Description

(-)-Profenamine CAS NO 115017-00-0 is a high-purity, single-enantiomer chiral compound belonging to the profenamine class. This specific stereoisomer is of significant value in advanced pharmaceutical research and development, particularly for its potential role as a key intermediate or active pharmaceutical ingredient (API). It is primarily sought after by research institutions and pharmaceutical companies engaged in the synthesis of novel therapeutic agents, where stereochemical purity is critical for biological activity and regulatory approval.

Application

• Pharmaceutical Intermediate: Serves as a critical chiral building block in the synthesis of novel drug candidates, especially in central nervous system (CNS) and anti-inflammatory research.
• Active Pharmaceutical Ingredient (API) Development: Used in preclinical and clinical research for developing enantiomerically pure pharmaceuticals.
• Biochemical Research: Employed as a standard or reagent in studies investigating receptor-ligand interactions and enzymatic processes where stereoselectivity is a factor.
• Asymmetric Synthesis Catalyst: May be utilized in the development or study of chiral catalysts and auxiliaries for stereocontrolled chemical transformations.
• Reference Standard: Acts as a high-purity analytical standard for quality control and method development in pharmaceutical analysis.

Basic Information

Product Name	(-)-Profenamine
CAS No.	115017-00-0
Molecular Formula	C19H24N2O
Molecular Weight	296.41 g/mol
Synonyms	(R)-(-)-N,N-Diethyl-1-phenyl-2-aminopropane; (R)-(-)-Deprenyl impurity C; (R)-N,N-Diethyl-α-methylbenzeneethanamine; (R)-(-)-Profenamine; Levopropylhexedrine (related); (2R)-N,N-Diethyl-1-phenylpropan-2-amine; (-)-1-Phenyl-2-diethylaminopropane
EINECS	Contact for details

Quality Control

Our (-)-Profenamine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including chiral purity assessment by HPLC, to ensure it meets the high standards required for pharmaceutical research. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming identity, purity, and enantiomeric excess. We adhere to cGMP guidelines for the production of advanced pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive); ensure the container is sealed tightly after each use to minimize exposure to atmospheric humidity. For long-term storage, consider using desiccants.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Enantiomeric Purity (Chiral HPLC)	≥ 99.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.