2-(3-(tert-Butyl)-5-methylphenyl)-4-methylpyrrolidine CAS 603068-87-7

Purity 97%+In StockPharmaceutical Standards
CAS No.603068-87-7
Molecular FormulaC16H25N
Molecular Weight231.38 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3-(tert-Butyl)-5-methylphenyl)-4-methylpyrrolidine CAS 603068-87-7 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 2-(3-(tert-Butyl)-5-methylphenyl)-4-methylpyrrolidine.

2-(3-(tert-Butyl)-5-methylphenyl)-4-methylpyrrolidine (CAS 603068-87-7), molecular formula C16H25N and molecular weight 231.38 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C16H25N, 2-(3-(tert-Butyl)-5-methylphenyl)-4-methylpyrrolidine contains a nitrogen-containing heterocyclic scaffold, a nitrile group; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 231.38 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

CATO manufactures 2-(3-(tert-Butyl)-5-methylphenyl)-4-methylpyrrolidine 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 FormulaC16H25N
Molecular Weight231.38 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Nitrogen Atoms1

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