Description

5,6,8,14-Tetradehydro-3,6-Dimethoxy-17-Methylmorphinan is a high-purity synthetic organic compound belonging to the morphinan class of alkaloids. This compound serves as a critical advanced pharmaceutical intermediate and a valuable reference standard in analytical chemistry. It is primarily required by research institutions, pharmaceutical R&D laboratories, and fine chemical manufacturers engaged in the development of specialized active pharmaceutical ingredients (APIs) and analytical methods.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of complex alkaloid-based active pharmaceutical ingredients (APIs).
• Reference Standard: Used as a certified reference material (CRM) for analytical method development, validation, and quality control in pharmaceutical testing.
• Chemical Research: Serves as a precursor or model compound in organic synthesis and medicinal chemistry research for studying structure-activity relationships (SAR).
• Analytical Applications: Employed in high-performance liquid chromatography (HPLC), gas chromatography (GC), and mass spectrometry (MS) as a calibration or identification standard.
• Academic Studies: Utilized in university and institutional research focused on alkaloid chemistry, pharmacology, and synthetic pathways.

Basic Information

Product Name	5,6,8,14-Tetradehydro-3,6-Dimethoxy-17-Methylmorphinan
CAS No.	1092-95-1
Molecular Formula	C19H23NO2
Molecular Weight	297.39 g/mol
Synonyms	3,6-Dimethoxy-17-methyl-5,6,8,14-tetradehydromorphinan; 17-Methyl-3,6-dimethoxy-5,6,8,14-tetradehydromorphinan; Thevinone; Thevinon; Thevinone (VAN); 5,6,8,14-Tetradehydro-3,6-dimethoxy-N-methylmorphinan; 3,6-Dimethoxy-N-methyl-5,6,8,14-tetradehydromorphinan
EINECS	Contact for details

Quality Control

Our 5,6,8,14-Tetradehydro-3,6-Dimethoxy-17-Methylmorphinan is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide a detailed Certificate of Analysis (COA) with each shipment, which includes data from HPLC, GC, NMR, and other relevant spectroscopic methods. Our quality commitment aligns with cGMP principles where applicable for pharmaceutical-grade material.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep the container sealed to protect the product from moisture and atmospheric contamination.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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