OxythiamineDISCONTINUED. Please see O878508. CAS 136-16-3

Purity 97%+In StockPharmaceutical Standards
CAS No.136-16-3
Molecular FormulaC12H16N3O2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

OxythiamineDISCONTINUED. Please see O878508. CAS 136-16-3 chemical structure

Description

OxythiamineDISCONTINUED. Please see O878508. (CAS 136-16-3) is a high-purity analytical reference standard with the molecular formula C12H16N3O2SHClCl and a molecular weight of 338.25 g/mol.

The molecular framework of OxythiamineDISCONTINUED. Please see O878508. (C12H16N3O2SHClCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

CATO manufactures OxythiamineDISCONTINUED. Please see O878508. under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC12H16N3O2S HCl Cl
Molecular Weight338.25 g/mol
Purity97%+
StorageStore at 2-8°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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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