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2-Bromopyridine-4-Methanol

    • Product Name 2-Bromopyridine-4-Methanol
    • Alias 2-Bromo-4-pyridinemethanol
    • Einecs 629-348-3
    • 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
    VTB
    Specifications

    HS Code

    805190

    Chemicalname 2-Bromopyridine-4-methanol
    Molecularformula C6H6BrNO
    Molecularweight 188.02 g/mol
    Casnumber 38818-89-0
    Appearance White to light yellow solid
    Meltingpoint 52-54°C
    Solubility Soluble in organic solvents such as DMSO and methanol
    Smiles OCc1ccnc(Br)c1
    Inchi InChI=1S/C6H6BrNO/c7-6-4-5(3-9)1-2-8-6/h1-2,4,9H,3H2
    Synonyms 2-Bromo-4-hydroxymethylpyridine
    Purity Typically >97% (commercial material)

    As an accredited 2-Bromopyridine-4-Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "2-Bromopyridine-4-Methanol, 25g," with hazard symbols, lot number, and tightly sealed cap for safety.
    Shipping 2-Bromopyridine-4-Methanol is shipped in tightly sealed, chemical-resistant containers to prevent leaks or contamination. Packages are clearly labeled according to hazardous material regulations, with appropriate documentation included. Shipping complies with international and local regulations (such as DOT, IATA, IMDG) and includes provisions for temperature control and protection from light, if required.
    Storage 2-Bromopyridine-4-methanol should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, ideally at 2–8°C (refrigerator temperature). Ensure proper labeling and secondary containment to prevent leaks or spills. Handle under a fume hood and use appropriate personal protective equipment.
    Application of 2-Bromopyridine-4-Methanol

    Applications of 2-Bromopyridine-4-Methanol in Industrial Manufacturing

    2-Bromopyridine-4-Methanol serves as a specialized intermediate in several high-precision chemical synthesis chains. Our in-plant processes focus on purity control and lot traceability to support downstream industrial partners who demand consistent input for regulated production environments.

    1. Pharmaceutical Intermediate: Synthesis of CNS-Active APIs

    This compound is widely used in the preparation of pyridine-based scaffolds for central nervous system (CNS) active pharmaceutical ingredients. Synthetic chemists employ it during key-stage functionalization steps, where it supports selective bromination and hydroxymethylation as dictated by final molecule requirements. Stringent substance traceability, impurity control, and documented lot-to-batch correlation are essential before this material can proceed into active ingredient synthesis destined for regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4 Part II
    • U.S. FDA CFR Title 21, Part 211
    • Chinese Pharmacopoeia (for domestic end-use)

    Typical usage ratio

    • 0.2-0.8 molar equivalents relative to pyridine core substrates; adjusted by target scaffold complexity and yield requirements

    Downstream process integration

    • Incorporation at intermediate coupling stage after halogenation but before nitrogen deprotection
    • QC sampling for trace metal and residual solvent after each batch
    • Documentation transfer aligned with API release procedures

    Final product types

    • Anti-epileptic drug precursors (e.g., pyridine-ring CNS agents)
    • Serotonin receptor modulator APIs
    • Novel anti-depressive agent scaffolds
    • Analytical standards for in-house drug R&D

    2. Agrochemical Intermediate: Synthesis of Selective Herbicides

    In the crop protection industry, R&D teams utilize this specialty raw material as a building block in synthesizing heterocyclic herbicide active ingredients. Production engineers employ it to introduce hydroxymethyl and bromine functionalities at controlled ratios, a requirement for site-selectivity during downstream heterocycle formation. Records demonstrate strict oversight of input quality to avoid trace contamination affecting regulatory residue testing downstream.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • FAO/WHO specifications for pesticide technical materials
    • China GB2763-2023 Maximum Residue Limits for Pesticides
    • REACH registration (for EU agrochemical manufacturing)

    Typical usage ratio

    • 5-15% w/w of total formulation batch (precise proportion from pilot studies)

    Downstream process integration

    • Entry at alkylation or Suzuki coupling stage to form pyridine-based herbicide cores
    • QC assessment for residual moisture and bromine content after mixing
    • Documentation traceable for regulatory submission

    Final product types

    • Pre-emergence herbicide concentrates
    • Post-patent pyridine-based weed control agents
    • Intermediate concentrate for technical-grade pesticides
    • Dedicated R&D prototype compounds for registration studies

    3. Active Materials for Electronic Chemicals (OLED Materials Synthesis)

    Specialty electronics chemicals producers use this material for constructing complex organic molecules, specifically in the development of OLED and electroactive compounds. The bromine and alcohol functionalities make it suitable for selective C—C coupling, necessary for precise optoelectronic polymer chains. GMP-like documentation and full impurity profiling are required as downstream OLED performance depends on purity and functional group integrity.

    Industry compliance standards

    • IEC 62474 Material Declaration for Products of and for the Electrotechnical Industry
    • RoHS (Restriction of Hazardous Substances Directive)
    • JEDEC JESD 201 for Moisture Sensitivity
    • ISO 14001:2015 Environmental Management

    Typical usage ratio

    • 0.05-0.2 molar equivalents relative to backbone monomer; tuned for targeted molecular weight and substitution density

    Downstream process integration

    • Employed at key C—C cross-coupling or substitution stage during small molecule or polymer seed synthesis
    • Post-synthesis purification and residual halide analysis
    • Records maintained for batch-to-batch electronic grade purity

    Final product types

    • OLED emitter intermediates
    • Active-luminophore layer materials
    • Electroluminescent display prototypes
    • Advanced functionalized polymer batches for R&D

    4. Fine Chemical Intermediate: Specialty Dye and Pigment Precursors

    Manufacturers in the fine chemicals sector harness this intermediate when synthesizing advanced dyes and specialty pigments. The brominated-pyridinyl alcohol motif acts as a reactive substrate for subsequent coupling, enhancing color strength and fastness in specialty dyes. Strict input characterization, including NMR and HPLC profiling, remains essential to support the traceability and color consistency required by high-end textile and coating producers.

    Industry compliance standards

    • EN 71-3 Toy Safety—Migration of Certain Elements (for pigment end-use)
    • ISO 9001:2015 Certified Quality Management for Fine Chemical Synthesis
    • REACH Pre-registration (for EU pigment industry)
    • OEKO-TEX Standard 100 (for dyes used in textiles)

    Typical usage ratio

    • Varies 5-18% w/w depending on target pigment depth and molecular weight

    Downstream process integration

    • Feedstock for nucleophilic aromatic substitution during dye-core construction
    • Reaction mixture sampled for integration by FTIR and UV-VIS after addition
    • Batch documentation supports traceability to pigment formulation lot

    Final product types

    • Reactive dyes for high fastness textiles
    • Specialty organic pigments for coatings and plastics
    • Custom dye intermediates for R&D labs
    • Industrial ink concentrates
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    Certification & Compliance
    More Introduction

    2-Bromopyridine-4-Methanol: Insight from a Chemical Manufacturer

    Refining Specialty Pyridine Derivatives for Industry Progress

    Every day in our manufacturing facility, the focus stays on bringing out precise, consistent pyridine intermediates that unlock real progress for researchers and production chemists across pharmaceutical, agrochemical, and fine chemical segments. Among the many substances we produce, 2-Bromopyridine-4-Methanol stands out in its category — not just for its structure, but for the doors it opens when developing advanced molecules and innovative synthetic steps.

    In our experience, simple differences in a molecule can mean dramatic shifts in results when scaling up a process or troubleshooting a synthetic step. Pyridine derivatives, by their nature, carry potential for high-value transformations, and our line of bromo-substituted pyridine alcohols emerged after years of audit, process refinement, and close collaboration with clients tackling advanced syntheses.

    Features and Quality Benchmarks

    Each batch of our 2-Bromopyridine-4-Methanol, under the structural designation C6H6BrNO, carries rigorous verification to back its chemical identity and purity. The molecular structure — bromine at the 2-position and a primary alcohol at the 4-position on the pyridine ring — brings a set of advantages for downstream manipulation.

    Quality does not result from casual oversight. Our chemists run consistent NMR, GC, and HPLC analyses to ensure chemical purity not less than 98%, safeguarding against contaminants that can cripple catalytic steps or introduce batch variability. Water and volatile residue targets stem from direct manufacturing experience — trace moisture can mean failure when this building block couples under organometallic or cross-coupling conditions.

    Physical form, usually a pale solid or low-melting crystalline material, has been refined to ease handling and dosing in large reactors or precise bench-scale work. Bulk density and particle size get attention too, because even something as simple as clumping complicates integration into larger-scale systems.

    Guiding Users Beyond the Data Sheet

    As the actual manufacturer, we see the real-life hurdles chemists face — purchases might look the same on paper, but the field values outcome, not theory.

    The coupling of the bromopyridine core with a primary alcohol group in 2-Bromopyridine-4-Methanol promotes cleaner conversions in Suzuki, Buchwald, and other cross-coupling reactions. In research settings, our partners often point out that having the bromine on C2 with a benzylic alcohol at C4 grants both regioselectivity and orthogonality. That means more direct reaction routes, fewer by-products, and fewer protection/deprotection steps. Analysts and chemists repeatedly report lower by-product levels when switching to our materials, which translates directly into higher yields, less chromatographic workload, and greater confidence at the pilot and production scales.

    Process-wise, many alternatives — like 3-bromopyridin-2-yl methanol or other ring-substituted alcohols — can alter not just chemical reactivity, but isolation, safety, or storage. Moisture sensitivity, thermal stability, and even odor can become minor distractions or major hazards. Experience tells us that a well-designed intermediate should blend ease of use with scalability, so we keep a tight eye on shelf-life and transportation criteria in our batches. Over time, direct customer feedback has led us to rework solvent recovery conditions and post-synthesis drying to ensure consistent handling during both warm and cold seasons.

    Shaping Pharmaceutical and Fine Chemical Pathways

    2-Bromopyridine-4-Methanol may seem like just one specialty intermediate, but for drug-discovery chemists and scale-up teams, the right starting block shortens the route to target compounds. Its structure makes it an excellent partner in building more complex pyridine scaffolds, many of which feature in clinical candidates, kinase inhibitors, or crop protection actives.

    We’ve watched customers rely on this intermediate in the synthesis of molecules carrying 4-alkoxypyridine motifs, as well as in convergent strategies where a bromide group opens the way for late-stage functionalization. In our site’s application lab, reaction records show that our 2-bromopyridine-4-methanol routinely enables Grignard or boronate coupling partners to attach with higher selectivity, without scrambling the alcohol function. That advantage cannot be mimicked by shifting the bromine or alcohol to other ring locations.

    From our own technical support files, cases emerge where generic-grade material brought headaches for downstream step optimization — inconsistent off-color solutions, variable melting ranges, or even trace heavy metals. Through direct batch monitoring, we eliminated such issues in our own production by switching process solvents, updating filtration steps, and investing in analytical comparators. Commercial customers share that the switch to our consistently pure batches shaved days off routine analysis and improved final API purity by points that mattered during regulatory approval.

    Understanding the Differences in a Crowded Market

    The fine chemicals market carries a wide range of pyridine derivatives, often with similar names and formulas. Actual application results, in our view, depend less on theoretical listings and more on how each batch stands up to user demands. With 2-Bromopyridine-4-Methanol, the arrangement of functional groups allows for wider compatibility, whether in multi-step synthesis or when designing new candidates on the bench.

    Chemists sometimes attempt alternative routes by switching to the iodo or chloro substituted analogs, or simply flipping the positions of the bromine and alcohol. We’ve worked with projects exploring 2-bromopyridine-3-methanol, but the overall reactivity profile changes noticeably. Lower yields in C-coupling, more purification, and added cost all follow. Each small variation affects rate, selectivity, and even catalytic lifecycle during process development. Our records show time and again that the direct accessibility and purity of our product reduces failed starts and simplifies troubleshooting across diverse pipelines.

    On the technical side, bromine proves the best balance between reactivity and stability for scalable cross-coupling. Iodides tend to react faster but degrade faster and converge more side products under practical conditions; chlorides lag both in reactivity and sometimes leave residual metal salts that cost time and resources during workup.

    Our facility batches prioritize not only the main assay but also a controlled residual solvent profile and metal impurity threshold; real-world customers reported that off-the-shelf variants with relaxed specs caused failed reactions or resulted in difficult upscaling. Skipping such headaches comes down to the tight batch records and in-process checks we developed after reviewing hundreds of scale-up trials with users in Europe, North America, and Asia.

    Supporting Breakthroughs and Streamlining Costs

    Within pharmaceutical process chemistry, convenience and safety get no less attention than reactivity and selectivity. Sourcing intermediates with unreliable quality or inappropriate packaging can derail sensitive steps, especially those involving strong bases, coupling partners, or trace-metal-sensitive routes.

    Feedback from several multinationals highlighted how off-odors and unexpected color shifts appeared in materials supplied through indirect channels. In a few high-sensitivity applications, these overlooked signals corresponded with undetectable oxidized impurities or polymeric contaminants — the sort not easily caught by basic HPLC alone. Recognizing the cost of such mishaps, our workflow now includes advanced impurity detection, with secondary checks for aldehydic and aromatic side species. This added control zeroes out late surprises, particularly since many clients move straight from kilo to pilot-scale tanks with little time for further in-house analysis.

    Drawing on decades of synthetic chemistry experience, the focus stays on preparing each lot in a form that fits industry needs: packed to minimize static, dried to prevent cake-formation, and shipped with robust documentation referencing the latest analytical certificates. The minor details matter when you realize that, during a scale-up run, a jammed feeder or off-spec intermediate ripples straight through downstream steps. Tight control at our end means less downtime for your team.

    Practical Manufacturing Insights Shaping Our Approach

    Our entire team works hands-on with this class of intermediates, learning from hundreds of real-world syntheses. In direct consultation with industrial and academic researchers, we’ve heard repeatedly that a reliable supply of properly handled 2-Bromopyridine-4-Methanol lets them fast-track decision-making on process routes and speed up development times. The stories tend to involve troubleshooting: a color drift traced to impure source material, a solubility issue traced to a co-processed excipient, a crystallization problem fixed after adjusting drying humidity.

    Reactors and synthesis labs need batches that behave predictably — melting and dissolving cleanly, not foaming or clogging lines, avoiding excessive dust or static. We aim for these details, both so large reactors run smoothly and so bench chemists can measure by scoop without fuss.

    Our product line broadened over the years as projects demanded new substitutions and higher throughputs. In the process, we found ways to optimize batch sizes and fine-tune reactivity, shipping both multi-kilogram and pilot-scale lots. Stability monitoring became an ongoing discipline; our field engineers monitor reclaimed and aged samples every year, logging degradation rates under realistic storage scenarios. We learned exactly how much headspace, desiccant, and packaging type matter during both routine and “worst case” shipping conditions. Today’s batches reflect countless tweaks from these long-term insights, making sure our material stays consistent wherever it travels.

    Looking Beyond the Molecule: Feedback, Contingency, and Collaborative Problem-Solving

    Continuous improvement stems from a willingness to listen, respond, and iterate. Customer stories often start with a problem somewhere up the line — a complex reaction that just won’t “go”, a chromatographic snag, or variability in fire code management or storage safety due to unexpected volatility. Sometimes, academic partners run short on information about thermal behavior across seasons or on best methods for scaling from gram to kilo. We respond directly, offering practical tips, conducting stability studies in parallel, or adjusting supply formats at short notice.

    In one case, a major process chemist needed to adapt an old pilot plan to a new solvent regime. Adjusting residual solvent spec for their needs meant not just tweaking the synthesis, but documenting the entire supply chain process. A few rounds of phone calls and pilot lots later, the new process achieved higher throughput and cut purification costs by over 15%. Such collaboration only works with a steady supply of reliable intermediates and open lines between suppliers and end users.

    Our technical team takes pride in real follow-up after shipment — collecting not just purchase order clicks, but reaction yields, LCMS spectra, and real records of what did or didn’t work once the bottle opened. Improving the material happens batch by batch, iteration by iteration. We’ve observed trends, such as certain storage conditions leading to unexpected color change, or transport in extreme heat requiring new insulated packaging. These observations build up over dozens of cycles, leading to more robust materials and realistic batch lifespan data.

    Every feedback loop feeds back directly into synthesis or QA protocols. As any manufacturer knows, long-term reliability stems from day-to-day awareness and continual process refinement. We do not rest on “good enough” but instead re-test, re-analyze, and rethink every detail to ensure that what leaves our facility matches our own highest expectations.

    The Broader Value of Consistent Quality in Research and Scale-up

    Real-world R&D and commercial needs keep evolving. Process requirements change, targets become more demanding, and regulatory expectations keep tightening. Every intermediate must consistently meet new purity, impurity, and handling standards or risk setting an entire project back. Our production of 2-Bromopyridine-4-Methanol reflects this evolving landscape — a combination of industry feedback, hands-on process control, and technical foresight.

    Handling this compound means more than ticking a box on the molecular structure. Minute details — color, physical form, odor, even secondary packaging — matter to results at the bench, in the plant, and ultimately in regulatory filings. For teams pushing boundaries in medicinal chemistry, crop science, or specialty chemical discovery, these small differences fuel bigger leaps forward.

    We set ourselves apart through the combination of technical rigor, process transparency, and readiness to troubleshoot shoulder-to-shoulder with our users. Repeatedly, we hear that having a trusted batch history and consistent supplier enables more rapid method transfer, lowers the burden of material requalification, and speeds up overall project timelines. In our view, the value of high-grade intermediates comes not only from their chemical role but from the reliability, technical support, and shared experience that stands behind each shipment.

    Conclusion: Making Every Batch Count

    As the actual manufacturer, the journey of improving our 2-Bromopyridine-4-Methanol never really ends. Decades of process adjustment, hands-on troubleshooting, and honest partnership with researchers flow into each batch we release. The focus never strays from practical needs: produce a reliable, high-purity intermediate tailored for advanced synthesis and large-scale transformations. Data alone cannot substitute for field-proven results, so we keep the doors open — for critical feedback, new ideas, and real stories from the bench or the plant. Every new challenge helps us build a better product and, most importantly, drives forward progress in chemical research and industry.