Products

Bromocyclopentane

    • Product Name: Bromocyclopentane
    • Alias: Cyclopentyl bromide
    • Einecs: 210-129-4
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    420401

    Cas Number 137-43-9
    Molecular Formula C5H9Br
    Molecular Weight 149.03 g/mol
    Iupac Name Bromocyclopentane
    Appearance Colorless liquid
    Boiling Point 132-134 °C
    Melting Point -71 °C
    Density 1.346 g/cm³ at 25 °C
    Refractive Index 1.4920 at 20 °C
    Flash Point 38 °C (closed cup)
    Solubility In Water Insoluble
    Odor Characteristic, sweet

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

    Packing & Storage
    Packing Amber glass bottle, 250 mL, tightly sealed with a screw cap; labeled with hazard warnings, product name, CAS number, and supplier details.
    Shipping Bromocyclopentane should be shipped in tightly sealed, appropriately labeled containers, conforming to hazardous materials regulations. Store and transport it upright, in a cool, well-ventilated area away from direct sunlight, heat, and incompatible substances. Ensure compliance with local, national, and international regulations regarding the handling and shipment of flammable and corrosive chemicals.
    Storage Bromocyclopentane should be stored in a tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Ensure the storage area is equipped for handling flammable and potentially harmful chemicals, with appropriate spill containment and fire suppression systems in place. Clearly label containers and restrict access to authorized personnel only.
    Application of Bromocyclopentane

    Applications of Bromocyclopentane in Industrial Manufacturing

    Bromocyclopentane serves as a highly specialized intermediate in advanced chemical synthesis, supporting the development and scale-up of downstream products across several tightly regulated industrial fields. We manufacture this raw material to meet strict global standards, ensuring consistent reactivity and reliable performance for each targeted application below.

    1. Pharmaceutical Intermediate Synthesis

    Our material is widely implemented as a building block in the synthesis of complex molecular structures for pharmaceutical actives where cyclopentyl moieties are introduced through substitution reactions. Chemists leverage its stable bromine leaving group to enable specific alkylation or cyclization steps within multistage API manufacturing, minimizing side products during critical bond formation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (FDA cGMP regulations)
    • European Pharmacopoeia, General Chapter 5.10 (Impurities in drug substances)
    • China Pharmacopoeia, Section 0401 (API synthesis controls)

    Typical usage ratio

    • 5–18% as a molar equivalent relative to core reactant, adjusted by route-specific stoichiometry, reaction scale, and targeted yield requirements in kilo- and ton-scale manufacturing

    Downstream process integration

    • Charged during intermediate coupling or nucleophilic substitution stage, entering after solvent charging and prior to temperature ramping
    • Reaction commonly proceeds in polar aprotic solvents with continuous analytical monitoring (GC/HPLC)

    Final product types

    • API intermediates for anticancer drugs
    • Cardiovascular therapeutic agent precursors
    • Central nervous system active molecule scaffolds

    2. Agrochemical Active Ingredients Manufacturing

    Bromocyclopentane functions as a core alkylating agent in downstream synthesis of select herbicide and insecticide actives, especially for introducing cyclopentyl residues into heterocyclic compounds. Downstream manufacturers value its predictable reactivity and low impurity profile for minimizing carryover to finished formulations and meeting strict residue requirements in food safety markets.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) requirements
    • ISO 9001:2015 Quality Management for agrochemical synthesis
    • EU REACH Regulation (EC) No 1907/2006 for raw material registration
    • US EPA Pesticide Chemical Regulations 40 CFR Part 158

    Typical usage ratio

    • 8–15% by mass fraction in active ingredient synthesis; ratio adjusted based on specific actives’ molecular design and desired conversion rates

    Downstream process integration

    • Added directly into closed reactor vessels after initial solvent charge, prior to catalyst addition, under temperature-controlled (typically 30–75°C) agitation

    Final product types

    • Herbicidal API intermediates (e.g., cyclopentylated triazines)
    • Synthetic pyrethroid precursors
    • Active ingredients for broad-spectrum insecticidal formulations

    3. Fine Chemical Synthesis for Fragrance Ingredients

    The chemical is integrated into the fragrance industry as a structural unit in the creation of musky and woody aroma compounds. Specialist producers use it to construct cyclopentyl-based keynotes via Grignard or Friedel-Crafts processes. The controlled introduction of a cyclopentyl group imparts desirable olfactory and volatility properties in downstream perfumery intermediates.

    Industry compliance standards

    • International Fragrance Association (IFRA) standards for material safety and use restrictions
    • ISO 9235:2013 (Aromatic Raw Materials—Definition)
    • REACH SVHC compliance for all precursors
    • IFRA Code of Practice for raw material traceability

    Typical usage ratio

    • 3–7% relative to reaction mass in ketone, aldehyde, or ester synthesis; ratio set based on olfactory purity targets and process selectivity

    Downstream process integration

    • Fed via metered addition into specialty reactors during early-stage Fragrance Intermediate Construction, in tandem with catalyst or after Grignard reagent formation

    Final product types

    • Ketonic musk fragrance ingredients
    • Woody cyclopentyl-derived aroma intermediates (e.g., cyclopentyl methyl ketone bases)
    • Compound perfume bases for fine fragrances

    4. Specialty Polymer Monomer Synthesis

    Our product is employed as a key halogenated feedstock for producing specialty monomers used in research-scale and commercial-grade polymers that require cyclopentyl ring incorporation for enhanced material properties such as flexibility and impact resistance. The halogen group enables controlled polymer chain initiation or bridging during ring-opening polymerization or via subsequent nucleophilic displacement methods.

    Industry compliance standards

    • ISO 9001:2015 (Polymer Production)
    • OECD Principles of Good Laboratory Practice for polymer R&D
    • REACH Monomer Registration Guidelines
    • ASTM D2569-07 (Polymer Raw Material Quality Control)

    Typical usage ratio

    • 2–10% molar input, depending on targeted copolymer composition and desired mechanical or thermal properties

    Downstream process integration

    • Dosed into high-purity reactors following initial pre-polymer precursor charging, frequently under inert gas atmosphere to prevent premature side reactions

    Final product types

    • Cyclopentyl-functionalized specialty copolymers
    • Modified engineering plastics with tailored flexibility
    • Elastomer precursors for advanced industrial applications

    5. Custom Synthesis in Agrochemical Contract Manufacturing

    Chemical contract manufacturing organizations (CMOs) utilize bromocyclopentane in custom production of novel agrochemical intermediates based on patented molecular frameworks. As a flexible alkyl source, it supports rapid route development cycles where proprietary substitution patterns are required to deliver client-specific regulatory dossiers and pilot batch data.

    Industry compliance standards

    • OECD Good Manufacturing Practices for pilot- and commercial-scale contract synthesis
    • FAO/WHO GMP for technical grade active substances
    • ISO 14001:2015 Environmental Management Systems for chemical plants
    • Japanese Agricultural Standards (JAS) for agro-intermediates

    Typical usage ratio

    • 6–22% by reaction yield, adjusted for molecular design, pilot batch size, and reaction conversion efficiency in multi-step synthetic routes

    Downstream process integration

    • Introduced post-catalyst activation during targeted alkylation, monitored for selectivity by in-process QA/QC as required by client specifications

    Final product types

    • Intellectual property-backed agrochemical intermediates
    • Regulatory submission intermediates (trial batches)
    • Custom active ingredient scaffolds for downstream formulation
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    Certification & Compliance
    More Introduction

    Bromocyclopentane: A Closer Look from the Manufacturer’s Perspective

    Introduction to Bromocyclopentane

    In the world of organic intermediates, bromocyclopentane stands out for its ability to deliver reliability in multiple synthetic routes. Our production teams handle this molecule daily, and its behavior in reactions has specific characteristics that make a difference when compared to many standard alkyl bromides. Although bromocyclopentane starts with a simple cyclopentane core, the addition of a bromine atom significantly alters its chemical profile. Practically, that one change gives chemists more tools than they might expect for what otherwise looks like a straightforward five-membered ring.

    Product Model and Batch Consistency

    We synthesize bromocyclopentane under controlled environments, always targeting a purity grade above 99%. Our batch processes, set up in glass-lined reactors, make use of high-purity cyclopentane and a carefully monitored bromination step. Models and designations in our company arise not from external standards, but from the eccentricities of real-world chemistry—specific batch numbers reflect not just traceability but variations in reaction time, temperature control, and feedstock consistency. This level of detail matters, as the downstream reactivity of bromocyclopentane in Grignard reactions depends on trace impurities—something often overlooked until an unexpected result ties up valuable production time.

    Specifications and Physical Properties Based on Direct Handling

    Day in and day out, our staff work with the colorless liquid in both small-scale and industrial setups. The boiling point of 118-120°C signals that you’ll rarely face difficulties handling vapor management in regular fume hoods or jacketed reactors. The compound’s low viscosity makes transfer and measurement straightforward, and the sharp, sweet odor alerts us quickly to leaks beyond expected industrial smells. Experience tells us—unless lines and valves are regularly flushed, you’ll find residue, because during regular bottling operations, even minimal splashes can build up and cause handling headaches down the line.

    Moisture content plays a role in stability. We continuously monitor water levels below 0.05% in final packaging, knowing even small moisture upticks introduce the risk of undesirable side-reactions, especially during lithium-halogen exchange reactions or when working with phenylmagnesium bromide synthesis. Regular testing in our own labs, not just outside QC contractors, guards against these kinds of surprises.

    Usage in Synthesis from a Manufacturer’s View

    Organic synthesis often benefits from molecules that provide both reactivity and stability in one package. Bromocyclopentane offers both, meeting the needs of research chemists and large production teams. Its reliability as an alkylating agent means it enters a wide array of reactions—alkylating amines, activating Grignard pathways, and even forming building blocks in pharmaceutical intermediate routes. Employees in our batching department will confirm: shipments bound for pharmaceutical clients almost always require the lowest levels of unreacted cyclopentane or overbrominated byproducts, so our teams constantly optimize column purifications and quick chill protocols to clear these impurities.

    We’ve shipped bromocyclopentane to contract manufacturers building new heterocyclic units for drug research—it forms a foundation in the construction of more complex molecules, such as spirocyclic compounds and new candidate antivirals. In pilot scale manufacturing, colleagues using bromocyclopentane report consistent yields and a lower incidence of troublesome side reactions.

    It’s common for newcomers to underestimate the variations in outcomes with different grades. Our technical support fields calls from labs that had relied on brokered or lower purity lots—sometimes they run into chain scission or unwanted oligomerization, problems not seen with higher grade material. Those real-world issues taught us to provide only material where we’ve directly overseen every stage, from distillation to drying to inert atmosphere shipping. This hands-on approach matters, as the molecule’s reactivity magnifies impurities.

    Comparison with Other Alkyl Bromides and Related Compounds

    If you line up bromocyclopentane against straight chain alkyl bromides—take n-butyl bromide, for instance—you’ll soon spot clear differences in lab and plant settings. Cyclopentane’s ring structure grants a predictable pathway for nucleophilic substitution: the SN2 pathway here sees less steric hindrance than bulkier secondary bromides but makes for better selectivity than some open-chain types. Our chemists often comment on the reduced formation of elimination side products, a stark contrast to what you find with more hindered or branched alkyl bromides.

    Bromocyclopentane also sets itself apart from aromatic bromides, such as bromobenzene, because it combines hydrocarbon flexibility with halogen reactivity, making it suited for ring-opening reactions and cycloaddition experiments. Several years ago, our R&D team collaborated with an academic group to examine cross-coupling efficiencies with palladium catalysts. Their findings—and our own follow-up process validations—showed higher yields in Suzuki and Heck reactions compared with some other alkyl and aryl bromides, due primarily to minimal byproduct formation and easier purification.

    Other cycloalkyl bromides, like bromocyclohexane, share some features but diverge in details that affect cost and performance. Our process engineers have tracked energy consumption closely: bromocyclopentane distills at a lower temperature, allowing for more economical reactor cycles, which has a direct impact on the bottom line of high-volume production. The smaller ring also enables access to unique carbocation intermediates under certain conditions—traits valued in specialty organic syntheses.

    Handling and Storage: Lessons from Day-to-Day Operations

    Our warehouse team stores bromocyclopentane in airtight, light-blocking steel drums with lined interiors. Based on years of storage trials, open plastic or unlined metal containers eventually lead to product degradation or increased impurity profiles—especially when temperature swings occur during seasonal transitions. For bulk users, this translates into an investment in compatible storage solutions, because in-transit degradation remains one of the most common sources of complaints. We deal with real metrics every year; trace water or exposure to ultraviolet light will start degrading the reagent, altering halide concentration and ruining careful stoichiometry.

    From the manufacturing floor’s perspective, safety always figures strongly in handling bromocyclopentane. The chemical’s volatility isn’t extreme by industrial standards, but leaks and spills require prompt action. Our crews use double-sealed transfer pumps and insist on splash shields and chemical gloves rated for brominated hydrocarbons—simple habits that prevent injuries from skin contact or inhalation. Plant managers ensure routine training covers the distinctive sharp aroma, since leaks, even at low parts per million, signal a need for immediate containment. We value hard-won lessons—spills in secondary containment units get priority cleanup, and routine calibration of vapor detection sensors further reduces risks.

    Reactors, lines, and storage vessels see routine cleaning cycles. We track cleaning solvent residues to prevent cross-contamination with other halogenated stock on site. There is a fine line between operational efficiency and residual contamination; leaving traces of other organohalides creates unpredictable results in future runs—a risk no serious producer accepts.

    Quality Assurance: Beyond the Standard Batch Release

    Many chemical firms rely on outsourced analysis, but our experience demonstrates the value of in-house testing. For every lot of bromocyclopentane, our lab team runs GC-MS, NMR, and Karl Fischer titration before authorizing release. This internal control process reveals minor byproducts most contract labs overlook and keeps our speculative error margin far below industry averages. Twice, over the last decade, we intercepted shipments destined for major pharmaceutical clients after in-house tests identified nonvolatile residue above our specifications—catching these issues before customers ever saw impact.

    Our senior chemists actively monitor trends in side reactions based on small differences in trace metals or unreacted bromine. In several cases, tweaking wash procedures and scheduling shorter reactor dwell times eliminated persistent ghost peaks in downstream chromatograms—directly improving both customer satisfaction and our own process yields. We document every adjustment and report findings internally, so improvements persist from batch to batch and operator to operator.

    Compliance with regulatory requirements forms part of our routine, but repeated experience shows that documentation alone never replaces actual quality. Each drum receives tamper-evident seals, with log numbers linking directly to analytical reports. We remain alert to evolving industry standards, and our technical files record adjustments made as clients’ needs change—especially as new pharmaceutical or agrochemical processes bring more exacting purity demands.

    Supporting Research and Process Development

    Bromocyclopentane occupies a unique space in process R&D setups. Synthetic routes employing this molecule facilitate rapid exploration of cyclopentane-modified motifs, granting access to structures found in several active pharmaceutical ingredients. Research groups contact us not for generic products, but seeking insight on downstream reactivity and application nuances. For example, cyclopentyl groups show up in pain management agents and certain agricultural fungicides. The flexibility bromocyclopentane brings to the table—allowing installation at different points in a molecule—lets synthetic chemists chase new analogs without major overhaul of established reaction conditions.

    Over the years, our technical advisors have helped troubleshoot common bottlenecks: one typical issue involves unexpectedly sluggish alkylations, usually traced to old or humidity-compromised stock. Quick resolution stems from practical experience with the chemical, sharing best practices for storage and prompt application after opening. Partners in scale-up projects often adapt their own worklists after observing our protocols, improving outcome predictability and minimizing trial-and-error cycles.

    Many researchers attempt direct bromination of cyclopentane on a small scale, but results often disappoint. In contrast, dedicated bromocyclopentane production using continuous flow setups and in-situ purification produces material free from the color and odor changes signaling incomplete reactions or overbromination. Our clients’ R&D chemists, aware of the purity challenges, recognize the value in sourcing from teams who control both reagent quality and logistical reliability.

    Rooted Differences from Brokered and Generic Materials

    Bromocyclopentane production, done with attention to every step in the line, produces a material that behaves more reliably across downstream processes than off-the-shelf or reseller inventory. Over many years, customers reported inconsistencies when they tried to switch to generic suppliers for cost savings. Reactions failed to scale efficiently, unwanted oligomers crept into NMR spectra, and final products lost yield or required additional purification. Feedback like this informs our process improvements—the value lies in doing the work directly and knowing the chemistry, not just moving drums through warehouses.

    Every solvent wash and every trace analysis tells a story—reactors must start clean, lines must run dry, and minimal oxygen ingress ensures predictability. Our production teams demand traceability all the way down to lot records on bromine sources, knowing fluctuations can change color, odor, or reactivity. Experience demonstrated repeatedly that what seems a minor variance in one batch influences outcomes for entire downstream campaigns, especially during late-stage scale up.

    Potential Hurdles and Solutions in Manufacturing and Application

    Consistently producing high-purity bromocyclopentane means keeping a sharp eye on process drift. Small temperature fluctuations in reactor cycles shift product distribution toward heavier byproducts, while subtle changes in bromine reagent quality create persistent odor or color. Our on-site process engineers monitor temperature, pressure, and bromine flow, using inline sensors and redundant checks—a necessary investment against otherwise silent product failures.

    Safety concerns always accompany volume manufacturing of alkyl halides. Several years ago, an unplanned valve release caused a small leak in one filling area. Actionable lessons came out of that day—new spill containment, tighter maintenance schedules, and a switch to more robust PPE. We learned to never undervalue training or backup equipment, and every annual review leads to further risk reduction.

    In end-use, one clear challenge for customers remains: inadvertent mixing with incompatible solvents or exposure to nucleophiles outside tightly controlled parameters leads to decomposition, introduced off-odors, or viscosity jumps. Our technical team recommends process audits—walkthroughs of plant lines and bottle handling protocols—to ensure storage and use keep up with process needs. Active conversations between supplier and end-user reduce waste and can reveal savings others miss.

    Documented experience also points to benefits in direct shipment scheduling. Contract manufacturers avoiding long storage times, especially through summer months, see reduced impurity accumulation. We prioritize freshly manufactured lots for critical applications and work closely with clients to communicate realistic shelf life and handling expectations.

    Environmental and Ethical Considerations

    Through decades of chemical production, environmental stewardship shaped our approach to bromocyclopentane manufacture. We capture bromine off-gas with advanced scrubbing systems and restrict waste streams through engineered containment. All production cycles emphasize solvent recycling, maximizing use of recovered diluents and minimizing landfill waste. Operators carry out routine environmental inspections—checking sump pumps, storage tank seals, and secondary containment units, ensuring compliance does not cut corners but actually reduces risk.

    The Responsible Care initiatives our industry promotes translate to concrete steps—hazardous waste tracking, internal audit teams, and continuous worker training keep both employees and the environment protected. Long-term investments in process optimization resulted in lower energy use per kilogram manufactured and fewer unscheduled flares or emissions incidents.

    Working closely with regulatory authorities and neighborhood advisory councils, we strove to keep open communication channels. Concerns about brominated waste, especially with past industry accidents making news, prompted us to become proactive—reducing incident response times and adapting best practices from leaders in chemical process safety worldwide.

    A Manufacturer’s View: Why Chemistry and Process Depth Matter

    Bromocyclopentane might look simple on a spec sheet, but real-world production experiences reveal the depth hidden behind each clear bottle. Chemists with hands in the process see, measure, and adapt to the nuances—the difference between reliable building block and unpredictable reagent comes down to the range of best practices built over years of repetition. Our process teams, lab staff, and logistics partners all share a stake in delivering a product that acts as more than another chemical—it becomes a foundation for better, safer, more effective chemical synthesis at every level of industry.

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