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6-Amino-3,7-Dihydro-2H-Purin-2-One

    • Product Name 6-Amino-3,7-Dihydro-2H-Purin-2-One
    • Alias Guanine
    • Einecs 207-487-7
    • 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
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    Specifications

    HS Code

    318867

    Iupac Name 6-Amino-3,7-dihydro-2H-purin-2-one
    Molecular Formula C5H5N5O
    Molecular Weight 151.13 g/mol
    Cas Number 73-24-5
    Synonyms Guanine
    Appearance White crystalline powder
    Melting Point 350 °C (decomposes)
    Solubility In Water Slightly soluble
    Density 2.2 g/cm³
    Pka 2.4, 9.2
    Pubchem Cid 135398633
    Structure Type Purine derivative
    Logp -1.2
    Usage Nucleobase in DNA and RNA

    As an accredited 6-Amino-3,7-Dihydro-2H-Purin-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g 6-Amino-3,7-Dihydro-2H-Purin-2-One is packaged in a sealed amber glass bottle with a white screw cap.
    Shipping **Shipping Description:** 6-Amino-3,7-dihydro-2H-purin-2-one is shipped in airtight, sealed containers to maintain stability and purity. Packaging complies with chemical safety regulations for secure transport. Ensure the product is kept dry and away from incompatible substances. Appropriate documentation and labeling are included for safe and traceable delivery.
    Storage 6-Amino-3,7-dihydro-2H-purin-2-one should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep in a cool, dry, and well-ventilated area, ideally at room temperature or as recommended on the chemical’s datasheet. Ensure the storage area is clearly labeled and complies with local chemical safety regulations.
    Application of 6-Amino-3,7-Dihydro-2H-Purin-2-One

    Applications of 6-Amino-3,7-Dihydro-2H-Purin-2-One in Industrial Manufacturing

    As the original manufacturer specializing in chemical raw material production, we supply 6-Amino-3,7-Dihydro-2H-Purin-2-One for several distinct industrial sectors. Drawing on direct feedback from producers and our experience with customer formulation development, we highlight how this purine derivative supports precise process requirements across regulated, high-value downstream manufacturing segments.

    1. Synthesis of Pharmaceutical Intermediates for Antiviral APIs

    This compound serves as a building block in multi-step synthesis routes for guanine-type nucleotide analogues used in antiviral active pharmaceutical ingredient (API) production. Manufacturers incorporate it during early-stage condensation and amidation steps, underpinning high-purity pharmaceutical intermediates under strictly controlled environments. Adjustments in input ratio directly respond to reaction scale and intended downstream molecule complexity, with process engineers monitoring impurity profiles and residue levels to fit regulated thresholds.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia – National Formulary) monographs for substances and intermediates
    • EU GMP (EudraLex Volume 4) guidelines
    • Chinese Pharmacopoeia standards for synthetic intermediates

    Typical usage ratio

    • Reactant input ranges from 0.8 molar equivalents up to 1.2 molar equivalents relative to coupling chlorides, varied by batch size and impurity removal needs
    • Adjustment depends on target yield and downstream step requirements

    Downstream process integration

    • Introduced at the nucleobase coupling phase after initial precursor activation in glass-lined reactors
    • Progresses via acid-base catalysis, followed by isolation and purification with chromatographic units

    Final product types

    • Intermediate substances for anti-viral agents (e.g., Acyclovir, Ganciclovir)
    • Synthons for nucleoside and nucleotide therapeutics

    2. High-Purity Reagents for Molecular Biology and Life Sciences

    Biotech laboratories and diagnostics manufacturers use this molecule as a nucleobase precursor in the large-scale synthesis of oligonucleotides and custom primer sets. Quality control protocols enforce ultra-low residual metal and endotoxin requirements, with incoming lots sampled for absorption spectra and impurity traceability. Purity and consistent performance remain key for end-use in PCR assays and gene sequencing kit production.

    Industry compliance standards

    • ISO 13485:2016 (Quality Management for Medical Devices and Diagnostics)
    • cGMP guidelines for molecular biology reagents
    • Certificate of Analysis (COA) with trace metal and microbiological limits based on customer protocols

    Typical usage ratio

    • Formulation levels typically between 0.2% to 1% w/w of total reagent blend, with scaling based on target oligonucleotide length and throughput
    • Adjusted according to desired batch volume and process scaling

    Downstream process integration

    • Dosed at the initial nucleoside assembly phase using automated synthesizers
    • Followed by solvent-based purification and lyophilization to achieve analytical purity

    Final product types

    • Synthetic primers and probes for PCR and qPCR kits
    • Custom DNA/RNA oligonucleotides for sequencing platforms

    3. Precursor in Agrochemical Synthesis (Plant Growth Regulators)

    Industrial agrochemical formulators rely on this purine structure as a core nucleobase precursor during controlled syntheses of certain cytokinin-type plant growth regulators. Purity and batch traceability strongly influence regulatory registration and environmental safety data. Process managers adjust input mass to match conversion rates during alkylation or glycosylation steps while minimizing structural byproducts prior to formulation.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • REACH (EU Regulation No 1907/2006) for chemical safety in agrochemicals
    • ISO 9001:2015 for agro-input quality assurance

    Typical usage ratio

    • Standard loading at 0.5–2% by weight in synthetic reaction vessels, modified according to batch conversion rates and target cytokinin compound yield

    Downstream process integration

    • Added during the precursor condensation phase prior to final cyclization and formulation
    • Subsequent purification through crystallization and solvent extraction units

    Final product types

    • Intermediate forms of synthetic cytokinins, such as 6-Benzylaminopurine (6-BA)
    • Bulk technical-grade plant growth regulators for crop formulation

    4. Electronic and Semiconductor Grade Precursors for Organic Synthesis

    Specialty electronics and semiconductor fabricators use this molecule as a traceable organic precursor in the manufacture of purine-based conducting polymers and advanced functional coatings. Engineering teams stipulate low ionic contaminant requirement, with dosing managed through automated powder feeders to support ultra-high-purity synthesis lines. Product managers adjust feedstock ratios to optimize conductivity and layer uniformity while controlling downstream polymerization kinetics.

    Industry compliance standards

    • SEMI C94 (Specifications for Electronic Chemical Purity Levels)
    • ISO 14644 (Cleanroom and controlled environment standards)
    • Internal customer validation protocols for trace organic compounds

    Typical usage ratio

    • Loaded at 0.1–0.5% by weight in functional organic synthesis, variably increased when higher layer conductivity or permittivity is targeted

    Downstream process integration

    • Fed during in situ polymerization or chemical vapor deposition stages within inert atmosphere modules
    • Integrated as a seeding agent for co-polymerization with aromatic or heterocyclic substrates

    Final product types

    • Electronically active thin films for microelectronic device packaging
    • Purine-based conductive polymer intermediates

    5. Specialty Ink and Dye Formulations for Secure Document Printing

    Producers of inks and specialty coatings for secure documents, such as passports or high-security certificates, integrate this compound as a molecular recognition element. Its purine ring is essential for the synthesis of proprietary dyes with anti-counterfeiting properties. Laboratory teams tightly monitor the input ratio to adapt to specific dye molecule requirements and fastness parameters. Quality protocols rely on batch-tested spectral profiles and migration data to meet end-user specifications.

    Industry compliance standards

    • ISO 14298 (Management of security printing processes)
    • EN 71-3 (Safety of toys – migration of certain elements, for ink material safety)
    • RoHS Directive (Restriction of Hazardous Substances)

    Typical usage ratio

    • Typical input between 0.05–0.2% by weight of total ink formulation, raised or lowered depending on targeted molecular dye intensity and process efficiency

    Downstream process integration

    • Introduced during pigment synthesis prior to dispersion in ink base
    • Processed via high-shear mixing and microfiltration for performance consistency

    Final product types

    • Security inks with anti-counterfeiting features
    • Document-grade dyes used in identification materials
    Free Quote

    Competitive 6-Amino-3,7-Dihydro-2H-Purin-2-One prices that fit your budget—flexible terms and customized quotes for every order.

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    More Introduction

    6-Amino-3,7-Dihydro-2H-Purin-2-One: Insights from the Laboratory Floor

    Introduction to 6-Amino-3,7-Dihydro-2H-Purin-2-One

    Standing on the manufacturing floor, 6-Amino-3,7-Dihydro-2H-Purin-2-One grabs attention not just for its structure, but for its pivotal role in pharmaceutical and biochemical research. Years of crafting purine derivatives taught us that fine margins in synthesis often decide the reliability and reproducibility of end products. This compound, often referred to under its purine scaffold code, builds the backbone for several key research ingredients and intermediates, supporting critical progress in laboratories across the world.

    Model and Specifications

    We produce 6-Amino-3,7-Dihydro-2H-Purin-2-One on-site, using batch synthesis processes that maintain batch-to-batch consistency in purity and physicochemical properties. Each lot passes HPLC and NMR checks to meet industry expectations for research-grade materials. We pay close attention to melting point, particle size offering, and impurity profiles, as our partners rely on unambiguous analytical fingerprints. Choices made at each synthesis step determine whether the molecules reach correct tautomeric form—an insight only clear after handling dozens of such heterocyclic systems in practice.

    Demand for clear characterization rises every year, so we fine-tune methods to attain sharper spectra and minimize trace contaminants. Our team checks not only for percent-purity but also for likely related compounds, residual solvents, and heavy metals—byproducts that often prove harder to spot than one expects. Experience tells us that rushing this part eventually causes setbacks downstream.

    Direct Applications and Usage Observations

    Chemists reach for 6-Amino-3,7-Dihydro-2H-Purin-2-One most often as a building block for creating nucleoside analogues and other modified purines. These form the framework for antiviral agents, targeted cancer therapies, and molecular probes. Decades into old methods, the subtle modifications enabled by this compound still draw renewed interest for next-gen therapeutic strategies. During scale-up or method transfer, its specific solubility and reactivity often dictate the range of possible reaction partners.

    In our process, storage and handling protocols have evolved alongside feedback from scientists who report on reactivity, stability, and ease-of-use at their own benches. Keeping the compound in carefully sealed environments reduces unwanted side reactions, especially in the presence of atmospheric moisture. This reduces batch failures and downstream purification headaches, which cascade into better experimentation for the scientists using our products.

    Over the years, we documented common pitfalls customers face—such as hydration states affecting weigh-outs and re-dissolution steps. Addressing such issues has shaped the way we package and QC each production lot. We often field questions about compatibility with different reaction media, so we maintain close records of solubility in a range of practical solvents, from DMSO to buffered aqueous systems, to keep advice grounded in trial and error rather than blanket statements.

    What Sets 6-Amino-3,7-Dihydro-2H-Purin-2-One Apart from Other Related Products

    Comparing this compound to other purine-derivatives in the lab draws lessons we’ve seen repeated, especially among research clients juggling synthetic planning. Purine core chemistry spans a spectrum of reactivity and selectivity; minor structural changes unlock or suppress desired reactions. The amino group at the 6-position, and the precise dihydropurine oxidation at positions 3 and 7, guides the formation of specific hydrogen-bonded scaffolds in new analogues. We have seen research teams confirm via crystallography how easily downstream products inherit precise stereochemistry, a trait often missing from more substituted or protected derivatives.

    Unlike bulk commercial analogues that favor lowest-possible manufacturing cost, our approach emphasizes lot consistency so core laboratories can repeat their experiments. Many of our colleagues in start-up biotechs or university groups share how an inconsistent supply chain derails timelines. By staying in control of every input raw material and hard-coding analytical release specifications, we see more successful scale-up stories coming from the field.

    Challenges During Manufacturing and How We Address Them

    Producing 6-Amino-3,7-Dihydro-2H-Purin-2-One in-house exposes both the joys and hurdles of chemical synthesis. Purine chemistry demands vigilance, especially given the compound's sensitivity to residual water or oxygen during key synthetic steps. Early in our production program, unintentional exposure would slow down reactions or force wasteful repurification. By pinpointing sources of microcontamination in reactors, we adopted new vessels, reworked moisture-exclusion strategies, and saw product yields and quality improve measurably.

    Our approach to scaling up remains hands-on. Lab observations guide the pilot runs, and even minor temperature variations can tip the balance away from the desired product. Lots of other manufacturers cut process corners or accept broader impurity ranges, but we’ve learned this only raises headaches later. As we see requests grow for kilo-scale and even larger runs, we invest in new monitoring equipment and recruit new process chemists trained specifically in purine system chemistry.

    Supply chain disruptions, particularly in starting amines and intermediates, cause downtime if not managed with advanced planning. Experience over the past few years, especially under pandemic-induced market stress, taught us to maintain multiple qualified sources and build redundancy in critical raw material inventories. Maintaining this buffer has allowed steady delivery commitments, which our regular clients highlight as a deciding factor for returning business.

    Supporting Scientific Progress with Reliable Materials

    Quality differences matter in research-grade supplies. One cannot count the projects derailed by questionable materials, yet researchers rarely publish such setbacks. We saw the urgency for better reproducibility in published results, so we tuned our internal practices to provide traceable documentation, open-feedback loops, and readily available technical support. Some scientists bring us feedback from failed experiments, and tracing these to manufacturing quirks drives our improvements.

    Our engagement with research consortia and academic labs gives direct exposure to evolving needs. The hunger for high-purity intermediates reflects the push toward more selective and high-throughput screening platforms. If even trace impurities drift between lots, biological assays risk false positives or negatives. By sharing real data from our own runs, we support open conversations about both strengths and pitfalls. This means disclosing real spectra, failure modes, and pathways to remediation if a batch falls outside expectations.

    Lessons in Scale, Packaging, and Delivery

    Producing 6-Amino-3,7-Dihydro-2H-Purin-2-One at significant scale while retaining lab-grade attention to detail took years of process refinement. Packaging emerged as a cornerstone for preserving quality. Bulk packaging in unsafe environments triggered hydrolytic breakdowns and angry phone calls early on. Now, we use moisture-proof, opaque containers, adapting fill quantities to maximize throughput while minimizing the risk of repeated exposure. Every return message from clients mentioning convenience or product longevity validates this investment.

    Shipping regulations for purine derivatives also impose constraints. Our logistics specialists have learned to navigate both domestic and international standards for chemical transport, reducing delays and reducing the risk of rejected shipments. Real-time tracking, responsible documentation, and regular training for hazardous materials handling support the safe, punctual arrival of our products on customer benches. Each point in this system stems from direct experience—the frustration of a ruined batch motivates process improvement better than any committee review.

    Clients switching from alternative sources express appreciation for responsive technical support rooted in lived production experience. Our chemists field questions about storage, handling, and synthesis tips, sometimes drawing on personal notebooks or long-form SOPs written up after late-night troubleshooting sessions. This feedback loop, where the producer and the end user communicate directly, has enriched both our internal knowledge base and customer outcomes.

    Differences Observed Between 6-Amino-3,7-Dihydro-2H-Purin-2-One and Other Purine Derivatives

    As the synthetic landscape matures, the need for subtle differences in activity and reactivity between purine base structures grows. 6-Amino-3,7-Dihydro-2H-Purin-2-One stands out for its reliable participation in targeted transformations, especially when constructing isosteric bases in complex oligonucleotide synthesis. Our collaborators report fewer side products and clearer separation profiles during downstream purification compared to other aminopurine analogues.

    Analysis reveals that substitution at the 6-position, combined with the specific hydrogenation at positions 3 and 7, tunes both the electronics and the three-dimensional profile. While less reactive alternatives struggle with nucleophilic aromatic substitution or cyclization steps, this compound offers better yields and cleaner reactions in non-aqueous media. We confirmed this in both bench-scale reactions and pilot plant runs for strategic partnerships, where upstream successes determined not only the fate of a batch, but the ability for teams to move forward with preclinical studies.

    A common story we hear is that batches sourced from the open market vary in color, solubility, or melting point—each a signature of sub-par purification or inconsistent synthesis. By anchoring all our production in-house, every deviation can be traced, halted, and corrected before reaching customers. That isn’t a luxury; it’s a necessity for sustaining partners in regulated or exploratory science.

    Pushing for Better, Not Just More

    Manufacturing 6-Amino-3,7-Dihydro-2H-Purin-2-One sometimes feels like a race between process improvement and rising customer expectations. Requests now reflect demands for even smaller impurity windows, advanced analytical documentation, and scalable production protocols adaptable from milligrams to multi-kilogram runs. We continue to tweak our processes based on field feedback and analytical advances, resisting the temptation to treat the compound as a generic intermediate.

    Some mistakes have proven more educational than costly. Early on, higher throughputs forced us to re-examine the impact of storage conditions and process vessel clean-outs. Residues invisible after initial washes register clearly during sensitive NMR runs or high-throughput bioassays. We now log every cleaning step and gather post-run contaminants for analysis, often learning from the outliers in process data. This feedback builds a culture of continuous improvement and open reporting among plant operators and QC staff.

    Answering Evolving Market and Research Needs

    Despite the recognition 6-Amino-3,7-Dihydro-2H-Purin-2-One now receives, the demands on its quality and traceability will only grow sharper as regulatory oversight and scientific replication priorities increase. Many biotech and pharmaceutical programs hinge on early research materials. By tracking global legislative changes and integrating quality assurance at all operations levels, we protect both our customers and our own reputation from supply-chain gaps.

    Sustained communication with regulatory bodies and third-party auditors helps align our technical documentation with established guidelines. This attention to transparency breeds repeat orders from experienced buyers who have yet to see the same rigor elsewhere. Keeping in touch with former clients informs us about any issues occurring years after initial shipment, speaking to our ongoing responsibility far beyond a sale.

    Each kilogram shipped represents a trust built on the sweat, knowledge, and adaptability of manufacturing teams over many seasons. Leaning on real experience gained from mistakes, successes, and persistent curiosity means every year brings higher standards and new technical solutions. The objective stays constant: reliable, reproducible, and trustworthy production of 6-Amino-3,7-Dihydro-2H-Purin-2-One for researchers on the frontlines of science.