(3S,4S)-1,2-Bis(tert-butoxycarbonyl)-4-methylhexahydropyridazine-3-carboxylic acid CAS 2641452-28-8

Purity 97%+In StockPharmaceutical Standards
CAS No.2641452-28-8
Molecular FormulaC16H28N2O6
Molecular Weight344.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3S,4S)-1,2-Bis(tert-butoxycarbonyl)-4-methylhexahydropyridazine-3-carboxylic acid CAS 2641452-28-8 chemical structure

Description

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

CATO supplies (3S,4S)-1,2-Bis(tert-butoxycarbonyl)-4-methylhexahydropyridazine-3-carboxylic acid (CAS 2641452-28-8), a certified reference material (molecular formula C16H28N2O6, MW 344.40 g/mol) for analytical method development and quality control.

Based on its molecular formula C16H28N2O6, (3S,4S)-1,2-Bis(tert-butoxycarbonyl)-4-methylhexahydropyridazine-3-carboxylic acid contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 344.40 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

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.

Physical & Chemical Properties

Molecular FormulaC16H28N2O6
Molecular Weight344.40 g/mol
AppearanceOff-white to pale yellow crystalline powder
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
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2002
Nitrogen Atoms2

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