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8-Bromoadenosine

    • Product Name 8-Bromoadenosine
    • Alias 8-Bromoadenosine;8-Br-Ado;NSC 148141
    • Einecs 225-895-7
    • 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

    466312

    Cas Number 2381-07-5
    Molecular Formula C10H12BrN5O4
    Molecular Weight 358.14 g/mol
    Appearance White to off-white powder
    Purity Typically ≥98%
    Solubility In Water Soluble
    Melting Point 205-210°C (decomposes)
    Storage Temperature -20°C
    Synonyms 8-Bromo-adenosine, 8-Bromoadenosine-9-β-D-ribofuranoside
    Chemical Structure Nucleoside analog with a bromine atom at the 8-position of adenosine
    Iupac Name 9-β-D-Ribofuranosyl-8-bromoadenine

    As an accredited 8-Bromoadenosine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 8-Bromoadenosine is supplied in a 100 mg amber glass vial with a tamper-evident cap, labeled with product and safety details.
    Shipping 8-Bromoadenosine is shipped in secure, sealed containers, protected from light and moisture. The chemical is handled according to applicable regulations, requiring appropriate hazard labeling and documentation. Shipments are typically sent via priority courier with temperature control if necessary, ensuring product integrity and compliance with safety standards during transit.
    Storage 8-Bromoadenosine should be stored in a tightly sealed container, protected from light and moisture, at -20°C. Avoid repeated freeze-thaw cycles to maintain chemical integrity. Store in a dry, well-ventilated area away from incompatible substances such as strong acids or bases. Proper labeling and handling precautions are essential to ensure safety and stability during long-term storage.
    Application of 8-Bromoadenosine

    Applications of 8-Bromoadenosine in Industrial Manufacturing

    8-Bromoadenosine serves as a critical chemical intermediate in several high-value downstream sectors. As a manufacturer, we deliver material tailored for advanced research, regulated pharmaceutical synthesis, diagnostic development, and academic supply. Below, we detail its industrial applications, industry-specific compliance, targeted dosing parameters, downstream process roles, and finished product categories.

    1. Pharmaceutical API Synthesis for Antiviral Research

    Pharmaceutical companies incorporate 8-Bromoadenosine as a nucleoside analog for early-stage antiviral compound development. The unique halogenated structure enables nucleoside modification required in experimental drug candidates targeting RNA polymerase and related viral enzymes. Our GMP-grade material integrates into high-purity multi-step organic syntheses, where each process demands precise molecular configuration tracking and strict impurity control. End products supply ongoing pre-clinical screening pipelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <823> Recombinant and Synthetic Nucleosides
    • 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • FDA Guidance for Industry: Drug Substance

    Typical usage ratio

    • Ranges from 0.05 molar equivalents to 0.15 molar equivalents; subject to process optimization by route and targeted nucleoside analog yield.

    Downstream process integration

    • Employed as a key reactant in the nucleoside functionalization stage.
    • Introduced during early-step halogenation or as an intermediate for phosphoramidite coupling.
    • Batch or continuous flow reactors apply real-time in-process QC for residue and reactivity.

    Final product types

    • Investigational antiviral drug candidates
    • RNA polymerase inhibitors for infectious disease trials
    • Nucleotide prodrugs for Phase I–II clinical evaluation

    2. Nucleic Acid Probe Manufacturing for Molecular Diagnostics

    Specialist diagnostic manufacturers use 8-Bromoadenosine to synthesize modified oligonucleotide probes for qualitative and quantitative nucleic acid testing platforms. Its bromine substitution enhances probe affinity and enables site-directed incorporation in labeled molecular beacons and reporter strands. The compound enters automated DNA synthesizer lines where precise chain assembly and post-coupling purification require trace water and metal control.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices Quality Management Systems
    • CLSI MM12-A Molecular Methods for Clinical Diagnostics
    • EU In Vitro Diagnostic Regulation (IVDR) 2017/746
    • FDA 21 CFR 809 In Vitro Diagnostic Products for Human Use

    Typical usage ratio

    • Utilized at 1.0–10.0 μmol per synthesis batch; actual dosing set per probe design and degree of labeling required.

    Downstream process integration

    • Fed into phosphoramidite chemistry during automated solid-phase synthesis.
    • Integrated as a site-specific nucleotide replacement in custom probe sequences.
    • Cleansing steps follow to remove residual halide and confirm substitution accuracy.

    Final product types

    • Custom qPCR probes
    • Fluorescent molecular beacons
    • Labeled nucleic acid detection kits

    3. Enzyme Substrate Development in Biochemical Research

    Biochemical and life science laboratories leverage 8-Bromoadenosine as a defined substrate or inhibitor in enzyme kinetics, particularly for adenosine deaminase and related transferase screening. Its selective modification alters enzyme recognition, permitting assay of catalytic mechanisms or new inhibitor scaffolds. Material specifications target high solubility and minimal byproduct content to support reproducible kinetic analysis and thermodynamic profiling.

    Industry compliance standards

    • ISO/IEC 17025:2017 General Requirements for the Competence of Testing and Calibration Laboratories
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH Regulation (EC) No 1907/2006 for Laboratory Chemicals
    • NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic Acid Molecules

    Typical usage ratio

    • Added at 0.1–1.0 mM final concentration in reaction mixtures; level depends on experimental design, enzyme turnover number, and inhibition constants.

    Downstream process integration

    • Direct addition to biochemical assay buffers or microplate reagent sets.
    • Used in substrate saturation curves, inhibition mapping, or enzyme fidelity testing.
    • Integrated with analytic HPLC/MS for substrate-product turnover monitoring.

    Final product types

    • Biochemical assay kits
    • In vitro enzyme research reagents
    • Reference standards for academic and industrial R&D

    4. Modified RNA Synthesis for Academic and Industrial Research

    RNA technology developers and academic core facilities source 8-Bromoadenosine to help synthesize site-specifically modified RNA oligonucleotides. The bromine atom enables incorporation at designated positions, supporting studies of RNA secondary structure, protein-RNA interaction, and synthetic biology constructs. Stringent batch controls ensure low-level organic residues and high lot-to-lot reliability for advanced RNA modification projects.

    Industry compliance standards

    • ISO 9001:2015 for Laboratory Production and Process Documentation
    • Guidelines for Synthetic Nucleic Acid Research (CDC NIH)
    • Supplier-specific quality control protocols for oligonucleotide building blocks
    • Relevant institutionally approved chemical safety and stewardship guidelines

    Typical usage ratio

    • Substituted at 1–2 sites per 15–100 base RNA sequence; actual incorporation level guided by experiment objectives and structural requirements.

    Downstream process integration

    • Added during automated or manual solid-phase RNA synthesis cycles.
    • Site identification and verification performed using MALDI-TOF or NMR post-synthesis.
    • Purification by preparative HPLC to yield analytical-grade RNA for downstream applications.

    Final product types

    • Synthetic modified RNA oligonucleotides
    • Research-grade RNA for NMR or X-ray crystallography
    • RNA probes for ribonucleoprotein interaction studies
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    More Introduction

    The Role of 8-Bromoadenosine in Modern Research Labs

    Tracking progress in research often means spending time with chemical compounds that promise to spark the next breakthrough. 8-Bromoadenosine is one of those compounds. Folks who work with cell signaling, metabolic studies, and RNA experiments have likely heard about it, if not already used it in the lab. It’s a synthetic analog of adenosine, which might not sound exciting at first, but that slight molecular twist – swapping a hydrogen for a bromine at the 8th position – changes how it interacts inside biological systems. Labs come to rely on this difference for tasks where standard adenosine just won’t cut it.

    The Unique Character of 8-Bromoadenosine

    The first thing people notice about 8-Bromoadenosine is how it stands apart from adenosine by resisting certain enzymes more effectively. This single change lets scientists study metabolic and enzymatic pathways without worrying about rapid breakdown. Experienced bench scientists trust this compound when they need a nucleoside that's a little more stubborn. Standard research-grade 8-Bromoadenosine usually appears as a white to off-white solid and dissolves readily in water or buffer, making it easy to handle without fuss. Purity can swing above 98 percent when sourced from a reputable provider. That level of consistency gives researchers peace of mind, as unexpected impurities can wreck a multi-day experiment.

    The model I’ve had success with usually ships as a powder in amber vials. Even after years of storing similar compounds, the extra care taken to avoid light exposure with brominated variants is worth noting. It keeps oxidation at bay. Those minor tweaks in handling mirror how small molecular changes have big impacts once this nucleoside is put into action.

    How Scientists Use 8-Bromoadenosine

    Looking at real use cases, 8-Bromoadenosine doubles as a valuable molecular tool. In my time working with it, I found its strength in modulating adenosine receptor activity really shines. By blocking or tweaking biological pathways, you can probe deeper into the signaling world, seeing how cells talk to each other under stress or in normal growth. This same property means researchers tap it for dissecting enzyme selectivity and understanding the nuts and bolts of nucleic acid metabolism. It’s more than a substitute for adenosine; it's a lens into cell behavior. Work published over the past decade credits 8-Bromoadenosine for clarifying the role of second messengers and shining a light into the varied lives of kinases and phosphatases.

    When pipetting out another batch, I noticed that unlike standard adenosine, the brominated analog rode through enzymatic modifications differently. Kinase assays react slow to it, which lets you pick apart phosphorylation patterns with precision. That detail makes it possible to model diseases or test new drugs with more confidence. In some metabolic studies, cells treated with this analog slow down their use of energy, a property exploited to model energy depletion or stress conditions without killing the cells outright.

    Comparing 8-Bromoadenosine and Other Adenosine Analogs

    I’ve had a chance to work with a few adenosine derivatives over the years: 2-chloroadenosine, N6-methyladenosine, and N6-benzyladenosine come up a lot when it’s time to study signaling or RNA modification. The distinction starts with stability. 8-Bromoadenosine sticks around; it’s not as prone to getting broken down by adenosine deaminase or other pesky enzymes in solution. That matters for anyone looking for sustained action during longer experiments, especially in cell culture or in situ tissue work.

    N6-substituted analogs often grab headlines for their role in epigenetic research, but they may interact with methyltransferases and enzymes in unpredictable ways. On the other hand, 8-bromo derivatives like 8-Bromoadenosine favor a straightforward course – they’re better for directly provoking or blocking specific receptor responses in a more controlled manner. This gives researchers a sharper edge when mapping out signaling cascades that don’t muddy the water with too many side-pathways. While 2-chloroadenosine may have its uses, it tends to be more potent in activating adenosine receptors broadly, which can complicate interpretation of results. Brominated analogs like this one show more selectivity, or at least a more manageable profile of action, which is essential for teasing apart layered cell responses.

    Why 8-Bromoadenosine Matters for Modern Science

    It’s easy to assume every nucleoside derivative is just another tool in a vast molecular toolbox, but anyone who spends time in a molecular biology or cell signaling lab sees the difference day to day. 8-Bromoadenosine stands out because of its predictability and resilience. Having a reliable compound that resists enzymatic decay lets scientists conduct experiments that reach further – longer time-lapses, repeated stimulations, or robust pathway probes.

    Beyond technical convenience, this analog fits inside the framework of rigorous science. Reproducibility is a big deal; too many promising results have faded in follow-up studies when variables like nucleoside breakdown go unaccounted for. My own attempts at repeating published kinase assays only started to succeed once I switched to 8-Bromoadenosine. It simplified workflow, cut down on annoying troubleshooting, and helped ensure the right controls held steady all the way through. More granular experiments, like slow titrations or kinetic progress curves, became much more practical.

    There’s also a trust factor involved. When I reach for a bottle of 8-Bromoadenosine, I know I'm working with a compound that's well-documented in literature and that my results won’t gather suspicion from colleagues or reviewers. Confidence in a material means fewer repeats and saves precious time – and in a research world where budgets get squeezed annually, that's no small gain. Choosing the right analog isn’t just about chemistry; it's about the pace and certainty of progress.

    Recent Breakthroughs and Applications

    It’s not all familiarity. Research communities using RNA-based drugs or modifying genetic circuits count on 8-Bromoadenosine as a sort of tuning fork. In cell culture, this analog fine-tunes receptor studies, acting almost like a dimmer switch rather than an on/off button. Neuroscience labs lean on it for teasing out the subtleties of neurotransmitter release and synaptic remodeling, since its resistance to adenosine deaminase means it sticks around long enough to be measured without heavy background noise.

    In metabolic research, 8-Bromoadenosine can dictate cell energy dynamics, showing its value in work involving AMP-activated protein kinase (AMPK) and related signaling pathways. Dissecting pathways like this is where small differences in nucleoside stability and behavior matter most. RNA studies add another layer: because of its unique structural twist, 8-Bromoadenosine helps demystify how ribozyme and riboswitch elements respond to modified substrates. Compared to standard adenosine, its signature allows targeted probes to trace activity and binding with more clarity. This is especially useful for groups experimenting with RNA-based therapeutics, as small differences picked up in the lab lay the foundation for later clinical work.

    On another front, some cancer research pivots on using 8-Bromoadenosine to slow proliferation in aggressive cell lines. This helps scientists single out which pathways matter most for unchecked cellular growth and what happens when energy management is disrupted. Reports from oncology teams keep emerging, showing that this analog is more than just a research curiosity; it acts as both a probe and a blocker, giving scientists a real shot at separating cause from effect in models of disease.

    Best Practices in Handling and Storage

    My shelves have seen their share of nucleoside analogs losing potency thanks to sloppy storage. 8-Bromoadenosine deserves the extra attention. Keeping it in tightly sealed vials away from sunlight extends its shelf life. That way, every batch keeps its promise, and reproducibility improves across repeated experiments. Water solubility simplifies prep work, but it’s worth using purified water to rule out issues from ions or contaminants.

    Once dissolved, it’s best to use this analog the same day. Repeated freeze-thaw cycles or sitting out at the bench often shortens the window for reliable results. Sets of aliquots stored at -20°C save time and cut down on wasted material. Following these habits isn’t just about being neat; it lets 8-Bromoadenosine perform at its peak and prevents a bad day’s data from creeping into big-picture interpretations.

    Challenges and Future Prospects

    Even good compounds have tradeoffs. One challenge with 8-Bromoadenosine comes up during scale-up. Pricing can swing depending on availability of high-purity starting material and expertise of suppliers. This sometimes puts a squeeze on small labs hoping to integrate it into larger screens. Sourcing only from reliable vendors becomes part of the experiment, as lower-cost, off-brand batches might carry impurities or lack the purity needed for downstream work.

    Waste management poses another issue. As with many halogenated organics, safe disposal needs more than just pouring unused material down the sink. Labs stick to local regulations and partner with certified waste handlers. Those grounded in the real world of hazard management know cutting corners threatens both health and environmental integrity. Regulatory scrutiny around brominated analogs also means researchers pay attention to batch documentation and track every gram that moves through the lab.

    Technology marches on, and future improvements might revolve around making synthesis cleaner and more sustainable. A push for greener chemistry already influences many suppliers, steering processes towards less toxic reagents and recyclable solvents. With market interest rising for nucleotide analogs in fields like synthetic biology and personalized medicine, availability of 8-Bromoadenosine in different forms – higher concentrations, sterile-stock solutions, or novel salt versions – could help shave time off workflows and open fresh possibilities for clinical translation.

    Training and Onboarding New Researchers

    Bringing in new grad students or staff means more than basic protocols; it includes mindset training for using compounds like 8-Bromoadenosine. It’s easy to miss the small decisions that drive reproducible, clear results. In my own labs, training sessions highlight why careful weighing, light protection, and labeling matter. Peer mentoring guarantees fewer mishaps, but having a culture of curiosity goes further. Newcomers find themselves drawn to 8-Bromoadenosine’s role in teasing out precise experiments and learning about how targeted molecular changes shift outcomes.

    Teaching with real examples helps - showing what happens to assay curves when using freshly prepared analog versus one that’s degraded in sunlight or suffered too many freeze-thaws. Building this awareness early prevents costly errors. Documentation, both in physical lab books and digital inventory, closes the loop so every experiment can be retraced if questions pop up later. Passing on these lessons secures a legacy of rigor with every new batch of researchers entering the field.

    Building a Collaborative Research Network

    8-Bromoadenosine fosters connections across scientific communities. Groups studying cardiovascular disease, oncology, and neurology use it as common ground. Sharing results and protocols in open forums helps keep progress moving. This compound’s clear documentation and wide citation base make it a convenient reference point for peer reviewers and collaborators alike. One of the great strengths is the way it acts as a bridge between biochemical studies, drug discovery, and applied cellular biology.

    Scientists benefit by staying plugged into ongoing discussions about best practices, troubleshooting rare issues, or even pooling purchasing power for bulk orders. Real-world science isn’t a solo pursuit, so routine communication ensures new findings and methods get vetted, refined, and shared quickly. This kind of open exchange helps turn basic chemical tools like 8-Bromoadenosine into conduits for collective discovery, where everyone shares in the responsibility and reward of pushing scientific boundaries.

    Final Thoughts: Value Beyond the Bench

    Whether the focus is on dissecting delicate molecular pathways or experimenting with RNA modification, 8-Bromoadenosine embodies the careful intersection of chemistry and biology. Its unique resilience, clear handling protocols, and broad applicability ensure it remains a favorite for those aiming to run reliable, reproducible experiments. From bench to publication, it enables a rare kind of confidence. Every researcher benefits from picking the right analog, and 8-Bromoadenosine often turns out to be the right choice for those who need a combination of stability, specificity, and documented performance in their chemical arsenal.