4-Chloro-3-(4-methyl-1-piperazinyl)aniline CAS 148547-10-8

Purity 97%+In StockPharmaceutical Standards
CAS No.148547-10-8
Molecular FormulaC11H16ClN3
Molecular Weight225.72 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-3-(4-methyl-1-piperazinyl)aniline CAS 148547-10-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 225.72 g/mol gives 4-Chloro-3-(4-methyl-1-piperazinyl)aniline distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-Chloro-3-(4-methyl-1-piperazinyl)aniline (CAS 148547-10-8) is a high-purity analytical reference standard with the molecular formula C11H16ClN3 and a molecular weight of 225.72 g/mol.

4-Chloro-3-(4-methyl-1-piperazinyl)aniline (C11H16ClN3) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, 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).

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

As a certified reference material (CRM), 4-Chloro-3-(4-methyl-1-piperazinyl)aniline meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H16ClN3
Molecular Weight225.72 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.)1999
Halogen ContentCl-containing
Nitrogen Atoms3

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