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2-(3-Bromopropoxy)Tetrahydro-2H-Pyran

    • Product Name 2-(3-Bromopropoxy)Tetrahydro-2H-Pyran
    • Alias THP-O-(CH₂)₃Br
    • Einecs 473-120-8
    • 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

    591952

    Iupac Name 2-(3-Bromopropoxy)tetrahydro-2H-pyran
    Molecular Formula C8H15BrO2
    Molecular Weight 223.11 g/mol
    Cas Number 142137-95-5
    Appearance Colorless to pale yellow liquid
    Boiling Point No reliable data available; estimated approx 90-100°C at 0.8 mmHg
    Density 1.286 g/mL at 25°C (estimated)
    Refractive Index 1.456 (estimated)
    Solubility In Water Insoluble
    Flash Point 79°C (estimated)
    Smiles BrccccOCC1CCCCO1
    Storage Conditions Store at 2-8°C, protected from moisture

    As an accredited 2-(3-Bromopropoxy)Tetrahydro-2H-Pyran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 50g of 2-(3-Bromopropoxy)tetrahydro-2H-pyran is securely sealed in an amber glass bottle with a tamper-evident cap.
    Shipping The chemical **2-(3-Bromopropoxy)tetrahydro-2H-pyran** is typically shipped in tightly sealed containers, protected from moisture and light. It is transported as a hazardous material, requiring appropriate labeling and documentation. The package should adhere to local and international regulations for brominated organic compounds, ensuring safety during handling and transit.
    Storage Store 2-(3-Bromopropoxy)tetrahydro-2H-pyran in a tightly sealed container under a dry, inert atmosphere such as nitrogen or argon. Keep it in a cool, well-ventilated area away from moisture, heat sources, and direct sunlight. Avoid storage with incompatible materials such as strong acids, bases, or oxidizing agents. Refrigeration (2–8°C) is recommended for prolonged storage.
    Application of 2-(3-Bromopropoxy)Tetrahydro-2H-Pyran

    Applications of 2-(3-Bromopropoxy)Tetrahydro-2H-Pyran in Industrial Manufacturing

    2-(3-Bromopropoxy)Tetrahydro-2H-Pyran is a specialized organobromine compound serving as a vital intermediate in several advanced chemical industries. As an original manufacturer, we supply this raw material to facilities engaged in high-value synthesis processes, focusing strictly on sectors where it has established industrial roles. Below, we detail core application scenarios, each reflecting industry-specific regulatory standards, formulation practices, integration points, and the nature of downstream commercial products.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Pharmaceutical manufacturers rely on this compound for the synthesis of key intermediates in the production of heterocyclic active pharmaceutical ingredients, particularly where selective alkylation of heterocycles or oxygen-protecting group strategies are required. Our clients in this segment value precise reactivity and the ability to control byproduct formation to support downstream GMP batch production.

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7A)
    • European Pharmacopoeia (Ph. Eur.) stipulations for raw materials
    • United States Pharmacopeia (USP) excipient requirements for process intermediates
    • Certificate of Suitability to the Monographs of the European Pharmacopoeia (CEP) consideration in API registration

    Typical usage ratio

    • Ranges between 5-20 mol% relative to core heterocycle or alcohol substrate, depending on protection or alkylation requirements; adjustment based on reaction scale and impurity thresholds

    Downstream process integration

    • Incorporated during the alkylation or O-protection stage within multi-step batch reactor synthesis sequences for non-sterile and sterile API manufacturing

    Final product types

    • Pharmaceutical active ingredients for CNS, cardiovascular, and antiviral drugs
    • Protected intermediate compounds dispatched for further downstream derivatization or deprotection

    2. Advanced Agrochemical Intermediate Production

    In agricultural chemical manufacturing, this compound enables the synthesis of novel protected alcohol intermediates and fungicidal precursors, valued for its selectivity in step-growth reactions and facilitation of downstream coupling steps critical to large-volume crop protection agents.

    Industry compliance standards

    • FAO/WHO specifications for pesticide intermediate purity
    • ISO 9001:2015 certified QC procedures for consistency in agro-intermediate supply
    • REACH registration for import and use in European Union agrochemical production
    • National Industrial Chemicals Notification and Assessment Scheme (NICNAS) listing for Australia

    Typical usage ratio

    • Typically 3-10% w/w in reaction mixtures; optimized to ensure complete conversion in etherification protocols for maximum crop protection agent yield

    Downstream process integration

    • Enters the synthesis flow in the formation of brominated intermediates prior to subsequent nucleophilic substitution or deprotection stages in herbicide and fungicide synthesis

    Final product types

    • Active intermediates for systemic fungicides and herbicides
    • Key building blocks for selective pre-emergent crop protection chemicals

    3. Custom Synthesis for Fine Chemical Libraries

    Contract research organizations and fine chemical producers source this material for core library synthesis, especially in discovery-phase small molecule projects where oxygen protection and bromopropyl introduction are required for SAR (structure-activity relationship) study compounds. These end-users demand batch-to-batch purity and reliable origin for regulatory submissions and patent support.

    Industry compliance standards

    • ISO 9001:2015 for custom fine chemical production traceability
    • OECD GLP (Good Laboratory Practice) compliance in library synthesis for preclinical candidates
    • Material transfer and chain-of-custody documentation under CMC regulations for pharmaceutical R&D
    • Hazardous chemicals handling standards for laboratory-scale synthesis (OSHA 1910.1200)

    Typical usage ratio

    • Variable between 2–15 mol% based on target structure requirements and complexity of combinatorial array; adjusted according to required substitution patterns and downstream reactivity

    Downstream process integration

    • Utilized in early-stage molecule construction, typically at the selective alkylation step in multistep synthesis protocols managed in parallel reactor arrays for high-throughput screening

    Final product types

    • Small molecule screening libraries for bioactivity and toxicology screening
    • Lead compound scaffolds for subsequent medicinal chemistry optimization

    4. Specialty Polymer Modifier Synthesis

    Producers in the specialty polymer market leverage this compound to introduce controlled functional groups within engineered polymers for performance additive development, including modifications aimed at improving surface properties, compatibility, or reactivity in block copolymers.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in specialty chemical processing
    • RoHS compliance for downstream use in electronics or automotive polymer systems
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) requirements for polymer precursors in European markets
    • ASTM D6288 for additives in plastics formulation

    Typical usage ratio

    • Typically incorporated at 0.5–3% by weight in modifier synthesis-stage reactor charge; application-specific ratio depends on polymer chain length and targeted functionalization degree

    Downstream process integration

    • Added at the monomer or oligomer feed stage during the formation of telechelic or block copolymer chains, where bromopropyl side groups are needed for further crosslinking or compatibilization reactions

    Final product types

    • Functionalized specialty polymers used in adhesives, sealants, and high-performance elastomer blends
    • Additive-modified engineering plastics with enhanced processing or physical properties for industrial and electronic applications
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    Certification & Compliance
    More Introduction

    2-(3-Bromopropoxy)tetrahydro-2H-pyran: A Practical Perspective from the Manufacturer’s Bench

    Getting to Know the Molecule

    2-(3-Bromopropoxy)tetrahydro-2H-pyran stands out both as a building block and as a tool for synthesis teams. Over years of direct production experience, every step of its manufacture reveals how details from raw material quality to purification quirks directly affect reliability in downstream chemistry. For us, its utility lies in more than a well-defined CAS or a melting point; it shows up where alkylating agents must combine tailored chain length with a cyclic ether scaffold.

    Chemists in pharma and specialty chemicals often seek out this molecule for constructing more complex frameworks. Its molecular structure, balancing hydrophobic and hydrophilic segments, offers solutions not easily replicated by simple bromoalkanes. With careful control of reaction conditions, its formation combines the bromopropanol chain and tetrahydropyran ring through selective etherification. Each batch reveals the challenge of keeping impurities like dibromides and unreacted alcohols below analytical detection, essential for high-yield coupling steps down the line.

    What We’ve Learned Production-Side

    Early in our scale-up efforts, small variations in temperature swings and the choice of acid catalyst could translate to off-color product or trace residual solvents after distillation. Our operators recognized quickly how tightly the synthesis process needed to be guarded — margins for error stay slim, whether running a 5-liter glass reactor or a 1,000-liter vessel. Direct handling offers a different understanding than reading a spec sheet; consistency never emerges by chance.

    Compared to classic bromoalkanes like 1-bromopropane or 3-bromopropanol, the presence of the tetrahydropyran ring stabilizes the molecule, making storage and transport much less tricky. We’ve monitored shelf stability both by NMR and through years of warehouse records and see less degradation and discoloration than with unprotected linear bromides. Shipments to customers rarely come back with complaints tied to off-odors or color shift, giving us a genuine appreciation for how the cyclic structure acts as a natural shield.

    Working knowledge tells us to set strict moisture controls. The cyclic ether resists hydrolysis, but repeated opening and closing of containers or shortcuts during drying create problems in subsequent use, especially for customers running moisture-sensitive palladium-catalyzed couplings. Teams using this intermediate call out its low water content and clarity — attributes not always obvious until they’re missing.

    Model and Specifications: Based in Experience, Not Templates

    We produce 2-(3-Bromopropoxy)tetrahydro-2H-pyran in a range of purities to suit different stages of research and manufacture, and the best uses stem from full clarity about real-world thresholds rather than chasing generic numbers. High purity (≥98% GC) supports pharmaceutical process development while research-use material may run slightly broader cuts to deliver economic value. In-house, the compound typically presents as a clear, nearly colorless to pale yellow liquid at ambient temperatures, matching what our customers see in their own fume hoods.

    The molecule’s distinct density and boiling point make it suitable for distillation-based purification, yet without the volatility problems of short-chain bromoalkanes. We identified early on that the intermediate volatility places practical boundaries on collection protocols and storage—run too hot, and losses spike, but stay too cold and you end up with sticky residues trapping impurities. Operators measure batch consistency not only by analytical readouts, but from practical handling — pouring, pumping, and filtering all matter for day-to-day reliability.

    One common misconception from outside labs is the belief any alkyl bromide in a homologous series will work the same. Our direct comparisons have shown differences in reactivity and selectivity during O-alkylation or nucleophilic substitution steps. The THP group, acting as a protected alcohol, offers steric bulk and electron-donating characteristics, tuning reaction rates and product profiles. We keep close track of byproduct formation, and our production notes routinely flag differences compared to neighbors like 4-bromobutanol or 3-bromopropyl acetate.

    Where It’s Used and Why It Matters

    Ask our technical team where 2-(3-Bromopropoxy)tetrahydro-2H-pyran goes, and a common reply is "wherever new carbon-oxygen bonds are needed without sacrificing selectivity or safety." The molecule serves as a starting point for introducing protected ether chains onto complex organics. For many pharma R&D groups, it fills a gap between easy-to-handle, short alkyl bromides and more reactive but troublesome alternatives. Its moderate chain length fits the needs of polyethylene glycol linkers and sidechains for API intermediates, as well as various agrochemical actives.

    Customers often report cleaner conversions and easier workup when using our product versus making in-house or substituting more basic bromoalkanes. The cyclic structure helps with solubility and viscosity in organic solvents, aiding downstream reactions. Since we handle requests for both milligram R&D batches and multi-ton commercial quantities, we see firsthand where supply consistency has downstream effects. Delays or failed reactions typically reach back to hidden variables like stabilizer content or contaminant build-up — problems much less common with this well-engineered intermediate.

    Specialty polymer producers highlight the value in using this molecule for introducing both flexibility and controlled polarity into their backbones. When grafting or endgroup modification is required, the predictable reactivity of the bromopropoxy group paired with the THP ether ensures smooth incorporation while minimizing side reactions that plague more basic alkyl halides. These production insights shift buyer preferences over time — what starts as a research curiosity becomes an industrial favorite once teams recognize improved yields and smoother purification.

    What Sets It Apart from Other Options

    We field many questions about why select 2-(3-Bromopropoxy)tetrahydro-2H-pyran over a simpler bromoalkane. Drawing from both customer feedback and process troubleshooting, the benefit emerges in its higher stability, easier crystallization of downstream intermediates, and lower rates of unwanted elimination in strong base. Compared to pure 3-bromopropanol, the THP protection blocks oxidation and polymerization, reducing downtime due to fouled reactors or clogged lines. We’ve had pilots report sharp drops in maintenance needs after switching, largely due to a decrease in gum and tar formation.

    Direct side-by-side testing in Suzuki or ether-forming reactions shows the protected alcohol substantially boosts selectivity, giving cleaner profiles on HPLC and mass spec. Our in-house analytical team developed specific impurity signatures unique to this molecule, allowing us to troubleshoot customer issues tied to unknown background peaks. No detail stays trivial when batches worth hundreds of thousands depend on consistency.

    What also earns repeat orders is handling safety. Free-flowing liquid in most climates, low odor, and relatively moderate hazard labels mean warehousing and shipping don’t demand specialty gear or high insurance premiums. Teams doing their own bulk storage appreciate the easier drum handling compared to more volatile, irritating bromoalkanes. The THP group reduces volatility, so ounces lost to headspace don’t add up; the payoff is straight product, not sticky residue, months after delivery.

    Manufacturing Insights: From Lab to Plant Floor

    Scaling up production for specialty organics like 2-(3-Bromopropoxy)tetrahydro-2H-pyran brings its own lessons. Unlike off-the-shelf bromoalkanes, this molecule tolerates neither shortcuts nor guesswork. Batch control begins with every incoming flask of raw materials: bromopropanol, tetrahydropyran, and acid catalyst each leave their own "fingerprints" on the final product. A minor impurity in the starting alcohol, for example, can lead to ghost peaks three steps downstream, only revealed after repeated chromatography. We put every employee onto shift teams with senior operators to pass down these practical lessons — details never show up on COAs but matter most for process reliability.

    Solvent selection, rate of base addition, and order of mixing all affect yield and side-product formation. We learned through costly missteps that running the etherification reaction at a single, steady temperature keeps the impurity profile tight and product color stable. Scaling pilots showed that small volumes of water can shift the outcome, so vacuum drying and Karl-Fischer measurements became non-negotiable at every stage. Our plant relies on continuous collaboration between R&D and QA; we bridge the gap with production notes, not just paperwork, and share real incident reports alongside best practices.

    Our technical crews spend time not only synthesizing and packing but also speaking directly with end users about their own plant experiences. Such conversations boost collective understanding and help us troubleshoot any unexpected challenges that come up, like colds ends after long-term storage or variable compounding behavior in large reactors. Every batch shipped gets tracked retrospectively in case later data show emerging trends — a level of transparency driven by our own interest in understanding molecular behavior over time.

    Meeting and Surpassing Customer Demands

    Demand often rises for higher-purity variants of 2-(3-Bromopropoxy)tetrahydro-2H-pyran as projects move from discovery to production. Our team draws on direct process history to address these unique requirements; the real work happens at points of practical difference, like ensuring low base-sensitive impurity content or packing only in metal-free containers for electronic-grade material. Whenever API developers push for nearly undetectable water levels, we double down on drying cycles and test for trace moisture by different techniques — not out of obligation, but because customer batch failures once taught us how even slight deviation can stall an inspection or fill.

    Researchers reaching out for analytical support find we provide not just a product, but a map of how it behaves under different storage and processing conditions. We log details from viscosity shifts before and after winter transport, to color changes after weekend downtime. This vigilant monitoring stands out to long-term partners, as does our willingness to substitute packing materials or shipping practices depending on their particular compliance needs. Working in the fine chemicals industry directly teaches that success means tracking both routine and rare scenarios, never assuming today's conditions will repeat without change.

    Many of the improvements in product performance come from operator suggestions. Increasing filtration surface area or tweaking the order in which washing solvents are applied makes for cleaner product, better yields, and time savings, both for our team and our customers down the line. Efforts large and small compound into trust, so much so that production managers or synthesis leads often consult our team for advice about tricky side reactions, contamination histories, or scale-up bottlenecks. Over time, this grows both expertise and a foundation for technical innovation.

    Continuous Learning from Real-World Applications

    The feedback loop between manufacturing and end use teaches us new lessons every month. Our molecule gets tested in so many environments — as part of a reaction in a pharma process plant, a coupling in a flavors lab, or a polymer modification experiment — that fresh questions often arise. When a client reports a surprise drop in coupling efficiency tied to some odd solvent effect or metal-catalyzed impurity, our lab can trace those issues directly back to the handling and chemistry observed at the source.

    Direct participation in root-cause analyses reveals new factors in performance, like how subtle shifts in pH during storage or slight overexposures to UV light can nudge degradation ceilings. Teams reporting unexpected foaming or resin gelling during large-scale runs have helped us modify our drying and packaging techniques. No problem stays theoretical for long; shared urgency to prevent downstream losses keeps us sharp, and each troubleshooting cycle improves the next batch.

    We approach future improvements by building on practical experience, not marketing promises. Production records, field reports, and analytical signatures all converge to highlight true product strengths and honest limitations. Collaboration goes both ways, as improvements in material purity or stability feed back into customer innovation, allowing end users to unlock new reaction pathways or meet tougher regulatory standards.

    Solutions Built on Shared Experience

    Material science advances keep raising the bar. To address stricter requirements, we've invested in analytical technology that helps us identify ultralow-level impurities no instrument could see just a decade ago. Understanding that our product will often be part of a larger system, we work to minimize hidden reactive contaminants at each point of manufacture — short alkyl bromides, unknown peroxides, or trace acid residues all get targeted routes for reduction.

    Every production campaign brings opportunities for process innovation. Handling 2-(3-Bromopropoxy)tetrahydro-2H-pyran in batch and continuous flow has highlighted the trade-offs in reactor design, heat management, and product isolation. By running side-by-side pilot trials and collecting user-driven feedback, we find new ways to cut batch times, boost yield, or trim solvent use, making for greener, more cost-effective processes. These on-the-ground insights shape the next generation of manufacturing protocols — less speculation, more evidence from repeated cycles.

    We believe the most useful solutions come not solely from in-house R&D or external consultants, but from the day-to-day knowledge that operators, QC analysts, and customer support engineers bring. That’s why process improvements flow from real engagement, whether during line audits or joint troubleshooting sessions. This direct visibility into challenges at every step of the chain leads to enhancements that stick, not just across our plant, but in our customers’ final products.

    Looking Ahead: The Value of Informed Manufacturing

    While every molecule might look like just another chemical on a catalog page, manufacturing 2-(3-Bromopropoxy)tetrahydro-2H-pyran proves how each step, each improvement, and every conversation shapes quality for the long run. We learned through our own process scale-ups, troubleshooting, and regular feedback what matters most: purity, stability, handling safety, and the ability to adapt. This product distinguishes itself not simply by analytical figures but by a track record of success across diverse applications, earned with real-world use and problem-solving.

    Our commitment comes from experience: every lot carries with it lessons from every drum filled, every customer call answered, and every successful scale-up. We innovate because demand calls for it, and we respond because years in the field have shown us how much value comes from a molecule that does what chemists actually need. By staying grounded in production realities and industry needs, we ensure 2-(3-Bromopropoxy)tetrahydro-2H-pyran stays a preferred choice for today’s challenges and tomorrow’s discoveries.