2-Methyl-5-(prop-1-en-2-yl)-3-(pyrrolidin-1-yl)cyclohexanone CAS 88718-04-1

Purity 97%+In StockPharmaceutical Standards
CAS No.88718-04-1
Molecular FormulaC14H23NO
Molecular Weight221.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Methyl-5-(prop-1-en-2-yl)-3-(pyrrolidin-1-yl)cyclohexanone CAS 88718-04-1 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-Methyl-5-(prop-1-en-2-yl)-3-(pyrrolidin-1-yl)cyclohexanone.

2-Methyl-5-(prop-1-en-2-yl)-3-(pyrrolidin-1-yl)cyclohexanone (CAS 88718-04-1) is a high-purity analytical reference standard with the molecular formula C14H23NO and a molecular weight of 221.34 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 2-Methyl-5-(prop-1-en-2-yl)-3-(pyrrolidin-1-yl)cyclohexanone is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 221.34 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

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 FormulaC14H23NO
Molecular Weight221.34 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Nitrogen Atoms1

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