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HS Code |
407959 |
| Product Name | 8-Bromoadenine |
| Cas Number | 4426-47-5 |
| Molecular Formula | C5H4BrN5 |
| Molecular Weight | 214.03 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 315-317 °C |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C |
| Iupac Name | 8-bromo-7H-purin-6-amine |
| Synonyms | 8-Bromo-6-aminopurine |
| Smiles | C1=NC2=C(N1)N=CN=C2Br |
| Inchi | InChI=1S/C5H4BrN5/c6-3-4-2(1-7-5(4)10)8-9-3/h1H,(H3,7,8,9,10) |
| Boiling Point | Decomposes before boiling |
As an accredited 8-Bromoadenine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Scientific tools help open doors in research, and 8-Bromoadenine stands out among the many compounds found in biochemical labs. With years spent in molecular biology, I’ve seen how vital it is to have specific reagents when digging into the mechanics of DNA and RNA. 8-Bromoadenine, a brominated derivative of adenine, serves a distinct role. In structure, it carries a bromine atom bonded at the 8th position of the purine ring, changing how it interacts in a biological context. This small modification brings about properties different from regular adenine and other analogs, making it useful in a variety of research settings.
Research-grade 8-Bromoadenine comes with a focus on purity and consistency. In a lab, even tiny impurities can throw off results, especially for experiments examining minute changes in nucleic acid structure or enzyme recognition. From experience, I’ve learned the importance of checking not just for high assay values—often well above 98%—but also ensuring free flow granules and reliable lot-to-lot performance. The compound is typically supplied as a powder or crystalline solid, with color ranging from white to slightly off-white. This visual simplicity hides the complex possibilities unlocked by its molecular tailoring.
There’s a reason 8-Bromoadenine draws researchers interested in genetics, pharmacology, and enzyme function. Its unusual structure allows it to serve as a probe when mapping out adenosine-related biological processes. It fits into DNA and RNA structures but brings along a twist—altered hydrogen bonding. In studies probing DNA replication or repair, replacing normal adenine with 8-Bromoadenine lets scientists see how cells cope with modified bases. This tool helps unravel the fidelity of DNA polymerases or the selectivity of repair enzymes, revealing weaknesses or fail-safes in the cell’s machinery.
This molecule isn’t confined to DNA work. It also appears in biochemistry for studying purine metabolism, where enzymes catalyze transformations between bases. By swapping out adenine for 8-Bromoadenine, biologists can track changes in binding specificity or catalytic rates. Studying these subtle differences often leads to breakthroughs in drug design or our understanding of inherited metabolic diseases.
Researchers have used a roster of adenine analogs—2-aminopurine, 6-methyladenine, N6-benzyladenine—to test theories about DNA structure, enzyme targeting, or cell signaling. Each analog brings a unique twist; for example, 2-aminopurine fluoresces under UV light, which suits imaging but not always studies of hydrogen bond pairing. 8-Bromoadenine’s distinct feature is its capacity to disrupt traditional base pairing without substantially altering the backbone of DNA or RNA. This feature offers an opportunity to examine how tiny chemical changes drive—or disrupt—normal function.
While 6-methyladenine plays a huge role in epigenetics studies, and N6-benzyladenine gets attention in plant biology as a cytokinin, 8-Bromoadenine finds its niche in mapping out base mispairing and sensitivity to DNA damage. The bromine atom isn’t massive—but it’s bulky enough to reduce hydrogen bonding efficiency and increase base mispairing rates during replication. This property helps simulate mutagenesis processes or stress-test error-correcting routines in cellular systems.
Labs get to know their reagents by how they work—whether the powder dissolves cleanly, whether every batch acts the same, whether hidden contaminants cause headaches months down the line. My best collaborations happened with reliable sources, who take stability and batch documentation seriously. High purity ensures that experimental changes come from planned modifications, not stray byproducts. 8-Bromoadenine, when sourced with rigor, fits this bill. Good storage practices—cool, dry, away from UV light—help maintain its performance, preventing slow degradation that can trip up precision experiments.
One critical use for this compound is in testing the selectivity of DNA and RNA polymerases. By inserting 8-Bromoadenine into controlled positions, researchers watch for changes in error rates or enzyme kinetics. This approach reveals how enzymes accommodate modified nucleotides or signal them as something foreign. My time studying polymerase fidelity showed just how revealing it can be—8-Bromoadenine challenges the system, showing weak spots in the enzyme’s ability to distinguish between closely related structures.
Beyond the test tube, scientists introduce this analog into living cells or cell-free systems to observe how well repair pathways respond. If a cell recognizes and excises 8-Bromoadenine, it gives insight into the defense mechanisms against abnormal DNA damage. In contrast, a failure can show where repair pathways struggle, hinting at susceptibility to genetic disorders or chemotherapeutic side effects. These lines of research guide both fundamental biology and applied medicine.
The field of pharmacology often borrows tools from molecular biology. 8-Bromoadenine, for instance, sometimes features as a model lesion in toxicity tests or as a probe to examine drug-DNA interactions. Because it subtly alters base pair stability, 8-Bromoadenine helps simulate the effect of environmental mutagens that modify DNA after exposure. It stands in as a surrogate, enabling safer, controlled studies into mutagenesis mechanisms without resorting to unpredictable or highly dangerous chemicals.
This analog also shows up in drug development as a building block for designing new molecules. Researchers look for analogs that modify enzyme targeting or signaling, hoping to either block viral replication or tweak cell cycle checkpoints. Using 8-Bromoadenine to screen for small molecule binders or to test compound specificity offers a window into the likely biological behavior of new therapeutic leads.
It’s easy to overlook how a single research reagent can shape years of discovery in multiple labs. While the broad strokes come down to technical compatibility and price, the deeper significance of 8-Bromoadenine rests in its reliability. Nobody wants surprises halfway through a multi-stage experiment. My former team once dealt with a poorly characterized batch—false negatives and days spent retracing steps. This kind of setback teaches the value of proper sourcing and strict verification, even for seemingly routine chemicals.
Another often underestimated aspect is regulatory and safety handling. While not as hazardous as some nucleobase analogs, this compound still deserves care. Proper labeling, equipped storage space, and clear training about handling go hand in hand with its scientific application. Labs keep safety data sheets on hand—not just as a formality, but to build a safe, functional working environment where accidents remain rare.
No single compound fits every experimental design. 8-Bromoadenine exemplifies how research tools must keep evolving. Challenges pop up—accuracy at low concentrations, solubility in non-standard buffers, interference with downstream assays. Part of the solution comes from open exchange in the research community. Forums, journals, and shared protocols let early career scientists learn from those with decades of hands-on experience.
Changing research needs mean suppliers face fresh demands. I’ve seen protocols shift toward greener chemistry, higher throughput, and digital verification. Some companies now offer real-time online analytics on lot consistency. While technology brings improvements, the core principle remains: a reagent that can be trusted, with transparent documentation.
Whether working in a university setting or biotech firm, the expectations remain similar. Researchers look for solvents and reagents that won’t bring hidden surprises into carefully controlled work. 8-Bromoadenine stands as a clear example of how quality control underpins scientific advance. Labs working with high-throughput DNA sequencing or custom enzyme screens require analogs that match strict performance parameters. The compound also finds use in teaching labs to illustrate the impact small changes in nucleotide structure have on biological outcomes.
Supplier support plays a role here. Researchers sometimes extend protocols to new enzymes or substrates. Access to technical support, real-life troubleshooting, and rapid replacement in case of unexpected issues creates an environment where exploration doesn’t get derailed by chemical inconsistencies.
With more emphasis on reproducibility, chemicals like 8-Bromoadenine land in the spotlight. Reports of irreproducible science trace back to mismatched stocks, hidden impurities, or poor documentation. Part of my own research training involved checking every detail from bottle label to final report. Reagents that supply detailed certificates of analysis, batch testing reports, and clear expiration dates help safeguard against these problems.
Careful record keeping, peer review, and transparent reporting work together to keep experiments grounded. It’s impossible to guarantee results without reliable reagents. In the case of 8-Bromoadenine, matching product documentation to batch use logs ensures a clear trail if questions come up during publication or review.
The sciences don’t stand still. I watch professional networks discuss new uses for purine analogs, testing modified forms under emerging reaction conditions or developing next-generation sequencing platforms. Synthetic chemists design analogs with even greater specificity or altered base-pairing abilities, hoping to tease further detail from nature’s language. As understanding of DNA and RNA continues to grow, compounds like 8-Bromoadenine will play a role both as blunt instruments and fine scalpels in molecular investigation.
Improvements in characterization methods offer hope for early detection of contaminants or slow shifts in reagent quality. Automated tracking and tighter feedback among suppliers, researchers, and peer reviewers can highlight problems before they ripple out. It’s a cooperative effort—from the point of synthesis to the final publication—anchored by consistent, open communication.
Unlike more common nucleobase analogs, 8-Bromoadenine holds its ground through its combination of accessible chemistry and targeted perturbation of the nucleotide world. It won’t fit every project, nor should it—but in the context of probing DNA fidelity, mutagenesis, base repair, and purine metabolism, it gives teams a sharper lens. Instead of overwhelming biological systems or introducing unrelated variables, 8-Bromoadenine applies precise, predictable pressure. This lets teams challenge biology without introducing chaos.
Real breakthroughs rely not just on discovering the right question, but on having the right tools to answer it. The analog’s long track record in scientific literature, along with the breadth of data published on its interactions, allows researchers to plan studies with fewer unknowns. Years of collective knowledge help new researchers avoid pitfalls and explore new frontiers.
From personal experience, value comes not from the lowest price per gram, but from overall project costs—experiment downtime, troubleshooting, repeat experiments, and overall confidence in data. By choosing a well-documented, high-purity batch, labs cut those hidden costs and focus on advancing research. Close collaboration with suppliers, transparent information flow, and regular validation testing form a safety net against wasted resources.
Scientists often share protocol tips—optimal solvent, gentle mixing to dissolve, order of addition in complex buffers. These seemingly minor details help protect both the compound’s stability and data quality. Small investments in researcher training and regular reviews of product documentation pay off through smoother progress.
There’s more to a research chemical than just its specs. One can trace the flow of impact from a bottle of 8-Bromoadenine to the stories that emerge in journals, student theses, and new drug candidates. To those outside the lab, it can look like one more powder among thousands. To scientists focusing on DNA mechanics, enzyme function, or cellular repair, it becomes a lens that clarifies or distorts reality, depending on its integrity.
The science community depends on mutual trust—between suppliers, scientists, publishers, and readers. 8-Bromoadenine won its place in research by meeting the challenge of reliability and specificity, proving itself as a tool that brings clarity, not noise, to tough scientific questions.
People often think progress requires only bright ideas and cutting-edge machines. In practice, it’s the steady march of reliable, high-quality reagents along with careful minds that drives discovery. 8-Bromoadenine, through its chemical precision and strong supporting data, continues to play its role in research labs worldwide. By focusing on sourcing, handling, and open sharing of results, labs can stretch the value of each gram, making every experiment count.
Ultimately, scientific progress builds on details—physical properties, documented origins, care in use—just as much as on vision. The lessons learned from tools like 8-Bromoadenine stay with researchers throughout their careers, shaping not just particular experiments but habits of rigor, caution, and pride in trustworthy results.