6-(4-(1H-Imidazol-1-yl)phenoxy)-N,N-dimethylhexan-1-amine dihydrochloride CAS 502656-68-0

Purity 97%+In StockPharmaceutical Standards
CAS No.502656-68-0
Molecular FormulaC17H25N3O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(4-(1H-Imidazol-1-yl)phenoxy)-N,N-dimethylhexan-1-amine dihydrochloride CAS 502656-68-0 chemical structure

Description

6-(4-(1H-Imidazol-1-yl)phenoxy)-N,N-dimethylhexan-1-amine dihydrochloride (C17H25N3OHCl) contains a steroid core, 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies 6-(4-(1H-Imidazol-1-yl)phenoxy)-N,N-dimethylhexan-1-amine dihydrochloride (CAS 502656-68-0), a certified reference material (molecular formula C17H25N3OHCl, MW 323.87 g/mol) for analytical method development and quality control.

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.

As a certified reference material (CRM), 6-(4-(1H-Imidazol-1-yl)phenoxy)-N,N-dimethylhexan-1-amine dihydrochloride 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 FormulaC17H25N3O 2*HCl
Molecular Weight323.87 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentCl-containing
Nitrogen Atoms3

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