|
HS Code |
342253 |
| Chemical Name | 2(1H)-Pyrimidinone, 4-amino-5-bromo- |
| Molecular Formula | C4H4BrN3O |
| Molecular Weight | 189.00 g/mol |
| Cas Number | 81569-42-6 |
| Appearance | Light yellow to off-white powder |
| Melting Point | 228-230°C |
| Solubility | Slightly soluble in water; soluble in DMSO and methanol |
| Pka | Approx. 9.1 (for pyrimidinone NH) |
| Smiles | C1=C(NC(=O)NC1N)Br |
| Inchi | InChI=1S/C4H4BrN3O/c5-2-1-7-4(9)8-3(2)6/h1H,(H3,6,7,8,9) |
| Storage Conditions | Store at 2-8°C, protected from light |
| Synonyms | 4-Amino-5-bromo-2(1H)-pyrimidinone |
| Purity | Typically ≥98% (as specified by suppliers) |
As an accredited 2(1H)-Pyrimidinone, 4-amino-5-bromo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with tamper-evident cap, labeled “2(1H)-Pyrimidinone, 4-amino-5-bromo-”, 10 grams, with hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL: Loaded in 25kg fiber drums, 9 MT per container, securely packed, ensuring safe handling and transport of chemicals. |
| Shipping | Shipping of 2(1H)-Pyrimidinone, 4-amino-5-bromo- requires secure, chemical-resistant packaging to prevent leaks or contamination. The compound should be shipped at ambient temperature unless otherwise specified and accompanied by appropriate documentation, including safety data sheets (SDS). Compliance with local and international hazardous materials regulations is mandatory during transport. |
| Storage | **2(1H)-Pyrimidinone, 4-amino-5-bromo-** should be stored in a tightly closed container, protected from light and moisture. Store in a cool, dry, and well-ventilated area, away from incompatible materials such as strong oxidizing agents. Ensure proper labeling and keep away from sources of heat and ignition. Follow standard laboratory chemical storage procedures for safe handling and storage. |
| Shelf Life | The shelf life of 2(1H)-Pyrimidinone, 4-amino-5-bromo- is typically 2–3 years when stored in a cool, dry place. |
Competitive 2(1H)-Pyrimidinone, 4-amino-5-bromo- prices that fit your budget—flexible terms and customized quotes for every order.
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In our labs, we constantly work to ensure every batch of 2(1H)-Pyrimidinone, 4-amino-5-bromo- meets strict quality targets. The structure sets this molecule apart—pyrimidinone as a core, with both amino and bromo substituents giving it unique reactivity. Chemists taking on heterocyclic compound synthesis or pharmaceutical discovery often ask about its differences compared to simple pyrimidinones or 5-unsubstituted analogs. The bromo group changes the electron distribution, making this compound an excellent intermediate for cross-coupling, halogen-exchange reactions, or modification by transition-metal catalysts. This is exactly why our production involves daily attention to recrystallization, purity control, and spectroscopic validation, going well beyond baseline industry methods.
Those familiar with active pharmaceutical ingredient research recognize the critical role of well-characterized heterocycles. In some cases, similar scaffolds without the bromine lack the same reactivity or selectivity. Our team consistently chooses 4-amino-5-bromo as a stepping stone toward more elaborate heterocyclic libraries. One misstep with trace metal contamination or over-bromination can throw off entire reaction schemes. By tuning each production batch to achieve narrow melting point ranges and maintaining tight control over moisture absorption, we prevent the degradation that may occur in lesser material. The result—predictable, reproducible performance in downstream chemistry.
Back in the early years of our manufacturing floor, we observed inconsistency among incoming raw materials not made to pharmaceutical grade. Yield losses spiked. Purity drifted from month to month. Researchers voiced frustration about ambiguous NMR patterns and irreproducible couplings. This led us to overhaul our purification equipment and bring spectrometers on site. Each run now receives full mass spectrometry and NMR checks before it leaves our walls, so the end-user sees only crisp, reliable compounds.
Customers often share their challenges sourcing meaningful quantities of 2(1H)-Pyrimidinone, 4-amino-5-bromo-. While resellers sometimes offer small samples of questionable lot history, our factory guarantees line-of-sight quality records and lot traceability. We make it clear to research teams that every step—solvent choices, drying times, ambient air controls—has a tangible impact on their own experimental outcomes. The days of mysterious decompositions and purity tails are gone here.
The pharmaceutical industry relies on heterocyclic motifs as bioactive backbones. Pyrimidinone derivatives, and especially halogenated variants, appear in kinase inhibitor research, antiviral leads, and libraries searching for antibacterials. This specific compound, with its amino and bromo arrangement, sees heavy use as a coupling partner in Suzuki-Miyaura and Buchwald-Hartwig reactions. Our customers come back to us because each gram translates into hours saved on failed optimizations. The presence of the bromo substituent unlocks Pd-catalyzed cross-couplings. The amino group lets chemists easily incorporate urea, amide, or other pivot groups for SAR expansions.
We receive feedback from both small startups and large pharma. They use our product to round out screening sets, develop diagnostic probes, or test new reaction conditions. While alternative pyrimidinones might exist without bromine, they simply do not respond in the same fashion to halogen exchange, Grignard additions, or site-directed halogenation. For some research groups, switching to a lesser grade or skipping the bromo allows alternative routes, but nearly always with lost time and less reliable endpoints.
More than a decade has passed since we scaled up from gram to multi-kilogram synthesis. That journey uncovered a hundred small details. We keep overhead-stirred reactors under dry nitrogen to stop hydrolysis. Our operators adjust pH and temperature profiles throughout condensation and bromination steps, isolating the purest product. Each operator learns our triple-point solvent system to ensure full precipitation and avoid oiling out in humid months. As a result, our batches show consistent white to off-white crystalline form and stand up under the toughest analytical scrutiny.
Some buyers wonder why manufacturing matters, when so many sources seem similar online. We try not to lecture, but facts from our daily practice make the case. We receive requests to rescue stalled syntheses built on low-grade 2(1H)-Pyrimidinone, 4-amino-5-bromo- from outside vendors. These rescue jobs often come after a competitor’s impure batch throws off an entire SAR campaign or fouls up a catalyst system. Simple contamination or unchecked manufacturing parameters have ripple effects in the lab. This is why transparent documentation, batch-to-batch consistency, and thorough quality review aren’t just regulatory boxes—they’re the core of our daily work. Customers lose far less time and money with something they can trust.
Every lot goes through LC-MS quantitation, water content verification, and visual inspection. We’ve set internal benchmarks above typical industry minimums. Purity often exceeds 98 percent. Stability checks include cyclic storage at different temperatures and humidity conditions—any signs of decomposition or color shift trigger a halt and review. By keeping all paperwork and QC data available, we offer transparency as part of the service.
Synthesis teams who select 2(1H)-Pyrimidinone, 4-amino-5-bromo- as an intermediate get more than just chemical feedstock. Our controlled crystallization avoids solvate entrapment, so no unknown peaks emerge during analytical qualification. Chemists scale up from milligrams to hundreds of grams without worrying about polymorph conversion, excess fines, or batch heterogeneity. This sort of reproducibility only comes from process control on the manufacturing side. In most of the screening runs we’ve seen downstream, this consistency prevents false negatives and improves hit rates.
The synthetic world abounds with pyrimidinone analogs, but not all are made equal. Unsubstituted 4-amino-pyrimidinones do appear in commercial catalogs, though without the bromine at position five, a host of cross-coupling strategies remain out of reach. Halogen placement matters, especially for selectivity in transition metal catalysis.
While some operations try to convert their own 4-amino-pyrimidinone to the bromo variant by crude bromination, many stumble into low yield or contamination from multiple regioisomers. This doesn’t seem a problem until a side-product poisons a catalyst or disrupts downstream purification. Our in-house expertise avoids these headaches. Having walked through many failed bromo-exchange reactions years ago, we learned that careful control over stoichiometry and reaction conditions gives better selectivity and a purer product straight out of the reactor. This means chemists relying on Suzuki, Buchwald, or Stille couplings no longer face unpleasant surprises.
Too many chemists recall weeks lost to repeating reactions where subtle impurity tails or incorrect melting points smashed synthetic plans. With tight timelines and dwindling R&D budgets, those delays eat away at productivity. Our clients send stories about gaining back time spent troubleshooting, ordering second batches, or running extra purification steps. They now reroute that time into new targets and expanded screens.
Academic groups and industrial teams alike highlight the peace of mind that comes with clean baseline chromatograms and exact NMR peaks. For teams using flow chemistry platforms or automated synthesis, small deviations sink entire design-of-experiments runs. It’s not just the loss of a single experiment—it’s the compounded cost of halted projects, reallocated staff, and months shaved off timelines. Our approach to controls, both in the pilot suite and full-scale line, ensures researchers never have to double-guess what’s in their bottle.
Our team pays close attention to trends in drug development and materials science to predict how demand for 2(1H)-Pyrimidinone, 4-amino-5-bromo- will evolve. With the rise of novel kinase inhibitors, molecular probes, and enzyme inhibitors, the demand for well-characterized heterocycles will only grow. Newer methods for late-stage functionalization, electrochemical halogen exchange, and green chemistry drive fresh research into scaffolds based on 5-bromo-pyrimidinones.
We invest regularly in reactor upgrades, analytical suites, and employee training. Our technical team collaborates with synthetic chemists, process development groups, and academic labs. By keeping direct lines to science innovators, we improve our own production and respond directly to end-user feedback—shorter delivery times, cleaner lots, or customized particle size. This partnership model benefits both sides, keeping our facilities aligned with where real-world chemistry happens.
Every operator on our floor sees daily reminders of how water- or air-sensitive certain intermediates can be. Unwanted hydrolysis, over-bromination, or exposure to light affects both yield and purity. Rather than hiding behind boilerplate, we engage directly with our customers. We explain our packaging strategy—triple-layer liners, inert-atmosphere filling, anti-static drums where necessary. Our logistics team audits every shipment before it leaves, logging photos and environmental monitors so customers never open a degraded drum.
Safety stays front of mind, both for our staff and users. We design our facilities around open airflow, isolated reactors, and digital process monitoring. All waste streams run through treatment protocols designed around the species unique to this substrate. While accidents can never be reduced to zero, every incident gets a full root-cause analysis and retraining to avoid recurrence. For users handling the compound, we supply detailed guidance on handling, spill control, and emergency response, shaped not just by generic templates but by field experience and ongoing consultation with health and safety experts.
Quality doesn't rest on a glossy certificate. Every incoming lot of reagents, solvents, and starting materials receive their own QC checks, flagged and blocked if they fall outside our tolerance windows. We pilot every new process change with a small team before rolling out line-wide, tracking data points for both process yield and product purity.
No two runs of 2(1H)-Pyrimidinone, 4-amino-5-bromo- are identical, though we strive to reach the closest possible margin by revalidating our critical process parameters. Over the past few years, customer feedback led us to refine purification steps, eliminate a previously used solvent to reduce residue risk, and entirely automate part of the weighing and transfer step. These ongoing efforts deliver a tighter product specification, reduce back-orders, and cut the carbon footprint of our production.
Research breakthroughs rarely happen with off-the-shelf solutions. As a manufacturer deeply invested in the science, we support R&D teams by delivering not just a chemical but a foundation for confidence. We maintain a buffer stock and prioritize recurring demand, so even as trends shift or discovery platforms accelerate, our material is there—ready, waiting, and up to spec.
Many chemists never see the factory work behind the products they depend on, but they know the difference. Clean analytical traces, repeatable yields, and clear SAR results speak volumes. Our facility has earned an ongoing reputation for trustworthy supply and unvarnished communication when challenges emerge. Whether the end-users are seeking kilograms for pilot API synthesis or milligrams for high-throughput screenings, they receive not just an SKU, but a partner invested in their scientific goals.
We stay in business not by chasing easy sales but by earning long-term trust through quality, transparency, and a commitment to shared scientific progress. The distinct structure of this compound makes it a useful springboard for chemical innovation across many disciplines. The manufacturing decisions made at the milligram and kilogram scale impact not just the shelf-life, but ultimately, the entire downstream research workflow.
As specialists focused on direct production rather than resale, we open our doors to open dialogue and collaboration. Our best improvements, year after year, come from customers willing to share tough problems—unexpected impurities, low-yield reactions, special application requirements. No catalog or search portal replaces these real-world stories, and no off-the-shelf offering can match the benefits of direct factory involvement.
For those who push the boundaries of molecular science, the difference is clear. Precision. Reliability. A principled, open partnership between chemical manufacturer and researcher makes higher-quality scientific progress possible, one molecule and one collaboration at a time.