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2,4-Dimethylphenyl Isothiocyanate

    • Product Name 2,4-Dimethylphenyl Isothiocyanate
    • Alias 2,4-Dimethylphenyl isothiocyanate
    • Einecs 221-606-6
    • 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

    427936

    Cas Number 10200-84-9
    Molecular Formula C9H9NS
    Molecular Weight 163.24 g/mol
    Appearance Pale yellow to yellow liquid
    Boiling Point 122-123°C at 9 mmHg
    Density 1.106 g/mL at 25°C
    Refractive Index n20/D 1.634
    Purity Typically ≥ 98%
    Solubility Insoluble in water; soluble in most organic solvents

    As an accredited 2,4-Dimethylphenyl Isothiocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a secure screw cap, labeled "2,4-Dimethylphenyl Isothiocyanate (CAS 3882-55-7)," hazard symbols included.
    Shipping 2,4-Dimethylphenyl Isothiocyanate should be shipped in tightly sealed containers under dry, cool conditions. It must be clearly labeled as a hazardous chemical and protected from moisture and incompatible substances. Comply with DOT and IATA regulations, ensuring secondary containment and appropriate safety documentation during transport to prevent leaks or exposure.
    Storage 2,4-Dimethylphenyl Isothiocyanate should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from moisture, heat, and sources of ignition. Keep away from incompatible substances such as strong oxidizing agents and acids. Store under inert atmosphere if possible. Always follow applicable regulations and consult the Safety Data Sheet (SDS) for detailed instructions.
    Application of 2,4-Dimethylphenyl Isothiocyanate

    Applications of 2,4-Dimethylphenyl Isothiocyanate in Industrial Manufacturing

    2,4-Dimethylphenyl Isothiocyanate serves as a key intermediate for the synthesis of specialty chemicals, especially in agrochemical, pharmaceutical, pigment, and polymer additive manufacturing. As the original manufacturer, we support regulated sectors with high-purity material and technical guidance throughout R&D and commercial-scale production.

    1. Agrochemical Intermediate Synthesis

    This compound is a core building block for sulfonylurea-based herbicides and certain fungicidal actives. Direct introduction during nucleophilic addition steps enables selective synthesis, minimizing by-product profiles. Agrochemical formulators use its reactivity to develop next-generation crop protection molecules with improved crop selectivity and environmental behaviors. Process QC requires continuous monitoring for trace-level impurities and batch-to-batch consistency to comply with both local and export regulatory regimes.

    Industry compliance standards

    • ISO 9001:2015 for quality management in chemical synthesis
    • Regulation (EC) No 1107/2009 for plant protection products (EU)
    • US EPA FIFRA registration standards for technical intermediates
    • China GB 2763 for maximum residue limits in agrochemicals

    Typical usage ratio

    • Employed at 0.8–1.2 molar equivalents relative to the nucleophilic partner in active ingredient core assembly
    • Ratio adjusted for desired selectivity and minimization of unreacted isothiocyanate residues

    Downstream process integration

    • Feeds directly into condensation reactions during batch or continuous active ingredient synthesis
    • Pre-mixed under inert conditions to control exothermicity and prevent hydrolysis
    • Integrated into multi-step synthetic flows for custom analog development (pilot to tonne scale)

    Final product types

    • Sulfonylurea herbicide technical concentrates
    • Custom fungicidal actives
    • Ready-to-spray and wettable powder agrochemical formulations

    2. Pharmaceutical API and Intermediate Manufacturing

    Pharmaceutical manufacturers use it to introduce isothiocyanate moieties in lead compound development, particularly when synthesizing candidate molecules for oncology and anti-inflammatory indications. The highly specific reactivity of this aromatic isothiocyanate provides targeted derivatization on aromatic rings. This enables access to libraries of potential active pharmaceutical ingredients and advanced intermediates with exacting process controls and GMP documentation to facilitate regulatory submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF, Ph. Eur., JP for impurities profiling and analytical method validation
    • 21 CFR Part 210 & 211 (US FDA) for pharmaceutical production controls
    • EDQM CEP or DMF filing requirements for advanced intermediates

    Typical usage ratio

    • Typically used at stoichiometric or slight molar excess (1.0–1.3 equivalents) depending on substrate availability
    • Ratio determined by impurity control and downstream purification strategies

    Downstream process integration

    • Charged in stepwise condensation protocols for heterocyclic core construction
    • Implemented in parallel-synthesis platforms for medicinal chemistry screening
    • Handled under nitrogen to control atmospheric moisture intake

    Final product types

    • NCE (New Chemical Entity) candidate molecules
    • GMP advanced pharmaceutical intermediates
    • Custom small-molecule APIs for clinical trial supply

    3. Organic Pigment Synthesis

    Pigment producers apply aromatic isothiocyanates to generate high-performance yellow and orange azo pigments with enhanced colorfastness. By precisely reacting with diazonium salts, formulating chemists achieve tailored chromophore stability and hue formation with predictable shade control. Process optimization focuses on batch reproducibility, filtrate clarity, and controlled particle size for downstream dispersion. Strict documentation assures compliance for both industrial coatings and select food packaging inks.

    Industry compliance standards

    • EN 71-3:2019 for pigment safety in toy applications (EU)
    • ISO 9001/14001 for pigment production QA and environmental management
    • REACH (EC 1907/2006) substance registration for colorant intermediates
    • FDA 21 CFR 178.3297 for pigments in food-contact polymers (US)

    Typical usage ratio

    • Applied at 0.95–1.05 molar equivalents vs. the diazo component during pigment coupling
    • Batch ratios optimized for desired pigment strength and minimized excess isothiocyanate traces

    Downstream process integration

    • Added directly into coupling reactors post-diazotization to ensure high coupling efficiency
    • Neutralization and filtration steps follow to isolate and purify pigment cake
    • Integrated with post-synthesis surface treatment for improved dispersibility

    Final product types

    • High-performance organic azo pigments
    • Dispersible pigment concentrates for plastics
    • Coating-grade pigment dispersions for paints and inks

    4. Polymer Additives and Crosslinking Agents

    Specialty resin and elastomer producers use aromatic isothiocyanates to introduce crosslinkable sites into polyurethane and synthetic rubber systems. The isothiocyanate end-groups react with tailored nucleophilic monomers, conferring enhanced chemical resistance and mechanical durability. Strict batching protocols, moisture exclusion, and traceability documentation are critical at industrial scale to meet automotive, electronics, or technical textile industry requirements.

    Industry compliance standards

    • ISO 14001 for environmental controls in specialty polymer production
    • RoHS (2011/65/EU) compliance for electrical/electronic polymer additives
    • ASTM D3574/D3575 standards for polyurethane foam characterization
    • OEM automotive specification protocols for under-the-hood elastomeric materials

    Typical usage ratio

    • Used at 0.5–2.0 wt% of total polymer mass, depending on targeted crosslink density and formulation type
    • Precise dosing determined by required balance of elongation and modulus in the end-use article

    Downstream process integration

    • Blended into polyol or prepolymer components before chain extension or curing steps
    • Monitored dosing via in-line flow meters and batch record-keeping for trace obligations
    • Supported with technical documentation for downstream compounding adjustments

    Final product types

    • Chemically crosslinked polyurethane foams
    • Technical elastomeric sheeting for automotive sealing
    • Adhesive-grade polymer binders for electronics assembly
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