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4-Amino-2-Chloropyrimidine-5-Carbonitrile

    • Product Name 4-Amino-2-Chloropyrimidine-5-Carbonitrile
    • Alias 4-Amino-2-chloro-5-cyanopyrimidine
    • Einecs 681-373-5
    • 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
    VTB
    Specifications

    HS Code

    224276

    Productname 4-Amino-2-Chloropyrimidine-5-Carbonitrile
    Casnumber 356783-16-9
    Molecularformula C5H3ClN4
    Molecularweight 154.56
    Appearance Off-white to light yellow solid
    Meltingpoint ≥180°C (decomposes)
    Purity Typically ≥98%
    Solubility Slightly soluble in DMSO, DMF
    Smiles C1=NC(=NC(=C1N)Cl)C#N
    Storagetemperature 2-8°C
    Synonyms 2-Chloro-4-amino-5-cyanopyrimidine

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

    Packing & Storage
    Packing The 100g bottle of 4-Amino-2-Chloropyrimidine-5-Carbonitrile comes in a sealed amber glass container with a tamper-evident cap.
    Shipping 4-Amino-2-Chloropyrimidine-5-Carbonitrile is shipped in a tightly sealed container, protected from moisture and light. The package complies with chemical safety regulations, labeled with hazard information. It is transported via certified carriers, ensuring secure handling, and typically dispatched within 2–5 business days. Safety data sheets are included with every shipment.
    Storage 4-Amino-2-Chloropyrimidine-5-Carbonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Properly label the container and keep it away from sources of ignition. Use appropriate personal protective equipment when handling and ensure good laboratory practices are followed.
    Application of 4-Amino-2-Chloropyrimidine-5-Carbonitrile

    Applications of 4-Amino-2-Chloropyrimidine-5-Carbonitrile in Industrial Manufacturing

    4-Amino-2-Chloropyrimidine-5-Carbonitrile serves as a key intermediate for several specialty chemical syntheses in pharmaceutical, agrochemical, pigment, and electronic material manufacturing. As a direct producer, we support precise formulation and integration of this intermediate into tightly controlled process chains.

    1. Pharmaceutical API Intermediate Synthesis

    This pyrimidine derivative functions as a critical starting building block in the assembly of antiviral and anticancer pharmaceutical ingredients. Leading pharmaceutical manufacturers employ the compound during multi-stage synthesis routes to introduce both amino and nitrile groups into heterocyclic scaffolds, using controlled reactions such as amidation, reductive amination, or cyclization. Reactant purity and stoichiometry must conform to validated batch protocols based on the final API target, with in-process QA/QC demanding low residual impurity levels.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance
    • EU GMP Part II (Basic Requirements for Active Substances)
    • US FDA cGMP 21 CFR Part 211 (Finished Pharmaceuticals)
    • Relevant pharmacopeial monographs (USP, EP, JP)

    Typical usage ratio

    • 5–15% molar basis as a precursor in the synthesis route; the exact ratio is set by the stoichiometry of the API structure being manufactured

    Downstream process integration

    • Enters after initial heterocycle formation, undergoes selective functional group transformations, and advances to further derivatization or coupling

    Final product types

    • Antiviral agents (e.g., nucleoside analogs)
    • Chemotherapeutic base compounds
    • Nonsteroidal anti-inflammatory drug (NSAID) precursors
    • Specialty pharmaceutical intermediates for custom synthesis

    2. Agrochemical Active Ingredient Synthesis

    Major crop protection producers utilize this compound in the preparation of pyrimidine-based insecticides and fungicides. It serves as a functionalized intermediate, participating in nucleophilic substitution and cyclocondensation reactions needed for active ingredient assembly. Batch records require tracking of residual starting material and byproducts, while national authorities mandate documented verification of all input chemicals.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Manufacturing
    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006
    • OECD Good Laboratory Practice for industrial chemicals

    Typical usage ratio

    • 5–12% weight basis of total reactants, adjusted depending on the crop protection molecule’s structural targets and required yield

    Downstream process integration

    • Acts as a core intermediate in early-stage synthesis, specifically before ring closure and halogenation steps in pesticide active ingredient production

    Final product types

    • Pyrimidinyl-based fungicides
    • Herbicide actives containing halopyrimidine motifs
    • Insecticide technical grade substances
    • Custom agrochemical intermediates for contract synthesis

    3. High-Performance Pigment and Dye Manufacturing

    Pigment and specialty dye producers use this compound to introduce nitrogen and halogenated pyrimidine units into advanced chromophores. This intermediate supports the production of structurally stable molecules for colorants used in inks, industrial coatings, and textile printing. Stringent quality systems control the synthetic route, with traceability of all raw materials and batch approval based on chromatic and purity criteria.

    Industry compliance standards

    • ISO 14001 (Environmental Management for pigment/dye manufacturing)
    • EN 71-3 (Safety of Toys—Migration of certain elements for colorants in children’s goods)
    • Swiss Ordinance on Materials and Articles (for food-contact inks and packaging)
    • REACH Annex XVII for restricted substances

    Typical usage ratio

    • 3–10% of total pigment batch, varying with colorant design and targeted molecular concentration

    Downstream process integration

    • Introduced in early or mid-stage cyclization reactions for pigment precursor synthesis, prior to azo coupling or metallization

    Final product types

    • High fastness azo and anthraquinone dyes
    • Metal-complex textile dyes
    • Inks for food packaging applications
    • Technical coatings pigments for automotive and industrial use

    4. Electronic and Optoelectronic Materials Synthesis

    Producers of organic semiconductors and liquid crystal materials employ this pyrimidine system as a building block for novel electron-transport and alignment layers. The structure and purity of the input material critically impact device performance, making process control and analytical batch release mandatory throughout the manufacturing lifecycle. Formulators tailor intermediate usage based on properties such as bandgap and carrier mobility in the finished product.

    Industry compliance standards

    • IEC 62679-2 (Display devices—liquid crystal panels—quality assessment)
    • ISO 9001:2015 (Quality management for electronic chemical production)
    • RoHS Directive (2011/65/EU) for electronic chemical restrictions
    • JIS C 61300 (Japanese standards for materials in electronics)

    Typical usage ratio

    • 8–22% of functional monomer input, depending on the synthesized optoelectronic material’s phase and electronic requirements; final composition optimized via lab verification

    Downstream process integration

    • Incorporated in primary organic synthesis, followed by further derivatization with other arenes or aliphatic units, prior to polymerization or device layer deposition

    Final product types

    • Active layers in organic thin-film transistors (OTFTs)
    • Alignment agents in LCD and OLED panels
    • Organic photovoltaic (OPV) sensitizers
    • Field-effect and charge-transport polymers

    5. Specialty Chemical Intermediate for Research & Custom Synthesis

    Chemical research institutes and custom synthesis partners integrate this compound into exploratory synthetic routes targeting novel heterocyclic analogs. Commonly, these workflows occur under controlled laboratory or pilot plant conditions, where traceability, starting material purity, and handling safety documentation remain essential for reliable scale-up and intellectual property approval. Its reactivity enables the development of structurally diverse end targets for specialty application evaluation.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and calibration in analytical research)
    • OECD Principles of Good Laboratory Practice
    • Material Safety Data Sheet (MSDS) provision under GHS
    • Proper licensing for regulated substance research (national/local)

    Typical usage ratio

    • 1–30% depending on the reaction protocol; dosage is driven by specific synthetic targets, route efficiency, and reaction scale

    Downstream process integration

    • Utilized in solution phase combinatorial synthesis, solid-phase screening projects, or pilot-stage custom route development

    Final product types

    • High-purity reference standards for analytical studies
    • Novel heterocyclic compounds for patent applications
    • SAR (structure-activity relationship) libraries for early-stage pharmaceutical and agrochemical testing
    • Technical-grade intermediates for subsequent scale-up studies
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