n-Isopropyl-3,5-dimethoxyaniline CAS 108103-33-9

Purity 97%+In StockPharmaceutical Standards
CAS No.108103-33-9
Molecular FormulaC11H17NO2
Molecular Weight195.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-Isopropyl-3,5-dimethoxyaniline CAS 108103-33-9 chemical structure

Description

The occurrence of n-Isopropyl-3,5-dimethoxyaniline is closely related to an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

n-Isopropyl-3,5-dimethoxyaniline (CAS 108103-33-9) is a high-purity analytical reference standard with the molecular formula C11H17NO2 and a molecular weight of 195.26 g/mol.

Owing to an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage, n-Isopropyl-3,5-dimethoxyaniline is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 195.26 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures n-Isopropyl-3,5-dimethoxyaniline 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.

Physical & Chemical Properties

Molecular FormulaC11H17NO2
Molecular Weight195.26 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
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.)1987
Nitrogen Atoms1

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