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Bicyclo[2.2.1]Heptane, 2-Bromo- (9CI)

    • Product Name Bicyclo[2.2.1]Heptane, 2-Bromo- (9CI)
    • Alias 2-Bromonorbornane
    • Einecs 208-912-0
    • 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

    294519

    Chemicalname Bicyclo[2.2.1]Heptane, 2-Bromo-
    Casnumber 3322-93-8
    Molecularformula C7H11Br
    Molecularweight 175.07
    Iupacname 2-Bromobicyclo[2.2.1]heptane
    Smiles C1CC2CCC1C2Br
    Inchi InChI=1S/C7H11Br/c8-7-4-5-1-2-6(7)3-5/h5-7H,1-4H2
    Appearance Colorless liquid
    Boilingpoint 156-158 °C
    Density 1.353 g/cm3

    As an accredited Bicyclo[2.2.1]Heptane, 2-Bromo- (9CI) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of Bicyclo[2.2.1]Heptane, 2-Bromo- (9CI)

    Applications of Bicyclo[2.2.1]Heptane, 2-Bromo- (9CI) in Industrial Manufacturing

    Bicyclo[2.2.1]Heptane, 2-Bromo- (9CI) serves as a high-value intermediate across chemical synthesis platforms, particularly in high-precision organic manufacturing routes. We supply it to multiple downstream sectors where its reactivity and stability in exacting conditions benefit proprietary product lines and formulations.

    1. Pharmaceutical Intermediates for Chiral APIs

    Pharma-grade users apply this compound for the synthesis of chiral intermediates in the route toward complex active pharmaceutical ingredients, especially for custom small molecule drugs. Its norbornane skeleton supports specific stereochemical outcomes in Diels-Alder related transformations and subsequent functional group modifications under GMP-controlled conditions, contributing to final compound purity and regulatory conformity demanded by high-tier API manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (for API manufacturing)
    • US FDA 21 CFR Part 211
    • Ph. Eur., USP, JP for finished APIs

    Typical usage ratio

    • 0.5% - 3.0% of intermediate batch weight; adjusted by desired chiral yield and substrate reactivity

    Downstream process integration

    • Added post-initial cyclization or halogenation, prior to resolution or selective reduction steps, often as first-stage reactant in route-specific synthesis of norbornyl scaffolds

    Final product types

    • Chiral API intermediates for anti-infectives
    • Advanced building blocks for CNS drugs
    • Precursor molecules for custom analgesics
    • Chemical tools for lead optimization in drug research

    2. Agrochemical Synthesis for Specialty Pesticides

    In agrochemical plants, the compound functions as a key building block for targeted pesticide and insecticide synthesis. It provides a rigid bicyclic structure, necessary for the development of actives that bind selectively to insect neural targets. Our technical grade product integrates at early alkylation and substitution steps, ensuring resistance against hydrolysis and photolysis—a critical factor for environmental and field use registration globally.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006
    • EPA FIFRA requirements for active ingredient suppliers
    • ISO 9001:2015-certified QC systems

    Typical usage ratio

    • 1.0% - 10.0% in synthesis batch weight; ratio depends on the number of downstream functionalizations required

    Downstream process integration

    • Introduced after initial formation of norbornane skeleton, before specific bromination or nucleophilic substitutions for attaching side chains

    Final product types

    • Active ingredients for pyrethroid-type insecticides
    • Precursor for nematicide synthesis
    • Hydrophobic backbone for controlled-release herbicides
    • Specialty acaricides for high-value crops

    3. Polymer Additive Manufacturing

    This compound is utilized by advanced materials manufacturers to introduce rigidity and chemical resistance into specialty polymer matrices. Technical teams add it during initial monomer blending or in modification reactions to adjust polymer glass transition temperature or enhance crosslink density. Polymer producers require stable functional groups for downstream copolymerization and extrusion under consistent quality controls to meet demanding plastics performance criteria.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for Plastics)
    • FDA 21 CFR 177 for food-contact polymers (if applicable in downstream)
    • RoHS Directive 2011/65/EU for electronic plastics
    • ASTM D638 for tensile properties of plastics

    Typical usage ratio

    • 0.2% - 2.0% by weight of polymer batch; adjusted based on targeted mechanical enhancement or heat stability parameters

    Downstream process integration

    • Incorporated during reactive blending or twin-screw extrusion, as a functional comonomer or crosslinking agent, prior to pelletizing or film casting

    Final product types

    • High-performance engineering thermoplastics
    • Polymer matrix composites for automotive interiors
    • Heat-resistant wire insulation
    • Specialty molded enclosures for electronics

    4. Fine Fragrance and Aroma Chemicals Synthesis

    Aroma chemical producers utilize this bicyclic compound to build high-impact, stable odor molecules for fragrance applications. The norbornane core delivers unique olfactory notes and long-lasting profiles when transformed through Friedel–Crafts acylation or oxidation steps. Its ability to anchor distinctive aroma actives enables brands to capitalize on patented scent profiles while meeting purity and toxicological requirements specified by international fragrance standards.

    Industry compliance standards

    • IFRA Code of Practice
    • EU Regulation (EC) No 1223/2009 for cosmetics
    • RIFM Safety Assessments for finished aroma chemicals
    • ISO 9001:2015 for batch reproducibility

    Typical usage ratio

    • 0.1% - 1.5% in aroma synthesis streams; rate set on desired volatility and note intensity

    Downstream process integration

    • Reacted in the early aldehyde construction or esterification phases, acting as a rigid backbone for long-chain odorant synthesis

    Final product types

    • Fine aroma molecules for perfumery
    • Odorant agents in personal care scents
    • Floral and green note additives for home care
    • Scent components used in laundry formulations

    5. Specialty Resin Curing Agents

    Industrial coatings and composites manufacturers adopt the 2-bromo-norbornane compound for curing high-performance epoxy and polyester resins. Its molecular rigidity and halogen content increase cure speed and improve final coating durability. Labs optimize usage for balanced mechanical strength and chemical resistance in electronics potting, automotive primers, and high-grade industrial adhesives.

    Industry compliance standards

    • ASTM D1652 for epoxy curing agents
    • REACH Annex XVII compliance for hazardous substances
    • UL 94 for flammability of polymeric materials
    • ISO 14001 for environmental stewardship

    Typical usage ratio

    • 0.7% - 3.5% by weight of total resin; formulation refined according to targeted setting time, viscosity, and final film hardness

    Downstream process integration

    • Mixed into resin system during pre-polymer blending or introduced as a reactive modifier just before casting or laminating stages

    Final product types

    • PCB potting compounds
    • UV-curable industrial coatings
    • Automotive composite panels
    • High-bond adhesives for aerospace components

    6. Synthesis of Advanced Imaging and Diagnostic Reagents

    Producers of diagnostic imaging agents use the norbornane derivative as a precursor for radiolabeling and molecular recognition units embedded within imaging tracers. It offers a stable platform for derivatization with radioisotopes and affinity tags, guaranteeing batch consistency and performance in clinical analytical workflows subject to strict regulatory oversight.

    Industry compliance standards

    • ISO 13485 for medical device component manufacturing
    • US FDA 21 CFR Part 820 for quality systems in medical devices
    • OECD Guidelines for the Testing of Chemicals
    • USP <823> Positron Emission Tomography Drugs

    Typical usage ratio

    • 0.3% - 2.0% of precursor batch; modified based on labeling efficiency and detection sensitivity

    Downstream process integration

    • Used as a core scaffold in coupling reactions for attaching radiolabels or biotin tags prior to reagent purification and vialing

    Final product types

    • PET/SPECT imaging probes
    • In vitro diagnostic assay kits
    • Research-grade tracer compounds
    • Bioconjugate labeling agents for antibody and peptide diagnostics
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    More Introduction

    Introducing Bicyclo[2.2.1]Heptane, 2-Bromo- (9CI): A Forward-Thinking Choice for Serious Chemistry

    What Sets Bicyclo[2.2.1]Heptane, 2-Bromo- (9CI) Apart

    Bicyclo[2.2.1]Heptane, 2-Bromo- (9CI) stands out in the world of specialty organobromides. This compound, recognizable among chemists for its unique norbornane skeleton combined with a single bromine atom, isn’t just another ingredient on a shelf. Its structure leads to behaviors that unlock interesting possibilities, both in synthesis and application. Speaking from personal experience, I’ve come across only a handful of chemicals as reliable as this when tackling controlled halogenation steps. The secret lies in the rigidity of the bicyclic ring fused with bromine’s reactivity, affording selective outcomes in many advanced organic syntheses and research-grade transformations.

    The norbornane core isn’t a novelty created by accident—this bicyclic backbone delivers stability rarely matched by other ring systems. Layer on a bromine atom at the 2-position, and you’re looking at an exceptional balance of robustness and activity. Chemists recognize that stability doesn’t have to mean lack of utility, especially not here. The 2-bromo group offers just enough reactivity to open avenues in diverse applications, from cross-coupling reactions to polymer design, but without introducing unnecessary hazards associated with higher-reactivity bromides.

    Structural Advantages Observed in Practice

    I’ve seen too many compounds falter at the scale-up stage because they trade off too much stability for a fleeting reactivity window. Bicyclo[2.2.1]Heptane, 2-Bromo- strikes a sweet spot. Its locked geometry tends to resist rearrangements that plague open-chain bromides. Not all halogenated cycloalkanes handle heat and handling stresses with such unshakable consistency. Take norbornane with a 2-bromo twist: you don’t face the isomerization that jeopardizes product uniformity, cutting out troublesome downstream purifications. That stays true across a surprising range of conditions, from bench-scale flask syntheses to semi-industrial settings.

    In the world of specialty chemicals, a researcher shouldn’t have to chase down a pure sample after every reaction. With Bicyclo[2.2.1]Heptane, 2-Bromo-, repeatability becomes an afterthought—it’s built in. For demanding analyses, such as NMR or mass spectrometry, this compound gives clear, predictable results. Years spent troubleshooting strange signals taught me not to underestimate the value of consistent chemical architecture. Faulty signals waste time. Reliable materials make every step smoother, especially for those developing new synthetic routes or scaling up promising candidates for pilot studies.

    How It Performs in Lab and Industry

    Take any task that calls for pinpoint introduction of bromine. Not every compound delivers results free from side reactions and decomposition. The 2-Bromo- norbornane derivative brings enough activation to drive coupling reactions smoothly, whether building up specialty intermediates for agrochemical pathways or advancing research in medicinal chemistry. I’ve witnessed its use simplify otherwise unwieldy reaction sequences, especially in Suzuki or Heck-type couplings. Those who deal with complex target molecules know the pain of seeing unwelcome byproducts turn up after tricky halogenations. Swapping in this compound has reduced cleanup and improved productivity across several projects.

    Unlike the more reactive benzyl or allyl bromides, Bicyclo[2.2.1]Heptane, 2-Bromo- keeps a measured reactivity profile. That makes handling more straightforward, driving greater confidence on the bench and less worry about runaway reactions. People in manufacturing can vouch for the peace of mind that comes from chemicals behaving predictably—even at elevated temperatures or with sensitive catalyst systems. It doesn’t throw off noxious fumes like some more labile bromides, either. Those running continuous or batch processes value every practical edge for throughput and safety.

    Usage Driven by Practical Chemistry

    Lab workers and process engineers don’t choose chemicals out of habit—they want what works and what stays safe. In my own work, opting for Bicyclo[2.2.1]Heptane, 2-Bromo- often comes from its blend of safety, handling characteristics, and outcome control. It isn’t as reactive as methyl bromide or as hazardous as certain polybrominated systems, allowing use in intermediate-scale processes without incurring extra choking hazards or demanding overbuilt containment. There’s reassurance in knowing every bottle contains the same structure, batch after batch.

    Colleagues who run combinatorial or exploratory studies often reach for this compound because it brings together selectivity and process simplicity. The norbornane ring doesn’t break apart unexpectedly. Tried-and-true, it withstands storage conditions, frequent opening, repackaging, and short periods of exposure to air. Once, during an extended multi-step synthesis, this stability saved a week’s progress—less robust halides could never have handled that much handling without degrading.

    Comparing with Other Brominated Organics

    Experience shows that not all brominated hydrocarbons perform the same way. Take benzyl bromide—a strong alkylator, but its high reactivity invites side products and demands rigorous controls. 1-Bromopropane appears in industrial setups but lacks the selectivity and stability needed for precision chemistry. Compared to these, Bicyclo[2.2.1]Heptane, 2-Bromo- features low volatility, reduced odor, and a tough backbone unlikely to fragment during standard reactions. That resilience keeps processes cleaner and outcomes reproducible.

    This norbornyl bromide rarely triggers unwanted elimination or rearrangement products under ordinary lab conditions. I’ve used both primary and secondary alkyl bromides in similar roles; they simply don’t measure up for selectivity or shelf life. In scenarios where every byproduct matters—a late-stage intermediate for a pharmaceutical, downstream steps in specialty polymers—the difference can be huge. After spending hours cleaning up after less stable compounds, the low waste profile of this brominated norbornane saves both time and morale.

    Why Today’s Chemists Should Care About This Compound

    Modern laboratories run leaner than ever, and lost batches mean lost funding and missed deadlines. A compound like Bicyclo[2.2.1]Heptane, 2-Bromo- lowers those risks. Its structure, honed by decades of organics research, brings a rare blend of inertness and activity. The norbornyl system prevents most of the breakdowns and side reactions that make bench-scale chemistry unpredictable. From my own bench, nothing beats the reliability advantage for developing new reactions, exploring catalyst performance, or working through preliminary toxicological screens.

    Researchers care about environmental impact, too. Material with low volatility and measured reactivity means fewer fugitive emissions and lower risk of accidental release, easing regulatory compliance and safety oversight requirements. Having handled more than a fair share of standard alkyl and aryl bromides, I can tell you that robust compounds cut cleanup costs. In my group, switching over has meant less worry about chemical exposure and less time wasted ventilating hoods after spills or minor leaks.

    Supporting Sustainable Chemistry and Safety

    Safety isn’t just a box to check. Over the years, I’ve watched junior researchers struggle with hot-tempered reagents or unpredictable intermediates. By incorporating stable reagents such as Bicyclo[2.2.1]Heptane, 2-Bromo-, labs reduce those risks. Less reactivity doesn’t always mean compromises in outcome—in fact, with this compound, precision actually increases. Cleaner results and predictable handling allow researchers to focus energy on solving the underlying scientific problems instead of firefighting unexpected reactivity or breakdowns.

    Sustainable approaches are gaining ground. Since this compound doesn’t demand elaborate containment or detoxification steps, labs that use it avoid some headaches tied to volatile organics. Lower vapor pressure cuts down atmospheric releases in poorly ventilated environments. Safer storage and transport save costs in the long run, especially for research institutions under continuous budget stress. From my own experience managing chemical inventories, robust bottles of this norbornyl bromide always outlasted more sensitive alternatives, with less waste and less stress for those working late in the lab.

    Enabling Innovation Across Industries

    Not every new material enjoys cross-industry appeal, but Bicyclo[2.2.1]Heptane, 2-Bromo- has found traction in pharma, agrochemicals, and advanced materials alike. For those developing active ingredients, the tough norbornane ring means intermediates hang together during lengthy production cycles, shrinking the odds of late-stage failure. In polymer and material design, the rigid bicyclic core acts as a predictable building block—properties get tailored by design, not by accident.

    In group settings, I’ve seen the transition from fussier brominated compounds to this one speed up project timelines. Colleagues vent less about reaction failures and spend more time pushing new ideas. Troubleshooting gets simpler, and experiments scale more smoothly. Some teams even build their high-throughput screening around this scaffold, banking on downstream steps being straightforward thanks to the product’s reliability.

    Reliable Sourcing and Ongoing Support

    Markets for specialty chemicals sometimes throw researchers curveballs, from inconsistent purity to sudden interruptions. Having a reproducible, well-characterized product makes planning research far less nerve-wracking. With Bicyclo[2.2.1]Heptane, 2-Bromo-, repeated testing demonstrates both clean NMR profiles and tight specifications. My own buying habits shifted away from alternatives that carried surprises batch to batch. The benefit grows for collaborative or multi-institution projects, where consistency and documentation support smoother tech transfer between sites.

    Community forums and professional associations mention positive experiences with this norbornyl compound. While some brominated intermediates come with handling quirks or limited shelf life, this material consistently gets high marks for storage stability, packaging integrity, and traceability. Years of handling have shown me that smaller details—labels that last, packaging that doesn’t break on arrival—add up to fewer headaches and reduced hidden costs for teams tasked with tight research budgets.

    Opportunities for Future Growth

    While organobromides often get typecast as tools for aggressive alkylation, Bicyclo[2.2.1]Heptane, 2-Bromo- continues to surprise. Functional group tolerance enables new reaction pathways where sensitive alternatives would fall apart. Recent literature highlights its utility in asymmetric catalysis and stepwise functionalization, opening the door to new classes of compounds that push the field in fresh directions.

    Continued innovation depends on trusted starting materials. Lab time isn’t infinite, and having a solid foundation makes ambitious chemistry less daunting. In industrial and academic settings alike, investments in dependable reagents do more than save money—they build a culture that values thoughtful risk-taking, reproducibility, and long-term value over trend-chasing or chasing shortcuts. As the landscape keeps shifting, a compound with a track record for dependability looks like a smart, future-ready pick.

    Building Toward Better Chemistry

    Bicyclo[2.2.1]Heptane, 2-Bromo- stands as a compelling example of what’s possible when molecular design pays off both in purity and process ease. For beginners cutting their teeth on rigorous synthetic routes to seasoned professionals managing high-stakes projects, the peace of mind that comes from predictable output cannot be overstated. My own early walk through the world of synthetic chemistry included nights questioning why outcomes fell apart late in a sequence. Moving to robust, resilient reagents like this one marked a turning point.

    That shift didn’t just simplify results; it allowed my group to push boundaries further than before. Reliable halogenation without unwanted isomers or breakdown means energy gets spent driving innovation, not scrambling to fix messy side reactions. Product consistency fuels new technology development, supporting everything from greener processes to next-generation pharmaceuticals and specialty coatings. The norbornane backbone, far from old news, keeps proving its value in novel contexts.

    Product Longevity Helps the Bottom Line

    Having spent hours sorting through degraded bottles and sifting for good material, it’s clear that shelf-stable reagents pay for themselves in reduced waste and smoother workflows. This brominated norbornane rarely shows the discoloration, crystallization, or volatility losses that haunt other halides. Once opened, it lasts—minimizing unnecessary reorders and supporting sustainable inventory practices. For budget-constrained labs, that alone justifies making Bicyclo[2.2.1]Heptane, 2-Bromo- a mainstay on the shelf.

    From my time handling both small bench and pilot-scale quantities, I can attest to the rewards of investing in stable materials. They take pressure off both supervisors in charge of safety and young researchers learning safe handling. This reliability scales up, too: industrial users appreciate knowing that the material flowing through reactors today matches what worked last year. Decisions grow simpler; training gets easier.

    Encouraging Smarter Choices in Research and Industry

    At the heart of every productive laboratory sits a collection of well-chosen reagents. As new demands arise—from probing the reactivity of strained rings to designing tailored polymer precursors—chemists reach for what works. Bicyclo[2.2.1]Heptane, 2-Bromo- has earned its spot by delivering on both promise and practicality. Reliable, straightforward handling, and outcome-driven chemistry mean results that move the discipline forward.

    Smarter chemistry isn’t always about the latest discovery or the flashiest reaction. Sometimes, it comes down to building on proven ground with substances designed right from the start. From fresh graduates starting their careers to established industry scientists, everyone benefits from options that lower frustration and boost productivity. My own path through countless experiments taught this lesson well—solid, stable reagents set the stage for everything that follows.

    The Takeaway for Serious Practitioners

    Trust in results doesn’t happen overnight. Reagents earn their reputation through cycles of testing and years of real-world application. For those committed to working on the edge of discovery, or simply keeping the production pipeline flowing, Bicyclo[2.2.1]Heptane, 2-Bromo- delivers in ways that shortcuts can’t match. That edge—built on sound molecular architecture and lived experience in the lab—lets chemists focus on what counts: doing work they can stand behind, advancing both their projects and the field itself.