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2-Amino-5-Bromo-4,6-Dimethylpyrimidine

    • Product Name 2-Amino-5-Bromo-4,6-Dimethylpyrimidine
    • Alias 5-Bromo-4,6-dimethylpyrimidin-2-amine
    • Einecs 263-832-2
    • 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

    220711

    Chemical Name 2-Amino-5-Bromo-4,6-Dimethylpyrimidine
    Molecular Formula C6H8BrN3
    Molecular Weight 202.05 g/mol
    Cas Number 23628-32-2
    Appearance Off-white to light yellow powder
    Melting Point 110-114°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles CC1=NC(=C(N=C1N)Br)C
    Inchi InChI=1S/C6H8BrN3/c1-3-4(2)10-6(8)5(7)9-3/h1-2H3,(H2,8,10)
    Storage Conditions Store in a cool, dry place, tightly closed container
    Synonyms 5-Bromo-4,6-dimethyl-2-aminopyrimidine

    As an accredited 2-Amino-5-Bromo-4,6-Dimethylpyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 25-gram amber glass bottle, tightly sealed, with clear labeling for 2-Amino-5-Bromo-4,6-Dimethylpyrimidine.
    Shipping 2-Amino-5-Bromo-4,6-Dimethylpyrimidine is shipped in sealed, chemical-resistant containers to prevent moisture and contamination. Packages comply with relevant safety regulations, featuring clear labeling for hazardous materials. During transit, the chemical is protected from extreme temperatures, direct sunlight, and physical damage. Shipping documentation includes safety data and handling instructions.
    Storage 2-Amino-5-bromo-4,6-dimethylpyrimidine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Protect from moisture and avoid extreme temperatures. Label the container clearly, and keep it in a secure chemical storage cabinet designed for hazardous laboratory chemicals.
    Application of 2-Amino-5-Bromo-4,6-Dimethylpyrimidine

    Applications of 2-Amino-5-Bromo-4,6-Dimethylpyrimidine in Industrial Manufacturing

    2-Amino-5-Bromo-4,6-Dimethylpyrimidine is a specialty intermediate produced in our controlled manufacturing facilities for precision use in critical downstream synthesis. The material serves as a core building block for various fine chemical and pharmaceutical sectors. Below we outline verified industrial applications, with sector-specific standards, process integration, and end products detailed for responsible B2B procurement.

    1. Pharmaceutical API Intermediate for Antiviral Drug Synthesis

    This compound is widely used as a functionalized pyrimidine intermediate in the preparation of pharmaceutical active substances targeting viral infections. It is utilized by major manufacturers during the development of non-nucleoside inhibitors and is essential for building complex heterocyclic structures during multi-step synthesis. Strict monitoring of residual levels, impurity profiles, and final integration into regulated API pipelines is required throughout the process. Customers often demand broad documentation, including full traceability and analytical support at every stage, to comply with regulatory filings.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monographs applicable to end API
    • USP General Chapters — Residual solvents and Purity testing

    Typical usage ratio

    • Usually dosed at 1.2–1.8 molar equivalents as a key intermediate; actual charge ratio is optimized based on downstream impurity controls and process yield requirements.

    Downstream process integration

    • Charged in the condensation or coupling step for assembling tricyclic/pyrimidine API backbones
    • Undergoes further halogen exchange or amination in flow or batch reactors
    • Subject to multi-step purification, including recrystallization or preparative chromatography
    • Final inclusion in GMP API batch record and full batch analytical verification

    Final product types

    • Antiviral actives (e.g., HIV non-nucleoside reverse transcriptase inhibitors, hepatitis C compounds)
    • Small molecule pharmaceutical APIs with substituted pyrimidine motifs
    • Investigational new drug (IND) substances in clinical development
    • Generic compounds compliant with regulated DMF filings

    2. Agrochemical Intermediate for Pyrimidine Herbicide Synthesis

    Leading crop protection companies use this material as a strategic key intermediate in the synthesis of substituted pyrimidine herbicides. The controlled introduction of bromine and methyl groups supports highly selective reactivity for further sulfonation, amidation, or etherification steps in plant protection agent development. Manufacturers require lot-specific quality documentation, low impurity grades, and stability data to meet the increasingly regulated agrochemical sector requirements.

    Industry compliance standards

    • FAO/WHO Specifications for plant protection products
    • REACH Regulation (EC) No 1907/2006 (EU registration for substances)
    • OECD guidelines for quality and environmental assessment
    • ISO 9001:2015 for production traceability and process control

    Typical usage ratio

    • Applied at 0.7–1.2 molar equivalents in pre-herbicide intermediate synthesis; adjusted depending on downstream coupling group requirements and byproduct minimization strategies.

    Downstream process integration

    • Fed into initial heterocycle building step for pyrimidine herbicide skeleton
    • Activated with chlorination, sulfonation, or etherification reagents
    • Process often involves continuous monitoring of unreacted bromine and methylated byproducts
    • Final intermediate isolated using controlled crystallization or liquid-liquid extraction

    Final product types

    • Pre-emergent or selective pyrimidine herbicides for cereal and rice crops
    • Combination herbicide formulations with dual-action activity
    • Registered export-grade agrochemical actives for global markets
    • Pyrimidine-based plant health promoters

    3. Chemical Intermediate in Dye and Pigment Synthesis

    The fine chemicals sector integrates this pyrimidine derivative into specialty dye and pigment synthesis, particularly where heterocyclic substitution provides lightfastness and specific tint properties. Industrial users leverage its unique reactivity for introducing donor or acceptor groups into pigment structures, targeting improved stability and color strength. Quality control focuses on minimizing contaminant breakthroughs and achieving set absorbance endpoints in finished pigment dispersions.

    Industry compliance standards

    • ISO 787 (General methods of test for pigments and extenders)
    • EN 71-3 (Migration of certain elements — for pigments destined for toys)
    • REACH registration certification (for handling and transport)
    • Customer-specified heavy metal impurity limits

    Typical usage ratio

    • Variable, typically 0.5–1.0 mass equivalents in pigment precursor batch; ratio set by target chromophore density and solubility characteristics in organic synthesis.

    Downstream process integration

    • Introduced into the condensation or coupling step during pigment molecule assembly
    • Reacted under temperature- and pH-controlled conditions to form heterocyclic structures
    • Mixture advanced to post-oxidation or reduction to achieve desired hue
    • Filtration, drying, and milling of final pigment powder

    Final product types

    • Specialty printing ink pigments with improved thermal stability
    • Plastics colorants with high lightfastness
    • Textile dyes for polyester or nylon fiber applications
    • Technical blends for electronics encapsulation colorants

    4. Electronic Chemical Intermediate for Organic Semiconductor Materials

    Advanced electronics and materials companies deploy this compound for the synthesis of organic semiconductor building blocks. Its functional group pattern supports tailored electronic properties, enabling downstream producers to fine-tune charge mobility or optical performance in display and sensor applications. These applications demand certified purity, trace metal testing, and documented absence of ionic contaminants, given the end-use in sensitive device fabrication.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for hazardous substance content
    • JEITA standards for organic electronic material quality
    • IEC 60068 (Environmental testing for electronic materials)
    • ISO 9001:2015 for quality-managed supply chains

    Typical usage ratio

    • Typically 0.3–0.7 molar equivalents per batch, depending on molecular architect design and device function; adjusted for target conductivity and process yield.

    Downstream process integration

    • Fed as a key starting block in Suzuki or Buchwald-Hartwig couplings
    • Reacted under inert gas with Pd-based catalysts for high-purity electronic intermediates
    • Batch output purified using sublimation or column chromatography to device-grade levels
    • Reviewed for trace ionic and heavy metal contaminants before wafer integration

    Final product types

    • Organic semiconductor films for thin-film transistors (TFTs)
    • Active layers in OLED displays
    • Photoactive sensor device components
    • Printed circuit board (PCB) surface modifiers
    Free Quote

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