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4-Hexyloxyphenol

    • Product Name 4-Hexyloxyphenol
    • Alias 4-(Hexyloxy)phenol
    • Einecs 307-636-2
    • 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

    730968

    Chemical Name 4-Hexyloxyphenol
    Molecular Formula C12H18O2
    Molecular Weight 194.27 g/mol
    Appearance White to off-white solid
    Cas Number 40286-39-7
    Melting Point 70-74°C
    Boiling Point 336.9°C at 760 mmHg
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.045 g/cm3
    Structure Phenol ring substituted at para position with a hexyloxy group
    Synonyms 4-(Hexyloxy)phenol, p-Hexyloxyphenol
    Pubchem Cid 175428

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

    Packing & Storage
    Packing The 100g of 4-Hexyloxyphenol is packaged in an amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 4-Hexyloxyphenol is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. The packaging complies with applicable safety regulations, protecting the chemical from light and moisture. During transit, containers are clearly labeled with hazard information, and shipping follows all local, national, and international guidelines for safe chemical transportation.
    Storage 4-Hexyloxyphenol should be stored in a tightly sealed container, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area. Ensure the storage area is equipped to contain spills, and label containers clearly. Avoid exposure to moisture and handle in accordance with standard chemical safety protocols.
    Application of 4-Hexyloxyphenol

    Applications of 4-Hexyloxyphenol in Industrial Manufacturing

    As a specialized manufacturer of 4-Hexyloxyphenol, we deliver this high-purity phenolic compound for advanced industrial production. With established performance in precise reaction systems, our material supports downstream processors in several regulated markets. Below are key application scenarios based on authentic industry adoption, reflecting best practices in process control and compliance.

    1. UV Absorber Intermediates for Polymer Additives

    Producers of high-performance polymer additives use our material as an intermediate in the synthesis of advanced UV absorbers. Its molecular structure permits targeted alkylation and etherification steps, enhancing UV stability in polyolefins, engineering plastics, and coatings. Accurate weighing and continuous mixing are critical for quality outcomes. Final product consistency depends on qualified raw input and inline analytical monitoring.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • ASTM D5204 for polymer additives
    • ISO 9001:2015 certified quality management systems
    • RoHS Directive 2011/65/EU (for electronics plastics)

    Typical usage ratio

    • 0.5%–5% in intermediate reaction mass (adjustable by UV absorption requirements and polymer base stability)

    Downstream process integration

    • Direct addition at the stage of phenol etherification during UV absorber synthesis
    • Inline blending with other functional group donors for targeted product profile
    • Final purification by distillation or crystallization post-reaction

    Final product types

    • Hindered amine light stabilizers (HALS)
    • UV absorbers for automotive coatings
    • Light-stabilized polypropylene resins
    • High-durability outdoor polycarbonate panels

    2. Specialty Pigment Synthesis for Printing Inks

    Ink manufacturers incorporate our phenolic compound as a tailored coupling agent or stabilizer in synthetic pigment production. The molecular scaffold aids dispersion, tint strength, and stability in pigment particles developed for demanding graphic and packaging applications. Compliance with food-contact regulations is essential for inks used in packaging. Production lines utilize controlled batch feeds for precision color consistency.

    Industry compliance standards

    • EN 71-3:2019 Safety of toys – migration of certain elements (food packaging inks)
    • ISO 2846 series for printing ink characterization
    • FDA 21 CFR 175.300 (indirect food additive regulations for coatings)
    • Good Manufacturing Practices (GMP) for printing ink production

    Typical usage ratio

    • 0.3%–1.2% by total pigment batch weight (modulated by pigment type and required particle size)

    Downstream process integration

    • Inserted during aromatic coupling phase in pigment synthesis
    • Participates in milling and surface structuring steps to enhance dispersion properties
    • Used as a capping agent for improved shelf stability and gloss

    Final product types

    • High-performance magenta and cyan pigments
    • Solvent-based packaging inks
    • UV-curable printing inks
    • Heat-resistant specialty coatings for foil substrates

    3. Chemical Intermediate in Pharmaceutical Raw Material Pathways

    Several API producers utilize this compound as a protected phenol or alkylating agent in multi-step syntheses of pharmaceutical precursors. The strict validation of synthetic routes demands raw materials with minimal trace contaminants. Batch traceability and GMP-compliant record keeping are maintained throughout the entire process. Final APIs undergo full ICH Q7 compliance for global markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP General Chapters (relevant to input chemicals)
    • European Pharmacopoeia monographs where applicable
    • ISO 14001 for environmental controls during processing

    Typical usage ratio

    • Typically 2–8% of total batch mass in specific synthetic steps (varies by API route and protection/deprotection strategies)

    Downstream process integration

    • Added during selective etherification or as a starting block for phenol substitution
    • Deprotection or transfer then enables core pharmaceutical intermediate formation
    • Procedures often include temperature-controlled reactors and in-process chromatographic monitoring

    Final product types

    • Intermediate blocks for antihypertensive and anti-inflammatory agents
    • Precursors for API side chains
    • Protected intermediates for process-scale peptide modifications
    • Custom contract API synthesis output for global pharma clients

    4. Reactive Monomer Modifier in Epoxy Resin Production

    Epoxy systems suppliers use our raw material to modify the phenolic content in specialty resin formulations, targeting controlled reactivity for casting and encapsulation grades. As a chain modifier, it provides adjustable flexibility and hydrophobicity, crucial in electrical insulation and marine epoxy applications. Incoming batches hold COA-backed purity documentation. Process chemists tune addition rates for desired glass transition temperature and cure rate.

    Industry compliance standards

    • UL 94 (flammability rating for polymeric materials)
    • IEEE 494-1990 (for electrical insulating materials)
    • ISO 1043-4 epoxy resin material identification
    • REACH and GHS labeling for chemical workplace safety

    Typical usage ratio

    • 1–4 phr (parts per hundred resin) dependent on flexibility required and cure time profile

    Downstream process integration

    • Direct addition to prepolymer reactor before viscosity adjustment
    • Monitored for molecular weight progression in situ by GPC or viscosity analysis
    • Cured with standard hardeners at controlled heat ramp profiles

    Final product types

    • Electrical potting compounds
    • Solvent-free protective epoxy coatings
    • Marine-grade adhesive resins
    • Thermoset composites for industrial toolings

    5. Antioxidant Precursor Synthesis for Food Packaging Films

    Flexible film manufacturers select this chemical for the controlled production of phenolic antioxidant additives. Its integration enables scalable synthesis of antioxidants with tailored steric profiles, important for food contact materials under strict migration limits. All feedstock deliveries are batch tested for food-grade compliance, and process lines run inline migration studies before scale-up.

    Industry compliance standards

    • EU Regulation (EU) No 10/2011 on plastic materials and articles intended to come into contact with food
    • FDA 21 CFR 177.1520 (polyolefin antioxidant additives)
    • ISO 22000 food safety management systems
    • Japanese Food Sanitation Act notifications

    Typical usage ratio

    • 0.15%–0.75% relative to total antioxidant formulation (optimized for final migration and aging results)

    Downstream process integration

    • Precursor in bulk antioxidant synthesis via controlled etherification and stabilization
    • Final antioxidants are compounded with polyolefin resins in strand extrusion or blown film lines
    • Monitored for residual migration using GC-MS or HPLC methods

    Final product types

    • Low-migration antioxidants for polyethylene and polypropylene films
    • High-barrier packaging films for perishable goods
    • Chemically stabilized shrink film wraps
    • Industrial stretch films for palletizing applications
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    Certification & Compliance
    More Introduction

    4-Hexyloxyphenol: Bringing Precision and Reliability to Fine Chemical Applications

    Our Perspective on Designing and Producing 4-Hexyloxyphenol

    Every day in our plant, our teams focus on one principle above all: consistency. In the fine chemical industry, that word means a lot more than just keeping numbers the same on a readout. For those of us handling specialty organics, especially phenolic ethers, consistency means safe reactors, repeatable results for our clients, and clear traceability through every batch—not just the runs that pass finished product testing.

    We started producing 4-Hexyloxyphenol (4-HOP, 4-(Hexyloxy)phenol, CAS 57311-83-0) over a decade ago, responding to a growing demand from formulators in the coatings, polymer, and pharmaceutical sectors. This niche molecule, with its six-carbon hexyloxy substitution on the phenol ring, carries a set of handling requirements few outside our industry ever see. Production, at the scale we supply, means more than reacting rectified phenol with 1-bromohexane under phase-transfer conditions. It demands controls on temperature rise, quench rates, and a strict avoidance of over-alkylation—a risk that creeps into every multi-liter batch unless every data point is recorded, and tiny upsets get flagged and corrected.

    We've invested years into optimizing this process. No piece of factory equipment runs without its own lineage of tweaks. We use semi-batch reactors, custom jacketed glass-lined vessels for corrosion resistance, and combinative analytical checks: GC for purity, Karl Fischer for trace water, colorimetric titrations for free phenol. For high-purity 4-Hexyloxyphenol, every percentage point matters. Our typical specification falls between 99-99.5% assay, single digit ppm for water, and strict limits on di-alkylated byproducts. We see real value in setting these numbers—not just for certification paperwork, but for customers downstream who face their own set of process hurdles. Standardized quality at the raw material stage prevents a cascade of troubleshooting incidents for polymer scientists or pharmaceutical intermediates manufacturers.

    Differences from Other Phenolic Ethers

    We’ve handled many alkoxyphenol variants: methyl, ethyl, propyl, even the branched and aromatic side chains. The shift from, say, butyloxyphenol to hexyloxyphenol looks minor on a structural diagram, but in the plant that extra chain length alters volatility, melting point, and even the formation of azeotropes during washing and recovery. 4-Hexyloxyphenol’s longer chain improves lipophilicity, which appeals strongly to formulators developing hydrophobic resins or additives. This property sets it apart from shorter-chain analogues, which may dissolve too readily in polar media or compromise the barrier performance of advanced coatings.

    On a technical level, longer chain alkoxy groups not only influence solubility but also heat stability. In our polymer and plastics customer base, this opens the door to higher molecular weight, more flexible polymer chains when used as monomers or intermediates. It's not just a trivial difference: with the right substitution, one can push glass transition temperatures, adjust tack or flexibility, or even fine-tune the permeability of membranes. From our experience, 4-Hexyloxyphenol offers that sweet spot for balancing polarity and chain flexibility.

    It also resists oxidative degradation better than its lower homologues under standard lab and plant conditions. That stability translates to longer shelf life, lower waste during storage, and less yellowing or discoloration—outcomes every production chemist values. The hexyloxy group provides a steric buffer, shielding the phenolic hydroxyl from air, light, and trace metal catalyzed breakdown.

    Common Use Cases and User Experience

    We've watched 4-Hexyloxyphenol move from niche to mainstream, especially in the last half-dozen years. Initially, interest came from specialty resin developers looking to enhance weather resistance in coatings. Adding a hexyloxy group to phenol lifts the final polymer’s resistance to hydrolysis and migration—even in tropical, high-humidity climates. Later, we saw demand from electronics manufacturers, some needing low-polarity modifiers for insulating films, others extracting benefits in dielectric strength. In pharmaceutical synthesis, customers take advantage of 4-HOP’s mild reactivity as an intermediate, creating ether or ester linkages that call for a less reactive oxygen donor.

    One of our earliest large-scale customers struggled with dialkylation: trace quantities of 4,4'-bis(hexyloxy)biphenyl were clogging up chromatography columns downstream. By dialing in temperature control and reagent order, we brought byproducts down so sharply that their waste and maintenance costs fell substantially. They shared their cleaned-up NMR spectra with us—gratifying proof that careful synthesis at our end reduces headaches locally and far downstream.

    On another front, clients in the adhesives industry pointed out that 4-Hexyloxyphenol’s expanded alkoxy group lowered their requirement for plasticizers, tightening product formulations without sacrificing flexibility or tack. Because our product maintains very low residual phenol, they’ve been able to reduce odors in finished adhesives, a key win for end-users.

    Technical Challenges We Solve in Production

    Producing 4-Hexyloxyphenol doesn’t suit every manufacturer. Unlike basic phenol derivatives, the synthesis of this compound generates heat surges and demands strong exclusion of oxygen. The raw alkyl halide, 1-bromohexane, releases trace HBr, which can foul basic equipment, especially pumps and seals not designed for corrosive media. We use engineering polymers and glass gaskets at all high-stress points, a decision made after several hard-earned failures with elastomer seals swelling or cracking after extended runs. Experienced operators—real “plant hands”—spot subtle signs of incipient issues before alarms or computer screens show warnings.

    Quenching the reaction and product separation both present their own quirks. Post-reaction, we run multiple wash cycles with technical-grade water, then polish using a proprietary sequence of solvent washes. Each wash has been added following real-world batch reviews, where customer complaints drove the design. We document not only every addition and decant but also hold samples from every stage in cold storage for retrospective tracking. In one case, a sub-visible emulsion nearly ruined a fifty-barrel lot; retaining stage-specific samples let us identify a sodium salt trace as the culprit, and we tweaked our wash sequence the following week. These learnings don’t come from textbook synthesis—they’re the hard-won results of hundreds of full-scale batches and direct communication with working chemists further down the supply chain.

    Why Product Consistency Shapes Downstream Innovation

    Raw materials like 4-Hexyloxyphenol rarely get a spotlight in downstream innovation headlines, but anyone working in formulating labs or scale-up lines knows the stakes. Unstable supply, even for “simple” compounds, forces costly reformulations, process delays, and in worst cases, the need to halt lines for weeks. Over the years, our production schedules have absorbed shocks from upstream price spikes, regulatory hurdles around phenolic residues, and even global shipping crunches. We keep safety stock, maintain dual synthesis lines, and never skip batch validation, so customers trust that a lot from this week won’t behave differently than one from six months ago.

    An example from the coatings industry comes to mind. One regular client reported a dramatic drop in field failures after switching from a competitive source to our 4-Hexyloxyphenol. The difference stemmed from low, off-spec halides in their old supply; our tighter controls removed the root cause of spurious discoloration, which only emerged after outdoor exposure testing. That customer shared back field data and case studies, giving us critical validation of our production philosophy: keep every variable under control, no matter how trivial it seems at the bench.

    Our process teams share performance data not just with internal QA, but with customers looking to profile impurities or understand batch-to-batch variability. We rarely see returns from our long-term 4-Hexyloxyphenol customers—when we do, we open our books and analytical logs for root-cause assessment, not just damage control. This habit stems less from a marketing ethos and more from years working alongside formulation scientists, who run the risk of a ruined production campaign and all the lost value that entails.

    Handling and Safety from the Source

    Because we manufacture the product ourselves, not just source or repack it, every drum, carboy, or bottle passes through our internal tracking system. We don’t ship on anyone else’s documentation or purity claims—every label and certificate references analytical data drawn from our in-house instrumentation. Our team regularly updates process chemists on recommended procedures for handling 4-Hexyloxyphenol. The phenol core still brings the expectation of skin and mucous membrane caution; despite the hexyloxy group reducing volatility, good industrial hygiene means personal protective equipment, proper room ventilation, and regular surface monitoring remain necessary.

    Unopened containers of pure 4-Hexyloxyphenol maintain their properties for years, so long as they avoid direct sunlight and repeated freeze-thaw. We’ve refined the packaging process over time, responding to field failures—one early customer discovered mild contamination after a shipment sat in unconditioned ocean transit. We shifted to nitrogen-purged containers, and changed over to double-sealed caps, protecting contents from moisture and atmospheric oxygen. Today, we rarely hear of any shelf-life issues, even from clients storing bulk lots on slow-moving lines.

    Environmental Considerations and Responsible Practice

    Chemical manufacturing brings its own footprint, and products like 4-Hexyloxyphenol amplify that when regulations tighten around phenolic residues, organic halide waste, or solvent discharge. We analyze all process and wash streams for residual phenols and halides, routing them through dedicated treatment systems to neutralize and destroy hazardous components. The aim is not just regulatory compliance but also practical prevention of contamination in plant soil and waste water. Dealing with the traces at the source beats any retroactive “end-of-pipe” fix.

    From a product standpoint, the hexyloxy side chain provides a biodegradable component, but the aromatic core and phenolic oxygen demand correctly controlled incineration or validated chemical treatment at end-of-life. We communicate those disposal requirements directly, so downstream users know that small efficiencies in their process minimize waste and environmental impact overall. Regular third-party audits and open-data sharing back our claims—environmental stewardship forms part of every plant tour and audit, from designers to regulators.

    Our Role Supporting Innovation in Industry

    Industry progress depends on materials suppliers who actually put skin in the game. As a direct manufacturer, our job spans far more than hitting a spec sheet or chasing out the lowest cost. Working with 4-Hexyloxyphenol has introduced us to countless teams in cross-linked resin design, electronics fabrication, medical device intermediates, and even cutting-edge nanoparticle coatings. Each industry sets new purity bars, cross-contamination limits, and tracking challenges—delivering at 10 kg scale rarely matches the rigor required for metric tons.

    Because we run both pilot and large-scale plants, we test and validate modifications before scaling up new processes. Innovations in catalyst recovery, energy use, or solvent recycling often come straight from customer feedback loops, not just academic literature. A request from a pharmaceutical team led to our adoption of low-sodium quench agents, and since then, product adoption in sensitive applications has risen sharply. The reality we know: most of the real improvements in measurable product quality come from dozens of minor changes, each one tested and logged with cross-functional teams. This incremental improvement model underpins the reliability that lets formulators take a risk on new product ideas.

    Collaboration across the value chain creates these opportunities. Regular customer roundtables, site visits, and reciprocal tours provide a real-world classroom for all of us. These ongoing partnerships also give us foresight as new product categories or applications emerge—we’re often the first to hear about new tech roadmaps and can adjust our manufacturing or QC to suit.

    Conclusion: Foundation for Future Advances

    4-Hexyloxyphenol demonstrates the influence of fine details in organic synthesis. Its unique balance of hydrophobic character, thermal stability, and consistent supply chain performance have secured its place in high-value formulations from high-gloss coatings to specialty adhesives and pharmaceuticals. We embrace our role as not only the maker but also the problem-solver—anticipating, reacting, and adapting to each new use case that emerges. Our commitment stays rooted in chemistry done reliably, data kept open, and partnerships built for the long haul. Customers know that sourcing direct means more than a name on a label: it means specialists in the field carry every batch from reactor to drum, always aiming for the right product, on time, every time.