2-Amino-1-(4-benzyl-1-piperazinyl)-3-methyl-1-butanone hydrochloride CAS 1236259-19-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1236259-19-0
Molecular FormulaC16H25N3O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Amino-1-(4-benzyl-1-piperazinyl)-3-methyl-1-butanone hydrochloride CAS 1236259-19-0 chemical structure

Description

Based on its molecular formula C16H25N3OHCl, 2-Amino-1-(4-benzyl-1-piperazinyl)-3-methyl-1-butanone 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 311.85 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.

2-Amino-1-(4-benzyl-1-piperazinyl)-3-methyl-1-butanone hydrochloride (CAS 1236259-19-0), molecular formula C16H25N3OHCl and molecular weight 311.85 g/mol, is a CATO reference standard with documented purity and traceability.

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 2-Amino-1-(4-benzyl-1-piperazinyl)-3-methyl-1-butanone 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.

Physical & Chemical Properties

Molecular FormulaC16H25N3O HCl
Molecular Weight311.85 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms3

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