Description

Lysergol is a naturally occurring ergoline alkaloid and a key intermediate in the synthesis of more complex ergot derivatives. Its unique tetracyclic ring structure makes it a valuable precursor for pharmaceutical research and development. This high-purity compound is essential for manufacturers and research institutions focused on developing new therapeutic agents and studying neurological pathways.

Application

• Pharmaceutical Intermediate: A critical building block for the synthesis of various ergot-based pharmaceuticals and novel drug candidates.
• Research & Development: Used in biochemical and pharmacological research to study receptor interactions and neurological mechanisms.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in laboratories.
• Chemical Synthesis: Employed in organic synthesis to construct complex molecular architectures containing the ergoline scaffold.
• Biocatalyst Studies: Investigated in enzymatic transformation studies due to its specific alkaloid structure.

Basic Information

Product Name	Lysergol
CAS No.	602-85-7
Molecular Formula	C16H18N2O
Molecular Weight	254.33 g/mol
Synonyms	9,10-Didehydro-6-methyl-8β-ergoline-8-methanol; D-Lysergol; Lysergol, D-; (8β)-9,10-Didehydro-6-methylergoline-8-methanol; Lysergol base; NSC 17693; Lysergol (D-); 8β-Hydroxymethyl-6-methyl-9,10-didehydroergoline
EINECS	210-034-8

Quality Control

Our Lysergol CAS NO 602-85-7 is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure it meets the stringent requirements for research and synthesis. A Certificate of Analysis (COA) detailing all test results is provided with every shipment.

Storage

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

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.