Lovastatin Impurity 41 CAS CATO-C4X-168441

Purity 95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-168441
Molecular Formula-
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Lovastatin Impurity 41 CAS CATO-C4X-168441 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Lovastatin Impurity 41.

CATO supplies Lovastatin Impurity 41 (CAS CATO-C4X-168441), a pharmacopoeial impurity reference standard (molecular formula N/A, MW N/A g/mol) used for the identification and quantification of trace impurities in APIs.

Lovastatin Impurity 41 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC8H17A C7H16 C4H10 C2H6
Molecular Weight301.62 g/mol
Purity95%
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityStable under recommended storage conditions
Degree of Unsaturation (DBE)-2.5

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