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HS Code |
547134 |
| Cas Number | 20721-46-2 |
| Molecular Formula | C11H12O3 |
| Molecular Weight | 192.21 g/mol |
| Iupac Name | 5,6-dimethoxy-2,3-dihydro-1H-inden-1-one |
| Appearance | White to off-white solid |
| Melting Point | 95-97°C |
| Boiling Point | Unknown |
| Solubility | Soluble in organic solvents such as ethanol and dichloromethane |
| Density | Unknown |
| Smiles | COc1cc2c(cc1OC)C(=O)CC2 |
| Inchi | InChI=1S/C11H12O3/c1-13-8-3-7-4-5-11(12)10(7)9(8)14-2/h3-4H,5-6H2,1-2H3 |
| Ec Number | 244-094-8 |
As an accredited 5,6-Dimethoxy-1-Indanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g quantity of 5,6-Dimethoxy-1-Indanone is packaged in a tightly sealed, amber glass bottle with clear hazard labeling. |
| Shipping | 5,6-Dimethoxy-1-Indanone is typically shipped in tightly sealed containers to protect it from moisture and light. It should be handled and transported in accordance with standard chemical safety protocols, including labeling and documentation. Shipping must comply with local and international regulations for non-hazardous laboratory chemicals. Store in a cool, dry place upon arrival. |
| Storage | 5,6-Dimethoxy-1-Indanone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Protect from moisture and incompatible substances such as strong oxidizers. Store at recommended room temperature, and always follow standard laboratory safety protocols when handling or storing this compound. |
Applications of 5,6-Dimethoxy-1-Indanone in Industrial Manufacturing5,6-Dimethoxy-1-Indanone functions as a key intermediate for multiple specialized sectors requiring rigorous quality, traceability, and reliable supply chain integration. Below we outline verified downstream applications, together with compliance, dosing, process stage, and end product details relevant to each manufacturing field. 1. Pharmaceutical Active Ingredient SynthesisPharmaceutical companies employ 5,6-Dimethoxy-1-Indanone as a core building block in the synthesis of complex indanone derivatives for anti-inflammatory and neuroprotective drug discovery. Its role is central in the formation of specific cyclic ketone scaffolds through substituted indanone condensation reactions. In R&D and commercial-scale GMP processes, precise stoichiometry and reaction control are required to ensure drug substance purity and batch-to-batch repeatability. This raw material is utilized for the preparation of small molecule drugs subjected to strict regulatory auditing. Industry compliance standards
Typical usage ratio
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2. Agrochemical Intermediate ManufacturingLeading agrochemical firms integrate 5,6-Dimethoxy-1-Indanone into synthesis pathways for pyridyl and indanone-based herbicide and pesticide actives. These structurally unique compounds target weed and pest resistance in crops. Manufacturers rely on this material for key condensation reactions enabling scalable production under rigorous quality and environmental controls. Trace level impurities must be managed due to their direct impact on final agrochemical efficacy and regulatory registration acceptance. Industry compliance standards
Typical usage ratio
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3. Fine Chemical Synthesis for Dye and Pigment BasesThe dye and pigment sector uses 5,6-Dimethoxy-1-Indanone as a precursor in the synthesis of advanced aromatic systems. These targeted syntheses produce colorants employed in specialty inks and high-stability coatings, where colorfastness and batch uniformity are critical. This intermediate participates in Friedel-Crafts acylation and cyclization schemes to introduce methoxy substituents that enhance pigment stability under UV exposure and in harsh process environments. Industry compliance standards
Typical usage ratio
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4. Fragrance and Aromatic Chemicals ManufactureFragrance compound producers use 5,6-Dimethoxy-1-Indanone as a core intermediate for synthesizing aromatic ketones and indanone derivatives found in fine fragrances, cosmetic aromas, and household scents. The methoxy-substituted structure enables downstream reactions yielding musky and woody base notes with high odor stability. Manufacturing lines must meet IFRA and REACH criteria for traceability and composition safety, and production teams control input ratios according to olfactory target profiles and consumer product safety data. Industry compliance standards
Typical usage ratio
Downstream process integration
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