Penethacillin Hydroiodide CAS 808-71-9

Purity >95%In StockPharmaceutical Standards
CAS No.808-71-9
Molecular FormulaC22H31N3O4S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Penethacillin Hydroiodide CAS 808-71-9 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 561.48 g/mol gives Penethacillin Hydroiodide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Penethacillin Hydroiodide (CAS 808-71-9), molecular formula C22H31N3O4SHI and molecular weight 561.48 g/mol, is a CATO reference standard with documented purity and traceability.

Penethacillin Hydroiodide (C22H31N3O4SHI) contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine 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. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 Penethacillin Hydroiodide 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 FormulaC22H31N3O4S HI
Molecular Weight561.48 g/mol
Purity>95%
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Halogen ContentI-containing
Nitrogen Atoms3
Sulfur Atoms1

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