Lusutrombopag Impurity 10 CAS CATO-C4X-208410
| CAS No. | CATO-C4X-208410 |
| Molecular Formula | C17H25ClO3 |
| Molecular Weight | 312.83 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Chemical Structure
Description
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 supplies Lusutrombopag Impurity 10 (CAS CATO-C4X-208410), a pharmacopoeial impurity reference standard (molecular formula C17H25ClO3, MW 312.83 g/mol) used for the identification and quantification of trace impurities in APIs.
Lusutrombopag Impurity 10 (C17H25ClO3) contains a steroid core, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).
CATO manufactures Lusutrombopag Impurity 10 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 | C17H25ClO3 |
| Molecular Weight | 312.83 g/mol |
| Appearance | Off-white to pale yellow crystalline powder. (slight halide-like odor) |
| Purity | 97%+ |
| Storage | Store at room temperature, keep sealed and dry |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 5.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| Halogen Content | Cl-containing |
Related Lusutrombopag Standards
- Lusutrombopag Impurity N1 (CAS 1110767-96-8)
- Lusutrombopag Impurity 11 (CAS CATO-C4X-208411)
- Lusutrombopag Impurity 18 (CAS 1110767-94-6)
- Lusutrombopag Impurity 68 (CAS CATO-C4X-208468)
- Lusutrombopag Impurity 30 (CAS 1110767-19-5)
- Lusutrombopag Impurity 87 (CAS CATO-C4X-208487)
- Lusutrombopag Impurity N3 (CAS 1110767-89-9)
- Lusutrombopag Impurity 47 (CAS CATO-C4X-208447)
Recommended Standards
- Mcpa-2-Ethylhexyl Ester (CAS 29450-45-1)
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- Iridium(2+),pentaamminechloro-,(OC-6-22)- (CAS 29589-09-1)
- Balsalazide Impurity 5 (CAS 1346606-53-8)
- N-Nitroso Ivabradine impurity 85 (CAS CATO-C4X-111985)
- Gemfibrozil EP Impurity H (CAS 415724-02-6)
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- 4-Amino-n-[1-(4-ethoxyphenyl)ethyl]butanamide hydrochloride (CAS 1384428-56-1)
- Heparan Sulfate (CAS 9050-30-0)
- 2-(6-Benzamido-9H-purin-9-yl)acetic acid (CAS 171486-04-7)
- Cholecystokinin, CCK Tetrapeptide (30-33) (CAS 35144-91-3)
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