2-(6-Iodobenzofuran-3-yl)propan-1-amine hydrochloride CAS 1363404-89-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1363404-89-0
Molecular FormulaC11H12INO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(6-Iodobenzofuran-3-yl)propan-1-amine hydrochloride CAS 1363404-89-0 chemical structure

Description

CATO manufactures 2-(6-Iodobenzofuran-3-yl)propan-1-amine hydrochloride 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.

2-(6-Iodobenzofuran-3-yl)propan-1-amine hydrochloride (CAS 1363404-89-0), molecular formula C11H12INOHCl and molecular weight 337.58 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 2-(6-Iodobenzofuran-3-yl)propan-1-amine hydrochloride (C11H12INOHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine/iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 337.58 g/mol, it falls into the moderately-high-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC11H12INO HCl
Molecular Weight337.58 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl/I-containing
Nitrogen Atoms1

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