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9-Ethylguanine

    • Product Name 9-Ethylguanine
    • Alias 9-Ethyl-2-amino-1,7-dihydro-6H-purin-6-one
    • Einecs 211-701-3
    • 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

    566502

    name 9-Ethylguanine
    cas_number 992-30-1
    molecular_formula C7H9N5O
    molecular_weight 179.18 g/mol
    appearance White to off-white powder
    melting_point 285-287 °C (dec.)
    solubility_water Slightly soluble
    chemical_class Purine derivative
    iupac_name 9-ethyl-1,9-dihydro-6H-purin-6-one
    pubchem_cid 6872

    As an accredited 9-Ethylguanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 9-Ethylguanine is supplied in a 1-gram amber glass vial, tightly sealed with a screw cap and labeled with safety information.
    Shipping 9-Ethylguanine is shipped in a tightly sealed container to protect it from moisture and light. The packaging complies with international regulations for chemical transport, ensuring safe delivery. It is typically dispatched via a reliable courier, with proper hazard labeling and supporting documentation, including a safety data sheet (SDS).
    Storage 9-Ethylguanine should be stored in a tightly sealed container, protected from light and moisture, at a temperature between 2-8°C (refrigerated conditions). Keep it in a dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Ensure proper labeling and limit exposure to air to preserve its stability and prevent degradation.
    Application of 9-Ethylguanine

    Applications of 9-Ethylguanine in Industrial Manufacturing

    As a purine derivative with nucleobase structure, 9-Ethylguanine serves specific functional roles in downstream chemical and pharmaceutical industries. We manufacture this compound for high-purity supply chains that rely on reliable performance in targeted applications. Below, we outline the practical scenarios where 9-Ethylguanine supports industrial workflows, detailing regulatory standards, integration ratios, processing stages, and resulting product types.

    1. Nucleic Acid Research Reagents and Oligonucleotide Synthesis

    Research reagent manufacturers and oligonucleotide synthesis facilities utilize 9-Ethylguanine as a reference standard and as a synthetic building block for modified nucleosides. Its unique ethylated position allows for studies on DNA/RNA structure and function, as well as the development of nucleic acid analogues for advanced biotech research.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • Good Laboratory Practice (GLP) for reagent production
    • IUPAC Nomenclature and Analytical Purity Verification
    • Applicable internal QC specifications for reference standards

    Typical usage ratio

    • 0.1–1.0 mol% as a reference or spike-in for analytical assays
    • 1–10 mol% in solid-phase synthesis for analog incorporation, adjusted per target oligonucleotide sequence requirements

    Downstream process integration

    • Prepared into buffer solutions or lyophilized mixtures for calibration and assay controls
    • Coupled during phosphoramidite synthesis, introduced in controlled cycle steps on DNA synthesizers, typically after base deprotection

    Final product types

    • Custom oligonucleotides containing ethyl modifications
    • DNA/RNA structure–activity relationship test kits
    • Analytical nucleic acid controls
    • Modified RNA therapeutics for structure-function studies (preclinical reagents)

    2. Pharmaceutical Intermediate for Antiviral and Antitumor API Synthesis

    Pharmaceutical API manufacturers employ 9-Ethylguanine as an intermediate in multi-step syntheses of nucleoside analog drugs, particularly in the preparation of certain acyclic guanine derivatives with established antiviral or antitumor profiles. The presence of the ethyl group modifies pharmacokinetic properties during lead optimization.

    Industry compliance standards

    • EU GMP (Good Manufacturing Practice) for Active Pharmaceutical Ingredients
    • ICH Q7 for Pharmaceutical Manufacturing
    • FDA 21 CFR Part 211 for API Process Validation
    • USP/EP monograph guidance for related substance control

    Typical usage ratio

    • Stoichiometric 1:1 molar ratio with halogenating agents in primary alkylation steps
    • 5–15% w/w relative to reaction mass when used as a feed intermediate in nucleobase modification stages

    Downstream process integration

    • Introduced in the alkylation or acylation phase, reacted under anhydrous or inert gas conditions prior to condensation for nucleoside analog formation
    • Subject to purification and crystallization before further conversion to active intermediates or final APIs

    Final product types

    • Prodrugs based on acyclic nucleoside structures
    • Experimental nucleoside antitumor agents
    • Selective antiviral therapy precursors
    • Active pharmaceutical ingredient batches pending scale-up and registration

    3. Synthetic Dye and Marker Precursor for Molecular Biology Diagnostics

    Producers of molecular diagnostic kits and life science dyes utilize 9-Ethylguanine as a precursor in the synthesis of guanine-based fluorescent labels and chromophores. The ethyl modification influences fluorescence spectra and facilitates specific coupling with reporter molecules.

    Industry compliance standards

    • IVD Regulation EU 2017/746 for in vitro diagnostic materials
    • ISO 13485:2016 for medical device and reagent quality
    • REACH Regulation (EC) No 1907/2006 on chemical safety
    • RoHS (Restriction of Hazardous Substances) for electronic diagnostic kit assembly

    Typical usage ratio

    • 0.2–2.0 mol% in chromophore synthesis reaction mixtures
    • Concentration optimized based on fluorescence yield and detection limit calibration (generally 0.05–0.5 mg/ml in working probe formulations)

    Downstream process integration

    • Undergoes direct coupling with label precursors via alkylation, reductive amination, or diazonium salt chemistry, most often prior to probe assembly
    • Components are purified by HPLC or flash column before being formulated into conjugated detection probes

    Final product types

    • Fluorescent oligonucleotide probes for PCR diagnostics
    • Nucleic acid hybridization marker kits
    • Guanine-derived dye labeled antibodies for immunoassay platforms
    • Research-use-only reporter molecule panels

    4. Chemical Reference Standards and Analytical Controls

    Accredited analytical laboratories integrate 9-Ethylguanine as a control sample or calibration standard for chromatographic and spectrometric method development, especially within purine quantification studies and purity assessments for pharmaceutical and research chemicals.

    Industry compliance standards

    • ISO/IEC 17025:2017 for laboratory competence
    • USP Section <1225> for Analytical Method Validation
    • Ph. Eur. and JP reference standard protocols
    • ICH Q2 (R1) for validation of analytical procedures

    Typical usage ratio

    • Prepared as 1–100 µg/ml stock solutions for HPLC, LC-MS, or UV-Vis quantitation
    • Applied at 0.1–10% as external or internal standard depending on target analyte level

    Downstream process integration

    • Weighed and dissolved into solvent systems prior to analytical run setup
    • Included in calibration curves or QC check batches according to validated method SOPs

    Final product types

    • Validated analytical standard kits
    • Certified reference material vials
    • Batch QC test solutions
    • Calibration blends for routine laboratory instrument performance testing
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    Certification & Compliance
    More Introduction

    Introducing 9-Ethylguanine: Building DNA Analogs with Confidence

    Our Hands-On Experience in Producing 9-Ethylguanine

    Making 9-Ethylguanine takes more than just a checklist and a supply of raw materials. Over years in the lab, our team developed a process that secures every atom’s right place. The result offers researchers and industry specialists a nucleotide analog where structure, reliability, and purity leave no room for doubt. Repeated, careful crystallizations, monitored each time by skilled chemists, produce a product recognized for its consistency batch after batch. Chemists blending knowledge and sweat behind each lot means you receive a compound that sets a standard you can build on, not guess at.

    Model and Specifications: Attention to Detail from Start to Finish

    Our production focuses on the flagship model: 9-Ethylguanine, CAS No. 15310-72-6, with a molecular formula of C7H9N5O. We supply this material in powder form, crystalline, ensuring sharp, well-formed edges and bright white color—sure visual cues that signal a product without contamination from synthesis byproducts.

    Trace impurities matter most at low concentrations, so our batches exceed the benchmark for high purity, typically above 99%. Our QC team crosschecks every lot for typical interferences such as alkali metal residues, heavy metals, and moisture, using well-calibrated HPLC and NMR protocols. Each bottle brings with it a chain of paperwork confirming traceability from lot number back to raw guanine sources and essential process chemicals.

    Why 9-Ethylguanine?

    Many projects call for 9-Ethylguanine as a core tool in studying DNA base pairing, mutagenesis, and nucleic acid analog design. The ethyl group at the 9-position alters hydrogen bonding compared to unmodified guanine, offering researchers a way to control base recognition and stacking in oligonucleotides. For years, the compound found steady demand in academic DNA studies, but recently, biotech and pharmaceutical sectors pushed requirements higher, demanding even tighter purity and fuller documentation. Not all sources can keep up. Consistency makes a difference: a batch made with less oversight brings mystery to your experiments, not answers.

    In our hands, 9-Ethylguanine exhibits stable handling and long shelf-life under appropriate conditions—dry and stored away from light at 2–8°C. Our production runs emphasize not just chemical correctness but also careful handling through every step, so the ethyl group remains perfectly positioned while the guanine ring keeps all tautomers in check.

    Differences from Other Guanine Analogs

    Competitors ship materials labeled 9-Ethylguanine, but our lineup stands apart in more ways than one. Experience reveals that some suppliers cut corners, skipping extra purifications or accepting low-level color and odor contaminants. Impurities of just a few tenths of a percent can change crystallization behavior or downstream reactivity, leading to confusing or irreproducible research data.

    Compared to 2-substituted or N7-alkylated guanines, the 9-position ethyl group gives unique steric bulk that modifies electronic distribution across the purine ring without excessive disruption of backbone configuration. The product dissolves cleanly in standard polar organic solvents like dimethyl sulfoxide and remains stable in buffered aqueous solutions, unlike several methyl or isopropyl derivatives that show drop-off in solubility or stability.

    No generic guanine source matches the selectivity profile of 9-Ethylguanine for certain DNA polymerase or synthetase assays, or for probing the mechanics of DNA repair. The molecule often serves as a control to identify subtle variations in hydrogen bonding, stacking energy, and base-pair discrimination. Reproducibility turns on the minute and the marginal. We keep our eye on the details.

    Common Usage: From Idea to Application

    Research groups use our 9-Ethylguanine in oligonucleotide synthesis, site-directed mutagenesis, and as a building block for nucleoside analogs. The ethyl group blocks certain enzymes from recognizing the guanine site, making this analog valuable in studies of DNA methylation, repair, and enzyme-substrate specificity.

    Biotech firms adopt it in proprietary workflows where precise base recognition creates or negates binding events. It allows for fine-tuning of enzyme selectivity in engineered polymerase systems. Some pharma development labs integrate our compound as a marker or probe that stands apart from endogenous bases under mass spectroscopy and chromatographic detection, eliminating the confusion that can come from broader-spectrum detection signals.

    Our customers return looking for the same predictable melting patterns, sharp NMR shifts, and clean UV absorbance they see each time with our 9-Ethylguanine. They point to fewer failed syntheses, better-defined intermediates, and fewer reruns of critical bioassays.

    University teams, who always question every material’s provenance, find our documentation stands up to peer review, reducing headaches and revision cycles later. Research managers gain confidence that data generated with our compound withstand scrutiny and find acceptance in high-impact journals.

    Managing Product Limitations and Process Challenges

    Unlike basic guanine salts, 9-Ethylguanine poses its own manufacturing challenges. Ethylation must achieve selectivity at the N9 atom, avoiding over-alkylation or side reactions involving exocyclic amino groups. Our process builds on mastery of protecting group chemistry and gentle reaction conditions—choosing solvents and bases that maintain molecule integrity without creating unwanted isomers.

    Some competitors source starting material from unvetted suppliers, risking introduction of organics that remain buried in the matrix. We’ve invested in upstream audits so every partner follows quality protocols for their own reagents. Inspecting early saves pain downstream.

    Drying after synthesis can change color or cause clumping, so we fine-tuned parameters for both vacuum and temperature. Even so, workers visually inspect each dried batch before a single gram goes to packaging. Automation helps, but the naked eye, trained and experienced, picks up on subtle cues.

    Ongoing Innovation Based on End-User Feedback

    Every year, project leaders and R&D directors send feedback after trying our 9-Ethylguanine in evolving workflows. Some requested higher concentration stock solutions in DMSO; others wanted reformulations for improved long-term storage stability. After running side-by-side studies, our own team qualified specific low-residual solvents and low-ion content to cut down on unwanted background signals in sensitive bioanalytical systems.

    The shift toward machine-assisted DNA synthesis and larger-scale enzymatic workflows brings new demands. Early, we realized even trace sodium or potassium can interfere with high-fidelity polymerase or ligase activity. So we invested in additional washes and microfiltration to push trace metal concentrations below 5 ppm in every lot. The switch eliminated hard-to-explain variability in next-generation sequencing applications, and letters of thanks flowed in from downstream tool providers who saw smoother ramp-up and easier troubleshooting.

    Storage protocols matter too. Researchers told us about previous experiences losing reactivity due to oxidation and humidity. We optimized container selection: certified glass vials with low-leach caps, nitrogen flush, and double vacuum packaging. Test samples stored for twelve months showed less than 1% change in assay performance.

    Environmental Responsibility and Worker Safety

    Handling guanine analogs requires strict attention to environmental controls and worker safety. Our synthesis lines use closed systems and fume extraction to keep airborne exposure low and to prevent trace residues from reaching outside waste streams. All reactions take place under scrupulous containment, and we treat effluents through a two-stage purification system before disposal, verified by routine testing for purine derivatives.

    Our plant operates under ISO 14001 guidance, which pushes us to reduce intermediates and solvents. Regular third-party audits reinforce that we don’t let byproducts or raw effluents leave the facility outside of allowable limits. We recycle significant fractions of solvents and collect residual materials for offsite energy conversion. Our staff undergoes regular health and safety training—a practice that not only keeps injury rates low but also helps maintain the culture of diligence each step really needs.

    Supporting the Community: Training and Collaboration

    Because chemists rarely work in isolation, we run technical seminars every spring and fall, open to both our employees and external researchers in related fields. Our trainers highlight not just the “how” but the “why” behind each step—raw material handling, purification troubleshooting, and final quality control. Attendees report fewer failed syntheses and more productive collaborations in their broader labs.

    Suppliers, academic groups, and competing firms have occasionally joined for process improvement workshops. Much of the best learning happens on the plant floor, sharing real cases rather than reviewing stale textbooks. While intellectual property merits respect, passing along hard-won process insights lifts the standard and helps everyone in the field.

    Regulatory Updates and Certification

    On the regulatory side, we keep pace with developing pharmacopeial guidelines and country-specific import controls. Detailed batch records, complete chain-of-custody, and comprehensive analytical certificates go out with every shipment. Our QA team meets regularly to anticipate new rules—from local workplace safety standards to international REACH compliance for handling bioactive purines.

    After recent updates in key markets, extra documentation became a must: full elemental analyses, in-depth impurity profiles, and evidence of environmental stewardship now form part of each standard shipment. From the outside, these may look like simple paperwork additions, but real effort underpins the authentication of origin, history, and process performance on every lot.

    Future Directions and Industry Demands

    Genomic research keeps evolving, and so do requirements for materials like 9-Ethylguanine. As new synthetic biology and diagnostic companies push into more complex nucleic acid systems, demand rises for analogs with tighter purity, new functional groups, and even longer-shelf-life under less-than-ideal lab conditions.

    To stay ready, we keep one foot in our production lab and the other in project meetings with key industry partners. If a polymerase in clinical diagnostics starts asking for unanticipated side chain tolerance, or a pharmaceutical development calls for fine-tuned solubility thresholds, our team stands prepared to isolate the bottleneck and adjust. Scaling up to kilogram or higher quantities—sometimes on short notice—means rethinking raw material supply chains, tightening cleaning cycles, and extending batch documentation. Again, years of experience paying close attention to customer results provide our best guide.

    Direct Dialogue with Researchers and Partners

    Years in manufacturing taught our team never to underestimate the advantage of direct communication with researchers. We don’t rely only on end-of-quarter surveys or filtered distributor reports. Once a project connects with our technical support—whether it’s troubleshooting a stalled synthesis, clarifying a spectral anomaly, or prepping a larger-scale shipment—we bring the actual process chemist, not just a generic support rep. This face-to-face, or at least scientist-to-scientist, dialogue breaks through many of the misunderstandings that come from second-hand communication.

    Requests for documentation, data about impurity profiles, or recommendations for solvent choice receive precise and timely answers. We don’t keep trade secrets about basic handling, as long as the questions come from genuine research pursuits. Our view is that transparency builds trust, and twice as many returning partnerships reflect this approach.

    The Road Ahead for 9-Ethylguanine

    Demand for high-quality guanine derivatives will only grow as synthetic biology, pharmaceutical design, and diagnostic technology keep pressing for better, faster, and more precise DNA analogs. 9-Ethylguanine, simple by structure but challenging in synthesis, plays an essential role for those experimenting at DNA’s cutting edge.

    Our team remains committed to refining each step—listening to the unexpected hurdles customers face, working with regulators to streamline approvals, and never cutting corners on raw material or process oversight. Chemical manufacturing doesn’t just stop with shipping a bottle; it lives in the trust forged between chemist and researcher, between every batch and every result.

    As our customers tackle more ambitious questions—whether developing cancer diagnostics or probing the fundamental rules of base pairing—our 9-Ethylguanine stands ready to keep up, every step of the way.