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2,2-Difluoroethylamine

    • Product Name 2,2-Difluoroethylamine
    • Alias DFEA
    • Einecs '700-150-9'
    • 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

    393923

    Chemicalname 2,2-Difluoroethylamine
    Casnumber 430-98-2
    Molecularformula C2H5F2N
    Molecularweight 81.06 g/mol
    Appearance Colorless liquid
    Boilingpoint 61-63 °C
    Density 1.099 g/mL at 25 °C
    Solubility Miscible with water
    Meltingpoint -80 °C
    Refractiveindex 1.349
    Flashpoint 6 °C
    Vaporpressure 171 mmHg at 25 °C

    As an accredited 2,2-Difluoroethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2,2-Difluoroethylamine, sealed with a red cap and labeled with hazard warnings.
    Shipping 2,2-Difluoroethylamine is shipped in tightly sealed containers, protected from moisture and incompatible substances. It should be transported under cool, well-ventilated conditions, clearly labeled as a hazardous chemical. All relevant safety and regulatory guidelines must be followed during shipping, including UN, DOT, and IATA regulations. Handle with appropriate personal protective equipment (PPE).
    Storage 2,2-Difluoroethylamine should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. It should be kept in tightly sealed containers, made of materials compatible with amines. Properly label the container and ensure it is stored at room temperature, protected from moisture and direct sunlight.
    Application of 2,2-Difluoroethylamine

    Applications of 2,2-Difluoroethylamine in Industrial Manufacturing

    Our 2,2-Difluoroethylamine (DFEA) is integral to advanced synthetic routes across multiple industrial sectors, powering the development of innovative fluorinated products. As a direct manufacturer specializing in high-purity sourcing and controlled batch processes, we support downstream partners with consistent material supply for reliable finished goods performance. All use examples below reflect authentic, validated applications in real-world production pipelines.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    DFEA is widely adopted by pharmaceutical manufacturers during the synthesis of fluorinated active pharmaceutical ingredients, where its unique difluorinated structure enables the creation of molecules with enhanced metabolic stability and bioavailability. It serves as a valuable alkylating agent or as a building block in Suzuki and other coupling reactions, especially when introducing selective difluoroethyl motifs crucial for next-generation CNS and antiviral agents.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Directive 2001/83/EC for medicinal products
    • USP-NF: United States Pharmacopeia, National Formulary monographs (for regulated APIs)
    • EDQM Certificate of Suitability (CEP) standards

    Typical usage ratio

    • 0.8% – 6% w/w based on total batch input, adjusted according to desired substitution level and scale of target moiety integration

    Downstream process integration

    • Enter in key intermediate coupling or alkylation step; often introduced after pre-activation of aromatic or alicyclic sites, followed by purification and crystallization sequences

    Final product types

    • Difluoroalkylated drug intermediates
    • CNS active APIs (e.g., fluorinated SSRIs, antiepileptics)
    • Antiviral compounds with improved oral bioavailability
    • Small-molecule enzyme inhibitors

    2. Agrochemical Synthesis (Pesticide and Herbicide Intermediates)

    Industrial agrochemical producers rely on DFEA when engineering advanced pesticides and herbicides containing difluoroalkyl functional groups. By facilitating the addition of unique fluoroethyl segments during molecular design, manufacturers strengthen environmental stability and selectivity in crop protection agents, particularly for actives requiring resistance to rapid biodegradation in field settings.

    Industry compliance standards

    • FAO/WHO JMPR pesticide specification standards
    • REACH Regulation (EC) No 1907/2006
    • OECD Guidelines for the Testing of Chemicals (for eco-toxicity and degradation)
    • ISO 17025 Laboratory Quality Systems (for analysis and batch release)

    Typical usage ratio

    • 1.2% – 7% w/w in the specific reaction step, depending on the desired functionalization density and crop protection profile

    Downstream process integration

    • Introduced during nucleophilic substitution or amination steps within multi-stage synthesis of core actives; followed by hydrolysis, extraction, and formulation into granules or wettable powders

    Final product types

    • Difluoroalkylated herbicide intermediates
    • Novel fungicidal actives for seed coatings
    • Systemic insecticide building blocks
    • Stabilized pesticide conjugates for extended field-release formulations

    3. Specialty Fluorinated Polymer Monomers

    Major polymerization plants incorporate DFEA as a monomeric precursor when producing high-performance fluorinated resins and coatings, where its difluoro functional group imparts improved chemical resistance, decreased surface energy, and superior weatherability. This strategy is especially relevant in the electronics, automotive, and industrial coating sectors, allowing the downstream production of specialty polymers tailored to demanding applications.

    Industry compliance standards

    • ISO 9001 Quality Management for polymer manufacturing
    • ASTM D6444-18 for fluoropolymer materials
    • RoHS Directive (EU) 2015/863: Restriction of Hazardous Substances
    • UL 94 Flammability Tests for polymeric materials

    Typical usage ratio

    • 0.3% – 3.5% per monomer feed, depending on targeted modification and copolymerization degree; precise level set according to desired resin properties

    Downstream process integration

    • Added directly into continuous or batch polymerization reactor as a functional monomer or chain extender; incorporated alongside fluorinated comonomers prior to initiation step

    Final product types

    • Fluorinated acrylate and methacrylate resins
    • Weather-resistant automotive topcoats
    • Antifouling electronic device coatings
    • Chemical-resistant floor sealants and linings

    4. Life Science Research Chemicals and Custom Synthesis

    Contract research organizations and life science manufacturers integrate DFEA into their workflow to streamline custom molecule development. Synthetic chemists benefit from its reactivity when building labeled compounds for NMR studies, medicinal chemistry screening, and radiolabel synthesis. Its compact structure and selective reactivity simplify the design of molecular probes and preclinical testing agents used in R&D pipelines.

    Industry compliance standards

    • ISO 13485:2016 for laboratory equipment and research reagent production
    • OECD Good Laboratory Practice (GLP) principles
    • Hazard Communication Standard (29 CFR 1910.1200) for chemical safety in laboratories
    • All relevant local occupational exposure limits (OELs) and waste handling regulations

    Typical usage ratio

    • Variable 0.1% – 5% per target compound, adjusted for labeling intensity, molecular scaffold, and detection requirements

    Downstream process integration

    • Applied during late-stage derivatization of molecular scaffolds; coupled with isotopic labeling, fluorination, or modification reactions, followed by chromatographic purification and analytical confirmation

    Final product types

    • Fluorine-labeled analytical standards (NMR, mass spectrometry)
    • Molecular probes for biochemical pathways
    • Radiolabeled trial compounds for preclinical ADME studies
    • Reference substances for drug metabolism research
    Free Quote

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