(5-(4-(Tert-butyl)phenyl)-1,2,4-oxadiazol-3-yl)methanamine hydrochloride CAS 1185294-12-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1185294-12-5
Molecular FormulaC13H17N3O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(5-(4-(Tert-butyl)phenyl)-1,2,4-oxadiazol-3-yl)methanamine hydrochloride CAS 1185294-12-5 chemical structure

Description

CATO manufactures (5-(4-(Tert-butyl)phenyl)-1,2,4-oxadiazol-3-yl)methanamine hydrochloride 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.

CATO supplies (5-(4-(Tert-butyl)phenyl)-1,2,4-oxadiazol-3-yl)methanamine hydrochloride (CAS 1185294-12-5), a certified reference material (molecular formula C13H17N3OHCl, MW 267.76 g/mol) for analytical method development and quality control.

Based on its molecular formula C13H17N3OHCl, (5-(4-(Tert-butyl)phenyl)-1,2,4-oxadiazol-3-yl)methanamine hydrochloride contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 267.76 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

Physical & Chemical Properties

Molecular FormulaC13H17N3O HCl
Molecular Weight267.76 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Nitrogen Atoms3

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