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N4-Benzoylcytosine

    • Product Name N4-Benzoylcytosine
    • Alias N4-benzoylcytidine
    • Einecs 209-096-5
    • 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

    751349

    Chemical Name N4-Benzoylcytosine
    Cas Number 1026-85-5
    Molecular Formula C10H9N3O2
    Molecular Weight 203.20 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 246-248°C
    Solubility Slightly soluble in water, soluble in DMSO and methanol
    Pka 8.8 (approximate, for cytosine moiety)
    Storage Temperature 2-8°C
    Purity Typically ≥98%
    Synonyms N-Benzoyl-4-aminocytosine
    Inchi InChI=1S/C10H9N3O2/c1-8(14)13-5-6-12-9(7-13)11-10(15)4-2-3-4/h2-7H,1H3,(H2,11,15)
    Smiles C1=CC=C(C=C1)C(=O)NC2=NC=CC(=N2)N
    Application Protecting group in nucleoside synthesis

    As an accredited N4-Benzoylcytosine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of N4-Benzoylcytosine, tightly sealed, labeled with product details, safety data, and hazard warnings.
    Shipping N4-Benzoylcytosine is typically shipped in tightly sealed containers, protected from moisture, light, and extreme temperatures. It is packaged according to chemical safety regulations and may require labeling for hazardous materials. Shipping is usually expedited and tracked, ensuring safe and timely delivery to laboratories or research facilities.
    Storage N4-Benzoylcytosine should be stored in a cool, dry place, away from light and moisture. Keep the container tightly closed under inert gas, such as nitrogen or argon, to prevent hydrolysis and degradation. Store at 2-8°C (refrigerated) if long-term storage is required. Handle in a well-ventilated area and avoid contact with incompatible materials, such as strong oxidizing agents.
    Application of N4-Benzoylcytosine

    Applications of N4-Benzoylcytosine in Industrial Manufacturing

    N4-Benzoylcytosine is recognized in industrial supply chains as a precision intermediate deployed within specialized sectors that demand stringent regulatory compliance and traceable raw material sourcing. As a direct manufacturer, we serve leading enterprises by facilitating workflow integration, performance consistency, and audit-ready supply assurance for real-world applications rather than speculative or marginal use cases.

    1. API Synthesis for Cytosine Derivative Antivirals

    Research-based pharmaceutical producers select N4-Benzoylcytosine as a protected nucleotide precursor in multistep syntheses of cytosine-analog antivirals, particularly for prodrug and pro-moiety modification routes requiring minimization of process by-products. Downstream, process chemists utilize N4-Benzoylcytosine to achieve higher selectivity during N-acylated nucleoside assembly, enabling better impurity control for subsequent deprotection and purification steps that meet regulatory toxicity thresholds necessary for market authorization in regulated territories.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/EP/JP raw material monographs and impurity thresholds
    • 21 CFR Part 211 Current Good Manufacturing Practice (CGMP) for Finished Pharmaceuticals
    • EMA Guideline on Setting Specifications for New APIs

    Typical usage ratio

    • 0.2 – 0.8 molar equivalents relative to target cytosine nucleoside backbone; actual ratio depends on route selection and protection requirements, optimized during scale-up to control over-acylation.

    Downstream process integration

    • Introduced at the acylation stage for temporary protection of the cytosine N4 amino group during nucleoside assembly, prior to catalytic hydrogenolysis or hydrolytic deprotection.

    Final product types

    • Bulk active pharmaceutical ingredients (e.g., Lamivudine, Emtricitabine intermediates)
    • GMP-grade cytosine nucleoside analogues
    • Intermediates for further linkage to proprietary prodrug carriers
    • Validated APIs for oral and injectable antiviral medications

    2. Oligonucleotide Manufacturing for Molecular Diagnostics

    In the oligonucleotide manufacturing sector, downstream integrators employ N4-Benzoylcytosine to synthesize modified RNA or DNA fragments with site-specific base modifications. By providing a temporary protective group compatible with automated solid-phase synthesis, this raw material enables efficient cycle chemistry, avoids undesired secondary acylations, and ultimately produces highly pure diagnostic probes for PCR and gene sequencing assays that must satisfy worldwide diagnostic kit regulatory reviews.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices – Quality Management Systems
    • CAP/CLIA Validation Guidelines for In Vitro Diagnostic Reagents
    • QSR 21 CFR 820 FDA Quality System Regulation for Medical Devices
    • REACH Annex XVII Raw Material Restrictions (for import/export)

    Typical usage ratio

    • 0.5 - 1.1 equivalents per cytosine residue during solid-phase synthesis cycles, adjusted to minimize incomplete coupling and maximize deprotection rates in high-throughput batch runs.

    Downstream process integration

    • Charged during the base protection cycle in automated DNA/RNA synthesizers; removed with ammonia or basic hydrolysis at the final cleavage step to yield the functionalized oligonucleotide with unprotected cytosine bases.

    Final product types

    • Custom DNA/RNA oligonucleotide probes for real-time PCR
    • Diagnostic primers and gene detection panels
    • Molecular barcodes for clinical genotyping kits
    • Sequencing adaptors for next-generation sequencing platforms

    3. Specialty Fine Chemicals for Agricultural Genetic Marker Development

    N4-Benzoylcytosine also plays a core role in the formulation of genetic marker kits used for plant variety verification and trait mapping in commercial agriculture. Biotech companies integrate the protected base into synthetic template oligonucleotides destined for use in agricultural PCR kits, facilitating robust sequence recognition and minimizing nonspecific base pairing under field-grade thermal cycling conditions. Its precise specification ensures batch reproducibility demanded by agrigenomics regulators for official seed, crop, and germplasm certification programs.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (Applied Genomics)
    • ISO 17034:2016 Reference Material Producers Standard
    • EC 2002/657/EC Analytical Methods Validation (Plant Tissue DNA Tests)
    • USDA Accredited Laboratory Protocols

    Typical usage ratio

    • Typically 0.7 - 1.0 molar equivalents relative to the target oligonucleotide chain per synthesis batch, with adjustments based on marker design and expected annealing characteristics.

    Downstream process integration

    • Integrated at the base protection phase in oligonucleotide manufacturing, followed by controlled deprotection and purification to obtain ready-to-hybridize genetic markers for downstream formulation into PCR master mixes.

    Final product types

    • Genetic identification kits for crop variety authentication
    • Trait mapping reagents for breeding programs
    • Germplasm barcode panels for plant genetic resource management
    • Field deployable DNA testing strips

    4. Precursor in Modified Nucleic Acid Therapeutics Research

    Innovators in pharmaceutical R&D and next-generation therapeutics utilize N4-Benzoylcytosine as a high-purity, acylated nucleobase precursor for the design and construction of chemically modified oligonucleotides, such as antisense agents and RNA interference (RNAi) molecules. This raw material supports structure-activity optimization at the nucleobase level, letting researchers fine-tune target affinity, stability, and off-target profile before scale-up for preclinical or clinical GMP production. Analytical teams leverage the material’s specification traceability to meet both internal and regulatory documentation standards.

    Industry compliance standards

    • USP General Chapter <1047> Gene Therapy Products
    • FDA Points to Consider for Nucleic Acid-Based Therapeutics (CBER)
    • GLP (Good Laboratory Practice) for Preclinical Safety Studies
    • OECD Principles of Good Laboratory Practice

    Typical usage ratio

    • Ranges from 0.4 to 1.0 equivalents per targeted cytosine depending on the degree and positioning of modification in the oligonucleotide sequence; selected based on in vitro screening and pharmacokinetic requirements.

    Downstream process integration

    • Dosed into base protection steps during solid-phase or solution-phase nucleic acid synthesis; subsequently deprotected at the final assembly or post-synthesis modification stage to generate modified backbones suitable for lead optimization studies.

    Final product types

    • Antisense oligonucleotide research compounds
    • RNAi lead compounds for gene-silencing assays
    • Preclinical candidates for nucleic acid drug pipelines
    • Modified synthetic guide RNAs for genome editing research
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    Certification & Compliance
    More Introduction

    N4-Benzoylcytosine: Perspective from the Manufacturer

    What We Create in Our Plant

    Our team synthesizes N4-Benzoylcytosine through a direct benzoylation route, using high-grade cytosine as a starting point. Instead of chasing high throughput alone, we keep a steady eye on purity, since every gram that leaves our purification line carries our reputation with it. We run this process under tight control, using analytical verification at multiple steps. Typical product runs reach at least 99% purity by HPLC, and we ship the powder as a fine, crystalline solid. Packing happens in controlled rooms to guard against moisture and contamination because water uptake can affect handling further down the supply chain.

    Most of what we sell weighs out into research labs or pilot-scale production. Chemists use N4-Benzoylcytosine to build modified nucleotides, antisense oligonucleotides, and a growing list of molecular tools in both academic and industry settings. DNA and RNA synthesis workflows often require protected bases, and we learned long ago from direct customer feedback that impurity profiles and batch consistency matter more than labels or flashy datasheets. An erratic side product can eat up days of work at the downstream synthesis stage.

    Down the Line: What N4-Benzoylcytosine Delivers

    This compound stands out in the protected nucleosides market. The benzoyl group shields the exocyclic amino function at the 4-position of cytosine, a step that cuts down on unwanted side reactions during chemical synthesis steps. By comparison, other protecting groups—acetyl, isobutyryl—come with different removal conditions and can often complicate deprotection processes with byproducts or incomplete removal. In our experience, the benzoyl group is robust during commonly encountered cleavage conditions, yet it strips away cleanly under mild base.

    We've learned from feedback in the oligonucleotide industry: this reliability keeps workflows predictable and simplifies troubleshooting. Other analogs still have a place, but N4-Benzoylcytosine walks a practical line between stability under acidic conditions and ease of deprotection without introducing extra steps or obscure reagents. Customers developing oligo therapeutics lean heavily toward this profile, given the tight regulations and qualification testing that follow.

    Real-World Experience: Batch Consistency and Analytical Support

    A lot of what matters doesn’t show up on the label. Buyers might see purity or loss-on-drying figures, but what often builds trust are small things: repeatable chromatography, no unexplained peak drift from one lot to the next, no surprises under LC/MS analysis. Poor reproducibility in raw materials ends up amplifying errors in later chemical sequences, costing not just material but labor and project timelines. We run in-process checks, not just on finished lots, to keep each batch within specification.

    Sometimes, clients ask about residual solvents or trace metal content. We keep data sets from every major run, and our QC lab keeps an open-door policy for third-party audits. Our goal isn’t just meeting pharmacopeia specs but helping clients map our material’s performance into their own documentation, easing regulatory reviews or method validation.

    Some research clients push us for smaller, highly customized lots, ranging from multi-gram batches for exploratory steps to kilogram batches for scale-up. Skills in precise weighing and blending become essential here—cross-contamination risks creep in at low scales, making careful handling even more critical. You get less crosstalk with equipment rinses, and this can make or break a customer's downstream process. The people in our team doing these jobs have handled these requests hundreds of times, and their practical know-how means mistakes rarely reach the customer.

    Applications: Serving Researchers Making a Difference

    N4-Benzoylcytosine supports a range of chemistries in nucleotide and nucleic acid modification. We’ve seen our material end up in custom DNA syntheses, CRISPR guide RNA engineering, and sequencing applications. Biotech firms building next-gen PCR kits or DNA-editing enzymes use our product when they require a stable, modifiable cytosine base. The trend toward more selective oligonucleotide therapeutics in diseases like cancer, rare genetic disorders, and viral infections has driven greater demand for dependable reagents like this.

    Researchers sometimes share their frustrations with low-quality nucleosides bought from generalist chemical suppliers. We try to fill that gap by offering transparency and technical support, not just a bucket of powder. If a customer’s reaction mix keeps generating unknown byproducts, we can check retention times or run NMR profiles alongside theirs to see if the source traces to our lot or another reagent. These exchanges help us improve our synthetic control and alert other customers in case something systemic is brewing.

    Our technical staff fields routine questions about application-specific details, like the compound’s stability under various coupling conditions. Years of internal testing around temperature, pH, and storage variables feed our user guides. We have compared N4-Benzoylcytosine to other protecting groups in-house, monitoring for base hydrolysis or incomplete deprotection. We answer detailed questions promptly, whether the customer is engineering novel nucleotides or replicating well-known sequences at scale.

    Comparing with Other Products: Key Distinctions

    Plenty of chemical suppliers pitch similar products, but manufacturing from the ground up has shown us where the devil sits—in the details. Some products appear alike at first glance but contain unaccounted isomeric byproducts or residual moisture, which disturbs downstream reactions. Experience tells us that end-users can’t afford inconsistent materials when pilot-scale batches decide the fate of a new therapy or a diagnostic tool.

    Other common protected cytosines—N4-isobutyrylcytosine, N4-acetylcytosine—follow comparable synthetic routes up to a point. Each protecting group suits a particular use-case, but benzoyl remains stable enough to survive the anhydrous acidic conditions in solid-phase oligo synthesis, then releases under milder alkaline exposure. Isobutyryl, favored mainly in classic phosphoramidite synthesis, still brings more difficult deprotection and sometimes lags behind in completeness. Scientists keen to avoid base damage frequently select our N4-Benzoyl product for maximum strand yield and fewer truncations.

    We maintain side-by-side test runs to compare our product with others in the market. Controlled lab notes have revealed that, under a broad range of pH and solvent conditions, our product’s shelf-life and performance stay consistent. An overlooked feature: the benzoyl group’s added aromaticity reduces reactivity during prolonged storage, cutting the risk of hydrolytic loss or ring-opening side reactions.

    We avoid the old industry game of marketing through technical jargon or inflated claims. Instead, repeat customers from both pharma and research settings say that clean NMR, batch traceability, and transparent supply matter well beyond price or immediate delivery. Data from repeated full-length oligo syntheses with our N4-Benzoylcytosine show side-product reduction up to 25% over in-market competitors using alternate protecting groups. These are figures we track and refine with every outgoing shipment.

    Quality Assurance as an Embedded Value

    No batch ships out until it clears a battery of physical and chemical tests. Using validated HPLC methods, we monitor not only for main peak purity, but for subtle contaminants like isomeric overreactions or early hydrolysis. Residual solvent data tracks to every batch code in our archives. Our line staff keep a detailed chain of custody per drum, so anything unusual gets caught before product release.

    Protocols matter less than operator attention to quality. Many of our team members have chemistry degrees, but hands-on experience with scaling sensitive syntheses often separates a smooth run from a recall. We calibrate balances against internal weights, and every blend receives spot checks for particle size and flow. Direct observation, repetition, and training build a culture where mistakes get fixed before product hits the warehouse.

    If an academic partner reports difficulty with a particular run, we’ll split their remaining sample side-by-side with an archived retention lot under lab conditions. This form of ongoing support keeps us sharp and sends a message to every buyer: if something goes wrong, we don’t dodge transparency. Analytical reports are shared openly because we want customers returning for reliability, not just price.

    Manufacturing Challenges and How We Address Them

    Controlled synthesis of N4-Benzoylcytosine comes with its own challenges. High-purity cytosine feeds, benzoyl chloride of fine enough grade, and effective moisture elimination matter on every run. Even a slight temperature drift during reaction can tilt impurity ratios, and we learned the hard way that trace acids or bases can cause side reactions that echo into later reprocessing.

    We employ closed-system reactions under dry nitrogen, cutting down on potential hydrolysis or oxidation. Reactors are glass-lined for easy cleaning between batches, and our solvent recovery protocols both save cost and reduce environmental impact. Filtration is monitored and validated per run with micron screening, which prevents fiber or particulate carry-through.

    Drying is a crucial step; our facility runs under regulated humidity, and we carefully track loss-on-drying figures per drum. Packages seal under vacuum or nitrogen flush and are stored in an environment with strict humidity and temperature settings until shipment. These field-tested controls help guarantee that what arrives in a client facility matches what left ours.

    Customer Support and Ongoing Communication

    Customers bring practical questions to our support staff—about reaction scale, storage, or analytical verification—and expect answers grounded in experience. We have technical staff available not just for email exchanges but for in-depth discussions on synthetic troubleshooting, regulatory compliance, or stability studies. A trusting relationship grows out of these ongoing conversations.

    Our customer support shares analytical data upon request so labs can match our standards with their in-house QC. We’ve worked with early-stage startups and established biotech companies refining processes for scale-up, adapting lots to match their workflow. If a researcher’s experiment fails, we pull archival samples and data to look for lab-to-lab variables, not just defects. This direct line of support separates us from traders with little knowledge of the product’s journey from raw material to final drum.

    We invite in-person or remote audits by customer QA teams. Our confidence in the product comes from the company-wide ethos: nothing leaves the warehouse without traceable documentation, and all analytic reports map to a verified batch code. If a client asks for a copy of a spectrum or a certificate review, we produce them within days, often faster. Consistency in documentation builds the kind of transparency regulatory authorities—and, in time, patients—depend upon.

    Looking Ahead: Meeting the Future of Protected Nucleosides

    Industry shifts toward stricter regulatory oversight, novel therapeutic pipelines, and rising demand for high-fidelity nucleic acids keep us innovating. We invest in periodic process reviews, quantifying not just yield per run but solvent use, byproduct minimization, and the environmental impact of each synthesis step. We actively test greener reagents and waste-reduction methods in pilot-scale reactors to cut process risk and stay compliant with evolving standards.

    Biotechnology continues to expand beyond classic DNA synthesis into RNA vaccines, gene therapy, and epitranscriptomic modification. Demand for more specialized and stable protected nucleosides climbs every year. Small experimental firms sometimes need microbatches, while larger biologics companies ramp up to pilot and commercial scale. Both rely on timely, candid feedback from suppliers that know the business end as well as the laboratory bench.

    Why We Choose to Stay Hands-On

    Staying in close touch with both synthesis and customer feedback keeps us tuned to the real needs of researchers and commercial manufacturers. Our best process changes come from conversations—hearing where pain points lie, finding which purification steps don’t translate outside of theory, and matching batch sizes to each client’s workflow. This continual engagement means we spot issues early and commit to resolving them head-on.

    Many competitors operate as brokers or outsource critical steps. By investing in our own manufacturing and analytics, we retain control and flexibility. If a field customer calls with a challenge—product instability, new impurity peaks, need for even higher purity—we test, adapt, and share insights back with the community. We take the view that trust, not marketing claims, leads to long-term customer relationships.

    N4-Benzoylcytosine demands attention and experience from the people producing it. Every challenge solved, every run refined, and every conversation with a fellow chemist improves both our product and the science carried out by those who rely on it. Our commitment is to continue setting a high bar—not through loud claims, but through the daily work of consistent, rigorous production and open support.