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1,5-Dibromopentane

    • Product Name 1,5-Dibromopentane
    • Alias Pentamethylene dibromide
    • Einecs 216-047-6
    • 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

    288499

    Iupac Name 1,5-Dibromopentane
    Molecular Formula C5H10Br2
    Molar Mass 229.94 g/mol
    Cas Number 111-24-0
    Appearance Colorless to pale yellow liquid
    Density 1.602 g/cm³
    Boiling Point 227 °C
    Melting Point -13 °C
    Solubility In Water Insoluble
    Refractive Index 1.499
    Flash Point 120 °C
    Vapor Pressure 0.041 mmHg at 25 °C

    As an accredited 1,5-Dibromopentane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500 mL amber glass bottle with a secure screw cap, labeled "1,5-Dibromopentane" and appropriate hazard warnings.
    Shipping 1,5-Dibromopentane is shipped in tightly sealed containers, typically made of glass or high-density polyethylene, to prevent leaks and contamination. It should be labeled as a hazardous material and stored in cool, dry, and well-ventilated conditions away from incompatible substances. Shipment must comply with local, national, and international regulations.
    Storage 1,5-Dibromopentane should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Store separately from strong oxidizing agents and incompatible materials. Ensure the area is equipped with spill containment measures and appropriate safety signage. Access should be restricted to trained personnel only.
    Application of 1,5-Dibromopentane

    Applications of 1,5-Dibromopentane in Industrial Manufacturing

    Our manufacturing expertise enables precise supply of 1,5-dibromopentane to verified downstream sectors where it serves as a key intermediate for advanced chemical synthesis. Below, we outline major industrial application scenarios, providing in-depth details on compliance, standard industry process integration, formulation specifics, and targeted end products.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Pharmaceutical manufacturers rely on 1,5-dibromopentane as an alkylating agent and bridging compound in the multi-step synthesis of complex active pharmaceutical ingredients, particularly for certain antiviral agents, antihistamines, and tailor-made specialty APIs. The material's two terminal bromine atoms offer high reactivity in nucleophilic substitution, making it indispensable for constructing nitrogen- or oxygen-bridged heterocycles. Consistent purity, traceability, and documentation are critical throughout the value chain to support downstream validation in clinical-grade product lines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • EU GMP – EudraLex Volume 4, Annex 8 for APIs
    • Applicable individual national pharmacopoeia (USP, EP, JP) monographs for intermediates, if designated

    Typical usage ratio

    • Dosage in multi-gram to multi-kilogram scale, typically 1.1–1.5 molar equivalents per reaction step, adjusted based on process yield and downstream impurity profiling

    Downstream process integration

    • Charged as a reagent in the alkylation step of pharmaceutical intermediate production, often dissolved in anhydrous polar aprotic solvents, followed by phase separation and further purification prior to conversion into the API structure

    Final product types

    • Antiviral active pharmaceutical ingredients (e.g., nucleoside analogues)
    • Antihistamine intermediates
    • Specialty amine-based pharmaceutical compounds

    2. Agrochemical Synthesis for Pesticide and Herbicide Intermediates

    Formulators in the agrochemical sector employ 1,5-dibromopentane as a chain extender and alkyl bridging unit in the synthesis of key intermediates for selective herbicides and insecticides. The compound’s bromo-functionality enables selective nucleophilic substitution reactions, providing unique building blocks for molecules with improved environmental degradation profiles. All inputs must be assessed and documented for regulatory compliance regarding environmental and toxicological impact, especially for global export of crop protection agents.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO and WHO)
    • OECD Guidelines for the Testing of Chemicals
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) for EU distribution
    • US EPA 40 CFR Part 174 and 180 for pesticide chemicals

    Typical usage ratio

    • 0.8–1.3 molar equivalents per synthetic step, modulated depending on targeted molecular scaffold and minimisation of byproduct levels, reaction scale ranges from pilot (multi-kg) to full tonnage for bulk actives

    Downstream process integration

    • Integrated at the nucleophilic substitution or SN2 alkylation stage in batch or continuous agrochemical intermediate production lines, followed by chromatographic purification and formulation into technical concentrates

    Final product types

    • Herbicide intermediates used in selective grass weed control
    • Organophosphorus and carbamate pesticide core synthesis
    • Precursor molecules for fungicides with tailored chain lengths

    3. Polymer Modification and Specialty Elastomer Cross-Linking

    Producers of specialty polymers and engineered elastomers utilize 1,5-dibromopentane as a functional cross-linking agent introduced during the compounding of advanced materials such as high-performance rubber seals, cable insulation, and automotive gaskets. The difunctional bromine groups enable bridging reactions which increase molecular weight and introduce flexible aliphatic linkages without excessive cure temperatures, supporting tailored mechanical and aging properties of robust elastomeric compounds.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for polymer production
    • UL 94 and IEC 60695 flame resistance for automotive and electronics applications
    • RoHS Directive 2011/65/EU (where applicable for downstream products)
    • OEKO-TEX® Standard 100 for textiles/consumer-facing elastomers

    Typical usage ratio

    • Typically 1.5–4.0 parts per hundred rubber (phr) in the formulation; actual ratio determined by targeted cross-link density, polymer type, and required thermal/mechanical specifications

    Downstream process integration

    • Added during mixing of base polymer and compounding ingredients prior to vulcanization; reacts during the curing stage to connect polymer chains in the extruder or compression mold process

    Final product types

    • Automotive O-rings and gaskets
    • High-voltage cable sheathing and insulation
    • Specialty hoses and vibration damping mounts

    4. Fine Chemical and Specialty Surfactant Synthesis

    Producers of surfactants and fine specialty chemicals incorporate 1,5-dibromopentane as an intermediate for the synthesis of gemini surfactants, where it links two hydrophilic head groups via the pentane chain, imparting distinct surface-active properties valued in oilfield chemicals, personal care emulsifiers, and advanced detergents. The synthesis route requires controlled nucleophilic substitution, and impurity levels must remain within limits to ensure surfactant performance and compliance for human/environmental safety.

    Industry compliance standards

    • OECD Guidelines for Acute Toxicity, Biodegradability, and Ecotoxicity testing
    • EU Regulation (EC) No 648/2004 on detergents
    • ISO 9001:2015 for chemical process management
    • US EPA Safer Choice Standard for surfactants in consumer products

    Typical usage ratio

    • Introduced at 0.9–1.2 molar ratio to the amine precursor in gemini surfactant synthesis; batch size varies with formulation, scaled from pilot to several metric tons annually depending on final surfactant demand

    Downstream process integration

    • Fed into the central linking step, where dibromopentane reacts with two moles of amine head group under controlled temperature, followed by neutralization, purification, and blending with other surfactant additives

    Final product types

    • Gemini-type surfactants for enhanced oil recovery fluids
    • Personal care emulsifiers for shampoos and conditioners
    • Formulated detergent blends for industrial and institutional cleaning

    5. Synthesis of Functionalized Organic Building Blocks for Dye and Pigment Manufacture

    Producers of specialty dyes and pigments manufacture various colorants and UV-stable solid solutions using pentamethylene-based linkers. 1,5-dibromopentane acts as a bridging molecule, allowing rapid substitution with chromophoric amines or phenols, thereby generating key dye intermediates for use in fiber, plastic, and ink formulations. The linker's structure imparts improved solubility and light fastness in the final pigment, with careful monitoring of reaction parameters to ensure batch-to-batch color consistency demanded by the industry.

    Industry compliance standards

    • REACH registration (EC/1907/2006) for imported and manufactured chemicals in the EU
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Product Stewardship
    • ISO 787 general methods for testing pigments and extenders
    • ISO 9001:2015 for manufacturing processes

    Typical usage ratio

    • Used at 1.0–1.4 molar ratios per functional group in the chromophore; scale up ranges from laboratory development (gram scale) to commercial synthesis (multi-ton) for large-volume dyes

    Downstream process integration

    • Charged into coupling reactors for the stepwise assembly of dye molecules, typically followed by isolation, purification, and downstream formulation into pastes, powders, or dispersions

    Final product types

    • Solvent-soluble dyes for plastics and fibers
    • UV-resistant pigments for automotive and textile coatings
    • Colorants for inkjet and industrial printing inks
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    Certification & Compliance
    More Introduction

    1,5-Dibromopentane: Practical Experience from the Manufacturer

    Introduction to 1,5-Dibromopentane

    Working as a chemical manufacturer, we encounter a diverse landscape of materials and processes. Among the multihalogenated alkanes that cross our production floor, 1,5-Dibromopentane (CAS 111-24-0) has a clear practical role in the modern chemical industry. This molecule, also called pentamethylene dibromide, offers more than just its two bromine atoms at each end of a five-carbon chain—it forms the backbone for specialty synthesis in pharmaceuticals, agrochemicals, and beyond. Our daily operations give us a firsthand look at how reliability and purity in such a building block can shape entire outcome chains.

    Why Pay Attention to Structure and Purity?

    Success in downstream reactions depends on key details, especially with linear dibromides like 1,5-Dibromopentane. We produce batches with controlled impurity profiles and maintain consistency across lots. In practice, this means focusing on parameters such as GC purity (often >99%), dryness, color (clear to faint yellow, with strict APHA standards), and absence of common side-products, especially 1-bromopentane or trace halogenated byproducts. Care has to be taken at every step, from raw bromine sourcing and pentane backbone control to purification and stabilized packaging. It’s easy to overlook how strongly the purity of a single intermediate can impact yields in nucleophilic substitution, macrocycle formation, or polymer chemistry, but in our facility, operators see it every day.

    Performance Compared to Other Dibromides

    1,5-Dibromopentane occupies a unique role distinct from shorter or longer dibromoalkanes. Bridging the gap between flexible yet too-short chains like 1,3-dibromopropane and more unwieldy ones like 1,6-dibromohexane, 1,5-dibromopentane introduces the right span for many five-membered and seven-membered ring syntheses. This length provides ideal spacing for producing macrocyclic compounds or acting as a linker in the assembly of complex molecules. Lab chemists mention the increased reactivity paired with a manageable boiling point, and process engineers notice how easily it integrates into closed production loops with standard halide handling equipment.

    Core Applications: Beyond Standard Reactions

    Over the years, we’ve seen 1,5-Dibromopentane used in a spectrum of fields. In alkylation chemistry, it forms a class of ditopic linkers, where spacing and reactivity allows attachment of different functional groups. Customers in the pharmaceutical industry rely on it for constructing nitrogen-containing heterocycles, piperidine rings, or specialty intermediates for APIs under patent. Beyond pharma, specialty polymer manufacturers value it as a chain-modifying unit, sometimes in the production of anti-static polymers or ion-conducting materials.

    Agrochemical developers use its dual bromine endpoints for bridging or capping in pesticide intermediates, often in scales ranging from 1 kg pilot lots to multi-ton reactors. In these environments, reliably handling a halogenated intermediate without major decomposition or off-gassing is crucial, both for safety and to limit contamination. Our experience shows that customers who tried analogous compounds—such as chlorinated or iodinated versions—often report troublesome by-product profiles or less manageable reactivity. For certain end uses, this difference becomes crucial, especially where downstream halogen displacement influences overall cost or yield.

    What Sets 1,5-Dibromopentane Apart in the Plant

    Chemists often focus on the molecular level, but plant operators see the differences play out in real time. 1,5-Dibromopentane is clear and nearly odorless under right conditions, though its halogen content demands proper care. During handling, it shows less volatility than the lighter homologues, reducing fugitive loss risks and making it more suitable for closed-transfer systems. Longer chain dibromides, on the other hand, introduce unwanted viscosity and slower reactivity. The five-carbon spacing hits a productive sweet spot: fluidity, reactivity, and easier containment.

    On storage, the product keeps stable under dry, inert gas. Operators report synergy with standard lined steel or glass containers. Reactive offshoots such as 1,4-dibromobutane sometimes have a tendency to build problematic residues in valves and lines; we haven’t run into such issues after years producing and moving 1,5-Dibromopentane—provided storage protocols are followed.

    Specification Review and Real-World Handling

    We target high GC purity in our 1,5-Dibromopentane—usually not less than 99%. This directly reflects in downstream conversion rates and helps those running multi-step syntheses avoid unnecessary purification stages. Trace moisture management cannot be neglected: even 100 ppm water content may cause phase issues in Grignard or sodamide reactions, leading to unexpected stoppages or color changes. Many commercial samples struggle to maintain this, especially if distribution or handling involves repeated tank opening. By controlling the production and packaging all the way to delivery at user’s premises, we avoid common pitfalls—off-smells, color drift, or polymerization in storage.

    For advanced uses, we sometimes produce material with tighter color and residue specs, demanded by those preparing chemical sensors or specialty monomers. Realistically, actual requirements vary: electronics industry clients seek dust-free, ultra-pure grades, while agricultural users often prioritize ease of pumping and minimal shelf-loss. Having scaled up production from kilogram to multi-ton batches, we invest in process robustness: continuous monitoring against hydrogen bromide evolution, careful in-line stripping for volatiles, and scheduled tank inspections all serve to keep final product dependable.

    Comparison with Alternative Products in Practical Terms

    Chlorinated or iodinated analogues might look similar on a blackboard, but operations reveal their drawbacks. Iodopentanes, for example, rarely justify their high reactivity except in niche syntheses, often bringing higher costs and difficult storage. Their rapid decomposition and tendency to color or haze after months of storage make them unpredictable. Chlorinated versions fall short in some nucleophilic substitutions, often leaving more unconverted material or sluggishly reacting under standard conditions. In actual plant runs, 1,5-Dibromopentane strikes a balance: strong halogen leaving groups that don’t degrade equipment or tax solvent recovery systems.

    Compared with shorter-chain relatves, the five-carbon backbone lowers the risk of side-alkylation and delivers the right extension for macrocyclization. Where a three-carbon bridge creates ring strain, or a six-carbon stretches beyond catalyst tolerance, five carbons often win favor. Many customers find that their yields lift simply by swapping in our dibromopentane for alternatives.

    Insights from Daily Production and QA

    Anyone running a chemical plant knows the difference between theoretical quality and genuine batch reliability. By manufacturing 1,5-Dibromopentane entirely in-house, we run every lot through sampling, in-line GC/FID analysis, and strict visual checks. By catching color drift, trace decomposition, or inconsistent moisture immediately, we head off downstream synthesis problems before they start.

    Waste minimization plays another role in our thinking. Dibromides tend to resist auto-oxidation, but each step demands vigilance against stray heat or light. One reason long-term clients stay with our product: tanks and drums last without significant residue, so transfer lines need less downtime for cleaning. Tighter spec material means users can push yields closer to full conversion without additional distillation. This has saved one polymer client two full purification steps over the course of a year—a real cost reduction.

    Safety and Rural Distribution Considerations

    Handling brominated organics calls for a steady hand and respect for hazards, especially in larger volume delivery. Plant personnel receive regular training on spill response, ventilation, and exposure avoidance, especially during loading. Our transfer systems use closed-loop pumps with scrubber backup, which keeps workplace air clean and minimizes contact risk.

    Rural or remote users in agriculture often need drums or tanks resistant to pressure and UV—so we ship in UN-compliance packaging, with full tracking. This avoids cross-contamination and secures the supply chain. Reporting from the field, clients mention fewer losses or upsets on arrival, because our quality carries through from first batch sample to final delivered drum. As demand increases seasonally, we ramp up in-house testing and on-site supervision.

    Feedback Directly from End-Users

    Long-standing customers in the pharmaceutical industry comment that switching to 1,5-Dibromopentane from older, less standardized sources immediately reduced variability in complex reactions. In macrocycle synthesis, every unwanted by-product means lost time. High-purity material increases their reaction success rate, confirmed both by HPLC and by actual final product yields. In polymer production, especially where chain-end fidelity matters, high-grade material prevents chain termination and boosts average molecular weight as measured by GPC.

    We also see analytical chemists calling for tighter impurity profiles for specialty building blocks. By investing in new column technology and vapor-phase drying, we match these needs while keeping scale-up practical. Regular communication with end-users informs our quality initiatives, so the product not only meets but improves reaction outcomes.

    Investing in Process Improvements Year After Year

    Production technology doesn’t stand still. In our facility, we regularly re-examine the core synthetic route to reduce by-product formation. Modernized reactors—double-sealed, jacketed, and equipped for vacuum stripping—allow more precise control over exotherm and reaction time, crucial for repeatability. We have also moved away from legacy storage methods, where atmospheric air led to hydrolytic breakdown. Now, nitrogen-purged containers keep product stable and colorless, even in high-humidity areas.

    On the analytical side, the introduction of real-time GC/FID and Karl Fischer titration enables rapid trouble-shooting. This means clients get product that meets the spec not just at the moment of filling, but throughout the container’s usable life.

    Sustainability, Compliance, and Supply Responsibility

    Beyond chemistry, the reality of chemical production in the twenty-first century involves environmental responsibility and regulatory transparency. Our manufacturing site maintains strict emissions controls, with abatement systems handling brominated off-gas before venting. Regular audits and transparent environmental impact reporting enable us to comply with local and international regulations, including REACH and TSCA listings for 1,5-Dibromopentane.

    We recycle bromine wherever possible, both from side streams and process water, closing the loop and reducing raw input costs. This matters not just for cost-saving, but as proof of stewardship. Taking pride in minimizing waste and ensuring safe operation becomes part of our everyday life, discussed as frequently as reaction yield or throughput.

    Common Questions Raised by Application Chemists

    Over the years, chemists from R&D groups approach us to discuss reactivity profiles or substitution rates. 1,5-Dibromopentane draws interest because its C-Br bonds activate easily under mild base, yet resist unwanted hydrolysis in storage. Many who use higher-reactivity iodides struggle to match this balance. Another common question focuses on regulatory purity for regulated markets—the reproducible sampling and thorough documentation at our plant supports advanced regulatory filings for companies entering advanced or medical markets.

    Others want to know about the impact of micro-contaminants. Here, practical experience counts: trace brominated side products can spell trouble in sensitive electronics, so we support users by pushing detection limits further and providing data from third-party labs.

    Anticipating Future Developments

    The trend toward greener chemistry and high-value specialty materials is only accelerating. Manufacturers who invest in process automation, improved waste neutralization, and sustainable packaging win customer trust. In the case of 1,5-Dibromopentane, legacy manual production methods simply can’t match precision or throughput requirements of modern synthesis. Automation in our plant closes the gap: less chance of contamination, faster turnaround, and a better fit with high-throughput R&D environments.

    We’re preparing for upcoming demands, adapting production to serve industries needing even tighter impurity limits or custom batch sizes. This keeps us relevant as a true manufacturing partner, not just a supplier.

    Conclusion: The Manufacturer’s Perspective on Reliable Chemical Supply

    Building reliability into the supply chain for advanced chemicals doesn’t come from paperwork or catalog promises—real consistency grows from hands-on experience, steady investment, and close attention to both plant operations and customer feedback. 1,5-Dibromopentane serves as a case study in the value of manufacturing control, purity focus, and responsiveness to application needs. Day in and day out, our team follows these principles not just for compliance or client reassurance, but because repeated success in each batch pays off in every downstream process run by our partners.