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6-Phenylhexanoic Acid

    • Product Name 6-Phenylhexanoic Acid
    • Alias 6-Phenylcaproic acid
    • Einecs 211-502-7
    • 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
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    Specifications

    HS Code

    878804

    Chemical Name 6-Phenylhexanoic Acid
    Molecular Formula C12H16O2
    Molar Mass 192.25 g/mol
    Appearance White to off-white powder
    Boiling Point 331.7 °C
    Melting Point 56-58 °C
    Solubility In Water Slightly soluble
    Density 1.047 g/cm3
    Cas Number 1676-90-8
    Smiles C1=CC=CC=C1CCCCCC(=O)O

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

    Packing & Storage
    Packing A 100g amber glass bottle labeled "6-Phenylhexanoic Acid," tightly sealed with a screw cap, includes hazard information and lot number.
    Shipping 6-Phenylhexanoic Acid is shipped in tightly sealed, chemical-resistant containers to ensure stability and prevent contamination. Packaging complies with regulatory guidelines for safe transport. The compound is dispatched via ground or air freight, accompanied by appropriate hazard labels, safety data sheets, and documentation for handling and storage upon arrival.
    Storage 6-Phenylhexanoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Keep it away from sources of ignition, heat, and incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Always follow standard laboratory safety procedures and store at recommended temperature, typically room temperature, unless otherwise specified.
    Application of 6-Phenylhexanoic Acid

    Applications of 6-Phenylhexanoic Acid in Industrial Manufacturing

    As a direct manufacturer of 6-Phenylhexanoic Acid, we have supplied this specialty intermediate to various advanced chemical sectors for over a decade. Its molecular structure, purity levels, and controlled production allow for performance-driven use in several key downstream applications, each governed by specific industry protocols and formulation requirements. Below, we detail selected industrial scenarios based on actual customer deployment, process flow, and regulatory adherence.

    1. Synthesis of Aromatic Plasticizers for Polyvinyl Chloride (PVC) Compounds

    6-Phenylhexanoic Acid functions as a key aromatic carboxylic acid building block during the manufacture of specialty plasticizers used in technical-grade PVC compounds. Its unique phenyl-alkyl structure improves compatibility and migration resistance when incorporated as an intermediate for polyester plasticizer synthesis. Manufacturers employ it at precise molar ratios during esterification with high-boiling alcohols to produce non-phthalate plasticizers for flexible PVC in wire, cable, and automotive sheathing applications.

    Industry compliance standards

    • EN 71-3:2019 Safety of toys - Migration of certain elements
    • RoHS Directive (EU) 2015/863 for electronic components
    • REACH Annex XVII Restrictions on phthalates
    • ASTM D2124 for plasticizer migration

    Typical usage ratio

    • Reacted at 7–12 mole% of total dicarboxylic acid input in polyester plasticizer synthesis batches; exact proportion adjusted based on final flexibility and migration resistance specifications for end-use compound

    Downstream process integration

    • Introduced at the initial esterification reactor step, typically under vacuum with multifunctional alcohols, followed by polycondensation and neutralization before downstream blending into PVC formulations

    Final product types

    • Flexible PVC cables and insulation
    • Automotive soft trims
    • Technical film and sheet for packaging
    • Non-phthalate wire coatings

    2. Production of Aromatic Fragrance Intermediates in Fine Chemical Synthesis

    The phenyl-hexyl backbone of this acid provides a tailored molecular scaffold for creating musky, woody aroma intermediates used in luxury and mass-market fragrance compositions. As an industrial aromatic intermediate, it undergoes downstream esterification or amidation with specific alcohols or amines, yielding stable, high-volume compounds for perfumers’ concentrate blends and fragrance oils for detergents and personal care.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • Cosmetic Ingredient Review (CIR) safety limits
    • EU Cosmetics Regulation (EC) No 1223/2009
    • JSCI (Japanese Standards for Cosmetic Ingredients)

    Typical usage ratio

    • Converted at 5–15% of total acid reactant charge in downstream esterification recipes; final inclusion in fragrance oil remains below 1% w/w, verified via organoleptic testing and regulatory submission

    Downstream process integration

    • Charged as a principal acyl donor during catalytic transformation, either in batch or continuous reactors, before purification and QC release for integration into fragrance compound compounding lines

    Final product types

    • Fragrance base intermediates
    • Scented detergent concentrate oils
    • Perfume and Eau de Toilette bulk formulas
    • Cosmetic and personal care fragrance components

    3. Custom Pharmaceutical Intermediate: Synthesis of CNS-Active Drug Substance Precursors

    For advanced pharmaceutical synthesis, 6-Phenylhexanoic Acid is used as a key intermediate in the multi-step production of active pharmaceutical ingredients (APIs) targeting the central nervous system (CNS). Its alkyl-aryl structure is uniquely positioned for selective coupling reactions, facilitating the downstream construction of advanced benzyl or aryl moieties in patented CNS drug scaffolds, particularly in the manufacturing of anti-epileptic and neuroprotective substances.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for active pharmaceutical ingredients
    • Ph. Eur (European Pharmacopoeia) monograph controls for chemical purity
    • US FDA 21 CFR Part 211
    • USP Residual Solvent Guidelines

    Typical usage ratio

    • Used at a stoichiometric input, typically 0.9–1.1 molar equivalents relative to target amine or alcohol in coupling stages; precise input determined by the required conversion rate and impurity profile through scale-up validation

    Downstream process integration

    • Supplied as a purified crystalline solid, introduced during controlled active site alkylation or acylation in pharmaceutical synthesis, with all steps monitored for traceability and batch record compliance

    Final product types

    • API intermediates for CNS therapeutic candidates
    • Reference standards for process development
    • Small-molecule drug precursor batches

    4. Synthesis of High-Performance Lubricant Additives

    This aromatic acid sees use in the formulation of synthetic ester lubricants for applications requiring excellent oxidative stability, such as high-temperature compressor oils and specialty greases. Through esterification with branched polyols, it contributes to lubricant additives with enhanced film strength and volatility performance, especially in demanding automotive and industrial lubrication environments.

    Industry compliance standards

    • API SN and ILSAC GF-6 automotive lubricant specifications
    • ACEA European lubricant sequences
    • ISO 6743 Lubricants, industrial oils classification
    • SAE J300 lubricant viscosity classifications

    Typical usage ratio

    • Charged at 3–9% w/w of total acid input in polyol ester base stock formulation; proportion varies with viscosity grade and additive compatibility testing

    Downstream process integration

    • Mixed with polyol and reacted under vacuum and temperature-controlled reactors for full conversion, followed by filtration and blending into finished lubricant base stocks before performance additive addition

    Final product types

    • Compressor and refrigeration synthetic oils
    • Automotive high-performance greases
    • Hydraulic and turbine lubricants
    • Specialty gear oils

    5. Manufacture of Polymeric Resin Modifiers for Coating Systems

    Selective use of the acid as a chain-modifying agent during polyester and alkyd resin production allows downstream manufacturers to tailor molecular weight and glass transition properties of coating resins. By adjusting addition levels, formulators achieve improved film hardness and chemical resistance for metal, wood, and automotive coating applications. Purity and consistency are crucial for maintaining batch-to-batch quality targets under regulatory inspection.

    Industry compliance standards

    • ISO 12944 for protective paint systems
    • ASTM D3029 for polyester resin impact resistance
    • EU REACH SVHC Compliance
    • US EPA TSCA Inventory Listing

    Typical usage ratio

    • Used at 2–8% by weight of total acid monomer content in alkyd and polyester resin kettle reactions; specific dosage is selected based on targeted film property profile and QC viscosity checks

    Downstream process integration

    • Added alongside polyacids and polyols at the resinification stage, undergoes controlled polycondensation, followed by downstream formulation into paint or varnish bases

    Final product types

    • Protective industrial coatings
    • Electro-deposition primers
    • Wood varnishes
    • Automotive body primers
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    Certification & Compliance
    More Introduction

    6-Phenylhexanoic Acid: Experience from the Production Floor

    Getting to the Heart of 6-Phenylhexanoic Acid Production

    Standing over steel reactors for over two decades, we see every raw material cross our doors. Few are as specific and quietly hardworking as 6-Phenylhexanoic Acid. In our process lines, batches of this specialty acid flow through jacketed systems, clearly different from your simpler straight-chain acids. The phenyl ring, coupled with its six-carbon backbone, doesn’t just shift molecular weight – it changes how chemists and downstream users interact with organic intermediates.

    On the production floor, a batch of pure 6-Phenylhexanoic Acid (CAS 2539-53-3, to be exact) is unmistakable: a white crystalline powder, not prone to clumping, with a faint aromatic scent drifting from the vessel the moment the vacuum pulls off residual solvents. Typical purity for us sits at 99% and above, reliably checked by both GC and HPLC before it even gets to packaging. Our model of the product currently sits under the code 6PHA-WS, recognizing our proprietary process which improves batch-to-batch color and odor consistency. These aren’t empty boasts – a visual check and a run through the analytical lab can verify that clarity, since downstream users in pharma and flavor chemistry can’t be bothered with off-odors or tints.

    Applications: From Lab Bench to Full Scale

    Talking about uses, it’s easy to list where 6-Phenylhexanoic Acid gets put to work, but the real sense comes from why formulators ask for this specific chain length and aromatic substitution. Researchers in flavor chemistry often rely on its role as both a precursor and a modifier. Small changes in an intermediate like this shift the character of a final compound – nothing dramatic, but a nuance that flavor designers notice. In pharmaceutical research, those same six carbons with a phenyl group create a more substantial backbone than simple hexanoic acid ever could. Modifying esters, amides, and further derivatives happens cleanly from our acid because we've ironed out residual solvents and trace organics.

    In polymer research, its backbone and hydrophobic phenyl group add bulk and modulate flexibility across different polymer matrices. The acid group tethers cleanly onto functionalized monomers. Direct feedback from a textile coatings partner made us realize how influential purity and physical form were on their process. Once we stopped using recycled solvents in this synthesis, their lot-to-lot variation nearly vanished.

    Real-World Distinctions: 6-Phenylhexanoic Acid Versus Standard Acids

    In the chemical world, people sometimes roll their eyes at subtle structural differences. Over years of handling nearly every straight-chain and branched acid from C4 to C12, the difference a single phenyl ring makes in compound properties became obvious. Standard hexanoic acid leans oily, smells sharp, and remains biologically active in ways that are limiting for some syntheses. It oxidizes easily and triggers off-flavors if exposed to air too long in flavor applications. 6-Phenylhexanoic Acid, after crystallization and purification, is far less volatile and shows a muted, more sophisticated aromatic note.

    Its reactivity changes, too – nucleophilic attacks on the carboxyl group proceed smoothly during amidation and esterification, but you get less side-product formation due to electronic stabilization from the phenyl ring. In practice, yields bump up a few points and purification costs drop. These benefits travel downstream, especially in pharma syntheses, where each extra purification step shaves profit and increases production lag. Where straight-chain acids offer no added stability, and branched acids sometimes add sterics at the wrong place in a molecule, the placement of the phenyl group in our 6-Phenylhexanoic Acid lends both rigidity and a friendlier disposition for subsequent transformations. These aren’t qualities a distributor or outside party can appreciate unless they’ve run the reactions themselves. We catch all sorts of solvent artifacts and degradation products from hexanoic acid sources elsewhere; with our internal process controls, customers stop reporting downstream surprises.

    Manufacturing Insights and Customer Feedback

    Each line technician and QC chemist here follows these batches with the kind of attention that comes from knowing a single off-specification can halt a client’s project. Our reactors, designed for aromatic acids, maintain temperatures to a half degree, and we never cut corners on vacuum drying steps. Most complaints we’ve heard from industry buyers center on inconsistent melting point and the presence of color bodies. Adjusting our workup over the years – including an extra filtration and a final carbon treatment – meant we moved away from the pale yellow hues seen in earlier market samples. Now, our acid runs closer to bright white. Seasoned flavor chemists prefer it, as even minor tinting changes the taste threshold in their systems.

    In process chemistry, mid-sized innovators look for acids like this to build block structures and introduce new aroma features; university partners told us after switching, their syntheses yielded less tar byproduct, which scaled up without fuss. We get regular calls for certifications and compliance. For our product, we guarantee absence of phthalates and low residual metals, as both these contaminants have caused problems during polymerization and flavor compound isolation.

    Challenges in Production: Learning from Batch Issues

    No one in our field walks past the topic of reproducibility. A batch of 6-Phenylhexanoic Acid isn’t routine in the same way a bulk commodity acid is. Temperature holds during Grignard reactions and oxidation steps never forgive distraction. We’ve learned, through painful batch write-offs, that controlling pH during workups makes all the difference for color and purity. On one occasion, solvent residue crept above 120 ppm, leading to downstream gelling in one customer’s esterification process. Since that episode, our plant adopted an extra pass in the rotary evaporator step, dropping residuals well beneath 50 ppm – we test each drum before packing.

    Analytical feedback from a pharmaceutical client once flagged a single drum with unexpectedly high UV absorbance. Following up, we discovered trace alkylbenzenes carried over from an impure starting reagent. This event prompted us to invest further in feedstock verification and unambiguous GC analysis before synthesis. That’s the difference between internal manufacturing and a third-party supplier’s approach: fixing the root, not glossing over it.

    Maintaining process documentation, lots of real-time data logging, and batch genealogy gives us not just GMP compliance, but an edge when customers cycle through lab trials and need root-cause troubleshooting. Our staff don’t just fill in checklists – they call out anomalies even on good days, since we all remember missed endpoints from years ago. This kind of simple, honest discipline makes the acid better, batch after batch.

    Quality Control: Beyond Certifications

    Market demand for rigorous QC has jumped in the last five years. Telling a customer you run HPLC and GC is just the entry ticket – supplying them with batch chromatograms, trace impurity specs, and repeatable melting point data sets the standard. We provide full spectral analysis for our 6-Phenylhexanoic Acid, so every formulator or research chemist can spot-check purity before they charge a reactor or prep their own derivatives.

    A few years back, one flavor house reported background bitterness in formulations that should have stayed neutral. We found the culprit: traces of an oxidized intermediate left from poor atmospheric control in the final dry-down. After changing our inert-atmosphere protocol, complaints disappeared and contracts expanded. We also field requests for extended stability testing and can quote real data over two-year storage.

    Perspectives on Supply Consistency and Industry Needs

    Within the specialty aromatics space, disruptions in raw material price and shipping delays have grown more common. We responded with an expanded inventory approach, keeping extra raw stock and finished acid on hand. As a result, most orders ship within two business days, and urgent requests from research labs can leave our dock the same shift. Here, our direct control over every synthesis – from weighing out benzene precursors to drumming the finished acid – gives clients a measure of predictability they haven’t found from agents or outside channels.

    Researchers in both flavors and pharmaceuticals come back for our acid because it means one less thing to troubleshoot in complex syntheses. They remind us frequently that switching to our batches eliminated whole downstream cleaning cycles and improved run times on pilot lines.

    Safety, Environmental Responsibility, and Community Experience

    Working with aromatic carboxylic acids, we always remind our team about safe handling. Gloves and decent ventilation go without saying, but we train for proper neutralization and containment. Each run ends with recorded disposal of solvent residues, spent filtrates, and minor offcuts. Most of our process wastewater returns through an on-site treatment unit, and all waste packages get categorized and logged according to hazard potential. Responsible disposal, not a marketing line, came from years of seeing what corners cut in rival facilities do to municipal systems.

    Our facility sits close to a community of small businesses and family homes – we field questions every few months about process odors and waste management, and give tours to local science teachers so kids understand what responsible chemical manufacturing looks like. Transparency with our material, from sourcing to product delivery, isn’t an afterthought here; it guards our reputation and the product’s acceptance with high-compliance chemists.

    Tackling Specific End-User Challenges

    Flavor chemists and fragrance designers push for acid grades low in volatiles. They remind us that even a trace of common process solvents leaves behind a lingering note during high-temperature blending. To reach top-tier purity, we cycle through two separate drying phases and tailor our packaging to minimize oxygen ingress. Extra steps mean higher production cost, but nobody returns drums for unwanted side-reactivity or strange flavors.

    Pharma clients chasing rare derivatives complain about metallic residues, which often come from poorly maintained reactor jackets or end fittings. As plant operators, we spent months inspecting and replacing vulnerable system components, as even parts-per-million contamination can stall a pilot run. Post-maintenance review now forms a regular part of our shift reports.

    In polymer research, the balance between functionality and side reactions really matters. We’ve seen teams lose valuable weeks substituting in commodity acids, only to watch polymer chains degrade or fail to incorporate cleanly. Early samples of our acid that contained color bodies once stained batches; process tweaks and finer filtration led to consistent, neutral-colored outputs. The difference is clear under a simple glass plate demo.

    Lessons Learned and Continuous Process Improvement

    Seasons change, but chemical consistency remains hard-won. Winter months demand adjustment in cooling rates, or else crystallization drags on and fines develop, slowing filtration. Summer humidity affects how the powder aggregates in drums, prompting a shift toward lined packaging. Our process control team collects real-world feedback: drum weights, pour speed, even how the powder flows during repackaging, and keeps refining small steps.

    Not all adjustments pay off, and sometimes trial batches lose time and money. But meaningful improvement only comes when line workers, supervisors, and QC chemists share real data and trust the management team. Over time, minor but persistent defects – like those undissolved specks in test solutions or the slightly tacky feel of a less-dried drum – fade away in favor of disciplined, documented best practices. This makes it possible for end users to depend on regular results without running extensive inbound checks themselves.

    Perspectives from Direct Manufacturer Experience

    Having real skin in the game makes every improvement tangible. Handling customer complaints, batch misses, and tough deliveries motivated us to tweak processes that never drew attention in official audits. Whenever a scientist calls up to ask why their retort won’t clean up after using another supplier’s acid, or why their crystallization stalls, the answer comes back to how much attention the manufacturer gave to fundamentals. That’s why, instead of marketing stories, we prefer to discuss the journey of every shipment – who signed off on the batch, which reactor produced it, how clean it left our floor.

    These conversations led to changes like moving from fiber drums to triple-lined poly carboys, swapping batch dry-down timing to avoid high atmospheric moisture, running split batches to troubleshoot troublesome input lots, and keeping notes on every variance. Seasoned technicians hold these lessons close, teaching each new worker that every step, down to how the drum loader positions sealing gaskets, affects the finished acid’s integrity.

    Collaboration and New Uses for 6-Phenylhexanoic Acid

    Over years in the field, collaborations between manufacturing, application chemistry teams, and process engineers have opened up new uses for this material. One university partner started from our sample drums and pivoted their research after discovering that 6-Phenylhexanoic Acid derivatives had stronger surfactant properties than initially reported. Another customer opened up a new fragrance line based on ester variations, winning a patent based on the confidence that our acid provided uncontaminated reactant every time.

    Projects like these circle back to the manufacturer, challenging us to refine our protocols, invest in better analysis, and build relationships that outlast price cycles or temporary industry panics. Every new application – whether in specialty resins, niche pharmaceuticals, household aromas, or emerging agricultural chemicals – grows from reliability and openness at the source. We keep up with these changes by reading process papers, attending technical conferences, and pulling line staff into training every quarter, not just to tick compliance boxes but to keep practical know-how sharp.

    Looking Forward with 6-Phenylhexanoic Acid

    The market for specialty acids like 6-Phenylhexanoic Acid keeps evolving. Every new regulation, raw material challenge, and research avenue brings another round of adjustments at the plant. What remains unchanged is our approach: vacuum out that last trace of solvent, check every drum against batch records, pick up the phone when chemists run into problems, and keep production as traceable as the first barrel we shipped.

    Long-term, we’ll keep expanding our quality commitments, double down on process transparency, and collaborate with new chemistry teams eager to trial this versatile acid. For anyone who works with it, especially those tired of off-flavors, inconsistent yields, or mysterious side reactions, our real manufacturing experience backs every shipment, batch, and drum. The difference is in the details – a difference that stacks up, not just for today’s order, but for every innovation made tomorrow.