Tert-butyl 3-(hydroxymethyl)-6-methoxy-1H-indole-1-carboxylate CAS 914349-08-9

Purity 97%+In StockPharmaceutical Standards
CAS No.914349-08-9
Molecular FormulaC15H19NO4
Molecular Weight277.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl 3-(hydroxymethyl)-6-methoxy-1H-indole-1-carboxylate CAS 914349-08-9 chemical structure

Description

As a certified reference material (CRM), Tert-butyl 3-(hydroxymethyl)-6-methoxy-1H-indole-1-carboxylate 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.

CATO supplies Tert-butyl 3-(hydroxymethyl)-6-methoxy-1H-indole-1-carboxylate (CAS 914349-08-9), a certified reference material (molecular formula C15H19NO4, MW 277.32 g/mol) for analytical method development and quality control.

Tert-butyl 3-(hydroxymethyl)-6-methoxy-1H-indole-1-carboxylate (C15H19NO4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 FormulaC15H19NO4
Molecular Weight277.32 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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