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9-Bromo-1-Nonene

    • Product Name 9-Bromo-1-Nonene
    • Alias 9-Bromonon-1-ene
    • Einecs 207-905-7
    • 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
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    Specifications

    HS Code

    996104

    Chemical Name 9-Bromo-1-Nonene
    Molecular Formula C9H17Br
    Molecular Weight 205.14 g/mol
    Cas Number 76319-27-6
    Purity Typically >98%
    Boiling Point 110-112°C at 15 mmHg
    Density 1.154 g/cm³ at 25°C
    Appearance Colorless to light yellow liquid
    Refractive Index 1.471 to 1.474 at 20°C
    Flash Point 88°C
    Solubility Insoluble in water, soluble in organic solvents
    Storage Conditions Store in a cool, dry place, keep container tightly closed
    Smiles C=CCCCCCCCBr
    Inchi InChI=1S/C9H17Br/c1-2-3-4-5-6-7-8-9-10/h2H,1,3-9H2
    Synonyms 1-Nonene, 9-bromo-

    As an accredited 9-Bromo-1-Nonene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 9-Bromo-1-Nonene

    Applications of 9-Bromo-1-Nonene in Industrial Manufacturing

    As the manufacturer of high-purity 9-Bromo-1-Nonene, we serve a global base of advanced material producers and specialty chemical formulators. This linear bromoalkene is a key intermediate in four real-world downstream sectors, each requiring stringent process integration, adjusted dosing, and adherence to specific industry protocols for the production of value-added derivatives. The following industrial applications outline typical compliance benchmarks, recommended formulation ranges, workflow stages, and representative end products incorporating this raw material.

    1. Pharmaceutical Intermediate Synthesis for API Sidechain Construction

    Leading pharmaceutical firms employ 9-Bromo-1-Nonene in the preparation of structural sidechains for complex Active Pharmaceutical Ingredients, particularly where n-nonyl substitutions confer bioactivity or improve drug delivery profiles. Manufacturers introduce the bromoalkene into multi-step synthesis, typically in nucleophilic substitution or cross-coupling reactions, producing functionalized alkyl chains incorporated into APIs targeting cardiovascular, antiviral, or CNS disorders.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 for Finished Pharmaceuticals
    • EU EMA EudraLex Volume 4 (GMP Guidelines)
    • USP/NF (United States Pharmacopeia/National Formulary) for impurity profiling

    Typical usage ratio

    • 0.4%–2.0% w/w relative to the total reaction mass; ratio is scaled based on target alkyl chain incorporation and yield optimization studies

    Downstream process integration

    • Introduced at the alkylation or cross-coupling stage within multi-step organic synthesis under inert atmosphere, with stoichiometry adjusted per batch size and target molecule requirements

    Final product types

    • Nonyl-derivatized antiretroviral intermediates
    • Side-chain modified antihypertensive actives
    • Intermediates for CNS pharmaceutical APIs

    2. Specialty Surfactant Raw Material in Alkylation Processes

    Producers of high-end surfactants downstream utilize 9-Bromo-1-Nonene to introduce controlled alkyl chains onto aromatic or heterocyclic backbones, especially in the synthesis of nonionic and cationic surfactants. Raw material incorporation supports precise hydrophobic-lipophilic balance adjustment, critical for detergents used in industrial and institutional cleaning, textile scouring, and agrochemical emulsification.

    Industry compliance standards

    • REACH (Registration, Evaluation, Authorisation, and Restriction of Chemicals) for raw material safety
    • OECD Guidelines for the Testing of Chemicals: Ready Biodegradability
    • ISO 9001 Quality Management Systems for surfactant manufacturing
    • EU Detergents Regulation (EC) No 648/2004 for finished formulations

    Typical usage ratio

    • 1.5%–6.0% w/w in the alkylation batch; proportions modified for target hydrophobe length and surfactant type

    Downstream process integration

    • Charged during the initial alkylation reaction with suitable nucleophiles or aromatic substrates, typically following phase-transfer or Lewis acid catalysis

    Final product types

    • Nonyl-based nonionic surfactants for textile auxiliaries
    • Specialty cationic surfactants for industrial cleaning
    • Agrochemical emulsifiers for pesticide formulations

    3. Organic Electronics Precursor for Functional Polymer Synthesis

    Advanced materials companies use 9-Bromo-1-Nonene to introduce pendant alkyl chains in the monomer design phase for conductive polymers and specialty elastomers, supporting improved solubility, film flexibility, and electrical properties in final products such as flexible circuit boards or organic LEDs. The controlled incorporation of nonenyl substituents is essential in tailoring polymer backbone architecture.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substances in electronics
    • ISO 14001 Environmental Management for specialty polymer operations
    • IPC-4101B standards for base materials in electronics
    • ETSI EN 301 489 for electronic compatibility in communication devices

    Typical usage ratio

    • Variable between 0.8%–4.0% w/w of total monomer loading, depending on polymer type and intended electronic property profile

    Downstream process integration

    • Added during Grignard or Suzuki coupling for side-chain attachment to thiophene, phenylene, or other arylene monomers; process designed for high-purity product streams

    Final product types

    • Pendant-alkylated polythiophenes for conductive inks
    • Flexible OLED emissive layer polymers
    • Functionalized elastomers for wearable electronic components

    4. Custom Fragrance Intermediates for Aroma Chemical Synthesis

    Fragrance and aroma compound producers employ 9-Bromo-1-Nonene as an alkylating agent in the synthesis of long-chain musk and specialty odorants, where the nonenyl group imparts unique volatility and release profiles in fine fragrance and cosmetic formulations. It enters etherification, cyclization, and esterification sequences under controlled conditions to ensure consistency in olfactory performance.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards for raw materials
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 9235 for natural aromatics characterization
    • Good Manufacturing Practice (GMP) for cosmetics (ISO 22716)

    Typical usage ratio

    • Generally 0.6%–2.3% w/w per batch, with fine adjustments according to GC-MS profiling and desired olfactory strength

    Downstream process integration

    • Alkylation or cyclization step in multi-stage synthesis of musk ketone and related aroma molecules; operations carried out under inert conditions for purity

    Final product types

    • Nonenylmusk bases for fine fragrances
    • Long-chain alkylated aroma modifiers
    • Cosmetic-grade fragrance intermediates
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    Certification & Compliance
    More Introduction

    Introducing 9-Bromo-1-Nonene: A Thoughtful Look at a Powerful Organic Intermediate

    What Sets 9-Bromo-1-Nonene Apart?

    I’ve spent years observing the role of specialty chemicals in research labs and manufacturing sites, and 9-Bromo-1-Nonene keeps cropping up more often in conversations among professionals. With its formula C9H17Br, this liquid compound brings a specific benefit to the people working on molecular frameworks and targeted modifications within the chemical industry.

    Ask anyone who has handled alkenyl bromides: 9-Bromo-1-Nonene isn’t just another intermediate. It has a chain length that appeals to designers of fine chemicals, allowing enough backbone flexibility while maintaining a single terminal double bond. The way that single nonene unit combines with bromine at a precise spot turns this molecule into a versatile platform for further functionalization. Chemists value the compound's reactivity, and manufacturers looking to diversify molecular scaffolds in pharmaceuticals, fragrances, or specialized polymers often gravitate toward it.

    Physicochemical Properties and Handling in Practice

    Every bottle of this compound calls for careful respect. Clear or pale yellow in appearance, its low viscosity and manageable boiling point support its use on both bench and pilot scales. Standard purity runs high—almost always above 95%—although many researchers prefer material exceeding 98%, confident that slight impurities won’t derail their process but still aiming for predictable reactivity. In any industrial or laboratory environment, staff wear gloves and goggles, not just because safety demands it but because respect for a compound’s power starts with the basics.

    My experience buying and handling similar organobromines has taught me that moisture control and temperature matter. Even trace water can alter outcomes, so sealed storage under dry nitrogen or argon is a regular sight. Glass containers, sometimes amber in color to shield from stray light, help keep the material in prime condition over weeks or even months. Nobody wants surprises when scaling a synthesis.

    Real-World Applications

    Chemists can be a picky crowd, and for good reason. They want intermediates that open doors rather than box them in. 9-Bromo-1-Nonene finds its main life in the synthesis of specialty surfactants, scents, and pharmaceutical building blocks. The compound’s double bond gives it a sort of chemical “handle” for further reactions—hydroboration, epoxidation, or cross-coupling have all featured in published literature. Each transformation takes advantage of the strategic placement of the bromine, letting one swap in a staggering variety of functional groups with minimal side reactions.

    Those looking for a more modern use might point out its role in the world of polymer science. Here, terminal alkenes let researchers anchor long chains to surfaces or build custom block copolymers. I remember a colleague using nonene derivatives for designing surface modifications on nanoparticles, searching for just the right spacing and reactivity. Every researcher looking to extend structures without fussing over secondary isomerism has run into the benefit of the terminal, linear nature of 9-Bromo-1-Nonene.

    Comparisons with Other Intermediates

    Plenty of organobromines fill catalogs, but not all of them match the attributes of 9-Bromo-1-Nonene. For someone used to working with bromoalkanes like 1-Bromooctane or ring structures such as bromocyclohexene, the difference is clear. Shorter homologs, for instance, often prove too volatile or suffer poor selectivity during further functionalization. Branched bromides create unnecessary byproducts in coupling reactions or iodine-metal exchange steps, making purification a headache.

    A linear chain of nine carbons—with a single site of unsaturation—lets chemists plot out functional transformations with few detours. Those same features produce sharper, more reliable NMR spectra, and who hasn’t struggled with ambiguous proton peaks from branched isomers? Compared with neighbors in the family, like 1-Bromo-1-octene or 10-Bromo-1-decene, 9-Bromo-1-Nonene fits as a "Goldilocks" solution: long enough to be useful, not so long as to reduce efficiency or complicate logistics.

    Sourcing and Quality Considerations

    In labs where every gram costs real money, and in factories where every kilogram represents trust in the supply chain, not all sources deliver the same experience. Having witnessed bulk purchases go sideways due to inconsistent purity or traces of isomerization, I’ve learned that due diligence pays off. Reputable suppliers publish detailed certificates of analysis, tracking not just main product content but also trace metals, halides, and water content.

    Staff with good habits verify results with their own analysis. Thin-layer chromatography and gas chromatography-mass spectrometry take on an everyday quality—not reserved for mystery samples, but integrated into routine checks. Stability over transit and storage matters, too. I’ve seen more than one well-packed shipment suffer excess pressure or exposure, weakening the compound’s clean reactivity. Temperature-controlled packaging costs a bit more but saves much grief.

    Economic Impact in Industry

    On the economic side, every custom synthesis company and chemical producer looks for reliable intermediates that won’t jeopardize yields. Demand for products such as synthesized fragrances, agrochemical actives, or medical research tools often comes down to small structural details embedded in molecules like 9-Bromo-1-Nonene. So much opportunity exists where an inexpensive, reactive, and predictable material forms the backbone of a downstream synthesis.

    The specialty nature of 9-Bromo-1-Nonene means prices can fluctuate, particularly if demand spikes for a novel polymer or drug intermediate. Yet, its widespread availability through global catalogs balances scarcity concerns. Well-established suppliers routinely keep plenty on hand, setting clear batch numbers and expiration dates. Knowing that a supply chain has redundancy buys peace of mind, and I’ve seen teams breathe easier when backup orders arrive without fanfare.

    Sustainability and Environmental Concerns

    Many in the chemical industry worry about the ecological downsides of organobromine chemistry. I share that concern; brominated byproducts have earned a reputation for persistence in the environment and potential health hazards. Synthetic routes that use 9-Bromo-1-Nonene generate hazardous waste, meaning labs and factories focus more and more on efficient reaction conditions and comprehensive waste treatment. Companies investing in green chemistry explore alternatives, but the specific reactivity of the bromide often remains hard to replace.

    Mitigating environmental impact starts with simple steps: tightly controlling reaction conditions, reusing solvents, and ensuring all halogenated wastes reach licensed disposal facilities. I’ve worked in research groups adding phase-transfer catalysts to squeeze more yield from every batch, minimizing excess use and heating. Upstream, some manufacturers transition to more sustainable bromination methods, using microreactor technology or greener solvents that minimize exposure and accidental releases.

    Professionals who coordinate closely with environmental, health, and safety teams build stronger, more responsible operations. Data sheets and audits extend beyond paperwork; chemists and facility managers regularly check local groundwater for traces of halogenated compounds, especially in regions with sensitive ecosystems. Advances in analytical techniques let us spot trouble before it grows, and every company has an obligation to pay attention to regulations and actual field conditions—not just what’s convenient.

    Opportunities for Safer, Smarter Use

    Having seen more than one accident caused by rushing through procedures or skipping PPE, I can’t stress enough the importance of ongoing safety training. People work best when they know the risks and trust management to invest in safer equipment—local ventilation, splash-resistant instrumentation, automated addition systems. Regular practice drills, proper signage, and up-to-date spill kits belong in every facility using this type of material.

    Training extends to proper labeling, inventory tracking, and protocol documentation. In a world where staff turnover happens, keeping institutional memory alive saves costly mistakes. Pairing new team members with experienced hands helps carry forward not just data but attitudes that value precision and clear judgment.

    Future Directions: Innovation and Research

    Researchers don’t just rest on tradition. New catalytic systems for cross-coupling and selective functionalization have appeared in respected journals, often making use of linear alkenyl bromides like 9-Bromo-1-Nonene. I remember a project where transition-metal-catalyzed couplings used this compound to anchor a tricky side chain in a bioactive molecule—a task that, with alternative approaches, would have taken months longer.

    Polymer chemistry continues to draw on the unique structure for the rapid assembly of terminally functionalized chains. In nanotechnology circles, tailored organic layers made from 9-Bromo-1-Nonene derivatives offer promising avenues for sensor design and surface patterning. There’s ongoing interest in redesigning reaction schemes to reduce waste and streamline carbon integration into complex targets.

    Mentorship and public sharing of new synthetic routes boost the whole field. Open-access publications and regular workshops break down barriers between academia and industry, encouraging smarter, more responsible use of such intermediates. Standards groups develop consensus protocols so everyone from start-up labs to multinational producers works from verifiable best practices.

    Why 9-Bromo-1-Nonene Matters

    Every scientist and engineer working with organic molecules comes to recognize certain building blocks as both a blessing and a challenge. 9-Bromo-1-Nonene occupies that space. Its distinctive structure, strategic reactivity, and reliability in crucial transformations give it a central role in many projects that drive innovation in pharmaceuticals, polymers, and materials science.

    From the technical staff that store and handle it, to the process engineers plotting out scale-up, to the researchers designing tomorrow’s molecules, each sees the material through slightly different eyes. Safe and effective use always comes down to practical decisions—purchasing from careful suppliers, using tried-and-true analytical methods, pursuing safer process improvements, and remembering environmental responsibility.

    People bringing new substances into our world need transparency, shared know-how, and real commitment to science and safety. 9-Bromo-1-Nonene offers both an opportunity and a responsibility, and how we handle it speaks to the quality of our labs, our products, and our stewardship of chemical innovation.