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HS Code |
213925 |
| Chemicalname | 8-Acetyl Dimethoxycoumarin |
| Casnumber | 26218-34-8 |
| Molecularformula | C13H12O5 |
| Molecularweight | 248.23 |
| Appearance | White to off-white solid |
| Meltingpoint | 188-191°C |
| Solubility | Soluble in DMSO, methanol |
| Purity | Typically ≥98% |
| Storagetemperature | 2-8°C |
| Smiles | COC1=CC(=O)OC2=C1C=C(C(=O)C)C=C2OC |
| Synonyms | 8-Acetyl-6,7-dimethoxycoumarin |
As an accredited 8-Acetyl Dimethoxycoumarin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25g of 8-Acetyl Dimethoxycoumarin; tightly sealed, clearly labeled with hazard warnings and chemical details. |
| Shipping | 8-Acetyl Dimethoxycoumarin is shipped in tightly sealed containers, protected from light and moisture. The packaging complies with chemical safety standards, ensuring secure transit. All shipments include appropriate labeling, documentation, and safety data sheets. Handling requires gloves and eye protection; the chemical is not shipped with food or consumables to avoid contamination. |
| Storage | 8-Acetyl Dimethoxycoumarin should be stored in a tightly sealed container, protected from light and moisture, at room temperature or as specified by the supplier. It should be kept in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances. Always follow safety protocols and local regulations for chemical storage. |
Applications of 8-Acetyl Dimethoxycoumarin in Industrial ManufacturingAs a producer specializing in coumarin derivatives, we focus on supplying 8-Acetyl Dimethoxycoumarin for select industrial sectors that rely on its unique molecular characteristics. Below are the principal application segments where this intermediate integrates into advanced manufacturing processes. Each section is based on direct market adoption and practical production experience. 1. Pharmaceutical Intermediate Synthesis for Anticoagulant Drug APIs8-Acetyl Dimethoxycoumarin acts as a critical intermediate in the synthesis of select coumarin-based anticoagulant active pharmaceutical ingredients (APIs), such as acenocoumarol and derivatives. Manufacturers incorporate it during the core condensation and acylation steps, where its distinct acetyl and methoxy substituents improve control over regioselective reactions. Maintaining consistency in the purity and isomer profile helps downstream pharmaceutical partners meet stringent validation and regulatory requirements for their drug API formulations. Industry compliance standards
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2. UV-Absorbing Additive for High-Performance Coatings and Industrial PaintsFormulators select this coumarin derivative as a light-stabilizing UV absorber in coatings targeting industrial surfaces, exterior automotive parts, and specialty wood finishes. The compound’s methoxy functionality enhances its UV absorption range and compatibility with both solvent- and water-based resin systems. Its integration helps manufacturers improve film durability and fade resistance, especially in clear coats and high-gloss protective layers where photodegradation must be minimized. Industry compliance standards
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3. Fluorescent Marker for Chemical and Biological Analytical ReagentsThis raw material frequently serves as a fluorescent tag or marker in the preparation of liquid chromatography reagents, protein assays, and environmental detection kits. Its rigid coumarin backbone, further substituted with acetyl and methoxy groups, provides sharp emission spectra, making it suitable for analytical protocols requiring high signal-to-noise ratios. Chemical reagent manufacturers prefer its stability under standard storage and its compatibility with established analytical dye synthesis workflows. Industry compliance standards
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4. Synthetic Building Block for Advanced Organic Electronics R&DMaterials science labs and specialty polymer developers incorporate this compound as a modular building unit during the synthesis of conjugated small molecules and advanced polymeric matrices for organic electronics. The molecule’s extended aromatic core, with functional acetyl and methoxy side chains, allows chemists to modify photophysical properties and improve charge transport in experimental organic semiconductors. Tight quality control on the batch spectrum profile supports reproducible optoelectronic device fabrication at pre-scale and pilot-line stages. Industry compliance standards
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