4-[2-(4-Iodophenoxy)ethyl]piperidine hydrochloride CAS 1112052-95-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1112052-95-5
Molecular FormulaC13H18INO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-[2-(4-Iodophenoxy)ethyl]piperidine hydrochloride CAS 1112052-95-5 chemical structure

Description

As a certified reference material (CRM), 4-[2-(4-Iodophenoxy)ethyl]piperidine 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.

4-[2-(4-Iodophenoxy)ethyl]piperidine hydrochloride (CAS 1112052-95-5), molecular formula C13H18INOHCl and molecular weight 367.65 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 4-[2-(4-Iodophenoxy)ethyl]piperidine hydrochloride (C13H18INOHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine/iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 367.65 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC13H18INO HCl
Molecular Weight367.65 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
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.)1989
Halogen ContentCl/I-containing
Nitrogen Atoms1

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