N-(5-(4-Aminophenoxy)pentyl)-2,2,2-trichloroacetamide CAS 106165-47-3

Purity 97%+In StockPharmaceutical Standards
CAS No.106165-47-3
Molecular FormulaC13H17Cl3N2O2
Molecular Weight339.65 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(5-(4-Aminophenoxy)pentyl)-2,2,2-trichloroacetamide CAS 106165-47-3 chemical structure

Description

CATO manufactures N-(5-(4-Aminophenoxy)pentyl)-2,2,2-trichloroacetamide 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 N-(5-(4-Aminophenoxy)pentyl)-2,2,2-trichloroacetamide (CAS 106165-47-3), a certified reference material (molecular formula C13H17Cl3N2O2, MW 339.65 g/mol) for analytical method development and quality control.

The molecular framework of N-(5-(4-Aminophenoxy)pentyl)-2,2,2-trichloroacetamide (C13H17Cl3N2O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC13H17Cl3N2O2
Molecular Weight339.65 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms2

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