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2-Chloro-5-Nitropyrimidine

    • Product Name 2-Chloro-5-Nitropyrimidine
    • Alias 2-Chloro-5-nitro-1,3-diazine
    • Einecs 221-592-0
    • 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

    860820

    Product Name 2-Chloro-5-Nitropyrimidine
    Cas Number 5470-18-8
    Molecular Formula C4H2ClN3O2
    Molecular Weight 159.53
    Appearance Yellow to brown crystalline powder
    Melting Point 95-97°C
    Solubility Slightly soluble in water
    Density 1.59 g/cm3
    Synonyms 2-Chloro-5-nitro-1,3-diazine
    Pubchem Cid 10622
    Smiles C1=CN=C(C(=N1)Cl)[N+](=O)[O-]
    Inchi InChI=1S/C4H2ClN3O2/c5-3-1-6-4(7-2-3)8(9)10/h1-2H
    Storage Temperature Store at 2-8°C
    Hazard Classification Harmful if swallowed, causes skin and eye irritation

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

    Packing & Storage
    Packing Amber glass bottle with screw cap, labeled “2-Chloro-5-Nitropyrimidine, 25g,” hazard warnings, and chemical structure, securely sealed.
    Shipping 2-Chloro-5-Nitropyrimidine is shipped in tightly sealed containers, protected from moisture and light. Transportation is conducted in compliance with local regulations for hazardous chemicals. Proper labeling, documentation, and handling procedures are ensured to prevent leaks, spills, or accidental exposure. Use appropriate safety measures and store in a cool, dry environment during transit.
    Storage 2-Chloro-5-nitropyrimidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from light, moisture, and ignition sources. Handle under a fume hood if possible, and ensure proper labeling. Store at room temperature and follow all regulatory and safety guidelines.
    Application of 2-Chloro-5-Nitropyrimidine

    Applications of 2-Chloro-5-Nitropyrimidine in Industrial Manufacturing

    2-Chloro-5-Nitropyrimidine plays a strategic role as a key intermediate in the synthesis of a variety of high-value fine chemicals. Our facility supplies this compound to specialized sectors where downstream processes demand high purity and consistent reactivity. Below, we outline its principal industrial application channels, highlighting processing specifics and market-focused compliance profiles.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers incorporate this compound during the route-selective synthesis of heterocyclic APIs, particularly in the production of antiviral, antifungal, and anti-inflammatory agents. Our clients utilize it as a starting structure for pyrimidine-based drug scaffolds, where controlled nucleophilic substitution and reduction steps are crucial for medicinal chemistry outcomes. At the batch level, process engineers monitor temperature and solvent polarity stringently to optimize yields and purity, adapting proportions according to the reactivity of substituted amines or aryl groups in downstream steps.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients (ICH Q7)
    • US Pharmacopeia (USP) standards for residual solvents (USP <467>)
    • European Pharmacopeia (Ph. Eur.) guidelines for intermediates
    • REACH pre-registration for pharmaceutical use

    Typical usage ratio

    • 0.8–1.3 molar equivalents for stepwise coupling; adjustments based on substrate substitution pattern and side reaction risk

    Downstream process integration

    • Introduced at the heterocycle formation or amination stage—used as a core building block before derivatization and salt formation
    • Purified by vacuum distillation or recrystallization immediately post-reaction to ensure QC release to next synthesis stage

    Final product types

    • Pyrimidine-based antiviral drugs
    • API intermediates such as substituted aminopyrimidines
    • Anti-inflammatory pharmaceutical compounds
    • Generic bulk drug actives

    2. Agrochemical Intermediate Manufacturing

    Formulators in the agrochemical sector employ this compound for the targeted synthesis of pyrimidine-derived herbicides and fungicides. Reaction flows typically involve nucleophilic aromatic substitution with specific amines or thiols, followed by nitro group transformations. Our technical team supports customers in optimizing throughput and batch purity under strict environmental health standards, ensuring safe handling and reproducibility at industrial scale.

    Industry compliance standards

    • ISO 9001:2015 certified Quality Management System for chemical intermediates
    • FAO/WHO specification for technical grade pesticide production
    • Compliance with EU Regulation (EC) No 1107/2009 for plant protection products
    • China National Standard GB 2763 for agrochemical residues in raw materials

    Typical usage ratio

    • 0.7–1.1 molar equivalents in relation to nucleophile or substrate; tuned for target molecule yield and solvent system efficiency

    Downstream process integration

    • Reacted during upstream intermediate synthesis—chlorine and nitro positions provide reactivity handles for further derivatization
    • Subjected to filtration and solvent washing to remove process residues before incorporation into formulation lines

    Final product types

    • Pyrimidine-derived herbicides
    • Fungicidal active ingredients
    • Insecticide intermediates
    • Custom plant protection molecule scaffolds

    3. Chemical Research & Fine Chemical Synthesis

    Chemical R&D divisions and fine chemical manufacturers use this compound as a versatile, stable substrate in the study and development of novel heterocyclic compounds. Research teams value its electrophilic positions—both chloro and nitro groups—for late-stage functionalization in structure-activity relationship (SAR) projects and preclinical studies for material science exploration. Our high-purity batches meet stringent academic and industrial lab requirements for controlled studies.

    Industry compliance standards

    • ISO 17025:2017 for laboratory quality assurance
    • Analytical purity validation under ASTM E2879/E2880
    • Globally Harmonized System (GHS) for reagent safety labeling
    • REACH compliance for research-grade chemicals

    Typical usage ratio

    • 0.05–1.0 molar equivalent depending on reaction design (exploratory synthesis vs. scale-up); subject to compound library diversity requirements

    Downstream process integration

    • Used in the early synthetic route as a core fragment for library expansions, or in late-stage derivatization of test compounds
    • Enters parallel synthesis reactors or combinatorial chemistry platforms for hit-to-lead optimization

    Final product types

    • SAR research libraries
    • Screening tool compounds for drug discovery
    • Custom heterocyclic analogs for advanced materials R&D
    • Reference standards for chemical validation

    4. Dye and Pigment Intermediates

    Selected dye manufacturers utilize this compound in the synthesis of specialty pyrimidine dyes and reactive pigment intermediates, particularly for application in textiles and technical fibers. Its functional groups facilitate nucleophilic and reductive colorant modifications, making it suitable for the preparation of dye molecules with high fabric binding properties and stability under wash and light stress. Production attention focuses on solvent compatibility and exhaust process management to meet environmental performance requirements.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances
    • Regulation (EC) No 1907/2006 (REACH) Annex XVII for dye ingredient restriction
    • ISO 9001:2015 for pigment and dye intermediate production
    • ZDHC Manufacturing Restricted Substances List (MRSL)

    Typical usage ratio

    • 0.65–1.2 molar equivalents in relation to chromophore core or amine co-reactant; adapted for desired color yield and fastness

    Downstream process integration

    • Integrated in the initial coupling or reduction steps during dye intermediate synthesis
    • Processed with controlled pH and temperature to achieve target substrate conversion and minimize unwanted by-products

    Final product types

    • Pyrimidine-reactive dyes for technical textiles
    • Specialty pigment intermediates
    • Colorfast textile auxiliaries
    • Luminescent dye components
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