C3H7NC2H6, MW 301.60 g/mol) used for the identification and quantification of trace impurities in APIs.
Lovastatin Impurity 17 (C10H22C5H12C3H7NC2H6) contains an organic framework. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.
Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.
CATO manufactures Lovastatin Impurity 17 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 | C10H22 2*C5H12 C3H7N C2H6 |
| Molecular Weight | 301.60 g/mol |
| Purity | 95% |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | -2.0 |
| Nitrogen Atoms | 1 |
Related Lovastatin Standards
- Lovastatin-d3 (CAS 1002345-93-8)
- Epi Lovastatin Hydroxy Acid Sodium Salt (CAS 101400-30-0)
- Lovastatin EP Impurity F (CAS 1048973-04-1)
- Lovastatin Impurity N1 (CAS 106909-04-0)
- Lovastatin EP Impurity C (CAS 109273-98-5)
- Lovastatin Acid Triol Sodium Salt (CAS 132294-94-1)
- Lovastatin EP Impurity D (Lovastatin Dimer) (CAS 149756-62-7)
- Lovastatin Anhydro Acid Sodium Salt (CAS 188067-71-2)
Recommended Standards
- Zidovudine Impurity 19 (CAS CATO-C4X-178319)
- Fludarabine Phosphate Impurity 13 (CAS 71261-44-4)
- Melphalan EP Impurity C DiHCl (CAS 896715-19-8)
- 4-(4-Bromo-3,5-dimethyl-1h-pyrazol-1-yl)butanoic acid (CAS 898050-16-3)
- 2-((Propan-2-ylideneamino)oxy)acetic acid (CAS 5382-89-8)
- 1-(3-Bromopyridin-2-yl)cyclopropanecarbonitrile (CAS 1876944-81-8)
- 4-Fmoc-3(S)-morpholine carboxylic acid (CAS 281655-37-6)
- (3-Nitrophenyl)(phenyl)methanone (CAS 2243-80-3)
- 5-Pyridin-2-yl-1,3,4-oxadiazol-2-amine (CAS 5711-72-8)
- Semaglutide impurity 202 (CAS CATO-C4X-2226202)
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