Tert-butyl 7a-phenyloctahydro-5H-pyrrolo[3,4-c]pyridine-5-carboxylate CAS 1251007-41-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1251007-41-6
Molecular FormulaC18H26N2O2
Molecular Weight302.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl 7a-phenyloctahydro-5H-pyrrolo[3,4-c]pyridine-5-carboxylate CAS 1251007-41-6 chemical structure

Description

Tert-butyl 7a-phenyloctahydro-5H-pyrrolo[3,4-c]pyridine-5-carboxylate (CAS 1251007-41-6), molecular formula C18H26N2O2 and molecular weight 302.41 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of Tert-butyl 7a-phenyloctahydro-5H-pyrrolo[3,4-c]pyridine-5-carboxylate (C18H26N2O2) 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 its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC18H26N2O2
Molecular Weight302.41 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 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms2

Recommended Standards

Why CATO?