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N-Benzoyl-2'-Deoxy-Adenosine

    • Product Name N-Benzoyl-2'-Deoxy-Adenosine
    • Alias Bz-dA
    • Einecs 607-443-5
    • 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

    348394

    Chemical Name N-Benzoyl-2'-Deoxy-Adenosine
    Molecular Formula C17H17N5O4
    Molecular Weight 355.35 g/mol
    Cas Number 28093-14-1
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in DMSO and methanol
    Storage Temperature -20°C
    Synonyms N6-Benzoyl-2'-deoxyadenosine
    Iupac Name N6-benzoyl-9-[(2R,3S,5R)-3,5-dihydroxyoxolan-2-yl]-9H-purin-6-amine
    Smiles C1=CC=C(C=C1)C(=O)N2C=NC3=C2N=CN=C3N[C@@H]4O[C@H](CO)[C@@H](O)[C@H]4O
    Application Used in nucleoside and oligonucleotide research

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

    Packing & Storage
    Packing White plastic bottle containing 1 gram, sealed with a screw cap. Labeled with product name, batch number, and hazard information.
    Shipping N-Benzoyl-2'-Deoxy-Adenosine is shipped in tightly sealed containers under cool, dry conditions to ensure stability. Packaging complies with local chemical safety regulations, typically using padded, leak-proof materials. Detailed labeling includes product identification, hazard warnings, and handling instructions. Expedited shipping with temperature control may be recommended for sensitive or high-value orders.
    Storage Store **N-Benzoyl-2'-Deoxy-Adenosine** in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep the container tightly closed and clearly labeled. Protect from incompatible substances such as strong oxidizers and acids. Recommended storage temperature is 2–8°C (refrigerated). Handle under an inert atmosphere if necessary, and follow all relevant safety protocols.
    Application of N-Benzoyl-2'-Deoxy-Adenosine

    Applications of N-Benzoyl-2'-Deoxy-Adenosine in Industrial Manufacturing

    N-Benzoyl-2'-Deoxy-Adenosine serves as a key intermediate and raw material for high-value sectors including pharmaceuticals, diagnostics, and specialty chemicals. The following sections detail core application areas, with precise compliance, ratio, processing, and downstream product information relevant to industry procurement and production teams.

    1. Nucleoside-Based Anticancer Drug Synthesis

    Pharmaceutical manufacturers use N-Benzoyl-2'-Deoxy-Adenosine as a protected intermediate during multi-step synthesis of nucleoside analogs for antitumor active pharmaceutical ingredients (APIs). The benzoyl group protects the amino group during glycosylation and phosphorylation reactions. Production facilities achieve high purity through dedicated crystallization and HPLC purification lines, ensuring reliable feedstock for subsequent deprotection and conversion steps. This intermediate’s stability supports efficient storage under GMP-controlled environments before downstream processing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) Reference Standards Where Applicable
    • European Pharmacopoeia Guidelines (Ph. Eur.)
    • FDA 21 CFR Part 211 Manufacturing Practices

    Typical usage ratio

    • Intermediate utilization in API synthesis: 0.8–1.2 molar equivalents per target nucleoside unit (ratio refined by desired yield and by-product minimization in each batch)

    Downstream process integration

    • Enter multi-step synthesis after sugar coupling, during nucleobase functionalization
    • Batch added to reactor vessel with base deprotection at final step
    • Purified and isolated under inert atmosphere before hydrolysis or activation
    • QC tested for residual benzoyl content before release to API finishing stage

    Final product types

    • Anticancer nucleoside analogs such as cladribine and related chemotherapeutics
    • Bulk nucleoside API lots for tableting and injectable formulation
    • Pharmaceutical finished dosage forms—oral tablets, IV solutions

    2. Oligonucleotide Diagnostic Probe Manufacturing

    Diagnostics labs and contract manufacturers leverage this compound during automated solid-phase synthesis of oligonucleotide probes, primers, and molecular diagnostics kits. The benzoyl-protected adenosine derivative enables batchwise, controlled deprotection on DNA synthesizers, ensuring minimal base damage and high coupling efficiency. High purity and low trace metal content are critical for sensitive PCR and hybridization applications, as downstream contamination affects assay reliability.

    Industry compliance standards

    • ISO 13485:2016 Quality Management for Medical Devices
    • CLSI MM13-A Standards for Nucleic Acid Amplification
    • EU In Vitro Diagnostic (IVD) Regulation 2017/746
    • REACH/CLP Safety Data and Purity Requirements

    Typical usage ratio

    • 0.95–1.05 equivalent per coupling step on solid-phase synthesis (adjusted by probe length and throughput)

    Downstream process integration

    • Automated loading to DNA/RNA synthesizers for chain assembly
    • Enters as protected nucleoside phosphoramidite or via pre-activation
    • Sequential deprotection under mild conditions to prevent sequence loss
    • Pooled and purified post-synthesis for custom oligo orders

    Final product types

    • PCR primers and DNA probes for clinical diagnostic kits
    • qPCR detection panels and gene panels
    • Next-generation sequencing barcodes and adapters
    • Custom research-grade oligonucleotides

    3. API Reference Standards & Analytical Controls

    Reference laboratories and pharmaceutical QC units employ N-Benzoyl-2'-Deoxy-Adenosine as a traceable analytical control for nucleoside analog quantification and identification. Its stability compared to unprotected analogues makes it suitable for calibrating HPLC, LC-MS, and NMR instruments during release testing. The material’s certified purity (typically >99%) supports robust analytical method validation under regulated conditions, backed by full spectral documentation and batch certification.

    Industry compliance standards

    • USP General Chapter <1225> Validation of Compendial Procedures
    • ICH Q2(R2) Analytical Method Validation
    • ISO/IEC 17025 Testing and Calibration Laboratories Accreditation
    • FDA 21 CFR Part 58 Good Laboratory Practice for Nonclinical Studies

    Typical usage ratio

    • Analytical control: 1–10 μg per analysis (referenced against calibration curve standards)

    Downstream process integration

    • Dissolved to prepare HPLC/LC-MS calibration samples
    • Sourced as reference for method validation during API development
    • Routine use in stability and degradation testing of nucleoside pharmaceuticals
    • Inclusion in laboratory standard operating procedures for batch release

    Final product types

    • Certified reference standard vials for QC laboratories
    • Analytical kits for nucleoside profiling in pharmaceuticals
    • System suitability reagents for method performance checks

    4. Modified Nucleoside Synthesis for Gene Therapy Research

    Biotech R&D teams integrate the benzoyl-protected derivative in the synthesis of chemically modified nucleosides for gene editing, antisense oligonucleotides, and siRNA candidates. The protective group ensures site-selective modification and prevents unwanted reactions, particularly during the introduction of 2'- or 5'-site modifications. Facilities employ continuous flow or small-batch reactors, optimizing yield by adjusting reaction time and temperature to the physicochemical profile of this intermediate.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • NIH Guidelines for Research Involving Recombinant DNA Molecules
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.7–1.3 equivalents per modification reaction (ratio standardized by sequence length and functional group)

    Downstream process integration

    • Dosed to microreactors for chemical modification steps
    • Incorporated after initial ribose protection, prior to labeling or functionalization
    • Reaction monitored to full consumption before purification
    • Deprotected as a last stage to yield the active nucleotide

    Final product types

    • Functionalized nucleoside analogs for gene therapy vectors
    • siRNA and antisense oligonucleotides for research and preclinical studies
    • Chemically modified mRNA and DNA constructs
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    Certification & Compliance
    More Introduction

    N-Benzoyl-2'-Deoxy-Adenosine: Shaping Progress in Modified Nucleosides

    True Value from the Manufacturer’s Floor

    Ask anyone who’s spent time on a plant floor where we handle nucleoside derivatives, and you’ll hear the same truth: tiny details in synthesis shape everything downstream. N-Benzoyl-2'-Deoxy-Adenosine stands as one of those compounds that demands respect for principles both scientific and practical. Not many compounds in the lab receive the same careful handling. Over years of large-scale production, small choices in temperature, solvent, and even storage conditions have taught us that reliable quality comes from more than printed specifications.

    What Sets N-Benzoyl-2'-Deoxy-Adenosine Apart

    Customers who look for 2'-deoxynucleoside derivatives often ask what makes benzoylation so important. It doesn’t matter if your lab is chasing next-generation oligonucleotides or fitting pieces into delicate nucleic acid chemistries—the need to protect the adenine amine function is essential. A benzoyl group secures this function, reducing side reactions during chain assembly, and makes the end product markedly cleaner during deprotection. Newcomers notice fewer impurities at the HPLC, and experienced eyes see higher reproducibility batch-to-batch. That isn’t just theory; it’s become part of the routine here after working with hundreds of runs through our reactors.

    Our production relies on high-purity starting adenosine and select reagents. We control moisture meticulously in each step, using validated instruments regularly audited for drift and calibration. Always, our technicians sample at intermediate steps. The impact shows up clearly: N-Benzoyl-2'-Deoxy-Adenosine rolls out of our crystallizers as sharp, white solids, meeting more stringent purity and identity criteria than many commercially available alternatives. Yield and conversion figures don’t tell the full story. Consistency matters more, and our clients would confirm—across pharmaceutical R&D or advanced materials—when a flask from a reliable batch saves days of troubleshooting downstream.

    The Backbone for Oligonucleotide and Diagnostic Research

    Whether assembling antisense oligos, exploring modifications in siRNA, or constructing chemical probes for diagnostics, researchers need modifications that offer precise control. N-Benzoyl-2'-Deoxy-Adenosine acts as a crucial building block, no matter if the final target is a phosphoramidite reagent for automated DNA synthesizers or a manually-assembled construct. In semipreparative synthesis, we’ve seen teams run into headaches with sub-par derivatives: small amounts of overreacted or underprotected nucleoside forcing labor-intensive cleanups. From a manufacturer’s seat, batch success starts with robust starting materials. We find that our benzoylated adenosine stays consistent through a wider range of temperatures and solvent systems, maintaining its integrity. The uniformity isn’t just about numbers; it translates to a more predictable synthesis experience in customer labs.

    Even outside classic oligonucleotide applications, new demand emerges from maturing fields. Chemical biologists in our network have extended usage of this modified base into enzyme evolution tests, aptamer screening, and even selective labeling in emerging diagnostics. Some choose it for improved compatibility with particular protecting group chemistry. Suppliers tightly control trace impurities—anionic, metallic, or organic—because side reactions can take weeks to spot once incorporated downstream. All lessons we have absorbed feeding this molecule into complexity, and all reflected in our own output.

    Product Model and Fit-for-Purpose Production

    We don’t see ourselves offering just a catalogue entry. Over time, adaptation has become our second nature; so if a customer requests gram-to-kilo scale, different grading for academic versus GMP pipelines, or tailored particle sizing for distinct reactors, we step up. Each model reflects raw analytics, but behind the scenes, there’s constant adjustment—solvent choices, residence times, process temperature—shaped by hands-on trial. In scaling up, volumetric yields grow, but process complexity does too. We rely on careful in-process analytics: NMR, HPLC, water content by Karl Fischer, and residual solvent checks. Our team won’t release a lot until multiple eyes—seasoned chemists, instrument techs, and compliance auditors—have signed off. That diligence never fades.

    Some clients benefit from smaller batch synthesis for method development. Here, minimizing cross-contamination and flexible scheduling top the list. For pharma clients biding by regulatory frameworks, documentation and supporting data flow seamlessly—each batch record meticulously reviewed. Our GMP and non-GMP lines remain physically distinct. Working decades in this field, we know trace contaminants can spark regulatory interruptions. Every minor adjustment, such as changing a water filter or rotating reactor staff, prompts an internal review to avoid incident. In our experience, customer trust grows from seeing traceable, well-documented material in hand, not generic paperwork.

    Specifications as a Living Standard

    Product specs aren’t just a one-off list on a datasheet for us; they’re living benchmarks. Typical product specs for N-Benzoyl-2'-Deoxy-Adenosine revolve around appearance, identification, assay (HPLC), individual impurities, total impurities, and water content. Our material routinely exceeds compendial numbers—purity by HPLC measuring well above 98%. Water content rarely rises beyond 1%. TLC, MS, and NMR reports sit with every release file and with client documentation.

    Batch differences happen in every chemical plant. Our operators flag unusual spectral peaks or color shifts immediately. Routine stability testing under controlled storage and intentional stress conditions back up shelf-life claims. Customers revisit these reports year over year. Off-spec batches rarely slip through, but when they do, they don’t make it into commerce. We communicate transparently, detail findings, and run corrective actions—an ethos learned from years navigating customer audits.

    Navigating Differences Versus Other Deoxyadenosine Derivatives

    Plenty of modified nucleosides appear similar on paper, but small variations in design make a world of difference. N-Benzoyl-2'-Deoxy-Adenosine sees regular comparison with analogues like N-acetyl, N-phenoxyacetyl, and unprotected 2'-deoxyadenosine. The driving difference? The benzoyl group’s stability under the acid and base conditions common in DNA and RNA synthesis. Protection is more robust than acetyl, and more easily removed under mild conditions than some bulkier alternatives. Researchers gain a wider window for assembly, particularly in long-chain solid phase synthesis, and the end products emerge easier to purify after deprotection.

    Customers who once tried cheaper, less-defined batches from traders often bring us up to speed on pitfalls: variable melting points, inconsistent response to deprotection, or unpredictable hydrolysis rates. From our own QC sampling, trace solvent contaminants or degradation byproducts contribute to these outcomes. High-throughput oligonucleotide synthesis centers—where productivity, yield, and reproducibility matter—won’t accept that unpredictability. For pilot-scale and scale-up studies, our regulars say the decision saves them both materials and time.

    Why In-House Manufacturing Matters

    Manufacturing modified nucleosides in-house, rather than drawing from third-party stock or trading networks, brings its own set of challenges. Yet we find few things more critical. Every step—from adenosine arrival, through benzoylation, neutralization, and crystallization—happens under our control and our eyes. Technicians rotate shifts to keep batch integrity consistent around the clock. Sourcing quality benzoyl chloride and ensuring no trace of catalyst carries over are basics, but years in the business show that only firsthand process knowledge offers the best long-term customer experience.

    Our labs collaborate closely with production teams. Small shifts in routine—from adjusting agitation rates to tweaking cooling curves—regularly come out of suggestions from staff who’ve seen what works. Frequent internal audits, compliance walkthroughs, and open-door policy for staff feedback let the organization catch risk before it grows. That process sits at the root of what customers appreciate: consistency and partnership. Many nucleoside suppliers claim purity, but longtime collaborators know the difference it makes when sourcing from an actual manufacturer, not a repackager or broker.

    E-E-A-T in the Real World: Depth, Responsibility, and Know-How

    Real expertise can't just be rehearsed for brochures. Every client comes in with a unique set of requirements. Some want academic small lots for research, others develop diagnostics under regulated conditions. Many have one thing in common: a no-tolerance policy for unknowns in their supply chain. Our staff brings not just academic degrees, but deep field experience. Many technicians started as apprentices and have moved through several process upgrades and scale expansions. That human knowledge—paired with a robust internal QA/QC process—shapes much of why our N-Benzoyl-2'-Deoxy-Adenosine stands out.

    Trust, responsibility, and transparency guide our choices. Mistakes in this sector show up quickly: dropped yields, ghost peaks in an impurity panel, tiny shifts in physical appearance. The only real answer is to deal with issues openly and to invite customers into the validation process. We regularly share batch sample reports, raw analytic data, and update on scale changes directly with our bigger partners, knowing that regulatory or scientific inspection may follow. Experience teaches that credibility is earned in repeated, real-world partnerships.

    Challenges and Solutions: Honest Lessons from the Plant

    Production rarely runs perfectly, and it’s a mistake to pretend otherwise. Over time, we see batches react differently to weather, raw material source, and even differences in process water. Troubleshooting starts with pattern-spotting. Staff uses real-time digital records to compare batches, spot deviation in yields, or track oddities. If an HPLC outlier appears, samples circulate for a second and third review. In some growing seasons, solvent recoveries or byproduct levels rise. Operators flag these for corrective actions, such as replacing adsorbents or running longer drying cycles.

    Inventory swings also create challenges in maintaining proper delivery schedules. Raw material purchasing works around long lead times, and though we stockpile essentials, occasional delays occur. Clients appreciate honest timelines. That transparency keeps schedules realistic and partners informed. A critical solution we’ve found is building strong, reliable relationships with a small number of trusted raw material vendors, including regular on-site visits. Cyclical demand from the life sciences sector adds pressure, yet we maintain buffer stock to level out the extremes as best as budgets allow.

    Safety and compliance have taken center stage. Regulators want clear records, stringent audits, and demonstrated control over cross-contamination, particularly in multi-product facilities. On the floor, our teams adhere to strict gowning, cleaning, and equipment rotation protocols. Audits occur not just on a scheduled basis but also as impromptu inspections. Problems become opportunities to learn. We’ve overhauled ventilation and solvent recovery several times over the past decade after identifying even a single near-miss. That focus on constant improvement impacts both product safety and ecosystem responsibility—signs of a responsible manufacturer.

    Direct Support—Expertise in Action

    Direct conversations with research scientists, formulators, and procurement professionals shape much of our process improvement. We host regular feedback calls and encourage open questions, sharing technical details openly within legal and compliance limits. These discussions surface recurring themes, from requests for lower water content to push certain solid-phase reagents, to the need for larger, purer lots to supply early clinical trials. Insights travel both ways: our staff learns about the latest challenges in downstream processing and can adjust routines to help.

    For particularly demanding projects—such as developing new phosphoramidite intermediates—we’ve joined client teams in adjusting synthetic routes, dosing schedules, and purification choices. Our chemical engineers adjust plant parameters, allowing new approaches to scale rapidly. We support novel method development, such as fragmentation or labeling studies, with samples and ongoing dialogue, not merely catalog quotes. That flexibility shapes our reputation and ensures materials function as designed in critical research settings.

    Conclusion: Advancing Research with Proven Quality

    N-Benzoyl-2'-Deoxy-Adenosine has moved from a niche reagent to an established backbone in nucleic acid chemistry. What lifts our offering above others isn’t only about purity figures or data points. It’s the combination of hands-on manufacturing experience, reliable supply, and a transparent, responsive partnership rooted in years of practice. In every bottle or bag sent out, our customers find the result of painstaking attention to detail and shared lessons from the real world of chemical manufacturing. The commitment stays the same: deliver excellent material, stand behind every batch, and propel research forward with a focus on integrity and knowledge.