6-Methylimidazo[2,1-b]thiazole-3-carboxylic acid hydrochloride CAS 1269052-79-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1269052-79-0
Molecular FormulaC7H6N2O2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Methylimidazo[2,1-b]thiazole-3-carboxylic acid hydrochloride CAS 1269052-79-0 chemical structure

Description

As a certified reference material (CRM), 6-Methylimidazo[2,1-b]thiazole-3-carboxylic acid hydrochloride 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.

6-Methylimidazo[2,1-b]thiazole-3-carboxylic acid hydrochloride (CAS 1269052-79-0), molecular formula C7H6N2O2SHCl and molecular weight 218.66 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 6-Methylimidazo[2,1-b]thiazole-3-carboxylic acid hydrochloride (C7H6N2O2SHCl) contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 218.66 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.

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

Physical & Chemical Properties

Molecular FormulaC7H6N2O2S HCl
Molecular Weight218.66 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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