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1,3-Dimethylurea

    • Product Name 1,3-Dimethylurea
    • Alias N,N'-Dimethylurea
    • Einecs 203-312-7
    • 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

    986094

    Cas Number 96-31-1
    Molecular Formula C3H8N2O
    Molecular Weight 88.11 g/mol
    Iupac Name 1,3-Dimethylurea
    Synonyms N,N'-Dimethylurea
    Appearance White crystalline powder
    Melting Point 107-110 °C
    Boiling Point 244 °C
    Solubility In Water Readily soluble
    Density 1.13 g/cm3
    Flash Point 115 °C
    Pubchem Cid 7231

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

    Packing & Storage
    Packing 1,3-Dimethylurea is packaged in a 500g sealed HDPE bottle with a screw cap, labeled with hazard and product information.
    Shipping 1,3-Dimethylurea is typically shipped in tightly sealed containers, protected from moisture and incompatible materials. It should be handled as a non-hazardous solid, kept in a cool, dry, and well-ventilated area. During transit, it must comply with relevant regulations to prevent contamination or spillage. Standard chemical labeling and documentation are required.
    Storage 1,3-Dimethylurea should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of heat, ignition, and incompatible materials such as strong oxidizers. Protect the chemical from moisture and direct sunlight. Ensure containers are clearly labeled and regularly inspected for leaks or damage to maintain safety and chemical integrity.
    Application of 1,3-Dimethylurea

    Applications of 1,3-Dimethylurea in Industrial Manufacturing

    1,3-Dimethylurea plays a significant role in specialty chemical synthesis and industrial production. As the direct manufacturer, we supply this intermediate to various sectors with established downstream protocols and validated compliance systems. Below, we detail key industry segments where our product integrates into manufacturing processes, accompanied by dedicated standards, formulation ratios, process entry points, and final products.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use 1,3-dimethylurea as a secondary amine reagent in the synthesis of certain API precursors, notably in the production of methylated hydantoin-based drugs and intermediate building blocks for cardiovascular and CNS therapeutics. Typical applications require hazard and traceability assessments built into validation batches, as end formulators must comply with international pharmacopoeias and local regulatory filings. Onsite QC checkpoints verify impurity profiles, with documentation supporting full batch-to-batch trace. Formulation teams integrate our material at controlled stages preceding catalytic cyclization or condensation reactions, directly affecting the downstream process yield and purity for further API conversions.

    Industry compliance standards

    • International Council for Harmonisation (ICH Q7) for API intermediates
    • Good Manufacturing Practice (GMP) guidelines (EU GMP, US FDA 21 CFR Part 210/211)
    • Relevant pharmacopeias, e.g., USP, Ph. Eur., JP (depending on the drug product)
    • Local Drug Master File (DMF) registration guidance if required

    Typical usage ratio

    • 0.45–1.2 molar ratio relative to target substrate, adjusted for process yield and impurity control

    Downstream process integration

    • Charged after solvent charging and before temperature ramp in multi-step synthesis
    • Participates in methylation or condensation step with process analytical technology monitoring

    Final product types

    • Hydantoin derivatives (e.g., anticonvulsant intermediates)
    • Pyrimidine and purine analogs
    • Custom methylated pharmaceutical intermediates

    2. Resin and Plastics Additive Manufacturing

    Resin producers employ 1,3-dimethylurea as a curing accelerator and latent hardener in phenolic and melamine resin systems for performance laminates and molded products. Our material supports stable storage of prepolymer mixtures before rapid in-mold curing under heat or pressure. Downstream users precisely meter dosage to control crosslinking rates and final product thermal profile, especially when balancing curing speed against fine surface finish requirements. We provide tailored technical support to ensure compliance with application-specific ISO standards and chemical control inventories.

    Industry compliance standards

    • ISO 9001 Quality Management Systems for manufacturing
    • EU REACH Regulation (EC 1907/2006) registration and supply chain traceability
    • RoHS Directive 2011/65/EU (for electronics uses)
    • Relevant ASTM resin standards, e.g., ASTM D7995 for melamine-formaldehyde-based laminates

    Typical usage ratio

    • 0.2–1.5 wt% on total resin solids, tuned based on ambient storage durations and curing conditions

    Downstream process integration

    • Blended downstream with formaldehyde and resin precondensates before molding or impregnation
    • Added during final resin mixing or as a post-add to adjust setting speed

    Final product types

    • Decorative laminates (e.g., high-pressure laminates for furniture panels)
    • Molded melamine dinnerware
    • Electrical insulation boards

    3. Pesticide Formulation Intermediate

    Agrochemical manufacturers source 1,3-dimethylurea as a synthetic intermediate for triazine-based herbicides and growth regulator molecules. With precise handling under exemption codes in pesticide technical material plants, our product enters nucleophilic substitution reactions in closed-reactor environments. Site-specific documentation for local and global chemical inventory registrations remains mandatory, and downstream formulators manage input levels tightly to meet sectorial residue guidelines and environmental health standards.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for agrochemical R&D
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • China MEE Environmental Management of New Chemical Substances Regulation
    • REACH Annex VII/VIII dossier requirements (where applicable)

    Typical usage ratio

    • 0.7–1.1 mol equivalents per triazine unit, adjusted for batch scale and process efficiency

    Downstream process integration

    • Merged into reaction scheme during early-stage build-up of herbicide ring structure
    • Fed continuously to maintain reaction kinetics in flow or batch synthesis set-ups

    Final product types

    • Triazine herbicides (e.g., simazine, atrazine synthesis intermediates)
    • Plant growth regulator intermediates
    • Further downstream specialty agrochemical actives

    4. Textile and Paper Chemical Synthesis

    Producers of textile finishing agents and paper strength additives integrate 1,3-dimethylurea in the manufacturing of non-formaldehyde resin crosslinkers and wet strength agents. Carefully metered addition allows for improved product handle, resilience, and anti-wrinkle performance for cellulosic fibers, meeting growing regulatory pressure on residual formaldehyde levels in consumer goods. Our technical collaboration covers both formulation development and batch-scale implementation aligned with EU and national chemical control rules.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for textile chemical residues)
    • European Regulation (EC) No. 1935/2004 for food contact materials (for paper and board)
    • ISO 9001 in chemical plants and downstream paper mills
    • REACH SVHC monitoring and safety assessments

    Typical usage ratio

    • 0.3–0.9 wt% for paper and textile auxiliary formulation, varied by fiber substrate and end-use requirements

    Downstream process integration

    • Added at polycondensation step of resin or during formulation of finishing agent concentrate
    • Applied via aqueous solution or directly into pulp sizing system

    Final product types

    • Wrinkle-free cotton finishes
    • Wet strength resins for tissue and specialty paper
    • Non-formaldehyde textile resin crosslinkers

    5. Specialty Fine Chemical Synthesis

    Fine chemical firms use our product in the construction of heterocyclic building blocks, especially for high-value dyes and specialty monomers. Chemists design custom reaction routes involving methylation or condensation, tightly controlled for impurity and conversion efficiency to satisfy customer audits and quality reviews. Downstream fine chemical processors operate under ISO or customer-specified quality programs and report input quantities for full supply chain documentation.

    Industry compliance standards

    • ISO 9001 certified production and documentation processes
    • Customer audit programs (global specialty chemical majors)
    • Compliance with GHS/CLP labeling for supplied raw materials
    • Applicable national chemical control lists

    Typical usage ratio

    • 1.0–1.5 molar equivalents relative to target aromatic or aliphatic substrate, adjusted by target yield and byproduct formation rate

    Downstream process integration

    • Charged as core reactant at starting step of heterocycle formation
    • Dosage adjusted at scale-up to ensure batch reproducibility

    Final product types

    • Industrial dyes with urea and amine substructures
    • Specialty monomers for high-performance polymers
    • Unique heterocyclic intermediates for global niche markets
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