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5-Bromo-2-(Dimethylamino)Pyrimidine

    • Product Name 5-Bromo-2-(Dimethylamino)Pyrimidine
    • Alias 5-Bromo-2-(N,N-dimethylamino)pyrimidine
    • Einecs EINECS 611-342-4
    • 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
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    Specifications

    HS Code

    434570

    Productname 5-Bromo-2-(Dimethylamino)Pyrimidine
    Casnumber 145373-34-4
    Molecularformula C6H8BrN3
    Molecularweight 202.05
    Appearance White to off-white solid
    Purity Typically ≥98%
    Meltingpoint 74-78°C
    Solubility Soluble in DMSO, DMF
    Smiles CN(C)C1=NC=NC(Br)=C1
    Inchi InChI=1S/C6H8BrN3/c1-10(2)6-8-3-5(7)9-4-6/h3-4H,1-2H3
    Storagecondition Store at 2-8°C, protect from light

    As an accredited 5-Bromo-2-(Dimethylamino)Pyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 5-Bromo-2-(Dimethylamino)Pyrimidine

    Applications of 5-Bromo-2-(Dimethylamino)Pyrimidine in Industrial Manufacturing

    As a direct manufacturer, we provide 5-Bromo-2-(Dimethylamino)Pyrimidine for established downstream industries with well-documented use cases. Below are key segments where this intermediate plays an integral role in the value chain, with sector-specific standards, practical usage ranges, integration points, and representative end products.

    1. Pharmaceutical Intermediate for Antiviral Drug Synthesis

    This pyrimidine derivative functions as a key building block in the synthesis of several antiviral drug candidates, particularly nucleoside analogues used in antiviral therapies. The compound typically enters synthesis routes during early-stage heterocyclic modifications, where its bromo and dimethylamino functional groups offer controlled reactivity for targeted ring functionalization. Quality control in these applications strictly follows regulatory processes to ensure batch-to-batch consistency and trace impurity levels as required for pharmaceutical raw materials.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) for starting materials requirements
    • USP General Chapters applicable to pharmaceutical intermediates

    Typical usage ratio

    • Employed at 0.1–0.4 molar equivalents relative to the core pyrimidine ring in multi-step synthesis; precise quantities vary based on target molecule structure and desired yield optimization.

    Downstream process integration

    • Introduced during initial heterocyclic intermediate formation, participating in direct halogenation or nucleophilic substitution steps before further functionalization and coupling with sugar moieties in nucleoside analogues synthesis.

    Final product types

    • Active pharmaceutical ingredients (APIs) for antiviral medications, such as modified cytosine or uracil analogues used in HIV or hepatitis C treatment formulations.

    2. Agrochemical Synthesis: Herbicide Active Ingredient Manufacture

    Producers of advanced agrochemicals rely on this pyrimidine intermediate for its ability to introduce precise halogen and amine functionality into heterocyclic scaffolds, which are central to herbicidal efficacy. Its use is well-documented in the construction of key pyrimidinyl-based herbicide actives, facilitating downstream transformations such as cross-coupling or selective amination. Compliance with agrochemical regulations is essential, with process and traceability controls confirmed during contractor audits and quality assurance reviews.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO specifications for pesticide active ingredients
    • REACH Regulation (EC) No 1907/2006 for chemical safety in the EU
    • National pesticide registration requirements (e.g., US EPA 40 CFR Part 158)

    Typical usage ratio

    • Applied at 0.8–1.1 mole ratio for heterocyclic core construction, with adjustments based on desired substitution density and structural requirements of the active molecule.

    Downstream process integration

    • Incorporated as a halogenated precursor during key amination or cross-coupling stages, enabling diversity in methylation and halide content for structure-activity relationship studies or final product development.

    Final product types

    • Technical grade herbicide active ingredients including pyrimidinylthioacetic acid derivatives, and further formulated crop protection products for cereal and vegetable applications.

    3. Chemical Intermediate for Dye and Pigment Manufacture

    This halogenated pyrimidine is valuable in pharmaceutical-grade dye synthesis, especially for production of stains and labeling agents with defined fluorescence or colorimetric properties. Its bromo group provides a reactive handle for coupling reactions, enabling substitution or derivatization under mild conditions. Manufacturers adhere to protocols applicable to high-purity colorants suitable for biomedical and chemical assay environments, addressing traceability and contaminant minimization at every production phase.

    Industry compliance standards

    • ISO 9001:2015 certified quality management systems in colorant production
    • REACH Regulation (EC) No 1907/2006 for dye and pigment registration
    • FDA 21 CFR Part 74 for color additives (applicable for certain diagnostic dye applications)
    • GMP guidelines for dye intermediates intended for pharmaceutical or diagnostic use

    Typical usage ratio

    • Utilized at 0.3–0.6 mole ratio as a modifying intermediate relative to the parent aromatic or heterocyclic substrate in dye synthesis; proportion depends on target chromophore development and downstream reactivity requirements.

    Downstream process integration

    • Reacted in controlled substitution or condensation steps, usually prior to final azo or fluorescent group introduction; positioned to offer functional group diversity essential for selectivity in staining and imaging applications.

    Final product types

    • Pyrimidine-based fluorescent dyes, analytical assay stains, high-purity pigment intermediates for diagnostic reagent manufacturing and labeling agents for research use.

    4. Advanced Material Synthesis in Organic Electronics

    In the production of organic semiconductors and materials for thin-film transistors, this pyrimidine intermediate provides the electronic properties necessary for charge transport and molecular organization. Manufacturers use it for constructing conjugated heterocyclic frameworks, critical for engineering the bandgap and performance characteristics of active layers in organic electronic devices. Raw material handling and synthesis protocols maintain consistency and reproducibility for downstream device manufacturers, with process documentation supporting traceability of functional groups introduced in early-stage electronic material development.

    Industry compliance standards

    • ISO/TS 80004-8:2013 Nanotechnologies — Part 8: Nanomanufacturing processes
    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • Customer-specific internal QC systems for high-purity organic materials
    • Trace metal and halide ion threshold limits based on end-use in electronics

    Typical usage ratio

    • Typically loaded at 0.5–0.9 equivalents in multistep coupling reactions when building extended conjugated systems; actual consumption may shift according to final molecular architecture and desired physical properties of the resulting film or device layer.

    Downstream process integration

    • Participates in cross-coupling or direct arylation steps during pre-polymerization of small-molecule semiconductors, often before solution processing or vapor deposition for device fabrication.

    Final product types

    • Organic field effect transistor (OFET) active layers, functionalized electronic inks, and conjugated oligomer intermediates for photonic device assemblies.
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    More Introduction

    Introducing 5-Bromo-2-(Dimethylamino)Pyrimidine: A Reliable Ally in Modern Chemical Synthesis

    Curiosity about new molecules sometimes starts at the bench in a university chemistry lab or in a conversation between scientists puzzling over reaction bottlenecks. 5-Bromo-2-(Dimethylamino)Pyrimidine has become a regular point of discussion among researchers and process chemists who absolutely demand consistency from their building blocks. Not all substituted pyrimidines offer the unique blend of reactivity and selectivity found here, and this compound plays a bigger role than its compact structure might suggest.

    A Closer Look at the Product

    At its core, 5-Bromo-2-(Dimethylamino)Pyrimidine combines a robust bromine group at the fifth position with a dimethylamino group at the second. Though this detail might sound technical, small shifts like this in structure can open doors to new reactions. The presence of two methyl groups on the amino substituent keeps it electron-rich, which often translates to heightened nucleophilicity and better control in substitutions or coupling reactions. The bromine placement confers other possibilities—researchers opt for this molecule again and again because the aromatic bromine invites selective cross-coupling, such as Suzuki-Miyaura or Buchwald-Hartwig reactions, under relatively mild conditions.

    As someone who’s worked both in a university lab and for pharmaceutical start-ups, I've seen how a single molecule like this can save a synthetic campaign. The frustration of a late-stage roadblock, where a slight change in reactivity can make or break a project, isn’t just a theoretical problem. Where other potential building blocks might stall or give poor yields, the combination of bromine and dimethylamino groups has moved projects from near-failure to smooth success.

    Specifications Matter—Purity, Form, and Handling

    People often focus on the supposed magic of new discoveries, yet day-to-day work with chemical reagents always starts with questions of quality. Analytical purity does not simply act as a marketing point; it directly impacts every experiment downstream. In the case of 5-Bromo-2-(Dimethylamino)Pyrimidine, the best batches on the market are routinely available at purities exceeding 98%. Fine powders in this range dissolve well in common organic solvents. This lets researchers avoid filtration headaches or unwanted by-products in later synthesis steps, which absolutely adds value to both bench chemists and scale-up teams.

    Many labs keep a dedicated cabinet for halogenated pyrimidines, and this molecule finds its home right alongside long-time favorites. One understated difference: 5-Bromo-2-(Dimethylamino)Pyrimidine resists clumping and degrades much more slowly with ordinary lab humidity than less-stable analogs. It’s an advantage that might go unnoticed—until a reagent bottle sits for a few weeks and the next reaction kicks off without hassle. Convenience like this translates to more reproducible results and fewer failed reactions, which builds trust over time.

    Uses in Research, Development, and Manufacturing

    As a seasoned researcher, I can say the utility of this molecule goes beyond simple coupling reactions. The bromine atom acts as a reliable “handle” for introducing new groups by palladium-catalyzed methods, a true workhorse approach in modern medicinal chemistry. Influence doesn’t stop there—many teams push further to form nitrogen-rich motifs, thanks in part to the electron-donating capacity of the dimethylamino group. In small-molecule synthesis, this translates to more varied scaffolds, faster route scouting, and reliable optimization cycles.

    Makers of candidate drugs seek out this intermediate for both diversity-oriented synthesis and focused library construction. More than once, I’ve watched this intermediate shorten timeline estimates by giving teams latitude in late-stage diversification. One pharmaceutical process switched to this compound after older synthons produced undesired impurities; project leaders credited that switch with shaving off several weeks of troubleshooting. Time is money, but reliability in chemical feedstocks often pays off most in project morale.

    Beyond the pharmaceutical sphere, specialty chemical manufacturers often require precise intermediates for pigment and dye design. The backbone of 5-Bromo-2-(Dimethylamino)Pyrimidine attracts chemists working in material science, who incorporate it into optoelectronic materials. Some research groups have described its use in small-scale synthesis of ligands or pre-catalysts, counting on that same bromine group for well-controlled follow-up steps. It wouldn't be overstated to call it a "small connector" that enables much larger ambitions in the lab.

    Comparison with Related Compounds

    Similar-looking pyrimidines sometimes don’t perform as well where it matters. Take 5-chloro-2-(dimethylamino)pyrimidine, a close relative. In reactions demanding swift cross-coupling, the bromine in 5-Bromo-2-(Dimethylamino)Pyrimidine outpaces chlorine analogs. The bond reactivity and ease of oxidative addition significantly impact yield and purity in these systems. Another point: analogs missing the dimethylamino group lose much of the synthetic flexibility offered here. Substituent effects are subtle but powerful, and this particular hybrid brings together favorable leaving-group ability with active site electron density.

    While both bromine and chlorine derivatives often serve similar synthetic purposes, differences start showing in difficult conversions. My own experience echoes what’s found throughout the literature: fewer incomplete couplings, easier purification, and less time spent justifying unexpected by-products. This molecule isn’t the only choice, but compared to other halogenated pyrimidines, it strikes a strong balance between reactivity and stability.

    Addressing Current Challenges and Building Confidence

    Uneven supply chains and uncertain regulatory climates have forced a lot of scientists and production managers to think hard about chemical procurement. A few years ago, sourcing high-quality halogenated compounds meant long waits from overseas or sudden changes in supplier standards. Now, with more consistent supply of 5-Bromo-2-(Dimethylamino)Pyrimidine, research planning becomes less of a gamble. The product’s robust specifications allow compliance with strict internal quality systems, which matters for everyone from the grad student running an exploratory reaction through to the quality assurance officer releasing final product batches.

    Stories circulate about rushed synthetic runs plagued by impurity peaks, many traced back to inconsistent feedstock. This isn't just a matter of yield—it determines whether precious time (and money) gets wasted or builds toward publishable results. In the compounds I’ve handled, including this one, top vendors now provide batch certificates documenting trace contaminants. This transparency builds trust between suppliers and researchers. Data-driven decisions, such as choosing a documented, high-purity intermediate, cut down on trial-and-error and let scientists focus on genuine innovation.

    Reputations get built on the back of reliable chemistry, and companies known for tight characterization standards have stepped up. Straightforward access to purity data, spectral signatures, and stability studies lets users determine suitability before a single reaction tube gets charged. I once met a colleague who refused to take on a new pyrimidine substrate until the supplier shared not only a CoA, but also recent NMR/LC-MS files—he remembered too many projects bogged down by volatility or mystery contaminants. A supplier able to anticipate these demands doesn’t just win business; they help raise the overall bar for chemical sourcing.

    Environmental and Safety Considerations

    Working with halogenated heterocycles always brings a few extra safety notes into daily practice. The bromine group in 5-Bromo-2-(Dimethylamino)Pyrimidine prompts the familiar caution, yet users report that the compound remains easier to contain and less volatile than some smaller halogenated aromatics. Standard practice means storing it in tightly sealed bottles away from light and excessive heat. Most modern labs—especially those experienced with similar materials—have hazard reviews and handling protocols in place; incorporating this molecule rarely requires special training.

    Environmental responsibility continues to shape how reagents get handled. Disposal and recovery programs for halogenated solvent waste now capture the trace by-products generated from reactions with compounds like this. Green chemistry isn’t just a catchphrase but a driving principle. Many institutions review every new molecule for lifecycle impact, and 5-Bromo-2-(Dimethylamino)Pyrimidine benefits from being manageable with existing containment waste solutions. This readiness means fewer regulatory headaches and supports the shift toward more sustainable habits.

    Global Reach and Local Value

    Lab stories echo around the world—everywhere that pharmaceutical and materials chemistry happens, teams push for reproducible, efficient reactions. When suppliers began offering this product in larger volumes and with certified purity, smaller research teams gained access to the same tools typically reserved for industry giants. Large-scale synthesis brings its challenges—especially with scale-up and process validation—but consistency in starting materials makes troubleshooting less daunting.

    Collaborations across countries now rely on predictable intermediates. If a lab in Boston makes a discovery and shares the route with colleagues in Berlin, shared access to reliable 5-Bromo-2-(Dimethylamino)Pyrimidine means those protocols transfer much more smoothly. I’ve witnessed partnerships flourish based on this simplicity; uniformity in research feedstocks cuts down on frustrating “what went wrong?” cycles that choke productivity and sour relationships.

    Supporting Ongoing Innovation

    Academic groups gravitate toward intermediates like 5-Bromo-2-(Dimethylamino)Pyrimidine for a reason—tighter budgets and faster timelines force scientists to get creative. The ability to quickly introduce substituents, ring systems, or linker groups directly impacts the reach of grant-funded projects. Many research proposals now mention such versatile building blocks, describing how they enable more targets with fewer steps. From generating analogs to exploring structure-activity relationships, this molecule is a catalyst for discovery, not just in the literal chemical sense, but also in the project acceleration it delivers.

    Consider a case from a university medicinal chemistry team. They aimed to create a focused library of kinase inhibitors with slight variations around the 5-position of pyrimidine. By starting with 5-Bromo-2-(Dimethylamino)Pyrimidine, the group easily introduced a range of functional groups using mild cross-coupling conditions. Traditional alternative routes required protecting groups or more laborious multi-step sequences. The streamlined pathway gave more time for biological evaluation, bringing hit compounds forward for funding renewal and further study.

    On a larger scale, contract manufacturing organizations turn to this intermediate as part of validated synthetic protocols. Competing CROs look for ways to minimize risk and maximize throughput, and that only happens when key building blocks don’t surprise users with batch-to-batch deviations or hidden instability. Continuous flow chemistry, an increasingly popular approach, leverages the reliable solubility and reactivity of this compound—less time spent tweaking, more product in the flask, more confidence from clients.

    What Could Be Improved?

    No chemical supply story is ever finished. Feedback from users points to the desire for even higher purity grades, especially for applications in ultra-sensitive electronic materials or biological screening. While current purity levels serve most research and commercial needs, the push for “zero unknowns” keeps analysts and production chemists busy toward ever-tighter control. The development of green halogenation routes—avoiding harsh reagents or hazardous solvents—also remains on many wish lists. Some research teams are exploring biocatalytic or low-waste methods for functionalizing pyrimidines, and success here would strengthen the case for more widespread application.

    Questions about long-term storage and degradation products still pop up in specialist circles. Most samples fare well over months if stored properly, but more detailed degradation studies build confidence for those working under regulatory oversight. It’s often the little details, like a transmittal note with actual storage condition data, that make users stick with one supplier over another. Openness about shelf life, lot variability, and physical form support smarter decisions across the industry.

    Building a Stronger Community Around Quality Chemistry

    The best innovations in synthetic chemistry have always been collaborative, grounded in shared experience and trust. The rise in available data about 5-Bromo-2-(Dimethylamino)Pyrimidine’s properties, methods of analysis, and stories of research success has grown alongside the molecule’s increasing use. Some chemists even publish case studies featuring the product—detailing not only breakthrough yields, but pitfalls and workarounds too. This cultural sharing helps new users avoid costly mistakes and gives experienced teams the tools to push boundaries.

    On discussion boards and at conferences, the merits and quirks of new reagents become familiar talking points. Feedback—positive and critical—shapes production priorities and leads to improvements in consistency and delivery. Just as the open exchange of NMR data or proof-of-concept experiments fuels innovation, transparency about limitations or areas for improvement earns lasting loyalty. The story of 5-Bromo-2-(Dimethylamino)Pyrimidine is not finished, but rather part of a bigger movement in scientific supply: data-driven confidence, rigorous quality, and real conversation between supplier and user.

    Anticipating the Future—Integration in New Technologies

    As digital tools, automated synthesis, and electronic lab notebooks become standard, compounds like 5-Bromo-2-(Dimethylamino)Pyrimidine integrate seamlessly into new workflows. Smart inventory management, tracked through barcodes and real-time usage logs, makes it easier to maintain quality standards and respond quickly to process deviations. Labs can monitor not only stock levels but also monthly performance data—detecting hidden patterns that help prevent issues before they start.

    Additive manufacturing and nanotechnology open further opportunities. With better controls over purity and documentation, this molecule could see use in producing high-specification electronics or as a precursor for next-generation imaging agents. Researchers at the boundaries of traditional chemistry and engineering need intermediates they can trust—variability in starting material causes headaches at every level, from R&D through scale-up and process validation.

    Final Thoughts on Value and Practice

    After years of running reactions, reviewing spectral data, and troubleshooting failed syntheses, reliability ranks above almost any other factor in reagent selection. For anyone who’s endured malfunctioning runs or unexplained contamination, a consistently high-quality intermediate like 5-Bromo-2-(Dimethylamino)Pyrimidine means less stress and more forward momentum. Upfront costs may run a bit higher than for lesser grades or obscure analogs, but the downstream benefits quickly stack up: simpler process development, more publishable results, and better chances of timely breakthroughs.

    While no chemical solves every synthetic problem, the thoughtful design, rigorous quality standards, and practical reliability found in this molecule support a pattern of excellence. As the chemical sciences move ever-faster—from university labs to high-volume industry—building blocks like this one enable speed without compromising trust. That’s the sort of reliability that lets real breakthroughs happen, experiment by experiment.