tert-Butyl ((6-(indolin-1-yl)-2-methylpyridin-3-yl)methyl)carbamate CAS 1355236-31-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1355236-31-5
Molecular FormulaC20H25N3O2
Molecular Weight339.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl ((6-(indolin-1-yl)-2-methylpyridin-3-yl)methyl)carbamate CAS 1355236-31-5 chemical structure

Description

CATO supplies tert-Butyl ((6-(indolin-1-yl)-2-methylpyridin-3-yl)methyl)carbamate (CAS 1355236-31-5), a certified reference material (molecular formula C20H25N3O2, MW 339.43 g/mol) for analytical method development and quality control.

The molecular framework of tert-Butyl ((6-(indolin-1-yl)-2-methylpyridin-3-yl)methyl)carbamate (C20H25N3O2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage. 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).

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.

CATO manufactures tert-Butyl ((6-(indolin-1-yl)-2-methylpyridin-3-yl)methyl)carbamate 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 FormulaC20H25N3O2
Molecular Weight339.43 g/mol
AppearancePale yellow to yellow crystalline powder
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
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms3

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