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4-Cyano-1-Cyclohexene

    • Product Name 4-Cyano-1-Cyclohexene
    • Alias 4-Cyclohexenecarbonitrile
    • Einecs 209-723-0
    • 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
    VTB
    Specifications

    HS Code

    332461

    Chemicalname 4-Cyano-1-Cyclohexene
    Molecularformula C7H9N
    Molarmass 107.15 g/mol
    Casnumber 1193-06-8
    Appearance Colorless to pale yellow liquid
    Boilingpoint 199-201 °C
    Density 0.976 g/mL at 25 °C
    Flashpoint 89 °C
    Refractiveindex 1.493
    Purity Typically ≥98%
    Smiles C1CC(C=CC1)C#N
    Solubility Slightly soluble in water

    As an accredited 4-Cyano-1-Cyclohexene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 4-Cyano-1-Cyclohexene, sealed with a white cap, labeled with hazard and safety information.
    Shipping 4-Cyano-1-Cyclohexene is shipped as a chemical reagent in tightly sealed, compatible containers, protected from light and moisture. During transport, it is classified and handled according to relevant regulations for hazardous materials. Proper labeling and documentation ensure safety, with care to avoid exposure to extreme temperatures, and compliance with all regulatory guidelines.
    Storage 4-Cyano-1-cyclohexene should be stored in a cool, dry, well-ventilated area away from sources of heat, ignition, and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protected from moisture. Store in a designated chemical storage cabinet and label appropriately. Use only with adequate ventilation and handle with suitable personal protective equipment.
    Application of 4-Cyano-1-Cyclohexene

    Applications of 4-Cyano-1-Cyclohexene in Industrial Manufacturing

    4-Cyano-1-Cyclohexene serves key roles in high-value chemical syntheses across multiple industrial sectors. Its cyano functionality and non-aromatic cyclohexene backbone allow downstream producers to develop advanced intermediates and specialty chemicals applicable in pharmaceuticals, agrochemicals, high-performance polymers, and specialty coatings. The following sections describe real-world usage scenarios, compliance protocols, and integration practices derived from direct collaboration with end users in the chemical industry.

    1. Pharmaceutical Intermediate Synthesis

    Producers of active pharmaceutical ingredients leverage this cycloaliphatic nitrile for the synthesis of piperidine and azacyclic moieties, particularly in CNS and cardiovascular drug manufacturing. Its role as a stable intermediate supports multi-step transformations such as partial reductions and nucleophilic additions tailored to GMP-compliant processes, prioritizing end-product purity and traceability demanded in regulated pharmaceutical environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for intermediates
    • US FDA 21 CFR Part 210/211 Production Controls
    • REACH Registration for chemical intermediates under ECHA

    Typical usage ratio

    • Applied at 0.15–0.35 molar equivalent in heterocyclic intermediate syntheses; exact charge adjusted based on yield optimization and impurity profile monitoring.

    Downstream process integration

    • Charged into the vessel following primary substrate dissolution, typically during Stage 1 of piperidine or related aza-cyclic intermediate synthesis.
    • Reacted under anhydrous conditions, with process control maintained for residual cyanide assays as part of intermediate release testing.

    Final product types

    • Piperidine-based drug intermediates
    • Pyrrolidine derivatives for pharmaceutical actives
    • Cardiovascular and CNS small molecule APIs (final transformation steps)

    2. Agrochemical Active Ingredient Manufacturing

    4-Cyano-1-Cyclohexene is an effective building block for the synthesis of cyclic nitrile-containing herbicides, fungicides, and miticide actives. Agrochemical formulators utilize its stable ring structure and nitrile reactivity to create highly specific functional groups through nitrile hydrolysis, Grignard addition, or catalytic hydrogenation, allowing for precise structural modification to meet bioactivity and environmental persistence requirements.

    Industry compliance standards

    • FAO/WHO Guidelines for the Registration of Pesticides
    • ISO 9001:2015 Quality Management in agrochemical production
    • National Institute for Occupational Safety and Health (NIOSH) exposure limits
    • EU-Regulation 1107/2009 for Plant Protection Products

    Typical usage ratio

    • Used at 0.10–0.28 molar equivalent as a cycloaliphatic backbone precursor; formulation labs adjust load ratio based on desired herbicide or insecticide chain length and substitution pattern.

    Downstream process integration

    • Dosed during early-stage active ingredient assembly, post-halide activation or inline with nitrile group transformation. Monitoring for residual unreacted material is maintained to ensure compliance with maximum residue limits.

    Final product types

    • Cyclohexenyl-based herbicides
    • Miticide and nematicide actives containing cycloaliphatic nitrile groups
    • Selective fungicidal intermediates for cereal and orchard protection

    3. Advanced Polymer Synthesis

    Specialty polymer producers incorporate this monomer to introduce nitrile-functionalized cyclic units into advanced polymer matrices. The compound’s structural features allow for controlled copolymerization and subsequent chemical modification, resulting in polymers that demonstrate enhanced chemical resistance, improved gas barrier properties, and unique mechanical flexibility for demanding packaging and engineering applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for polymer manufacturing
    • ASTM D638 (Standard Test Method for Tensile Properties of Plastics)
    • RoHS Directive (2011/65/EU) for restricted substances in electrical/electronic equipment
    • Global Automotive Declarable Substance List (GADSL) for automotive polymers

    Typical usage ratio

    • Introduced at 0.5–3.5% by weight into copolymerization reactors. The exact percentage depends on the target polymer weight-average molecular weight and desired end-use performance parameters.

    Downstream process integration

    • Fed to the polymerization step during copolymer production. May be subject to post-polymerization modifications, including hydrolysis and crosslinking, to introduce functional groups or adjust polymer end properties.

    Final product types

    • Nitrile-functional copolymers for food packaging
    • Barrier films for pharmaceutical and industrial storage
    • Technical components in automotive and aerospace assemblies

    4. Specialty Coating and Adhesive Formulation

    Resin and adhesive formulators utilize the cyclohexenyl nitrile as a specialty crosslinking monomer for high-performance coatings where chemical resistance and adhesion to non-polar surfaces are critical. Chemical conversion of the nitrile group offers further adjustment of coating surface energy and adhesion profile, supporting multi-substrate industrial bonding applications and corrosion-resistant coatings.

    Industry compliance standards

    • ISO 12944 (Paints and varnishes: Corrosion protection)
    • UL 746C (Polymeric Materials: Use in Electrical Equipment Evaluations)
    • ASTM D3359 (Standard Test Methods for Measuring Adhesion by Tape Test)
    • REACH Annex XVII - Substances restricted in coating products

    Typical usage ratio

    • Used at 1–8% by weight in coating or adhesive converters. Dosage is tailored to base resin elasticity and target crosslinking density for the finished system.

    Downstream process integration

    • Mixed as a co-monomer during resin letdown stage or as a functional modifier in the final blending step before application.

    Final product types

    • Chemical-resistant industrial coatings
    • Adhesives for plastics and composites assembly
    • Multi-substrate bonding agents for automotive and aerospace industries

    5. Fine Chemical Building Block for Flavor and Fragrance Intermediates

    Manufacturers in the aroma chemicals sector apply the cyclohexene nitrile to synthesize high-value intermediates for musk and floral note creation. Controlled catalytic transformation maintains the cycloaliphatic structure, enabling synthesis of stable, low-volatility intermediates for downstream blending in F&F compositions, with all production steps adhering to food and cosmetic additive regulatory controls.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association) for formulated compositions
    • US FDA 21 CFR Part 172.515 for synthetic flavoring substances
    • EU Regulation (EC) No 1334/2008 for flavoring substances and food ingredients
    • ISO 9001:2015 for aroma chemical quality management

    Typical usage ratio

    • Employed at 0.02–0.18 mole ratio in aroma intermediate synthesis, depending on target musk or lactone backbone derivatization reactions.

    Downstream process integration

    • Introduced after catalyst selection and solvent charge in the initial blending phase. Purification and olfactory assessment follow prior to downstream incorporation in perfumery bases or flavor accords.

    Final product types

    • Cyclohexyl-based musk fragrance intermediates
    • Stable aroma lactone building blocks
    • Blending ingredients for high-end perfumery and food flavoring bases
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    Certification & Compliance
    More Introduction

    4-Cyano-1-Cyclohexene: A Product Born from Experience in Chemical Manufacturing

    A Closer Look at 4-Cyano-1-Cyclohexene

    After years working hands-on with cycloaliphatic intermediates and refining process chemistry, I have grown to appreciate the utility and versatility of a molecule like 4-Cyano-1-Cyclohexene. Its unique structure balances reactivity and selectivity, giving chemists and manufacturers alike real opportunity to push the boundaries of innovation. In our facility, designing and producing this material means thinking through every detail—from raw material sourcing to rigor in purification and control—because every batch can define the outcome of a downstream process.

    The 4-cyano functionality tacked to the cyclohexene ring isn’t just a subtle tweak; it gives the molecule a specific polarity and reactivity that opens new doors. Compared with its isomers or homologues, the position of that cyano group sets this compound apart. We’ve put in years fine-tuning our selective hydrogenation and ring modification protocols. We rely on an arsenal of reactors engineered for precise temperature and pressure control, since keeping byproducts in check is never simply about luck—experience tells us what contaminants will appear and how to address them quickly.

    Specifications: Shape, Purity, and Character

    In my daily rounds, I see the need for both consistency and adaptability. 4-Cyano-1-Cyclohexene comes to us as a colorless to slightly pale liquid, and getting the color right really means controlling potential side reactions during preparation. There are countless times I’ve checked a fraction and picked up signs of ring-opening or dimerization, making a mental note to adjust the feedstock drying sequence or catalyst selection. Trace water can wreak havoc—not just on purity, but on yield and reproducibility. That’s why every lot goes through rigorous GC and NMR screening. Any hint of saturated or aromatic impurity is flagged and tracked.

    Purity targets usually exceed 98%. We go beyond that in many runs, because downstream applications—whether pharma intermediate synthesis or advanced materials work—demand closer control. Minor components, even at the half-percent level, translate into complications during scale-up. We've learned to trace sources of unwanted byproducts, whether they arise from residual solvents, catalyst residues, or incomplete reaction. Careful vacuum stripping and distillation in glass-lined columns help achieve a clean cut.

    Real Uses: Value Across the Industry

    People in labs and plants choose 4-Cyano-1-Cyclohexene for the way it enables transformations that would be too hindered using benzene derivatives or fully saturated alicyclics. For several specialty polymers, the ability to introduce a cyano group under mild conditions adds reactivity precisely where it’s needed. As a seasoned manufacturer, I can remember the pain points in nitrile chemistry—unstable intermediates, finicky ring closures. This cyclohexene version can streamline certain cyclizations or functional group attachments, sidestepping the harsher reagents needed with other cores.

    Fine chemicals is where the product really shines. Customers in crop protection and custom synthesis reach out with requests: “I need a ring construction route that won’t poison downstream steps with unwanted aromatics.” That’s one thing our process for 4-Cyano-1-Cyclohexene can offer: you avoid the persistent, hard-to-remove aromatic residues that plague many classical nitrile approaches. Over time, we’ve seen customers apply the material in chiral resolution schemes, molecular electronics, and as coupling partners in metal-catalyzed cross-coupling. Each application teaches us something about process tolerance, solubility, and safe handling.

    What Sets It Apart: Differences in Performance and Processability

    There’s a world of difference between 4-Cyano-1-Cyclohexene and simpler cyclohexene analogs. Many buyers come to us after struggling with isomerization, conjugation issues, or incompatibility with organometallic reagents seen with substituted cyclohexenes. The cyano group at the 4-position changes the electronic landscape—something our R&D team explored for years. With alternative products like 1-cyano-cyclohexene or 3-cyano-variants, the outcome in reactivity, melting and boiling point, and downstream functionalizations diverges in meaningful ways.

    We found that the 4-positioned cyano imparts greater balance—enough distance from the double bond to avoid over-reactivity, but close enough to be easily incorporated into further transformations. This means fewer popped seals, less fouling in transfer lines, and reduced risk of uncontrolled side-reactions. Cyclohexene itself, with no cyano group, struggles to offer this breadth of reactivity. Alternatives, such as aromatic nitriles, fall short in processes that need lower toxicity or reduced environmental load.

    Manufacturing Practice: Lessons from the Plant Floor

    There’s no substitute for direct experience, and handling 4-Cyano-1-Cyclohexene builds deep intuition about cycloaliphatic chemistry. Over time we noticed that the raw material sourcing—the right grades of cyclohexanone or cyclohexenone—matters as much as reactor design. In our early days, backflow from too-basic cleaning solvents led to partial hydrolysis. After troubleshooting, switching to buffered washes and nitrogen blanketing carried a big payoff, not only in yield but in reducing trace amines that compromise product stability.

    Production volumes can vary widely, but we keep process flexibility at the core. High-purity, small batch for pilot-scale drug development. Bulk runs for agrochemical intermediates. I’ve watched colleagues manage each scale shift in real time, chasing pressure drops, tweaking reflux ratios, and verifying that preps are “on spec” well ahead of dispatch. Customers rely on us for repeat deliveries, so we tie documentation, batch release protocols, and sample archiving directly into our logistics chain.

    A common challenge in manufacturing involves heat transfer and gas evolution. With 4-Cyano-1-Cyclohexene, the underlying chemistry can lead to runaway polymerization if a jacket temperature sensor drifts out of calibration. We've evolved a practice of cross-checking sensors daily during critical runs and using heat transfer fluids with rapid response profiles. On the analytical side, having a well-calibrated GC setup ensures the product never leaves the gate until those last few peaks line up with our internal reference library.

    Supporting Quality: Analytical Rigor and End-Use Considerations

    Almost every customer who visits our site asks to see the analytical data, right down to the residual solvent scores. This hands-on approach builds trust—you can talk through the challenges with people who rolled up their sleeves themselves. I recall an instance where a minor unknown peak appeared at the tail end of our chromatogram. Rather than just discounting it, our QC manager ran additional analyses at different detector wavelengths, zeroed in on a rare side reaction, and adjusted the post-reaction workup. That cross-functional vigilance keeps our product a reliable choice for demanding applications.

    Our experience points to one trend: end-users want more than purity alone. They ask about shelf life, storage recommendations, and long-term compatibility with planned synthetic schemes. 4-Cyano-1-Cyclohexene stores best in dark, airtight containers, at modest temperatures. Direct sunlight can promote slow polymerization or color shift, so packaging means as much as chemical purity. I remember the first time we shipped a summer batch cross-country, only to find that the quality dipped from lengthy exposure during transit. From then on, we switched to insulated, UV-resistant drums and built storage time tracking directly into our barcode management.

    Handling safety always remains front of mind. The cyano group adds reactivity, so proper ventilation and personal protective equipment are essentials on the plant floor. In larger charge sizes, vapor containment and secondary containment systems keep everything stable in case of an incident. All of these steps reflect lessons learned—not out of a company playbook, but from regular feedback and direct problem-solving on the job.

    Partnerships and Collaborative Problem-Solving

    Manufacturing rarely stays static. New requests, pilot runs with novel catalysts, or a custom specification for a pharmaceutical startup can push us to rethink everything from order of addition to downstream purification strategy. We’ve worked side by side with process chemists, patent attorneys, and plant engineers to hit yield targets or reduce environmental impact. Sometimes that means running parallel preps to dial in the best protocol; other times it requires revisiting waste stream management because a customer’s plant downstream lacks sophisticated scrubbing or incineration.

    It’s not unusual to get feedback from a specialty polymer customer asking, “We’re getting haze in our end product. Can you trace any residuals on your end?” That sends us back through our own process records and analytical history, seeking any signature left by auxiliary solvents or byproducts. It’s part of the craft—continuous loop between producer and end-use team. Transparency, clear reporting, and thorough understanding of our product’s journey translates into real-world benefits for people working to create new materials.

    Improvements Based on Feedback

    Customer needs change with every season. Cropping up recently, there’s greater interest in sustainable production. 4-Cyano-1-Cyclohexene manufacturing involves reagents and energy input that leave a footprint. Over the last few years, our team invested in greener solvent systems for the core steps, and piloted reactor setups that regenerate and recycle process gases. It didn’t come from boardroom mandates, but from the practical realization that solvent costs and regulatory restrictions are only trending up.

    Another area of feedback centers on process flexibility. Some customers requested higher concentration batches or alternative solvent carriers for easier integration into their existing formulations. Our approach has been to adapt reaction workups and drying steps, while staying alert to the possibility that tweaks may introduce new side products. It takes active experimentation, not just desk research, to balance yield, purity, and compatibility. Sometimes the biggest innovations come from these small, unplanned changes—solutions built in the lab or on the plant floor rather than commission from outside consultants.

    Challenges Ahead: Risk Management and Regulatory Changes

    Every change in chemical regulation, whether it’s limits on handling of nitrile-bearing materials or on VOC emissions, lands directly on our production desk. 4-Cyano-1-Cyclohexene sits at a crossroads in this respect—it avoids some of the strictest controls, thanks to its non-aromatic nature and relatively low vapor pressure, but ongoing attention is always needed. We keep an eye on updates across multiple jurisdictions, especially as our clients export finished formulations globally.

    Our regulatory staff works with production to align documentation and batch release with regional requirements. Over time, tracking supply chain origins and tracing intermediates became a necessary discipline: from verifying the integrity of our starting materials to validating the recyclability of packaging. With new pressures pushing the industry, strong documentation and full traceability prove more important than ever. Through audits and regular self-assessment, we stay prepared for whatever challenges might arise tomorrow.

    Innovation from the Plant Floor: Where the Future Leads

    Research into new applications and derivatives of 4-Cyano-1-Cyclohexene never stops. Our technical group spends a slice of every week testing novel catalysts, exploring alternate nitrile substituents, or working up new step-economical synthetic routes. Over the last year, we’ve been able to shorten the number of unit operations needed for purification, lowering energy use and shrink waste. Long nights spent scaling up a reaction teach you real process optimization faster than any seminar or textbook.

    Every improvement, whether a tweak in palladium-catalyzed addition or a new approach for decolorization, comes from lessons in the real world. Sometimes a test run goes sideways—overheating, or a stalled hydrogenation that needs quick diagnosis—but more often, careful attention and cumulative experience win out. The aim remains constant: more reliable supply, tighter quality, and real value for every person downstream.

    Building for the Long Term

    4-Cyano-1-Cyclohexene’s impact reaches across industries, from specialty chemicals to pharmaceutical intermediates and niche materials development. Our job, as manufacturer, is to bring every tool—analytical, mechanical, and experiential—to bear on every batch. We know that small changes in process flow, raw material grade, or post-processing have consequences in the field. As needs in pharma and materials science evolve, we rely not on generic routines, but on grounded, human judgment, built from thousands of hours spent handling this molecule in all its forms.

    Manufacturing this compound has taught us lessons about chemical craft, about the value of direct engagement with customers, and about always keeping an eye out for both problems and opportunities. Our approach combines hard experience, continuous learning, and a stubborn insistence on getting things right, even if it means going the extra mile on a late shift or overhauling a familiar process as demands shift. This is the everyday reality of chemical manufacturing that underlies every drop of 4-Cyano-1-Cyclohexene we send out the door.