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3-Fluorobenzylamine

    • Product Name 3-Fluorobenzylamine
    • Alias 3-FBA
    • Einecs 218-699-8
    • 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

    882747

    Productname 3-Fluorobenzylamine
    Casnumber 456-83-1
    Molecularformula C7H8FN
    Molecularweight 125.14
    Appearance Colorless to pale yellow liquid
    Boilingpoint 193-196°C
    Meltingpoint -21°C
    Density 1.13 g/cm3
    Purity Typically >98%
    Refractiveindex 1.540
    Flashpoint 76°C
    Solubility Soluble in water and organic solvents
    Synonyms m-Fluorobenzylamine; 1-(3-Fluorophenyl)methanamine
    Smiles C1=CC(=CC(=C1)F)CN
    Inchikey NAXHZMAWOKSPIM-UHFFFAOYSA-N

    As an accredited 3-Fluorobenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle of 3-Fluorobenzylamine is sealed, amber glass with a screw cap, labeled with safety and product information.
    Shipping 3-Fluorobenzylamine is shipped in tightly sealed, chemically resistant containers to ensure product integrity and safety. The chemical should be handled and transported in compliance with local, national, and international regulations, including labeling for hazardous materials. It usually ships via ground or air freight as a chemical substance, with appropriate documentation provided.
    Storage 3-Fluorobenzylamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and acids. Protect from moisture and direct sunlight. Store at room temperature or as recommended by the manufacturer, and ensure appropriate labeling and secondary containment to avoid accidental spills or exposure.
    Application of 3-Fluorobenzylamine

    Applications of 3-Fluorobenzylamine in Industrial Manufacturing

    As a direct manufacturer, we supply high-purity 3-Fluorobenzylamine for a range of industrial sectors. This raw material supports innovation in process chemistry, enabling precise integration into demanding downstream syntheses. Below we detail major application scenarios, their technical and regulatory context, and their specific requirements in large-scale production environments.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediates

    Innovators in small-molecule pharmaceuticals use 3-Fluorobenzylamine as a key intermediate, especially in synthesis routes for fluorinated phenethylamine derivatives, kinase inhibitors, and neurological agents. Production facilities employ it in amide coupling, reductive alkylation, and heterocyclic assembly steps, demanding tight impurity control and full traceability. Our material supports pilot and commercial-scale batch reactions meeting regulatory filing standards for the US, EU, and Asian markets.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for APIs
    • 21 CFR Part 210/211 (US FDA)
    • EU EudraLex Volume 4 GMP
    • Ph. Eur. monographs for medicinal chemistry intermediates

    Typical usage ratio

    • 5–22 mol% relative to core synthesis reactants, adjusted for step conversion and impurity profile

    Downstream process integration

    • Enters stagewise in multi-step batch or flow reactors as an amination or alkylation agent within the lead compound or side chain assembly

    Final product types

    • Targeted APIs in oncology and CNS therapy
    • Fluorinated benzylamine-based small molecules
    • Registered pharmaceutical intermediates (DMF/CEP supported)
    • Proprietary fluorinated building blocks for custom pharma R&D

    2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    Leading crop protection formulators incorporate 3-Fluorobenzylamine to construct key intermediates for selective herbicide and fungicide synthesis. It participates in nucleophilic aromatic substitution, forming fluorinated amine linkers that improve metabolic stability in field formulations. Control of trace metal and amine impurities remains critical for achieving government registration and maintaining product performance during field application trials.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Annex VIII–X registration (EU)
    • EPA 40 CFR 158 (US Federal Insecticide, Fungicide, and Rodenticide Act)
    • IS 6940:2002 Indian Standard for Pesticide Intermediates

    Typical usage ratio

    • 8–18 mol% relative to substituted benzene/formulated active ingredient backbone, dependent on desired substitution pattern and process yield

    Downstream process integration

    • Enters continuous or batch fine chemical reactors as an aminating agent prior to cyclization or further substitution steps

    Final product types

    • Fluorinated aromatic herbicide actives (e.g., phenoxyalkylamine class)
    • Benzylamine-derived fungicidal intermediates
    • Precursor compounds for selective insecticides
    • Registered technical concentrates for large-scale formulation

    3. Specialty Polymer Monomers and Modifiers

    Polymer producers use 3-Fluorobenzylamine as a functionally substituted building block in specialty polyamides, polyimides, and epoxy curing agents. Its presence imparts thermal and chemical resistance, lowers surface energy, and enhances dielectric performance in advanced polymers for electronics and aerospace materials. Strict control of residual fluorinated amines supports UL certification for electrical safety and performance validation in end-uses requiring long-term reliability.

    Industry compliance standards

    • UL 94 Flammability for Plastics
    • RoHS (Restriction of Hazardous Substances Directive)
    • IEC 60601 for electronic component materials
    • ISO 9001:2015 for quality management of polymer manufacturing

    Typical usage ratio

    • 2–8 wt% in monomer blend for specialty polyamides
    • 1.5–4 mol% as chain extender or side group modifier

    Downstream process integration

    • Introduced during copolymerization or polycondensation steps for backbone or side chain functionalization

    Final product types

    • Fluorinated engineering plastics for electronic housings
    • Specialty thermoset resins for circuit encapsulation
    • Modified polyimide films for aerospace insulation
    • Low-absorption coatings for optical devices

    4. Liquid Crystal Material Synthesis

    Display technology manufacturers source 3-Fluorobenzylamine for use in synthesizing anisotropic fluorinated liquid crystal aligners and mesogenic compounds. Its role in the alkylation and substitution of biphenyl and phenylcyclohexane frameworks enables precise control of dipole moments and transition temperatures, supporting mass production of high-definition LCD and OLED panels. R&D and production lines demand lot-to-lot consistency for panel uniformity and stable device operation.

    Industry compliance standards

    • RoHS and REACH for display material safety
    • IEC 62321 analysis for hazardous substances
    • ISO/TS 16949 for automotive display supply chain quality
    • JEITA Display Material Guidelines

    Typical usage ratio

    • 1.2–6 mol% in the mesogenic core synthesis step, depending on the desired birefringence and alignment properties

    Downstream process integration

    • Added as an amine source in multi-step synthesis of liquid crystal precursors and final formulation via coupling or nucleophilic substitution

    Final product types

    • High-birefringence LC compounds for TFT-LCD panels
    • Fluorinated mesogens for advanced OLED alignment layers
    • Automotive display-grade liquid crystal materials
    • Wearable device liquid crystal fluids

    5. Fine Fragrance and Aroma Intermediate Synthesis

    Manufacturers specializing in specialty aroma chemicals and fine fragrances include 3-Fluorobenzylamine in the preparation of fluorinated benzyl derivatives for unique scent profiles. Its use in reductive amination and acylation enables the creation of novel aromatic ingredients with enhanced stability, volatility, and olfactory character. Consistent low-odor, low-residual solvent content is crucial for high-specification fragrance compounds supplied to regulated consumer markets.

    Industry compliance standards

    • IFRA Standards for Fragrance Safety and Allergens
    • EU Regulation 1223/2009 on Cosmetic Products
    • RIFM Safety Assessment Guidelines
    • ISO 9235 Natural Raw Materials (for supporting documentation on synthetic intermediates)

    Typical usage ratio

    • 3–12 mol% per batch, typically in pilot to multi-ton fine chemical aroma synthesis, adjusted for specific scent molecule design

    Downstream process integration

    • Used as a feedstock in batch fine fragrance synthesis during primary amination or as an intermediate for subsequent fatty acid or aldehyde coupling

    Final product types

    • Fluorinated benzyl aroma ingredients for perfumery
    • Specialty flavor intermediates for food and beverage
    • Functional additives in personal care fragrance bases
    • Custom aroma molecules for specialty chemical blenders
    Free Quote

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    Certification & Compliance