2-(Piperazin-1-yl)thiazole-4-carboxylic acid dihydrochloride CAS 2138098-59-4

Purity 97%+In StockPharmaceutical Standards
CAS No.2138098-59-4
Molecular FormulaC8H11N3O2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(Piperazin-1-yl)thiazole-4-carboxylic acid dihydrochloride CAS 2138098-59-4 chemical structure

Description

Structurally, 2-(Piperazin-1-yl)thiazole-4-carboxylic acid dihydrochloride (C8H11N3O2SHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 249.71 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies 2-(Piperazin-1-yl)thiazole-4-carboxylic acid dihydrochloride (CAS 2138098-59-4), a certified reference material (molecular formula C8H11N3O2SHCl, MW 249.71 g/mol) for analytical method development and quality control.

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

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 FormulaC8H11N3O2S 2*HCl
Molecular Weight249.71 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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