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2'-Deoxyadenosine-5'-Triphosphate Disodium Salt

    • Product Name 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt
    • Alias dATP
    • Einecs 206-220-7
    • 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
    VTB
    Specifications

    HS Code

    723009

    Product Name 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt
    Cas Number 5957-13-9
    Molecular Formula C10H14N5Na2O12P3
    Molecular Weight 507.17 g/mol
    Appearance White to off-white powder
    Solubility Soluble in water
    Storage Temperature -20°C
    Purity ≥98%
    Synonyms dATP, Deoxyadenosine triphosphate disodium salt
    Application DNA synthesis, PCR, sequencing
    Ph 1 Solution 7.0-8.0
    Ec Number 209-870-7

    As an accredited 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Clear, labeled plastic vial containing 100 mg of 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt, securely sealed, packaged in a protective box.
    Shipping 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt is shipped at ambient temperature or on dry ice, depending on stability requirements. The product is securely packed to prevent degradation and contamination, with appropriate documentation and safety labeling to ensure compliance with regulatory standards during domestic and international transit.
    Storage 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt should be stored at -20°C, protected from light and moisture. Keep the container tightly closed in a dry, well-ventilated area. Avoid repeated freeze-thaw cycles to maintain stability. Use only with proper personal protective equipment under suitable laboratory conditions. Proper storage ensures the integrity and efficacy of this nucleoside triphosphate.
    Application of 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt

    Applications of 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt in Industrial Manufacturing

    2'-Deoxyadenosine-5'-Triphosphate Disodium Salt serves as a fundamental nucleotide source used by industry leaders in biotechnological and molecular diagnostics production. Its performance in precision processes such as PCR, DNA sequencing, molecular diagnostics, cell-based manufacturing, and pharmaceutical synthesis has earned its role in downstream workflows requiring high purity and batch-to-batch consistency. The following sections detail core application scenarios where this material features prominently in real industrial practices.

    1. Molecular Diagnostics: PCR Kit and qPCR Reagent Manufacturing

    Leading diagnostics producers rely on our nucleotide for master mix production in quantitative PCR (qPCR) and conventional PCR kits. It is incorporated in enzymatic reaction systems to support DNA amplification and target sequence detection, where formulation integrity directly impacts cycle efficiency, target specificity, and reproducibility across multiplexed clinical and research applications.

    Industry compliance standards

    • ISO 13485 Medical Devices – Quality Management Systems
    • European In Vitro Diagnostic Regulation (IVDR 2017/746)
    • United States FDA 21 CFR Part 820 (QSR for Diagnostics)
    • Chinese YY/T 0287—2017 for Medical Devices

    Typical usage ratio

    • 200–1000 µM in enzyme reaction buffer, adjusted by primer/probe design and downstream template requirements. Manufacturers may optimize within this range based on enzyme activity and cycle protocol.

    Downstream process integration

    • Nucleotide is dosed into dNTP blends during master mix formulation, prior to aliquoting and lyophilization or liquid fill of PCR kit components.

    Final product types

    • qPCR diagnostic kits
    • Endpoint PCR assay kits
    • Isothermal amplification reagents
    • DNA-based disease detection panels

    2. DNA Sequencing Reagents for Sanger and Next-Generation Platforms

    Reagent manufacturers use this material as an essential building block in both Sanger and next-generation sequencing workflows, ensuring high signal clarity and minimizing background noise in template elongation cycles. Its sourcing and purity are critical for sequencing accuracy, troubleshooting, and long-read performance in clinical genomics and industrial-scale bioinformatics pipelines.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • OECD Principles of Good Laboratory Practice (GLP)
    • Herstellerzertifikat nach IVDR für In-vitro Diagnostika (where relevant)
    • CLSI MM09-A: Nucleic Acid Sequencing - Approved Guideline

    Typical usage ratio

    • 50–500 µM per sequencing reaction, titrated depending on template type, polymerase fidelity, and detection chemistry (fluorescent/labeled ddNTPs).

    Downstream process integration

    • Blending into dNTP reagent cocktails during multi-stage kit assembly followed by quality control assays for contaminant nucleotides and high-throughput fill-and-cap automation.

    Final product types

    • Sanger sequencing reagent kits
    • Library prep kits for NGS
    • Barcoded sequencing master mixes
    • Custom nucleic acid synthesis panels

    3. In Vitro Transcription and Cell-Free Protein Synthesis Systems

    Producers of cell-free expression kits and in vitro transcription reagents require precise nucleotide supply for enzymatic reactions synthesizing high-purity RNA or proteins in controlled environments. The compound’s role as a substrate guarantees transcript integrity without RNA contamination, a non-negotiable in mRNA vaccine or research-use reagent manufacturing.

    Industry compliance standards

    • European Pharmacopoeia monograph 2.6.32
    • 21 CFR Part 211 (GMP for Finished Pharmaceuticals)
    • EU GMP Annex 1 & Annex 15
    • ICH Q7 Good Manufacturing Practice Guide for APIs

    Typical usage ratio

    • 1–5 mM in cell-free reaction buffers, adjusted per lot for polymerase/transcriptase activity and final desired transcript length.

    Downstream process integration

    • Added as part of standardized or optimized nucleotide pools to in vitro transcription setups after template DNA and RNA polymerase precursors, followed by purification steps to remove unincorporated nucleotides.

    Final product types

    • mRNA synthesis kits
    • Cell-free protein synthesis kits
    • Transcription enzyme reagent sets
    • Gene editing research reagents

    4. Pharmaceutical API Synthesis: Antiviral & Anticancer Drug Manufacturing

    Intermediate manufacturing for selected active pharmaceutical ingredients (APIs) employs deoxynucleotide triphosphates as precursors or enzymatic feedstocks in the synthesis of nucleotide analogues. Rigorous contamination control prevents by-product formation which could compromise drug safety or batch uniformity, demanding nucleotides with traceable purity and validated production records.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF Monographs (where specified)
    • European Pharmacopoeia 2.2.46 (Chromatographic Purity)
    • Japanese Pharmacopoeia (JP XVII) for nucleotides used in API manufacturing

    Typical usage ratio

    • Concentration varies by synthetic route, typically 1–10 mmol/L within enzyme-mediated or chemical addition processes, with precise ratios specified in validated API manufacturing protocols.

    Downstream process integration

    • Introduced as a substrate or reactant in the nucleotide modification stage, prior to further derivatization and isolation during the production of therapeutic analogues.

    Final product types

    • Nucleotide-based antiviral agents (e.g., lamivudine analogues)
    • Chemotherapeutic precursor intermediates
    • Investigational nucleotide pharmaceuticals

    5. Biotechnology Research-Use-Only (RUO) Buffers and Enzyme Kits

    Life science and academic R&D suppliers require bulk nucleotide loading for buffer and enzyme kits specified for in vitro experimentation and protocol development. The adoption focuses on reproducibility, contaminant-free formulation, and compatibility with multiple enzymatic assays in both automated and manual workflows used by end research labs and contract research organizations.

    Industry compliance standards

    • ISO 9001:2015 (for RUO grade reagents)
    • OECD Good Laboratory Practice (GLP) as applicable
    • REACH Regulation (EC 1907/2006) for chemical supply
    • Material certificate traceability according to customer QC system

    Typical usage ratio

    • 100–1000 µM, modifiable to fit protocol-based enzyme or DNA template concentration requirements as specified by downstream users.

    Downstream process integration

    • Incorporated during buffer assembly or enzyme cocktail blending, followed by filtration and small-scale packaging adapted for laboratory end users.

    Final product types

    • Research-use-only PCR buffer kits
    • Enzyme mix packs for laboratory applications
    • Preformulated dNTP blends for R&D screening
    • Academic molecular biology kit sets
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    Certification & Compliance
    More Introduction

    2'-Deoxyadenosine-5'-Triphosphate Disodium Salt: A Manufacturer’s Perspective

    Seeing the Production Floor Through the Prism of Real Demand

    From the start, manufacturing 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt (dATP-Na2) means shouldering the daily reality that the accuracy of a single nucleotide touches everything from the reliability of DNA polymerase reactions to the performance of high-throughput sequencing machines. Each batch cannot stray from the set path by even a fraction. Researchers, technicians, and diagnostic developers count on us to deliver a compound that stays consistent, from the crystallization tank to the final vial, every time.

    About dATP-Na2: What Sets It Apart

    Our dATP-Na2, offered under the model D02013, has become an anchor for countless molecular biology protocols. Months of precision chemical synthesis and purification go into each lot. The molecular formula C10H13N5Na2O12P3 ensures that every molecule entering a PCR, dNTP mix, or sequencing process supports accurate data. We manufacture the powder under controlled humidity, using strict temperature parameters to protect the labile triphosphate group.

    The product leaves our plant as a white, crystalline powder, free from detectable contaminants. UV analysis, HPLC and mass spec all work double-duty, confirming each run’s purity exceeds 98 percent and nucleotide content remains stable for months when stored at −20°C. These tests take time and expertise, and in our experience, skipping one step in the hope of increasing output usually sets off a cascade of costly errors.

    Why Reliability Remains the Real Value-Add

    Manufacturing a pure nucleotide triphosphate means more than mixing reactants and capturing a yield. Any drop in purity can sabotage an entire batch of Taq reactions or cause peaks to blur in sequencing chromatograms. For years, we have watched customers trust a cheaper dNTP source, only to return when ambiguous bands, low-amplitude signals, or unexpected sequence artifacts undermine weeks of research. In the world of genomics, false data does more than waste time—sometimes it misdirects entire projects.

    We take stability just as seriously. Most users realize that hydrolysis of triphosphate groups happens all too quickly with even small temperature fluctuations or trace metal contamination. We verify stability with accelerated testing, exposing samples to temperature and storage stress. Our teams regularly revisit the entire chain, from raw material qualification to final packaging, ensuring no overlooked variable slips through.

    Solving Common Challenges and Handling User Concerns

    Scale brings surprises, and dATP-Na2 is no different. As output rose over the years, we learned firsthand that even minor changes—a filter swapped for a “compatible” alternative, a new cleaning solvent introduced, or a batch of sodium ion solution with slightly different pH—can throw off the entire process. Some competitors, drawn by the demand for cheaper nucleotides, will trim steps or relax their controls. That’s never led to long-term customer satisfaction.

    Every time a client flags lot-to-lot inconsistency or finds spurious bands in their PCR products, we dig in and simulate the protocol, sometimes using their precise primer-template systems in our QC labs. These case studies show the true cost of quality lapses. It often stems from invisible process shortcuts—skipped lyophilization cycles, chelation steps missed, or poor cold-chain management in transit. Investing in robust systems pays off, and feedback from skilled scientists helps us tune every stage.

    Model, Specifications, Usage

    We provide dATP-Na2 as D02013, bundled in vacuum-sealed amber vials to shield from moisture and UV. Working scientists want short rehydration times, so we optimize lyophilization and granule sizing for quick dissolution. For those setting up qPCR plates at 6 a.m., this matters. Our standard offering comes at 100 mM concentration levels upon reconstitution with molecular biology-grade water, which is ideal for dNTP mixes. The compound dissolves easily, remains clear in solution, and doesn’t precipitate out even if the protocol demands lengthy storage on ice. We track each lot’s pH, matching guidelines set by leading enzyme suppliers.

    Researchers rely on this triphosphate for everything from routine PCR to whole genome amplification, Sanger sequencing, and newer third-generation sequencing platforms. Its role as a building block in DNA synthesis remains critical. In enzymatic reactions, the extra purity means less inhibition. No unexpected inhibitors sneak in—false starts, delayed extension, and incomplete amplification get traced back to trace impurities more often than most researchers realize. Our quality standards are tuned against the most sensitive downstream applications, including high-fidelity polymerases and clinical diagnostic kits.

    The Difference from Off-The-Shelf Alternatives

    Some nucleotides, offered by smaller operations, make cost the central pitch. But the trade-off becomes clear when inspecting the data. Our experience shows that dATP-Na2 batches from less-controlled sources can introduce metal ions, pyrophosphate contamination, or remnants of synthetic byproducts. Harsh purification saves pennies in the short term but creates headaches later. Small labs chasing fast results sometimes risk it, but the problems emerge quickly—usually in the form of weak bands, laddering, poor yield, or outright reaction failure.

    We have run competitive sampling, testing market-sourced dATP-Na2 alongside our own. The majority do not meet the claimed purity, instead hovering below the threshold vital for high-sensitivity work. Reverse transcription, library prep, and multiplex PCR applications demand higher standards. Trace metals, often invisible on basic QC screens, will cripple high-fidelity enzymes or light-up negative controls.

    Quality Control: What Actually Works

    Every batch undergoes a sequence of high-pressure liquid chromatography, UV absorbance checks at 260 nm and 280 nm, and negative-control PCR on in-house reference templates. Re-processing happens if any parameter falls out of our accepted range—a lesson learned after an early run sent incomplete material to a pilot client more than a decade ago. We maintain a central repository of test data for post-market traceability.

    Supply chain complexity sometimes injects unexpected variables. Over the years, we have received feedback from labs battling with inconsistent dNTPs that forced them to run batch-specific positive and negative controls, wasting hours on troubleshooting. These stories reinforce the importance of supplier transparency. Our records stretch back for years, and product traceability is non-negotiable.

    Scalability and Ongoing Improvements

    Maintaining quality at growing volumes is its own challenge. We redesigned aspects of the process—switching to closed-loop systems and more sensitive analytical methods. Now, every purity and contamination threshold is double-checked at two stages. Tight scheduling in the plant avoids crowding batches, so there’s never a race to wind up one cycle to start another.

    Recent upgrades to our purification suite allowed us to cut run times without cutting corners. The new high-resolution columns outperform older ones, catching minor byproducts that eluded us in the past. Sometimes, we test new buffer recipes submitted by customer labs, helping us tweak for even better compatibility. The product adapts alongside scientific progress—especially as synthetic biology and diagnostics shift demand from bulk nucleotides to more specialized, consistent reagents.

    Supporting Tomorrow’s Lab Innovations

    Researchers increasingly push for longer read lengths, lower input DNA concentrations, and higher throughput. Triphosphate purity has emerged as a limiting variable that only a few pay close attention to until problems arise. With clinical diagnostic regulations tightening, especially for in vitro diagnostics, maintaining both high purity and complete documentation determines a supplier’s reputation. We field requests for variant dNTP mixes, smaller packaging for automated liquid handlers, and tailored packing for field-ready PCR units. Our production lineup now accommodates these new needs, backed by robust change-control logs for every tweak.

    As a manufacturer, adapting rapid QC release protocols and reducing bottlenecks without lapsing into rushed production stays front-of-mind. After several years of feedback from laboratories working with decaying dNTP stocks because of excess freeze-thaw cycles, we moved to smaller aliquots on request and invested in more reliable low-temperature logistics.

    Minimizing Downstream Headaches: Real-World Results

    Critical endpoint PCRs for Clostridium-detection, rapid SARS-CoV-2 test development, and CRISPR gene-editing validation all run on time because of reliable nucleotide supplies. Attention to material and process control raises the reproducibility across labs—valuable for high-stakes clinical studies and academic research alike. After incorporating more rigorous endotoxin screening prompted by feedback from a vaccine manufacturer, our dATP-Na2 consistently meets or exceeds assay requirements for sensitive diagnostic kits.

    We invest in routine post-sale support for troubleshooting, and maintain frequent communication with bioinformatics and wet lab teams running into protocol-specific issues. This hands-on approach has helped our product avoid the common pitfalls of more generic alternatives that miss the mark when protocols grow more demanding.

    The Importance of Open Data and Testing Collaboration

    Key to reliable production is close work with early adopters and advanced testing labs. Some of our most significant improvements have come from partnerships with reference labs who probe lots with advanced NGS-based tests or employ capillary electrophoresis for impurity mapping. They flag subtle stability differences across supplier lots, helping us refine our purification protocols further.

    We see value in keeping open conversations. Whether a customer needs a nucleotide to work seamlessly in a multiplex PCR or for high-throughput sequencing, we support their protocol development with real QC data, not just certificates that tick regulatory boxes. Transparency builds trust much faster than glossy marketing ever could.

    What Sets True Manufacturers Apart

    As the field grows, more startups and academic spinoffs join the molecule supply race. The reality remains: only a few handle the complexity of scale, quality, and continuous improvement all at once. Handling the whole process—ordering raw nucleoside, synthesizing triphosphate, purifying via ion-exchange and HPLC, freeze-drying in controlled cycles, then sampling every lot in actual application scenarios—means every failure lands squarely in our lab, not a distributor’s.

    Traders and repackagers cannot match the level of insight that comes from solving manufacturing problems in real time. Every failed reaction their product causes erodes a researcher’s time, budget, and confidence. Our direct manufacturing approach keeps lines of responsibility clear and makes technical support relevant to real-world application, not just theoretical specifications.

    Shaping the Next Era of Nucleotide Manufacturing

    With the advancements in gene editing and ultrasensitive molecular diagnostics, the margin for error grows thinner. We see protocols moving toward ever-higher amplification efficiency and lower artifact tolerance. Our plant is preparing to handle future iterations of dNTPs that may carry specialized labels, isotopic signatures, or stricter contaminant thresholds, building on the foundation established by years of working directly with industry needs.

    Growth in demand never justifies relaxing quality standards. Each vial that leaves our facility has been checked against practical, not just regulatory, expectations. We field questions about lyophilization residual moisture, trace metal impact on enzyme complexes, and packaging material compatibility for automated handling. Each answer reflects hands-on lab experience: choosing a manufacturer rather than a repacker ups the likelihood that issues get solved efficiently.

    Keeping an Eye on Impact

    Every time a new diagnostic test wins approval or an academic team reports a breakthrough, attention returns to the subtle molecular building blocks that enable this work. Manufacturing 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt isn’t glamorous, but the precision, care, and construction behind each microgram matters more than ever. Researchers ask the right questions—about lot numbers, impurity testing, and application trials—making our commitment to total traceability and open technical support indispensable.

    By investing in process improvement, quality control, and hands-on troubleshooting, we ensure the scientific community gets a nucleotide triphosphate it can count on, year after year. In a field where reproducibility, accuracy, and time-to-result decide success or failure, these efforts count far more than ever before.