Diethyl 3,3'-(disulfanediylbis(methylene))bis(5-methyl-1H-pyrazole-4-carboxylate) CAS 296266-49-4

Purity 97%+In StockPharmaceutical Standards
CAS No.296266-49-4
Molecular FormulaC16H22N4O4S2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Diethyl 3,3'-(disulfanediylbis(methylene))bis(5-methyl-1H-pyrazole-4-carboxylate) CAS 296266-49-4 chemical structure

Description

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.

Diethyl 3,3'-(disulfanediylbis(methylene))bis(5-methyl-1H-pyrazole-4-carboxylate) (CAS 296266-49-4), molecular formula C16H22N4O4S2HCl and molecular weight 434.95 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C16H22N4O4S2HCl, Diethyl 3,3'-(disulfanediylbis(methylene))bis(5-methyl-1H-pyrazole-4-carboxylate) contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 434.95 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC16H22N4O4S2 HCl
Molecular Weight434.95 g/mol
Purity97%+
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms4
Sulfur Atoms2

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