Tert-butyl 3-(aminomethyl)-1H-indole-1-carboxylate hydrochloride CAS 1401425-95-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1401425-95-3
Molecular FormulaC14H18N2O2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl 3-(aminomethyl)-1H-indole-1-carboxylate hydrochloride CAS 1401425-95-3 chemical structure

Description

The molecular framework of Tert-butyl 3-(aminomethyl)-1H-indole-1-carboxylate hydrochloride (C14H18N2O2HCl) 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.

Tert-butyl 3-(aminomethyl)-1H-indole-1-carboxylate hydrochloride (CAS 1401425-95-3) is a high-purity analytical reference standard with the molecular formula C14H18N2O2HCl and a molecular weight of 282.77 g/mol.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), Tert-butyl 3-(aminomethyl)-1H-indole-1-carboxylate hydrochloride 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 FormulaC14H18N2O2 HCl
Molecular Weight282.77 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms2

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