Description

9-Oxaergoline, 6-Propyl-, Monohydrochloride is a high-purity, synthetic ergoline derivative, a class of compounds known for their significant biological activity. This monohydrochloride salt form offers enhanced stability and solubility for advanced research and development applications. It is a critical intermediate and reference standard for pharmaceutical research, particularly in the development of central nervous system (CNS) agents and other specialized therapeutics. Global suppliers and R&D institutions rely on this compound for its consistent quality in process development and analytical studies.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel ergoline-based active pharmaceutical ingredients (APIs).
• Neurological Research: Used as a reference standard and tool compound in studies targeting serotonin and dopamine receptor pathways.
• Process Development & Scale-up: Serves as a critical material for optimizing synthetic routes and manufacturing processes in a GMP environment.
• Analytical Standard: Employed in HPLC, LC-MS, and NMR for method development, validation, and quality control of related substances.
• Preclinical Studies: Utilized in pharmacological and toxicological evaluations during early-stage drug discovery.
• Chemical Reference Material: Provides a certified standard for identity and purity confirmation in regulatory filings and quality assurance laboratories.

Basic Information

Product Name	9-Oxaergoline, 6-Propyl-, Monohydrochloride
CAS No.	85351-27-5
Molecular Formula	C16H20N2O•HCl
Molecular Weight	292.80 g/mol
Synonyms	6-Propyl-9-oxaergoline Hydrochloride; 6-n-Propyl-9-oxaergoline HCl; 9-Oxa-6-propylergoline Hydrochloride; Cabergoline Impurity; Cabergoline Related Compound; (8β)-6-Propyl-9-oxaergoline Monohydrochloride; Pergolide Related Compound; Ergoline-9-one, 6-propyl-, hydrochloride
EINECS	Contact for details

Quality Control

Our 9-Oxaergoline, 6-Propyl-, Monohydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR spectroscopy, and stringent control of residual solvents and related substances. We provide full traceability and Certificates of Analysis (COA) are available for every shipment, ensuring compliance with the rigorous standards required for pharmaceutical development and research applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under inert conditions or in a desiccator after opening to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white 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%
Single Maximum Unknown Impurity	≤0.5%
Water Content (KF)	≤1.0%
Residue on Ignition	≤0.1%

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