Rupatadine Fumaric Acid CAS 182349-12-8

Purity >95%In StockPharmaceutical Standards
CAS No.182349-12-8
Molecular FormulaC26H26ClN3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Rupatadine Fumaric Acid CAS 182349-12-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 532.04 g/mol gives Rupatadine Fumaric Acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Rupatadine Fumaric Acid (CAS 182349-12-8), a certified reference material (molecular formula C26H26ClN3C4H4O4, MW 532.04 g/mol) for analytical method development and quality control.

Rupatadine Fumaric Acid (C26H26ClN3C4H4O4) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), Rupatadine Fumaric Acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC26H26ClN3 C4H4O4
Molecular Weight532.04 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity>95%
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)17.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2009
Halogen ContentCl-containing
Nitrogen Atoms3

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