1,2,3,3-Tetramethyl-5-sulfo-3H-indol-1-ium iodide CAS 644979-02-2

Purity 97%+In StockPharmaceutical Standards
CAS No.644979-02-2
Molecular FormulaC12H16NO3S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,2,3,3-Tetramethyl-5-sulfo-3H-indol-1-ium iodide CAS 644979-02-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 381.22 g/mol gives 1,2,3,3-Tetramethyl-5-sulfo-3H-indol-1-ium iodide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

1,2,3,3-Tetramethyl-5-sulfo-3H-indol-1-ium iodide (CAS 644979-02-2), molecular formula C12H16NO3SI and molecular weight 381.22 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine substitution, 1,2,3,3-Tetramethyl-5-sulfo-3H-indol-1-ium iodide is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 381.22 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures 1,2,3,3-Tetramethyl-5-sulfo-3H-indol-1-ium iodide 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 FormulaC12H16NO3S I
Molecular Weight381.22 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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.)1985
Halogen ContentI-containing
Nitrogen Atoms1
Sulfur Atoms1

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