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HS Code |
925268 |
| Chemical Name | 2,8-Dimercapto-6-Hydroxypurine |
| Cas Number | 570-69-2 |
| Molecular Formula | C5H4N4OS2 |
| Molecular Weight | 200.24 g/mol |
| Synonyms | Thiopurinol; 6-Hydroxy-2,8-dimercaptopurine |
| Appearance | White to off-white solid |
| Melting Point | Above 300°C (decomposes) |
| Solubility In Water | Slightly soluble |
| Pubchem Cid | 68695 |
| Iupac Name | 6-hydroxy-2,8-dimercaptopurine |
| Smiles | C1=NC(=NC2=C1N=CN2S)S |
| Inchi | InChI=1S/C5H4N4OS2/c10-3-2-4(12)8-1-7-5(2)11/h1,10,12H,(H3,7,8,11) |
As an accredited 2,8-Dimercapto-6-Hydroxypurine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,8-Dimercapto-6-Hydroxypurine is supplied in a 5-gram amber glass vial, tightly sealed and labeled with safety information. |
| Shipping | 2,8-Dimercapto-6-Hydroxypurine is shipped in tightly sealed containers under ambient or refrigerated conditions to prevent degradation. The packaging complies with relevant chemical safety regulations, using appropriate hazard labeling. It is transported as a non-bulk chemical and handled with care to avoid exposure, spillage, and environmental contamination. |
| Storage | 2,8-Dimercapto-6-hydroxypurine should be stored in a tightly sealed container, protected from light and moisture, and kept at a cool temperature (typically 2–8°C). Store in a well-ventilated, dry area designated for chemicals, away from incompatible substances such as strong oxidizers. Use only with proper personal protective equipment and ensure the container is properly labeled at all times. |
Applications of 2,8-Dimercapto-6-Hydroxypurine in Industrial ManufacturingAs the direct producer of 2,8-Dimercapto-6-Hydroxypurine, we supply this raw material for several specialized industrial domains. Its well-documented coordination chemistry and functional group reactivity drive precise roles in complex manufacturing chains. Below, we detail four distinct application scenarios, covering regulated compliance frameworks, typical addition rates, integration points in your production sequence, and resulting downstream product forms. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisOur material serves as a sulfur-rich heterocyclic intermediate in the synthesis of selective APIs for chronic heavy metal poisoning treatments. Downstream pharmaceutical operations routinely demand stringent impurity profiles, dictated by licensing authorities. Manufacturers leverage the precise thiol and purine functionalities for targeted metal chelation agent formation, entering multi-step organic syntheses to yield injectable or oral antidote formulations for mercury and arsenic toxicity. Industry compliance standards
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2. Heavy Metal Analytical Reagent ManufacturingExtensive laboratory test kit producers utilize this compound as a selective metal chelator in heavy metal detection systems, particularly for spectrophotometric and electroanalytical assays identifying mercury, cadmium, and arsenic contaminants. Its dual thiol groups enable strong complexes at trace levels, forming critical agents in high-sensitivity field and industrial testing devices required for regulatory compliance in waste management and pharmaceutical QC labs. Industry compliance standards
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3. Process Chemical for Semiconductor Wet Etching2,8-Dimercapto-6-Hydroxypurine features as a functional additive in custom chemical formulations for the microfabrication sector, specifically as a complexing agent for non-oxidative wet etching baths aimed at selective removal of metal contaminants from semiconductor wafers. Its thiol functionality delivers robust copper and precious metal complexation, facilitating precise control in high-purity electronic chemical supply chains for logic and memory fabrication plants. Industry compliance standards
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4. Catalyst Ligand in Precious Metal RecoveryIn precious metal recycling operations, hydrometallurgical refineries use this thiol-purine compound as a complexing ligand during the selective extraction and recovery of gold or platinum group metals from electronic waste solutions. The material forms stable, extractable complexes under controlled pH and redox environments, improving both metal selectivity and environmental compatibility compared to older chelators. Industry compliance standards
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