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6-Phenyl-1-Hexanol

    • Product Name 6-Phenyl-1-Hexanol
    • Alias 6-Phenylhexan-1-ol
    • Einecs 223-686-7
    • 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

    818565

    Cas Number 1632-17-9
    Molecular Formula C12H18O
    Molecular Weight 178.27 g/mol
    Iupac Name 6-Phenyl-1-hexanol
    Appearance Colorless to pale yellow liquid
    Boiling Point 292-294 °C
    Melting Point -10 °C
    Density 0.973 g/cm3
    Flash Point 144 °C
    Refractive Index 1.505
    Solubility In Water Insoluble
    Smiles C1=CC=CC=C1CCCCCO

    As an accredited 6-Phenyl-1-Hexanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mL amber glass bottle with screw cap, chemical label displaying "6-Phenyl-1-Hexanol," CAS number, hazard symbols, and safety information.
    Shipping 6-Phenyl-1-Hexanol is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is transported according to standard chemical safety protocols, with appropriate labeling for flammable or irritant substances. All shipping complies with local and international regulations for the safe handling and transport of organic chemicals.
    Storage 6-Phenyl-1-Hexanol should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture, heat, and direct sunlight. Use appropriate chemical storage cabinets if available, and ensure all containers are clearly labeled and handled by trained personnel using suitable protective equipment.
    Application of 6-Phenyl-1-Hexanol

    Applications of 6-Phenyl-1-Hexanol in Industrial Manufacturing

    6-Phenyl-1-Hexanol occupies a critical role in several advanced manufacturing sectors, serving as a specialty intermediate and a performance-building block. Our B2B partners leverage this material to add specific functional properties in syntheses that require high reliability, regulatory compliance, and precision. Below, we detail verified downstream application scenarios that reflect actual market usage.

    1. Fragrance Ingredient Synthesis for Fine Perfume Manufacturing

    Perfume producers utilize 6-Phenyl-1-Hexanol primarily as a key intermediate for the synthesis of complex aroma molecules, especially those with floral or fruity notes because of its distinctive olfactive profile. Large-scale fragrance formulators incorporate it into fine perfume compositions that demand unique aromatic signatures, and the alcohol group allows for further chemical derivatization during the creation of proprietary fragrance accords and aroma chemicals for luxury personal care items.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • European Cosmetics Regulation (EC) No 1223/2009
    • REACH Registration (Europe)
    • US Food and Drug Administration (FDA) 21 CFR 700–740 for fragrance use

    Typical usage ratio

    • 0.1%–3% by weight in fragrance oil concentrates, with final loading adjusted based on desired aroma intensity and IFRA dermal limits

    Downstream process integration

    • Direct incorporation into aroma molecule synthesis during Grignard, Friedel–Crafts alkylation, or esterification stages followed by compounding in fragrance blends

    Final product types

    • Luxury fine fragrances
    • High-end eau de parfum and eau de toilette
    • Scented body lotions and creams
    • Perfumed hair care spray

    2. Plasticizer and Modifier Intermediate for Specialty Polymer Production

    Chemical manufacturers apply 6-Phenyl-1-Hexanol as a co-monomer or chain modifier in the synthesis of certain specialty polyesters, acrylics, or copolymers, exploiting its aromatic ring and alcohol functionality to manipulate compatibility, plasticization characteristics, and impact resistance of engineered plastics. Its controlled reactivity enables production of advanced plastics used in demanding packaging, automotive, and electronics components.

    Industry compliance standards

    • EU Regulation (EU) No 10/2011 on food contact plastics
    • US FDA 21 CFR 177.1660 for polyesters in food packaging
    • ISO 9001:2015 quality management for polymer processing
    • RoHS Directive (2011/65/EU) for electronics plastics

    Typical usage ratio

    • Up to 5% by weight relative to total monomer input; polymer producers calibrate precise dosage according to target mechanical and thermal properties

    Downstream process integration

    • Incorporation into polycondensation or free-radical polymerization step as a functionalized alcohol modifier, either by direct batch addition or via pre-reacted building block

    Final product types

    • High-performance polyesters and copolymers
    • Flexible food packaging films and trays
    • Impact-resistant automotive interior parts
    • Electronic device housings

    3. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Pharmaceutical manufacturers value 6-Phenyl-1-Hexanol as an intermediate for the controlled introduction of a phenyl-hexyl moiety within custom molecule synthesis. This role is fundamental in several patented routes where the alcohol group is essential for subsequent oxidation, derivatization, or as a chiral auxiliary. Such syntheses are commonly encountered in the development of analgesics, CNS agents, and select APIs where FDA and ICH guidance must be strictly followed.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) guidelines (ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) relevant monographs
    • FDA Drug Master File (DMF) requirements
    • REACH compliance for pharmaceutical chemical use

    Typical usage ratio

    • Stoichiometric or slight molar excess depending on the specific synthetic route and controlled process yield, often 1–1.2 equivalents

    Downstream process integration

    • Introduction as an alcohol substrate during multi-step organic synthesis (alkylation, oxidation, or reductive amination), feeding into subsequent formation of API core or side-chain, followed by purification under GMP

    Final product types

    • Pharmaceutical active ingredients (APIs) for CNS drugs
    • Precursors for synthetic analgesics
    • Intermediates for patent-protected therapeutic molecules

    4. Specialty Surfactant and Emulsifier Manufacturing

    Producers of specialty surfactants incorporate 6-Phenyl-1-Hexanol as a structurant to introduce hydrophobic aromatic character into nonionic, amphoteric, or cationic surfactant frameworks. This supports the manufacture of high-performance emulsifiers for agrochemicals, inks, and lubricants, where fine balancing of solubility and persistence is key. The compound’s backbone also enables the production of surfactants with tailored partition coefficients.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals (for environmental impact)
    • Regulation (EC) No 1907/2006 (REACH) for surfactants
    • ISO 14001 environmental management for chemical production
    • EPA Title 40 CFR regulations on emulsifier use in pesticides

    Typical usage ratio

    • 1%–7% by weight, optimized per surfactant structure and application system (water/oil, oil/water, or complex blends)

    Downstream process integration

    • Added during etherification, esterification, or quaternization stage to generate surfactants of defined hydrophilic-lipophilic balance (HLB); batch or continuous processes may be employed

    Final product types

    • Emulsifiers for crop protection formulations
    • Ink dispersants for industrial printing
    • Specialty lubricants and anti-statics
    • Wetting agents for paints and coatings
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    Certification & Compliance
    More Introduction

    6-Phenyl-1-Hexanol: Precision in Chemical Craftsmanship

    Introduction to 6-Phenyl-1-Hexanol

    Chemists who spend their days troubleshooting reactions and scaling new heights in organic synthesis quickly learn to recognize the value of good building blocks. 6-Phenyl-1-Hexanol belongs in this category. Our team produces this specialty alcohol with consistency as the top priority, a decision rooted in years of feedback from formulators and process engineers who know that minor impurities introduce headaches down the road. Each batch leaves our factory following thorough purification and analytical checks because even at sub-percent tolerances, certain byproducts can sabotage performance in downstream applications. In the past, we dealt with customer reworks and frustration traced to careless manufacturing. Since implementing tighter controls on source materials, our current process maintains a purity profile that has become a hallmark for the chemistries that count on 6-Phenyl-1-Hexanol as a backbone.

    Model and Specifications

    In the world of fine chemical synthesis, transparency about inputs pays dividends. We prepare our 6-Phenyl-1-Hexanol to suit both research and scale-up needs, typically offering the product in a liquid form with purity above 99%. Routinely, our analytical lab subjects samples to GC and NMR scrutiny to catch any off-notes in the carbon chain or unwanted aromatic impurities. Most labs come to us with specific requirements about water content or trace catalysts, and we shape our purification schedule around these facts. Small-batch orders often go out in amber glass, using PTFE-lined closures to preserve integrity during long storage. We publish exact assay results and typical spectroscopic fingerprints alongside each shipment, so QC managers at our customers’ sites don’t gamble with assumptions. Any variation in the hexanol's chain length or residual aromatic content can disrupt specialty perfumery, liquid crystal alignment, or pharmaceutical intermediate synthesis.

    User Experience in Lab and Industry

    Years of shipping 6-Phenyl-1-Hexanol to diverse customers—academics chasing new reaction mechanisms, industrial manufacturers developing complex polymers, fragrance formulators adjusting the backbone of a new scent—gives us a unique seat to feedback cycles. Nearly every customer operates under time and cost pressures. One of the recurring messages: avoid surprises. A polymer researcher might only run three trials before a production deadline. A formulator in cosmetics requests surplus material to account for batch loss. Over time, these stories shaped our practice of consistency: each order should match the last, making scale-up smoother for those who rely on rigorous recordkeeping.

    During the early days in this industry, superficial specification tables sufficed. Today, the regulatory and performance landscape looks different. Customers want reassurance that each bottle contains what we promise. In response, we established baseline thresholds for aromatic residue, moisture, and oxide byproducts, reducing the risk that invisible culprits cause batch failures farther down the processing line. Industry partners working in pharmaceutical intermediates have grown wary of supply chain substitution, so we maintain traceability of every batch back to specific feedstocks. These practices weren’t part of the original plan but grew from direct requests. Making a specialty alcohol like this available with full spectrum data adds days to our preparation cycle, but reliability saves headaches for everyone.

    Technical Profile: Why 6-Phenyl-1-Hexanol Matters

    Organic synthesis professionals look at a structure like 6-Phenyl-1-Hexanol and see a platform for diverse transformations. Technicians in our own labs have used it to anchor reactions via the terminal alcohol, introducing selectivity into multi-step routes. The phenyl group at one end makes this alcohol behave differently from simple linear hexanols; reactivity tuning comes into play both in nucleophilic substitutions and in esterification series. Colleagues in the fragrance industry value how the same motif imparts a subtle, persistent note different from related alcohols. Used as a component in higher-performance lubricants, it confers a degree of thermal stability and viscosity control that plain aliphatic alcohols rarely manage.

    We’ve sat through discussions with development teams seeking compact “modular” molecules that enable rapid screening through chemical space. 6-Phenyl-1-Hexanol, by virtue of its chain length and aromatic substitution pattern, performs well in these studies. Its solubility profile enables good blending in a range of non-polar and polar systems. Colleagues in pharmaceutical R&D have highlighted the way it supports precise modification—for instance, alkylation of the hydroxyl end, or aromatic ring functionalization. This flexibility enables lead optimization and rapid SAR exploration.

    Differences from Other Hexanols and Alcohols

    Our experience bears out that not all hexanols behave the same. The introduction of a phenyl group changes vapor pressure, boiling point, and reaction profile. Customers who tried to substitute less expensive aliphatic alcohols or shorter-chain analogs into protocols sometimes call us asking why their yield plummeted, or why a fragrance base no longer radiates the same note after aging a few weeks. The key lies in the interplay between the nonpolar hexyl backbone and the aryl group.

    Compared to common 1-hexanol, 6-Phenyl-1-Hexanol delivers improved substrate compatibility in Suzuki couplings and offers enhanced performance in specialty coatings that demand migration resistance. While isohexanols or branched alcohols may seem interchangeable in cursory screens, applications that rely on a particular viscosity or miscibility quickly expose the differences introduced by aromatic substitution. In our own tests, blends using 6-Phenyl-1-Hexanol outperform their straight-chain counterparts in maintaining clarity and fragrance longevity after thermal cycling.

    For processes such as resin modification or advanced material synthesis, our chemists experimented with both para-substituted and meta-substituted phenyl hexanols. Over several production runs, even a shift between 5-Phenyl and 6-Phenyl positional isomers created noticeable changes in polymer matrix performance. The particular placement at carbon six provides an optimal balance of flexibility and ring-induced rigidity. In high-performance lubricants, customers relate that the phenyl group helps retard oxidative breakdown, giving their blends a competitive edge—something we validate both in our lab and through customer field data.

    Ensuring Purity and Process Control

    Any specialty chemical manufacturer faces a fundamental question: how much control can be exercised over the input stream and the final output? The journey to consistently clean 6-Phenyl-1-Hexanol started for us with a stretch of complaints about color drift, strange odors, and mysterious “ghost peaks” in chromatograms that showed up only after customers heated solutions or tried scale-up. Early batches from less selective processes produced side-products—like dialkylated phenyl compounds or oligomeric alcohols—that tested our patience and strained client trust.

    We responded by redesigning the synthesis loop. Every hydroxy functionalization step gets close monitoring to head off side reactions. After years of refining the purification, we now freeze preliminary batches at decision gates—sample, analyze, and course-correct before proceeding. Every time we run a batch, seasoned operators and chemists walk the line, sampling solvent drains, confirming GC retention times, and flagging any deviations in viscosity or color. With this approach, complaints about crystal formation, haze, or shifting refractive index have faded to rare exceptions. Down-stream users benefit from this vigilance, especially those building polymers or synthesizing pharmaceutical candidates where trace contaminants can derail a project.

    Perspectives on Application: What Industry Needs

    Interactions with customers reveal distinct priorities depending on the application. In perfumery, scent longevity, purity, and stability under ambient storage matter most. Some fragrance houses order pilot lots, running side-by-side scent panels to gauge subtle differences over aging. Here, even a percentage point of unrelated hexanol isomers can skew results, resulting in reformulations that slow down development for months.

    In advanced coatings, formulators focus on migration resistance and optical stability—properties deeply influenced by molecular structure. Our batches have been compared alongside other phenyl alcohols; the consensus: 6-Phenyl-1-Hexanol preserves performance after UV exposure and maintains clarity better than para-substituted relatives. Polyol producers interested in tailored reactivity note the ease with which terminal functionalization proceeds, whether for urethane linkages or crosslinking with isocyanates. Pharmaceutical chemists tell us that the chain length and aromatic character anchor further transformations (such as etherification or oxidative conversion) with less fuss about unwanted side reactions.

    Those new to the field might underestimate the impact of minor batch-to-batch variation until a process shuts down because a property like solubility or miscibility diverges. Over the years, we’ve collaborated with process engineers troubleshooting these off-spec challenges, offering technical support and sharing our quality data for root cause analysis. This transparency builds confidence and lays the groundwork for trust in long-term supply relationships.

    Challenges and Practical Solutions

    Every chemical producer faces cycles of supply constraints, regulatory shifts, and rising expectations. Sourcing precursors for 6-Phenyl-1-Hexanol requires agility because global aromatics markets swing in both price and purity. To buffer these risks, we expanded relationships both upstream and downstream, recruiting suppliers who prioritize transparency over spot pricing games. Traceability for each lot now reaches back to source benzene and hexanol providers, giving our customers confidence their products originate from stable, ethically managed supply chains.

    Recycling and waste minimization took patience and investment. Our original process left behind sizable streams of solvent and side-products, some of which could not be reused or sold. Tightening yield at each step, and engineering effective purification train, cut costs and aligns with sustainability demands from major partners—especially in personal care or pharmaceutical markets facing stricter oversight. More recently, we adopted monitoring protocols that detect impurities as soon as a deviation occurs, reducing rework and waste.

    Collaboration outside our own plant makes a difference. Customers working at scale often run trials that catch subtle off-flavors, unanticipated haze, or reactivity shifts before they become problems for end users. We review their data, adjust our process, and feed the lessons back into production. This feedback loop—company to customer and back—sets the standard for continuous improvement.

    Quality as the Buyer's Guarantee

    Through the years, we’ve seen the fate of many “good enough” intermediates on the market. They attract budget-driven buyers at first, but weak documentation and underwhelming performance catch up fast. We have observed competitors cut corners on drying steps, sometimes packaging product with high water content that causes confusion for buyers later. In contrast, our commitment is to continuous refinement of batch protocols and open sharing of all relevant analytical data. We provide the numbers—assay results, IR/NMR spectra, color and odor reports—the same data our own chemists use to sign off on each shipment.

    Some customers seek only basic alcohols for blending. These situations highlight the non-interchangeable nature of specialty molecules. For polymer or pharmaceutical work, even seemingly redundant details in our batch reports prove valuable for R&D teams troubleshooting inconsistent results. In our experience, large buyers in regulated industries don’t want promises alone; they demand proof, and our approach gives them the reassurance needed for approval steps and long-term contracts.

    This openness particularly benefits labs scaling a process from milligrams up to hundreds of kilos. As product demand takes off, so does the risk profile around error or inconsistency. We built our support systems—return procedures, batch cross-checks, expedited troubleshooting—to catch and fix problems before they impact production. Several key accounts testify to the value of transparency over short-term savings, knowing that an extra day of quality assurance today shields them from long-term supply risk.

    6-Phenyl-1-Hexanol in the Era of Stringent Standards

    Modern industry tolerates less ambiguity. Compliance teams pore over every detail, from residual solvent ranges to elemental traces. We have watched the regulatory environment tighten, especially for substances destined for European and North American markets. Our adjustments include documentation at each process step and additional testing to confirm compliance with new and anticipated standards. This approach ensures global customers gain a future-proof source that adapts to changing rules rather than playing catch-up.

    Specialty alcohols like 6-Phenyl-1-Hexanol, once considered “niche,” occupy an expanding footprint across markets. Whether as links in polymer chains, anchors in pharmaceuticals, or fixatives in fragrances, their importance grows each year. Forward-looking customers scrutinize each ingredient in their supply chains, pushing us further than ever in product stewardship. Safety data, impurity breakdown, and environmental reporting—these documents now move with every delivery, backed by batch traceability built into our systems.

    Final Thoughts: Building Trust Through Chemistry

    Years of reflection across countless batches inform one truth: none of us works in isolation. As manufacturers, responsibility doesn’t end with shipping a drum or bottle. We see our products in the hands of researchers solving medical challenges, in start-ups inventing better plastics, and in artisans blending new scents. Each use case carries its own risks and rewards, but all of them rest on the foundation of quality, reliability, and open communication.

    6-Phenyl-1-Hexanol exemplifies the result when a manufacturing company listens, adapts, and perseveres. Trust, once won, motivates every member of our team to maintain both the honesty in every assay sheet we sign and the craft in every batch we deliver. In the evolving landscape of specialty chemicals, a reputation for diligence and collaboration makes all the difference—not just for us, but for the countless chemists, engineers, and innovators who depend on our work.