tert-Butyl (5-(hydroxymethyl)pyridazin-3-yl)carbamate CAS 2452465-22-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2452465-22-2
Molecular FormulaC10H15N3O3
Molecular Weight225.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (5-(hydroxymethyl)pyridazin-3-yl)carbamate CAS 2452465-22-2 chemical structure

Description

Based on its molecular formula C10H15N3O3, tert-Butyl (5-(hydroxymethyl)pyridazin-3-yl)carbamate contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 225.24 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

tert-Butyl (5-(hydroxymethyl)pyridazin-3-yl)carbamate (CAS 2452465-22-2), molecular formula C10H15N3O3 and molecular weight 225.24 g/mol, is a CATO reference standard with documented purity and traceability.

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 tert-Butyl (5-(hydroxymethyl)pyridazin-3-yl)carbamate 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 FormulaC10H15N3O3
Molecular Weight225.24 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2000
Nitrogen Atoms3

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