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2'-Deoxycytidine-5'-Triphosphate Trisodium Salt

    • Product Name 2'-Deoxycytidine-5'-Triphosphate Trisodium Salt
    • Alias dCTP
    • Einecs 207-987-2
    • 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

    421739

    Product Name 2'-Deoxycytidine-5'-Triphosphate Trisodium Salt
    Abbreviation dCTP trisodium salt
    Chemical Formula C9H12N3O13P3Na3
    Cas Number 102783-51-7
    Purity ≥98% (HPLC)
    Appearance white to off-white powder
    Solubility water-soluble
    Storage Temperature -20°C
    Usage biochemical research, DNA synthesis
    Synonyms 2'-deoxycytidine 5'-triphosphate sodium salt
    Stability stable under recommended storage conditions
    Ph Range pH 7.0-8.0 (aqueous solution)
    Lambda Max 271 nm (UV absorption)
    Ec Number 213-022-2

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

    Packing & Storage
    Packing The 2'-Deoxycytidine-5'-Triphosphate Trisodium Salt is supplied in a 25 mg white, tamper-evident, amber glass vial, tightly sealed.
    Shipping 2'-Deoxycytidine-5'-Triphosphate Trisodium Salt is shipped in tightly sealed, moisture-resistant containers with appropriate labeling. It is packed with cold packs or dry ice to ensure stability during transit and to maintain its quality. Handling complies with chemical safety regulations and includes Material Safety Data Sheet (MSDS) documentation.
    Storage 2'-Deoxycytidine-5'-Triphosphate Trisodium Salt should be stored at –20°C, protected from light and moisture. Keep the container tightly closed when not in use and avoid repeated freeze-thaw cycles. Store in a dry, well-ventilated area away from incompatible materials. For optimal stability, aliquot the reagent to minimize contamination and degradation.
    Application of 2'-Deoxycytidine-5'-Triphosphate Trisodium Salt

    Applications of 2'-Deoxycytidine-5'-Triphosphate Trisodium Salt in Industrial Manufacturing

    2'-Deoxycytidine-5'-Triphosphate Trisodium Salt (dCTP·3Na) supports advanced biotechnology and pharmaceutical production. As a manufacturer, we supply high-purity dCTP·3Na for specific downstream industrial applications requiring strict quality controls and adherence to relevant compliance standards.

    1. DNA Polymerase Chain Reaction (PCR) Reagents Manufacturing

    Pharmaceutical ingredient producers rely on dCTP·3Na as a key nucleotide for formulating PCR master mixes. These mixes enable diagnostic kit manufacturers to conduct DNA amplification for clinical, forensic, and research use. The compound’s purity and stability ensure minimal background signals in high-sensitivity PCR systems. Customization of nucleotide balance directly impacts enzyme kinetics and reproducibility in large-scale reagent blending and fill-finish operations.

    Industry compliance standards

    • ISO 13485:2016 for medical device quality management
    • Current Good Manufacturing Practice (cGMP), 21 CFR Part 820
    • European IVDR (EU) 2017/746 for in vitro diagnostic raw materials
    • US FDA’s QSR for reagent manufacturing

    Typical usage ratio

    • 100–250 µM per reaction for PCR master mixes, adjusted according to polymerase class and DNA template length; bulk blend tanks scaled up to mmol/L, concentration detailed in product-specific protocols.

    Downstream process integration

    • Nucleotide mixing during master mix formulation
    • Batch-wise or continuous inline addition before sterile filtration
    • Co-packaging with other dNTPs and stabilizers
    • Transferred to automated filling lines for single-use reagent kits

    Final product types

    • PCR diagnostic reagent kits for clinical laboratories
    • Dye-based qPCR mixes for gene quantification
    • Research-use only (RUO) nucleic acid test reagents
    • Custom DNA analysis solutions for contract manufacturing partners

    2. DNA Sequencing Reaction Mixtures Production

    dCTP·3Na acts as a building block for Sanger and next-generation sequencing (NGS) reaction mixtures. Contract manufacturers and kit developers utilize high-purity nucleotides to achieve accurate readouts in capillary electrophoresis and NGS workflows. Formulation technicians monitor each nucleotide’s relative purity to suppress sequencing noise and maximize base-calling accuracy, especially during bulk and batchwise process upscaling.

    Industry compliance standards

    • ISO 9001:2015 for quality management systems
    • GMP EU Annex 1 (sterile manufacture)
    • EN ISO 18385:2016 for forensic laboratory consumables
    • USP General Chapter <1046> for biotechnology products

    Typical usage ratio

    • 50–500 µM concentration per sequencing reaction, with precise titration based on DNA read length and polymerase system; large-production lots may require quality release at each batch concentration point.

    Downstream process integration

    • Direct addition during reaction mix formulation
    • Integration into pre-dispensed plates or sequencing cartridges
    • Staged quality checks for nucleotide profile analysis
    • Final assembly and packaging into sequencing kits

    Final product types

    • DNA sequencing reagent kits for clinical genomics
    • Forensic genetic identification kits
    • NGS library preparation kits for research and diagnostics
    • Companion diagnostics for precision medicine

    3. In Vitro Diagnostic (IVD) Assay Kit Development

    IVD manufacturers employ dCTP·3Na within nucleic acid-based test kits for disease detection, genetic screening, and pathogen identification. Stringent quality checkpoints verify nucleotide identity and lot-to-lot consistency, as regulatory filings require tracking every raw material input. Scale-up engineers adjust nucleotide blends to match each diagnostic system’s enzyme and detection format, as errors in ingredient proportions can affect signal specificity and test accuracy.

    Industry compliance standards

    • ISO 13485:2016 for medical device quality
    • CE IVDD/IVDR conformity assessment (EU)
    • US FDA 21 CFR Part 820 for IVD medical devices
    • WHO Prequalification requirements for critical diagnostics

    Typical usage ratio

    • 80–300 µM per reaction, tailored to test panel design and polymerase activity; bulk blending strategies follow kit manufacturer’s technical files.

    Downstream process integration

    • Dispensing into multi-well plate formats for high-throughput screening
    • Automated reagent addition during diagnostic panel production
    • In-process QC verification for each kit batch
    • Integration with liquid handling robots on manufacturing lines

    Final product types

    • Multiplex nucleic acid testing kits for infectious diseases
    • Companion diagnostic kits for gene mutations
    • High-throughput genotyping panels
    • Point-of-care molecular diagnostic devices

    4. Cell-Free DNA Synthesis Platforms

    Contract research and industrial synthetic biology labs utilize dCTP·3Na for enzymatic synthesis of custom DNA constructs using cell-free systems. Pure nucleotides are added at production scale in continuous or fed-batch reactor setups, enabling the controlled elongation of DNA strands for gene synthesis services and nucleic acid therapeutics. Documentation on purity and endotoxin levels accompanies every supply, meeting customer and regulatory audit requirements during platform qualification and technology transfer.

    Industry compliance standards

    • ISO 9001:2015 for chemical and biological R&D
    • IPEC-PQG GMP Guide for pharmaceutical excipients
    • USP <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • REACH registration for chemical safety in the European Union

    Typical usage ratio

    • 0.2–1.0 mM final concentration in reaction, based on DNA assembly protocol and desired fragment length; process engineers may further adjust for kinetic optimization.

    Downstream process integration

    • Reagent feed into DNA synthesis bioreactors or microfluidic devices
    • Pooling with other dNTPs for cassette or scaffold assembly
    • Automated system monitoring of nucleotide depletion rates
    • Immediate downstream purification and product QC

    Final product types

    • Synthetic DNA fragments for gene editing
    • Plasmid libraries for functional screening
    • CRISPR guide RNA templates
    • Nucleic acid therapeutics research materials

    5. Laboratory-Scale DNA Labeling and Probing Chemicals

    Research institutions and reference laboratories require high-quality dCTP·3Na as a substrate for labeling DNA probes with fluorescent or radioactive tags. During probe synthesis, controlled incorporation of labeled dCTP ensures detection sensitivity and specificity in downstream hybridization and microarray applications. Batch documentation supports method validation and reproducibility for regulatory or GLP-compliant projects.

    Industry compliance standards

    • GLP (Good Laboratory Practice) OECD Principles
    • ISO/IEC 17025 for testing and calibration laboratories
    • USP <1058> Analytical Instrument Qualification
    • Relevant national regulations for radiolabeled reagent handling

    Typical usage ratio

    • 50–200 µM dCTP in enzyme-based labeling protocols, with the proportion of labeled to unlabeled dCTP typically ranging from 1:4 to 1:20 depending on sensitivity requirements.

    Downstream process integration

    • Direct addition during chemical or enzymatic labeling setups
    • Mixing with labeled nucleotides and incorporation enzymes
    • Hybridization or microarray printing post-labeling
    • Method-specific cleaning and validation procedures

    Final product types

    • Fluorescently labeled DNA hybridization probes
    • Radioactively labeled DNA standards
    • Calibrator materials for molecular diagnostics
    • Chemically synthesized oligonucleotide markers
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    Certification & Compliance
    More Introduction

    2'-Deoxycytidine-5'-Triphosphate Trisodium Salt: Experience from the Production Floor

    About the Product

    In our years manufacturing nucleotides, we have learned to recognize not just the value of purity, but also the many real-world uses and the exacting standards of researchers around the world. 2'-Deoxycytidine-5'-Triphosphate Trisodium Salt, often referred to as dCTP, belongs to the group of deoxyribonucleotide triphosphates essential for DNA polymerization reactions. Researchers in genetics, molecular biology, diagnostics, and biotechnology have relied on our dCTP, and every batch reflects our commitment to hands-on, detail-oriented production.

    We produce dCTP as a white to off-white crystalline solid, well suited for common laboratory applications. Its model number in our line-up represents a standardized synthesis process. What that means in simple terms: the chemical maintains the same characteristics and performance across every lot. The specification sheet confirms a minimum purity of 98% by HPLC, and our records show actual values rarely drift near the lower edge. The batch-to-batch consistency results from rigorous raw material vetting, tight environmental controls, and equipment maintenance that goes beyond regulatory minimums.

    What Sets Our dCTP Apart

    It is easy to talk about the purity percentages and analytical instruments, but that misses the lived experience. We know that researchers face a world of DNA sequencing kits, PCR setups, and cloning experiments that simply do not forgive impurities or buffers that shift pH over time. We choose trisodium salt form for the strong solubility in water-based systems and the stable integration into both manual and automated protocols.

    Real life in the lab rarely happens under textbook conditions. Trace metallic contaminants or inconsistent hydration can derail expensive assays. Every round of synthesis involves steps to scavenge and test for transition metals and other interfering ions. Our in-house team runs both HPLC and spectrophotometric checks, then double-checks with beta-propeller assays for pyrophosphate when needed. Procurement chooses raw cytidine that meets set UV and IR spectra, never just the generic pharmaceutical grade.

    Where others might trim back calcium and magnesium checks to save on reagents, we stick with the standard because it is cheaper to maintain good habits than troubleshoot ruined PCRs. We check for residual organic acids that can muddle up high-fidelity enzymes. And because we've seen frustrated grad students pacing over a failed experiment, we work to keep endotoxin levels low. It is not a regulatory headline; just something we know can ruin a day or a whole week of progress.

    How 2'-Deoxycytidine-5'-Triphosphate Trisodium Salt is Used

    Most of the dCTP we send out ends up in DNA amplification. PCR — both classical and in real-time qPCR setups — remains the largest use, though we see researchers requesting bulk for isothermal amplification, cloning, genetic labeling, and library preparation for high-throughput sequencing. Some customers use it in mutagenesis workflows or for labeling reactions since natural deoxynucleotides work seamlessly with high-fidelity and mutant polymerases.

    We pay attention to solubility profiles and buffer compatibility, constantly fielding questions about dCTP’s interaction with magnesium or combinations in custom nucleotide mixes. Our team deals often with order notes that call out for re-solubilization steps at specific pH or blending with custom buffer salts to fit protocols that are anything but generic.

    One practical issue that crops up: stability of the nucleotide in solution. dCTP in trisodium form resists hydrolysis better than the dipotassium or ammonium counterparts under standard freezer conditions, which gives our users a longer window for their master mixes and kit components. The trisodium salt format holds up through repeated freeze-thaws. We know researchers will cycle their stocks through a series of enzymes, chelators, and freeze-thaw regimes; we are no strangers to unexpected feedback when other salt forms fall short under such stress.

    Working With dCTP in the Factory and the Lab

    Inside our facility, strict climate and moisture controls are the rule, not the exception. We manufacture in small lot sizes by modern standards, which lets us monitor every critical step and cut down on aging inventory. Every container gets a detailed lot record, with documentation for critical control points and actual test results.

    The drying phase takes place under vacuum so residual water content stays consistently low. Handling crystalline dCTP requires care; it absorbs ambient moisture and can clump if exposed too long. Lab experience shows quick weighing and sealing in dry boxes keeps downstream processes easier. To every order, we recommend aliquoting into single-use vials once dissolved to prevent repeated freeze-thaw cycles. Long-term users tend to store their working stocks between –20°C and –70°C; from our own archive studies, we confirm little loss in activity over six months under proper conditions.

    Our blending protocols strip out chances for mixed-salt contamination. We run long rinse cycles between lots, and we test for phosphate carryover. Good practice, proven by direct feedback from clients who notice the lack of trace artifacts in Sanger sequencing or conversions between 96-well plate runs and larger fermenters.

    Solving Customer Challenges Through Manufacturing Choices

    Researchers have complained to us in the past about colorless particles and faint yellow hues in solutions from other suppliers. Many root causes point to incomplete purification or improper storage during warehousing. Our response was to audit our handling procedures, add more frequent inspection steps, and invest in shielding our raw material storage from light and humidity.

    Questions about salt form come up a lot. Trisodium versus dipotassium or lithium salts: most end-users want stable pH and reproducible solubility. Trisodium salts dissolve easily in water, avoiding tough chelation problems with magnesium or potassium, a recurring pitfall in sensitive DNA polymerase reactions. We see far fewer complaints about precipitation or opalescence compared to non-sodium salts.

    Careless handling in distribution can sometimes spoil a perfectly good product. We went to tamper-evident, moisture-barrier sealing some years ago. Regular audits catch deviations in packaging that could expose the powder to humidity swings during transit. We emphasize quick transfer to –20°C freezers upon arrival, and our technical bulletins reinforce swift, airtight handling through final user preparation.

    Comparisons With Other Nucleotide Triphosphates

    Making dCTP is not quite the same as producing the other deoxynucleotide triphosphates, although initial steps share similarities. The challenge with dCTP comes from its sensitivity to pH drifts and the need to match the base’s natural chemical environment. We calibrate our processes using standard curves and reference grades of ATP and GTP, but tailor the final purification to cytidine’s distinct binding affinity and solubilization behavior.

    Compared to dGTP, dCTP shows a slightly higher rate of hydrolysis at pH above 8.0, one reason we push for slightly acidic to neutral storage buffers in customer labs. As for dTTP, the major difference comes from feedback inhibition in multi-enzyme setups; minor impurities in dCTP more quickly lead to enzyme poisoning. That’s why our batch records flag even minor side products, pushing yield loss over salvage of risky fractions.

    End users report that the trisodium form consistently offers better reproducibility, particularly in kit assembly for diagnostic PCR and next-gen sequencing prep. We monitor news in the synthetic biology world and research consortia regularly push onto salt forms tailored for ultra-high-throughput needs. In our shop, we stick with what brings fewer headaches, higher reliability, and easier downstream process controls.

    Serving the Research and Diagnostic Community

    We listen carefully to customer stories. One long-time user shared how a run of low-quality dCTP from another source spun out an entire week’s worth of inconclusive qPCR results. Tests traced the issue back to high chloride and trace nickel. It reinforced what we already believed: purity and transparency in reporting come ahead of chasing the largest possible lots or bulk discounts. We have built our process to address documented challenges instead of chasing trends that only fill marketing slides.

    Our technical liaison group provides protocols, handles real lab questions, and tracks outcomes when researchers push our dCTP under non-standard setups. We expect to answer questions about integrating dCTP with proprietary polymerases, dealing with pH drift after repeated usage, and recommendations for aliquoting that fit into demanding robotics applications.

    Quality Control and Continuous Improvement Lessons

    Each new run brings a chance to refine. Operator notes track challenges in freeze-drying, and lab techs flag any signs of powder browning or inconsistencies in crystal formation. Our best improvements have come from noticing patterns in cap failures or slow resuspension rates, not from tinkering with headline-grabbing additives.

    We tailor our documentation and reporting to what working scientists need. Our certificates go into the specifics: pyrophosphate content, residual transition metals, trace phosphate, endotoxin. We add these details since they address active concerns in high-throughput, high-fidelity reaction setups. We run regular reference checks against NIST standards, maintaining a tight calibration schedule. None of that floats into the marketing copy, but it ends up in fewer troubleshooting emails, more repeat customers, and new collaboration opportunities.

    Looking Forward: New Research, Same Core Principles

    Demand for dCTP changes every year. Some seasons researchers leap into new diagnostic fields and automation platforms, stretching both our production schedules and inventory planning. Larger batch sizes tempt shortcuts, but our experience says small, consistent lots match the needs of the fast-changing laboratory world.

    Some emerging protocols use custom nucleotide analogs, yet basic dCTP in trisodium form remains the backbone for most DNA-related reactions where fidelity, yield, and reproducibility trump the latest trends. End-users tell us they value knowing their supplier runs the same hands-on, cautious approach every day, no matter the production batch size or regulatory focus.

    From the Manufacturer’s Perspective: Why It Matters

    On the shop floor, the lesson is clear: real researchers and lab techs count on their chemicals behaving every time, in every experiment, across disciplines. Fluctuating results kill research momentum, spike costs, and drain trust. Buying standardized dCTP from a bulk catalog does not promise the same outcome as manufacturing each lot with direct accountability. We have learned from every customer question, every batch deviation, and every protocol that flagged even the smallest out-of-spec result.

    We stand behind our approach to making 2'-Deoxycytidine-5'-Triphosphate Trisodium Salt the way we do, not only because it results in fewer problems, but because our own techs would not want to run an experiment on anything less reliable. It isn’t just about purity or consistency on paper; it’s about building trust with the researchers who stake their results, and their reputations, on invisible details that add up in every test tube.