Description

6-Propyl-8-Ergolinylacetamide is a high-purity synthetic ergoline derivative, a key intermediate in advanced pharmaceutical research and development. This compound is valued for its precise molecular structure, which is critical for producing active pharmaceutical ingredients (APIs) with specific neurological and receptor-targeting activities. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of novel therapeutic agents, particularly within the central nervous system (CNS) and endocrine therapy domains. Consistent quality and reliable supply are paramount for ensuring the integrity of downstream R&D and production processes.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of novel ergot alkaloid-based APIs.
• Neurological Research: Used in preclinical studies targeting dopamine, serotonin, and other neurotransmitter receptors.
• Endocrine Therapy Development: Applied in research for developing treatments related to prolactin inhibition and other hormonal pathways.
• Reference Standard: Functions as an analytical standard for quality control and method validation in pharmaceutical laboratories.
• Chemical Synthesis: Employed in organic synthesis for creating more complex ergoline structures with tailored biological activities.
• Biochemical Assays: Utilized as a ligand or probe in receptor binding studies and high-throughput screening (HTS) platforms.

Basic Information

Product Name	6-Propyl-8-Ergolinylacetamide
CAS No.	67658-45-1
Molecular Formula	C19H25N3O
Molecular Weight	311.42 g/mol
Synonyms	6-Propyl-8-ergolineacetamide; 8β-[(Aminocarbonyl)methyl]-6-propylergoline; 6-n-Propyl-8-ergolinylacetamide; Cabergoline Impurity; Cabergoline Related Compound A; (8β)-6-Propylergoline-8-acetamide; Pergolide Related Compound
EINECS	Contact for details

Quality Control

Our 6-Propyl-8-Ergolinylacetamide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, IR and NMR for structural confirmation, and residual solvent analysis, to ensure it meets stringent specifications for research and pharmaceutical use. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance with your quality requirements.

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) and must be kept in a desiccated environment to maintain stability and purity. Avoid prolonged exposure to air during handling.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Maximum Impurity	≤ 0.5%
Loss on Drying	≤ 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.