3-(4-Bromo-1H-indol-3-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid CAS 691885-26-4

Purity 97%+In StockPharmaceutical Standards
CAS No.691885-26-4
Molecular FormulaC16H19BrN2O4
Molecular Weight383.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Bromo-1H-indol-3-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid CAS 691885-26-4 chemical structure

Description

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

3-(4-Bromo-1H-indol-3-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid (CAS 691885-26-4), molecular formula C16H19BrN2O4 and molecular weight 383.24 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 3-(4-Bromo-1H-indol-3-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid (C16H19BrN2O4) is characterized by a flavonoid core, an amide group, a hydroxyl group, an ether linkage, bromine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures 3-(4-Bromo-1H-indol-3-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid 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 FormulaC16H19BrN2O4
Molecular Weight383.24 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentBr-containing
Nitrogen Atoms2

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