|
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 | 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. |
Applications of 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt in Industrial Manufacturing2'-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 ManufacturingLeading 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
Typical usage ratio
Downstream process integration
Final product types
2. DNA Sequencing Reagents for Sanger and Next-Generation PlatformsReagent 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
Typical usage ratio
Downstream process integration
Final product types
3. In Vitro Transcription and Cell-Free Protein Synthesis SystemsProducers 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
Typical usage ratio
Downstream process integration
Final product types
4. Pharmaceutical API Synthesis: Antiviral & Anticancer Drug ManufacturingIntermediate 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
Typical usage ratio
Downstream process integration
Final product types
5. Biotechnology Research-Use-Only (RUO) Buffers and Enzyme KitsLife 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
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2'-Deoxyadenosine-5'-Triphosphate Disodium Salt prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.