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5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid

    • Product Name 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid
    • Alias 5-Bromo-2-methylpyrimidine-4-carboxylic acid
    • Einecs 'EINECS 693-327-6'
    • 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
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    Specifications

    HS Code

    991978

    Product Name 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid
    Cas Number 877399-37-6
    Molecular Formula C6H5BrN2O2
    Molecular Weight 217.02 g/mol
    Appearance White to off-white powder
    Melting Point 215-219 °C
    Purity Typically >98%
    Solubility Slightly soluble in water, soluble in DMSO and methanol
    Storage Conditions Store at 2-8°C, keep tightly closed
    Synonyms 5-Bromo-2-methylpyrimidine-4-carboxylic acid
    Smiles Cc1ncc(C(=O)O)nc1Br
    Inchi InChI=1S/C6H5BrN2O2/c1-3-8-4(6(10)11)2-9-5(3)7/h2H,1H3,(H,10,11)

    As an accredited 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid 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-Methyl-4-Pyrimidinecarboxylic Acid

    Applications of 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid in Industrial Manufacturing

    As the original manufacturer, we supply 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid to leading enterprises in the pharmaceutical, agrochemical, and specialty chemical sectors. Our production focuses on the stringent requirements and integration points of each downstream industry, ensuring that each batch meets the real-world needs of formulation, process efficiency, and regulatory compliance. Below we highlight several key industrial applications where this material has proven essential in supporting innovations and manufacturing scale-up.

    1. Pharmaceutical API Intermediate for Antiviral Drug Synthesis

    This compound serves as a crucial pyrimidine building block during the multi-step synthesis of nucleotide analog APIs, especially for antiviral medications targeting hepatitis viruses. The unique structure supports regioselective functionalization in intermediate stages, directly impacting yield and impurity profile management under cGMP constraints. Our clients employ it to achieve high-purity synthons for regulatory submissions in major markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monograph guidance for APIs
    • China Pharmacopoeia (ChP) for raw pharmaceutical materials

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to nucleoside precursor in batch processes
    • The precise addition rate depends on target compound structure and required purification complexity

    Downstream process integration

    • Incorporation during intermediate coupling or cyclization step
    • Used in protected pyrimidine ring modifications before API finalization
    • Sampling and in-process controls at coupling completion phase

    Final product types

    • Antiviral nucleotide analog APIs (e.g., tenofovir intermediates)
    • Pharmaceutical intermediate products for regulatory submittal
    • Export-grade bulk API for finished dosage manufacturers

    2. Agrochemical Active Ingredient Synthesis

    Major crop protection chemical producers source this material for use as a precursor in synthesizing pyrimidine-based herbicides and fungicides. The specific bromine substitution pattern enables tailored substitution reactions critical to downstream ring functionalization, supporting products targeting resistance management in field applications. Process selectivity and residue controls depend on precise raw material handling aligned to agricultural chemical safety guidelines.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical manufacturing
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • REACH (EC 1907/2006) registration for ingredient use in Europe
    • China ICAMA registration for agrochemical intermediates

    Typical usage ratio

    • 0.5–1.5 molar equivalents, adjusted for the specific ring closure or substitution reaction
    • Variation based on target yield and downstream application spectrum

    Downstream process integration

    • Charged into multi-step organic synthesis as an early-stage intermediate
    • Utilized in halogen exchange or further substitution to form key agro-active scaffolds
    • Purified through industry-standard crystallization before formulation

    Final product types

    • Selective pyrimidine herbicides for cereal and broadacre crops
    • Fungicidal active ingredients for seed treatment formulations
    • Technical-grade pesticide intermediates for global supply chains

    3. Pharmaceutical Research: Heterocyclic Scaffold Modification

    Innovative drug development projects use this compound as a source for targeted substitution onto the pyrimidine core, supporting lead candidate optimization for oncology and CNS indications. The brominated position allows medicinal chemists to introduce various nucleophiles, expanding SAR (structure-activity relationship) exploration. Our reliable quality and consistent assay support rapid scale-up from medicinal chemistry bench top to process development pilot scale.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for research compound tracing
    • Internal R&D raw material acceptance specifications
    • RoHS/REACH compliance for laboratory chemical supply
    • Corporate new molecule regulatory workflow protocols

    Typical usage ratio

    • Stocks prepared at 0.1–0.5 mmol scale for screening; 1–8 mmol for scaling-up candidate compounds
    • Amount adjusted per desired substitution degree and library design

    Downstream process integration

    • Engaged in Suzuki, Sonogashira, or Buchwald-Hartwig cross-coupling pipelines
    • Direct halide substitution to diversify libraries for lead selection
    • Integrated with HPLC/LC-MS for inline purity checking

    Final product types

    • Reference standards and analog libraries for SAR studies
    • Milligram to gram-scale drug development candidates
    • Early-phase non-GMP clinical trial supplies

    4. Specialty Chemical Synthesis for Dye and Pigment Manufacturing

    5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid marks a key intermediate for synthesizing specialty dyes where custom pyrimidine motifs are needed to impart specific light absorption or fastness profiles. Leading pigment manufacturers use the material’s brominated structure to enable high efficiency in nucleophilic aromatic substitution, producing advanced intermediates for electronic and textile dye applications under closely controlled conditions to minimize off-target residue and color shift.

    Industry compliance standards

    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) for textile chemicals
    • Oeko-Tex Standard 100 for dye components in textiles
    • EN ISO 105 family (color fastness testing protocols)
    • ISO 14001 (environmental management for chemical production)

    Typical usage ratio

    • Ratios from 1.0–1.5 molar equivalents relative to nucleophile in aromatic substitution steps
    • Fine-tuned depending on batch scale and dye chromophore yield targets

    Downstream process integration

    • Introduced as a nucleophilic aromatic substitution substrate at pre-chromophore stage
    • First engaged in pilot-scale synthesis before full production ramp-up
    • Incorporated with strict monitoring of residual bromine content

    Final product types

    • Pyrimidine-based dyes for textile and synthetic fiber coloration
    • Specialty pigment intermediates for electronic inks
    • Light-fast and wash-fast colorants for industrial coatings
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    More Introduction

    Introducing 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid: A Fresh Look at Its Applications and Value

    Understanding This Compound’s Role in Modern Chemical Synthesis

    Chemists and researchers don’t often get the chance to work with compounds that truly shift the direction of a project, but 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid offers something distinct. As a heterocyclic aromatic acid with the bromo and methyl groups positioned on the pyrimidine ring, I have seen this molecule prove its usefulness in a variety of synthesis challenges, especially in the pursuit of complex pharmaceuticals and advanced materials. The real-world benefits come forward in its clean reactivity and reliability, which stem directly from its structure and purity level.

    This acid isn’t simply another reagent on the shelf. The structure—5-bromo on the ring, a methyl at position 2, and the carboxyl at position 4—creates a foundation for building blocks that tackle hurdles in creating nucleoside analogs, kinase inhibitors, and other small molecules aimed at tackling diseases. In my time in organic and pharmaceutical chemistry, robust starting materials shape research momentum. This compound brings that dependability, day in and day out.

    Model and Purity: Consistency Matters

    Every batch of 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid I’ve handled has come in crystalline form. White to off-white appearance signals strong purity, which is key when trace impurities can complicate downstream work. Typical specifications see purity assessed by HPLC, running at 98% or above. Moisture content falls well below levels that might cause hydrolysis or instability. In weighing out quantities, I find it straightforward to handle, and the gram-to-milligram scale works for both library synthesis and larger pilot batches.

    Robust documentation backs up the product: NMR, MS, and other analytical data confirm its identity. While this attention to purity might look like overkill to an outsider, rigorous verification spares labs from the headaches of repeating failed reactions due to hidden contaminants.

    Key Usage Scenarios

    The acid group at position four allows easy conversion to esters and amides, so I use 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid as a starting point for coupling reactions. For those projects where clients request halogenated scaffolds or need the pyrimidine motif, this compound fits right in. Used as a precursor for medicinal chemistry programs, its bromo group enables Suzuki, Stille, and Buchwald-Hartwig couplings with a wide range of aryl and alkyl partners. Medicinal chemists appreciate this sort of flexibility because it jump-starts SAR studies by letting them quickly introduce a variety of substituents on the core ring.

    From my experience, the methyl group on the ring brings metabolic stability. In drug discovery, small substituents like this can block unwanted biotransformations, helping those new analogs last longer in biological systems. That helps researchers get more predictive data from in vitro and in vivo tests.

    I’ve also seen this acid play a role in agrochemical research. The same features that appeal to pharmaceutical labs—straightforward derivatization, robust purity, and a scaffold compatible with numerous transformations—help agrochemical teams develop crop protection agents and plant activators. The presence of both the carboxylic acid and bromo group isn’t just for show: it allows quick construction of a huge number of derivatives, and in small-scale, high-throughput syntheses, these time savings become cost savings.

    Real-World Differences from Other Pyrimidinecarboxylic Acids

    Comparing 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid with other pyrimidinecarboxylic acids, the value often lies in the combination of the bromo and methyl groups. Plenty of pyrimidine acids show up in catalogs, many with substituents at various positions. Some have chlorine, others might carry further alkylation or bulkier aryl groups. What sets this one apart is the way the 5-bromo group opens up cross-coupling chemistry without causing deactivation or unneeded side reactions at the other positions. Labs short on time need predictable, selective coupling reactions, and this compound delivers, where extra functional groups can sometimes complicate purification or downstream modifications.

    The methyl group contributes to improved solubility in organic solvents compared to some unsubstituted or bulkier derivatives. Handling gets easier, and the isolation step often yields cleaner products, reducing time spent on silica columns or repeated crystallizations. During years working with heterocyclic intermediates, I’ve gotten a feel for which derivatives make scale-up an ordeal, and which cooperate with minimal fuss; 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid finds itself in the latter category.

    Meeting Industry Demands for Reliability and Scalability

    For companies working at the intersection of medicinal, material, or agrochemical innovation, reliability counts. I have seen projects stall over inconsistent batches, poor solubility, and even just minor shifts in melting point or impurity content. Organizations gain an edge when they depend on starting materials produced to tight specs and documented with analytical support. In this context, 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid consistently pulls its weight.

    As projects scale up, labs need more than just proof-of-concept quantities. This is where access to robust kilogram-scale production makes a difference. Suppliers who focus on reproducibility and tight process controls become partners, not just vendors. That reduces risks of late-stage surprises that can burn budgets and morale alike. Over close collaboration, a reliable partner can offer rapid batch-to-batch analysis, flexibility in packaging, and re-assessment or re-purification as needed. Labs benefit by getting exactly what they ordered—every single time.

    The Compound’s Place in Research and Development

    Chemistry research isn’t just about hitting milestones; it’s also about avoiding setbacks. In lead optimization or early-stage medchem, an interrupted supply chain or erratic reagent quality can halt months of work. Reliable materials give teams the headspace and security to push forward new ideas. In my own experience, small changes in building block quality ripple through the whole project more than outsiders realize. If a project relies on Pd-catalyzed couplings of a pyrimidine core, and the input material brings in trace metals or organic impurities, extra purifications and checks start eating up time and money.

    That’s one reason so many researchers come back to molecules like 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid. It performs in diverse settings: classic solution-phase synthesis, microwave-promoted reactions, automated liquid handlers, and even solid-phase strategies. Automated workflows depend on predictable results; every missed coupling or spurious side product triggers diagnostic runs and wasted reagents. Straightforward, validated materials keep research moving instead of mired in troubleshooting.

    Improving Transparency and Trust in Chemical Sourcing

    One improvement I’ve pushed for—across years of purchasing in academic and industrial environments—is greater transparency in sourcing and manufacturing. For specialty chemicals like 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid, genuine batch-to-batch data builds trust. Documentation should include not just the standard MS and NMR, but moisture and elemental analysis, ideally with retention samples reserved for problem-solving. When a supplier makes this level of detail available, it signals a commitment to accountability. Scientists, in turn, get reliable performance for their money.

    Open reporting of issues and willingness to troubleshoot recalls a lost era of customer service. Reliable partners keep reference standards and provide timely updates on supply constraints, so users aren’t caught off-guard. Given the current global supply challenges, transparent manufacturing details—solvent residues, origin of raw materials, storage, and shelf-life—matter more than ever. I’ve learned to reward suppliers who share these details up front.

    Trends in Building Block Development

    Innovation in chemical building blocks shapes the direction of discovery. Demand for bromo-substituted pyrimidines keeps growing, thanks to their compatibility with modern cross-coupling techniques. The best labs don’t just follow catalog trends; they look for scaffolds with proven track records. Over the past decade, 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid moved from niche curiosity to a reliable contributor in many drug design campaigns, especially where early hits relied on 2,4-disubstituted cores.

    Efforts in green chemistry are also reshaping expectations for these reagents. Clients and production teams increasingly ask about sustainable methods of synthesis, preference for lower-waste or solvent-minimized routes, and options for recyclable packaging. For 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid, suppliers who back up quality with attention to green credentials stand out. In my circles, I’ve watched teams switch suppliers for the sake of process transparency, not just price or purity.

    Challenges for Users and the Wider Industry

    Even a reliable intermediate isn’t free of challenges. If upstream suppliers shift synthetic routes, trace impurities from new reagents or solvents might slip by, undetected until a downstream reaction fails. Teams must remain vigilant, both by running their own standard checks and by choosing partners who welcome feedback and quality audits. Negative surprises do more than affect chemistry output—they disrupt timelines, budgets, and sometimes professional reputations. I’ve staffed more than one rescue operation to clean up after a bad batch.

    Intellectual property is another factor. In current IP landscapes, unique building blocks with both halogen and carboxylic functionality can tip the balance on patent scope. Using a less-common substitution pattern adds a layer of complexity to competitive filings. Buyers of 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid must weigh how unique their end products might be, and whether freedoms-to-operate match their goals. Legal teams, not just chemists, play a growing role in reagent selection.

    The Road Ahead: Smarter, Safer, and More Sustainable Practice

    The story of 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid reflects broader changes in the chemical and pharma research world. Quality, traceability, and responsible sourcing—these aren’t just bureaucratic checkboxes, but critical advantages. I’ve seen firsthand how proactive communication between chemistry teams and suppliers heads off problems before they start. Continuous improvement through tighter partnerships, digital tracking, and open lab notes turns each run of synthesis into shared progress.

    Looking at the pipeline ahead, improvements in green production—more efficient bromo introductions, lower-waste carboxylations, minimized solvent load—all matter for scale-up and regulatory filings. Producers who commit to full disclosure, responsive customer support, and transparent manufacturing meet needs in ways one-off catalog sales can’t. Chemists who value purposeful purchasing and track core building blocks with a critical eye secure smoother project advancement and ultimately, quicker routes to publication and product launch.

    Final Thoughts on Choosing 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid

    Across diverse projects, this acid proves itself with consistent batches, straightforward handling, and broad compatibility in modern synthetic methods. Its distinct substitution pattern brings both chemical utility and regulatory depth, supporting researchers in the pursuit of new medicines and advanced materials. By aligning choice of chemical building blocks with principles of quality, sustainability, and transparency, the research community can drive more meaningful innovation and tackle unmet scientific needs head-on.

    Those who invest in proven intermediates and foster real partnerships with reliable suppliers position their organizations for long-term impact, well beyond the next publication or product launch. 5-Bromo-2-Methyl-4-Pyrimidinecarboxylic Acid stands as a testament to the difference that true reliability can make in discovery and development.