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2'-Deoxyguanosine Monohydrate

    • Product Name 2'-Deoxyguanosine Monohydrate
    • Alias 2dG
    • Einecs 242-367-9
    • 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

    615431

    Product Name 2'-Deoxyguanosine Monohydrate
    Cas Number 959-24-0
    Molecular Formula C10H13N5O4·H2O
    Molecular Weight 299.26 g/mol
    Appearance White to off-white crystalline powder
    Purity ≥98%
    Solubility Soluble in water
    Melting Point Approx. 172-176°C (dec.)
    Storage Temperature 2-8°C
    Synonyms 2'-Deoxyguanosine hydrate; Deoxyguanosine monohydrate
    Inchi Key SWNQRMELNAXCMP-REOHCLBHSA-N
    Canonical Smiles C1=NC2=C(N1)N=C(NC2COC3C(C(C(O3)CO)O)O)N

    As an accredited 2'-Deoxyguanosine Monohydrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, tamper-evident plastic bottle labeled "2'-Deoxyguanosine Monohydrate, 1g," with chemical details, hazard symbols, and storage instructions.
    Shipping **Shipping Description:** 2'-Deoxyguanosine Monohydrate is shipped in secure, moisture-resistant packaging to maintain product integrity. The chemical is transported at ambient temperature, unless otherwise specified, with clear labeling. Compliance with local and international chemical transport regulations ensures safe and prompt delivery. Documentation such as safety data sheets accompanies every shipment.
    Storage 2'-Deoxyguanosine Monohydrate should be stored in a tightly sealed container, protected from light and moisture. Keep at 2-8°C (refrigerator temperature) in a dry, well-ventilated area, away from incompatible substances. Avoid excessive heat and ensure the container is clearly labeled. Proper storage helps maintain its stability and purity for research or laboratory use.
    Application of 2'-Deoxyguanosine Monohydrate

    Applications of 2'-Deoxyguanosine Monohydrate in Industrial Manufacturing

    2'-Deoxyguanosine Monohydrate serves as a specialized nucleoside raw material in several strictly regulated industrial sectors. Its high purity level and defined molecular character suit it for use in nucleic acid synthesis, quality-driven diagnostics, pharmaceutical intermediate production, molecular research, and other biotechnological manufacturing pathways. Below are key industrial applications, including compliance requirements, manufactured product types, and technical integration details.

    1. Oligonucleotide Synthesis for Molecular Diagnostics

    Our material forms a critical precursor during solid-phase chemical synthesis of DNA oligonucleotides used in diagnostic kits. Manufacturers select high-purity grades to ensure low background signal and accurate hybridization with clinical samples. The batching process incorporates the nucleoside at the early coupling step, and sequence fidelity directly relies on the starting purity.

    Industry compliance standards

    • ISO 13485 for medical device quality management
    • US Pharmacopeia (USP) standards for diagnostics raw materials
    • 21 CFR Part 820 (FDA cGMP for medical devices)
    • IVD Directive (EU 98/79/EC) for in vitro diagnostic substances

    Typical usage ratio

    • Batch ratios: 0.1–1.0 mmol per 1 mmol total nucleoside input, adjusted by oligonucleotide sequence requirements and synthesis scale

    Downstream process integration

    • Material is loaded onto automated DNA synthesizers at the first step after support attachment, proceeding through coupling, oxidation, and deprotection cycles for full oligo chain assembly.

    Final product types

    • Short DNA oligonucleotides for PCR and qPCR assays
    • Gene probes for infectious disease diagnostics
    • Clinical genotyping test kits
    • Pathogen detection arrays

    2. API Intermediate for Antiviral Nucleoside Analogues

    2'-Deoxyguanosine Monohydrate is widely used as an essential starting material in the industrial synthesis of nucleotide analogue active pharmaceutical ingredients (APIs), such as acyclovir and ganciclovir. Manufacturing sites utilize the nucleoside for regioselective modifications, which require consistent impurity profiles and batch traceability. Preparation steps focus on maintaining chiral integrity and chemical purity, critical for subsequent downstream derivatization and final API quality.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for all API materials
    • FDA Drug Master File (DMF) referencing
    • WHO GMP and PIC/S guidance for ingredient manufacturing

    Typical usage ratio

    • Material input: 1 mol per target API synthesis, with reaction stoichiometry adapted to downstream protecting group strategy (typically in 1:1 with core reactants)

    Downstream process integration

    • Charged into the first or second step of the API precursor route, followed by protection, selective activation, and further functional group transformation.

    Final product types

    • Acyclovir API for herpesvirus treatment
    • Ganciclovir bulk for cytomegalovirus infection control
    • Other guanosine-analogue antivirals

    3. Standard Material for Pharmaceutical Analytical Method Development

    Industrial laboratories employ our material as a certified reference or calibrant for high-performance liquid chromatography (HPLC), capillary electrophoresis, and mass spectrometry method validation. Its well-characterized profile helps laboratories verify method accuracy when quantifying nucleoside levels in formulated drug and research products. Traceability and purity documentation ensures seamless integration within regulated analytical environments.

    Industry compliance standards

    • USP Reference Standard requirements
    • ISO 17025 accreditation for laboratory testing
    • FDA and EMA guidelines for analytical performance qualification
    • Good Laboratory Practice (GLP) regulations for pharmaceutical analysis

    Typical usage ratio

    • Solution standard preparations: 10–100 μg/mL for calibration, as per specific instrument sensitivity or regulatory method protocol

    Downstream process integration

    • Nucleoside reference standard is dissolved and diluted to create standard curves for quantitation of pharmaceutical impurities and active contents in analytical assays.

    Final product types

    • Validated pharmaceutical assay kits
    • Certified laboratory analytical reference solutions
    • Quality control calibrators for nucleoside APIs

    4. Substrate in Genomic DNA Labeling for Biotechnology Research Tools

    Genomic researchers and life science tool makers chemically modify our material to create labeled nucleosides for incorporation in DNA sequencing and fluorescent in situ hybridization (FISH) workflows. High nucleoside quality supports reproducible labeling efficiency and minimal background. Manufacturers covalently attach fluorescent, biotin, or digoxigenin tags, requiring controlled reaction and purification steps adapted to the specific downstream assay.

    Industry compliance standards

    • ISO 9001 for quality management in life science component production
    • OECD Principles of Good Laboratory Practice (GLP)
    • Relevant REACH pre-registration for research chemical supply in the EU
    • Consignment compliance with applicable transport and handling regulations (IATA, DOT)

    Typical usage ratio

    • Substrate input: Up to 0.25–2.0 mmol per labeling prep, ratio is optimized for label incorporation yield and enzymatic polymerase compatibility

    Downstream process integration

    • The nucleoside is dissolved in activation buffer before being subjected to derivatization steps (e.g., NHS-ester or click chemistry reactions), then purified and formulated for labeled DNA synthesis or direct FISH application.

    Final product types

    • Fluorescent nucleotide reagents for DNA sequencing
    • Labeled dNTPs for PCR and RT-PCR kits
    • FISH probe reagents for cytogenetic analysis

    5. Nucleoside Substrate for Enzymatic Synthesis of Modified Nucleotides

    Enzyme-catalyzed synthesis platforms use our material as a substrate to generate specialty triphosphates and other modified nucleotides for downstream applications in DNA polymerase and ligase reaction systems. This application places stringent requirements on trace metal contamination and enzymatic compatibility, as even minor grades of impurities can inhibit polymerase or kinase activity and affect product yield or activity profile.

    Industry compliance standards

    • ISO 9001 for nucleic acid reagent manufacturing
    • Custom specifications matching enzyme manufacturer's QC protocols
    • Controlled documentation for batch traceability under laboratory GMP
    • Material Safety Data Sheet (MSDS) compliance for enzyme production environment

    Typical usage ratio

    • Input: 1.0–3.0 mmol per batch, precisely controlled for stoichiometry in kinase or polymerase-catalyzed conversion reactions

    Downstream process integration

    • Loaded into reaction vessels after pH adjustment, then subjected to enzymatic phosphorylation and further converted to dGTP or specialty derivatives for use in highly regulated reagent kits.

    Final product types

    • Enzymatically synthesized dGTP for RT-PCR and sequencing kits
    • Specialty nucleotide analogues for DNA repair and epigenetics research
    • Custom nucleotide mixtures for commercial biotech reagent manufacturers

    6. Feedstock for GMP-Grade Nucleotide Formulation in Cell Therapy Media

    Cell therapy manufacturing operations require defined and GMP-validated nucleotide sources to supplement culture media. Our material fulfills this demand by providing a traceable and consistent guanosine source with lot analytics to meet regulatory expectations. This role involves direct dissolution into sterile, pyrogen-free media preparations to support ex vivo expansion of patient-derived cells, with close control over batch composition and impurity profile.

    Industry compliance standards

    • GMP for cell therapy starting materials (21 CFR 210/211)
    • USP and Ph. Eur. monographs for pharmaceutical-grade nucleosides
    • ISO 14644 for cleanroom production environments
    • Comprehensive Certificate of Analysis (COA) documentation for batch release

    Typical usage ratio

    • Formulation input: 10–100 mg/L final media concentration, adjusted for cell type and growth-stage specific requirements

    Downstream process integration

    • Dissolved directly into sterile media formulations pre-filtration, with subsequent gamma irradiation or autoclave sterilization depending on end-use protocol.

    Final product types

    • GMP cell therapy expansion media
    • Stem cell and primary cell proliferation supplements
    • Clinical-grade cell culture kits for autologous or allogeneic cell preparation
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    Certification & Compliance
    More Introduction

    Understanding 2'-Deoxyguanosine Monohydrate: From Our Process to Your Laboratory

    Real Experience: Creating a Product that Chemists Count On

    At our production site, every batch of 2'-Deoxyguanosine Monohydrate passes through equipment and hands that belong to people who know its importance from years of experience. When our staff steps into the plant, they see rows of reactors charged with carefully chosen raw materials. The people who run these lines understand that chemists, biologists, and researchers around the world are looking for more than a white powder. They need a compound that meets predictable physical, chemical, and biological standards—I’ve watched colleagues discard batches due to minor variances, because consistent nucleoside quality helps underpin reliable scientific work. Not every manufacturer is interested in these headaches, but we’ve spent years refining purification, crystallization, and hydration steps to get what we believe is a top-tier product.

    What Sets 2'-Deoxyguanosine Monohydrate Apart

    2'-Deoxyguanosine Monohydrate is not just another component in a catalog. It matters for DNA synthesis and analytical studies because of the specific way it behaves. The monohydrate form locks in a certain ratio of water, one mole of water per mole of 2'-deoxyguanosine, which can make a significant difference in downstream work. That hydration shields the compound from breaking down, especially during long storage or rigorous handling. Our technicians keep an eye on both the moisture level and the crystalline structure as part of our quality checks. Other suppliers sometimes push out a crude product—dry, brittle, or with uncertain purity. Their powder may look the same by eye, but the HPLC traces, melting point, and moisture content tell you the truth. Our standard model, which typically falls under catalog code DG-01, lists a purity above 99%, with the monohydrate content closely controlled batch-to-batch.

    Why Our Approach to Specification Matters

    Many companies chase low cost and fast throughput, but that route carries a risk of impurities, variable hydrate content, and unpredictable behavior in synthesis protocols. Experienced chemists know that hidden contaminants, like residual solvents or trace nucleobase impurities, can throw off DNA polymerizations or cause reactions to stall. In our lab, we notice the difference right away—crystals grown from truly clean material come out flawless, and the melting point sits squarely where published values say it should. That’s not just bragging; it results from meticulous solvent selection, slow crystallization, and individually checked hydration. We keep tabs on every lot through HPLC, NMR, moisture analysis, and melting point determination—not just for regulatory compliance but because our colleagues use this same 2'-deoxyguanosine monohydrate in their own research. If we cut corners, they catch it in a heartbeat.

    The Real-World Uses: How It Gets Put to Work

    Researchers use this compound as a building block for DNA oligonucleotide synthesis, but it finds its value across areas like diagnostics, therapeutics, and molecular biology. In our own collaborations, we see teams relying on our batches to create custom primers or gene editing sequences. In diagnostics, degraded or impure material leads to ambiguous results. If you work with polymerase chain reaction or next-generation sequencing, the upstream nucleoside quality can steer whole project trajectories. Over the years, we’ve seen researchers hit roadblocks after purchasing lower-grade products, only to resolve weeks of troubleshooting by switching back to a highly controlled monohydrate source. Real-life experiments don’t forgive sloppiness in reagent preparation.

    The Challenge of Getting Monohydrate Exactly Right

    Anyone can grind crude deoxyguanosine and weigh in a splash of water, but the actual crystal lattice incorporates water very specifically. The monohydrate offers remarkable stability during storage and less static clinging during weighing and transfer. To get the monohydrate form right, we dial humidity, temperature, and rate of crystallization so the water nests perfectly in the structure—not just left outside or bound loosely. Some labs in the field work with anhydrous 2'-deoxyguanosine and see more dust, static loss, faster decomposition, or unexpected reaction rates. Sometimes a customer will ask why our powder pours so smoothly or why their protocols finally started delivering clean bands on a gel. The process of achieving the correct hydration level every time isn’t simple; it involves a mix of old-fashioned patience and investments in real-time monitoring equipment.

    Differences from Other Deoxyguanosine Compounds

    Not all “2'-deoxyguanosine” offered in the market is truly comparable. Some powders arrive unlabeled regarding hydration or with vague references to “technical grade.” Using those products, researchers sometimes find that their results drift over time, or that small changes in water content throw off their yields. Anhydrous forms tend to cake or degrade if the storage environment varies. Some manufacturers may dry the product at elevated temperatures or under vacuum, pulling out all moisture, but the stability drops as a result. Mixed hydrates or amorphous intermediates cause even more unpredictability—sometimes a small shift in moisture absorbs into their glass vials before the product even hits the bench. Our monohydrate has a crystal structure characterized by X-ray diffraction, a stable moisture content checked by Karl Fischer titration, and is supported by hundreds of researcher success stories.

    What Our Experience Has Taught Us About Handling and Storage

    We started by storing product in standard polypropylene bottles years ago, but soon learned that trace leaching or static charge throws off high-precision uses. Now, HDPE bottles with tamper-evident seals serve as the norm. During transit, we recommend cool, dry conditions because a hot, humid supply chain can trigger hydrate loss or promote clumping. We’ve worked with couriers to minimize temperature shocks, and if a shipment runs across a scorching summer, our staff adds thermal insulation to the packaging. Once opened, chemists in our own labs keep the container tightly capped and store at 2-8°C. Anyone in the nucleic acid synthesis field knows that even a few hours uncapped in a humid room can knock a percentage point off purity, or leave the weighed powder feeling gummy. These are boring details until you’re troubleshooting a stalled DNA synthesis—then they’re everything.

    Our Manufacturing Line: People, Processes, and Commitment

    Walking the floor during a batch run, you’ll see operators in clean hoods, working alongside up-to-date environmental controls. Each step, from the first dissolution in solvent through fine filtration and second crystallization, relies on careful measurement, calibrated glassware, and an eye for detail honed by years of mistakes and improvements. Batch records capture every part: exact temperature, pH, time, even notes on crystal appearance. We don’t trust a batch to its certificate alone—a laboratory tech takes samples to confirm the data matches reality. All this effort means we stand behind every bottle sent out. I’ve spent afternoons digging up archived chromatograms to settle a customer’s question, and our team is always listening for feedback that could improve the process. Many of the suggestions we implement come directly from researchers or internal production chemists—nobody knows a nucleoside’s quirks like someone who works with it every day.

    Practical Differences that Influence End Results

    Differences in crystallinity, particle size, and purity show up most in specialized applications. Oligonucleotide manufacturers demand that solid support coupling yields not drift from lot to lot. Some customers who attempted side-by-side comparisons with products from alternative sources sent us their results: an extra impurity at 262 nm or a slightly shifted retention time on reversed-phase HPLC. A single extra peak is the difference between an interpretable result and wasted synthesis cycles. Even small labs building DNA standards or running high-sensitivity tests can’t afford rolled dice with every reagent order. We’ve noticed many academic groups track down our technical team for advice not just on the product, but on troubleshooting sequences that aren’t behaving as expected. Every deviation they mention traces back, eventually, to a step where quality control went lax, or someone assumed all monohydrates are equivalent. They aren’t.

    Our Take on Batch Consistency and Traceability

    Every bottle of 2'-deoxyguanosine monohydrate that leaves our facility can be traced down to the smallest detail. We rely on digital batch logs, lot-specific test results, and archived reference samples for years after production. When we get a question about performance in a demanding application, we access historical data: yield, purity, XRD patterns, even operator notes. Our team doesn’t rest easy with “close enough.” The same product that fills orders for a university lab may go to an industrial-scale DNA manufacturer the next day, so no shortcuts get tolerated. If any issue pops up, we dig in and find root causes—sometimes a cracked gasket, sometimes a shipment sat too long on a loading dock, sometimes a new analytical standard.

    Facing the Tough Problems: Purity and Contaminant Control

    Nucleoside manufacturers run a daily battle against impurities. Things like dimers, guanine leachates, and trace metals have all shown up in inferior batches. Fighting these requires more than a good supply of chemicals or an automated purification skid—you spot trouble through hands-on TLC checks, additional washes, and ongoing method refinement. Our QC laboratory has pulled product for additional purification on several occasions, even when the impurity sat below published specification limits, just because a staff scientist didn’t like what the spectral data suggested. We catch things early because people keep their eyes and intuition tuned—chemistry is touch as much as number.

    Responsiveness to Customer Needs

    Science doesn’t rest, and neither can supply chains. Some customers call for custom particle sizes, so we run extra sieving or controlled milling. We’ve fulfilled requests for certificates listing extra analytical markers, or for pyrogen-free batches aimed at clinical work. We’ve learned that flexibility, fast feedback, and openness to troubleshooting usually matter more to a bench scientist than a minor difference in invoice price. If a problem turns up, we invite customers to walk us through their process, compare data, and, if needed, escalate for replacement or adjustment. That partnership over years has led to many product adaptations—tighter controls, changes in bottle size, or tweaks to drying protocols—all of which add up to a smoother research experience.

    Building Knowledge: Supporting New Applications

    Every year, we hear from groups looking to push 2'-deoxyguanosine monohydrate into new territory: modified nucleoside analog synthesis, DNA repair assays, antiviral drug research. Each time an application extends beyond standard DNA synthesis, the importance of known hydration, impurity profile, and handling becomes clear. Researchers share challenges—maybe a modified base that’s unstable unless paired with a specific hydrate, or an enzymatic reaction that fails unless the nucleoside is ultra-clean. We collect this feedback, use it to test secondary parameters, and advise future customers based on real experience. Chemistry isn’t static, and new uses often reveal old problems. Over decades, the bank of practical trial-and-error guides both production and how we suggest researchers approach their work.

    Ensuring Reproducibility and Transparency

    Too many chemical producers rely on opaque supply deals or repackaged bulk material, and researchers downstream bear the risk. We control every stage: procurement of raw guanine, conversion and protection, hydrolysis, neutralization, purification, and final crystallization. At every step, samples get checked not just for finished purity but for unseen variables like trace borates, remaining residuals, or moisture uptake. Reproducibility means answering for every batch, good or bad. We share analytical data, certificate details, and even answer in-depth technical questions routinely. Science relies on repeatability, and our team brings results from our QC lab directly to the customer’s bench.

    Why Source 2'-Deoxyguanosine Monohydrate from a Reliable Manufacturer

    Having produced and shipped this compound to hundreds of labs and manufacturing sites worldwide, we’ve observed a clear pattern: those who stick with consistent supply from knowledgeable manufacturers spend less time troubleshooting, get better yields, and rarely need to compensate for reagent anomalies. Early in our company’s history, we fielded calls about failed experiments, only to realize the market overflowed with gray-market products. Some lacked proper labeling, others showed visible yellowing or caking. Once groups switched to batches with detailed traceability and proven batch records, success rates rose sharply.

    What We Believe: Science Built on Trust

    Behind every bottle of 2'-deoxyguanosine monohydrate stands a team of process chemists, analytical specialists, and logistics planners who have seen what goes wrong when shortcuts get taken. Our commitment comes from direct lab experience, not from copywriters or sales brochures. Every gram dispensed carries the quiet testimony of hours spent correcting, refining, and recording methods that lead to reliable research. The most important part of our job may be keeping science predictable so problems at the bench come from real questions, not from doubts about a reagent’s basic quality.

    A Path Forward: Helping You Succeed in Nucleic Acid Work

    If your work demands reliable, fully characterized nucleosides, we’re happy to talk details, share protocols, and help optimize handling steps according to your context. Our knowledge stems from years of trial, correction, and partnership with scientists who ask tough questions. We’ve learned that supplying high-quality 2'-deoxyguanosine monohydrate isn’t just about a product line—it’s about supporting discoveries that depend on rock-solid foundations.