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2-Cyclohexen-1-ol

    • Product Name 2-Cyclohexen-1-ol
    • Alias 2-Hydroxycyclohexene
    • Einecs 208-628-2
    • 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

    831467

    Name 2-Cyclohexen-1-ol
    Cas Number 2919-23-5
    Molecular Formula C6H10O
    Molecular Weight 98.14
    Appearance Colorless liquid
    Boiling Point 168-170°C
    Melting Point -74°C
    Density 0.951 g/cm3
    Refractive Index 1.466
    Flash Point 64°C
    Solubility In Water Slightly soluble
    Smiles C1CC=CCC1O

    As an accredited 2-Cyclohexen-1-ol 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 mL of 2-Cyclohexen-1-ol, securely sealed, labeled with hazard symbols and chemical identification.
    Shipping **2-Cyclohexen-1-ol** is shipped in tightly sealed containers compatible with organic solvents, protected from light, moisture, and heat. It should be labeled according to regulatory requirements, with safety data included. During transport, maintain upright positioning, avoid physical damage, and comply with all local and international chemical transportation regulations.
    Storage 2-Cyclohexen-1-ol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from direct sunlight and moisture. Use appropriate, chemical-resistant containers and clearly label them. Store in accordance with local regulations for flammable or reactive organic chemicals.
    Application of 2-Cyclohexen-1-ol

    Applications of 2-Cyclohexen-1-ol in Industrial Manufacturing

    As a direct producer of 2-Cyclohexen-1-ol, we focus on established downstream markets where this specialty raw material is integrated into advanced formulating and synthesis environments. Our production supports sectors with strict compliance demands, verified process controls, and high-value end use, spanning fine chemicals through functional polymers.

    1. Agrochemical Intermediates for Fungicide Synthesis

    Leading agrochemical formulators incorporate 2-Cyclohexen-1-ol as a critical building block during the synthesis of protective fungicide actives, especially those relying on cyclohexenyl structural motifs to disrupt fungal metabolism. Production must address stringent European REACH and China CCPA compliance for traceability and contaminant limits. Process control begins with preliminary esterification or alkylation, followed by precise transformation at the intermediate stage of active compound assembly. Academic work and pilot plant validations have established 2–7% w/w input relative to main-cycle intermediates, subject to target molecule yield optimization or regulatory thresholds for residuals. Continuous monitoring of solvent, temperature, and reactant / by-product flows secures both consistent batch quality and regulatory audit readiness.

    Industry compliance standards

    • EU REACH Regulation (EC) No. 1907/2006
    • China Crop Protection Industry Association (CCPIA) Product Quality Standards
    • OECD Good Laboratory Practice (GLP) for pesticide R&D phases
    • US EPA 40 CFR 180 for pesticide residue limits

    Typical usage ratio

    • 2–7% by weight of the reaction feed, adjusted according to target fungicide structure and process optimization studies

    Downstream process integration

    • Precursor input for multi-step catalytic condensation and functional group modification during the core assembly of fungicidal actives

    Final product types

    • Triazole-based fungicides
    • Strobilurin analog intermediates
    • Cyclohexene-based seed treatment agents
    • Protective spray concentrates for cereal and oilseed crops

    2. Intermediate in Fragrance and Flavor Ingredient Manufacture

    Perfume and flavor houses select 2-Cyclohexen-1-ol as an intermediate for producing aroma molecules, capitalizing on its ability to introduce green, floral, or balsamic notes via oxidation or acetalization. Only suppliers with ISO 9001-certified traceability and compliance to EU Regulation (EC) No. 1334/2008 for flavorings ensure the material enters scalable synthesis for high-volume production lines. Typically, processors convert the alcohol in step one via oxidative or reductive pathways depending on the target. Customer-formulated batch cycles call for 0.5–2.5% by weight depending on intended olfactory impact and compatibility with carrier bases. Each addition undergoes HPLC and GC-MS quality checks before final blending and bottling of concentrate compounds.

    Industry compliance standards

    • EU Regulation (EC) No. 1334/2008 (Flavorings and Certain Food Ingredients Regulations)
    • IFRA (International Fragrance Association) Standards
    • ISO 9001:2015 Quality Management System for flavor and fragrance manufacturers
    • US Food Chemicals Codex (FCC) for flavoring ingredients

    Typical usage ratio

    • 0.5–2.5% w/w in reaction batch, adjusted based on required fragrance intensity or flavor effect

    Downstream process integration

    • Entered during the initial synthesis step, followed by oxidation, acetalization, or cyclization depending on final aroma chemical design

    Final product types

    • Jasmine aroma intermediates
    • Balsamic flavor bases
    • Fine fragrance raw materials for colognes and perfumes
    • Food flavor compound bases for beverages and confectionery

    3. Functional Monomer in Specialty Polymer Synthesis

    Polymer manufacturers leverage the cyclic structure of 2-Cyclohexen-1-ol to introduce controlled flexibility or adhesion features into specialty acrylic and polyurethane prepolymers. Its use demands alignment with ISO 14001 for eco-management and specific toxicology documentation under global GHS and REACH protocols. During batch polymerization, technical managers dose the material at 1–6% w/w relative to the total monomer input, finetuned via pre-reactor trials to balance molecular weight distribution and end-use mechanical targets. Precision feeding ensures downstream extrusion or dispersion steps perform reliably for customer material warranties.

    Industry compliance standards

    • EU REACH Regulation (EC) No. 1907/2006—Substance Registration and Testing
    • ISO 14001 Environmental Management for chemical polymerization
    • Globally Harmonized System (GHS) for chemical safety labeling and handling
    • RoHS (Restriction of Hazardous Substances) for appliance component applications

    Typical usage ratio

    • 1–6% by weight of total monomer charge, dependent on specific chain modification objectives and pre-polymer characteristics

    Downstream process integration

    • Fed into the main polymerization reactor for chain extension, side-group introduction, or crosslink control in base resin formation

    Final product types

    • Pressure-sensitive acrylic adhesive bases
    • Functionalized polyurethane coatings and sealants
    • Responsive hydrogels for technical textiles
    • Elastomeric shoe sole compounds

    4. Pharmaceutical Intermediate in Cardiovascular Drug Synthesis

    Pharmaceutical synthesis routes for select antihypertensive and antianginal agents use 2-Cyclohexen-1-ol as a starting material for constructing saturated or unsaturated nitrogen heterocycles, subject to strict cGMP controls and pharmacopeia monographs. Production managers rely on tight raw material QC under USP and Ph. Eur. guidelines for identification and purity. Dosing is tightly controlled, typically 0.8–3% by mass in the intermediate stage, with variations reflecting target molecule scale and yield step-up requirements. All critical process phases—including Grignard reaction or reductive amination—require full traceability and released batch records prior to active substance isolation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) and European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • WHO GMP Certification for API production sites
    • FDA 21 CFR Part 210/211 for finished pharmaceutical products

    Typical usage ratio

    • 0.8–3% by mass of batch input at designated intermediate construction stage, adjusted per in-process analytical outcomes

    Downstream process integration

    • Prepared in the synthesis suite during heterocycle backbone assembly, often via Grignard, alkylation, or bridge-building steps feeding into core drug structures

    Final product types

    • Calcium channel blocker intermediates
    • Beta-blocker key starting materials
    • Cyclohexene-based secondary pharmaceutical intermediates
    • Stable salts of antianginal APIs
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    Certification & Compliance
    More Introduction

    2-Cyclohexen-1-ol: Insights From the Production Floor

    Our Experience with 2-Cyclohexen-1-ol

    As chemical manufacturers, we spend much of our time looking for subtle differences in otherwise similar molecules. It’s these differences that create value for a formulator, a plant engineer, or a team with strict requirements. With 2-Cyclohexen-1-ol – also known by its CAS 822-67-3 and the formula C6H10O – we’ve learned through years of synthesis and quality control that this material has a unique place among cyclohexene derivatives. Through careful selection of raw materials, controlled reaction conditions, and stringent purification, we work to produce this product at a consistent standard so it can meet a wide range of end-user needs.

    Specifications Stem From Practical Demands

    2-Cyclohexen-1-ol appears as a clear, colorless to slightly yellow liquid under most storage conditions. Our standard produces a purity exceeding 98%. Small amounts of water and related cyclohexenols can develop if improper distillation occurs, but regular gas chromatography separates genuine product from unwanted side products. Boiling point centers around 158-162°C at atmospheric pressure, and care during transfer or blending prevents contamination by more volatile or less stable species. Our plant invests in glass-lined reactors and stainless-steel transfer lines to preserve integrity batch after batch.

    Because this substance is a sensitive intermediate, we track peroxides and aldehyde impurities closely. On the shop floor, alarms for temperature hikes or lean nitrogen purges alert us long before natural degradation becomes a risk. A well-maintained storage drum, fitted with nitrogen headspace, extends shelf life for months. Lighter oxygenates and tars, if detected, are quickly traced back and removed at source. Our operators know the odor shifts dramatically if contamination creeps in, so quality assurance remains a hands-on, real time effort.

    Key Uses in Manufacturing and Formulation

    Daily, our shipping dock sees outgoing drums bound for customers synthesizing pharmaceuticals, fragrances, agrochemicals, and specialty polymers. 2-Cyclohexen-1-ol’s value lies in the dual presence of an alcohol and an alkene group. This lets chemists modify it at either site depending on their needs. For example, acylation of the alcohol group can create building blocks for pheromones and insecticides. Hydrogenation yields cyclohexanol, a staple precursor for plastics, coalescents, and resins.

    Thanks to its reactivity, production teams often use enol forms directly in Diels-Alder reactions or further oxidize it to cyclohexenone—an important intermediate found in vitamin synthesis and certain anti-inflammatory agents. Laboratories that demand consistent color and low aldehyde impurity see better results with fresh, carefully monitored material than with off-the-shelf stocks prone to instability.

    Perfumery often explores this alcohol for its green, slightly floral nuances, contrasting with the more intense notes from aromatic alternatives. Synthetic pathways for natural product analogues benefit from the predictable reactivity profile offered by unadulterated 2-Cyclohexen-1-ol. Years of customer feedback make it clear: ease of downstream chemistry improves dramatically with tight controls at the synthesis stage.

    Learning from User Experience: Why Consistent Quality Matters

    Technical departments call us directly when slight variations in impurity levels affect the performance of their R&D batches. If much odor or color change shows up in a delivered drum, it suggests either unexpected side reactions or exposure during filling. Our design of closed, inerted transfer systems grew out of these conversations, not from any textbook recommendation. Most common complaints don’t relate to theoretical properties, but to real-world challenges like poor long-term storage or batch-to-batch variability.

    On the production side, we pay close attention to drying and deoxygenation steps. Even subtle lapses can introduce peroxides, which occasionally trip up new operators who grew too comfortable with automatic process controls. A senior technician once pointed out that a mere 0.05% water pickup altered reactivity in downstream pharmaceutical syntheses, so now new hires start on batches with high traceability so any slip is caught early. Consistency comes from experience and humility, not from a process flowchart.

    How 2-Cyclohexen-1-ol Differs from Other Cyclohexenols and Cyclohexanols

    Chemically, 2-Cyclohexen-1-ol occupies a distinct spot between saturated and unsaturated cyclohexyl alcohols. Cyclohexanol (fully saturated) offers stability but lacks the reactive diene needed for advanced synthetic steps. On the other hand, cyclohex-2-enone brings a more pungent odor and increased sensitivity to oxidation—challenging for anyone without air-free facilities.

    Our technical contacts report that 2-Cyclohexen-1-ol provides an optimal balance: it resists rapid decomposition yet remains reactive enough for selective functionalization. It avoids the instability associated with phenolic or conjugated enol forms, while outperforming pure alkanols on reactivity and versatility. For bulk manufacturing—where minor process inefficiencies multiply—differences like lower volatility, lower peroxide formation, and fewer regulatory constraints translate to smoother plant operation and reduced risk.

    We find its viscosity and surface tension fit well into blends requiring good miscibility with aromatics and aliphatics alike, something not always possible with more highly substituted congeners. This makes it suitable for specialty ink vehicles, semi-volatile carrier solvents, and controlled-release encapsulation, where both evaporation rate and interaction potential matter more than headline chemical descriptions.

    Troubleshooting and Overcoming Challenges in Real-World Production

    Unlike commodity solvents, the synthesis of 2-Cyclohexen-1-ol demands nuance. High-pressure hydrogenations and selective reduction steps can yield differing ratios of isomers if not managed skillfully. We trained our staff not to rely solely on automated sampler readings—olfactory and visual checks have stopped bad batches from leaving the plant more than once.

    Once, an operator flagged a shift in refractive index, despite all purity metrics reading within specification. Investigation traced it back to a raw material drum left exposed in summer heat, catalyzing formation of byproduct tars. Now, all critical raw stocks arrive on temperature-logged trucks, and storage depots come equipped with alarms for sudden ambient swings. These kinds of real-world challenges rarely show up on product bulletins, but they define success for anyone moving from lab scale curiosities to hundred-kilogram lots.

    Another lesson—users working in fine fragrances have different demands than those in bulk chemical synthesis. Trace aromatic contamination might go unnoticed by a plastics line, yet it spells disaster for a perfumery customer where pure note delivery drives product acceptance. We now tag every drum for batch history, including subtle odor or color notes, so a formulator can anticipate surprise changes before they waste valuable time or raw material.

    Our lab began offering hands-on training with every new outlet—sharing not just data but anecdotes from years of mishaps and improvements. Collaborating with end users gave us the motivation to revise protocols each season to match evolving regulatory or process expectations.

    End-User Applications: Where Fine Tuning Matters

    Manufacturers making pharmaceuticals often ask for the lowest possible metal content and ultra-low water. Our distillation lines use advanced separation columns and multiple freeze-drying cycles to reach technical targets. Research departments in agrochemical firms request drums with trace impurity profiling, so they can optimize catalytic studies for new herbicide pathways.

    Polymer scientists have taught us that even minimal color bodies, invisible in lab assays, can taint a blend’s end-use clarity in transparent plastics. By building trace-impurity libraries and archiving samples from every run, we let customers calibrate expectations for their unique downstream processes, not just off-the-shelf uses. Decades of data allow us to spot trends long before formal recalls or product re-certification become necessary.

    We’ve seen large improvements in customer satisfaction after inviting visiting technicians to audit our lines directly. Letting users compare analogues side by side—pure 2-Cyclohexen-1-ol against related isomers—translates theory into tactile feedback and sharpens everyone’s sense for what matters in daily production. Labs unfamiliar with these details sometimes struggle to scale up reliably, so we offer not just raw product but shared experience drawn from our own development history.

    Continuous Improvement and Ethical Responsibility

    In recent years, attention to sustainability and compliance inspired us to overhaul both material sourcing and energy management systems. Our procurement teams look past lowest-cost sources, focusing on suppliers with proven records of environmental and social good practices. All waste processing routes meet local and international guidelines, with direct oversight from both operations and regulatory staff.

    From the earliest design stage, we plan for closed-loop waste capture and recovery, minimizing emissions from purifications and storage. Instead of relying exclusively on batch sampling, we implement real-time monitoring across all critical stages, feeding data to an archive accessible by quality and compliance teams simultaneously. This network of transparency shortens response time if a deviation occurs—and builds trust with downstream buyers who need to certify product origins.

    Human experience shapes every aspect of our operation. From hands-on training to regular audits and ethical procurement, our approach arises from continual adaptation, not from fixed blueprints. As a team, we remember the lessons learned from unforeseen process challenges, batch deviations, and direct feedback from users. All these elements turn a specialty chemical like 2-Cyclohexen-1-ol from a theoretical reagent into a reliable workhorse supporting creative work in pharmaceuticals, agriculture, flavor, and material science.

    Why Real Manufacturing Experience Matters

    The world of specialty chemicals grows more dynamic and demanding year after year. Recipes shift, process windows tighten, and regulatory obligations expand. As a manufacturer, our responsibility lies not just in making a product that tests well at dispatch, but in supporting the ambitions, safety, and creativity of the customers who rely on us. 2-Cyclohexen-1-ol’s quality only carries value if backed by visible process vigilance, acceptance of feedback, and openness to improvement—traits rooted in decades on the factory floor.

    Our perspective on 2-Cyclohexen-1-ol stems from long hours among reaction vessels, filtration units, and the sharp eye of a technician who’s seen chemical production at every scale. The stories we share with users, from dealing with trace impurities to preventing runaway reactions, help both sides anticipate surprises and deliver better science. The future of this molecule depends less on theoretical purity figures than on practical reliability, transparent communication, and a shared commitment to excellence.