Lovastatin Impurity 19 CAS CATO-C4X-168419

Purity 95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-168419
Molecular Formula-
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Lovastatin Impurity 19 CAS CATO-C4X-168419 chemical structure

Description

CATO manufactures Lovastatin Impurity 19 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.

Lovastatin Impurity 19 (CAS CATO-C4X-168419) is a certified pharmaceutical impurity reference standard with the molecular formula N/A and a molecular weight of N/A g/mol.

Lovastatin Impurity 19 is supplied as a fully characterized reference material; its structural identity, assigned purity, and stability data are documented in the batch-specific Certificate of Analysis (COA).

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.

Physical & Chemical Properties

Molecular FormulaC24H41AO4 2*C2H6 CH3A
Molecular Weight438.69 g/mol
Purity95%
StorageStore at room temperature, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing

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