|
HS Code |
886889 |
| Cas Number | 7697-46-7 |
| Molecular Formula | C5H5BrN2O2 |
| Molecular Weight | 205.01 |
| Iupac Name | 5-bromo-6-methyl-1,3-dihydropyrimidine-2,4-dione |
| Appearance | Off-white to light yellow powder |
| Melting Point | 254-256 °C |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8 °C |
| Synonyms | 5-Bromo-6-Methyl-2,4(1H,3H)-Pyrimidinedione |
| Pubchem Id | 11687 |
As an accredited 5-Bromo-6-Methyluracil factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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5-Bromo-6-Methyluracil (also known by its short name, 5-BMU) steps into the lineup of nucleobase analogues with its unique balance of purity, chemical stability, and specific functional profile that’s hard to match. I have spent years in laboratories working with different pyrimidine derivatives, and this one always draws attention from both new researchers and seasoned chemists. Its chemical formula, C5H5BrN2O2, and a molecular weight near 205.01 g/mol make it easy to handle and incorporate into a variety of bio-organic workflows without the fuss of special equipment. It dissolves decently in common solvents and minimizes surprises during reactions, a trait any experienced bench scientist appreciates when racing against the clock.
Inside each molecule, the bromine at position five, alongside a methyl group at six, changes the game. These groups alter the hydrogen bonding and electron distribution across the pyrimidine ring, which plays a big role in DNA synthesis, PCR, and other nucleic acid-based protocols. I remember one project where swapping out ordinary uracil for 5-BMU helped resolve persistent replication slippage in synthetic oligo construction. That methyl group isn’t just chemical decoration—it shields parts of the ring, making 5-BMU more selective in base pairing and sometimes resistant to enzymatic cleavage, depending on the system. Whenever scientists talk about tweaking fidelity or boosting selectivity, the structural quirks matter, and 5-BMU brings the right kind of difference.
5-Bromo-6-Methyluracil finds its place in research labs that focus on DNA labeling, mutation studies, and polymerase chain reactions. I’ve seen it used to track DNA incorporation across cellular systems, revealing processes in a way that standard uracil simply can’t. Its ability to substitute for thymine or uracil in oligonucleotide synthesis hands researchers extra flexibility—an invaluable asset for anyone fine-tuning the stringency of hybridization reactions or probing the subtleties of genetic editing. During my own work on DNA-protein interaction assays, 5-BMU-labeled strands added a layer of clarity to footprinting analyses, especially when trace detection became a challenge. The presence of bromine also makes this compound suitable for X-ray crystallography work, providing clear signals in electron density maps. That’s a boon for labs mapping out nucleic acid-protein complexes or identifying drug binding pockets in nucleic acid-based therapeutics design.
Plenty of choices crowd the nucleobase market, but 5-Bromo-6-Methyluracil holds some unique ground. Compared to its close cousin, 5-bromouracil, 5-BMU brings extra specificity and sometimes better biological compatibility in engineered systems. The methyl group at position six slows down certain side reactions, limiting off-target mutation rates in controlled genetic experiments. I have relied on this property in mutation detection protocols: getting fewer background events means drawing more reliable conclusions, and that speeds up publication timelines. Other analogues can fall short. For example, 5-fluorouracil disrupts normal processes more aggressively, which may not suit every system. I remember troubleshooting weeks of unexpected results until the right analogue made all the difference. For teams focused on balancing selectivity and practical workflow, 5-BMU’s profile makes life easier.
Laboratories with strict purity standards rarely face letdowns with reputable batches of 5-BMU. Quality benchmarks usually hit 98–99% or higher, verified using high-performance liquid chromatography and spectral analysis. Each batch deserves close attention, but widely available analytical data make cross-checking easy for careful scientists. The compound typically presents as an odorless, white to off-white crystalline powder, stable under ordinary storage in sealed containers and indifferent to short-term exposure to room temperature. Out on the bench, 5-BMU resists light-induced degradation far better than some less robust analogues. I’ve stored open bottles for weeks during intense research cycles and never noticed a drop in reactivity, which can’t be said for every nucleobase out there.
Teaching labs demand safe, repeatable experiments where learners can test theories without the risk of hazardous byproducts or short shelf-lives. 5-BMU regularly appears in practical curricula for undergraduate molecular biology and biochemistry. Its well-defined melting point, generally reported in the 280–285°C range (with decomposition), offers a visible benchmark for experimental methods exercises. Chemistry students practicing thin-layer or column chromatography can reliably separate 5-BMU from close relatives, reinforcing important lab skills with a compound that doesn’t break the budget or require tricky waste disposal. From my own teaching days, having a compound that students could actually “see” under UV—thanks to bromine’s properties—made lessons stick much faster.
Interest in 5-Bromo-6-Methyluracil isn’t limited to bench research. Pharmaceutical teams exploring new antibiotics, antimetabolites, or nucleoside-based therapies sometimes select 5-BMU for its altered physiological effects. This analogue shows patterns of action distinct from widely used chemotherapeutic agents. Those characteristics matter during early-stage drug screening when unwanted cytotoxicity or metabolic instability can sink a project. 5-BMU often appears in enzyme inhibition screens and tests of DNA-binding ligand affinity because the bromine atom shifts electronic behavior in ways that open up fresh possibilities without causing disruptive biological responses. In diagnostic assay development, I’ve seen 5-BMU make target labeling more robust, supporting new platforms that need clear, specific signals.
Researchers who work routinely with nucleobase analogues will find 5-Bromo-6-Methyluracil simple to weigh, dissolve, and aliquot. Unlike more fragile or toxic compounds, it doesn’t require special atmospheric controls or sophisticated safety gear beyond the basics: gloves, eye protection, and well-ventilated workspaces. The powder dissolves in heated water, DMSO, or methanol, lending itself to fast stock solution preparation. The limited volatility cuts down on accidental loss even in a busy shared laboratory. I’ve transferred dozens of samples for international collaborations without worrying about spoilage or import headaches due to dangerous goods restrictions. That peace of mind streamlines logistics and keeps research projects on schedule.
Anyone aware of environmental stewardship wants to know how their lab choices stack up in terms of waste management. 5-BMU rates among the less problematic pyrimidines. Standard protocols recommend collection of pyrimidine wastes for chemical disposal rather than simply releasing them with other aqueous solutions. Aside from that, there’s no evidence of especially persistent or bioaccumulative properties in the small quantities used for research. My university’s safety office has incorporated 5-BMU into standard waste guidelines without red flags, making this a responsible choice for labs aiming to lower their environmental footprint without sacrificing experimental outcomes. It always feels good to wrap up a project knowing the chemical trail left behind won’t become a headache for the next generation.
As gene synthesis methods scale up, and as CRISPR tools move from buzzwords to routine practice, nucleobase analogues like 5-BMU will shape the next wave of genetic engineering. Experienced researchers see the trend: more work focuses on expanding the genetic alphabet, improving error-checking in artificial DNA assembly, and introducing targeted modifications for synthetic biology. 5-BMU’s mix of selectivity and resilience finds it well-placed for these developments. I’ve listened to graduate students present data on site-specific mutagenesis that relied on 5-BMU-labeled probes, and the clarity of their results makes a strong case for wider adoption. With industry pushing for faster and more reliable test kits and pharmaceutical teams needing better quality control in oligonucleotide production, analogues that boost precision and simplify workflow will keep finding fans.
Scientists often face a tradeoff between cost, ease of use, and experimental reliability. 5-BMU earns its spot because it rarely throws curveballs during scale-up or validation checks. In my own group projects, swapping to cheaper compounds sometimes cut corners that led to months of repeat experiments. The higher up-front cost of 5-BMU often balances out against time and material savings since reruns rarely happen. Friends working in high-throughput screening have shared the same feedback: sticking to validated, stable nucleobase analogues like this one makes big data projects achievable without calling for endless troubleshooting. Even at clinical scale, feedback from diagnostic laboratory staff tells a similar story, as batches incorporating 5-BMU pass regulatory scrutiny with fewer questions.
Pricing for 5-Bromo-6-Methyluracil can vary depending on the source, region, and current global demand. Reliable supply chains still matter. Labs working out of North America or Western Europe usually report consistent access, but in smaller research economies, shortages occasionally lead to increased prices. I’ve encountered this in joint projects overseas, where placing a consolidated order weeks in advance keeps everything on track. For teams on a budget, it pays to check local regulations and purchasing guidelines since certain import categories can slow down procurement. There’s the usual balance between quality and price, but the peace of mind that comes with high-purity, batch-consistent material usually outweighs minor cost differences, especially for grant-funded work where outcomes matter more than line item savings.
With all its advantages, 5-Bromo-6-Methyluracil does demand careful recordkeeping and attention during storage. Even stable compounds degrade slowly under rough handling—leaving containers unsealed, running unnecessary freeze-thaw cycles, or keeping it near reactive solvents eventually shows up in reduced assay performance. My own experience has shown the value in prepping workable aliquots, minimizing needless temperature swings, and logging every freeze-thaw event. These basic habits protect long-term study validity and keep expensive reagents from turning into indistinct, unreliable powders. Documented chain-of-custody protocols in our group dramatically cut down on batch-to-batch inconsistencies over years of research, and younger lab members pick up the right habits quickly when the consequences are clear.
With synthetic biology continuing to expand, 5-BMU could play a bigger role in RNA technologies, antiviral research, and gene therapy vectors. Oligonucleotide therapeutics rely on modified nucleobases to evade immune surveillance or to persist longer in vivo. The unique double modification of 5-BMU draws attention from groups optimizing RNA interference or antisense platforms. I recently attended a conference session where researchers used 5-BMU to map new areas of mRNA decay and processing—finding it easier to spot subtle interactions using this analogue’s built-in detection advantages. As the underlying chemistry evolves, more innovation is likely coming, with new kit formats, faster assays, and streamlined manufacturing chasing better patient outcomes.
The drive toward open science, reproducible research, and environmental mindfulness puts new pressure on every lab to make careful choices about reagents. 5-Bromo-6-Methyluracil stands out by consistently backing up its reputation with solid data and dependable results. Whether it’s the quiet confidence that comes from clear experimental lanes or the relief of easy compliance with safety audits, these everyday wins matter. Over the years, watching students and junior researchers grow confident as their experiments succeed—without roadblocks or surprise contamination—reminds me how much a single, well-chosen compound can impact scientific careers and discoveries. 5-BMU may not appear in every headline, but its understated role across hundreds of papers and countless experiments keeps science moving forward.
Choosing the right nucleobase analogue always starts with a conversation between the project team, procurement, and safety offices. For groups weighing the merits of 5-BMU, running a dry run with small batches can settle many open questions about process compatibility and downstream detection. I’ve helped coordinate method validation where a few pilot reactions with 5-BMU confirmed its value before any big investment. Keeping vendors accountable—for purity, batch documentation, and on-time delivery—helps maintain research momentum. Backups matter too: splitting orders across more than one supplier prevents single-point failures, especially during crunch periods near funding deadlines. Teaching best practices to every lab member, from proper weighing to diligent waste collection, keeps the entire workflow safer and smoother for everyone involved.
5-Bromo-6-Methyluracil carves out a respected spot in the toolkit of modern molecular biology by focusing on details that matter: structure-driven selectivity, chemical stability, and compatibility with the routines of daily research. Its impact reaches across disciplines, from forensic science to pharmaceutical discovery, from undergraduate classrooms to custom DNA synthesis foundries. By making high specificity possible without high risk, it answers the call for both innovation and responsibility in the laboratory. Drawing on years of real-world experience with this compound, and stories from colleagues pushing boundaries in science and health care, 5-BMU’s track record sets a strong example for what well-designed analogues can deliver to the scientific community both now and in the future.