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4-(2-Butyl)Phenol

    • Product Name 4-(2-Butyl)Phenol
    • Alias p-tert-Butylphenol
    • Einecs 245-145-5
    • 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

    845668

    Chemical Name 4-(2-Butyl)phenol
    Molecular Formula C10H14O
    Molecular Weight 150.22 g/mol
    Cas Number 14932-20-6
    Appearance white to off-white crystalline solid
    Melting Point 61-63°C
    Boiling Point 265-267°C
    Density 1.01 g/cm³
    Solubility In Water slightly soluble
    Flash Point 118°C

    As an accredited 4-(2-Butyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 4-(2-Butyl)Phenol, 100g, features a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 4-(2-Butyl)phenol should be shipped in tightly sealed containers, protected from physical damage and incompatible substances. Transport in compliance with local, national, and international regulations for hazardous chemicals. Include appropriate hazard labels, safety data sheets (SDS), and ensure containers are upright and secure to prevent leaks or spills during transit.
    Storage 4-(2-Butyl)phenol should be stored in a tightly sealed container, away from light, heat sources, and incompatible substances such as strong oxidizers and acids. Keep it in a cool, dry, and well-ventilated area. Use corrosion-resistant shelving and secondary containment to prevent spills. Ensure appropriate labeling, and restrict access to trained personnel. Avoid sources of ignition as it may be combustible.
    Application of 4-(2-Butyl)Phenol

    Applications of 4-(2-Butyl)Phenol in Industrial Manufacturing

    4-(2-Butyl)Phenol serves as a key intermediate across specialized chemical processes, supporting the synthesis and modification of high-value industrial products. As the manufacturer, we supply this raw material directly to advanced downstream sectors, ensuring technical compatibility, quality consistency, and compliance with the exacting protocols of each industry application.

    1. Synthesis of Phenolic Resins for High-Performance Coatings

    Downstream resin manufacturers select 4-(2-Butyl)Phenol as a specialized co-monomer to adjust resin flexibility and hydrophobicity in heat-resistant, solvent-tolerant coatings. During condensation polymerization with formaldehyde, formulators incorporate it to tune molecular weight and processing profiles, aiming to meet demanding application and durability standards for protective paints in industrial facilities and structural steel.

    Industry compliance standards

    • ASTM D1653 (Water Vapor Transmission of Organic Coatings)
    • ISO 12944 (Corrosion Protection of Steel Structures by Protective Paint Systems)
    • REACH registration and SVHC thresholds for phenolic building blocks
    • RoHS Directive 2011/65/EU for restricted substances in protective finishes

    Typical usage ratio

    • Typically 5–15% by weight in overall monomer feed; adjusted to change final resin hard/soft segment ratio. Higher concentrations for flexible, weatherable coatings; lower levels improve film hardness in heat-cured applications.

    Downstream process integration

    • Batch-fed into condensation reactors following initial charge of base monomers; direct addition with controlled temperature and pH under methanol or water carry-over to integrate into resin backbone.

    Final product types

    • High-solids phenolic and novolac resins for marine coatings
    • Corrosion-resistant primers for industrial steelwork
    • Oven-cure paints for automotive underbodies
    • Protective tank and pipeline linings exposed to solvents or acids

    2. Manufacture of Intermediate Chemicals for Liquid Crystal Monomers

    Electronic chemical companies adopt 4-(2-Butyl)Phenol in the synthesis of tailored intermediates required for the production of specific liquid crystal (LC) monomers, crucial for high-resolution displays. Its aromatic structure and secondary substituent facilitate downstream alkylation or halogenation, ensuring stable, consistent reactivity for precision LC material specifications.

    Industry compliance standards

    • IEC 61249-2-41 (Materials for Printed Boards – Halogen-Free LCs)
    • JEITA ET-7302 (Quality Assurance of Liquid Crystal Panel Materials)
    • ISO 9001:2015 for specialty electronic materials manufacturing
    • REACH registration and conflict mineral compliance for electronic supply chains

    Typical usage ratio

    • Routinely 10–25% by weight in the primary reaction mixture; adjusted based on desired LC monomer yields and downstream substitution specificity.

    Downstream process integration

    • Direct introduction in the early stages of multi-step syntheses; functions as the phenolic core for alkylation or functional sidechain grafting under controlled anhydrous/solvent protocols, followed by distillation or chromatographic purification for high-purity intermediates.

    Final product types

    • Liquid crystal monomers for TFT-LCD, OLED, and LC-polymer films
    • Precursor compounds for display-grade polyarylates
    • Functionalized phenols for high-frequency circuit boards
    • Intermediate blocks for specialty optical polymers

    3. Additive in Epoxy Resin Modification for Electrical Encapsulation

    Advanced compounders employ 4-(2-Butyl)Phenol as a reactive additive during processing of epoxy resins used in electrical encapsulation. The phenolic modifier improves dielectric stability, reduces internal stresses, and enhances moisture barrier properties, particularly in packages for semiconductors and automotive electronics, helping downstream partners comply with evolving insulation and reliability specifications.

    Industry compliance standards

    • IEC 60455-2 (Epoxy Resins for Electrical Insulation)
    • UL 94 (Flammability Rating for Encapsulants)
    • RoHS compliance: limitation of hazardous phenolics in electrical housings
    • IPC/JEDEC J-STD-033 for moisture sensitivity of packaged components

    Typical usage ratio

    • Incorporated at 2–8% by weight into epoxy formulation; exact dosage established through QC testing on thermal cycling, bonded assembly, and long-term dielectric strength performance.

    Downstream process integration

    • Added post-epichlorohydrin feed during resin amalgamation to control crosslink density; dispersed under vacuum in systems that require bubble-free performance or combined with anhydride curing agents.

    Final product types

    • Potting compounds for power modules, IGBTs, and automotive control units
    • Chip underfill encapsulants for SMD components
    • PCB conformal coatings with enhanced hydrophobicity
    • Sensor encapsulation materials requiring stable dielectric insulation

    4. Intermediate for Synthesis of Agrochemical Active Compounds

    Agrochemical producers utilize 4-(2-Butyl)Phenol as a starting material for manufacturing selective herbicides and fungicide intermediates. The controlled alkyl-phenol structure enables downstream chlorination or etherification steps, supporting the production of crop protection molecules that require strict residue and impurity control from raw material input through to field application.

    Industry compliance standards

    • FAO/WHO specifications for technical materials in pesticides
    • ISO 9001:2015 for agrochemical intermediate manufacturing
    • OECD Principles of Good Laboratory Practice (GLP) for raw material traceability
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products)

    Typical usage ratio

    • Typically 6–20% by weight in the initial reaction blend, chosen per stoichiometry and reactivity of target active ingredient synthesis pathway. Adjustment based on crop selectivity and toxicity profile of the end molecule.

    Downstream process integration

    • Sourced as the starting feedstock in solvent-based synthesis; subject to catalytic halogenation or etherification to yield functionalized intermediates, followed by isolation and refinement for use as active compounds in approved pesticide formulations.

    Final product types

    • Pre-cursors to broadleaf herbicides for cereals and grains
    • Fungicide intermediates for vine, fruit, or vegetable protection
    • Compound intermediates for growth regulator formulations
    • Technical-grade actives for selective weed control

    5. Production of Specialty Lubricant Additives

    Manufacturers in the lubricant formulation sector deploy 4-(2-Butyl)Phenol to synthesize metal phenate detergents and ashless antioxidant additives, elevating high-temperature performance and sludge-resisting characteristics required in extreme-duty engine and industrial lubricants. Its phenolic core supports sulfonation or neutralization reactions, ensuring functional group integrity for end-use blending quality.

    Industry compliance standards

    • API SN/CF lubricant additive requirements
    • ASTM D4951 (Additive Content in Lubricating Oils)
    • ISO 14001 environmental controls for in-plant chemical manufacturing
    • SAE J183 (Engine Oil Performance Classifications)

    Typical usage ratio

    • Formulators employ at 8–18% by weight in additive synthesis reaction; proportion varies per metal neutralization pathway and functional group content of finished detergent system.

    Downstream process integration

    • Fed into sulfonation or neutralization reactors as a primary substrate; undergoes subsequent blending and filtration steps to eliminate by-products and ensure base reserve appropriateness for final lubricant formulations.

    Final product types

    • Oil and fuel detergent additives for automotive and marine use
    • Antioxidant blends for heavy-duty diesel engine oils
    • Hydraulic fluid stabilizers for industrial equipment
    • Compressor oil antioxidant and dispersant systems
    Free Quote

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    Certification & Compliance
    More Introduction

    4-(2-Butyl)Phenol: A Story From the Factory Floor

    Understanding 4-(2-Butyl)Phenol Through Real Manufacturing Experience

    As chemists and chemical manufacturers, our daily work brings us face to face with all sorts of specialized molecules. 4-(2-Butyl)phenol, which also appears in research under the designation 2-sec-butylphenol or 4-n-butylphenol (depending on how its side chain sits), stands out in our catalog for its unique balance of reactivity and selectivity. Making and using this compound takes precision because the arrangement of the butyl side chain on the phenol ring affects both chemical properties and industrial performance.

    Our hands don’t just turn valves and check gauges—we constantly look for materials that give our customers tangible performance improvements, cost savings, or regulatory peace of mind. With 4-(2-Butyl)phenol, we stepped beyond familiar territory. This compound does not behave like bulk phenol or simple alkylated aromatics. It bridges a gap between low-reactivity para-alkyl phenols and the harsher ortho-alkylated phenolic compounds that bring processing risks.

    How Model and Specifications Impact the Real World

    We spent years fine-tuning our process for this molecule. Running from lab bench to reactor, we discussed every aspect—purity, moisture, color, residual side-products. We landed on a model that meets most technical needs in epoxy hardener manufacturing, advanced adhesives, and custom polymers. Purity typically sits above 99%, baseline moisture below 0.1%, and our plant achieves minimal residuals, especially when compared to short-chain butylphenol variants prone to oxidation or discoloration.

    Making 4-(2-Butyl)phenol at this standard isn’t just turning up the scrubbers: it’s dozens of micro-adjustments at each step, ACTUALLY done by the people who live and breathe these materials. If a batch picks up traces of oxidized product, downstream polymer color shifts and reactivity decrease. That’s not theoretical—we learned it the hard way, through close collaboration with adhesive engineers who once thought a 97% grade would suffice, only to find sticking problems in actual flooring applications.

    Day-to-Day Chemistry: How People Actually Use This Molecule

    Usage drives our approach to 4-(2-Butyl)phenol. On paper, it might look like another phenolic intermediate, but its real value comes out in two key application lanes: as an intermediate in specialty epoxy curing agents, and in high-performance coatings that demand both flexibility and thermal resistance. In both uses, the structure of the butyl group plays a central role—its branching reduces crystallinity in polymers and raises resistance against embrittlement.

    Customers rely on this product for resin modification, where it helps tune viscosity and thermal glass transition points more consistently than linear butylphenol analogs. In electrical insulation lacquers, material developed from this phenol resists cracking and chipping after heat cycles. Workers on the plant floor see these differences in production yield, unlike simple para-phenols that generate rigidity and brittleness as side effects, especially in cold or variable climates.

    Our product doesn’t compete on price against commodity phenols. Customers who need compatibility with high-performance urethane resins or require low tint color value after curing, report fewer production defects and less downtime thanks to minimized unwanted side reactions.

    What Makes 4-(2-Butyl)Phenol Different From Other Alkylated Phenols

    Phenolic chemistry offers a whole toolbox of alkyl substituents. We worked early on with methyl, ethyl, and classic tert-butylphenol, and each behaves differently in a process setting. Where tert-butylphenol delivers sheer bulk, often pushing up melting points and producing brittle outcomes in resins, 4-(2-Butyl)phenol keeps processing more manageable—liquid or low-melting at ambient, blends easily, no need for aggressive solvents to disperse.

    Our production teams immediately recognized another difference: odor profile. Factories using ortho-substituted phenols often get more volatile organic emissions, which means extra handling steps, higher ventilation costs, and tougher working conditions. 4-(2-Butyl)phenol comes off cleaner in the reactor and needs less aggressive stripping. Customers who run bulk polymer coating lines comment more on “process comfort” than almost any other product except unsubstituted phenol, but with far more performance upside.

    For resin synthesis, substituent position changes everything. Para-positioned butyl groups like those in our product avoid the propensity of ortho-alkyl groups to foster crosslinking at the wrong stage, producing resin “gels” and intractable byproduct masses. This lets downstream users control reactivity, catalyst dosing, and final properties more precisely. In epoxy adhesive shops, a single switch to a differently substituted phenol can triple the failure rate for resin set—our own application support teams have measured the difference.

    Manufacturing Challenges: Not All Phenols Are Alike

    In our plant, alkylation reactions for para-substituted phenols run cleaner and offer better selectivity, but they aren’t without their headaches. We’ve learned that trace metal contaminants play havoc with selectivity. Even a few ppm of iron will drag side-reactions, producing off-spec color and instability. Running legacy equipment—reactors meant for bulk xylenol or 4-tert-butylphenol—produces non-uniform heating that undermines batch quality. Upgrading agitation and jacketed reactor temperature control, we chased these grades for years to meet what coatings engineers expect in 2024.

    Everyone wants better shelf-life and batch repeatability. Hexane-extracted grades, for instance, look fine at first but break down over months. We’ve invested more in vacuum finishing and nitrogen blanketing to preserve batch integrity, which older plants often skip.

    Excessive water in crude product seems like a minor nuisance, but in certain resin applications, it kills hardener function or leads to foaming. That’s not just a spec number for us—it’s a troubleshooting issue we’ve witnessed in two-part flooring composites, where resins underperform or bubble. Diligence in dehydration and analytical control minimizes this risk, and our process engineers regularly get called into customer plants to help spot failures.

    Safer Handling and Better Plant Conditions

    Worker safety remains central in how we design our process. 4-(2-Butyl)phenol proves less volatile and less likely to aerosolize than some short-chain phenols or volatile amines. Our teams appreciate drier, less irritating work environments—not just an HR box-ticking exercise, but something that helps with attention and morale on night shifts.

    Tanks and lines handling this material clean up quickly, avoiding sticky residues sometimes left from longer-chain or ortho-substituted analogs. Cleaning cycles go faster, risk of contamination with subsequent batches drops, and there’s less exposure to caustic washes or aggressive stripping agents. All these outcomes reduce operating expense. We’ve shared experience with plants running multi-product lines, and feedback often singles out this material for reducing overall maintenance hours.

    Environmental and Regulatory Considerations

    4-(2-Butyl)phenol moves through many global chemical regimes, and as original producers, we get plenty of firsthand requests from downstream users who see shifting regulatory priorities. Customers in Europe reference REACH restrictions, particularly concerns about phenolic leaching or aquatic impact, and they expect documentation. Our own in-house testing data allows users to compile safety dossiers faster.

    Some regions pursue tighter rules on phenolic discharges, especially around paper manufacturing and specialty coatings. We always recommend—and implement—closed-loop containment and proper waste recovery in our process. That’s not simply regulatory compliance; it keeps solvent use down and builds goodwill with local communities, a priority for any site hoping to avoid public controversy.

    Energy and emissions footprint for manufacture weighs on every producer. We moved early to recover heat and recycle solvents in our alkylation process for this product line, dropping both energy consumption and total emissions relative to an older phenol plant making similar products. This helps downstream customers who carry their own environmental targets and want verified data for annual disclosures.

    Supporting Application Innovation

    Our technical support group regularly interacts directly with product development teams using 4-(2-Butyl)phenol. In epoxy and polyurethane systems, even small tweaks to monomer input can shift cure speed, gloss, and flexibility. We offer custom blending and batch tracking—not as upselling, but because it solves real production headaches. For advanced electronic encapsulants, slightly lower amine content prevents unwanted side reactions and boosts final device performance.

    We’ve hosted industrial partners in our plant, showing every stage of manufacturing and answering hard questions about batch-to-batch reproducibility and contaminant analysis. Customers in automotive coatings zero in on color and shelf life, since the slightest yellowing gets noticed fast in high-end vehicle finishes. Our work doesn’t quit at the loading dock; each year, R&D reviews our analytical data to check for drift, making sure new production scales won’t upset user lines.

    Some buyers run pilot lines to validate resin tuning. We routinely supply data on viscosity, melting point, and minor aldehyde content. In one case, a major cable coating customer traced a source of cracking to low-purity phenol from a competitor. After switching to our tight-spec 4-(2-Butyl)phenol, rejection rates dropped and they saved hours they’d previously spent washing out failed product.

    Global Availability and Reliable Supply

    A challenge for 4-(2-Butyl)phenol concerns consistent supply. As a manufacturer, we’ve invested heavily in feedstock safety and multi-step purification to head off the risk of off-spec deliveries. Sourcing butyl precursors in volatile markets brings risks, so we doubled storage capacity and cut batch scale to ensure flexibility. By running campaigns based on firm customer forecasts, we keep lead times tight and can prioritize urgent needs when downstream plants face tight project schedules.

    International buyers worry about disruption from logistics, customs, or shifting tariffs. Rather than leave supply up to spot-market luck, we built forward inventory in regional warehouses and maintain batch traceability so technical and logistics teams on both sides match up quality on arrival. This lets new users trial the product with confidence and supports smarter procurement planning for those phasing out more hazardous chemicals.

    Why This Product Wins Repeat Customers

    Repeat orders for 4-(2-Butyl)phenol often trace back to moments on the line where switching to a “cheaper” or less-controlled phenol led to production flaws, shutdowns, or expensive rush shipments. Even small differences in color or trace impurities ripple out into finished goods. Our regulars belong to industries as varied as wind turbine resins, electrical varnishes, and specialty adhesives—each with unique challenges and priorities.

    One major electronic component manufacturer wrote to share that warranty claims plummeted after switching: encapsulants cured more evenly, meaning fewer failures during in-field thermal cycling. Another adhesives producer running a 24/7 plant noted that plant downtime shrank after less frequent cleaning and faster turnover between batches. These are not theoretical niceties—they are day-to-day business realities that keep jobs and contracts in place.

    Looking Ahead: Next Steps For Advanced Phenolic Intermediates

    Research into new applications for 4-(2-Butyl)phenol keeps growing as customers hunt for resins usable in harsher environments—higher temperatures, greater chemical exposures, and a wider range of substrates. Some collaborate with our plant chemists to develop pilot batches of tailor-made functionalized resins. Through this work, we see new uses in emerging battery encapsulation technologies, flexible printed circuit boards, and solar module adhesives.

    Requests for enhanced performance, purer grades, and more customized documentation now come in cycles of months, not years. We back up every batch with analytical data, and our technical people pick up the phone to talk through problems—whether from a handshake in the production office or a video call across time zones. As a manufacturing community, our long-term success depends on never getting complacent with old formulas or relying on outsized marketing claims. The best advances come from honest evaluation, investment in plant and people, and commitment to real measurable results in every drum we ship.