Timepidium Bromide Hydrate CAS 116383-38-1

Purity 97%+In StockPharmaceutical Standards
CAS No.116383-38-1
Molecular FormulaC17H22NOS2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Timepidium Bromide Hydrate CAS 116383-38-1 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 418.41 g/mol gives Timepidium Bromide Hydrate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Timepidium Bromide Hydrate (CAS 116383-38-1), a certified reference material (molecular formula C17H22NOS2BrH2O, MW 418.41 g/mol) for analytical method development and quality control.

Timepidium Bromide Hydrate (C17H22NOS2BrH2O) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. Halogen substitution raises its density and boiling point, 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

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 FormulaC17H22NOS2 Br H2O
Molecular Weight418.41 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms2

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