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4-Butoxyphenylacetonitrile

    • Product Name 4-Butoxyphenylacetonitrile
    • Alias 4-Butoxybenzeneacetonitrile
    • Einecs 249-971-7
    • 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

    960828

    Chemical Name 4-Butoxyphenylacetonitrile
    Molecular Formula C12H15NO
    Molar Mass 189.25 g/mol
    Cas Number 35184-42-4
    Appearance White to off-white solid
    Boiling Point 359.6 °C at 760 mmHg
    Melting Point 45-47 °C
    Density 1.07 g/cm³
    Solubility Slightly soluble in water
    Smiles CCCCOc1ccc(CC#N)cc1

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

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed with screw cap, white hazard label displaying chemical name, formula, and safety precautions.
    Shipping 4-Butoxyphenylacetonitrile is shipped in tightly sealed containers, protected from moisture and light. It should be packed in compliance with local and international hazardous material regulations, ensuring secure transport and labeling. Transport is typically arranged via ground or air freight, with accompanying safety documentation and adherence to all chemical shipping guidelines.
    Storage 4-Butoxyphenylacetonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong oxidizers and acids. Protect the container from physical damage and direct sunlight. Always ensure proper labeling and handle using appropriate safety precautions including the use of gloves and eye protection.
    Application of 4-Butoxyphenylacetonitrile

    Applications of 4-Butoxyphenylacetonitrile in Industrial Manufacturing

    4-Butoxyphenylacetonitrile serves as an advanced specialty intermediate in several chemical manufacturing sectors. Its unique structural properties and high purity profile anchor its usage in downstream production routes requiring precise molecular modification or functional group integration. The following segments detail real, established application scenarios based on formulation standards, integration points, and end-use product classes.

    1. Pharmaceutical Intermediate for Sartan Antihypertensive Synthesis

    4-Butoxyphenylacetonitrile plays a key role as a building block in the production of biphenyl-tetrazole-based sartans, including candesartan and olmesartan. Used at scale by API manufacturers, it enters directly into the coupling and conversion steps for tetrazole motif attachment. Production teams choose this intermediate to ensure compliance with impurity controls and batch-to-batch consistency, especially under rigorous cGMP regimes. The input ratio varies based on targeted yields and stoichiometric efficiency, subject to reaction process validation and impurity profiling.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II – Basic Requirements for API Manufacture
    • USP/NF and Ph. Eur. monograph specifications for intermediates (in relevant registrations)
    • FDA 21 CFR Part 211 for finished dosage forms

    Typical usage ratio

    • 0.85–1.08 molar equivalents per target sartan API intermediate, adjusted for conversion efficiency and impurity control; precise proportion determined by downstream synthetic step requirements

    Downstream process integration

    • Reactant input for nucleophilic substitution and nitrile group transformation steps
    • Integration during early-stage intermediate synthesis for biphenyl system construction
    • Batch charging under inert atmosphere with high purity monitoring (HPLC, GC-MS)
    • Subsequent conversion in the tetrazole ring-forming stage of multi-step API synthesis

    Final product types

    • Candesartan cilexetil (API)
    • Olmesartan medoxomil (API)
    • Other related sartan API intermediates
    • Registered pharmaceutical bulk substances

    2. Agrochemical Intermediate for Selective Herbicide Synthesis

    Large-scale agrochemical producers incorporate 4-butoxyphenylacetonitrile as a strategic intermediate for synthesizing aryloxyphenoxypropionate herbicides. This raw material enables structure-specific modifications necessary for achieving target activity spectra and selectivity in weed control agents. Its inclusion requires close management of additive ratios to prevent formation of unwanted by-products while meeting environmental and agricultural product guidelines.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 certified process controls for manufacturing inputs
    • Regulations (EC) No 1107/2009 (EU plant protection product approval)
    • China GB/T 1603–2018 (Pesticide intermediates quality standard)

    Typical usage ratio

    • 0.65–0.95 equivalents per final herbicide molecule, optimized for target isomer formation and process efficiency; subject to herbicidal active concentration requirements and downstream step yield

    Downstream process integration

    • Initial condensation step for etherification reactions in aryloxy chain formation
    • Continuous or semi-batch reactor feeding, often under controlled temperature and catalytic conditions
    • Reactive precursor charging ahead of chlorination or carboxylation for active core construction
    • QC monitoring for residual unreacted nitrile by wet chemistry and LC analysis

    Final product types

    • Clofop-methyl and related herbicidal actives
    • Custom-formulated pre-emergent and post-emergent herbicide concentrates
    • Granular and liquid herbicide technical materials
    • Intermediates for selective grass weed control formulations

    3. Liquid Crystal Monomer Precursor in Electronic Displays

    The specialty electronics sector sources this compound as a core precursor in the synthesis of custom monomers for liquid crystal compounds. Manufacturers integrate this nitrile-based intermediate in the initial steps of producing high-performance nematic or smectic liquid crystals, where the precise electronic and steric properties critically affect display response times, colour stability, and electrical alignment in LC cells destined for advanced LCD panel technologies.

    Industry compliance standards

    • IEC 62321 (Screening of substances in electrical and electronic products)
    • RoHS 2011/65/EU directive (Restriction of hazardous substances)
    • ISO 9001:2015 for electronics materials traceability
    • Customer-specific QMS (Quality Management Systems) in the liquid crystal supply chain

    Typical usage ratio

    • 0.25–0.5 mole per mole of custom mesogen designed for final LC composition; usage based on electronic transition requirements and targeted birefringence

    Downstream process integration

    • Advanced organic synthesis stages for mesogenic core assembly
    • Functional group derivatization via hydrogenation and etherification
    • Purification via column chromatography for electronic applications
    • QC on monomer precursors by NMR and mass spectrometry prior to LC blend formulation

    Final product types

    • Nematic and smectic liquid crystals for LCD modules
    • Active matrix and passive matrix display materials
    • LC mixtures for TFT-LCD, OLED, and automotive display panels
    • Customized LC module blends for high-definition and high-speed applications

    4. Fragrance Intermediate in High-Performance Aroma Chemicals

    Aroma chemical producers deploy this intermediate for constructing alkylated phenylacetonitrile derivatives used in fine fragrance and specialty perfumery niches. The controlled alkylation and subsequent functional group transformation steps leverage its molecular backbone to build complex aromatic profiles with desired volatility and persistence. This application necessitates adherence to stringent volatile organic compound limits and IFRA guidelines, particularly in formulations destined for high-value end markets.

    Industry compliance standards

    • IFRA Standards for fragrance ingredient safety
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • REACH (EC) 1907/2006 for registration of chemical substances
    • ISO 9235:2013 (Aromatic natural raw materials and related products)

    Typical usage ratio

    • 0.1–0.18 equivalents in core aroma chemical formation; finalized by batch-specific headspace GC and olfactory panel testing

    Downstream process integration

    • Input to Friedel–Crafts alkylation step for scent performance tuning
    • Conversion during key-chain elongation and esterification for fixative synthesis
    • Fractional distillation and purity assays aligned with fragrance industry guidelines
    • Organoleptic evaluation prior to downstream blending into master fragrances

    Final product types

    • High-performance aroma base chemicals
    • Custom fragrance intermediates for fine perfumes and luxury personal care products
    • Functional fragrance compounds for detergents and consumer goods
    • Long-lasting fixatives for premium scent delivery
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    Certification & Compliance
    More Introduction

    4-Butoxyphenylacetonitrile: Manufacturing Insights, Uses, and Practical Advantages

    Rooted in Performance: What Sets Our 4-Butoxyphenylacetonitrile Apart

    In the chemical manufacturing field, few things matter as much as reliability paired with consistent purity. 4-Butoxyphenylacetonitrile, with the model name BPAN-03, stands as a durable choice for customers needing a phenylacetonitrile with a butoxy group at the para position. Across almost two decades of manufacturing experience, overseeing thousands of batches in our facility, I have seen this compound step up as both a niche specialty and a practical building block across challenging synthesis projects.

    There’s no substitute for hands-on processing. Every ton we produce goes through purification above 99%, with moisture and ash standards tighter than what’s found in bulk intermediates. Our chemists rely on gas chromatography and HPLC validation to confirm batch-to-batch reproducibility, something that matters for those scaling up into fine chemicals, pharmaceuticals, or advanced materials. We use only direct phenol butoxylation and cyanomethylation onto high-purity feedstock to give tighter isomeric profiles and almost zero residual reactants.

    Differences from other aromatics in this class show up not just in the numbers, but also out on the plant floor. During process scale-up, we tracked reaction kinetics for both the phenylacetonitrile and the substituted butoxy variants, finding that 4-Butoxyphenylacetonitrile tolerates higher thermal ranges without significant side reactions, compared to ortho or meta isomers. This gives formulators more leeway in acid/base equilibria, which helps custom manufacturers design more robust downstream reactions.

    Pushing Boundaries in Application: Real-World Usage

    As a starting intermediate for synthesis, this compound covers several demanding roles in API research, agrochemical exploration, and materials development. One specific case that stands out involved a customer developing a kinase inhibitor. Their route needed tight control over side-chain functionalities, especially avoiding cross-polymerization and unwanted branching during scale-up. Our 4-Butoxyphenylacetonitrile delivered the result. We traced their batch yields throughout the pilot phase. The structures built from our crystals gave the required substitution with negligible by-products, something not seen when they tried third-party supplies.

    On the agrochemical side, another partner pushed for higher stability in phenylacetic acid derivatives. Comparisons with traditional phenylacetonitrile and ethoxy-substituted versions showed lower thermal decomposition in stress testing for the butoxy product. The compound’s longer alkoxy chain offers not just electronic effects but also notable changes in solubility across solvents. In practical terms, this means easier formulation for both solvent-borne and suspension products. Since the demand from crop science ventures continues rising, performance on this front can’t be substituted by cheaper, less pure grades.

    Industrial coatings and specialty polymers pursue molecular rigidity as well as functional group compatibility. During certain polymerizations, our 4-Butoxyphenylacetonitrile outperformed its branched isomers, closing the risk of unwanted chain transfer. Manufacturers leveraging emulsion or solution-based techniques benefit from its controlled reactivity and lower formation of colored by-products post-cure.

    A Manufacturer’s Perspective: Stability, Handling, and Batch Verification

    The best lessons about chemical handling come from first-hand challenges. 4-Butoxyphenylacetonitrile presents fewer volatility issues compared to lower-substituted precursors. Its higher boiling point means safer charging in semi-continuous reactors. On occasion, during high-humidity days, we’ve seen caking if exposed too long outside its moisture-resistant packaging; that’s why our operations team reinforces sealed storage and argon blanketing.

    Consistency stays top of mind—not only purity but also granular flow and filtration performance. Some customers run it through high-shear mixers for custom formulations. Many suppliers neglect bulk bag screening, but we added inline sieving after years of fielding customer feedback. That helps avoid blockages and dusting during downstream weighing and blending. Simple quality-of-life improvements like these save time and mess. Our hands-on approach means plant technicians aren’t battling lumps or powder fly-off during charging.

    One difference from commodity phenylacetonitrile relates to how end-users perceive trace impurities. Over the years, researchers and process chemists reported that minor traces of unreacted phenol or residual halides can wreck lab reactions—even at levels considered “acceptable” under general standards. This is why our verification doesn’t stop at a single assay value. We archive certificate values for each shipment, and invite partners to audit our incoming feedstock and finished product analytics. In more than a thousand supply runs, we handled customer method development and transfer with transparent data to head off surprises.

    For customers scaling into cGMP or regulatory-restricted domains, reproducibility and traceability are absolute. Our records stretch back years, and we offer batch history and full sample retention. I recall supporting a customer’s DMF filing, navigating one regulator’s request for source chain documentation and stability records—because of that, our protocols now include extended shelf-life profiling under both light and dark conditions. The compound’s performance held steady, unlike less stable, shorter-chain homologues, which showed early yellowing and detectable degradation products.

    Supply Chain and Global Challenges

    Supply disruptions, especially for aromatic intermediates, created major shockwaves these last few years. When large factories shuttered or started capacity cuts, some buyers chased third-party traders promising expedient lead times and generic grades. With 4-Butoxyphenylacetonitrile, that risk carries real weight; inconsistent purity from resellers can mean downstream rework and qualification failures. Our approach stays rooted in primary manufacturing—controlling feedstock, synthesis, purification, and packaging under one roof.

    We source high-purity raw phenols and butyl intermediates from credentialed suppliers, performing incoming identity and contaminants screening to prevent right at the earliest stage. This tightens the supply chain to reduce contamination risks, maintains traceability, and simplifies regulatory reporting. We’ve worked with logistics partners to build temperature-stable, documented freight lanes, ensuring product safety from our warehouse to a customer’s dock. On occasion, end-users have asked us to organize on-site support to adapt to stricter storage protocols—our technical team answers those calls, sharing practical advice gained from field experience, addressing handling risks directly rather than pushing papers.

    Every change in chemical regulatory landscapes, whether by REACH, TSCA updates, or local equivalents, requires diligent review and real-world adaptation. For 4-Butoxyphenylacetonitrile, stability and registration support mean market access and operational compliance. Our regulatory support staff actively monitor changing requirements and liaise with regulators when new rules emerge on data transparency, batching, or waste management. Our facility responded to one audit by updating documentation practices and fortifying our waste capture systems based on best available technology benchmarks.

    Waste management for this compound follows applied benchmarks. Where possible, we recover solvents and minimize organics to reduce landfill impact. Slurry residues pass through incinerators engineered for aromatic by-products, minimizing air emissions and monitoring output in real-time. These investments matter long term—costly, but essential in responsible manufacturing.

    Comparative Advantages: What Practical Chemistry Has Taught Us

    Over many manufacturing cycles, careful control provides results not achievable with off-the-shelf or mass-batch chemical sources. We’ve done side-by-side trials with our 4-Butoxyphenylacetonitrile against meta- and ortho-butoxy analogues, as well as non-butoxy-phenylacetonitriles. The para-substituted version proved more stable to UV stress, resisted discoloration, and, in field trials, extended product shelf life by over 20% versus its closest isomeric cousins.

    In some API development campaigns involving nucleophilic substitutions, the steric profile of the butoxy group at the para position led to cleaner reaction profiles. Our in-house team has documented over forty substitutions using this molecule as a nodal intermediate, ranging from anti-cancer raw materials to fixed-dosage veterinary actives. Experience showed that customers achieved higher conversions, with less need for post-reaction scavenging, compared to products of lesser purity or alternate ring substitution.

    We engaged several partners in pilot trials, helping them resolve bottlenecks in their late-stage purification schemes. A recurring theme emerged: impurities typical in commodity routes—chlorinated organics, oxidized residuals, or unknown side products—poisoned catalysts and led to off-color batches. By deploying multiple adsorbent and crystallization steps, we lessened catalyst fouling, and with less residual color so the finished products met pharmaceutical appearance standards. No short cuts happened here; practical, methodical improvements build trust batch after batch.

    Continuous Improvement, Direct Dialogue

    Every manufacturer can talk up quality. But fielding feedback, then acting on it, makes the practical difference. Over years of direct exchange with chemists and engineers, we fortified our practices with real suggestions. One example: a customer working on ion-exchange applications reported micro-particle retention beyond their filter capability during a batch run. Instead of simply logging the complaint, we reworked our milling and sieving system, then followed up with batch samples and on-site trials.

    Another partner scaling up solvent-based formulations faced challenges in keeping the product in solution at low temperatures. Drawing on our bench-scale solubility plots and in-house thermal cycling, we gave clear guidance on optimal solvent pairing and storage conditions. These steps can’t be replicated by trading houses or generic resellers simply repacking bulk shipments. Our organization’s role is to support direct technical transfer, troubleshoot batch issues, and back up each shipment with a record extending to original feedstock.

    Our ongoing plant improvements come from both industry benchmarking and personal lessons. Whenever process incidents happened—whether from packing line mishaps or isolated feedstock events—our plant teams reviewed root causes and implemented practical fixes. Over time, that diligence reduced rework rates and improved on-time delivery.

    Looking at 4-Butoxyphenylacetonitrile across years, I see less of a commodity and more of a toolbox essential that keeps R&D, pilot, and production workflows running smoothly. Unlike disposable reagents or low-purity solvents where end-users settle for “good enough,” this compound rewards those who demand consistent performance batch after batch.

    Looking Ahead: Market Evolution and Practical Adaptation

    The landscape of specialty chemicals grows ever more complex. Demand for custom intermediates like 4-Butoxyphenylacetonitrile reflects the shifting needs of the pharmaceutical, agrochemical, and materials industries. Each year, stricter regulations, higher purity standards, and increasing performance requirements challenge manufacturers to keep pace. We approach this by investing in process optimization, personnel training, and active communication with users.

    Our laboratory staff continually explore route improvements—streamlining purification steps, recovering more solvent, or raising yields from available feedstocks. This isn’t change for its own sake; it’s rooted in responding to the realities of our customers’ operations: unpredictable demand spikes, tighter spec boundaries, and the need for absolute product traceability. Some improvements come from formal process improvement cycles, others just from a technician’s suggestion after a messy transfer. That open culture lets us stay flexible without compromising quality.

    Regulatory scrutiny will only increase: transparency around residual impurity profiles, validated stability data, and environmental impact. We have responded with ongoing investments in analytical infrastructure, tracking batch histories with more nuance, and integrating best practices for sustainable waste processing. Customers can expect even greater openness around source data and material history, steps we’ve anticipated because regulators, partners, and end-users all want verifiable information, not just promises.

    By maintaining full process control in-house—not splitting synthesis and purification across contractors or regions—we keep direct oversight, minimize chain-of-custody gaps, and respond faster to customer inquiries. This matters especially in a world where “minor” impurities can trigger major regulatory or operational headaches.

    A Down-to-Earth Commitment

    Reflecting on years of direct experience manufacturing 4-Butoxyphenylacetonitrile, the story comes down to more than a chemical name or purity number. Each batch carries the decisions, vigilance, and lessons from every preceding run. Customers have backed our approach with years of repeat orders, site visits, and feedback that keep us on course. For anyone seeking a robust, high-purity version with verified background, practical support, and documented improvements, we stand ready—not as an anonymous source but as a partner who’s lived the challenges and solved problems in real time.

    The journey continues as we map new applications, resolve emergent use-case hurdles, and raise the bar for what specialty intermediates should deliver. We embrace every challenge, answer every technical call, and document every improvement for a reason: real-world trust grows only from real-world experience, and nobody values that more than a manufacturer who stands behind every shipment.