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2,4-Diamino-6-Mercaptopyrimidine

    • Product Name 2,4-Diamino-6-Mercaptopyrimidine
    • Alias 2,4-Diamino-6-mercapto-pyrimidine
    • Einecs 212-844-2
    • 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

    273260

    Cas Number 1906-16-3
    Molecular Formula C4H6N4S
    Molecular Weight 142.18 g/mol
    Appearance White to off-white powder
    Melting Point 275-278°C (decomposes)
    Solubility In Water Slightly soluble
    Iupac Name 2,4-diamino-6-sulfanylpyrimidine
    Synonyms 6-Mercapto-2,4-diaminopyrimidine
    Storage Conditions Store at room temperature, protect from moisture

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

    Packing & Storage
    Packing 100 grams of 2,4-Diamino-6-Mercaptopyrimidine is packaged in a sealed amber glass bottle with clear labeling and hazard warnings.
    Shipping 2,4-Diamino-6-Mercaptopyrimidine is shipped in tightly sealed, chemical-resistant containers to prevent moisture or air exposure. Packaging complies with relevant hazardous material regulations. Containers are clearly labeled and cushioned to avoid breakage during transport. Shipping is typically performed by certified carriers, ensuring safe and compliant handling for laboratory or industrial use.
    Storage 2,4-Diamino-6-Mercaptopyrimidine should be stored in a cool, dry, and well-ventilated area, away from sources of moisture and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Store in a tightly sealed container and clearly label the storage area to avoid accidents. Follow all relevant safety guidelines for handling hazardous chemicals.
    Application of 2,4-Diamino-6-Mercaptopyrimidine

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

    2,4-Diamino-6-Mercaptopyrimidine serves as a critical intermediate in advanced chemical manufacturing. Our factory-scale production supports specialized industrial sectors that demand precise quality control and consistent supply. Below, we outline core segments where this compound directly enables downstream innovation and differentiated product value.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical intermediates manufacturers use 2,4-Diamino-6-Mercaptopyrimidine for the construction of heterocyclic scaffolds in antiviral and anticancer active pharmaceutical ingredients (APIs). It acts as a nucleophilic building block in multi-step synthesis, often forming the core of pyrimidine-based molecules via precise substitution and coupling reactions. This compound’s purity and reactivity directly influence downstream batch validation, regulatory audits, and process yield.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP; FDA 21 CFR Part 211)
    • ICH Q7 Guideline for Active Pharmaceutical Ingredient Manufacturing
    • USP/NF standards for intermediates and final APIs
    • European Pharmacopoeia (Ph. Eur.) where applicable in synthesis

    Typical usage ratio

    • 5%–15% by molar ratio relative to main substrate; precise charge depends on target API structure and protection/deprotection sequence

    Downstream process integration

    • Introduced after initial ring-forming steps as the nucleophilic agent
    • Batch-fed in reactors during condensation and amination transformations
    • Reacts under controlled pH (7–9) and solvent conditions
    • Critical for maintaining compound chirality in step-growth polymerizations

    Final product types

    • Antiviral drug APIs (e.g., certain nucleoside/tide analogues)
    • Anticancer agent intermediates
    • Pyrimidine-based diagnostic reagents
    • Second-generation heterocyclic pharmaceuticals

    2. Inhibitors for Industrial Enzyme Formulation

    Producers in the biochemical sector employ this compound to synthesize selective pyrimidine-based inhibitors that modulate key enzymatic pathways used in fermentation and biotechnology. By precisely introducing the mercapto group, formulators adjust molecular affinity for specific enzyme targets, improving downstream process selectivity while controlling unwanted side reactions during batch or continuous operations.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for Bioprocess Manufacturing)
    • OECD Guidelines for Testing of Chemicals (where inhibitor action is validated)
    • REACH Regulation (EC) No 1907/2006
    • Product-specific safety data sheets and process hazard analysis documentation

    Typical usage ratio

    • 0.01%–0.5% by weight in enzyme inhibitor formulation; adjusted according to activity assay and enzyme kinetics

    Downstream process integration

    • Added during final synthesis stage of inhibitor molecules
    • Key reactant in substitution/coupling steps within R&D or pilot fermentation trials
    • Directly impacts yield and selectivity indices in scale-up
    • Integrated into liquid or lyophilized enzyme inhibitor products

    Final product types

    • Enzyme inhibitor cocktails for industrial fermentation
    • Research-grade enzymatic assay reagents
    • Process aids for biosynthetic manufacturing lines
    • Fermentation-stability additives

    3. Corrosion Inhibitor Additives in Metal Processing

    Metal surface treatment facilities use 2,4-Diamino-6-Mercaptopyrimidine as a functional moiety in the synthesis of organic corrosion inhibitors, specifically for copper and aluminum alloys. Formulators leverage its mercapto functionality to create compounds with high affinity for metal ions, effectively passivating surfaces in acid-cleaning or pickling baths. PRODUCT ensures minimized residue, predictable layer thickness, and compatibility with downstream plating or painting steps.

    Industry compliance standards

    • ISO 8044:2020 (Corrosion of Metals and Alloys—Basic Terms and Definitions)
    • RoHS Directive 2011/65/EU for allowable additive levels in electronic and metal assemblies
    • Production safety requirements under OSHA 29 CFR Part 1910
    • Local environmental discharge standards for process chemicals

    Typical usage ratio

    • 200–600 mg/L in inhibitor concentrate; diluted 1:100–1:1000 in metalworking baths based on alloy type and bath volume

    Downstream process integration

    • Pre-mixed with aqueous corrosion inhibitor concentrates
    • Meter-fed into surface treatment tanks after cleaning but before passivation
    • Maintained at target pH (1.5–4) and monitored by in-line sensors
    • Followed by rinsing and downstream metal finishing

    Final product types

    • Acidic corrosion inhibitor blends for copper circuits
    • Pickling inhibitors for automotive and aerospace aluminum
    • Electronic component cleaning solutions
    • Corrosion-prevention fluids for export packaging

    4. Dye Intermediate for Specialty Hair Colorants

    Manufacturers in the cosmetic dye sector select this compound as a high-purity intermediate in oxidative hair colorant production. It forms part of advanced pyrimidine chromophore systems, reacting with specific developers to yield stable, non-fading color molecules. Batch-to-batch uniformity in input quality allows precise control of shade development and mitigates allergenic risk in finished oxidative dyes formulated for global compliance.

    Industry compliance standards

    • EU Cosmetics Regulation EC No 1223/2009
    • U.S. Food, Drug, and Cosmetic Act (21 CFR Parts 70, 73) for hair dye precursors
    • Japanese Standards of Quasi-drug Ingredients (JSQI)
    • Product-specific IFRA standards and global cosmetic ingredient inventories (CosIng, IECIC)

    Typical usage ratio

    • 0.1%–2.5% by weight in final hair dye formulation, adjusted based on shade, base formula, and regional safety limits

    Downstream process integration

    • Converted into chromophore intermediate in stage two or three of multi-step batch synthesis
    • Mixed with color developer and coupler components under controlled pH (8–10)
    • Subjected to color yield and safety/irritancy testing before final blending
    • QC testing for impurity profile and regulatory conformance

    Final product types

    • Permanent oxidative hair colorants
    • Specialty tone-correcting creams
    • Professional hair bleaching agents with chroma stabilization
    • High-resistance hair coloring kits for retail and salon use

    5. Thio-Functionalized Monomer for Polymer Modification

    Specialty polymer manufacturers utilize 2,4-Diamino-6-Mercaptopyrimidine as a thio-containing comonomer in advanced resin synthesis. Its introduction imparts tailored cross-linking, improved chemical resistance, and defined mechanical flexibility in engineered polymer matrices. Input consistency from our manufacturing process provides downstream processors with predictable molecular weight distribution and reactivity for both solution and melt-phase polymerization.

    Industry compliance standards

    • ISO 9001:2015 (for polymer production/quality control)
    • FDA 21 CFR 177 (Polymers for indirect food contact, where applicable)
    • ASTM D256 and D638 for mechanical testing of modified polymers
    • RoHS and REACH compliance for downstream electronic and packaging applications

    Typical usage ratio

    • 0.5–3% by molar content as monomeric modifier; adjusted based on polymer backbone structure and application performance target

    Downstream process integration

    • Meter-fed into reactor during pre-polymerization or chain extension stage
    • Blended into bulk monomer feed in solution or melt phase
    • Monitored via in-process NMR or GPC to optimize distribution
    • Contributes active thio site for post-polymer functionalization

    Final product types

    • Flexible printed circuit board (FPCB) adhesives
    • Specialty coatings with enhanced chemical resistance
    • Chemical-resistant membranes and films
    • Elastomer-modified engineering plastics
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    Certification & Compliance
    More Introduction

    2,4-Diamino-6-Mercaptopyrimidine: Real-World Insights from a Manufacturer’s Floor

    Getting to Know 2,4-Diamino-6-Mercaptopyrimidine

    Making 2,4-Diamino-6-Mercaptopyrimidine is not straightforward, but after years of refining the synthesis steps and troubleshooting bottlenecks, a routine has taken hold in our production line. We recognize this compound by its off-white to pale yellow crystalline appearance—a reliable standout from the closely-related pyrimidine derivatives lining our storage shelves. Each batch delivers a distinct sulfur note, unmistakable whether you’re in the lab filling jars or out on the operations floor.

    Chemists who work with this product know its structure up close: a pyrimidine ring with amino groups at positions 2 and 4, and a mercapto group at the 6 position. This arrangement creates a platform for robust nucleophilic substitution reactions, often asked for in custom synthesis projects, and a go-to intermediate for novel heterocyclic scaffolds. We rely on high-purity standards, and use our in-house chromatographic and spectroscopic equipment to verify every lot exceeds 98% purity as determined by HPLC. This attention to quality has practical results—with predictable crystalline form, manageable flowability, and minimal fines, handling large batches doesn’t demand specialized containment beyond our safety best practices.

    Practical Applications and Industry Feedback

    Over the years, our customer base has brought this compound into pharmaceutical research most often, where its core structure fits well as a building block in the synthesis of antimetabolites, kinase inhibitors, and other pyrimidine-based drug candidates. Research groups often modify the thiol or amino groups to introduce additional biological activity or to link the molecule to other pharmacophores. Biotech clients reach out for kilogram quantities for lead optimization campaigns, while agrochemical R&D labs look for high-quality intermediates for the development of crop protection actives.

    This product found its way into organic electronics labs, too, where the thiol handles enable covalent attachment to gold surfaces or metal nanoparticles. Device engineers appreciate a product that doesn’t vary in crystal size from order to order, reducing headaches from inconsistent solubility or film formation in test batches.

    Differentiating from Related Pyrimidine Compounds

    Our experience has shown that 2,4-Diamino-6-Mercaptopyrimidine stands apart from other pyrimidine derivatives such as 2,4,6-triaminopyrimidine or mercaptopurines. The presence of the mercapto group at position 6 opens doors for derivatization that aren’t possible with an amino group or simple hydrogen. For example, this thiol group forms disulfides under mild conditions, supporting straightforward conjugations that many downstream developers require.

    Comparing to standard diaminopyrimidine salts, 2,4-Diamino-6-Mercaptopyrimidine requires tighter moisture control during storage. Our production line addresses this by nitrogen-purging the packaging station and maintaining relative humidity below 30% in the packaging suite. Shipment in lined, air-tight containers has reduced product clumping and preserved batch quality for clients with extended development timelines.

    Process chemists from several partner facilities highlight the difference in reactivity: 2,4,6-triaminopyrimidine tends to favor substitution on the ring, while 2,4-Diamino-6-Mercaptopyrimidine allows sulfur-centric transformations, which are critical for certain enzyme inhibitors and labeling studies. For direct gold-thiol binding, few alternatives hold up to the stability and reliability we see with this compound.

    Production Insights and What Drives Stable Quality

    In-house production cuts out delays and variability caused by outsourcing most steps. Starting with pyrimidine-2,4,6-triol, we carry out amination under controlled temperature and pressure, then introduce thiol via chlorination followed by thiourea substitution. An on-line process analyzer checks by-products mid-run, and our experienced shift operators fine-tune pH and reflux conditions to maintain high conversion rates while keeping side reactions in check.

    Routine difficulties, like sulfur oxidation or overamination, are minimized by closely monitoring batch progression instead of relying on “set and forget” automation. The final isolation by filtration, washing, and vacuum drying ensures the product comes off the line at low residual solvent and consistent particle size. Every kilo packaged has been handled by a production team member who knows the purpose of each process parameter. This is not simply a “commodity chemical”—every lot reflects incremental improvements drawn from feedback, both internal and from our partners.

    Challenges with Stability, Handling, and Downstream Use

    Freshly produced 2,4-Diamino-6-Mercaptopyrimidine holds up well under dry, room temperature storage. Several years ago, we learned that careless packaging leads to subtle caking and eventual loss of free-flowing quality—something researchers notice as soon as a container is opened. For solvent-based reactions, clumped powder creates uneven dissolution, so we spent months revising drying and sieving steps until particle aggregation problems dropped noticeably.

    Safety is always part of our consideration. While this compound has not demonstrated acute toxicity typical of some analogs, its sulfur group leads to a mild odor and the potential for skin or eye irritation. Our production and QA staff use full PPE during handling and packaging, and recommend similar controls for users. Bulk storage in our facility uses stainless steel bins and sealed containers to minimize cross-contamination with related intermediates.

    Supporting Custom Applications

    Each year brings requests from formulators and researchers needing new variations on 2,4-Diamino-6-Mercaptopyrimidine. The mercapto group placement, combined with the diamino configuration, makes it a strong candidate for metal coordination chemistry. We frequently collaborate with development chemists who incorporate the product into screening libraries using standard coupling or thiol-click methods. Some of these collaborations have led to improvements in our isolation steps, making the transfer from bench-scale to pilot runs more efficient.

    For clients who require analytical documentation, our quality control group provides NMR, IR, HPLC, and elemental analysis certificates on request. In recent years, we’ve participated in round-robin proficiency testing with university labs to further validate our sample consistency and reliability, a step that helps us respond promptly to customer inquiries with data drawn from our regular QC archive.

    What Sets Our Product Apart

    Routine testing and customer feedback highlight distinct differences between 2,4-Diamino-6-Mercaptopyrimidine and other pyrimidine derivatives currently in the market. Many of our competitors, including global trading houses, do not synthesize in-house, and their products often show inconsistent purity or contamination with isomeric by-products such as 6-thioxo-2,4-diaminopyrimidine. This inconsistency can mean unexpected reactivity in downstream applications, a headache we have managed to avoid with strict batch-level checks.

    Our commitment to supporting scale-up has made a difference in several multi-year projects. Providing reproducible, kilogram-scale orders over many batches allows our customers to focus on developing new synthetic routes without worrying that a subtle impurity will throw off critical experiments. When difficulties arise with solubility or downstream reactivity, we work directly with partners to pinpoint any production factors at play, revisiting each step to optimize particle size or impurity content where needed.

    Pursuing Sustainability and Safe Manufacturing

    The chemical industry faces growing scrutiny regarding environmental footprint and waste stream regulation. We see challenges ahead, especially for sulfur-based intermediates, which can produce malodorous emissions if handled without care. Over the past decade, we have progressively replaced traditional chlorinated solvents with recoverable alternatives and use closed-system batch reactors to minimize operator exposure and fugitive emissions.

    Waste minimization hasn’t just been a regulatory concern—it has led to real cost savings on the ground. By recapturing thiourea from mother liquors and using onsite solvent distillation, we have nearly halved the volume of hazardous waste per kilogram produced compared to numbers from a decade ago. These adjustments forced us to reconsider certain long-standing steps, but now pay dividends in both equipment longevity and staff safety.

    Future Opportunities and Ongoing Learning

    The landscape of functionalized pyrimidines continues to evolve, and we continuously track publication trends and patent activity to anticipate the directions of demand. In the coming years, we expect more targeted applications of 2,4-Diamino-6-Mercaptopyrimidine in the areas of sensor technology, bioorthogonal chemistry, and potentially new classes of antifolates or allosteric enzyme modulators. By maintaining in-house technical expertise and open lines of communication with formulation partners, we can respond swiftly as the market shifts.

    Each process improvement or efficiency tweak traces back to hands-on troubleshooting—observing a filtration issue, reviewing purity profiles, or discussing solubility quirks directly with users. The lessons learned from past missteps inform ongoing process validation and operator training, and we maintain an archive of “lessons learned” case notes that assists new technical staff and project leads to build from succeeded, failed, and adapted approaches.

    Conclusion: Manufacturing Experience Defines Product Reliability

    Supplying 2,4-Diamino-6-Mercaptopyrimidine has sharpened our awareness of how bench-scale results differ from full-run manufacturing. By taking charge of synthesis, purification, packaging, and support, we have seen the difference consistent manufacturing can make for our partners. Our team brings both broad chemical know-how and direct familiarity with the day-in, day-out challenges of producing specialized building blocks for science-driven industries. The experience we’ve built with 2,4-Diamino-6-Mercaptopyrimidine doesn’t just show in our finished product; it informs the way we troubleshoot, collaborate, and keep pushing for better reliability in every order shipped out the door.