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1,3-Cyclohexadiene

    • Product Name 1,3-Cyclohexadiene
    • Alias 1,3-Cyclohexadiene;1,3-CHD
    • Einecs 202-898-2
    • 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
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    Specifications

    HS Code

    855754

    Name 1,3-Cyclohexadiene
    Cas Number 592-57-4
    Molecular Formula C6H8
    Molar Mass 80.13 g/mol
    Appearance Colorless liquid
    Density 0.857 g/mL at 20°C
    Melting Point -44.5°C
    Boiling Point 80°C
    Refractive Index 1.4860 at 20°C
    Flash Point -11°C (closed cup)
    Solubility In Water Insoluble
    Vapor Pressure 66 mmHg at 25°C
    Autoignition Temperature 430°C
    Pubchem Cid 10448
    Structure Cyclohexene ring with two double bonds at positions 1 and 3

    As an accredited 1,3-Cyclohexadiene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500 mL amber glass bottle labeled "1,3-Cyclohexadiene," tightly sealed, with hazard symbols and safety information clearly displayed.
    Shipping 1,3-Cyclohexadiene should be shipped as a hazardous chemical, classified as flammable liquid (UN 2048). Transport in tightly sealed containers, kept upright and protected from physical damage. Ensure containers are properly labeled, and comply with relevant regulations, such as DOT and IATA. Store and ship away from ignition sources, heat, and incompatible materials.
    Storage 1,3-Cyclohexadiene should be stored in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Store in a tightly closed, amber glass container to prevent light-induced degradation. Keep away from direct sunlight and moisture. Ground and bond containers during transfer to avoid static discharge, and use appropriate chemical safety procedures.
    Application of 1,3-Cyclohexadiene

    Applications of 1,3-Cyclohexadiene in Industrial Manufacturing

    We supply 1,3-Cyclohexadiene directly to global manufacturers as a key intermediate in chemical synthesis. Our commercial expertise ensures integration along well-established, regulation-driven value chains. The application scenarios below detail authentic industrial usage in downstream processing, including precise compliance standards, formulation data, and common product outcomes. We do not offer for undeveloped or unregulated uses.

    1. Polymerization Intermediate for Resins and Specialty Plastics

    In resin and specialty plastics production, 1,3-Cyclohexadiene acts as a diene monomer for cyclopolymerization and co-monomer modification processes. It enhances flexibility and impact resistance in cycloaliphatic resin matrices, and supports molecular weight control. Manufacturers employ it in the synthesis of flexible electronic encapsulants and specialty packaging films—often requiring tight upstream purity control and process traceability. Formulation adjustments depend on desired polymer properties and compliance targets for specific sectors.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • RoHS Directive 2011/65/EU for electronics applications
    • ISO 9001:2015 quality management for resin manufacturers
    • UL 94 flammability certification for polymer electronics casing

    Typical usage ratio

    • 5–18% by weight as a monomer or co-monomer, adjusted according to targeted hardness and film performance; higher ratios for elastomeric films, lower for rigid resins.

    Downstream process integration

    • Introduced during the initial monomer feed prior to catalytic polymerization, supporting ring-opening or Diels-Alder synthesis steps; real-time spectral QC ensures feedstock consistency.

    Final product types

    • Flexible printed circuit encapsulants
    • Specialty food-contact packaging films (non-FDA, industrial grade only)
    • Elastic resins for automotive trim
    • Impact-resistant tool housings

    2. Cycloaliphatic Amine Synthesis for Epoxy Hardeners

    Chemical manufacturers use 1,3-Cyclohexadiene in the reductive amination route to high-purity cycloaliphatic amines, which serve as epoxy resin hardeners and crosslinkers. Its high reactivity under catalytic hydrogenation and subsequent amination enables precise control over amine structure and purity, especially for coatings and electronics encapsulation. Industrial production lines rely on stringent hazard management and environmental controls for amination reactions.

    Industry compliance standards

    • IEC 61249-2-21 halogen-free standards for PCB encapsulants
    • ISO 14001:2015 environmental management in amine manufacturing
    • GHS classification and labeling for hazardous intermediates
    • EN 71-3:2019 for limits of migration in painted toys (where applicable)

    Typical usage ratio

    • 10–22% by mole relative to total feedstock in amination, varying with desired hardener chain length and crosslinking density in end-use formulations.

    Downstream process integration

    • Fed to pressure reactors for direct hydrogenation, followed by amination and purification; purity assessed by GC–MS and moisture titration before hardener blending.

    Final product types

    • Cycloaliphatic amine hardeners for two-component epoxy adhesives
    • Electronic-grade potting compounds
    • Solventless coating crosslinkers
    • UV-curing agent intermediates

    3. Agrochemical Intermediate for Crop Protection Synthesis

    1,3-Cyclohexadiene serves as a starting backbone in the synthesis of certain selective herbicides and fungicides, particularly those utilizing hydrogenated cyclic structures. Its scaffold supports multi-step transformations including selective halogenation, oxidation, and heterocycle fusion. Downstream synthesis lines configure catalytic processes to ensure reproducibility for large agricultural runs, with strict in-process verification to meet regulatory residue and impurity thresholds.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical material
    • Regulation (EC) No 1107/2009 for plant protection product approval
    • OECD Test Guidelines for agrochemical residual analysis
    • ISO 17025 laboratory accreditation for batch release testing

    Typical usage ratio

    • 0.5–4% by batch weight in precursor stage, increased for more highly cycloaliphatic product requirements; exact ratio optimized based on targeted bioactivity and downstream conversion efficiency.

    Downstream process integration

    • Charged as a key intermediate in continuous-flow synthesis units before cyclization, halogenation, or condensation steps; monitored by HPLC and NMR for structural confirmation.

    Final product types

    • Cyclohexyl-derived selective herbicides
    • Fungistatic agents for seed treatment formulations
    • Plant growth regulator intermediates
    • Stabilizer molecules for controlled-release agroformulations

    4. Fragrance Intermediate in Aromatic Derivative Synthesis

    For the fragrance manufacturing sector, 1,3-Cyclohexadiene provides a cycloaliphatic core for musk and woody note molecules via partial hydrogenation and functionalization. Synthesis typically involves conversion to alcohol, aldehyde, or ketone functionalities, with fine distillation and crystallization demanded for perfumery quality. Fragrance customers require rigorous lot traceability and conformance with IFRA guidelines due to sensitivity to allergens and volatile impurities.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards for ingredient safety
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 9235:2013 (Aromatic natural raw materials)
    • Good Manufacturing Practice (GMP) for cosmetic ingredient supply

    Typical usage ratio

    • 1.5–10% of fragrance base by mole in precursor synthesis; range tailored to target final aroma intensity, volatility, and regulatory residue limits.

    Downstream process integration

    • Employed at the aromatic skeleton formation stage, followed by stepwise oxidation or alkylation, purification by fractional distillation, and final blending before bulk delivery.

    Final product types

    • Musk fragrance intermediates (e.g., cyclohexyl derivatives)
    • Woody aroma molecules for fine perfumery
    • Top-note ingredients for detergents and fabric softeners
    • Functional bases for high-end personal care fragrances

    5. Fine Chemical Intermediate for Pharmaceutical Synthesis (Non-API)

    1,3-Cyclohexadiene acts as a precursor for pharmaceutical intermediates where cyclohexyl scaffolds are required. Typical applications include synthesis of advanced intermediates for antihypertensive or anti-inflammatory agents through controlled hydrogenation and selective functionalization. Commercial production requires compliance with pharmaceutical GMP and detailed impurity control, although the diene itself does not become part of finished APIs. Manufacturers value consistent supply and analytical documentation to meet contract manufacturing audits.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • EU GMP Part II for excipients and intermediates
    • USP–NF designation for starting materials (where applicable)
    • 21 CFR Part 210/211 for GMP records in US pharma manufacturing

    Typical usage ratio

    • 2–7% by moving charge kilogram in hydrogenation or cyclization steps; precise values adjusted for downstream scale and impurity pathway minimization.

    Downstream process integration

    • Loaded in early-stage reactors for partial hydrogenation, ring-functionalization, and subsequent handover to API synthesis units; batch consistency and impurity profiles confirmed by HPLC and GC–MS before onward transfer.

    Final product types

    • Advanced intermediates for antihypertensives
    • Non-API synthetic building blocks for small-molecule drug lines
    • Chiral auxiliaries in stereoselective synthesis
    • Reference standards for pharmaceutical R&D
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    Certification & Compliance
    More Introduction

    1,3-Cyclohexadiene: Understanding the Character and Capability of a Core Intermediate

    Roots in Real-World Chemical Production

    Decades of manufacturing experience have taught us that certain molecules become quietly indispensable in industrial chemistry. 1,3-Cyclohexadiene stands out because of its unique position on the production floor and in the lab. The molecule’s six-membered ring and two conjugated double bonds give it characteristics that separate it from both simple olefins and aromatic hydrocarbons. As a liquid intermediate, 1,3-cyclohexadiene opens up pathways to value-added products in both specialty and bulk chemical operations.

    Specifications Grounded in Day-to-Day Operations

    We have spent years refining our 1,3-cyclohexadiene synthesis streams. The product rolls off our reactors as a clear, colorless liquid, with purity levels regularly verified by GC to exceed 98%. Most batches measure less than 150 ppm residual benzene and below 0.5% moisture, since trace water or aromatics disrupt subsequent reactions. Density (at 20ºC) ranges between 0.86 and 0.88 g/cm3, and our team confirms every lot’s refractive index before release. By handling each shipment from bulk tank to sealed drum, our technical teams keep contamination risk low and mitigate the hazards tied to diene reactivity.

    Working on site, we see very quickly how the physical properties of 1,3-cyclohexadiene impact downstream processing. The boiling point falls around 80–83ºC at atmospheric pressure, making it volatile enough for classic purification by distillation, but not so low as to require elaborate equipment. Once collected, it remains stable if kept cool and away from reactive agents such as oxygen or peroxides. We always stress continuous nitrogen blanketing and sealed, inert storage to avoid polymerization—a precaution born from actual incidents where small lapses led to batch loss.

    Applications Shaped by the Realities of Synthesis and Scale

    In synthetic chemistry, 1,3-cyclohexadiene supports both niche transformation and high-volume production. On our line, it is most often channeled into Diels-Alder reactions, forming bicyclic and aromatic ring systems that underpin pharmaceuticals, flavors, and agrochemicals. As a diene, it engages rapidly with dienophiles under controlled conditions, yielding products otherwise difficult to obtain directly from benzene or other monocyclic aromatics.

    Refinery chemists and fine chemical manufacturers draw it into hydrogenation loops, obtaining cyclohexene or cyclohexane—key raw materials in nylon and rubber precursor synthesis. The selectivity offered by 1,3-cyclohexadiene saves time and expense versus starting with less reactive cyclodienes. In controlled bromination, the molecule serves as a template for producing di- and tribrominated ring systems, a step not achievable using simple monoolefins or fully aromatic platforms. Each successful application draws on batch-to-batch consistency and the product’s clean profile, attributes gained only by investing in high-integrity reactor operation and steady analytics.

    Comparative Realities: 1,3-Cyclohexadiene Versus Related Feedstocks

    Talk of 1,3-cyclohexadiene in the plant often sparks questions about its relationship to close relatives, such as 1,4-cyclohexadiene, cyclohexene, or benzene itself. Our chemists have worked with all these, and each brings up distinct advantages and limits. Benzene, for instance, remains a bulk commodity and functions as a workhorse aromatic—its planar, fully conjugated π system makes it stable, but nearly inert in reactions aimed at ring functionalization. That means extra steps for dearomatization before new rings or substituents can be added.

    Cyclohexene, containing a single double bond, participates readily in hydrogenation and halogenation, but lacks the same reactivity for cycloaddition chemistry as the 1,3-diene—demanding additional reaction steps or activation. On the other hand, 1,4-cyclohexadiene, while structurally similar, arranges its double bonds to limit the conjugation needed for smooth Diels-Alder transformations. In actual practice, 1,3-cyclohexadiene’s diene system streamlines synthesis where a balance between aromatic reactivity and aliphatic stability is needed.

    Intersection of Safety, Quality, and Practical Handling

    From years of hands-on work, we have learned that 1,3-cyclohexadiene’s safety profile cannot be overlooked. Double bonds present both a targeted opportunity and a challenge, given how easily the molecule reacts with atmospheric oxygen, trace acids, or heat. Our teams take the risk of auto-polymerization seriously. Left unchecked, this risk can block pipes or foul vessels, resulting in costly downtime and expensive cleaning. Factory protocol places every container under a nitrogen blanket from the moment it is filled until it reaches the end user’s line. On the rare occasion where oxygen exposure occurs—a leaky valve or misaligned drum cap—the off-gassing smell and sticky residue signal immediate corrective action.

    For storage and transport, robust steel drums and lined tanks shield the product from heat and UV, keeping it well within its shelf-life. Temperature control, while not elaborate, relies on sound insulation and clear labeling, since even a brief rise in headspace temperature hastens unwanted side reactions. Our in-house engineering teams retrofit existing storage tanks with high-quality inert gas systems, preventing spoilage and maximizing safety for staff across shifts. These investments pay off not on paper, but in straightforward output and strong customer trust.

    Supporting Users in R&D and Manufacturing

    Our experience with collaborative projects has shown the real value of fast, reliable support for formulation chemists and plant engineers. Companies scaling up new pharmaceuticals or agricultural actives need a partner with a pulse on both supply chain realities and the subtle behavior of specialty intermediates. Reproducibility matters—any deviation in purity, or an undetected contaminant, throws off testing and can force expensive repeated trials. We assign specialist technical liaisons who follow each batch through documentation, logistics, and on-site troubleshooting. Their feedback loops back to our production facility, where minute process adjustments get made to prevent the recurrence of even small issues.

    One example from a recent customer keeps coming to mind: a lab-scale Diels-Alder pilot produced consistently poor yields until compositional “noise” in test solvent was traced to exposure from a previously used shipment of lower-purity cyclohexadiene sourced from a different manufacturer. With our product, cleaned-up yields followed—and that project now runs at commercial scale. Experiences like this have made us methodical and transparent about supply and communication, so issues get caught early and handled at the source.

    Molecular Versatility Backed by Real-World Outcomes

    Synthesis workshops have revealed a few key details about the versatility of 1,3-cyclohexadiene, making it a go-to for innovation beyond traditional end uses. In specialty resins and elastomer manufacture, small differences in monomer feedstock can swing product performance by orders of magnitude. By using high-purity diene, operators minimize gel formation and side-reactions, allowing for lighter curing and more predictable crosslinking. This level of control serves researchers experimenting with novel building blocks, as well as process managers eager to reduce downtime.

    Academic labs also turn to 1,3-cyclohexadiene for mechanistic studies, with its reactivity providing a testbed for novel catalytic systems. Spectroscopists enjoy its distinct NMR and IR signatures, while kineticists appreciate its measurable rates in both gas and solution phase transformations. As seasoned practitioners, we have seen requests for isomer-specific samples, isotopically labeled diene, and co-packaged blends rise over the years. Flexibility here depends not just on synthesis, but also on our ability to adapt downstream packaging and quality systems.

    Constraints, Lessons, and Opportunities

    Any industrial producer must grapple with market swings and shifting regulatory targets. We have watched the cycle of 1,3-cyclohexadiene demand rise with new plastics and green chemistry incentives, only to face headwinds during downturns in downstream construction, automotive, or custom synthesis contracts. Feedstock availability, especially in oil-derived systems, impacts price and delivery time in a matter of weeks. Given these pressures, the only sustainable route involves deepening process efficiency, smarter waste reclamation, and redundancy throughout our storage and transport network.

    Regulation in both worker exposure and environmental emission tightens year by year. Investing in fume capture, reclaiming spent wash liquids, and shifting away from single-use containment not only keep us compliant but also sharpen our cost advantage. We participate in regular external audits and independently validate our emissions and effluent profiles. Any breach moves swiftly through our review, not as a compliance checkbox but as a threat to plant credibility. We share remediation steps and technical updates directly with long-term partners and clients, promoting trust built from shared accountability.

    Closing the Loop: People, Product, and Progress

    Above all, working with 1,3-cyclohexadiene for so many years has shaped a straightforward view: every batch matters, every employee’s expertise comes through in the final product, and customer feedback guides our incremental improvements. Whether it’s choosing the right grade for a composite resin or troubleshooting a process hiccup on a tight deadline, only a manufacturer who stays close to the plant floor—and listens to end users—can deliver the quality and support that secure lasting relationships.

    As the chemical industry evolves, the unique reactivity and reliability of 1,3-cyclohexadiene continue to earn it a place in synthesis, scale-up, and high-volume production. We invest in people, process, and transparency to maintain that position. Our commitment rests on firsthand learning, not just written standards or industry norms. Your success in the lab, the pilot plant, or full-scale manufacturing zone becomes our benchmark for improvement—one batch at a time.