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Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane

    • Product Name Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane
    • Alias cis-Hexylhydroxydioxane
    • Einecs 405-040-6
    • 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

    235838

    chemical_name Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane
    molecular_formula C10H20O3
    molar_mass 188.27 g/mol
    appearance Colorless to pale yellow liquid
    boiling_point Estimated ~270°C
    density Approx. 1.01 g/cm3
    solubility_in_water Slightly soluble
    flash_point Estimated >100°C
    CAS_number 60909-27-9
    stereochemistry Cis configuration
    functional_groups Dioxane ring, hydroxyl group
    refractive_index Approx. 1.45
    storage_conditions Store in a cool, dry place
    synonyms cis-2-Hexyl-5-hydroxy-1,3-dioxane

    As an accredited Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane is supplied in a 25g amber glass bottle with a secure, tamper-evident screw cap.
    Shipping Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane should be shipped in tightly sealed containers, protected from light, moisture, and excessive heat. Transport according to local and international regulations for chemicals. Ensure labeling with proper chemical identification and hazard information. Handle with appropriate safety precautions, including secondary containment to prevent leaks or accidental exposure during shipping.
    Storage Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong acids or oxidizers. Keep the chemical away from direct sunlight and sources of heat. Store in an area equipped for chemical storage, following appropriate safety guidelines and labeling for laboratory or industrial chemicals.
    Application of Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane

    Applications of Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane in Industrial Manufacturing

    Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane is a specialized chemical intermediate with performance characteristics valued by diverse industrial manufacturers. As the original producer, we support key markets using this compound in targeted formulations and precision-engineered processes for high-value end products.

    1. Flavor and Fragrance Production

    Producers in the fine chemicals sector utilize this compound for its unique green, slightly fruity aroma character in the synthesis of specialty fragrance ingredients. Formulators add it to complex flavor blends as an intermediate in creating lactone-rich profiles. The material integrates into controlled reactions, supporting selective modification of top-note volatiles and ensuring sensory consistency in mass-market and bespoke fragrances.

    Industry compliance standards

    • IFRA (International Fragrance Association) standards for ingredient traceability and purity
    • EU Regulation (EC) No 1334/2008 on flavorings and certain food ingredients
    • Food Chemicals Codex (FCC) for food-grade aroma applications
    • ISO 9235:2013 for definition and labeling of natural aroma substances

    Typical usage ratio

    • 0.01%–0.2% of total fragrance composition
    • Up to 15% in concentrated aroma intermediates depending on targeted olfactory characteristics
    • Adjustment based on solvent polarity and co-ingredient volatility

    Downstream process integration

    • Added at the reactive blending or compounding stage
    • Employed before distillation in headspace-controlled reactors
    • Purified via fractional distillation prior to final blending

    Final product types

    • Consumer and luxury perfumes
    • Food and beverage flavors
    • Air care formulations
    • Candles and home fragrance systems

    2. Pharmaceutical Chemical Synthesis

    This intermediate supports synthesis workflows in manufacturing active pharmaceutical ingredients and specialty excipients. Its stable dioxane ring and secondary alcohol group allow for strategic modifications in advance steps such as acylation, alkylation, or enzymatic transformation. Process chemists rely on its reproducibility and low impurity profile to ensure consistent batch-to-batch reproducibility in high-purity pharmaceutical manufacturing.

    Industry compliance standards

    • ICH Q7 GMP (Good Manufacturing Practice) for APIs
    • USP-NF (United States Pharmacopeia–National Formulary) for relevant monographs
    • EDQM CEP (Certification of Suitability to European Pharmacopoeia)
    • 21 CFR Part 210/211 US cGMP for finished pharmaceuticals

    Typical usage ratio

    • 0.5–5 mol% as an intermediate, depending on route yield and impurity control
    • Specific ratios dictated by stoichiometry and route optimization studies

    Downstream process integration

    • Introduced during early or mid-step functionalization reactions
    • Subjected to multi-stage purifications including recrystallization and column chromatography
    • Included in multi-step synthesis, followed by hydrolysis and coupling reactions

    Final product types

    • Specialty pharmaceutical intermediates
    • Modified-release matrix excipients
    • Targeted active pharmaceutical ingredients (APIs)
    • Chiral chemical building blocks

    3. Specialty Polymer Additive Manufacturing

    Materials engineers in the polymer industry blend this compound as a niche plasticizer and reactivity modifier in high-performance resins. The dioxane structure and hydrophobic hexyl side chain deliver targeted flexibility and compatibility in copolymer networks. Its use enhances low-temperature processing and imparts specific migration or release characteristics without compromising mechanical integrity or VOC compliance.

    Industry compliance standards

    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • RoHS Directive (2011/65/EU) for restrictions on hazardous substances
    • ISO 9001 quality system in polymer compounding facilities
    • ASTM D638 for mechanical properties of plastics

    Typical usage ratio

    • 0.3%–2% by weight in final polymer blends
    • Evaluated based on flexibility or migration profile targets in end-use testing
    • Larger amounts during masterbatch preparation, diluted at compounding stage

    Downstream process integration

    • Added during extrusion or melt compounding alongside primary polymers
    • Can be pre-blended with co-additives or dispersants
    • Dispersed under inert atmosphere in moisture-sensitive systems

    Final product types

    • Flexible polyurethane foams
    • Specialty polyvinyl chloride (PVC) sheets
    • High-performance adhesives and sealants
    • Elastomeric coatings for automotive or industrial equipment

    4. Agrochemical Synthesis and Formulation

    Technical teams at agrochemical plants select this intermediate for precision synthesis of lactone-based crop protection actives. Its controlled reactivity, enabled by the hydroxy and dioxane functionalities, supports coupling and cyclization reactions fundamental to modern pesticide or plant regulator architectures. It contributes to enhancing formulation stability and improving shelf-life of sensitive active ingredients.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • OECD Guidelines for the Testing of Chemicals
    • ISO 17025 accreditation for agrochemical quality control labs
    • National chemical control regulations (e.g., FIFRA – USA, Regulation (EC) No 1107/2009 – EU)

    Typical usage ratio

    • 1–7% of synthetic reaction mixtures depending on desired product class
    • Adjusted by process mass balance and yield optimization trials

    Downstream process integration

    • Added at the staged coupling or ring formation step in fine chemical synthesis
    • Handled under controlled temperature to maintain functional stability
    • Subjected to post-reaction phase separation and solvent washing steps

    Final product types

    • Systemic fungicides
    • Selective herbicides
    • Plant growth regulators based on lactone derivatives
    • Seed coating agents

    5. Food Additive Intermediate Processing

    Food ingredient manufacturers use this specialty dioxane derivative during synthesis of certain permitted aroma and flavor precursors, particularly for bakery, confectionery, and beverage sectors. Its role as a lactone precursor provides key flavor nuances in heat-aged or enzymatically treated food matrices, enabling formulators to match natural profiles while staying compliant with food safety frameworks.

    Industry compliance standards

    • FDA 21 CFR §172.515 (Synthetic Flavoring Substances and Adjuvants)
    • EU Regulation (EC) No 1333/2008 on food additives
    • Codex Alimentarius Standard 192-1995 for food additives
    • ISO 22000:2018 Food Safety Management Systems

    Typical usage ratio

    • 0.01–0.05% of targeted food additive preparations
    • Subject to maximum allowed limits in finished foods; levels set by sensory evaluation and regulatory exposure assessment

    Downstream process integration

    • Participates in enzymatic or thermal cyclization steps in food additive synthesis
    • Purified by aqueous extraction and vacuum distillation before QC release
    • Stabilized by adding natural antioxidants prior to blending in finished flavor bases

    Final product types

    • Compound food flavor bases
    • Aroma ingredient concentrates for bakery fillings
    • Beverage and dairy flavor top-notes
    • Specialty functional food ingredients

    6. Fine Chemical Building Block for Specialty Surfactants

    Formulation chemists incorporate this raw material as a hydrophobic-hydrophilic balance contributor in custom surfactant synthesis. Its dioxane core and secondary alcohol functional group make it suitable for ring-opening processes or unblocking reactions, modifying surface activity in non-ionic surfactant molecules designed for demanding cleaning, textile, or emulsion applications.

    Industry compliance standards

    • REGULATION (EC) No 648/2004 on detergents and surfactants
    • ISO 14001 Environmental Management Systems for chemical sites
    • ASTM D4265-14 for surfactant solutions
    • OECD Test Guidelines for surfactant biodegradability

    Typical usage ratio

    • 1–5% of the total surfactant batch
    • Adjusted during pilot scale according to desired hydrophobic-lipophilic balance and CMC targets

    Downstream process integration

    • Dosed during the surfactant reaction phase, especially for non-ionic variants
    • Mixed with ethoxylation or propoxylation agents under controlled pH
    • Purified from by-products via phase separation techniques

    Final product types

    • Technical cleaning agents
    • Emulsion polymerization aids
    • Textile processing surfactants
    • Specialty foaming agents for industrial applications
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    Certification & Compliance
    More Introduction

    Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane: Real-World Insights from the Production Floor

    Introduction to Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane

    At our manufacturing facility, our day-to-day focus stays grounded in the realities of chemical synthesis. Among the specialized cyclic acetals that pass through our reactors, Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane stands out. This molecule first earned its place in our lineup as chemists began demanding an acetal with an unbranched, midchain hexyl group and a secondary alcohol function. Its structure delivers more than predictable stability; the combination of the cis orientation and six-carbon chain brings interesting characteristics to several niche markets. We developed this model through a sequence of acetylation, cyclization, and subsequent hydrolysis, results of plenty of iterative trials and process scrutiny.

    Specifications and Characterization

    In production, consistency separates a research curiosity from a reliable specialty chemical. Our Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane meets a minimum purity of 98%, with most batches reaching higher, as measured by GC-MS and NMR. Impurity profiling isn’t simply a box-checking exercise; decades in the field taught us small variations in process parameters―such as reaction temperature curves or phase separation times―make the difference between high-performance material and out-of-spec waste. Analytical patterns for this compound show clear singlets for the acetal ring hydrogens, and the secondary alcohol’s proton is distinct, letting us spot deviations early.

    We ship Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane as a colorless or nearly colorless liquid, sometimes with a faint ester-like aroma depending on the micro-oxidation state. Standard packaging involves HDPE drums sealed under dry nitrogen; for research quantities, we rely on amber glass. Each drum includes a certificate of analysis confirming both chemical identity and residual solvent content. Downstream customers in odorous synthetics or pharmaceutical intermediates expect clarity and reproducibility, so we run comparison checks against industry benchmarks with every lot.

    Practical Uses: Where Performance Outweighs Theory

    Our main customers learned long ago that lab experiments do not always translate to production reliability, particularly when scaling flavor, fragrance, or intermediate synthesis. Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane does not belong to the commodity chemicals found in bulk shipments; its value emerges in applications where minor molecular differences mean measurable impacts on end results.

    In fragrance engineering, a single molecule can help balance complex bouquets or fix fleeting notes. The hexyl group here imparts both substantive and diffusive character, while the cis configuration assists with thermal stability in formulations that run through hot oil baths or distillation columns. We have seen perfumers combine this acetal with green, grassy aldehydes to produce long-lasting, crisp top notes that carry through even persistent fragrances. By adjusting batch purity, we ensure that residual aldehydes and ketones do not muddy olfactory profiles.

    Outside the realm of scent, our pharmaceutical clients integrate Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane in multi-step syntheses, sometimes as a protected form for unstable carbonyl intermediates. Typical acetals often fail under acidic or basic workups; here, the five-membered dioxane ring holds together, minimizing unintentional hydrolysis and improving overall yield. In a hands-on sense, our quality team maintains close communication with process chemists at customer sites, troubleshooting whenever process scale-up reveals unexpected side reactions. Exchange of spectral data, minor procedural tweaks, or even advice on solvent choice can reduce delays that cost clients real money.

    Comparing to Similar Compounds: What We See on the Production Side

    Real experience with a full range of 1,3-dioxane derivatives brings perspective. If you consider simple 1,3-dioxanes or those with branched alkyl substituents, the differences become clear both at the reactor and in the finished product. For example, we used to generate 2-ethyl-5-hydroxy-1,3-dioxane variants for smaller projects. Analysis showed branched side chains brought increased volatility and, sometimes, a tendency to exude unwanted by-products on standing.

    Linear, mid-chain hexyl substituents do more than extend lipophilicity—they alter both reactivity in subsequent syntheses and partition coefficients, which directly affect blending with oils, alcohols, or complex esters. Many customers, especially in fine fragrance bases, reported noticeably longer shelf life, less discoloration, and more consistent volatility when switching to Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane in their mixtures.

    Comparisons to trans isomers reveal other advantages. We have investigated both cis and trans forms under identical storage and processing conditions. The cis isomer tends to show greater physical stability, causing fewer precipitation or crystallization problems where strong cis interactions help keep the molecule dispersed at typical usage concentrations. If you plan to substitute with a trans analog, you may need to accept a shorter timeframe to process or risk batch rejection due to solids formation. Both options remain technically available, but process feedback from decades of contract manufacturing convinces us—cis offers more predictability in complex, performance-sensitive formulas.

    Downstream Handling and Processing Experience

    Part of our role as a manufacturer involves direct troubleshooting with users; some requests land in our technical support inbox at all hours. End users often underestimate the handling quirks of specialty acetals, especially cis-2-Hexyl-5-Hydroxy-1,3-Dioxane. Solubility shifts in mixed solvent systems or undesired phase separation can cut yield or foul equipment, facts only appreciated after running full-scale blends. Cold weather handling or prolonged storage can sometimes induce partial crystallization. For this reason, we document optimal storage above 18°C and advise gentle warming with mixing if haze develops in drums left static for many months.

    Commercial blenders seeking to emulsify this molecule into oil or alcohol matrices often need to tune pH and monitor for trace water or adventitious acids that would promote unwanted ring opening or reversion to aldehydes. We recommend a basic dryness check and tight control of all container surfaces. Our on-site blending specialists have run stability panels in both micro- and macro-lots, real tests that beat simple bench chemistry, simulating warehouse and transport cycles.

    In manufacturing, good process hygiene pays dividends. Tanker-to-kettle lines require passivation with non-reactive fluids, and exhaustive flushing routines clear out residuals from prior runs. The acetal ring here resists most casual hydrolytic breakdowns, but years of experience tell us no specialty molecule benefits from cross-contamination. Regulatory traceability forms the backbone of our documentation, letting downstream users link every drum to a well-defined process history. We maintain ready access to full synthesis trace analytics to satisfy both internal audits and customer inspections.

    Safety, Environmental, and Regulatory Factors from a Manufacturer’s Perspective

    Working daily with Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane means living with its challenges, both technical and regulatory. Our operators receive hands-on briefings about the irritant properties and the solvent-handling precautions in real warehouse and blending bay conditions. Common scents in the production area often include reminders: this chemical, while low in acute hazard, can irritate mucous membranes or the upper respiratory tract at higher vapor concentrations, particularly in enclosed spaces. Gloves, splash goggles, and local exhaust ventilation lessen everyday issues and support long-term safety compliance.

    Environmental stewardship matters, since some fraction of every production run may end as off-spec or rinse waste. Our facility adheres strictly to industry wastewater guidelines, capturing and neutralizing process stream residues prior to biological treatment. Real efforts go into closing the process loop, lowering both water and atmospheric releases. Analytical monitoring, not just paperwork, reinforces our commitment; we regularly check effluent levels and vapor stack losses via on-site gas chromatography, well above basic permit documentation.

    Challenges of Scale: What Mass Production Teaches

    Scaling Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane production from kilogram trials to full multi-ton runs always reveals new hurdles. It’s easy to overlook subtle impurities at bench scale; one batch that failed a pharmaceutical client’s QC showed how minor contamination, undetectable in earlier pilot runs, created a persistent off-odor. We learned to monitor aldehyde carry-over with sharper focus, leading to process upgrades and tighter supplier quality standards for solvents and reagents.

    Ongoing collaboration with equipment suppliers made a major impact. Our batch reactors operate under programmable controls that track temperature, pressure, and pH in real time, but equipment wear and tear remains a daily concern. Decades of operation prove that mechanical reliability equals product consistency; materials of construction must resist both acid wash and organic solvents, especially in impeller and seal areas. Maintenance crews routinely review lines, and we rotate stock to prevent any risk of contamination from corroded connections, an issue seen too often in less-established plants.

    Feedback Loops: Learning from Users and Adjusting Production

    Direct lines to customers create a constant feedback loop. Fragrance houses and pharmaceutical labs send us complaints and praise alike. Several years ago, a run of dioxane batches held marginally higher water content, and customers responded quickly with data on solubility shifts and changes in finished goods. These reports drive continuous improvement; we adjust drying protocols, modify storage atmospheres, and revise leak testing for every outgoing drum.

    Celebrating successful partnerships matters as much as fixing mistakes. One major wine flavoring producer reported a clear jump in long-term aroma persistence after shifting their base from a trans analog to our cis-hexyl product, attributing less seasonal batch-to-batch drift in the end formula. Transparent communication, backed with clear analytical evidence, turns these trials into lessons for both sides, building trust and refining overall process efficiency.

    Market Shifts and New Demands: Staying Ahead with Flexible Manufacturing

    The demand for Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane shifted regularly over the past decade. Downstream regulatory changes, such as new REACH requirements or updates in IFRA guidelines, prompted internal revisions in synthesis and quality protocols to keep end products sellable in global markets. Where some molecules faced outright restriction, thorough documentation and analytical validation of every contaminant helped keep our lots compliant. We retain digital batch records and scan for emerging contaminants, including trace catalysts or unexpected breakdown products, long before new rules demand them.

    Sometimes seasonal swings in demand, triggered by a new trend in fine perfumery or a change in pharmaceutical intermediate lists, forced us to flex batch sizes on short notice. Our reactors, designed for both short-run and continuous operation, let us meet sudden volume spikes without falling into the quality dips that plague so much line switching. Years in business taught us the cost of turning down high-quality repeat orders far outweighs the extra effort required to support emergent projects or custom syntheses.

    Technical Evolution: Updates to Processes and Instrumentation

    Continuous improvement underlies our approach to Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane production. Chemists and engineers collaborate on process updates, implementing incremental changes in reagents, catalysts, and purification methods based on both data and hands-on shopfloor feedback. Bringing in new analytical techniques such as advanced NMR or rapid GC-MS allowed us to spot column bleed, unreacted starting materials, and trace by-products more quickly. Investment in more precise temperature and pressure monitoring at every stage reduced off-spec rates by double-digit percentages across critical production windows.

    Scaling these technical advances across the facility does not happen overnight; we train operators and QA analysts on every new protocol, keeping process documentation current and emphasizing real situational awareness over rote compliance. Technical meetings allow direct discussion of both quality failures and success stories, allowing continuous adaptation to meet evolving customer requirements.

    Concluding Thoughts on the Value of a Specialist’s Molecule

    Not every chemical manufactured at scale receives the same care and scrutiny as Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane. The effort poured into synthesis, purification, and analytical confirmation reflects both external market pressure and our internal culture of pride in production. This molecule represents a point where precise chemistry, knowledgeable operators, and close customer relationships intersect—creating a product that holds real value in its consistency and specificity.

    Many competitors could offer a nominally similar compound on paper, but what sets ours apart is the rigor and transparency rooted in decades of manufacturing culture. Every drum tells the story of process improvement, equipment maintenance, and continual feedback with the end user community. Our commitment extends beyond routine supply; we invest in understanding evolving technical requirements, responding to unforeseen issues, and sharing best practices developed through long-term experience on the chemical production floor.

    Invitation for Collaboration

    Whether you approach us as a R&D chemist looking for reliability in small pilot batches, or as a high-volume customer with strict process parameters, our history with Cis-2-Hexyl-5-Hydroxy-1,3-Dioxane supports both technical complexity and operational dependability. If you need integration advice, troubleshooting help, or even co-development of custom derivatives, our technical team engages at the level that today’s specialty chemical market demands. Our process extends far beyond the drum and keeps you a phone call away from the people who actually make the molecule, not just move it.