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3-Methyl-1,1-Diphenylurea

    • Product Name 3-Methyl-1,1-Diphenylurea
    • Alias Monuron
    • Einecs 221-607-4
    • 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

    345595

    Chemical Name 3-Methyl-1,1-Diphenylurea
    Molecular Formula C14H14N2O
    Molar Mass 226.28 g/mol
    Cas Number 13114-72-2
    Appearance White to off-white solid
    Melting Point 132-135°C
    Solubility In Water Slightly soluble
    Structure Diphenylurea core with a methyl group at the 3-position
    Iupac Name 1,1-Diphenyl-3-methylurea
    Smiles CN(C(=O)NC1=CC=CC=C1)C2=CC=CC=C2
    Storage Conditions Store in a cool, dry, well-ventilated place
    Synonyms 3-Methylcarbanilide

    As an accredited 3-Methyl-1,1-Diphenylurea factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 3-Methyl-1,1-Diphenylurea, screw cap sealed, labeled with hazard and identification details.
    Shipping 3-Methyl-1,1-Diphenylurea should be shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture absorption. Transport under cool, dry conditions with appropriate labeling in compliance with local and international regulations. Ensure packaging is secure to avoid spills or leaks during transit, and include a Material Safety Data Sheet (MSDS).
    Storage Store 3-Methyl-1,1-diphenylurea in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Protect from moisture and direct sunlight. Use secondary containment to prevent spills. Ensure storage area complies with relevant chemical safety regulations and provide easy access to safety data sheets.
    Application of 3-Methyl-1,1-Diphenylurea

    Applications of 3-Methyl-1,1-Diphenylurea in Industrial Manufacturing

    3-Methyl-1,1-Diphenylurea serves as a functional intermediate across specialized chemical manufacturing sectors where performance, purity, and regulatory compliance remain critical. Our direct manufacturing experience informs precise allocation and quality assurance for targeted downstream integration.

    1. High-Resilience Polyurethane Elastomers

    Manufacturers apply 3-Methyl-1,1-Diphenylurea as a chain extender in the formulation of high-resilience polyurethane elastomers. The material enables improved flexural strength, compression set performance, and durability in dynamic load environments. Validation in this use requires strict batch-to-batch consistency and pre-dispersion in polyol components. Downstream processors focus on sports shoe soles and industrial wheels with exacting impact resistance.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • ISO 20743:2017 Determination of Antibacterial Activity—Textiles (for components in wearables)
    • REACH Regulation (EC) No 1907/2006—Substance Registration for European distribution
    • US EPA TSCA Inventory listing

    Typical usage ratio

    • 1.0–3.5% by weight of total polyurethane formulation
    • Adjusted according to targeted hardness and reactivity profile of the finished elastomer

    Downstream process integration

    • Pre-mixed with liquid polyol under strictly controlled temperature
    • Added before isocyanate injection in high-pressure metering units
    • Material QC includes HPLC purity confirmation before compounding

    Final product types

    • High-impact shoe soles for athletic and safety footwear
    • Industrial castor wheels and rollers
    • Automotive bushings and vibration dampers
    • Flexible foam components for heavy equipment seating

    2. Advanced Polymer Additives for Engineering Plastics

    In the plastics sector, this specialty urea derivative acts as a nucleating agent and crystallinity modifier in engineering thermoplastics like polyamide and polycarbonate compounds. Compounders incorporate it to increase crystallization rates, dimensional stability, and heat deflection temperatures in demanding automotive and electronics applications. We guarantee traceability and batch homogeneity required for large-volume compounding operations.

    Industry compliance standards

    • ISO 1043-1 Identification and Marking of Plastics—General Principles
    • ISO 9001:2015 Quality Management Systems
    • UL 94 Flammability Safety Certification for End-use Devices
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)

    Typical usage ratio

    • 0.2–1.0% by weight in target polymer blends
    • Adjusted for polymer base type and crystallization requirements

    Downstream process integration

    • Direct incorporation during compounding using twin-screw extrusion
    • Melt mixing with precise temperature control (200–260°C range)
    • Continuous monitoring for dispersion during pelletizing stage

    Final product types

    • Polyamide automotive structural parts
    • Electrical and electronic device housings
    • High-temperature connectors and switches
    • Handheld electronic enclosures

    3. Specialized Rubber Accelerators

    Chemical processors use 3-Methyl-1,1-Diphenylurea as a secondary accelerator in the vulcanization of certain high-performance rubber compounds, specifically for products requiring improved tensile strength and controlled cure kinetics. Blends with thiazole primary accelerators allow custom tuning of cure rates for complex rubber profiles and seals. Our production system supports major tire and industrial rubber lines, with emphasis on strict impurity control and proactive technical data support.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems (production)
    • ISO 14693:2003 Specifications for Elastomers and Vulcanization (oilfield use)
    • ASTM D3182 Standard for Rubber Compounding Equipment
    • REACH Pre-registration for EU Markets

    Typical usage ratio

    • 0.5–2.0 phr (parts per hundred rubber)
    • Tuned according to required cure time and crosslink density

    Downstream process integration

    • Added at mixing step with accelerator blend in open mill or internal mixer
    • Temperature maintained below 120°C pre-curing
    • Accelerator dispersion tested by rubber mill shrinkage and tensile properties

    Final product types

    • Industrial tire treads and sidewalls
    • Sealing gaskets for pipeline and automotive assembly
    • Technical rubber components for hydraulic systems
    • Oilfield packers and high-pressure seals

    4. Crop Protection Formulation Intermediate

    This compound is selectively used in the synthesis of advanced herbicide and fungicide active ingredients where high purity and reactivity are necessary for downstream efficacy and shelf-life stability. Agrochemical manufacturers often integrate it in multi-step syntheses that lead to urea-based crop protection agents. We maintain precise batch records and advanced analytical validation as demanded by global regulatory authorities.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines for Pesticide Purity
    • ECHA CLP Regulation (EC) No 1272/2008 for Chemical Classification
    • ISO 17025 Laboratory Testing Accreditation
    • China GB2763—National Food Safety Standard for Maximum Residue Limits in Food

    Typical usage ratio

    • Utilized as a stoichiometric reactant, typical range 5–12% by molar ratio in final active ingredient synthesis
    • Adjustment based on synthetic route and desired bioavailability of actives

    Downstream process integration

    • Reacted with acid chlorides, isocyanates, or other functionalized intermediates in closed reactor systems
    • Pre-purification by recrystallization or preparative chromatography to ensure chemical structure integrity
    • Tested for residual solvents and heavy metals before formulation fencing

    Final product types

    • Herbicide active ingredients for broadleaf weed control
    • Systemic fungicides for grains and horticultural crops
    • Ready-to-use pesticide formulations (EC, SC types)
    • Crop-specific granules for direct field application
    Free Quote

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