1-(3-Hydroxypropyl)-2,4,6-triphenylpyridin-1-ium perchlorate CAS 69821-55-2

Purity 97%+In StockPharmaceutical Standards
CAS No.69821-55-2
Molecular FormulaC26H24NO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(3-Hydroxypropyl)-2,4,6-triphenylpyridin-1-ium perchlorate CAS 69821-55-2 chemical structure

Description

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

1-(3-Hydroxypropyl)-2,4,6-triphenylpyridin-1-ium perchlorate (CAS 69821-55-2) is a high-purity analytical reference standard with the molecular formula C26H24NOClO4 and a molecular weight of 465.93 g/mol.

1-(3-Hydroxypropyl)-2,4,6-triphenylpyridin-1-ium perchlorate (C26H24NOClO4) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. 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.

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 FormulaC26H24NO ClO4
Molecular Weight465.93 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1976
Halogen ContentCl-containing
Nitrogen Atoms1

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