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2,4-Dichloro-5-Methylpyrimidine

    • Product Name 2,4-Dichloro-5-Methylpyrimidine
    • Alias 2,4-DCMP
    • Einecs EINECS 217-804-4
    • 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

    369079

    Chemical Name 2,4-Dichloro-5-Methylpyrimidine
    Cas Number 69045-84-7
    Molecular Formula C5H4Cl2N2
    Molecular Weight 163.01 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 57-61°C
    Purity Typically ≥98%
    Solubility In Water Slightly soluble
    Density 1.39 g/cm³
    Synonyms 2,4-Dichloro-5-methyl-1,3-pyrimidine
    Smiles CC1=CN=C(Cl)N=C1Cl

    As an accredited 2,4-Dichloro-5-Methylpyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed in a 500g amber glass bottle, 2,4-Dichloro-5-Methylpyrimidine is labeled with hazard warnings and chemical details.
    Shipping 2,4-Dichloro-5-Methylpyrimidine is shipped in tightly sealed containers, protected from moisture and light, and securely packed to prevent damage or leaks. It is classified as a hazardous material and should be transported according to local, national, and international regulations, including appropriate labeling and documentation to ensure safety during transit.
    Storage 2,4-Dichloro-5-Methylpyrimidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure the storage area is equipped for handling hazardous chemicals and is appropriately labeled. Use proper personal protective equipment when handling.
    Application of 2,4-Dichloro-5-Methylpyrimidine

    Applications of 2,4-Dichloro-5-Methylpyrimidine in Industrial Manufacturing

    2,4-Dichloro-5-Methylpyrimidine serves as an essential intermediate in the synthesis of value-added compounds across agrochemical, pharmaceutical, and specialty chemical industries. With direct integration into high-standard manufacturing lines, its purity and consistent performance support advanced processing demands in global downstream applications.

    1. Herbicide Active Ingredient Synthesis

    Agrochemical companies use our product as a core building block in the production of selective herbicide actives, particularly for pyrimidine-based formulations. It supports coupling reactions such as nucleophilic aromatic substitution and is often introduced in steps that define final molecular structure. Product quality and controlled impurity profiles ensure compliance with international registration requirements for crop protection products.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) Specifications
    • United States Environmental Protection Agency (US EPA) Registration Data Requirements (40 CFR 158)
    • REACH Regulation (EC 1907/2006) for chemicals in the EU
    • China ICAMA Product Registration Technical Requirements

    Typical usage ratio

    • 5–20% by weight in target herbicidal active ingredient synthesis batch; adjusted based on target molecule and co-reactants.

    Downstream process integration

    • Enters the nucleophilic aromatic substitution stage with amine or alcohol reagents for heterocyclic assembly.
    • Pre-purification occurs prior to final crystallization stage to remove unreacted materials.
    • Monitored for residual chlorine content during process analytics.
    • Supports scale-up in continuous or batch production blocks.

    Final product types

    • Pyrimidine-based herbicides (e.g., florasulam, flumioxazin intermediates)
    • Post-emergent weed control granules
    • Suspension concentrates for row crop application
    • Granular/SC/EC herbicidal formulations for cereals and soybean fields

    2. Pharmaceutical Intermediate for Antiviral and Anticancer Agents

    Leading pharmaceutical firms source this raw material for the fabrication of regulated drug intermediates, especially concerning nucleoside analogues and heterocyclic scaffolds in clinical development. The compound is reacted using highly monitored conditions and controlled pH, entering condensation and amination protocols for API generation. Batch record traceability, impurity limits, and solvent residues receive dedicated QC oversight according to pharmacopeial and GMP norms.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP), relevant monographs for APIs and intermediates
    • European Pharmacopoeia (Ph. Eur.) High-Purity Intermediate Listings
    • China GMP (2010 Edition) for Raw Material Management

    Typical usage ratio

    • 3–10% of the total molecular mass in synthetic routes for pyrimidine and triazine drugs; adjusted for molar excess based on stoichiometric calculation in condensation or alkylation reactions.

    Downstream process integration

    • Charged into closed reactors during initial condensation with amine or amino alcohol partners
    • Intermediate isolation through solvent extraction under inert atmosphere
    • Follows analytical verification by HPLC/GC for stage release
    • Feeds into downstream steps for ring modification or halogen exchange, as specified by synthetic route

    Final product types

    • API intermediates for antiviral agents (e.g., favipiravir intermediates)
    • Anticancer bulk drug intermediates with pyrimidine cores
    • Generic and branded pharmaceutical synthons for clinical supply
    • Advanced research chemicals for drug discovery support

    3. Synthesis of Plant Growth Regulators

    Plant growth regulator manufacturers utilize this chemical for constructing pyrimidine-derived control agents designed for yield improvement and stress mitigation in field crops. The key step involves selective substitution and ring closure using protected amines. The application requires strict raw material traceability, impurity containment, and batch reproducibility in compliance with national agricultural inputs regulations.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals, Section 5: Plant Protection Products and Pesticides
    • China Pesticide Registration Requirements (ICAMA GBT 1605-2001)
    • FAO/WHO Joint Meeting on Pesticide Residues Specifications
    • ISO 17025 Laboratory Management for Traceability and Analysis

    Typical usage ratio

    • 1–7% by weight of total charge in synthesis, depending on design of active molecule and scale of application.

    Downstream process integration

    • Introduced in the initial condensation or nucleophilic substitution stage with plant-safe functional groups
    • Followed by controlled crystallization and filtration for technical grade regulator isolation
    • QC evaluation for uniformity of active element distribution in end-use formulations
    • Final formulation into liquid concentrates or wettable powders

    Final product types

    • Pyrimidine-type plant growth regulators for cereals, vegetables, and horticulture
    • Stress tolerance enhancers in compatible field mixes
    • Yield boosting additives for row crops
    • Seed treatment actives and pre-germination stimulants

    4. Production of Specialty Dyes and Optical Brighteners

    Specialty chemical manufacturers add this compound into their synthetic pipelines to construct dye intermediates and optical brighteners for textiles and plastics. Electrophilic aromatic substitution and ring derivatization steps rely on high-purity feedstock to maintain brightness and fastness properties. Formulation stability, controlled color shade, and batch reproducibility form the basis for product release in global textile markets.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textiles free from harmful chemicals
    • EU REACH Annex XVII restrictions for azo colorants
    • ISO 105 Series (Textiles—Tests for Colour Fastness)
    • ASTM D7063-20 Specification for Optical Brightening Agents

    Typical usage ratio

    • 2–8% by mass for chromophore formation; adjusted by target brightness and desired hue intensity in the final formulation.

    Downstream process integration

    • Engaged during heterocyclic ring formation for the dye or brightener backbone
    • Subject to refluxing in polar aprotic solvents for substitution with electron-donating groups
    • Followed by condensation with sulfonic acid derivatives for performance enhancement
    • QC analysis using UV-Vis spectrophotometry to control color parameters and purity

    Final product types

    • Fluorescent brighteners for synthetic fibers and plastics
    • High-fastness dyes for cotton, polyester, and nylon fabrics
    • Color developers in ink and anti-counterfeiting printing
    • Brightness enhancers in detergents and paper coatings

    5. Manufacture of Heterocyclic Polymer Additives

    Polymer additive producers use 2,4-dichloro-5-methylpyrimidine to synthesize functionalized additives, which are employed to enhance flame retardancy and UV stability in engineering plastics. The product gets incorporated during the preparation of pyrimidine-based stabilizers or halogenated monomers for copolymerization. Regulatory control is maintained for trace-level migration and interaction with major resin systems such as polyamides and polyesters.

    Industry compliance standards

    • European Union Regulation (EU) No 10/2011 on plastic materials and articles
    • UL 94 Flammability Standard for Plastic Materials
    • ISO 4892 Weathering Tests for Plastics
    • FDA 21 CFR 177.2600 for indirect food additive compliance in relevant applications

    Typical usage ratio

    • 0.5–5% by mass in monomer or additive batch; fine-tuned to balance thermal stability and compatibility with core resin.

    Downstream process integration

    • Charged during closed kettle preparations for additive synthesis
    • Grafted via solution polymerization or melt blending with core polymers
    • Monitored by GPC or NMR for incorporation efficiency and chain length
    • Integrated into blended pellets or masterbatch for downstream extrusion/molding

    Final product types

    • Flame-retardant masterbatches for PA, PE, and PET
    • UV-stable additives for outdoor polymer products
    • Technical grade plastic compounding intermediates
    • Polymer stabilizer blends for specialty engineering plastics
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