Decarboxylated (S)-Adenosyl Methionine Trifluoromethanesulfonic Acid CAS CATO-CCHM706003

Purity 97%+In StockPharmaceutical Standards
CAS No.CATO-CCHM706003
Molecular FormulaC14H23N6O3S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Decarboxylated (S)-Adenosyl Methionine Trifluoromethanesulfonic Acid CAS CATO-CCHM706003 chemical structure

Description

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.

CATO supplies Decarboxylated (S)-Adenosyl Methionine Trifluoromethanesulfonic Acid (CAS CATO-CCHM706003), a certified reference material (molecular formula C14H23N6O3SCF3O3S, MW 504.50 g/mol) for analytical method development and quality control.

Decarboxylated (S)-Adenosyl Methionine Trifluoromethanesulfonic Acid (C14H23N6O3SCF3O3S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 FormulaC14H23N6O3S CF3O3S
Molecular Weight504.50 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Halogen ContentF-containing
Nitrogen Atoms6
Sulfur Atoms2

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