N-(3-Isopropoxybenzyl)-1-hexadecanamine CAS 1040688-12-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1040688-12-7
Molecular FormulaC26H47NO
Molecular Weight389.66 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Isopropoxybenzyl)-1-hexadecanamine CAS 1040688-12-7 chemical structure

Description

The occurrence of N-(3-Isopropoxybenzyl)-1-hexadecanamine is closely related to a steroid core, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

N-(3-Isopropoxybenzyl)-1-hexadecanamine (CAS 1040688-12-7) is a high-purity analytical reference standard with the molecular formula C26H47NO and a molecular weight of 389.66 g/mol.

Structurally, N-(3-Isopropoxybenzyl)-1-hexadecanamine (C26H47NO) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. 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 389.66 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.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC26H47NO
Molecular Weight389.66 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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