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8-Azaguanine

    • Product Name 8-Azaguanine
    • Alias 8-Azaguanine
    • Einecs 202-489-8
    • 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

    809014

    Cas Number 134-58-7
    Molecular Formula C4H4N6
    Molecular Weight 136.12
    Iupac Name 7H-pyrrolo[2,3-d]pyrimidin-8-amine
    Appearance Yellow crystalline powder
    Melting Point 320-325°C (dec.)
    Solubility In Water Slightly soluble
    Synonyms 8-Aza-guanine, Azaguanine
    Pubchem Cid 9469
    Storage Temperature 2-8°C
    Pka 1.4 (approximate)
    Chemical Class Purine analogue

    As an accredited 8-Azaguanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 8-Azaguanine, 1g: Supplied in a sealed amber glass vial with a tamper-evident cap, labeled with product details and hazard warnings.
    Shipping 8-Azaguanine is shipped in tightly sealed containers, protected from light and moisture. It is handled as a hazardous material, following all relevant regulations for transportation of chemicals. Shipping includes appropriate labeling and documentation to ensure safe handling and compliance with international, national, and local guidelines. Temperature-sensitive packaging may be used if required.
    Storage 8-Azaguanine should be stored in a tightly closed container, away from moisture, light, and incompatible substances. Keep it in a cool, dry, and well-ventilated area, ideally at 2-8°C (refrigerated). Ensure it is clearly labeled and protected from physical damage. Follow all safety guidelines for hazardous chemicals to prevent contamination or accidental exposure.
    Application of 8-Azaguanine

    Applications of 8-Azaguanine in Industrial Manufacturing

    As a direct manufacturer of 8-Azaguanine, we supply this high-purity heterocyclic base primarily for niche segments in advanced industrial chemistry, especially in regulated and quality-critical areas. Below we outline specific implementation scenarios in core downstream sectors where our material supports established production processes, clear compliance frameworks, and specialized end-use requirements.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antineoplastic Agents

    8-Azaguanine serves an established role as a key intermediate in the synthesis of guanine-analog APIs used in anticancer formulations, particularly for leukemia and lymphoma research and treatment. Its reliable integration into multi-stage small-molecule pharmaceutical synthesis makes it vital for process-scale manufacturing under strict quality environments, contributing directly to the molecular architecture of marketed cytostatic drugs.

    Industry compliance standards

    • US FDA Current Good Manufacturing Practice (cGMP), 21 CFR Parts 210/211
    • EU EudraLex Volume 4 GMP
    • ICH Q7 Good Manufacturing Practice Guidance
    • Ph. Eur., USP, JP monographs as applicable to drug substances

    Typical usage ratio

    • Used at 0.8–3.5% molar ratio in multi-step synthetic pathways; actual concentration aligns with the target API's process yield optimization and impurity profile controls.

    Downstream process integration

    • Fed into nucleophilic substitution or condensation reactions during early or intermediate synthesis cycles, followed by purification stages such as crystallization or chromatography in GMP suites.

    Final product types

    • Bulk APIs for injectable cytostatic pharmaceuticals
    • Formulated anticancer tablets and capsules

    2. Reference Compound Production for Clinical Research Diagnostics

    Academic and clinical laboratories employ 8-Azaguanine as a certified reference material (CRM) for quantifying purine analogs in biological assays and calibrating analytical instrumentation. Consistent batch quality and traceability to formal standards underpin its use in regulated environments for the validation and control of diagnostic and pharmacokinetic procedures.

    Industry compliance standards

    • ISO 17034: General Requirements for the Competence of Reference Material Producers
    • ISO/IEC 17025: Laboratory Accreditation
    • FDA/EMA bioanalytical method validation guidance
    • CAP Clinical Laboratory Improvement Amendments (CLIA)

    Typical usage ratio

    • Diluted and reconstituted at 50–500 μmol/L range depending on calibration curve and matrix specification set by analytical protocol.

    Downstream process integration

    • Processed during CRM formulation and spiked into matrix-matched media for proficiency testing, then aliquoted into vialed formats for distribution as analytical kits or standards.

    Final product types

    • Certified reference materials for laboratory QC
    • Analytical calibration standard sets for LC-MS, HPLC, and immunoassays

    3. Molecular Biology Reagent Formulation

    Life science reagent manufacturers include 8-Azaguanine as a selective agent in cell culture media, exploiting its antimetabolite properties to regulate gene expression in mutant selection protocols. High batch purity, precise assay, and minimal trace contaminants ensure compatibility with sensitive cell-based and in vitro genetic manipulation workflows.

    Industry compliance standards

    • ISO 13485: Medical Device Quality Management Systems for reagent manufacturers
    • OECD Principles of Good Laboratory Practice (GLP)
    • US NIH Recombinant DNA Advisory Guidelines
    • ATCC cell culture certification requirements

    Typical usage ratio

    • 0.5–10 μg/mL in prepared cell culture media, with concentrations adjusted to organism sensitivity and selection pressure required in screening assays.

    Downstream process integration

    • Introduced post-sterilization into nutrient-rich growth media, followed by filtration and packaging into ready-to-use bottles or amphorae for research use.

    Final product types

    • Custom selective growth media for bacteria, fungi, or mammalian cell lines
    • Genetic engineering screening kits

    4. Genotoxicity and Cytotoxicity Testing Controls

    Regulated contract laboratories and in-house QA groups use 8-Azaguanine as a positive control in genotoxicity screening, specifically evaluating cellular response via forward mutation assays. The material supports protocol consistency across research institutions, ensuring inter-laboratory data comparability and regulatory submission integrity.

    Industry compliance standards

    • OECD Test Guideline 476: In Vitro Mammalian Cell Gene Mutation Test
    • GLP Compliance (21 CFR Part 58, Directive 2004/10/EC)
    • EPA Good Laboratory Practice Standard
    • ICH S2(R1) Guidance on Genotoxicity Testing

    Typical usage ratio

    • 10–150 μM in suspension or monolayer cell test environments; range adjusted based on cell species and exposure protocol per GLP method SOPs.

    Downstream process integration

    • Dosed directly into control wells or flasks during the cell culture pre-exposure phase, with downstream collection post-assay for analysis by flow cytometry or microscopy.

    Final product types

    • Positive control panels for in vitro genetic toxicology test kits
    • OEM cytotoxicity assessment reagents
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    Certification & Compliance
    More Introduction

    8-Azaguanine: Stepping Into the Details of a Key Antimetabolite

    What 8-Azaguanine Brings to the Table

    Over many years, our team has had the chance to see questions and requests roll in for 8-Azaguanine from scientific groups and pharmaceutical developers around the world. This molecule is anything but an everyday chemical. As a factory manufacturer, we’ve seen first-hand how its special construction—bearing a nitrogen atom that disrupts the guanine ring—makes it stand out among purine analogues. People often look for it under the CAS number 134-58-7 or by its systematic name, but for us, it is the unique chemistry and value it contributes to ambitious projects in research and medicine that matter the most.

    8-Azaguanine, in our hands, comes out as a white to faintly off-white crystalline powder. Attention to detail matters at every stage, and we always make sure the purity surpasses the 98% mark as checked by HPLC. Some clients have asked for higher specs for certain clinical or research protocols, and these demands help us sharpen our process—always refining, always learning. Moisture content and particle size matter a lot for stability and processability, so our teams keep both under check during packaging.

    Uses We’ve Witnessed and Supported Directly

    What separates 8-Azaguanine from more common reagents and building blocks is the way it zeroes in on metabolic pathways. Its greatest role comes in biomedical research as an antimetabolite, where it serves as a useful tool for scientists trying to understand or disrupt nucleic acid biosynthesis. Since it inhibits nucleotide synthesis, it is often used in cell culture protocols for selecting genetically engineered cells by causing death in cells that don’t carry a specific resistance. Research hospitals and universities order it for preclinical studies on leukemia and other malignancies, while pharmaceutical labs have explored its value for crafting new mechanistic insights into tumor resistance and purine analog engagement.

    For us, packing and shipping 8-Azaguanine means engaging with groups who run clinical labs, university departments, and biotech research teams. It isn’t intended for end-use in humans as a finished pharmaceutical, but it forms the backbone of significant steps taken in the direction of new therapy discovery and mechanism validation. Tailoring batch sizes to the scope of the project—whether it’s a few grams for an exploratory assay or kilo quantities for a sustained R&D pipeline—we’ve watched teams leverage this compound to move cancer cell research forward.

    The Experience and Vigilance Behind Each Batch

    Manufacturing 8-Azaguanine differs from turning out standard reagents. The precursor inputs need scrutinizing—impurity profiles in the aza series often lead to troublesome downline issues if not carefully managed. Our facility has invested in additional steps, extending synthesis and purification so protein or nucleic acid-bound byproducts don’t sneak through and complicate downstream cell biology work. We've set up our own standards for residual solvents and heavy metals, following up with external tests to satisfy the protocols universities and pharma companies often share with us.

    We ensure that our 8-Azaguanine holds to narrow melting range requirements and clean NMR profiles, points that rarely get their due credit unless you’ve watched an inconsistent batch throw off a critical research sequence. Each time a batch leaves our facility, it carries the mark of our own process validation—a record that most academic or research customers choose to review before signing on for recurring orders. These are not regulatory box-ticking routines; these come from repeated questions we’ve faced from research groups who learned the price of cutting corners in purity or handling.

    Solubility, Storage, and Stability as Lived by Lab Teams

    The practicalities of working with 8-Azaguanine lie in something more concrete than spec sheets. Most of our clients dissolve the powder in dilute sodium hydroxide or DMSO for cell culture and selection assays. It's not the most water-soluble base compound, making careful handling and dissolution protocols essential for getting reliable results. We archive feedback from client labs and share pointers on temperature and humidity management to prevent degradation; we’ve found it best kept in well-sealed containers away from light and high temperatures, usually in cold storage under dry conditions.

    In rare cases, clients report slight yellowing during prolonged storage because of trace moisture or slow oxidation. For these customers, we discuss options for vacuum-packing or nitrogen-flush packaging to push out shelf life, especially for researchers making bulk orders that last a full academic year. Few suppliers account for these needs. They only surface after someone’s experiment is set back a month waiting for a new lot to ship out.

    8-Azaguanine vs. Other Guanine Analogues: A Direct Perspective

    People often ask us how 8-Azaguanine compares to related compounds such as 6-mercaptopurine, azathioprine, or other aza-substituted purines. The core distinction lies in the mechanism. By substituting at the 8-position on the purine ring, 8-Azaguanine interferes with DNA and RNA synthesis in ways different from the thiopurine compounds or standard guanine analogues. Some researchers expect overlapping results between analogues, but as several studies in the literature show, resistance profiles, cytotoxicity, and methylation patterns diverge once the analogues are put through their paces in cultured cells.

    Handling also makes a difference. 6-Mercaptopurine may degrade faster if left at room temperature, while 8-Azaguanine’s stability under dry refrigeration gives longer shelf life between uses. In our experience, solvent choice becomes more important with 8-Azaguanine compared to other antimetabolites, so users should double-check their experimental design against published protocols.

    From a manufacturing point of view, synthesizing pure 8-Azaguanine takes extra caution compared to guanine or adenine derivatives. False positive peaks often turn up during analytical testing, misread as product, unless you fine-tune your HPLC and set up the right reference standards. Compared to nucleoside analogues, 8-Azaguanine doesn't need the extra glycosylation step, but that simplification is offset by more complex workup requirements to exclude closely related impurities.

    Cost, too, is a concern for users deciding between alternatives. 8-Azaguanine runs higher per gram than other guanine derivatives due to demanding purification and the smaller market footprint. But for researchers, this upfront investment reduces experimental uncertainty or contamination-driven batch failure. The real cost often shows up only downstream, when a slightly cheaper benchmark leads to data that can't be replicated or interpreted with confidence.

    Guidance Rooted in Real-World Demands

    Our experience supplying 8-Azaguanine paints a clear picture: educational teams, research consortia, and industrial innovators rarely look for a ‘plug-and-play’ material. They reach out with case-specific questions, seeking batch records, performance histories, or tailored logistics for storage and handling. We walk them through packaging choices, split shipments, and validated cold chain logistics when needed.

    Each year, demand shifts. Some years, more orders come in from oncology labs exploring resistance mechanisms; in other cycles, molecular biology and genetics departments use it for selection protocols. Requests for documentation—the actual chromatograms, thermal scans, or impurity studies we keep on hand—track closely with new journals or grant proposals. There’s a natural ebb and flow, and as a manufacturer rooted in chemical synthesis, every query helps us tune future production and client support.

    Environmental considerations have changed in recent years. Our facility keeps a keen eye on waste minimization and water usage in each synthetic campaign. We collect feedback on packaging waste and look for more sustainable forms and recyclable vials where possible. Some universities request batch-specific origins and greener chemistry validation, giving us a chance to highlight low-solvent protocols that trim down environmental load. These aren’t sales pitches—they come from student and faculty priorities, echoed as procurement policies shift toward lower-impact chemistry.

    Challenges Our Partners Face (and How We Work With Them)

    The journey of 8-Azaguanine from lab bench to procurement isn’t always smooth. Universities, in particular, face longer timelines for customs clearance and inventory accounting. Delays in order processing force researchers to rethink study timing, laboratory workflow, and sometimes even results reporting. We engage with these partners to pre-book batches, offer rolling stock storage, or keep standby lots for tight project deadlines. Flexible logistics aren’t just a convenience—they keep essential projects moving instead of stalling out.

    Research staff often request reassurance that the supplied 8-Azaguanine will behave as expected in their hands. To answer those concerns, we routinely test random reserve samples from past production runs and track any deviation from previously reported assay or impurity results. When problems arise—such as solubility issues in specific media or unexplained color changes—we don’t send off a form letter or blame shipping: our chemists work directly with the customer to puzzle through the steps, sometimes reproducing their protocol in our own application lab. Hearing an end-user describe an unexpected hiccup has led us to tweak our own process on several occasions.

    The Human Element: Batch-to-Batch Consistency Beyond Certificates

    People in research work hard for their funding and build timelines around each delivery. As a manufacturer, we know that the most valuable ‘feature’ of our 8-Azaguanine lies in consistency and the human attention behind each lot. Purity isn’t about one-off numbers—it’s about predictable outcomes, project after project. Failing to hit the mark leads to trouble far beyond a returned order: it sidetracks research programs and makes for wasted work. Every certificate of analysis is more than just paperwork; it is a sign of accountability to those relying on our production integrity.

    Several repeat customers have told us how disruptions from inconsistent suppliers in the past forced them to halt studies mid-way. Our premise is straightforward: maintain a rigorously documented production system, keep retention samples from every lot, and publish the full analytical record upon request for academic and industry users alike. The traceability connects lot records back to every shift on our manufacturing floor and every maintenance interval on our reactors. It’s a level of transparency that requires more work, but trust takes years to earn and only a shipment or two to lose.

    Tracking the Bigger Trends: Regulatory, Safety, and Scientific Progress

    We stay aware of the landscape around 8-Azaguanine. KYC and controlled substance reviews come into play in some regions due to its clinical history, though it isn’t subject to the strict regulations of anticancer drugs currently on the market. Safety documents and shipping certifications update every time new rules get published, and we make sure both lab and logistics staff train and verify before every international delivery.

    In the broader world, more journals and grant-making bodies are calling for higher traceability and verifiable impurity profiles. Researchers expect more than a PDF datasheet—they look for real analytical traces, method summaries, and post-shipping stability data. As academic science aligns with transparency mandates, our workflow adapts: retaining long-term samples, rechecking lots years after production, running blind duplicate tests, and enabling scientists to compare test runs from 8-Azaguanine with other analogues directly with their own equipment and protocols.

    Future Directions: Scaling Production, Supporting Breakthroughs

    We hear regularly from customers planning extensive genetic selection campaigns, multi-year studies, or even pilot-scale process development for novel therapeutics. Their needs call for repeat supply and uniform performance. Scaling up production of 8-Azaguanine, though challenging, fits this collaborative model: the more we standardize and automate purification and analysis, the easier it becomes for research teams to forecast, replicate, and publish results based on trusted input material.

    As our own process chemists keep pace with evolving synthesis tech and analytical tools, we invest in both equipment and people. We monitor growing demand in Asia and North America and commit to batch reservation for those with grant-linked timelines. We invite researchers to share their findings, point out where actual vs. stated performances diverge, and partner with us to reshape our production and data management. Every kilogram that ships from our facility carries a record of the work behind it, and every report back from the field helps guide how we improve next time.

    Closing Thoughts: The Value of Experience Over Hype

    With every lot of 8-Azaguanine we produce, the core driver remains the same: trust. We have seen how genuine relationships and attention to detail save money, prevent repeat experiments, and push research toward real progress. There’s no one-size-fits-all solution in specialty chemicals—especially those as challenging and as valuable as antimetabolites like 8-Azaguanine. By sticking close to the needs and feedback of the end users, keeping batch histories transparent, and refusing to cut corners, we know the work we put into each order will help further discoveries in cancer biology, genetics, or drug design for years to come.

    For all the new techniques and ambitions research teams are bringing to the table, success keeps coming back to the reliability of starting materials. We see our work as more than supply—it’s about mutual confidence, steady quality, and giving science a foundation to build on, molecule by molecule.