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4,6-Diamino-2-Mercaptopyrimidine

    • Product Name 4,6-Diamino-2-Mercaptopyrimidine
    • Alias 2,4-Diamino-6-mercaptopyrimidine
    • Einecs 219-006-2
    • 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

    522794

    Name 4,6-Diamino-2-Mercaptopyrimidine
    Chemical Formula C4H6N4S
    Molecular Weight 142.18 g/mol
    Cas Number 56-06-4
    Appearance White to slightly yellow crystalline powder
    Melting Point > 300°C (dec.)
    Solubility In Water Slightly soluble
    Boiling Point Decomposes before boiling
    Density 1.73 g/cm³
    Synonyms 2-Mercapto-4,6-diaminopyrimidine
    Storage Conditions Store at room temperature, keep container tightly closed
    Pka 7.70 (for mercapto group)
    Smiles C1=NC(=S)N=C(N1)N
    Inchi InChI=1S/C4H6N4S/c5-2-1-7-4(9)8-3(2)6/h1H,(H6,5,6,7,8,9)

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

    Packing & Storage
    Packing A 25g amber glass bottle with a tightly sealed screw cap, labeled "4,6-Diamino-2-Mercaptopyrimidine" and safety information.
    Shipping 4,6-Diamino-2-Mercaptopyrimidine is typically shipped in tightly sealed containers to prevent moisture and air exposure. It should be packaged following hazardous chemical regulations, clearly labeled, and accompanied by safety documentation. Transport must comply with local and international guidelines for handling chemicals, ensuring protection from extreme temperatures and physical damage during transit.
    Storage **4,6-Diamino-2-Mercaptopyrimidine** should be stored in a tightly sealed container, away from light and moisture, at room temperature or as specified by the manufacturer. Keep in a cool, dry, well-ventilated area, separate from incompatible substances like strong oxidizers. Avoid prolonged exposure to air to prevent degradation. Always label containers clearly and follow all relevant safety guidelines.
    Application of 4,6-Diamino-2-Mercaptopyrimidine

    Applications of 4,6-Diamino-2-Mercaptopyrimidine in Industrial Manufacturing

    As the direct manufacturer of 4,6-Diamino-2-Mercaptopyrimidine, we support multiple specialized segments in industrial production. This pyrimidine derivative provides unique reactivity profiles in pharmaceutical intermediates, hair dye formulations, metal surface technologies, and specialized polymer systems. Below we outline select industry scenarios, with focus on compliance, dosage, process positioning, and downstream finished goods.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical manufacturers employ this compound for advanced heterocyclic building blocks, especially in small-molecule active pharmaceutical ingredient (API) development. Its primary amine and mercapto functionalities enable selective functionalization and ring closures in late-stage synthesis. Strict regulatory environments require exacting sourcing, documentation, and quality traceability from raw material delivery through API release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) monograph verification for residuals
    • European Pharmacopoeia (Ph. Eur.) Chapter 5.10 compliance
    • FDA 21 CFR Part 211: Pharmaceutical cGMP regulations

    Typical usage ratio

    • Applied at 0.08–0.25 molar equivalents per API synthetic step, varying with targeted substitution and desired intermediate purity. Adjustment according to route efficiency and impurity control protocols.

    Downstream process integration

    • Introduced during secondary amination or sulfur incorporation stages in the main reaction vessel. Batch or fed-batch addition, under nitrogen blanket at 40–80°C with continual in-process HPLC purity checks.

    Final product types

    • Pyrimidine-based pharmaceutical actives for anti-infective and anti-cancer treatments
    • Patented drug intermediates for metabolic disease APIs
    • Research chemicals for medicinal chemistry projects
    • Diagnostic reagent standards

    2. Oxidative Hair Dye Formulation

    Leading cosmetic and personal care companies use this material to introduce desirable tone and shade depth in permanent hair coloration systems. The diamino substitution pattern produces strong color density under oxidative conditions, while the mercapto group influences stability and hair fiber interaction. Strict cosmetic regulatory frameworks dictate raw material acceptance and batch consistency through finished product release.

    Industry compliance standards

    • EU Cosmetics Regulation EC No. 1223/2009 Annex III/V (restricted substances)
    • International Fragrance Association (IFRA) standard ingredient disclosures
    • ISO 22716:2007 (Cosmetics GMP)
    • CTFA/INCI nomenclature registration

    Typical usage ratio

    • Commonly used at 0.2–0.8% by weight in finished colorant cream, modulated within product line according to developer and shade profile. Ratio depends on depth/intensity specification and compatibility with other dye precursors.

    Downstream process integration

    • Pre-dissolved into aqueous or hydroalcoholic base during pre-mix blending. Incorporated before addition of oxidizing agents and thickeners. Quality control includes dye-stability and allergen screening of each batch.

    Final product types

    • Permanent and semi-permanent hair color creams
    • Salon professional hair coloring kits
    • Retail consumer-grade hair dye products
    • Specialty ethnic hair care color systems

    3. Metal Surface Corrosion Inhibition

    Specialty coating and oilfield service formulators utilize this compound as a selective corrosion inhibitor for ferrous and non-ferrous alloys. The sulfur and nitrogen atoms enable coordination with metal substrates, reducing corrosion rates and improving protective film uniformity. Deployment requires adherence to sector-specific environmental and occupational safety regulations.

    Industry compliance standards

    • ASTM G31–72: Laboratory Immersion Corrosion Testing of Metals
    • REACH EC 1907/2006 registration for downstream use
    • OSHA Chemical Safety Standards (29 CFR 1910.1200)
    • API RP 582: Corrosion Control in Oil & Gas Process Equipment

    Typical usage ratio

    • Dosages range between 15–150 ppm in recirculating water systems; adjustment based on water chemistry, temperature, and fluid velocity for optimal surface protection and minimal fouling.

    Downstream process integration

    • Metered injection into closed-loop cooling or process water streams using automated dosing systems. Monitored through routine inline corrosion coupon analysis and elemental residue checks.

    Final product types

    • Closed-system circulating water corrosion inhibitor packages
    • Oilfield corrosion control additives for enhanced equipment life
    • OEM-formulated industrial metal protection fluids
    • Specialty metalworking coolants

    4. High-Performance Polymer Modification

    Polymer and fiber manufacturers introduce this compound as a reactive chain modifier or cross-linker, mainly in specialty engineering plastics and high-performance coatings. The dual amino and mercapto reactivity facilitates chemical bonding during condensation or post-polymerization steps. This allows precise adjustments to mechanical, thermal, and chemical resistance properties.

    Industry compliance standards

    • ISO 9001:2015 certified manufacturing and traceability
    • ISO 14001:2015 for environmental management in polymer production
    • Directive 2011/65/EU (RoHS) substance declaration during electronics applications
    • Internal corporate restricted substance lists for major automotive and aerospace OEMs

    Typical usage ratio

    • Formulators use between 0.1–1.5% by weight, calculated relative to primary monomer or resin system. Selection based on end-use mechanical targets, with higher ratios for network density and solvent resistance improvements.

    Downstream process integration

    • Dispersion into polymer melt or formulation blend prior to extrusion or casting. Addition occurs at intermediate compounding step or inline reactive extrusion, with monitoring for cross-link uniformity and absence of residuals.

    Final product types

    • Engineering-grade thermoset and thermoplastic composites
    • Flame-retardant fiber reinforcements
    • High-durability industrial coatings
    • Adhesive films for electronics and automotive applications

    5. Analytical and Biochemical Reagent Production

    Diagnostic reagent and reference standard producers employ this compound as a key reference and derivatization agent in biochemical assays and analytical method development. Its unique structure offers selectivity in nucleic acid and protein labeling, improving assay sensitivity. Material control and batch-to-batch reproducibility are critical for compliance and reliability in laboratory use.

    Industry compliance standards

    • ISO 13485:2016 for medical device and IVD reagent production
    • USP Reference Standards–compendial purity requirements
    • CLSI (Clinical and Laboratory Standards Institute) guidelines for reagent validation
    • ISO/IEC 17025 laboratory quality management

    Typical usage ratio

    • Final assay preparations use 0.005–0.2 mmol per test batch, determined by required detection limits and assay format. Laboratory optimization ensures yield, reproducibility, and signal clarity.

    Downstream process integration

    • Weighing and dissolving into assay buffer during reagent solution preparation, followed by filtration and aliquoting into diagnostic test kits or calibration standards.

    Final product types

    • Biochemical assay reagent kits
    • Instrument calibration standards
    • Nucleic acid/protein labeling solutions
    • Specialized chromatography detection reagents
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