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4-Bromopyrazine

    • Product Name 4-Bromopyrazine
    • Alias 4-Bromopyrazin
    • Einecs 209-795-9
    • 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

    731268

    Cas Number 2070-41-5
    Molecular Formula C4H3BrN2
    Molecular Weight 158.98
    Iupac Name 4-Bromopyrazine
    Appearance White to pale yellow solid
    Melting Point 73-77°C
    Boiling Point 240°C
    Density 1.81 g/cm³
    Solubility In Water Slightly soluble
    Smiles C1=CN=CN=C1Br
    Inchi InChI=1S/C4H3BrN2/c5-4-1-6-3-7-2-4/h1-3H
    Pubchem Cid 17060

    As an accredited 4-Bromopyrazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 4-Bromopyrazine

    Applications of 4-Bromopyrazine in Industrial Manufacturing

    We supply 4-Bromopyrazine in large volumes to certified facilities worldwide. This intermediate finds strict end-use in several regulated industries. Below, we detail verified downstream applications, including compliance requirements, industrial formula ratios, integration process, and finished products as delivered by chemical, pharmaceutical, and material manufacturers.

    1. Pharmaceutical API Synthesis

    4-Bromopyrazine acts as a key intermediate during the preparation of novel anticancer and antimicrobial substances. Many leading pharma producers use it in Suzuki coupling and nucleophilic substitution steps to introduce substituted pyrazine rings. Our technical team frequently supports validated manufacturing protocols according to regulatory submissions, with full traceability and lot-specific QC analytics on every drum supplied to cGMP sites.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • US FDA 21 CFR Part 211
    • EU EMA Guidelines on GMP Parts I & II
    • Chinese Pharmacopeia (for domestic applications)

    Typical usage ratio

    • 0.8–1.2 molecular equivalents relative to final API scaffold; precise stoichiometry determined by downstream catalyst system and conversion efficiency.

    Downstream process integration

    • Charged during early-stage heterocyclic assembly in batch or continuous reactors prior to target molecule construction; often deprotected or cross-coupled using palladium catalysts.

    Final product types

    • Small-molecule APIs (oncology, anti-infective)
    • Intermediate building blocks for clinical candidates
    • Regulatory drug substances for Phase I-III trials
    • Reference standards for analytical labs

    2. Agrochemical Intermediates

    Crop protection and seed-treatment chemical producers leverage 4-Bromopyrazine for the targeted synthesis of heterocyclic actives and precursor molecules. It particularly supports the downstream preparation of pyrazine-based fungicides and insecticides that must pass national chemical safety and residue evaluation programs. All product batches maintain IR and NMR analysis records, provided together with supply chain and REACH compliance documentation.

    Industry compliance standards

    • EU Regulation 1107/2009 for Plant Protection Products
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act)
    • ISO 9001:2015 (Quality Management for Manufacturing)
    • OECD GLP for analytical laboratories

    Typical usage ratio

    • Typically 1.0–1.3 molar equivalents relative to final pesticide skeleton, dependent on targeted residual halide content and coupling efficiency.

    Downstream process integration

    • Used in the nucleophilic aromatic substitution step, prior to amination or ring modification; dosage adjusted for single- or multi-step syntheses per customer specification.

    Final product types

    • Fungicidal actives with pyrazine motifs
    • Pyrazinyl-based insecticide precursors
    • Seed-protectant intermediates
    • Research actives for new agrochemical development

    3. Specialty Dye and Pigment Synthesis

    Manufacturers in specialty colorant sectors select 4-Bromopyrazine as a controlled functionalizing agent in the synthesis of high-purity dye molecules. These applications demand batch uniformity, REACH compliance, and trace metals residuals below specification limits. Our production batches undergo standardized HPLC and trace contaminant profiling according to major pigment and dye manufacturers’ procurement requirements.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006
    • ISO 14001 (Environmental Management)
    • EN 71-3 for pigments intended for toys
    • GB/T 2417-2009 (China Pigment Standard)

    Typical usage ratio

    • 0.5–1.1 molar equivalents relative to chromophore base; optimized through pre-screening to achieve required spectral properties or color fastness.

    Downstream process integration

    • Added to reaction vessels during condensation with amines, or during halogen exchange to produce azo, anthraquinone, or phthalocyanine derivatives with tailored properties.

    Final product types

    • Specialty pharmaceutical dyes
    • Industrial pigment dispersions
    • Color additives for electronic displays
    • High-stability printing inks

    4. Electronic Material Intermediates

    4-Bromopyrazine supports the electronics industry as a rigid linker for advanced functional materials. Downstream producers use it for the precision construction of pyridine and pyrazine-based OLED emitters and battery electrolyte additives. All lots deliver under full COA, with compliance for heavy metal and particle size limits required by electronic material specification. Facilities producing these advanced intermediates maintain cleanroom QC protocols and comprehensive material traceability.

    Industry compliance standards

    • RoHS Directive (2011/65/EU)
    • IECQ QC 080000 for Hazardous Substance Process Management
    • ISO 14644 Cleanroom Standards
    • Customer-specified technical grades for electronics

    Typical usage ratio

    • Reacted in 0.7–1.1 equivalents versus core monomer or acceptor block during material backbone assembly.

    Downstream process integration

    • Fed into multi-step organic synthesis upstream of oligomer or copolymer formation; precise input required for device-grade uniformity.

    Final product types

    • OLED intermediate building blocks
    • Charge transport materials for displays
    • Lithium battery additive precursors
    • Specialty conductive polymers

    5. Fine Chemical Building Block for Research

    Commercial R&D laboratories and scale-up pilot plants regularly purchase this intermediate for the exploration of new catalysts and ligands in materials science and medicinal chemistry studies. Its high reactivity and availability from GMP-inspected lines enable researchers to expedite structure-activity studies and SAR optimization programs. All shipments include tracking and batch release certificates reviewed by our internal compliance auditors.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice
    • ISO 17025 Certification (Testing Laboratories)
    • GHS Labeling for Laboratory Chemicals
    • Hazardous Goods Transport Regulations (UN 3265)

    Typical usage ratio

    • Commonly employed at 0.2–2.0 equivalents relative to test substrate; specific loadings adjusted based on target library diversification or discovery route.

    Downstream process integration

    • Introduced at early or late-stage research synthesis—especially useful for assembling diversity-oriented libraries via cross-coupling and substitution reactions.

    Final product types

    • Structure-activity relationship libraries
    • Model compounds for synthetic optimization
    • Academic benchmark targets
    • Feasibility-scale intermediates for technology transfer
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    Certification & Compliance
    More Introduction

    Looking at 4-Bromopyrazine: Precision, Reliability, and What Sets It Apart

    Exploring the Substance: 4-Bromopyrazine by Name and Structure

    Chemical research depends on the quality and consistency of its building blocks. 4-Bromopyrazine stands out as a halogenated pyrazine with a noteworthy spot in laboratories and production settings. This compound, known by its CAS number 2072-81-9, features a bromine atom attached directly to the fourth position on the pyrazine ring. This minor shift in molecular architecture transforms a basic heterocycle into a much more versatile synthetic partner. Labs value this because subtle changes at the molecular level can produce dramatically new results downstream.

    Anyone who's worked with small-molecule synthesis understands that reliability isn’t negotiable. When relying on intermediates like 4-Bromopyrazine, the conversation usually revolves around reactivity, purity, and availability. The impact of a reagent’s quality ripples through every stage of work, and nobody wants to spend hours troubleshooting unexpected byproducts or inconsistent yields. My own experience in academic chemistry labs and fine chemical startups taught me to be picky: a small impurity that slips by at the beginning can snowball into costly purification work or a failed batch six steps later. So, the difference between a generic product and a carefully specified lot means more than a line on a specification sheet.

    Getting Specific: Physical Profile and Analytical Details

    Lab stock 4-Bromopyrazine usually arrives as an off-white crystalline powder. Its melting point often sits between 53 and 57°C, and its molecular weight clocks in at 157.01 g/mol. These things matter beyond trivia: dealing with compounds near their melting points changes how you handle, store, and process them. The physical state and purity directly shape workflow and results.

    I remember my first run with pyrazine derivatives during a medicinal chemistry internship. Access to a fresh, high-purity supply made downstream NMR and mass spec reads almost boring because peak assignments came out clean and clear. Life’s trickier with older, yellowed stock or questionable sources—analytical profiles get blurry fast, loss during workup creeps up, and collaborators start to question the reliability of your process.

    High-purity 4-Bromopyrazine typically boasts a purity above 98 percent. Analytical labs back this up with HPLC and GC traces, usually offering supporting data such as IR and NMR documentation. Trace moisture content can shift the scale for certain air-sensitive reactions, but a solid supplier keeps it within tight specs and runs Karl Fischer analysis to confirm. Quality assurance teams track batch-to-batch consistency to weed out low-weight lots—practices that should be standard, but not everyone delivers. These details sound routine, yet they’re often the dividing line between a smooth, reproducible synthesis and an ongoing troubleshooting session with your supervisor breathing down your neck.

    Applications: Where 4-Bromopyrazine Fits in the Workspace

    4-Bromopyrazine has earned its reputation because of how it links research and product development. Users tap into its aryl halide function for cross-coupling chemistry, notably Suzuki, Buchwald–Hartwig, and Stille reactions. These reactions might sound like insider talk, but their products shape modern pharmaceuticals, agrochemicals, dyes, and advanced materials.

    Looking back at my first complex synthesis, I learned quickly that switching from a chloro- to a bromo-pyrazine boosted my overall yield and saved me from an extra step on the bench. The bromine atom offers greater reactivity under standard conditions compared to chlorine, giving synthetic chemists easier access to previously challenging derivatives. For labs pressed for time and budget, this jump in efficiency frees up resources for deeper studies or pilot-scale production.

    Drug discovery outfits rely on scaffold hopping, tinkering with core molecular structures to unlock new bioactive compounds. The pyrazine core provides a privileged, drug-like motif. 4-Bromopyrazine doesn't just act as a static building block; it opens the door to new analogues with better solubility, metabolic stability, or biological activity. Talking to a friend from a contract research organization, I realized that hundreds of commercial screens start by quickly accessing similar scaffolds through robust halogenated intermediates like this one.

    On the other side of the research spectrum, material scientists go after new light-emitting diodes or charge-transport layers for electronics. Pyrazine rings, functionalized through bromination, become launchpads for more elaborate, conjugated systems. My time spent shadowing synthetic teams in a startup showed how the ease of aryl-bromide cross-coupling turned three-week syntheses into projects that could scale in days, not months.

    What Sets This Compound Apart from Alternatives?

    Some may scratch their heads wondering why not stick with cheaper chloro- or fluoro-pyrazines, or skip straight to amines or boronic acids. The answer comes down to reactivity and flexibility. In classic cross-coupling, bromides come across as the sweet spot for both cost and chemical responsiveness. Aryl chlorides might knock a few bucks off the invoice, but they demand harsher conditions and more expensive catalysts. In real-world settings, this means more time optimizing conditions and more money spent on specialty reagents.

    Aryl iodides react even faster, but at a significant hit to cost and stability. When overseeing a scale-up project, I saw our procurement team fight for every dollar—iodides often priced us out, while bromides balanced the budget and performance. Bromopyrazines offered a backdoor to broadening compound libraries without overcomplicating purification and waste management.

    Switching from unactivated pyrazines or lower-reactivity analogues drags down the yield and purity of your target molecules. You also risk picking up unknown side products that not only drain time to identify but can pose safety challenges. By leveraging the well-studied pathways accessible to 4-Bromopyrazine, synthetic teams can draft reliable routes and minimize ugly surprises.

    Likewise, the difference in trace impurities between 4-Bromopyrazine from established suppliers versus generic vendors affects endpoint reproducibility. In my own work, a well-documented lot history and regular certificate-of-analysis reviews proved key. Unexpected signals in downstream NMR or LCMS readouts almost always traced back to earlier-stage reagent quality—avoid the headache by starting with a clean slate.

    Quality and Trust in Chemical Sourcing

    Sourcing reliable chemicals has never been a mere formality. Questions about trace contaminants, solvent residues, and lot consistency make or break the success of a project. Recalling a time running a series of pilot syntheses, I watched two batches behave entirely differently—one consistently clean, the other clogged by persistent impurities. The difference traced straight to the vendor’s lot-to-lot variation in starting material. This isn’t an isolated story.

    Moving forward, researchers and process chemists gravitate to supplies that offer transparency with each shipment. Detailed certificates of analysis, routine analytical backing, and technical support build trust. I’ve dealt with suppliers that not only delivered what the spec promised but offered guidance on handling, storage, and even troubleshooting reaction issues. They empowered our teams to keep progress on track, rather than spending energy untangling sourcing problems.

    The best suppliers keep communication lines open beyond the original purchase order. If you catch a minor impurity or run into a handling hiccup, swift response and willingness to address problems matter. Many teams, myself included, stash contact details of go-to reps exactly for this reason. When deadlines close in and reproducibility is under scrutiny, relationships built on reliability pay back in peace of mind and project momentum.

    Safe Handling and Challenges in Storage

    Anyone actively using pyrazine derivatives knows storage isn’t a “set and forget” affair. 4-Bromopyrazine holds up well under dry, cool conditions, away from direct sunlight and moisture. Like many halogenated aromatics, exposure to high humidity brings the risk of degradation, yellowing, or even formation of trace acids. More than once, I’ve seen overlooked reagents transformed from clean crystals to a sticky, off-color mess overnight in a poorly sealed container.

    It pays to keep stocks in tightly sealed glass vials backed by desiccant packs, with access limited to trained handlers. Regular spot-checking prevents headaches, especially in team settings where turnover can mean lapses in protocol. Even a small amount of contamination—like accidental water exposure from pipetting or ambient humidity—rapidly reduces shelf life and reliability. I picked up a habit early on: weigh what you need, recap immediately, and keep everything clean. These little disciplines insulate teams from setbacks that domino across expensive project timelines.

    Chemical safety culture underscores everything. Proper labeling, up-to-date MSDS access, and safe waste disposal protocols cut down on risk. I’ve witnessed teams challenged during audits because of careless storage or missing documentation. In one such case, flagging a bottle of 4-Bromopyrazine stored alongside incompatible reagents averted a messy investigation. Vigilance pays back many times over, not just in safety but in smoother project flow.

    Environmental and Regulatory Considerations

    The world of chemistry has shifted in recent years, with labs and companies thinking hard about sustainability and compliance. Halogenated compounds draw scrutiny given their persistence in the environment. While 4-Bromopyrazine enjoys broad utility, disposal procedures and effluent controls must align with local requirements. My work with environmental health teams highlighted how improper solvent or reagent disposal can risk hefty fines and community backlash.

    Modern labs look beyond cost-per-gram calculus, now measuring impact from sourcing to post-use treatment. Full traceability—from production site audits to end-of-life waste management—raises the bar on responsible chemical use. Suppliers with clear environmental and sustainability policies stand out; their practices protect users and surrounding communities. When choosing between two almost-equivalent products, the one with credible stewardship usually wins.

    There’s an opportunity here for everyone—producers, researchers, and procurement leaders—to collaborate on greener practices. Innovations in recycling brominated solvents or adopting cleaner synthetic pathways give organizations a leg up. Sometimes, alternative reaction conditions can use less hazardous bases or greener solvents, shaving off environmental risk without trimming performance. Having a voice in industry forums and regulatory discussions proved rewarding in my career; it’s how practices improve for the next generation.

    Solving Common Challenges with 4-Bromopyrazine

    No product or reagent is without its wrinkles. Users sometimes run into solubility challenges—pyrazine derivatives don’t always play nice with polar or protic solvents. Conscious solvent selection saves hours on reaction workup and purification. In the field, I’ve seen DMSO, DMF, and acetonitrile provide reliable starting points, though solvent screening remains a lab bench staple.

    Another catch comes during cross-coupling sequences. If catalysts or ligands aren’t up to the task, brominated substrates sometimes lag in conversion or trigger unwanted side reactions. My team learned to vet new reactions fully at micro- and mini-scale before scaling up, saving us thousands on wasted metal catalyst or substrate. Open dialogue with technical reps from suppliers also pointed us toward robust, literature-backed conditions that smoothed out persistent bottlenecks.

    Contamination from airborne particles or mishandling cropped up now and then, especially during busy weeks in shared labs. Regular audits, strict inventory management, and batch segregation pulled us back from the edge several times. The discipline around small-molecule management rarely gets the fanfare of headline projects, yet it’s critical for success. Looking back, every protocol tweak and investment in better containers or labeling paid dividends by nipping problems in the bud.

    The Road Ahead: Innovation, Efficiency, and Collaboration

    Working with 4-Bromopyrazine brings more than technical advantage—it ties into a larger story about how the chemical sector adapts and evolves. At the cross-section between innovation and daily lab work, every small tweak in building block reactivity, purity, and sourcing reverberates through many industries. Strong coordination between suppliers, researchers, and regulatory bodies plays a direct role in driving safer, more effective science forward.

    New catalytic systems and more sustainable synthetic routes continue to reshape what’s possible. Projects that once struggled with harsh reagents or poor scalability now push the limits of rapid prototyping and agile production schedules. Looking at ongoing advances in medicinal and material chemistry, the quest for faster, cleaner access to advanced heterocycles stays front and center. 4-Bromopyrazine, for all its apparent simplicity, holds an outsized position in these changes.

    End-users, myself included, benefit from advances in analytical verification, documentation, and open data sharing. The global science community values not just the latest breakthrough, but the ability to reliably reproduce, iterate, and build on each other’s work. This ethos shapes how I select reagents, navigate supplier options, and collaborate with cross-functional teams. Looking back at successful projects, the most memorable always linked back to trusted basics—consistent chemicals, transparent communication, and a shared drive to improve.

    By understanding both the strengths and challenges of 4-Bromopyrazine, scientists and innovators keep pushing the boundaries. Creative use, careful handling, and ongoing dialogue ensure that this unassuming pyrazine variant continues fueling discovery, progress, and smarter chemical stewardship.