Tretinoin EP Impurity F (4-Methoxy Retinoic Acid) CAS 81121-20-2

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.81121-20-2
Molecular FormulaC21H30O3
Molecular Weight330.46 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Tretinoin EP Impurity F (4-Methoxy Retinoic Acid) CAS 81121-20-2 chemical structure

Description

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.

CATO supplies Tretinoin EP Impurity F (4-Methoxy Retinoic Acid) (CAS 81121-20-2), a pharmacopoeial impurity reference standard (molecular formula C21H30O3, MW 330.46 g/mol) used for the identification and quantification of trace impurities in APIs.

Tretinoin EP Impurity F (4-Methoxy Retinoic Acid) (C21H30O3) contains a steroid core, a hydroxyl group, an ether linkage. 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).

This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.

Physical & Chemical Properties

Molecular FormulaC21H30O3
Molecular Weight330.46 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity>95%
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1980

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