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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 | 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. |
Applications of 4,6-Diamino-2-Mercaptopyrimidine in Industrial ManufacturingAs 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 SynthesisMajor 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
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2. Oxidative Hair Dye FormulationLeading 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
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3. Metal Surface Corrosion InhibitionSpecialty 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
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4. High-Performance Polymer ModificationPolymer 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
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5. Analytical and Biochemical Reagent ProductionDiagnostic 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
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