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5-Methyl-2-Furanmethanamine

    • Product Name 5-Methyl-2-Furanmethanamine
    • Alias 5-Methyl-2-furfurylamine
    • Einecs 681-440-8
    • 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
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    Specifications

    HS Code

    154633

    Chemical Name 5-Methyl-2-Furanmethanamine
    Molecular Formula C6H9NO
    Molecular Weight 111.14 g/mol
    Cas Number 938-88-9
    Appearance Colorless to light yellow liquid
    Boiling Point 65-67°C at 16 mmHg
    Density 1.07 g/cm3
    Solubility Soluble in water
    Smiles CC1=CC=C(O1)CN
    Purity Typically ≥98%
    Synonyms 5-Methylfurfurylamine
    Storage Conditions Store at 2-8°C

    As an accredited 5-Methyl-2-Furanmethanamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "5-Methyl-2-Furanmethanamine, 25g." Features hazard symbols, CAS number, lot number, expiration date, and manufacturer details.
    Shipping Shipping of 5-Methyl-2-Furanmethanamine requires proper labeling and packaging, complying with relevant chemical transport regulations. Use leak-proof, chemically compatible containers. Include safety data sheets, and ensure carriers are authorized for chemical shipments. Protect from heat, moisture, and direct sunlight. Handle with appropriate personal protective equipment during loading and unloading.
    Storage 5-Methyl-2-Furanmethanamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as oxidizing agents. Avoid moisture and ensure the storage area is equipped with appropriate spill containment. Clearly label the container and restrict access to trained personnel only. Always follow local safety regulations when handling.
    Application of 5-Methyl-2-Furanmethanamine

    Applications of 5-Methyl-2-Furanmethanamine in Industrial Manufacturing

    Our facility produces 5-Methyl-2-Furanmethanamine for direct integration into key industries requiring precise intermediate synthesis. We ensure all shipments comply with stringent manufacturing and application protocols demanded by commercial end users. Below are the principal application sectors, with technical breakdowns for compliance, dosing, process design, and outcome.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers deploy 5-Methyl-2-Furanmethanamine as a key intermediate in the production of furan-based drug molecules, such as substituted amine-containing antivirals and anti-inflammatory compounds. The compound is introduced during stepwise synthetic routes, where process control and impurity management are central. Operators verify conformity with global pharmacopeia standards during the synthesis, isolation, and purification stages to maintain robust batch-to-batch consistency for active pharmaceutical ingredient (API) precursors.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary)
    • Ph. Eur. (European Pharmacopoeia) monographs on intermediates
    • FDA cGMP 21 CFR Part 211

    Typical usage ratio

    • 0.8–1.5 molar equivalents relative to precursor ketones or aldehydes, adjusted for target molecule requirements and route efficiency

    Downstream process integration

    • Feeds into amination reaction vessels following solvent pretreatment
    • Participates in condensation and ring-closure steps under controlled temperature
    • Affects downstream chromatographic purification and crystallization
    • Elaborated to advanced intermediates for subsequent API finishing

    Final product types

    • Substituted furan pharmaceuticals (e.g., antiviral and anti-inflammatory agents in clinical trials)
    • Intermediate building blocks for CNS drugs
    • API-related research candidates
    • GMP-compliant intermediates for regulatory submission

    2. Agrochemical Intermediate Production

    Agricultural chemical producers utilize 5-Methyl-2-Furanmethanamine as a building block for selective herbicides and insecticides that rely on furan moieties for specific bioactivity. Process chemists incorporate the raw material into multi-step synthesis schemes where its unique amine functionality enables downstream urea, alkylation, or acylation reactions. Stringent QC measures ensure traceability across lot mixing and reaction scaling, particularly for compounds heading toward regulatory approval.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Good Laboratory Practice (GLP)
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 for quality management in chemical manufacture

    Typical usage ratio

    • 10–20% mass-to-mass with respect to the main substrate in early-stage synthesis; adjusted based on final pesticide structure and conversion yield

    Downstream process integration

    • Added to synthesis reactors for nucleophilic addition or amination
    • Incorporated before formulation or coupling with chlorinated intermediates
    • Managed with in-line process controls to monitor amine purity and residuals
    • Feeds into formulation tanks for subsequent suspension concentrates or emulsifiable concentrates development

    Final product types

    • Furan-based selective herbicides (e.g., for cereal and maize markets)
    • Precursor amines for novel insecticidal active substances
    • Seed treatment additives for targeted pest resistance
    • Fungicidal ingredient intermediates

    3. Specialty Polymer Additives Synthesis

    Polymer additive producers select 5-Methyl-2-Furanmethanamine for integration into polyimide and polyurethane specialty resin systems, exploiting its aromatic amine reactivity and thermal stability. The compound enters pre-polymer mixers where it participates in controlled chain extension and crosslinking. Precise metering is required to balance mechanical properties and ensure compliance with downstream user standards, particularly for applications in electronics and automotive spacers demanding low outgassing and high-performance metrics.

    Industry compliance standards

    • ISO 9001:2015 (Quality management systems for chemical intermediates)
    • RoHS Directive 2011/65/EU (for electronics applications)
    • UL 94 for flame-retardant plastics (if relevant)
    • REACH SVHC screening requirements

    Typical usage ratio

    • 0.5–5 phr (parts per hundred resin), dependent on crosslink density and polymer matrix requirements; routine laboratory titration defines exact input

    Downstream process integration

    • Dosed during liquid resin pre-polymerization
    • Mixed under inert atmosphere to minimize side reactions
    • Reacted at 70–120°C for amine-epoxy or amine-isocyanate coupling
    • Integrated with in-line viscosity and gel-time monitoring

    Final product types

    • Modified polyimide insulating films
    • Specialty polyurethanes for electronics dam and fill applications
    • High-performance adhesives and coatings for automotive electronics
    • Custom engineered plastics for aeronautics

    4. Fine Chemical Building Blocks for Flavors & Fragrances

    Producers in the aroma chemicals sector rely on 5-Methyl-2-Furanmethanamine as a precursor for constructing high-value furan derivatives that impart nutty, caramel, or roasted notes when formulated for use in food flavors or fragrance blends. Chemists introduce the amine in regioselective functionalization steps under GMP-like controls for food ingredient production, followed by mild purification to eliminate off-odors or byproduct amines before downstream esterification or acylation.

    Industry compliance standards

    • FCC (Food Chemicals Codex) for food-grade processing aids
    • IFRA Standards (International Fragrance Association Code of Practice)
    • ISO 22000 (Food safety management systems)
    • FSSC 22000 for food ingredient manufacturers

    Typical usage ratio

    • 0.1–0.8 weight% based on total batch mass for targeted reaction specificity; minimized to reduce residual amine in organoleptic testing

    Downstream process integration

    • Introduced at early-stage amidation or reductive amination reactions
    • Purified via distillation and crystallization ahead of blending into food or fragrance systems
    • Strict process hygiene and odor monitoring throughout handling and packaging
    • Storage and material tracking per food additive regulations

    Final product types

    • Furan-based aroma chemicals for flavor houses
    • Fragrance intermediates for perfumery compounds
    • Caramel-type flavoring ingredients
    • Toasted, roasted, or nutty note enhancers in food manufacturing

    5. Research Reagents and Life Science Applications

    Contract research organizations and biotechnological laboratories source 5-Methyl-2-Furanmethanamine for small-scale synthesis of reference compounds, novel amino-furan scaffolds, and as a diagnostic reagent in bioconjugation protocols. The compound's defined purity and batch reproducibility are critical, with single-use or small-batch protocols subject to rigorous documentation and handling procedures for downstream characterization and regulatory compliance, especially in translational research initiatives or life science screening assays.

    Industry compliance standards

    • ISO 13485 for medical device and research reagent quality management
    • GLP (Good Laboratory Practice) for preclinical laboratory use
    • REACH (EC) No 1907/2006 registration for laboratory chemicals
    • Sigma-Aldrich Research Chemical Quality Standards

    Typical usage ratio

    • Microgram to gram-scale, precisely weighed according to experimental protocol; concentration varies from millimolar to molar solutions in analytical labs

    Downstream process integration

    • Dissolved into aqueous or organic solvents for synthesis or assay set-up
    • Derivatized in situ for scaffold-linker chemistry
    • Incorporated at bench-scale for standard compound generation
    • Handled with strict documentation for traceability and reproducibility

    Final product types

    • Novel chemical entities for screening libraries
    • Bioconjugation reagents for diagnostics and molecular probes
    • Reference standards for chromatographic and spectrometric analysis
    • Custom small-molecule tools for medicinal chemistry
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