tert-Butyl 6-methyl-2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate CAS 2385503-17-1

Purity 97%+In StockPharmaceutical Standards
CAS No.2385503-17-1
Molecular FormulaC18H24N2O3
Molecular Weight316.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 6-methyl-2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate CAS 2385503-17-1 chemical structure

Description

tert-Butyl 6-methyl-2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate (C18H24N2O3) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

tert-Butyl 6-methyl-2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate (CAS 2385503-17-1) is a high-purity analytical reference standard with the molecular formula C18H24N2O3 and a molecular weight of 316.39 g/mol.

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.

As a certified reference material (CRM), tert-Butyl 6-methyl-2-oxospiro[indoline-3,4'-piperidine]-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.

Physical & Chemical Properties

Molecular FormulaC18H24N2O3
Molecular Weight316.39 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999
Nitrogen Atoms2

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