3-{2-[4-(tert-Pentyl)phenoxy]ethyl}piperidinehydrochloride CAS 1220032-17-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1220032-17-6
Molecular FormulaC18H29NO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-{2-[4-(tert-Pentyl)phenoxy]ethyl}piperidinehydrochloride CAS 1220032-17-6 chemical structure

Description

CATO manufactures 3-{2-[4-(tert-Pentyl)phenoxy]ethyl}piperidinehydrochloride 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.

CATO supplies 3-{2-[4-(tert-Pentyl)phenoxy]ethyl}piperidinehydrochloride (CAS 1220032-17-6), a certified reference material (molecular formula C18H29NOHCl, MW 311.89 g/mol) for analytical method development and quality control.

Structurally, 3-{2-[4-(tert-Pentyl)phenoxy]ethyl}piperidinehydrochloride (C18H29NOHCl) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine 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 311.89 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

Physical & Chemical Properties

Molecular FormulaC18H29NO HCl
Molecular Weight311.89 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 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.)1990
Halogen ContentCl-containing
Nitrogen Atoms1

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