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4-Methoxyphenylthiourea

    • Product Name 4-Methoxyphenylthiourea
    • Alias Aniline, 4-methoxy-, thiourea
    • Einecs 221-876-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    609994

    Name 4-Methoxyphenylthiourea
    Cas Number 6321-15-5
    Molecular Formula C8H10N2OS
    Molecular Weight 182.24 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 142-145 °C
    Solubility In Water Slightly soluble
    Boiling Point Decomposes before boiling
    Density 1.22 g/cm³ (estimated)
    Smiles COC1=CC=C(C=C1)NC(=S)N
    Inchi InChI=1S/C8H10N2OS/c1-12-7-4-2-6(3-5-7)10-8(9)11/h2-5H,1H3,(H3,9,10,11)
    Storage Conditions Store in a cool, dry place, away from light
    Purity Typically ≥98% (commercial sources)
    Hazard Statements May cause skin and eye irritation
    Synonyms 1-(4-Methoxyphenyl)-2-thiourea

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

    Packing & Storage
    Packing The 4-Methoxyphenylthiourea is packaged in a 50-gram amber glass bottle, labeled with chemical name, purity, and hazard warnings.
    Shipping 4-Methoxyphenylthiourea is shipped in sealed, clearly labeled containers suitable for chemicals, protected from moisture and light. The package complies with relevant transport regulations. Handling includes use of personal protective equipment. Accompanying documentation provides safety and handling information. Transport is arranged to avoid high temperatures, impact, or exposure to incompatible substances.
    Storage 4-Methoxyphenylthiourea should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as oxidizing agents and strong acids. Protect from moisture and direct sunlight. Proper labeling and secondary containment are recommended to prevent spills. Follow local safety regulations and consult the Safety Data Sheet (SDS) for specific storage requirements.
    Application of 4-Methoxyphenylthiourea

    Applications of 4-Methoxyphenylthiourea in Industrial Manufacturing

    4-Methoxyphenylthiourea serves as a specialty intermediate in multiple chemical sectors. It is favored for its reactivity and selectivity in controlled synthesis routes. The following sections detail core downstream applications supported directly by high-purity grades from our own manufacturing lines.

    1. Pharmaceutical API Synthesis (Sulfonylurea Antidiabetic Intermediates)

    Major pharmaceutical manufacturers utilize 4-Methoxyphenylthiourea as a defined intermediate for the synthesis of certain sulfonylurea-based antidiabetic drug APIs. Its methoxy and thio functional groups facilitate targeted substitutions critical in the stepwise construction of the active ingredient backbone. Purity and batch traceability remain key to securing regulatory submission files and supporting audit trails throughout the drug substance manufacturing flow.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs (for related substances control)
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • EDQM CEP Submission traceability requirements

    Typical usage ratio

    • Mol ratio: 0.95–1.10 relative to target API precursor. Final charge depends on impurity profile and conversion yield tests.

    Downstream process integration

    • Enters at nucleophilic coupling or condensation stage in multi-step organic synthesis (after activation of aromatic ring substrates)
    • Subject to HPLC/GC incoming inspection
    • Used in reaction vessels with accurate stoichiometric dosing under nitrogen
    • By-product filtration and recycling steps integrated post-reaction to recover unreacted material

    Final product types

    • Bulk sulfonylurea API for type 2 diabetes medications
    • Regulatory-submitted API lots for ANDA and DMF
    • Intermediates for contract research and scale-up
    • Reference standards for pharmaceutical QC labs

    2. Crop Protection Chemical Synthesis (Herbicide Intermediate)

    Agrochemical processors integrate 4-Methoxyphenylthiourea as a targeted nucleophile in assembling selective herbicide scaffolds. Its structural motif enables downstream chloro- or amino-functionalizations, which are essential in generating crop-specific actives. Processing protocols mandate real-time analytics to maintain consistent isomeric form and impurity control appropriate for agricultural registration worldwide.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems for agrochemical manufacture
    • OECD Test Guidelines for pesticide residues
    • REACH Regulation (EC) No 1907/2006 for safe handling and environmental compliance

    Typical usage ratio

    • Charged at 0.85–1.2 molar equivalents per herbicide batch, fine-tuned according to impurity cut-off and conversion efficiency tracked by LC-MS

    Downstream process integration

    • Charged during intermediate coupling with chlorinated precursor in continuous or batch-mode reactors
    • Recovered from mother liquor and recycled for cost efficiency
    • Subject to in-process QC monitoring (KF titration, NMR verification)
    • Separation and purity enhancement by crystallization or process chromatography

    Final product types

    • Raw herbicidal actives (preformulation grade)
    • Technical concentrate intermediates for final formulation
    • Reference impurity markers for registration dossiers
    • Analytical standards for agriscience labs

    3. Rubber Vulcanization Accelerator Manufacturing

    Manufacturers in the rubber and elastomer sector use 4-Methoxyphenylthiourea in synthesis routines for specific vulcanization accelerators. Its electron-donating properties help control cure rates and cross-linking in sulfur-based systems. This enables tailored mechanical performance and processibility of automotive, industrial, and specialty rubbers. All raw material lots trace to full polymer batch production records under strict QA protocols.

    Industry compliance standards

    • ASTM D4678: Standard Guide for Rubber Compounding Materials—Processing, Safety, and Handling
    • ISO 9001:2015 for tire-grade elastomer processes
    • REACH Regulation for restricted chemicals in elastomeric products
    • Automotive OEM chemical compliance documentation

    Typical usage ratio

    • Introduced at 0.1–0.6% of total rubber compound weight, depending on cure kinetics and required compression set properties

    Downstream process integration

    • Dosed into banbury mixers along with primary accelerators and curatives
    • Melt blended prior to network formation in open mills
    • Integrated tracking for batch traceability and off-spec correction
    • Undergoes secondary QC prior to final compounding and extrusion

    Final product types

    • Tire tread compounds (PCR, TBR grades)
    • Industrial belts and hoses (chemical-resistant grades)
    • Specialty elastomer parts for machinery damping
    • Rubber laboratory masterbatch standards

    4. Specialty Dyes and Pigments Manufacturing

    Colorants manufacturers employ 4-Methoxyphenylthiourea in synthesizing sulfur-containing azo and benzothiazole dyes. Its selective nucleophilicity steers the formation of bright, lightfast pigment molecules, critical in textile, leather, and plastic masterbatch industries. Ingredient origin, specification adherence, and waste minimization guide its adoption in modern colorant production lines.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for finished textile dyes)
    • EN 71-3: Safety of Toys—Migration of Certain Elements (for colorant residues)
    • ISO 14001:2015 (for waste and effluent management)
    • REACH Annex XVII restrictions on aromatic amines

    Typical usage ratio

    • Standard charge: 0.5–1.5 molar equivalents in azo or thiazole dye condensation stages, depending on target pigment hue and brightness

    Downstream process integration

    • Added at the nucleation stage for dye molecule construction
    • Subject to in-process LC-HRMS verification for chromophore integrity
    • Efficiency monitored by color strength and fastness bench testing
    • Accompanied by effluent treatment protocols to capture thiourea derivatives

    Final product types

    • Textile reactive and vat dyes
    • Polymer masterbatch pigments
    • Direct dyes for leather finishing
    • Research-grade colorant standards for quality benchmarking
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