Cholesterol Impurity 35 CAS 64519-14-8

Purity ≥95%In StockPharmacopoeial Impurity Standards
CAS No.64519-14-8
Molecular FormulaC29H50O
Molecular Weight414.71 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Cholesterol Impurity 35 CAS 64519-14-8 chemical structure

Description

CATO manufactures Cholesterol Impurity 35 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.

As a process- or degradation-related impurity, Cholesterol Impurity 35 (CAS 64519-14-8, C29H50O) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Cholesterol Impurity 35 (C29H50O) contains a steroid core, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; 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).

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 FormulaC29H50O
Molecular Weight414.71 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity≥95%
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityStable under recommended storage conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1975

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