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(4-Amino-2,3-Difluorophenyl)Acetic Acid

    • Product Name (4-Amino-2,3-Difluorophenyl)Acetic Acid
    • Alias (4-Amino-2,3-difluorophenyl)glycine
    • Einecs 822-551-2
    • 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
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    Specifications

    HS Code

    474755

    Productname (4-Amino-2,3-Difluorophenyl)Acetic Acid
    Casnumber 1430184-77-4
    Molecularformula C8H7F2NO2
    Molecularweight 187.15
    Appearance Off-white to beige solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO, slightly soluble in water
    Smiles C1=CC(=C(C(=C1F)F)N)CC(=O)O
    Inchikey ICWQGNPZINXKFS-UHFFFAOYSA-N
    Synonyms 2,3-Difluoro-4-aminophenylacetic acid
    Storagetemperature 2-8°C

    As an accredited (4-Amino-2,3-Difluorophenyl)Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram sample of (4-Amino-2,3-Difluorophenyl)acetic acid, securely sealed in an amber glass vial with a tamper-evident cap.
    Shipping (4-Amino-2,3-Difluorophenyl)acetic acid is shipped in tightly sealed, chemically resistant containers, protected from moisture, heat, and direct sunlight. The package complies with regulatory standards for handling chemicals. Proper labeling and documentation ensure safe transport. Shipping is via approved carriers, suitable for laboratory and research chemicals, with appropriate hazard and handling instructions included.
    Storage (4-Amino-2,3-difluorophenyl)acetic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizing agents. The storage area should be designated for chemicals, clearly labeled, and protected from extreme temperatures and moisture to prevent degradation and ensure stability of the compound.
    Application of (4-Amino-2,3-Difluorophenyl)Acetic Acid

    Applications of (4-Amino-2,3-Difluorophenyl)Acetic Acid in Industrial Manufacturing

    As a specialized manufacturer, we supply (4-Amino-2,3-Difluorophenyl)Acetic Acid to leading industrial partners engaged in advanced synthesis workflows. This raw material supports critical transformations within pharmaceutical intermediate production, agrochemical research, pigment synthesis, and high-performance material development. The following scenarios detail its actual integration points, formulation ratios, relevant compliance frameworks, and the end-use products enabled by its use at scale.

    1. Pharmaceutical Intermediate Synthesis for Non-Steroidal Anti-Inflammatory Agents

    Major pharmaceutical organizations adopt this acid as a key building block in the multi-step condensation processes required for producing fluoro-phenylacetic derivatives used as core scaffolds in certain non-steroidal anti-inflammatory drug (NSAID) compounds. Integration occurs at the acylation stage, where its difluoro-amino substituents impart the molecular properties necessary for target selectivity and metabolic stability.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 – Current Good Manufacturing Practice (cGMP)
    • European Pharmacopoeia (Ph. Eur.) Reference Standards for Intermediates
    • USP Chapter <795> – Pharmaceutical Compounding

    Typical usage ratio

    • Ranges from 0.8% to 2.2% w/w of total batch mass depending on target API yield; process control engineers adjust based on desired purity and required downstream functionalization.

    Downstream process integration

    • Introduced mid-synthesis following initial aromatic activation, typically via acylation or amide coupling under controlled pH and temperature; subsequently subjected to further substitutions to finalize API precursor.

    Final product types

    • Drug substance intermediates (regulatory-filed precursors)
    • Final Active Pharmaceutical Ingredients (e.g., NSAID molecules with modified phenylacetic backbone)
    • Pilot clinical batch materials for R&D
    • Commercial finished oral solid dose formulations (after further processing)

    2. Agrochemical Intermediate for Herbicide Research & Production

    R&D centers in the agrochemical industry integrate this specialty acid as a nucleophile in the development of selective herbicidal molecules. The electron-withdrawing fluoro groups aid in fine-tuning biological activity for new-generation pre-emergent herbicides. The acid is incorporated during the early active intermediate synthesis stage, playing a direct role in creating molecules optimized to control resistance in target weed varieties.

    Industry compliance standards

    • ISO 9001:2015 – Quality Management Systems
    • GLP (Good Laboratory Practice) OECD Guidelines
    • FAO/WHO Specifications for Plant Protection Products
    • ECHA REACH Registration for Agrochemical Raw Materials

    Typical usage ratio

    • Blend ratios of 1.5%–3.0% by mass of active ingredient, specification depends on the type of coupling reactions and efficacy target set by downstream formulation chemists.

    Downstream process integration

    • Added to reaction vessels during nucleophilic aromatic substitution or amidation, prior to final cyclization and formulating into active technical concentrate.

    Final product types

    • Pre-emergence and post-emergence herbicide technical powders
    • Soluble concentrate intermediate compounds for bulk active manufacturing
    • Research-scale biological screening samples
    • Regulatory submission samples for active ingredient registration

    3. Specialty Dye & Pigment Intermediate

    Manufacturers in the specialty chemical sector utilize this difluorinated building block in the synthesis of high-performance azo and azo-anthraquinone dyes, particularly where colorfastness and chemical resistance are required for technical textiles and polymer applications. The material is introduced during the diazotization and subsequent coupling reactions, where fluorine incorporation delivers unique chromatic properties and lightfastness enhancements.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Certification (for textile dyes)
    • EU REACH Annex XVII – Restrictions on Dyes and Pigments
    • ISO 14001 – Environmental Management Systems for Chemical Manufacturers
    • EN 71-3:2019 – Safety of Toys: Migration of Certain Elements (for pigment use in toys)

    Typical usage ratio

    • Direct addition at 0.2%–1.0% by weight in pigment or dye intermediate synthesis step. Concentration controlled relative to intended absorption spectrum and final shade requirements.

    Downstream process integration

    • Introduced post-nitration and reduction for diazotization; forms stable diazonium salts that then undergo coupling to create the final chromophores or pigment bases.

    Final product types

    • Technical textile dyes with enhanced fastness
    • High-performance polymer system pigments
    • Color masterbatches for plastics
    • Special coatings for industrial finishing applications

    4. Advanced Electronic Material Synthesis for Specialty Polymers

    Leading manufacturers of advanced polymers and specialty electronics precursors use this raw material for the synthesis of fluorinated co-monomers and chain extenders, enhancing the dielectric and chemical resistance properties of engineered thermoplastics. The amino and carboxylic sites allow precise grafting during oligomerization, optimizing polymer chain configuration for semiconductors and insulation materials.

    Industry compliance standards

    • IPC-4101C – Specification for Base Materials for Printed Boards
    • ISO 9001 – Quality Assurance for Polymer Manufacturing
    • RoHS Directive (2011/65/EU) – Restrictions on Hazardous Substances
    • UL 94 – Flammability Standard for Plastic Materials for Parts in Devices and Appliances

    Typical usage ratio

    • Addition rates from 0.3%–1.8% by weight, determined by the degree of desired fluorination and target molecular weight distribution in the copolymerization stage.

    Downstream process integration

    • Charged into the polymerization reactor at early copolymer formation; participates directly in condensation or addition polymerization, subsequently guiding microstructure tuning during catalyst-driven chain assembly.

    Final product types

    • High-frequency PCB substrate resins
    • Optoelectronic films for display and solar panel encapsulation
    • Formulated engineering thermoplastics with advanced dielectric properties
    • Electronic insulating coatings for microeletromechanical systems (MEMS)
    Free Quote

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