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4-Bromomethyltetrahydropyran

    • Product Name 4-Bromomethyltetrahydropyran
    • Alias THP-bromide
    • Einecs EINECS 614-105-2
    • 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

    620985

    Chemical Name 4-Bromomethyltetrahydropyran
    Molecular Formula C6H11BrO
    Molecular Weight 179.06 g/mol
    Cas Number 131179-43-2
    Appearance Colorless to pale yellow liquid
    Boiling Point 92-94°C at 13 mmHg
    Density 1.31 g/cm³
    Refractive Index 1.473 (at 20°C)
    Purity Typically ≥ 95%
    Solubility Slightly soluble in water; soluble in organic solvents
    Storage Temperature Store at 2-8°C
    Smiles C1CC(OCC1)CBr

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

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 4-Bromomethyltetrahydropyran, labeled with hazard warnings and chemical identification details.
    Shipping 4-Bromomethyltetrahydropyran is shipped in tightly sealed containers, protected from moisture, light, and incompatible materials. Transport complies with relevant hazardous materials regulations, including proper labeling and documentation. Handle with care to prevent leaks or spills. Store at room temperature or as specified by the supplier, ensuring restricted access to authorized personnel only.
    Storage 4-Bromomethyltetrahydropyran should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon, to prevent hydrolysis and degradation. Keep it in a cool, well-ventilated area, away from direct sunlight, heat sources, and incompatible substances like strong bases or oxidizers. Store at room temperature or as recommended by the manufacturer’s safety data sheet (SDS).
    Application of 4-Bromomethyltetrahydropyran

    Applications of 4-Bromomethyltetrahydropyran in Industrial Manufacturing

    4-Bromomethyltetrahydropyran serves as a specialized intermediate in several advanced synthesis pathways across fine chemical and pharmaceutical manufacturing. The following sections detail its established roles, compliance frameworks, usage benchmarks, processing steps, and end-use product formats in different industrial verticals.

    1. Pharmaceutical Active Ingredient Synthesis

    Within pharmaceutical intermediate synthesis, manufacturers apply 4-bromomethyltetrahydropyran as an alkylating agent or protected pyran ring source during the multi-step construction of complex molecules. The material enters the production train where controlled alkyl substitutions are essential, for example, in the assembly of tetrahydropyran moiety-containing APIs used for central nervous system and antiviral drugs. Accurate batch records must trace raw material addition to comply with validation protocols. Usage depends on the molecular target’s synthetic route, with continuous monitoring to maintain low impurity profiles required by major authorities.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) GMP standards
    • EU EudraLex Vol. 4 GMP Guidelines
    • National authority requirements (FDA, EMA, NMPA) for traceability and purity control

    Typical usage ratio

    • 0.08 – 0.35 molar equivalents per step, determined by the target API synthesis pathway and protecting group strategy
    • Adjustment according to the number of alkylation sites and desired regioselectivity

    Downstream process integration

    • Stepwise introduction in multi-enzyme or multi-reagent sequences during protected group installation
    • Careful addition during Grignard, Suzuki, or S_N2 reactions prior to deprotection and final API isolation
    • Quality control with in-process HPLC analysis to confirm intermediate integrity

    Final product types

    • Neurology drug intermediates
    • Hepatitis antiviral intermediates
    • Chemical building blocks for branded pharmaceuticals
    • Reference standards for drug substance manufacturing

    2. Agrochemical Intermediate Manufacturing

    Agrochemical producers use 4-bromomethyltetrahydropyran as a functionalized pyran building block in the creation of select herbicide and fungicide actives. Industrial facilities incorporate it at the commencement of pyran ring-derivative synthesis, providing key structural diversity for the development of crop-protection actives addressing specific resistance mechanisms. Downstream analysts apply comprehensive purity and residual bromide testing to uphold regulatory requirements before releasing bulk products to formulation lines.

    Industry compliance standards

    • ISO 9001:2015 quality management for chemical synthesis
    • REACH Regulation (EC) No 1907/2006 for chemical registration and documentation
    • FAO/WHO specifications for technical grade pesticides
    • OECD Principles of Good Laboratory Practice (GLP) for development batches

    Typical usage ratio

    • 5 – 15% w/w based on active ingredient synthesis scale and overall molecular design
    • Adjusted for yield optimization and downstream conversion efficiency

    Downstream process integration

    • Charged as a starting material in heterocyclic ring-forming reactions
    • Feeds into condensation, alkylation, and cyclization steps alongside amines or acid chlorides
    • Batch monitoring with GC-MS for impurity mapping before integration with bioactive moieties

    Final product types

    • Selective herbicide intermediates
    • Systemic fungicide building blocks
    • Chemical precursors for seed treatment actives
    • Intermediates for insecticide synthesis

    3. Fine Chemical and Specialty Material Synthesis

    In the fine chemical segment, our raw material functions as a pyran-based linker or intermediate for producing custom specialty chemicals, especially where scalable alkyl bromide chemistry is vital. Clients deploy it in nucleophilic substitution, cyclization, or protective group chemistry performed in controlled reactors with automated addition to enable precision in batch reproducibility. The downstream risk of unreacted organobromine species requires scheduled safety and environmental compliance checks, particularly before solvent recovery or waste treatment.

    Industry compliance standards

    • ISO 14001: Environmental Management System for chemical plants
    • Responsible Care® chemical industry initiative compliance
    • Internal material balance and mass flow documentation for hazardous intermediates
    • National hazardous waste and discharge regulations

    Typical usage ratio

    • Typically 3 – 12% w/w as process intermediate
    • Adjusted for targeted product yield, end-application performance requirements, and batch scale changes

    Downstream process integration

    • First-stage reactant in nucleophilic substitution or etherification
    • Inline monitoring for conversion with real-time spectroscopic analysis
    • Serves as a protected functional group donor enabling staged functionalization

    Final product types

    • Pyran-containing specialty resins
    • Heterocyclic structure intermediates for advanced chemistry
    • Fine chemical building blocks for contract synthesis (CDMO) clients
    • Intermediates for specialty surfactants or lubricants

    4. Advanced Polymer Modification

    Application engineers employ this bromomethylated pyran as a reactive functional monomer for advanced polymer chain-end modification, imparting specialty chemical reactivity or facilitating further post-polymerization derivatization. The monomer is introduced as a minor component in copolymerization or as a post-polymer functionalization agent, with stringent control to prevent premature degradation or over-functionalization. QC departments routinely perform NMR and elemental analysis to control substitution levels in the modified polymer and to guarantee end-use performance in demanding environments such as electronics and medical devices.

    Industry compliance standards

    • ISO 9001: Quality management for polymer manufacturing
    • RoHS Directive 2011/65/EU regarding restricted substances for electronics
    • ASTM D638 and ASTM D256 for mechanical property testing of final polymers
    • REACH and CLP Regulations for chemical handling and pre-registration

    Typical usage ratio

    • 0.5 – 2.5 mol% as chain-end modifier in specialty copolymers, adjusted according to desired reactivity and properties
    • For post-polymer functionalization: 1 – 8% w/w, based on target substitution density

    Downstream process integration

    • Metered dosing into reactive extrusion, solution polymerization, or melt blending units
    • Batch and continuous process options available depending on polymer type
    • Post-modification purification and analysis to control functional group content

    Final product types

    • Reactive functional polymers for electronics encapsulation
    • Medical-grade copolymer intermediates
    • Specialty surface modifiers
    • Research-grade polymeric reagents
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    Certification & Compliance
    More Introduction

    Meet 4-Bromomethyltetrahydropyran: A True Workhorse in Organic Synthesis

    Direct from Our Plant: Attention to Purity, Every Step of the Way

    We have spent years fine-tuning the synthesis and purification of 4-Bromomethyltetrahydropyran in our own facilities. Instead of outsourcing any part of production, our chemists handle raw material selection, catalytic steps, and meticulous fractionation on-site. Working up the bromo-derivative from tetrahydropyran alcohol, we watch every reaction profile from batch to batch, knowing the smallest shifts can have real downstream effects when the product reaches your flask.

    Our current production model 4-Bromomethyltetrahydropyran delivers material as a colorless liquid, free from colored byproducts or water traces. Typical GC results show a single major peak, with side products below detection in regular runs. All finishing is done in closed systems, and when demand climbs, we adjust the cycle time—not the controls. Because everything happens under one roof, we troubleshoot each step personally and validate the purity ourselves before signing off on the shipping drum.

    A Springboard for Building Complexity: Why the Market Cares

    Many routes in pharmaceuticals, crop protection, and advanced materials depend on reliable access to functionalized pyran building blocks. 4-Bromomethyltetrahydropyran’s bromoalkyl handle carries plenty of reactivity for nucleophilic displacement, Grignard work, or Suzuki couplings. Out of all the alkyl bromide building blocks, this compound brings something special: a robust tetrahydropyran protected system, where the cyclic ether backbone stabilizes sensitive moieties during later synthetic transformations.

    People often ask about the difference between this product and plain alkyl bromides, or even 4-chloromethyl derivatives. Based on what we observe in lab prototypes and pilot plant upscales, the bromomethyl group unlocks stronger leaving group effects, making nucleophilic substitution faster and milder, even when working with aryl, azide, or strong base partners. The tetrahydropyran ring is not just a bystander—its oxygen atom influences electron distribution in transition states and helps to shield sensitive intermediates. Over years of running multistep campaigns, we’ve learned that skipping or switching the protection group can increase downstream impurity counts, reduce overall yields, or trigger instability. Sticking with genuine 4-bromomethyltetrahydropyran avoids those headaches.

    Our Observations on Handling, Storage, and Reactions

    You can't gauge the future steps of an intermediate like this without experience in your own labs. After several scale-ups, we can tell the difference between a fresh batch that has seen minimal air and UV, and a sample that sat in a poorly sealed bottle. Our team mans every hand-off point, using low-light transfers and nitrogen blankets during bottling to avoid tiny but cumulative oxidative degradation. We ship drums in lined containers, so that even after months in storage, incoming QC at customer sites shows unchanged purity and consistent starting material profile.

    In use, the reactivity profile stands up to its reputation. Whether you’re introducing heterocycles, pushing reductive aminations, or using the compound in preparation of advanced glycosides, we see higher conversions compared to analogous chlorinated or methylated pyran derivatives. Because our batches run free of common byproducts—like polybromo side chains or ring-opened fragments—users rarely report loss in selectivity or the appearance of trace contaminants down the line.

    On temperature sensitivity, our experience tracks with what literature reports. The bromomethyl group, once installed, holds up under moderate heat, but will talk back if heating rates spike or if acids are left in contact too long. We've worked with several process chemists over the years to tweak solvent choices, minimize exotherm, and keep product loss low during stress steps. These tweaks have filtered into our standard operating map, saving time and trouble for everyone who relies on the product mid-synthesis.

    Larger Perspectives: What Sets It Apart in Practice

    Real distinctions appear once projects move from bench to pilot reactor. In the market, plenty of alkyl bromides circulate from importers, each one labeled “high purity,” yet true quality shows itself under real-world strain. We recognize the temptation to use lower-cost alternatives, but from bitter experience, low spec grades introduce extra tars and halide byproducts—costing more later through clean-up and lower yield.

    Several chemists have called, weeks after ordering from non-manufacturer sources, to talk through batch-to-batch variation or double peaks in NMR traces. With material from our reactors, the spectrum remains exact, peak for peak, and you don’t have to compensate for hydrolysis fragments or tailing spots. The bromine atom profile, critical for sequences like phase-transfer alkylations, comes out crisp, letting users work with tighter process windows without the drift you get from recycled or warehoused inputs.

    Compared to 4-chloromethyltetrahydropyran, the brominated version shows sharply higher substitution yields when paired with hard nucleophiles and delivers surface-cleaner results if you’re introducing bulky or hindered partners. Multiple clients in the agrochemical sector reported improved batch consistency for pyrethroid intermediates when switching to bromomethyl over chloromethyl variants, even when resin loads or column requirements were fixed.

    The story changes again if you look at methylated variants where the halogen is swapped for a hydrogen. Those compounds, while stable on paper, don’t activate as handily, and often end up requiring longer run times, broader temperature ramps, or more aggressive partners—risky propositions in scale-up, which tend to spike operational costs and bog down the whole campaign.

    End-User Applications: Hearing From Colleagues in the Field

    The most common uses we see draw on the combination of reactivity and protection. Medicinal chemists gravitate toward 4-bromomethyltetrahydropyran for making modified nucleosides, protected carbohydrates, and as a bridgehead for late-stage functionalization. Process teams send questions about compatibility: Will it handle two-step displacements, can it tolerate flash chromatography, will trace base degrade the ring? Over and over, we see the same answer—efficient reaction, resilient protection, minimal waste.

    There’s tangible payoff as well in pilot manufacturing for actives, where trace halogens or residual tars can undercut regulatory filings. With our own tight process controls, we supply batches where every drum matches the next, all backed by datasets from the same columns and same glassware used for daily QC. This translates directly to less fire-fighting mid-process, fewer lost cycles, and more straightforward regulatory discussions.

    Anecdotally, one mid-sized pharma partner made the leap from open-market bromomethylpyran to our domestically manufactured material after three failed syntheses—each breakdown traced to inconsistent bromine distribution and upstream ring scission. With consistent supply lines, the same partner shortened campaign time by almost thirty percent, avoided double reactions, and saved on purification. Performance in the flask doesn’t lie, and we stand by the hands-on routine that goes into keeping our drums up to snuff.

    What We Prioritize in Every Batch

    From start to finish, we keep eyes on more than just yield or assay. Moisture control, trace metal analysis, and extrusion purity all matter. We train every new technician to spot subtle visual changes: cloudiness, odor, viscosity variance, which signal handling or shipping mishaps sometimes before the numbers do. Reactivity can shift after exposure, but rigorous pack-off and direct feedback loops catch problems before they reach end-users.

    On the regulatory front, we use a plant-wide batch tracking system that logs every charge, transfer, and sample. Certificates go out with each order, but the real assurance comes from knowing no third parties have cut corners. Our batch records reflect everything, from reaction conditions to final test data, logged and stored, so repeat orders get repeat results. This discipline has paid off in supply contracts with partners whose audits weigh stability and reproducibility as highly as cost.

    As the market tightens and regulatory hoops increase, buyers steer away from repackaged intermediates or generic vendors with mismatched documentation. Instead, they push for provenance and chain-of-custody, which only true manufacturers can supply. We open our doors for audits, answer technical back-and-forth with plant managers, and share protocols that have proven robust in multiple customer reactions.

    Facing Future Challenges: Quality, Scalability, and Collaboration

    Markets continue to shift, and new applications for 4-bromomethyltetrahydropyran crop up yearly. Lately, we’ve supported green chemistry studies exploring alternative solvents and milder nucleophile partners, and technical teams hungry for ever-purer intermediates send us performance requests—from 13C purity data to specific crystalization techniques. The main challenge lies in keeping process efficiency high while meeting stricter customer and regulatory requirements.

    We don’t chase lowest-cost production at the expense of consistency or safety. Instead, upgrades to our reactors, expansion of in-house testing capabilities, and continuous operator training rank as our main insurance. Every new demand—be it a more stringent water spec, lower halide residue, or expanded NMR library—is met head-on, since we believe every technical detail can impact the outcome far downstream of our own gates.

    As product needs evolve, we invest in scale-up tools designed for both flexibility and reproducibility: jacketed vessels, energy-efficient distillation set-ups, and in-line pure nitrogen transfers. These tools allow us to customize runs without undercutting baseline quality. Supply chain stability matters, but so does transparency. We lay our process data bare, so anyone using our intermediate can see exactly what they’re starting with—and can build their own data packages on top.

    Industry forums and technical working groups discuss at length the shifting landscape of pyran chemistry. Our testimony carries the weight of years spent solving practical process problems: ways to detect hidden instability, optimize throughput, or strip stubborn byproducts. We see the same recurring theme—solid manufacturing experience consistently delivers stronger outcomes than a reliance on piecemeal outsourcing or third-tier raw material sources.

    Our People Make the Difference

    The final product reflects every technician and chemist who’s joined the plant, each one contributing practical improvements or error traps that keep mistakes from snowballing. Routine on-site tests, paired with insight from real synthesis campaigns, mean we catch issues—sometimes before they even arise—and pass along those benefits to every customer. We keep staff up to date with technical seminars and benchmark studies, continuing to raise the bar for what this intermediate can offer.

    We answer technical support calls directly, not through intermediaries. Some of our closest customers started out with cautious pilot runs; now, they pull their main supply direct from our lines, after seeing side-by-side improvements in purity, reactivity, and yield. One-on-one exchanges about process bottlenecks, material handling, and optimal storage conditions help both teams grow, and over time we’ve built a library of common troubleshooting tips and best practices for new adopters.

    Compared to players who outsource or repackage, we take pride in solving supply shocks ourselves. Raw bromine availability, unexpected energy policy changes, rising environmental standards—these all cause headaches across the world. Because we own the process end-to-end, from procurement through to the last filter, we can adapt production before bottlenecks turn into missed deadlines or quality concerns.

    Supporting Innovation and Meeting Tight Deadlines

    Demand for 4-bromomethyltetrahydropyran spikes during regulatory submissions, synthetic route changes, or scale-up deadlines. We witness the impact first-hand when a customer faces a tight schedule for a new API launch or plant validation. Our plant runs in parallel with changing market needs: fast shipments, new format drums, or custom labeling requirements. Keeping enough stock for surge orders comes down to our capacity planning and direct communication channels with buyers.

    As routes and applications broaden, we don’t shy from collaboration. We field requests for higher purities, or for experimental grades with adjusted impurity profiles for research teams who want to probe new chemistries. Real innovation comes out of close feedback loops—sharing batch data, running split sample tests, hashing out process tweaks. Few competitors keep the same open channels between laboratory, plant, and customer. Our team thrives on these challenges, treating every order as an opportunity to refine and push the limits of the product’s reliability.

    Colleagues in process R&D often need to move quickly from idea to kilogram scale. With flexible batch sizes, on-demand production, and support for both routine and one-off requests, we smooth out any bumps along that road. Our input doesn’t stop with shipping; we troubleshoot problems with customers until they disappear, no matter how specialized the synthesis.

    Environmental Focus and Process Responsibility

    Producing specialty intermediates like 4-bromomethyltetrahydropyran means being accountable for everything leaving the plant—runoff, vent gas, packaging remains. We cap bromine emissions, treat waste streams to eliminate organics, and recover solvents for reuse wherever practical. These investments in environmental control stem not only from external regulation but from a belief in responsible stewardship for both our facility and our community. Every new piece of equipment is vetted for both output efficiency and reduction of unwanted byproducts.

    We offer returnable packaging and encourage bulk orders that shrink the environmental footprint per kilo delivered. Our laboratories switch out hazardous cleaning agents for greener alternatives whenever possible, observant that both regulatory agencies and customers want to track every step with full disclosure. This makes it easier to provide data for sustainability audits, trace contaminant studies, and even life cycle analysis for major downstream projects.

    Summary: Real Results Through Real Accountability

    All the care that goes into manufacturing, packaging, and delivering 4-bromomethyltetrahydropyran reflects our core approach to chemical production. The same hands who synthesize, purify, and pack the compound also deal with technical queries, resolve scale-up bottlenecks, and confront regulatory questions—all in the pursuit of reliability and performance. Through rigorous in-process controls, close customer cooperation, and continual technical development, we support everyone building new products or pushing the frontiers of chemical synthesis. For us, this compound’s journey doesn’t end at the shipping dock; it continues through every experiment, every process scale-up, every new application it powers.