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HS Code |
968966 |
| Cas Number | 359-13-7 |
| Molecular Formula | C2H4F2O |
| Molecular Weight | 82.05 g/mol |
| Iupac Name | 2,2-Difluoroethanol |
| Appearance | Colorless liquid |
| Boiling Point | 93-94 °C |
| Melting Point | -70 °C |
| Density | 1.247 g/cm3 at 25 °C |
| Solubility In Water | Miscible |
| Refractive Index | 1.324 |
| Flash Point | 22 °C |
| Vapor Pressure | 45.9 mmHg at 25 °C |
As an accredited 2,2-Difluoroethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,2-Difluoroethanol is supplied in a 100 mL amber glass bottle with a secure screw cap, featuring safety and hazard labels. |
| Shipping | 2,2-Difluoroethanol should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be labeled as a hazardous material and transported according to relevant regulations (e.g., DOT, IATA). Store and ship at room temperature, ensuring proper ventilation and spill containment measures are in place during transit. |
| Storage | 2,2-Difluoroethanol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat, sparks, open flames, and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Store in a corrosion-resistant container with a resistant inner liner. Ensure proper labeling and follow all regulatory and safety guidelines for flammable and toxic chemicals. |
Applications of 2,2-Difluoroethanol in Industrial Manufacturing2,2-Difluoroethanol plays a significant role as a process intermediate in specialty chemical production. Its chemical properties enable high-value transformative reactions across select industrial sectors. Below, we detail key downstream applications, regulatory requirements, usage ratios, process steps, and resulting end products. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical manufacturers use 2,2-difluoroethanol to introduce fluoroethyl groups during targeted API synthesis, including antivirals and CNS agents. Its selective reactivity allows precise alkylation under controlled conditions, followed by downstream purification and validation. Dedicated synthesis lines monitor the introduction of the functional group for compliance and product traceability. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Compound ManufacturingAgrochemical producers leverage 2,2-difluoroethanol as a key alkylating agent to synthesize fluoro-containing herbicides and fungicides. Its inclusion into bioactive scaffolds enhances environmental persistence and target specificity. Production environments require closed system handling and verified residue control. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Monomer Production for FluoropolymersChemical manufacturers incorporate 2,2-difluoroethanol as a unique monomer precursor to design custom fluorinated polymers and copolymers. Its dual fluorine groups introduce controlled polarity and hydrophobicity, benefitting polymer performance in demanding chemical environments. Automated feeding ensures consistent polymer architecture during scale-up. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Intermediate for Anti-Corrosion AgentsProducers of fine chemicals use 2,2-difluoroethanol as a precursor to synthesize fluorinated anti-corrosion additives employed in industrial lubricants and protective fluids. The presence of two fluorine atoms imparts high chemical stability and resistance to oxidative breakdown, enhancing the durability of formulated fluids under harsh conditions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Solvent Component in Analytical Reagent FormulationProducers of certified chemical reagents and analytical standards use 2,2-difluoroethanol as a specialty polar protic solvent or as a derivatization agent. The solvent provides unique partitioning properties for GC-MS and NMR sample preparations, delivering reliable solubility and minimal background interference necessary for high-purity analysis. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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