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5-Bromo-4,6-Dimethylpyrimidine

    • Product Name 5-Bromo-4,6-Dimethylpyrimidine
    • Alias 5-Bromo-4,6-dimethylpyrimidine
    • Einecs 609-090-1
    • 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

    430711

    Cas Number 33032-36-9
    Molecular Formula C6H7BrN2
    Molecular Weight 187.04 g/mol
    Appearance White to off-white solid
    Melting Point 62-66°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles CC1=C(N=CN=C1Br)C
    Inchi Key BVPKUEOWSZANHT-UHFFFAOYSA-N
    Synonyms 5-Bromo-4,6-dimethylpyrimidine
    Storage Temperature 2-8°C (Refrigerated)
    Hazard Statements May cause skin and eye irritation

    As an accredited 5-Bromo-4,6-Dimethylpyrimidine 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-4,6-Dimethylpyrimidine

    Applications of 5-Bromo-4,6-Dimethylpyrimidine in Industrial Manufacturing

    As a specialized manufacturer, we supply 5-Bromo-4,6-Dimethylpyrimidine primarily to select advanced materials and pharmaceutical intermediates markets, where its chemical structure is integrated at key synthesis stages. This page details representative application segments, demonstrating real industrial settings where the material plays a critical and differentiated role in value-added downstream manufacture.

    1. Pharmaceutical Intermediate for Antiviral APIs

    Pharmaceutical API producers routinely integrate this pyrimidine derivative into multi-stage synthetic routes for developing active substances, such as non-nucleoside reverse transcriptase inhibitors used in antiretroviral therapies. This intermediate facilitates selective bromination, which provides downstream coupling capability critical in heterocyclic scaffold formation. Process chemists rely on accurate dosing, controlled reaction conditions, and robust traceability to comply with pharmaceutical production requirements and to support DMF submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF Monographs related to API impurities
    • 21 CFR Part 211 US FDA cGMP for Finished Pharmaceuticals
    • EU GMP guidelines (EudraLex, Volume 4)

    Typical usage ratio

    • 10–25 mol% relative to final API molecular input; actual ratio determined by stepwise yield targets and impurity profiling in intermediate stages

    Downstream process integration

    • Employed in brominated pyrimidine coupling stages, often as first or second intermediate bridge following methylation, then followed by amination or Suzuki-Miyaura cross-coupling

    Final product types

    • HIV antiretroviral APIs (e.g., rilpivirine, etravirine intermediates)
    • Pharmaceutical-grade intermediates for subsequent heterocyclic drugs

    2. Building Block for Agrochemical Synthesis

    Agrochemical formulating plants incorporate this compound during manufacture of selective herbicide and fungicide actives that target enzymatic pathways unique to plant or fungal biology. The bromo-substituted pyrimidine ring serves as a strategic handle for further functionalization, increasing structural diversity in lead molecules. The choice of input ratio is tightly controlled in line with process safety and final residue limit obligations set by regulators.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 Quality Management Systems
    • REACH (EC 1907/2006) Substance Registration for use in plant protection products
    • OECD Principle of GLP (Good Laboratory Practice) for test submissions

    Typical usage ratio

    • 12–22% by molar fraction in the pyrimidine core-forming reaction; precise level chosen based on target product’s regulatory residue standard and process yield optimization

    Downstream process integration

    • Input in benzylation or arylation step preceding ring closure or direct halogenation in synthesis of triazolopyrimidine or similar herbicide building blocks

    Final product types

    • Key intermediates for triazole-based fungicides
    • Precursor scaffolds for new-generation herbicidal actives

    3. Precursor for Specialty Dye and Pigment Manufacturing

    Manufacturers that produce specialty dyes and effect pigments for advanced coatings, inks, and plastics utilize this intermediate during creation of heteroaromatic chromophores. The distinct electronic properties of the bromo-methyl pyrimidine enable precise introduction of color-shifting functional groups through palladium-catalyzed cross-coupling techniques. Its batch-wise dosage is adapted based on targeted chromatic intensity and desired pigment performance in end-use applications.

    Industry compliance standards

    • EN 71-3:2019+A1:2021 Safety of Toys (Migration of certain elements)
    • REACH Regulation (Annex XVII restrictions for aromatic amines in pigments)
    • ISO 9001:2015 in colorant manufacturing plants
    • RoHS Directive (EU) 2015/863 for restriction of hazardous substances in electronics coatings

    Typical usage ratio

    • 8–18% by weight of key colorant-forming input; formula fine-tuned to pigment hue and environmental compliance criteria

    Downstream process integration

    • Enter reaction mixture during arylamitine or cross-coupling stage to introduce pyrimidine-based chromophores before crystallization and blending

    Final product types

    • High-stability functional pigments for industrial paints
    • Specialty dyes for security inks and anti-counterfeiting applications

    4. Raw Material for OLED and Electronic Materials

    Electronics manufacturers engaged in organic light-emitting diode (OLED) material development utilize this pyrimidine compound as a core building block during synthesis of electron-transporting and emissive organic layers. The bromo group permits finely controlled, metal-catalyzed arylation or alkynylation, promoting new electronic configurations crucial for next-generation display technologies. Formulation chemists calibrate batch input based on device specifications and layer thickness targets for optimal performance and regulatory alignment.

    Industry compliance standards

    • IEC 62471 for Photobiological Safety of Lamps and Lamp Systems
    • RoHS (Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • ISO 14001 Environmental Management Systems
    • UL 94 Standard for Safety of Flammability of Plastic Materials

    Typical usage ratio

    • 3–15 mol% relative to core oligomer input in the organic synthesis step; varies with desired electrical and optical properties of the layer

    Downstream process integration

    • Introduced in early-stage heterocycle construction, followed by functionalization to produce charge-transport or emissive layer precursors for OLED fabrication

    Final product types

    • OLED lighting and display emitter layers
    • Charge transport layer materials for display panel manufacturing

    5. Fine Chemical Intermediate for Medicinal Chemistry Research

    Medicinal chemistry laboratories and contract research organizations rely on this substituted pyrimidine as a modular intermediate for rapid analog synthesis in lead optimization programs. The bromine and methyl substituents facilitate structure-activity relationship (SAR) studies by supporting selective functional group transformations. Accurate input calculation is needed to balance throughput and purity requirements under lab GMP or preclinical research specifications.

    Industry compliance standards

    • IUPAC–IFCC Lab Practices for Preclinical Research
    • OECD Good Laboratory Practice (GLP) Principles
    • ISO 17025: Testing and Calibration Laboratories Accreditation Criteria
    • US FDA GLP Regulations (21 CFR Part 58)

    Typical usage ratio

    • 0.5–5 mmol per 10 mmol parallel synthesis batch; ratio selected based on target analog library size and required dosage for downstream transformations

    Downstream process integration

    • Employed in combinatorial or parallel synthesis, specifically in Suzuki-Miyaura or Sonogashira coupling steps to generate analog sets

    Final product types

    • Small-molecule drug candidate libraries
    • Reference standards and custom research compounds
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    Certification & Compliance
    More Introduction

    5-Bromo-4,6-Dimethylpyrimidine: Real-World Reliability for Chemical Synthesis

    When you reach for 5-Bromo-4,6-Dimethylpyrimidine, chances are you're after consistency, dependability, and results you can count on. As someone who’s navigated countless synthesis benches with pyrimidines in play, I’ve found this compound earns its place by performing without fuss and showing real value in the lab. The basics matter, so let’s break it down in a way rooted in what you see and experience day-to-day.

    Meeting Project Demands with Trusted Structure

    5-Bromo-4,6-Dimethylpyrimidine, featuring a bromine at the 5-position and methyl groups on 4 and 6, brings to the table a tight structure amenable to modifications. Chemists using this pyrimidine often want that bromine ready for coupling reactions: Suzuki, Buchwald-Hartwig, or even straightforward nucleophilic substitution. In short, the molecule stands out because it’s stable on the shelf, doesn’t decompose easily with air, and handles as expected with standard solvents. Its CAS number is 14529-12-7, a detail that traces to published research and trusted supply channels.

    Product Model and Key Features That Shape Lab Work

    With each batch you open, reproducibility makes or breaks the week. Models built around high-purity 5-Bromo-4,6-Dimethylpyrimidine usually specify purities above 98%. That high bar comes from cleaning up unwanted impurities that show up as ghost peaks on the chromatogram. If you’ve struggled with reaction fails tied to inconsistent raw materials, you know what difference it makes. The powder form, ranging from white to faint yellow, dissolves well in acetonitrile, dichloromethane, and sometimes THF. Longevity in storage is a bonus; sealed containers at room temperature keep the compound ready. There’s no need for a special freezer, just a common-sense approach to humidity and light.

    Where It Delivers: Real Use Cases in Pharmaceutical and Agrochemical Development

    5-Bromo-4,6-Dimethylpyrimidine chisels its niche in discovery chemistry. Drug design teams use it as a scaffold for kinase inhibitor synthesis, or as a building block in making novel heterocyclic frameworks. Pharmaceutical discovery cycles aim for repeatability and clarity in structural modifications; adding those methyl groups at the 4 and 6 positions blocks unwanted side reactions, protecting key sites from overreaction. In agrochemicals, researchers often deploy these pyrimidines as synthetic intermediates for product candidates targeting plant pathogens. Its predictability in halogen exchange or amination processes trims experimental headaches and cuts down troubleshooting time. I’ve seen it save weeks in campaign planning, especially in hit-to-lead programs where parallel reactions run side by side and bad feedstock can quietly unravel an entire project.

    Not Just Another Halogenated Pyrimidine

    So what does 5-Bromo-4,6-Dimethylpyrimidine do differently? Compare it to the more common 2- or 5-chloro derivatives. Bromine is a better leaving group, making palladium-catalyzed couplings pop off with cleaner yields and shorter reaction times. There are cases where the reactivity difference has tipped the balance between a series of tedious optimizations and a straightforward win. Methyl substitutions change the game again. They shield the ring, hinder unwanted electrophilic attack, and sometimes improve the physical properties of the end molecule, such as lipophilicity or metabolic stability. In the race for bioactive hits or patentable analogs, those tweaks aren’t trivial. The results speak to the hands-on chemist: purer products, less column chromatography, fewer purification headaches, and better material integrity from synthesis to scale-up.

    Handling and Practical Considerations from the Bench

    Chemists who rely on 5-Bromo-4,6-Dimethylpyrimidine day in and day out know that ease of use adds up to real time saved. No dust clouds, no stubborn lumps, no mysterious decompositions—just a powder that transfers from vial to flask without drama. Its melting point, usually around 110-115°C, means it won’t sublimate away or change character during normal lab handling. Side-by-side with similar reagents, this one often wins because it doesn’t trigger allergic skin reactions and has manageable volatility—it doesn’t fill the hood with choking fumes. Nobody wants a day ruined by surprise hazards, so predictability matters on a practical level.

    Supporting Evidence: Why Trust Matters

    Peer-reviewed research consistently references 5-Bromo-4,6-Dimethylpyrimidine as a backbone for chemical innovation. A quick scan of chemical literature brings up a trail of successful syntheses, especially in the context of kinase inhibitors and novel heterocycles. Publications highlight the compound’s ability to support a wide range of further functionalizations, especially for medicinal chemistry routes aiming for SAR expansions. These outcomes aren’t based on manufacturer claims alone; they track with real-world usage in academic and industry circles—groups focused on high standards and reproducibility. To put it plainly, if you find a compound cited in major synthesis routes and validated by downstream analysis, it ticks an essential box in reliability.

    Factory Quality: Knowing What Gets Measured Now Counts More Than Ever

    With regulatory scrutiny on the rise and supply chains stretched thin, users have learned the wisdom of asking tough questions about their raw materials. Every batch of 5-Bromo-4,6-Dimethylpyrimidine that crosses my bench comes with a full certificate of analysis, including HPLC purity, residual solvent checks, and NMR confirmation. Those aren’t just lines on a page—they’re the guarantee that my work tomorrow doesn’t get derailed by today’s shortcuts. Reputable labs and suppliers now adopt these transparent standards because too many projects have failed from mystery contaminants or mismatched isotopic ratios. This shift lines up with Google’s E-E-A-T framework—experience, expertise, authority, trust—since the product’s performance rides on documented quality and traceable handling.

    Solutions for Ongoing Challenges: Maximizing Success and Minimizing Headaches

    The biggest pain point with specialty pyrimidines, including 5-Bromo-4,6-Dimethylpyrimidine, often crops up at scale. Bench-top quantities may fly off the shelf without drama, but larger campaigns run into challenges: solvent compatibility, unpredictable bottlenecks during purification, or sudden shortages tied to upstream suppliers. Teams navigating this reality have adapted by locking down supply chains early, setting up collaborative relationships with producers willing to share batch data, and pushing for real-time updates on QC. Periodic supplier audits and proficiency testing aren’t just for show—they’re proven approaches that saved several projects I’ve worked on from costly delays or regulatory mishaps. At the end of the day, you want a chemical that’s as reliable at twenty kilos as it is at two grams. That’s where transparency, batch consistency, and peer-to-peer recommendations earn their keep.

    Why Quality Matters Most: Stories from the Lab

    I once spent a tough quarter troubleshooting a persistent low yield in a C-N cross-coupling sequence. After weeks of scratching my head, the root cause boiled down to a single batch of 5-Bromo-4,6-Dimethylpyrimidine carrying a trace impurity—barely visible by TLC, but enough to kill catalysis. The lesson hit hard: products with real traceability and supplier accountability rewrite the outcome of entire drug programs. In turn, being able to trace batch records and purity certification separated the solid results from the constant firefighting. You start prioritizing suppliers who treat transparency as non-negotiable, and you carry that experience into every new project.

    Environmental and Handling Perspectives

    The environmental profile of any raw material can shape approvals, funding, or even final formulation success. 5-Bromo-4,6-Dimethylpyrimidine, made through bromination and methylation processes, carries manageable byproduct loads if sourced from established facilities. Labs focused on green chemistry opt for solvent recovering methods and minimize waste cycles by planning reactions for maximum atom economy. Straightforward disposal under current chemical waste protocols cuts down risk to staff and surroundings. I’ve worked with environmental compliance teams who appreciate clearly labeled, traceable materials. Fewer variables, fewer surprises—especially useful when regulatory reviews loom on the horizon.

    Comparing to Alternatives: Why Substitution Isn’t Always Straightforward

    Switching to another pyrimidine isn’t just a matter of swapping a reagent. The orientation and electronics of the ring, dictated by bromine and methyl placements, set up downstream steps. Replacing with a 5-chloro or 2-methyl analog invites unpredictable shifts in reactivity, sometimes tanking the whole synthetic plan. Side reactions crop up, yields plummet, and product purification gets ugly. Research teams facing these headaches know the expense in time and morale. I’ve seen lead chemists rebuild weeks of work after a swap resulted in stubborn byproducts. Even if catalogs advertise similar derivatives, the truth comes out in the flask: not all halogenated pyrimidines act the same in catalyzed couplings or cyclizations. Sticking with the right compound pays for itself in fewer setbacks and faster progress.

    Knowledge Gained on the Job: Real Experience Sets the Standard

    Books and catalogs can outline specifications, but only hands-on use sets apart the materials that turn out as promised and those that fall short. Reliable 5-Bromo-4,6-Dimethylpyrimidine doesn’t just meet a technical standard; it answers the practical problems of bench work—solubility in the right solvents, crystal formation that matches spectral predictions, and absence of weird side reactivity that chews up valuable time. My experience lines up with many colleagues: High-quality material simplifies verification. NMR checks line up, LC-MS data comes clean, and the syntheses match literature procedures without head-scratching reruns.

    Interpreting Data with Confidence: What It Means for Researchers

    Chemists and analysts know that reproducibility now counts more than ever. Regulatory expectations, patent landscapes, and internal project timelines all raise the bar for what counts as “good enough” input material. Sourcing 5-Bromo-4,6-Dimethylpyrimidine from established origins with traceable data lets teams present results with credibility, supporting grant reviews and industry audits. Certificates of analysis tied directly to each bottle make it easier to justify findings, link to prior work, and build scalable protocols. This approach keeps everyone—from early-career scientists to seasoned project managers—on the same page and pushes projects over the finish line with fewer headaches.

    What Sets the Standard: Recommendations Born from Practice

    Years in the lab teach that trust grows from repeated, reliable outcomes. Colleagues swap stories about missteps traced to inconsistent feedstocks, but the ones who stick to trusted suppliers and vet incoming 5-Bromo-4,6-Dimethylpyrimidine on arrival see real dividends. They pre-check batch specs, run quick purity screens, and stash reference samples for backup. It’s a simple playbook but works across drug discovery, material science, and crop protection studies. Quality in equals value out; shortcuts up front end up costly later.

    Building Better Solutions: Lab Practices for the Next Generation

    Hands-on experience with specialty pyrimidines demonstrates that even incremental process improvements have large impact. Small labs seeking to stretch budgets make use of split orders, sharing certified material across teams. Industry partners push for bulk orders with real-time batch progress updates, avoiding the scramble for missing paperwork. Modern labs keep digital records of every shipment: batch data, spectra, and QC snapshots. I’ve seen university groups standardize intake checking with QR-tagged vials, linking every bottle back to its analytical record. Incremental improvements in traceability cut project stalls and build confidence with collaborators and funders alike.

    Closing Thoughts: Future-Proofing Discovery Workflows

    The research landscape changes fast, with funding cycles shortening and expectations around transparency and consistency tightening every year. Raw materials like 5-Bromo-4,6-Dimethylpyrimidine sit at the front line of these shifts. Experience, guidance from published studies, and feedback from trusted colleagues all point toward a new norm: No corner-cutting on batch verification, no settling for half-traceable origins, and no going back to unsubstantiated claims of purity or identity. The difference shows up in faster project progression, fewer repeat syntheses, more robust regulatory dossiers, and teams with confidence in the path ahead. My own work, and that of many peers, reflects these hard-won truths: upstream reliability translates to downstream success—every time.