|
HS Code |
243358 |
| Cas Number | 2296-83-7 |
| Molecular Formula | C8H8F2O2 |
| Molecular Weight | 174.15 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 94-96°C at 15 mmHg |
| Density | 1.204 g/cm³ |
| Refractive Index | 1.513 (at 20°C) |
| Solubility In Water | Insoluble |
| Flash Point | 110°C |
| Smiles | COC1=CC(F)=C(F)C=C1OC |
| Inchi | InChI=1S/C8H8F2O2/c1-11-7-3-6(9)4-8(10)5-7-12-2/h3-5H,1-2H3 |
As an accredited 1,4-Difluoro-2,5-Dimethoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed with a PTFE-lined cap, white printed hazard label, and CAS number for identification. |
| Shipping | **Shipping Description:** 1,4-Difluoro-2,5-Dimethoxybenzene should be shipped in tightly sealed chemical containers, protected from moisture, heat, and direct sunlight. The package must be clearly labeled, handled as a laboratory chemical, and transported according to relevant national and international regulations for hazardous materials. Ensure appropriate documentation accompanies the shipment. |
| Storage | **Storage for 1,4-Difluoro-2,5-Dimethoxybenzene:** Store in a tightly closed container, in a cool, dry, well-ventilated area away from direct sunlight, heat, and incompatible substances such as strong oxidizers. Keep away from sources of ignition. Avoid moisture exposure. Label the container clearly and ensure appropriate safety measures (gloves, goggles) are available for handling. Store under recommended chemical storage protocols. |
Applications of 1,4-Difluoro-2,5-Dimethoxybenzene in Industrial Manufacturing1,4-Difluoro-2,5-Dimethoxybenzene serves as a key intermediate in several specialized chemical manufacturing processes. Our experience as an integrated production site ensures precise quality management and full traceability from upstream synthesis to shipment. Below, we detail real downstream industrial applications, including sector-specific standards, practical formulation ranges, relevant process stages, and typical end products. 1. Advanced Lithium-Ion Battery Electrolyte AdditivesProducers of high-performance lithium-ion batteries utilize this compound to modify electrolyte compositions for enhanced cycle life, stability, and safety. Using controlled dosing, formulation chemists integrate it during the wet mixing phase, optimizing electrochemical properties in both consumer electronics and automotive-grade batteries. This compound’s stability under electrochemical stress meets the requirements of next-generation battery cells. Industry compliance standards
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2. Pharmaceutical Intermediate for Active Compound SynthesisThe molecule functions as a critical intermediate in synthesizing certain fluorinated API precursors and research drugs, especially in the neuropharmaceutical and oncology fields. Process chemists introduce it during multi-step organic synthesis, controlling reaction kinetics and purity through established GMP protocols. The structural motif contributes to specific receptor affinities and metabolic profiles in the final active compounds. Industry compliance standards
Typical usage ratio
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3. Organic Electronic Material Synthesis (OLED & OPV)Researchers and manufacturing chemists in organic electronics use this benzene derivative as a core fragment for constructing electron-transport layers and host materials in OLED (organic light-emitting diode) and OPV (organic photovoltaic) devices. It is introduced at specific condensation or polymerization steps to modulate bandgap and film-forming characteristics, enhancing charge-carrier mobility and device longevity in display and solar panel applications. Industry compliance standards
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4. Agrochemical Intermediate for Advanced FungicidesAgrochemical formulators utilize this aromatic compound as a core intermediate to construct complex active ingredients for systemic fungicides. Its difluoro and methoxy substitution enable precision incorporation into target molecules, improving bioactivity and photostability. Integration occurs during key cross-coupling and chlorination steps under validated process controls to ensure compliance with pesticide regulations. Industry compliance standards
Typical usage ratio
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