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4-Tert-Butylbenzoylacetonitrile

    • Product Name 4-Tert-Butylbenzoylacetonitrile
    • Alias p-tert-Butylbenzoylacetonitrile
    • Einecs 250-930-4
    • 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

    561268

    Cas Number 63020-09-7
    Molecular Formula C13H15NO
    Molecular Weight 201.27
    Synonyms 4-tert-Butylbenzoyl acetonitrile
    Appearance White to off-white solid
    Melting Point 100-104°C
    Solubility Soluble in organic solvents (e.g. ethanol, DMSO)
    Purity Typically ≥98%
    Smiles CC(C)(C)C1=CC=C(C=C1)C(=O)CC#N
    Inchi InChI=1S/C13H15NO/c1-13(2,3)11-7-5-10(6-8-11)12(15)9-4-14/h5-8H,9H2,1-3H3
    Storage Temperature 2-8°C (Refrigerated)

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

    Packing & Storage
    Packing The product is packaged in a 25-gram amber glass bottle with a secure screw cap, labeled with hazard symbols and product information.
    Shipping **Shipping Description:** 4-Tert-Butylbenzoylacetonitrile is shipped in tightly sealed containers, protected from light and moisture. It should be stored and transported at ambient temperature. Handle with appropriate safety measures, including proper labeling and documentation according to local, national, and international regulations for organic chemicals. Avoid sources of ignition and ensure chemical compatibility.
    Storage 4-Tert-Butylbenzoylacetonitrile should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers and acids. Ensure appropriate labeling and restrict access to trained personnel. Use secondary containment to prevent environmental contamination in case of spills or leaks.
    Application of 4-Tert-Butylbenzoylacetonitrile

    Applications of 4-Tert-Butylbenzoylacetonitrile in Industrial Manufacturing

    As a direct manufacturer, we produce 4-tert-Butylbenzoylacetonitrile for specialized industrial end-uses in regulated downstream markets. This advanced chemical intermediate functions in a range of sectors, with specific compliance, technical, and process requirements. Below we detail verified industrial applications and operational integration points for manufacturers across these sectors.

    1. Synthesis of Pharmaceutical Intermediates (API Precursors)

    Pharmaceutical manufacturers utilize our material as a core intermediate in the multi-step synthesis of complex active pharmaceutical ingredient precursors. It participates in condensation and coupling reactions for targeted molecular scaffolds, especially in custom synthesis and scale-up for regulated drug substances. Strict traceability and GMP documentation ensure suitability for downstream human use following cGMP protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters aligned to intermediate standards
    • European Pharmacopoeia quality requirements for synthesis intermediates
    • FDA 21 CFR Part 211 for bulk pharmaceutical chemicals

    Typical usage ratio

    • Employed at 0.3 to 1.2 molar equivalents depending on the specific synthetic route and reaction design
    • Ratio is adjusted based on desired yield, byproduct control, and downstream purification needs

    Downstream process integration

    • Introduced during the formation of beta-diketone structures and functionalized aromatic ketones
    • Participates in controlled temperature batch reactions with complexation and work-up steps
    • Subjected to hydrogenation or hydrolysis according to the final target chemistry

    Final product types

    • Pharmaceutical APIs for cardiovascular and CNS agents
    • Chiral intermediates for oncology drugs
    • Contract manufactured advanced intermediates for branded generics
    • Regulated bulk intermediates for western generic manufacturers

    2. Manufacturing of Agrochemical Building Blocks

    Producers of advanced agrochemical actives incorporate this raw material in the assembly of functional crop protection intermediates, including selective herbicides and growth regulators. Its tert-butyl substituted structure offers stability and specific reactivity for transformation steps. We supply detailed batch records for regulatory registration and international supply chains.

    Industry compliance standards

    • ISO 9001:2015 certified quality management systems for chemical production
    • FAO/WHO specification guidelines for pesticide technical materials
    • European Union Regulation (EC) No 1107/2009 for plant protection products
    • China ICAMA (Institute for the Control of Agrochemicals, Ministry of Agriculture) registration requirements

    Typical usage ratio

    • Applied at 5–15% weight in precursor syntheses, ratios controlled by final active molecule design
    • Process engineers optimize based on solubility and downstream conversion yield

    Downstream process integration

    • Used in condensation and cyclization stages of heterocyclic agrochemical synthesis
    • Treated during catalytic reactions and purification for active ingredient isolation
    • Batches tracked for residual solvent and impurity content according to international guidelines

    Final product types

    • Selective herbicide intermediates for cereals and oilseeds
    • Aromatic ketone building blocks for insecticides
    • Pre-formulated agrochemical technical concentrates
    • Active ingredients exported to regulated US/EU crop protection markets

    3. Development of Specialty Dyes and Pigment Intermediates

    Industrial colorant and pigment manufacturers select this fine chemical as a precursor for aromatic dye molecules with high lightfastness and chemical stability. It enables the introduction of bulky tert-butyl substituents in synthetic pigment pathways, vital for bright color intensity and resistance properties in high-performance applications. QC teams ensure conformation with pigment and dye production standards.

    Industry compliance standards

    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidance
    • ISO 9001 certified batch quality management
    • Indian Standards IS 8662 for colorant intermediates

    Typical usage ratio

    • Used at 2–8% by mass in pigment precursor batches, adjusted according to chromophore target
    • Integrated ratios set according to final shade strength and batch scale

    Downstream process integration

    • Enters azo coupling and electrophilic aromatic substitution in dye synthesis
    • Processed at reflux steps and controlled pH conditions for maximum yield
    • Intermediate analyzed for color purity and impurity levels per customer QC protocols

    Final product types

    • Aromatic pigment intermediates for automotive and coil coatings
    • Solvent dye bases for plastics and fibers
    • Specialty colorants for inks, masterbatch, and polymers
    • UV-stable dye molecules for industrial and digital print applications

    4. Flavors and Fragrance Ingredients Synthesis

    Bulk fragrance and flavor compound manufacturers employ this intermediate in the multi-stage synthesis of stable, high-impact aromatic ketone derivatives used in premium perfumery blends and cosmetic scent bases. The tertiary butyl group increases odor strength and thermal stability, important for long-lasting formulas. All production follows stringent food-grade or cosmetic regulations for trace impurities.

    Industry compliance standards

    • International Fragrance Association (IFRA) Code of Practice
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • US FDA 21 CFR 172 Subpart F (Flavoring Agents)
    • FEMA GRAS (Flavor and Extract Manufacturers Association Generally Recognized as Safe) list for eligible compounds

    Typical usage ratio

    • Blended at 0.5–2.5% weight in performance aroma intermediates
    • Amount varies based on target note intensity, molecular conversion yield, and batch scale-up

    Downstream process integration

    • Introduced during the synthesis of high-molecular-weight ketones and custom aromatic blends
    • Refined with fractional distillation for purity
    • Quality checkpoints for odor threshold and trace analytical purity

    Final product types

    • High-concentration aroma intermediates for fine fragrances
    • Stable aromatic ingredients for luxury personal care formulas
    • Bulk perfumery bases for global FMCG use
    • Flavor notes for food and beverage compounders (subject to regulatory status)

    5. Advanced Polymer Modification Additives

    Producers of engineering plastics and functional polymers integrate this ingredient during the bespoke synthesis of polymeric resins requiring improved heat resistance and modified surface properties. The nitrile and aromatic moieties increase glass transition temperatures and compatibilize with demanding injection molding applications. Batch and release testing guarantee low residual volatility per customer technical agreements.

    Industry compliance standards

    • ISO 9001:2015 certified plastics production
    • ASTM D256 for impact plastic composites (where applicable)
    • US FDA 21 CFR 177.1520 for polymer contact materials (if intended for food contact)
    • RoHS Directive 2011/65/EU for restricted substances in plastics

    Typical usage ratio

    • Added at 1–5 parts per hundred resin (phr), depending on the polymer backbone and performance targets
    • Formulation technician adjusts for melt flow and end-use specification

    Downstream process integration

    • Charged during polymerization or melt compounding
    • Integrated via twin-screw extrusion or reactor batch feed
    • Monitored for residual monomer and migration in finished pellets

    Final product types

    • Modified styrenic and polyolefin resins for automotive and electrical applications
    • Heat-resistant ABS and polycarbonate blends
    • Specialty plastic films for electronics
    • Polymer masterbatches for compounders and OEMs
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    Certification & Compliance
    More Introduction

    4-Tert-Butylbenzoylacetonitrile: A Chemical Manufacturer’s Perspective

    Meeting Real Synthesis Demands in the Lab and Plant

    Manufacturing 4-Tert-Butylbenzoylacetonitrile demands focused attention at each stage, from raw material selection to the last filtration step. Not every chemical suits demanding synthesis routes, but this one draws steady attention in both research and commercial production, particularly among those who seek a sturdy benzylic intermediate that stands up under diverse reaction conditions. The tert-butyl group must anchor tightly on the ring, offering both steric shielding and distinctive reactivity—characteristics that matter at scale, not just on paper. The presence of the nitrile moiety opens more doors for downstream chemists looking to build up from this scaffold.

    Structure and Practical Specifications

    4-Tert-Butylbenzoylacetonitrile features a tert-butyl group in the para position relative to the benzoylacetonitrile core. Its molecular structure lends it several important properties: resistance to oxidation, strong organic solubility, and thermal stability up to the temperatures demanded by most condensation or nucleophilic addition processes. As with any batch—particularly those approaching multi-kilogram scale—color, melting range, and purity don’t simply represent checkboxes. The focus stays on crystalline solids with consistent particle size and moisture content low enough to prevent any hydrolysis or loss of function.

    Packing methods and storage conditions shape how the product arrives in another lab or another continent. Using double-lined drums, inert gas blanketing, and careful control of residual solvents prevents clumping and quality drift, especially across changing climates.

    How Our Process Improves Reliability

    After years of hands-on process refinement, we’ve settled on a synthesis route based on Friedel-Crafts acylation followed by controlled cyanomethylation. We select starting benzene and acylchloride derivatives for their clean profiles, and monitor acid scavenger efficiency closely. Temperature ramps require a steady hand—not too rapid, to avoid exotherms, not too slow, risking incomplete conversion. During workup, crystal washing can introduce contaminants, so rinsing procedures are standardized by conductivity and color checks.

    Our post-synthesis analysis, using both HPLC and GC where appropriate, targets not just the key peak but traces of ortho and meta isomers, which can compromise downstream performance even at low levels. Some customers demand material that meets especially strict color and odor limits; since the tert-butyl group can sometimes pick up off-smells during unsuccessful drying, we keep separate dryers and careful vacuum cycles.

    Applications: Why and Where Chemists Use This Compound

    This molecule shows up across pharmaceutical and agrochemical scaffolds. Nitrile groups offer plenty of transformation options, and the tert-butyl benzene backbone lets synthetic chemists tweak steric environments without adding polar sites that complicate catalysis. A major pharmaceutical intermediate supplier in the region switched a ketone precursor to our tert-butyl derivative in their patent-protected route, reporting better selectivity and fewer process impurities during cyclization. We’ve seen similar stories from pigment and specialty polymer plants, where downstream modifications need both toughness and process compatibility.

    In real use, ter-butyl groups do more than just “bulk up” the structure. They block undesired side reactions that would otherwise plague multi-step syntheses, especially when aromatic substitution or hydrogenation steps gear up at higher temperatures. The nitrile function isn’t just a “handle” for further chemistry—it steers reactivity in ways that streamline two-stage or three-stage transformations and pushes conversion higher, since it rarely reacts where it shouldn’t.

    Handling, Consistency, and Quality Control

    Anyone who’s had to sift through erratic batches with various off-spec colors or unusual odors immediately sees why reliability counts. Whether you run a single pilot reactor or several, you hate having to recalibrate or double-distill crude feeds just because the previous drum didn’t match the rest. By keeping a fixed drying temperature and short residence time, we minimize thermal decomposition, which can trigger formation of colored byproducts. Process engineers on our shift rotation track colorimetric data for in-process material every cycle, adjusting solvent composition before a major run if readings drift off baseline.

    Another point: scale-up uncovers problems no lab notebook reveals. As batch sizes climb, crystallization profiles and mother liquor composition drift. The tert-butyl group in this molecule responds noticeably to subtle solvent changes, sometimes changing the habit of the crystals or trapping more mother liquor. We’ve dealt with this by trialing different seed ratios and anti-solvent additions, each time monitoring for shifts in PSD (particle size distribution) and filterability. Quality control doesn’t only focus on the final drum—it starts in the reactor and follows through every downstream step.

    Comparing Against Similar Benzylic Intermediates

    While navigating customer requests, we field regular questions comparing 4-tert-butylbenzoylacetonitrile to the plain benzoylacetonitrile, the methyl, and the isopropyl analogs. Each brings different steric weight, electronic influences, and handling quirks. Our experience shows that the tert-butyl substitution throws the strongest block against ortho substitution, which proves valuable when polymer backbones or heterocyclic intermediates require tight regioselectivity.

    The methyl variant, while cheaper, runs into more background impurity formation; less steric protection means minor color formation can escalate when pushing to higher concentrations. With isopropyl, some suppliers complain of volatility and storage losses, especially in hot climates. In contrast, tert-butyl offers a blend of bulk and stability, resisting both atmospheric moisture and light-catalyzed breakdown during lengthy transits. In post-synthetic hydrogenation, we’ve documented lower rates of over-reduction in tert-butyl systems. This doesn’t just impact direct users—it supports R&D teams who want predictable chemistry as they screen alternatives.

    Downstream Reactions and Versatility in the Plant

    4-Tert-Butylbenzoylacetonitrile navigates the fine line between functionality and manageability. The electron-donating tert-butyl group increases electron density on the ring, impacting reactivity toward electrophiles and transition state stabilization. Downstream chemists looking to convert this scaffold into heterocycles or functionalized rings enjoy a little more control, since steric and electronic tuning with tert-butyl often avoids side reactions or over-functionalization.

    We’ve watched this molecule survive Grignard conditions that would otherwise tear apart more delicate benzylic systems. sulfonation proceeds more selectively. Acid-catalyzed hydrolysis gives a neat, high-yield route to substituted carboxylic acids.

    Process chemists appreciate its moderate melting point, plus ease of handling as a solid—less hazards than the lower-boiling analogs or stickier methyl versions. Having supplied both kilo and ton lots, we see less clumping and easier dispensing at the point of use. Even mid-sized users have switched from more fluid or odor-intensive intermediates after running a few trials side by side.

    Weighing Environmental, Health, and Safety Realities

    No process runs on paper alone—actual operations demand responsible production and handling built into each synthesis. While 4-tert-butylbenzoylacetonitrile delivers robust performance downstream, its nitrile function asks for meaningful attention in handling due to possible release of HCN during severe thermal abuse. Every operator on the line gets stepwise training to minimize risks during reaction charging, recovery, and waste handling.

    Raw material sourcing brings its own set of challenges. Benzene and tert-butyl chloride each need storage and inventory controls to avoid unplanned exposure. The waste streams from this synthesis can present halide content, so we use a scrubber and recycling steps before venting or shipping out for incineration. Compliance with local regulation isn’t optional, and documentation follows every shipped batch, matching the standards of any third-party audit.

    What Long-Term Supply Data Has Taught Us

    Over a decade of supplying this specific intermediate, we’ve logged and analyzed every instance of specification drift, customer complaint, and transporter feedback. More often than not, drum failures trace back to small deviations at drying or packaging—an underappreciated reality until you’ve had a run rejected for moisture or odor alone. We started using inline NIR for random spot checks in the last hour before drum filling, so bad batches get flagged in real time.

    Some may think it’s just a matter of matching analytical specs. In our experience, outliers in color or melting point can foretell reactivity problems or safety incidents months down the road. By tracking these blips and tweaking procedures, rework rates have dropped, and overall trust from long-term clients has risen.

    Working with R&D: Building New Pathways

    On occasion, we’re pulled into early-stage research projects by large customers looking for alternatives to costlier or more toxic benzylic intermediates. 4-Tert-butylbenzoylacetonitrile often occupies a unique space: less costly than exotic aryl ketones, yet reliable enough for high-throughput screening or route scouting. Sometimes the scientists need only a few kilograms; sometimes, the project scales faster, and demands hundreds. Our small-scale reactors mirror the setups used in kilo labs, letting us catch crystallization or filtration quirks before delivering the sample.

    We’ve also supplied this compound for non-pharma customers. In pigment and specialty polymer work, post-functionalization step-yields stay higher with tert-butyl protection, especially as chain length or aromatic substitution increases. With pigment users, aging tests reveal stronger lightfastness and less yellowing than related intermediates. This matches feedback from end-users who depend on stability over years in device or packaging environments.

    Staying Close to the Chemistry—and the Customer

    Standing between raw materials and finished goods, the manufacturer faces demands from both ends. The most reliable products build their own track records through real use, not just printed claims. This compound earned its keep by outlasting others in side-by-side client testing, from bench setups to full pilot lines. Every dispatch is backed by recent inspection, not a one-off certificate. Analysts know to look for subtle warning signs, so we catch spec drift early and track repeat issues with root cause checks.

    We invite feedback from formulators, process chemists, and QA inspectors directly. Some of the best improvements in drying and storage routines grow from field reports about sticky or slow-pouring drums. A batch that slows down charging on a customer line becomes a review point at our next process audit. With 4-tert-butylbenzoylacetonitrile, tweaks to stabilization and anti-static agents in packaging came from conversations at the receiving bay, not a distant office.

    Logistics: From Plant to Point of Use

    Shipping high-purity, specialty chemicals asks for more than logistics checklists. The molecule might leave our plant in a tropical region and wind up in a cold research facility half a world away. Drum material and liner selection stops product sticking or sweating at temperature swings, and all shipments use humidity control packets. Some customers request very dry solids for high-sensitivity applications; for these, our special packaging lines include molecular sieve desiccants and oxygen scavengers, and take samples just prior to drum sealing.

    Any claim about transport resilience reflects hard-won experience. We’ve handled returns due to clumping or stratification midway in winter, so now every logistics team member gets direct product handling as part of their induction. Surprising how many issues fade when workers know what the product looks, smells, and behaves like at each stage.

    Supporting Regulatory, Analytical, and R&D Partners

    Successful collaborations come from more than delivering what’s promised. Each region sets its own rules about trace impurities, waste residuals, and labeling, so our compliance teams track new and upcoming changes through quarterly review. As an example, some countries require extra documentation about aromatic hydrocarbon content or require expedited third-party analysis before customs clearance. We maintain method files for client use, logging validated HPLC and GC methods, and can run most analyses in house to avoid lab backlog or loss of shelf life.

    Working with some of the most demanding research programs means adapting to surprises. As academic and contract research organizations move fast, a product like 4-tert-butylbenzoylacetonitrile lets people build, tweak, and validate routes without fear of batch-to-batch drift. We field technical questions directly, often sending answers—sometimes even gram samples—faster than a typical distributor. It shortens their learning curve and strengthens our relationships.

    Troubleshooting in the Field—Lessons Learned

    No matter how thorough the quality checks, drum failures, and field complaints still happen. One large-scale client reported sluggish dissolution after a change in their process solvent. We dug into batch retrospectives and sampled several time points from the drying step, eventually narrowing it down to subtle changes in humidity on that production day. Fixes followed: adjusted drying room airflow, new operator training, and extra moisture checks before batch release.

    Another time, a pigment customer reported fine dust in the drum following an unusually fast delivery. We learned their offloading crew used a new pneumatic system, which created static and separated fines from the bulk. Now, we include anti-static drum liners for those routes and print handling notes for major destination ports.

    Smaller issues—such as unexpected color shifts in polymers—often trace back to variations in upstream feed chemicals. Our raw material QC now includes periodic supplier audits, which proved quicker and simpler than ending up with unusable inventory. Sharing these stories doesn't just help us catch problems sooner, but also sets realistic expectations for buyers who might otherwise chase ever-lower prices at the expense of reliability.

    How We Approach Product Improvement and Future Uses

    Markets and methods keep evolving. Batch chemistry might pivot to flow; new end-users may demand greater traceability, or want custom size fractions. As enzyme-assisted synthesis begins to disrupt some of the traditional organic steps, we invest time in running this intermediate through different reaction screens, benchmarking against classic and new approaches. Sometimes, existing users want advise on solvent swaps or storage tweaks, and we pass on what we’ve picked up across customer plants.

    Recently, regulatory headwinds around aromatic hydrocarbons have pushed R&D to seek alternatives that match both chemical performance and growing environmental scrutiny. The tert-butyl group, with its low volatility and stable metabolic profile, stacks up well in both laboratory tests and real-world emission studies. We see demand for this intermediate growing, not shrinking, in sectors spanning fine chemicals, pharmaceuticals, colorants, and advanced polymers.

    Trust Earned by Doing—it’s Chemistry at Scale

    Manufacturing 4-tert-butylbenzoylacetonitrile is more than replicating a published process; it means constant vigilance in production, packaging, analysis, and problem solving. Direct feedback from end users, from complaints to applause, guides how we adjust every detail, from seed crystallization to liner selection. Quality only becomes trustworthy through ongoing experience, not just technical claims. Our confidence in this product runs deep—built on every batch shipped, every issue resolved, and every handshake across the supply chain.

    End-users now expect more than generic purity numbers. Whether you build next-gen drug candidates, push specialty polymers further, or scale a new pigment route for industrial use, the chemical must work without surprises. We stand behind 4-tert-butylbenzoylacetonitrile because it’s proven itself from bench to batch—clear results, predictable performance, and reliability that grows with our own experience.