Description

n-(Cyclopropylmethyl)Normorphine is a specialized opioid derivative and a key synthetic intermediate in advanced pharmaceutical research. This compound is of significant interest for its role in the development and study of novel analgesic agents and receptor modulators. It is primarily utilized by research institutions and pharmaceutical companies engaged in neuropharmacology, medicinal chemistry, and the synthesis of controlled substances for therapeutic evaluation.

Application

• Pharmaceutical Intermediate: A critical precursor in the synthesis of novel opioid analgesics and receptor-targeting compounds.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies to explore modifications of the morphine scaffold for enhanced efficacy or reduced side effects.
• Neuropharmacology Studies: Serves as a reference standard or tool compound in investigations of opioid receptor binding and signal transduction pathways.
• Analytical Reference Standard: Employed in analytical laboratories for method development, validation, and quality control testing of related substances.
• Controlled Substance Synthesis: Used under appropriate regulatory licenses for the legal production of scheduled pharmaceutical agents for clinical research.

Basic Information

Product Name	n-(Cyclopropylmethyl)Normorphine
CAS No.	1976-45-0
Molecular Formula	C20H25NO3
Molecular Weight	327.42 g/mol
Synonyms	N-Cyclopropylmethylnormorphine; 17-Methyl-7,8-didehydro-4,5α-epoxymorphinan-3,6α-diol, N-(cyclopropylmethyl)nor-; Normorphine, N-(cyclopropylmethyl)-; N-CPM-Normorphine; Cyclopropylmethylnormorphine; N-(Cyclopropylmethyl)norcodeinone (related precursor); N-CPM-NM
EINECS	Contact for details

Quality Control

Our n-(Cyclopropylmethyl)Normorphine is produced under strict quality management systems to ensure batch-to-batch consistency and high purity, suitable for research applications. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles as determined by advanced chromatographic and spectroscopic methods. We adhere to cGMP principles where applicable for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). The product is light-sensitive and should be handled accordingly to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH guidelines
Water Content (KF)	≤ 0.5%

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