tert-butyl 4-(cyclobutoxy)-4-(iodomethyl)piperidine-1-carboxylate CAS 1698154-00-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1698154-00-5
Molecular FormulaC15H26INO3
Molecular Weight395.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-butyl 4-(cyclobutoxy)-4-(iodomethyl)piperidine-1-carboxylate CAS 1698154-00-5 chemical structure

Description

tert-butyl 4-(cyclobutoxy)-4-(iodomethyl)piperidine-1-carboxylate (CAS 1698154-00-5) is a high-purity analytical reference standard with the molecular formula C15H26INO3 and a molecular weight of 395.28 g/mol.

Owing to an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, tert-butyl 4-(cyclobutoxy)-4-(iodomethyl)piperidine-1-carboxylate is typically white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 395.28 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

As a certified reference material (CRM), tert-butyl 4-(cyclobutoxy)-4-(iodomethyl)piperidine-1-carboxylate 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 FormulaC15H26INO3
Molecular Weight395.28 g/mol
AppearanceWhite to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1994
Halogen ContentI-containing
Nitrogen Atoms1

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