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Isofumigaclavineb CAS NO 58800-20-7


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CAS No.:58800-20-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Isofumigaclavineb CAS NO 58800-20-7 is a specialized ergot alkaloid derivative of significant interest in advanced research and development. This compound serves as a crucial intermediate and reference standard for the synthesis and study of complex bioactive molecules. It is primarily utilized by the pharmaceutical and biotechnology sectors for its potential in neurological and receptor-targeting applications. Our supply ensures high purity and batch-to-batch consistency for critical R&D and manufacturing processes.

Application

  • Pharmaceutical Research: Acts as a key intermediate in the synthesis of novel ergot-based therapeutics and reference compounds for pharmacological studies.
  • Neurological Studies: Used as a research tool to investigate interactions with serotonin and dopamine receptor systems.
  • Biochemical Reference Standard: Serves as a high-purity analytical standard for method development and quality control in laboratories.
  • Academic Research: Employed in university and institutional labs for studying the biosynthesis and chemical properties of clavine alkaloids.
  • Process Development: Utilized in scaling up synthetic routes for complex alkaloid derivatives in pilot and commercial manufacturing.

Basic Information

Product Name Isofumigaclavineb
CAS No. 58800-20-7
Molecular Formula C₁₆H₁₈N₂O
Molecular Weight 254.33 g/mol
Synonyms Isofumigaclavine B; (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-Octahydro-7-methylindolo[4,3-fg]quinoline-9-carboxaldehyde; 9-Formyl-6-methyl-8,9-didehydroergoline; 9-Formyl-6-methylergoline-8-ene; 9-Formyl-6-methyl-δ⁸,⁹-ergolene
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Quality Control

Our Isofumigaclavineb is manufactured under strict quality management systems to ensure the highest standards of purity and identity. Each batch is subjected to comprehensive analytical testing, including HPLC for purity determination, IR and NMR for structural confirmation, and residual solvent analysis. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting all critical quality attributes. We adhere to cGMP principles for active pharmaceutical ingredients (APIs) and fine chemicals.

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 under inert atmosphere or in a desiccator after opening to prevent degradation. Keep away from incompatible materials.

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%
Loss on Drying ≤ 0.5%
Residual Solvents (GC) Complies with ICH Q3C guidelines

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

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Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.