1-(4-Chlorophenyl)-2-(piperazin-1-yl)ethan-1-one dihydrochloride CAS 1073155-04-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1073155-04-0
Molecular FormulaC12H15ClN2O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Chlorophenyl)-2-(piperazin-1-yl)ethan-1-one dihydrochloride CAS 1073155-04-0 chemical structure

Description

1-(4-Chlorophenyl)-2-(piperazin-1-yl)ethan-1-one dihydrochloride (C12H15ClN2OHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; 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).

CATO supplies 1-(4-Chlorophenyl)-2-(piperazin-1-yl)ethan-1-one dihydrochloride (CAS 1073155-04-0), a certified reference material (molecular formula C12H15ClN2OHCl, MW 275.17 g/mol) for analytical method development and quality control.

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 1-(4-Chlorophenyl)-2-(piperazin-1-yl)ethan-1-one dihydrochloride 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 FormulaC12H15ClN2O 2*HCl
Molecular Weight275.17 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms2

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