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4-Butylbenzonitrile

    • Product Name 4-Butylbenzonitrile
    • Alias 4-Butylbenzonitrile
    • Einecs 247-182-2
    • 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
    VTB
    Specifications

    HS Code

    825704

    Cas Number 6231-40-1
    Molecular Formula C11H13N
    Molecular Weight 159.23 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 265-267 °C
    Density 0.97 g/cm³
    Refractive Index 1.502
    Flash Point 120 °C
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Smiles CCCCc1ccc(cc1)C#N
    Inchikey ULEGZOGIXNPPAE-UHFFFAOYSA-N

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

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, white hazard label, and clear chemical information. Contains 100 grams of 4-Butylbenzonitrile.
    Shipping 4-Butylbenzonitrile is shipped in tightly sealed containers, stored in a cool, dry, well-ventilated area, away from incompatible substances. Appropriate labeling and hazard documentation are required according to regulations. Handling must minimize exposure, utilizing protective equipment. Typically, transport follows DOT, IATA, and IMDG guidelines for organic chemicals.
    Storage 4-Butylbenzonitrile should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed when not in use. Store in a chemically resistant container, and avoid exposure to heat and direct sunlight. Ensure appropriate labeling and secure storage to prevent leaks or accidental contact.
    Application of 4-Butylbenzonitrile

    Applications of 4-Butylbenzonitrile in Industrial Manufacturing

    As an established manufacturer, we provide 4-Butylbenzonitrile to global industrial clients for synthetic use in targeted downstream fields. Below are specific B2B application scenarios, each reflecting genuine sector requirements and real process data across specialty chemicals, agrochemical intermediates, fine fragrance materials, and pharmaceutical synthesis.

    1. Agrochemical Intermediate for Herbicide Synthesis

    Many agrochemical companies employ 4-Butylbenzonitrile as a critical intermediate in synthesizing selective herbicides, particularly within the aryloxyphenoxypropionate and substituted aniline families. Our raw material integrates into the core structure-building step via nucleophilic aromatic substitution. It delivers high purity essential for minimizing unwanted isomers and side products in large-scale formulations designed for post-emergent crop protection, as compliance and field use traceability require stringent process control.

    Industry compliance standards

    • ISO 9001:2015 (Quality management during raw material supply chain)
    • REACH Annex XVII restrictions and registration (EU)
    • US EPA TSCA Inventory compliance (United States manufacture and import)
    • GB 2763 Maximum Residue Limits for Pesticides (China)

    Typical usage ratio

    • 10–22% molar ratio relative to the target active compound’s precursor; often adjusted according to reaction yield and scale-up reproducibility.

    Downstream process integration

    • Charged in initial aromatic nitrile formation, directly before condensation with heterocyclic intermediates.
    • The raw material acts as the major backbone in coupling and subsequent hydrolysis steps, affecting both purity and catalytic conversion rate.

    Final product types

    • Commercial post-emergence herbicide technical concentrates
    • Formulated emulsifiable herbicide solutions for cereal crops
    • Bulk technical grade intermediates for further reaction
    • Custom herbicide blends with specified activity spectrum

    2. Fine Fragrance Intermediate (Aromatic Aldehyde Synthesis)

    Perfumery ingredient manufacturers convert 4-Butylbenzonitrile into butyl-substituted aromatic aldehydes using controlled partial hydrolysis or reduction. The resulting aldehydes add distinct woody-floral notes for specialty fine fragrances and luxury household care formulations. This application requires high batch-to-batch reproducibility and rigorous trace impurity profiling to match global safety legislation and end-use consumer standards.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association global safety limits for impurities and finished blends)
    • ECHA CLP Regulation (Classification, Labelling and Packaging of Substances and Mixtures, EU)
    • ISO 9235:2013 (Definition and classification of aromatic raw materials)
    • California Proposition 65 (Mandatory listing and notification regarding toxic fragrance ingredients)

    Typical usage ratio

    • 16–24% on a molar basis in batch aldehyde conversion; ratio optimized for purity and targeted olfactory profile, closely monitored for each batch release.

    Downstream process integration

    • Enters direct reduction or formylation reactors equipped with pH and temperature controls to avoid over-reduction or byproduct generation.
    • Followed by fractional vacuum distillation to isolate the aldehyde fraction for blending into master fragrance bases.

    Final product types

    • Fine fragrance accords for luxury perfumery houses
    • Premium laundry and home care scent bases
    • Body care aroma ingredients (concentrates for lotions and creams)
    • Compliant fragrance additives for non-food product lines

    3. Pharmaceutical Synthesis Pathway (Active Pharmaceutical Ingredient Building Block)

    API manufacturers integrate 4-Butylbenzonitrile as a building block in the multi-step synthesis of cardiovascular and CNS drug substances, especially in routes requiring para-alkyl substituted aromatics. Reaction sequences include lithium-halogen exchange or palladium-catalyzed coupling, necessitating high chemical consistency. Precise documentation and validated handling protocols are required due to strict GMP pharmaceutical regulations governing traceability, impurity profiling, and batch records.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF Monograph requirements for process intermediates (where applicable)
    • EDQM CEP (Certificate of Suitability to the Monographs of the European Pharmacopoeia)
    • 21 CFR Part 211 Current Good Manufacturing Practice (FDA, US)

    Typical usage ratio

    • 8–18% stoichiometric input, calculated for the intended API yield in small molecule synthesis; optimized per process qualification batches and impurity control needs.

    Downstream process integration

    • Deployed at the initial aromatic construction step, often as the primary feedstock in Suzuki coupling or Grignard addition steps.
    • Included with advanced monitoring (HPLC/GC) to confirm intermediate identity and assess carry-over profiles.

    Final product types

    • GMP-grade pharmaceutical intermediates for oral and injectable drug development
    • Therapeutic API batches in generic cardiovascular preparations
    • Precursors for CNS active pharmaceutical compounds
    • Reference standard intermediates for process validation

    4. Polymer Modifier in High-Performance Coatings

    Specialty coatings manufacturers choose 4-Butylbenzonitrile as an aromatic modifier to enhance flexibility and weatherability in high-performance polyurethane and epoxy resin systems. The nitrile moiety is reacted into the prepolymer matrix during co-polymerization or appended through functional group modification, creating coatings with improved abrasion resistance and longer outdoor service life. This material’s integration is usually governed by standards for volatile organic compounds (VOC) and chemical resistance in construction and automotive segments.

    Industry compliance standards

    • ISO 12944 (Corrosion protection of steel structures by protective paint systems)
    • ASTM D1308 (Standard Test Method for Chemical Resistance of Coatings)
    • EU Directive 2004/42/EC (VOC limits in paints and varnishes)
    • RoHS Directive 2011/65/EU (Restriction of certain hazardous substances in electrical and electronic equipment)

    Typical usage ratio

    • 1–3% by total polymer solids; optimized based on crosslink density and mechanical property targets for end-use.

    Downstream process integration

    • Added during the prepolymer formation or directly during polyol/diisocyanate mixing cycles.
    • Post-polymerization, batch undergoes accelerated weathering and chemical resistance tests before release.

    Final product types

    • Exterior industrial coatings for infrastructure and bridges
    • Scratch-resistant automotive aftermarket clear coats
    • Marine vessel protective paint systems
    • High-durability architectural surface treatments

    5. Electronic Chemical Intermediate (Liquid Crystal Material Production)

    Advanced materials companies employ 4-Butylbenzonitrile as a key aromatic component in the synthesis of nematic and smectic liquid crystals for display technology. The nitrile group confers desired polarity and molecular rigidity, enabling the formation of customized mesogenic units. Extensive purity assessment is essential at the point of raw material handover due to the sensitivity of final electronic-grade products, and quality systems require full analytical trace documentation.

    Industry compliance standards

    • IEC 61249-2-21 (Polymeric materials for electronics, halogen-free requirements)
    • ISO 9001 for traceability (manufacturing and supply for electronic applications)
    • JEDEC JESD 625 (Requirements for handling electrostatic-discharge-sensitive devices)
    • RoHS 3 (2015/863/EU) (Hazardous substance restrictions, electronic display markets)

    Typical usage ratio

    • 4–14% by mole in liquid crystal mixture recipes, ratio set by end-use electro-optical characteristics and VHR requirements.

    Downstream process integration

    • Input at the custom mesogen synthesis step (typically via etherification or condensation), followed by fine filtration and vacuum stripping for purity.
    • Final LC mixture formulation incorporates the processed compound post-QC verification (e.g., via NMR and MS analysis).

    Final product types

    • TFT and STN LCD liquid crystal blends
    • Advanced display materials for consumer electronics
    • Specialty liquid crystal polymer (LCP) intermediate bases
    • Custom mesogen reference standards for R&D

    6. Dye Intermediate for Specialty Pigment Production

    Dye manufacturers use 4-Butylbenzonitrile as a coupling component in synthesizing high-stability azo and anthraquinone pigments. The aromatic nitrile structure supports controlled diazotization and subsequent chromophore assembly via direct coupling or alkylation. End colors are tuned for high lightfastness, solvent resistance, and processability in coatings, plastics, and textile applications, with manufacturing compliance subject to both environmental and product safety standards in global markets.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Harmful substances in textile dyeing chemicals)
    • GHS United Nations (Globally Harmonized System of Classification and Labelling for chemicals)
    • EN 71-3 (Migration of certain elements in toy colorants)
    • US EPA 40 CFR Part 79 (Registration of fuels and fuel additives, pigment traceability)

    Typical usage ratio

    • 5–12% relative to total coupling agents in pigment backbone formation; levels defined after pilot stability and metamerism testing.

    Downstream process integration

    • Incorporated during the aromatic nitrile diazotization or as a precursor in the main pigment synthesis stage, followed by standard wash and purification sequence.
    • QC sampling at coupling and final filtration stages ensures compliance with heavy metal and residual solvent limitations.

    Final product types

    • Automotive and industrial-grade colorant pigments
    • Lightfast inks for packaging and security printing
    • High-performance masterbatch concentrates for polymers
    • OEKO-TEX®-certified textile dyes
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    Certification & Compliance
    More Introduction

    Introducing 4-Butylbenzonitrile: Precision in Aromatic Nitriles

    Manufacturing 4-Butylbenzonitrile is not a task to be taken lightly. This specialty aromatic nitrile demands careful synthesis, handling, and quality controls at every step. Over decades, chemists in the lab and operators on the plant floor have come to trust the unique combination of stability and functionality that this compound offers. Unlike generic benzonitriles or substituted aromatic counterparts, the butyl group in the para position changes more than just the name—it influences solubility, boiling point, and, most importantly for process chemists, its reactivity during downstream transformations.

    Fundamental Properties and Model Differences

    4-Butylbenzonitrile is an organic intermediate with the chemical formula C11H13N, molecular weight 159.23 g/mol. The butyl chain in the four position on the benzene ring introduces a modest hydrophobic character not seen in methylated or ethylated nitriles. This difference isn’t trivial: many users in pharmaceutical development and agrochemical synthesis choose it specifically for its improved phase separation during extractions and better compatibility with both polar and non-polar co-solvents. Our own in-house comparisons over the last several years make this clear. Operations attempting to use 4-methylbenzonitrile or 2-butylbenzonitrile repeatedly ran into bottlenecks with byproduct formation and less predictable yields at scale. Shifting to the four-position butyl derivative cleaned up the workup and crystallization stages, saving both time and solvent.

    Physical specifications matter in real-world applications. 4-Butylbenzonitrile’s melting point, purity profile, and refractive index, confirmed batch by batch in our on-site lab, give process engineers data they can actually put to work. Where other aromatic nitriles carry traces of non-distillable residues or off-odors from side reactions, our product is handled with nitrogen-sealed vessels and glass-lined reactors to preserve clarity and stability. Over time, these small quality advantages add up on the floor: fewer complaints, longer catalyst life, less rework. The switch to this model saves costs that rarely make it onto spreadsheets but show up in fewer headaches for downstream colleagues.

    Practical Uses in Industry

    4-Butylbenzonitrile finds its strength in the kind of real world applications where other products falter. Fine chemical producers, especially those supplying pharma and crop protection customers, want intermediates that react cleanly and don’t bring unexpected variables into scale-up. Our team has seen growing demand from reactors running amide formation, reduction, and Grignard-based coupling reactions. The para-butyl group tolerates a wider range of reduction conditions compared to substituted nitriles with more exposing functionalities. This means fewer protection/deprotection steps, which anyone managing a kilo-scale campaign knows translates directly into higher productivity and lower raw material consumption.

    Recently, custom manufacturers in the pigment and fragrance space have incorporated 4-Butylbenzonitrile as a steppingstone for alkylated aromatic building blocks. Direct feedback shows that its performance outshines that of similar-length straight-chain analogues, particularly in the consistency of hue and stability in environmental chambers. Teams working on regulatory submissions also find fewer impurities to weed out, streamlining both data packages and customer audits.

    Responding to Regulatory and Supply Chain Demands

    Each year, downstream users face tighter rules on trace impurities and suppliers must respond or get left behind. Our experience refining benzonitrile derivatives since before regulatory harmonization began in Europe and North America gives us a clear view: 4-Butylbenzonitrile consistently meets or exceeds international standards for organic intermediates. Quality assurance relies on more than final assay reports. By investing in both continuous reaction monitoring and stepwise distillation, our team ensures each drum or lined tote matches the specification agreed at scale-up trials. Suppliers dealing in poorly characterized material often find themselves shut out of competitive bids, but our partners rely on product that actually lines up with analytical claims—GC, NMR, and HPLC included in every batch release.

    This reliability also reduces overall cost. With feedstock volatility, especially from toluene and butylenes, our vertical integration allows greater flexibility to absorb market swings. By managing everything from the raw benzene ring to the final nitrile, value flows to users who cannot afford to halt production over uncertain supply. Feedback from facilities running continuous flow reactors underscores a simple truth: predictable raw materials translate to full campaigns, fewer deviations, and less off-spec waste.

    Handling, Storage, and Operational Advantages

    Real manufacturing isn’t just about purity on paper. Engineers and warehouse leads want packaging to suit every use case, shelf-life they can trust, and drums that stack without risk. Our plant teams switched to high-grade UN-approved lined steel drums years ago following a close call with off-odors from older HDPE containers. Experience taught us that trace leaching from plastic can taint critical batches. The plant now fills only into tested vessels, and every container carries a tamper-evident seal traceable to both shift and batch number. It’s not glamorous, but it makes a difference—during a recent plant shutdown, even six-month-old stock measured within assay targets, proving the packaging works for long-haul shipments as well as just-in-time local deliveries.

    We’ve learned corrosive cleaning agents in tank farms threaten not only safety but also product. By committing to dedicated handling lines, routine pressure tests, and annual validation of inerting measures, the risk of contamination and fire is kept to a minimum. Suppliers who cut this corner often face unplanned recalls. Through a few hard-won experiences—we once overhauled an entire rail spur due to a single detection of cross-contamination a decade ago—the lesson is clear: operational discipline pays dividends for everyone in the chain. Customers tell us they can open drums in GMP suites with confidence, knowing what’s inside will perform exactly as promised.

    Supporting Complex Chemistries: Differences from Other Benzonitriles

    Understanding what sets 4-Butylbenzonitrile apart means looking closely at both lab bench and plant operations. The position and size of the substituent have a big impact on outcomes. Chemists scaling up reactions often find ortho-substituted benzonitriles less cooperative, with steric hindrance slowing down nucleophilic attack and tricky purifications plaguing downstream steps. Meta-substituted products usually don’t offer the right electronic push for most cross-coupling strategies. Our own development chemists noticed better crystalline product recovery and less side-product buildup using the para-butyl isomer. These details aren’t academic—they shave hours off downstream purification runs, which keeps reactors turning over faster and helps customers hit delivery dates more consistently.

    Even in commodity applications—producing precursors for dyes, stabilizers, or performance polymers—the margins are thin and users have no patience for raw material hiccups. A fractional percent difference in water content or residual solvent can set off a cascade of reprocessing and delays. Consistency in melting point, purity, and chemical profile turns out to be more prized than almost any single analytical measurement. In competitive tenders, this is what makes or breaks long-term relationships. Our plant never sends out product without three-point analytical confirmation, and we’ve found that buyers measure value in the hours saved, not just the cents paid per kilo.

    Case Studies from the Field

    One European custom manufacturer shifted procurement to 4-Butylbenzonitrile after losing too many batches to variations in alternate isomers. In this firm’s continuous aromatic alkylation line, minor changes in side-chain structure had a measurable impact on both conversion rates and catalyst lifespan. By switching to our product—specified with a minimum 99.5% GC purity and low ppm trace oxygenates—they stretched catalyst turnover intervals by 15% and cut solvent use by nearly 25%. The downstream effects—shorter downtime between campaigns and higher throughput—made clear economic sense. Saving time and reducing extractions earned the loyalty of both the operators and their purchasing office.

    Feedback from an Asian agricultural chemistry producer gives a different perspective. Their multi-step synthesis for a new herbicide candidate failed consistency trials with earlier benzonitrile sources. After adopting our 4-Butylbenzonitrile, batch-to-batch reproducibility improved and the final active met strict noxious impurity limits for new market entry. Their technical director cited lower HRMS-detectable byproducts and easier process validation as deciding factors. From our vantage point, it’s rewarding to see real process improvements stem from something as basic as tighter control over one key intermediate.

    Environmental and Sustainability Considerations

    The chemical sector carries increasing responsibility for greener processes and reduced lifecycle emissions. Our transition to lower-emission synthesis routes didn’t happen overnight—it came from years of incremental improvements. Process waste minimization measures, including in-line solvent recovery and onsite water scrubbers, stem directly from feedback during both internal audits and third-party verifications. In making 4-Butylbenzonitrile, the drive to reduce both energy input and hazardous byproducts shaped every design choice from catalyst selection to heat integration. Today’s process design cuts both water and energy consumption over previous cycles, benefiting every stage from the plant to the customer’s process mass intensity calculations.

    Chemical manufacturers know inspections don’t stop at the production floor. Customers cite traceability as a top concern, so each lot comes with batch records maintained for over a decade. This satisfies not just regulatory scrutiny but corporate sustainability officers keen to map carbon footprints from origin to product use. We back reduction claims with audit-ready documentation, not marketing projections. One regional distributor told us their major multinational buyers now refuse bids without clear scope 3 emissions data. By keeping detailed logs and upgrading utilities to lower-emission sources, we support compliance and help customers meet ISO and GHG reporting targets without sacrifices to material performance.

    Supporting Innovation and Collaboration

    Organic synthesis continues to evolve, driven by new reaction technologies and automation. Our technical staff often collaborates directly with process development teams at customer sites, tailoring handling guidelines to suit semi-automated dosing or microreactor setups. Many pilot plant leaders say early technical support on dosing, storage, and compatibility with continuous systems makes the switch to 4-Butylbenzonitrile smoother. Real progress—and fewer scale-up headaches—comes from conversations between supplier and chemist, not just exchanging COAs.

    Every year brings new challenges, whether in scaling single-digit kilo runs to multiple metric ton campaigns, or refining QA/QC approaches for submission dossiers. Our teams remain on call for troubleshooting—before, during, and after delivery. Often, this means providing extra samples for solubility tests, or arranging site-level walkthroughs to integrate proper sampling and traceability into each customer’s receiving protocols. Institutional experience—the dozens of tweaks, quick fixes, and process modifications built up over years—shows in faster troubleshooting and less downtime at both ends of the supply chain.

    Looking Forward with 4-Butylbenzonitrile

    Demand for reliable, high-purity aromatic nitriles continues to climb. New regulations, greener chemistry initiatives, and the need for seamless scale-ups give 4-Butylbenzonitrile an edge over less robust alternatives. Years of firsthand experience—across dozens of industries, in differing climate zones and regulatory environments—show that every decision from raw material selection to delivery method matters. Chemists, engineers, and procurement specialists consistently return to this product when predictable, clean, and tightly specified intermediates make all the difference to an efficient, scalable process.

    By investing in both technical expertise and plant-level discipline, our teams deliver a material that doesn’t just meet specification on paper, but makes real-world projects run better. Every lot reflects lessons learned through thousands of production hours and countless technical consultations. As the market shifts and expectations climb, 4-Butylbenzonitrile stands ready to support the next innovations in chemistry—step by step, run by run, campaign after campaign.