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2,2-Difluoroethanol

    • Product Name 2,2-Difluoroethanol
    • Alias Difluoroethyl alcohol
    • Einecs 206-649-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 2,2-Difluoroethanol

    Applications of 2,2-Difluoroethanol in Industrial Manufacturing

    2,2-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 Synthesis

    Pharmaceutical 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

    • ICH Q7 GMP for APIs
    • USP/NF monographs for related drug substances
    • 21 CFR Parts 210/211 cGMP for finished pharmaceuticals
    • EMA Guidelines on Impurities: Guideline for Residual Solvents

    Typical usage ratio

    • 0.8–1.5 molar equivalents relative to target API moiety, adjusted according to alkylation efficiency and required conversion rate

    Downstream process integration

    • Introduced post-primary ring formation for fluoroalkylation
    • Reacted in anhydrous or aprotic solvents under catalytic control
    • Followed by in-process analytical monitoring using HPLC/GC-MS
    • Final product isolation via crystallization or chromatographic separation

    Final product types

    • Antiviral drug intermediates
    • Neuropharmaceutical actives with improved metabolic stability
    • Experimental oncology compounds featuring difluoroethyl modification
    • Fluorinated building blocks for drug discovery pipelines

    2. Agrochemical Active Compound Manufacturing

    Agrochemical 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

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems
    • OECD Guidelines for Testing of Chemicals: Residues in Crops
    • REACH Regulation (EC) No 1907/2006 for chemical registration

    Typical usage ratio

    • 5–15% by weight in combined reactant feed, optimized by active molecule structure and crop safety profile validation

    Downstream process integration

    • Charged during alkylation or fluorination stage following core structure assembly
    • Solvent-based reactions with continuous agitation
    • QC by GC-MS for residue verification
    • Neutralization and phase separation pre-formulation

    Final product types

    • Difluoroalkylated herbicides (e.g., for resistant weed strains)
    • Fungicides with controlled release profiles
    • Seed treatment actives with enhanced shelf life
    • Plant growth regulators incorporating fluorine motifs

    3. Specialty Monomer Production for Fluoropolymers

    Chemical 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

    • ASTM D3677 for polymer monomer purity analysis
    • ISO 14001:2015 Environmental Management Systems
    • EPA TSCA Inventory listing and reporting requirements
    • EU Regulation (EC) No 1272/2008 CLP classification

    Typical usage ratio

    • 2–10 mol% relative to total monomer blend; adjusted based on chain length target and required polymer properties

    Downstream process integration

    • Reactive feed in batch or continuous monomer polymerization lines
    • Initiator and catalyst addition post-charged
    • Molecular weight control via in-line concentration monitoring
    • Post-polymerization solvent stripping and pelletization

    Final product types

    • Fluorinated acrylic copolymers
    • Oil- and chemical-resistant films and coatings
    • Membrane-grade fluoropolymers for chemical processing industry
    • Surface treatment resins for electronics

    4. Fine Chemical Intermediate for Anti-Corrosion Agents

    Producers 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

    • ASTM D7548 Standard for Lubricant Additive Testing
    • ISO 21469:2006 for Hygiene Requirements in Manufacturing
    • SAE AMS 3150 for corrosion-inhibiting compounds
    • Directive 2011/65/EU (RoHS) for restricted substances

    Typical usage ratio

    • 0.5–3% by weight as intermediate in additive synthesis; altered according to targeted corrosion protection and solubility requirement in finished lubricant

    Downstream process integration

    • Condensation or etherification to introduce difluoroethyl group into additive backbone
    • Solvent phase reaction under controlled temperature and agitation
    • Post-synthesis blending with carrier oils and antifoam agents
    • Filtration and quality control prior to packaging

    Final product types

    • Engine oil additives for automotive and industrial machinery
    • Hydraulic fluid anti-corrosion packages
    • Industrial grease protectants
    • Rust-preventive coatings for metalworking fluids

    5. Solvent Component in Analytical Reagent Formulation

    Producers 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

    • ISO/IEC 17025:2017 Laboratory Competence
    • ACS Reagent Chemicals Specifications
    • Ph. Eur. Reagent Monograph Compliance
    • EPA Method 8270 for Semi-Volatile Organics by GC/MS

    Typical usage ratio

    • 1–20% v/v as solvent modifier or derivate; dilution varies depending on analyte and analytical procedure

    Downstream process integration

    • Added to reagent matrix during formulation of trace-analytical kits
    • Mixed directly with analytical standards to enhance solubility or reactivity
    • Used as derivatization reagent for GC or NMR sample preparation prior to instrumental analysis
    • Final blending and filtration before packaging for certified reference use

    Final product types

    • Certified analytical grade reagent kits
    • GC and LC sample preparation solutions
    • Calibration standards for instrument validation
    • Derivatization agents for complex organic analysis
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