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2-Chloro-N-(2-Furylmethyl)Acetamide

    • Product Name 2-Chloro-N-(2-Furylmethyl)Acetamide
    • Alias N-(Furan-2-ylmethyl)-2-chloroacetamide
    • Einecs 248-173-5
    • 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

    700465

    Productname 2-Chloro-N-(2-Furylmethyl)Acetamide
    Casnumber 68787-98-2
    Molecularformula C7H8ClNO2
    Molecularweight 173.6
    Appearance White to off-white solid
    Meltingpoint 76-78°C
    Solubility Soluble in organic solvents
    Purity Typically ≥98%
    Storagetemperature Store at 2-8°C
    Smiles ClCC(=O)NCC1=CC=CO1
    Inchikey NZWYZUVOMIABLC-UHFFFAOYSA-N

    As an accredited 2-Chloro-N-(2-Furylmethyl)Acetamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed, labeled amber glass bottle containing 25 grams, with hazard warnings and handling instructions clearly visible.
    Shipping Shipping for 2-Chloro-N-(2-Furylmethyl)acetamide is conducted in accordance with applicable chemical safety regulations. The compound is securely packaged in appropriate, labeled containers to prevent leakage or contamination. All shipments include safety documentation and are typically dispatched via certified carriers specializing in hazardous or specialty chemicals. Delivery timelines depend on destination and compliance checks.
    Storage 2-Chloro-N-(2-Furylmethyl)acetamide should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong oxidizing agents. Ensure proper labeling and access only to trained personnel. Always follow local regulations and chemical safety guidelines during storage and handling.
    Application of 2-Chloro-N-(2-Furylmethyl)Acetamide

    Applications of 2-Chloro-N-(2-Furylmethyl)Acetamide in Industrial Manufacturing

    As an established manufacturer of 2-Chloro-N-(2-Furylmethyl)Acetamide, we support specialized downstream industries that require this material for advanced synthesis and the development of distinct chemical-based products. Below we outline key industrial applications based on data from our long-standing partnerships with sector-leading producers. Each scenario focuses on core compliance, recipe inclusion, integration into the client’s facility, and the resulting finished goods.

    1. Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Major pharmaceutical API producers rely on this compound as a key intermediate during the preparation of certain heterocyclic and furanyl-derived therapeutic molecules, especially antimicrobial or anti-inflammatory agents. The compound offers specific reactivity that allows regioselective substitution during multi-step organic synthesis, especially when introducing chloroacetyl side chains onto a furyl-based core. Process chemists adjust concentration according to conversion rate, impurity profiles, and target batch size, optimizing purity to meet regulatory filing requirements.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) guidelines (ICH Q7, US FDA 21 CFR Part 210/211)
    • European Pharmacopoeia (Ph. Eur.) API monographs where applicable
    • ICH Q3A/B for impurity limits in intermediates and raw materials
    • REACH Annex XVII (EU) for handling of specialty chemicals in drug synthesis

    Typical usage ratio

    • 5-18% molar equivalent, calculated against target core structure; chemists adjust depending on targeted API yield and side product minimization

    Downstream process integration

    • Material introduced at Step II or Step III during multi-stage organosynthetic routes after initial furanyl core building
    • Dosed in jacketed reactors under inert atmosphere for controlled nucleophilic acyl substitution
    • Pre-treated with base in solvent system (e.g., DMF or acetonitrile) for chloride activation

    Final product types

    • Generic and proprietary APIs with furanyl-chloroacetyl structures
    • Bulk pharmaceutical intermediates for contract development and manufacturing (CDMO) supply
    • Finished tablets, capsules, or injectable vials post downstream processing

    2. Agrochemical Synthesis Intermediate

    Manufacturers in the crop protection sector use this compound as a building block in the synthesis of selective fungicides and bactericides, specifically those leveraging furyl-acetamide scaffolds for targeted activity. Downstream formulators prefer this raw material due to its consistent reactivity and purity, which allow controlled chlorination and amidation steps in custom pesticide synthesis.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical material (FAO Manual, WHO Guidelines)
    • Regulation (EC) No. 1107/2009 for plant protection product approval in the EU
    • US EPA FIFRA requirements (US 40 CFR Part 158)
    • ISO 9001:2015 for agrochemical manufacturing quality systems

    Typical usage ratio

    • 2-12% by weight of the synthetic batch; adjusted based on fungicide or bactericide required potency and backbone modification

    Downstream process integration

    • Charged during Stage I or Stage II for coupling with other heterocyclic intermediates
    • Typically dissolved in polar aprotic solvents for direct amidation
    • Monitored via HPLC for conversion rate before downstream chlorination/aromatization

    Final product types

    • Technical-grade fungicide actives
    • Bactericide concentrates for agricultural dilution
    • Ready-to-use granule or suspensible powder formulations

    3. Chemical Synthesis Intermediate for Specialty Polymers

    Producers of niche polymers and specialty resins use this material as a crosslinking or functionalizing intermediate, taking advantage of its unique furylmethyl acetamide motif to impart hydrophilicity and chemical resistance to final polymer matrices. Production engineers tailor charge levels in formulation to achieve desired molecular weight and branching.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical manufacturing
    • ASTM D638, D790 testing for physical polymer properties
    • Restriction of Hazardous Substances (RoHS) for electronics-grade resins
    • REACH registration for polymer intermediates within the EU

    Typical usage ratio

    • 1.5-7% by mass, relative to total monomer content; adjusted according to target molecular architecture and solubility requirements

    Downstream process integration

    • Fed as a co-monomer or crosslinker during bulk or solution polymerization
    • Introduced after main chain monomer addition to control end-group functionality
    • Post-polymerization purification to remove unreacted residues, ensuring stability

    Final product types

    • Engineering plastics with enhanced chemical and heat resistance
    • Coatings with improved barrier and adhesion characteristics
    • Polymer films for specialty packaging and electronics applications

    4. Fine Chemical Intermediate for Dye and Pigment Manufacturing

    Advanced dye and pigment factories utilize this compound to synthesize high-value furan-based chromophores and intermediates for specialty colorants. Its electron-rich furan ring and reactive chloroacetamide group enable it to participate in ring-closure and acylation reactions that generate intensely colored molecules for dyes, plastics, and inks.

    Industry compliance standards

    • EN 71-3 for migration of certain elements in toys and inks
    • ISO 9001:2015 for dye and pigment manufacture
    • Standard Methods for the Examination of Water and Wastewater (SM 2018) regarding effluent colorant load
    • US TSCA Section 8(b) inventory listing for industrial colorants

    Typical usage ratio

    • 3-10% batch mass, modulated per chromophore backbone and color intensity target

    Downstream process integration

    • Reacted during coupling or condensation steps with aromatic amines or aldehydes
    • Used in solvent-mediated acylation for pre-chromophore construction
    • Subsequently purified using column chromatography to isolate high-purity intermediates

    Final product types

    • Furan-based organic pigments for textiles and plastics
    • Specialty dyes for inks, markers, and industrial colorants
    • UV-resistant colorant additives
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