Ethyl 2-(4-bromophenyl)ethanimidate hydrochloride CAS 51627-99-7

Purity 97%+In StockPharmaceutical Standards
CAS No.51627-99-7
Molecular FormulaC10H12BrNO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 2-(4-bromophenyl)ethanimidate hydrochloride CAS 51627-99-7 chemical structure

Description

As a certified reference material (CRM), Ethyl 2-(4-bromophenyl)ethanimidate hydrochloride 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.

Ethyl 2-(4-bromophenyl)ethanimidate hydrochloride (CAS 51627-99-7) is a high-purity analytical reference standard with the molecular formula C10H12BrNOHCl and a molecular weight of 278.57 g/mol.

Ethyl 2-(4-bromophenyl)ethanimidate hydrochloride (C10H12BrNOHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine/bromine 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

Physical & Chemical Properties

Molecular FormulaC10H12BrNO HCl
Molecular Weight278.57 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1971
Halogen ContentCl/Br-containing
Nitrogen Atoms1

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