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4-(Tert-Butoxy)Benzaldehyde

    • Product Name 4-(Tert-Butoxy)Benzaldehyde
    • Alias tert-butyl 4-formylphenyl ether
    • Einecs 630-461-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    440390

    Productname 4-(Tert-Butoxy)Benzaldehyde
    Casnumber 5162-68-7
    Molecularformula C11H14O2
    Molecularweight 178.23
    Appearance White to off-white solid
    Boilingpoint 332.2 °C at 760 mmHg
    Meltingpoint 57-60 °C
    Density 1.038 g/cm3
    Smiles CC(C)(C)COC1=CC=C(C=O)C=C1
    Inchi InChI=1S/C11H14O2/c1-11(2,3)13-10-6-4-9(8-12)5-7-10/h4-8H,1-3H3
    Synonyms 4-(tert-Butoxy)benzenecarbaldehyde
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Refractiveindex 1.522

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

    Packing & Storage
    Packing Brown glass bottle with secure cap, labeled "4-(Tert-Butoxy)Benzaldehyde, 25g," includes hazard warnings, supplier information, and batch number.
    Shipping 4-(Tert-Butoxy)Benzaldehyde is shipped in tightly sealed containers to prevent contamination and moisture exposure. It should be handled with care and transported according to standard chemical regulations, ensuring protection from heat and direct sunlight. Packaging complies with relevant safety standards for organic chemicals. Shipping documents include all pertinent safety and handling information.
    Storage 4-(Tert-Butoxy)benzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep away from strong oxidizers and acids. Store at room temperature, protected from moisture. Follow standard chemical storage guidelines and ensure all containers are properly labeled to prevent accidental misuse or exposure.
    Application of 4-(Tert-Butoxy)Benzaldehyde

    Applications of 4-(Tert-Butoxy)Benzaldehyde in Industrial Manufacturing

    As a direct manufacturer of 4-(Tert-Butoxy)Benzaldehyde, we work with key sectors that utilize this compound in well-established downstream processes. Below, we detail specific industrial scenarios based on verified applications, covering industry standards, recommended formulation ratios, process points, and corresponding end products.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    This compound functions as a critical building block in the synthesis of specialty aromatic intermediates for various APIs, especially where steric protection and selective reactivity are required. It often appears at key condensation or alkylation steps in the preparation of advanced pharmaceutical chemicals, aiding in the production of high-purity molecular structures for further derivatization.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs (as applicable for subsequent API)
    • 21 CFR Part 210 & 211 (US cGMP guidelines for finished pharmaceuticals)
    • Chinese Pharmacopoeia 2025 Edition for regulated API starting materials

    Typical usage ratio

    • 5–20 mol% relative to coupling partners in condensation or alkylation reaction steps; exact proportion based on target API molecular design and batch scale.

    Downstream process integration

    • Added directly to the reactor as starting aldehyde component during multi-step organic synthesis, frequently following in-situ deprotection, then advanced via reductive amination or selective hydrogenation to yield key intermediates.

    Final product types

    • Advanced API intermediates for antihypertensive, antiviral, or CNS-active drugs
    • Benzylamine derivatives for further pharmaceutical processing

    2. Synthesis of Specialty Aromatic Resins

    This material serves as a protected aromatic aldehyde functionality, facilitating the preparation of modified phenolic or polyvinyl-based resins with tunable thermal and chemical performance. It allows downstream users to precisely introduce tert-butoxy substitution for targeted resin structure-property relationships, especially in electronics encapsulants and high-end coatings.

    Industry compliance standards

    • UL 94 Standard for Safety of Flammability of Plastic Materials
    • RoHS Directive (2011/65/EU)–restrictions on hazardous substances
    • ISO 14001:2015 for environmental management in resin production
    • REACH Regulation (EC) No 1907/2006 for downstream registration

    Typical usage ratio

    • 1–6 wt% of total monomer mass in aromatic resin formulation, depending on final crosslinking density and desired resin thermal performance. Formulators adjust ratio for electrical insulation vs. mechanical strength targets.

    Downstream process integration

    • Introduced during batch monomer blending prior to acid- or base-catalyzed polymerization; participates in the initial polymer-forming reaction and remains chemically incorporated in the cured matrix.

    Final product types

    • Electronic encapsulation resins for circuit board protection
    • Specialty coatings for industrial machinery with chemical resistance requirements
    • Molded insulating parts for electrical components

    3. Advanced Organic Synthesis for Agrochemical Intermediates

    4-(Tert-Butoxy)Benzaldehyde is utilized in the stepwise preparation of functionalized aromatic compounds for agrochemical active development. Its use enables downstream producers to prepare masked aldehyde intermediates, contributing to selective structural modifications critical in the synthesis of next-generation fungicides and herbicides.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)–for regulated agrochemical R&D
    • ISO 9001:2015 for process and quality management in chemical ingredient production
    • FAO Guidelines on Pesticide Specifications and Quality Control
    • REACH Regulation (EC) No 1907/2006 pre-registration for agrochemical intermediates

    Typical usage ratio

    • 2–8 mol% relative to the primary agrochemical precursor, modulated based on scale-up batch size and downstream route complexity.

    Downstream process integration

    • Dosed at the protected aromatic step prior to functionalization, followed by unmasking and conversion (e.g., via hydrolysis or oxidative cleavage) in later synthesis stages to yield the target aldehyde intermediate.

    Final product types

    • Key intermediates for selective herbicides and crop protection active ingredients
    • Building blocks for specialty agrochemical discovery libraries

    4. Fine Fragrance and Aroma Intermediate Synthesis

    Downstream fragrance compound suppliers employ this raw material in the controlled synthesis of advanced aroma chemicals, leveraging the tert-butoxy group’s steric hindrance to guide desired reaction selectivity within aromatic frameworks. Careful utilization in multi-step synthesis routes leads to improved yields in valuable aldehyde- and alcohol-type aroma actives.

    Industry compliance standards

    • IFRA Global Fragrance Ingredient Standards (latest amendment)
    • ISO 9001:2015/ISO 22716 for quality management in fragrance intermediate production
    • EU Regulation (EC) No 1223/2009 on cosmetic products (for fragrance safety assessment)
    • US Food and Drug Administration (21 CFR) for fragrance ingredients in flavor use

    Typical usage ratio

    • 0.2–2 mol% relative to the total aromatic precursor mass, adjusted for pathway selectivity and specific end-odorant creation requirements.

    Downstream process integration

    • Integrated at the selective aromatic modification stage, typically as a protected aldehyde during Friedel–Crafts acylation or subsequent reduction for multi-functional aroma material synthesis.

    Final product types

    • Specialty aldehyde aroma chemicals for fine fragrance blends
    • Precursor stocks for olfactory ingredients in functional consumer goods

    5. Laboratory Reagents for Academic and Industrial R&D

    Research departments and industrial R&D centers employ this compound in method development for new catalytic, condensation, and protection strategies. Controlled addition allows researchers to explore sterically hindered aromatic chemistry and generate reference samples for reaction optimization.

    Industry compliance standards

    • ISO/IEC 17025:2017 General requirements for laboratory competence
    • GLP compliance for relevant regulated laboratory studies
    • Hazard Communication Standard (OSHA 29 CFR 1910.1200) for chemical labeling and MSDS

    Typical usage ratio

    • 0.1–10 mmol scale per laboratory protocol; precise ratio varies by experimental design, reaction type, or synthetic target.

    Downstream process integration

    • Weighing and solution preparation at the design-of-experiment phase for reaction development, mechanistic studies, or high-throughput screening in research environments.

    Final product types

    • Reference material archives for synthetic method validation
    • Custom aromatic intermediates for patent filing or process innovation
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    Certification & Compliance
    More Introduction

    4-(Tert-Butoxy)Benzaldehyde: Reliable Building Block for Modern Synthesis

    Introduction From the Factory Floor

    Standing on our production line, you get a deep appreciation for what separates a reliable specialty chemical from a constant source of frustration. We know 4-(tert-Butoxy)benzaldehyde not as an abstract commodity, but as a daily reality: a pale yellow crystalline solid with the kind of subtle aroma that makes you certain you’re dealing with a true aromatic aldehyde. Every batch we produce follows a route we’ve refined for over a decade, using controlled environments, locally sourced raw materials, and a systematic multi-step synthesis that minimizes waste.

    This compound, shaped by the para-substitution of tert-butoxy on a benzaldehyde backbone, helps synthetic chemists build a cleaner, more responsive platform for complex molecules. Isolation and purification play out on our site with attention to trace contaminants, not just because paperwork demands it, but because small impurities in a core building block can sabotage the next stage of any downstream process. For anyone scaling up or fine-tuning a transformation, knowing the real factors behind a consistent aldehyde supply can make the difference between a workhorse and a bottleneck.

    Our Process and Product Guarantee

    Take it from the folks measuring and monitoring at every control point: we maintain 4-(tert-Butoxy)benzaldehyde above 99% purity, verified by HPLC and NMR alongside standard gas chromatography. You won’t find phthalic or other aromatic byproducts in any of our outgoing drums because the column operations always receive hands-on oversight, not just automated feedback. Consistency grows from batch accuracy, from managing exothermic control during formylation to ensuring that every drum shipped looks and behaves as expected in your own glassware.

    Our product arrives dry, with minimal residual moisture to avoid hydrolysis, and stays stable during transit. From the start, we chose packaging in high-density polyethylene pails or steel containers depending on lot size, always lined and sealed. Whether you work with kilogram lots for pilot work or need ton-class supply for plant-scale production, our storage and transport teams understand their job isn’t over until our aldehyde blends seamlessly into your workflow.

    Why 4-(Tert-Butoxy)Benzaldehyde Matters in Real Synthesis

    Synthetically, the tert-butoxy group on the aromatic ring plays a crucial role in protecting, activating, or steering selectivity. Research chemists and scale-up teams gravitate toward this compound because the electron-donating effect increases nucleophilicity at certain positions, lending unique access to derivatives like substituted cinnamaldehydes, benzyl alcohols, and various heterocycles. Our direct customers run advanced cross-couplings, fragmentations, and even photoinduced ligations that require tolerating and pacifying many reactive intermediates found only at this position.

    The aldehyde function, as always, serves as a site for Wittig, Knoevenagel, or even classic Grignard reactions—each one is sensitive to both steric and electronic tweaks produced by the para-tert-butoxyl group. This arrangement opens new opportunities for step-economic access to fluorinated intermediates or for bioconjugations that otherwise stall with less forgiving aldehydes. We’ve supported one customer with continuous-flow routes for medicinal fragments, and another looking to install protected aldehydes into OLED precursors where decomposition is a show-stopper.

    What Sets Our Material Apart

    There’s no shortage of benzaldehyde derivatives on the market. Compare what you see under the microscope or take a sample to TLC—some generic products show micro-residues, ghost colors, or broad peaks in the NMR spectrum. We double-check every lot, not because regulations demand it, but because even barely-there side products leave a fingerprint that disrupts precise reactions: a key difference noticeable to anyone who’s had a reaction ruined by inconsistent suppliers.

    Our process engineers use a fine-tuned order of addition to reduce the formation of ortho-isomers or polymeric side chains. Every bottle comes from a single verified batch, never cobbled together from leftovers. If you notice unusually slow reaction onset or have cleanup headaches, recall that some room-temperature processes use recycled solvents or improperly dried acids. We stick with fresh, high-grade inputs for each run. This extra step raises our costs a little, but we see the benefit every time a returning customer tells us about clean conversion and reproducible results.

    Those who run large-scale reactions know only too well that a drum tainted with trace acids or chlorinated side products can throw out entire reaction sequences. That’s why we check for halides and peroxides by precise spot tests and keep a low-waste policy throughout multi-stage cleaning. For sensitive chemistries, this extra level of scrutiny gets your process closer to right-first-time.

    Handling, Shelf Life, and Practical Experience

    If you open a jar in our lab, you won’t catch a powerful stench—the tert-butoxy benzaldehyde grants a muted, almost sweet odor that won’t overpower an enclosed space. Our team stores it at 2–8°C during longer-term holding, but the compound holds up under ambient shipping, so you won’t see clumped or oxidized product even after weeks on the road.

    The main pitfall in extended storage is the slow oxidation typical for aromatic aldehydes. We ship in air-tight, inerted vessels, and recommend closing every cap promptly. Exposure to air or a hot workspace triggers peracid formation, which can cause headaches downstream especially if your reaction uses sensitive transition metal catalysts. For smaller scale work, we see customers storing test lots under nitrogen or argon. We do the same during initial dispatch.

    Our material remains free-flowing and easy to weigh, with a melting point around 51–52°C. Anyone handling aldehyde derivatives learns quickly to minimize exposure by using gloves and standard lab PPE—our product falls well inside accepted industrial safety norms with no unusual toxicity below gram scales. For bulk operations, the usual air extraction and spill management apply, not because this benzaldehyde is wildly hazardous but because all aromatic aldehydes deserve respect for their irritant properties.

    Applications From Polymers to Pharmaceuticals

    Most of the outgoing orders head to research, pilot plants, and manufacturers targeting demanding syntheses. In pharmaceutical R&D, our 4-(tert-butoxy)benzaldehyde anchors key steps in the assembly of scaffolds where functional group protection matters—think boron-rich intermediates or precursor synthons which must survive a gauntlet of reagents before the protection is stripped away at just the right moment.

    In agrochemical routes, this aldehyde serves as a portal for delivering protected aromatic rings, with the bulky butyl group staving off unwanted ring substitutions and adding a blocking effect that standard benzaldehydes lack. We’ve supported teams who push reaction cleanliness: partial hydrogenations proceed more predictably without side-chain overreduction, and the ortho-para directing effect isn’t just a textbook principle, but a lived experience with our benzaldehyde as the reagent of choice.

    Some of our largest lots move into the hands of polymer chemists who take advantage of the steric freedom imparted by the tert-butoxy group. When making prepolymers or photoresists, our customers run condensation and addition reactions where electron-rich aromatics are essential. Yields climb and batch reproducibility soars thanks to our consistently pure starting material. In the electronics field, several partners use our benzaldehyde in the base synthesis of OLED matrix intermediates or light-sensitive imaging chemicals—the para-tert-butoxy group proves less prone to unwanted side reactions, making for sharper, longer-lived photoinitiators.

    One of the unique stories from our own team came out of working with a specialty flavors company striving to synthesize complex fragrance aldehydes. They repeatedly hit purity plateaus with commodity benzaldehyde sources, fighting a losing battle against aldehyde dimerization. After switching to our 4-(tert-butoxy)benzaldehyde, reaction selectivity improved and downstream distillation required fewer stages, which cut both time and solvent use. Real process data outpaces literature speculation when it comes to the cost savings of a reliable, pure input.

    What We’ve Learned Supplying This Aldehyde

    Our years in the business show that no two customers use this material in quite the same way. Some focus on the synthetic latitude the tert-butoxy group introduces, especially in producing fine chemicals, liquid crystals, or advanced dyes. Others come back for the confidence that each order will match the last—measured by retention time, not just label claims. Over the years, we’ve tracked yield improvements, cleaner spectra, and fewer purification steps among experienced users compared to companies relying on lower-grade imports or questionable resellers.

    Global supply chain headaches can tempt buyers toward cheap, unverified product; bitter experience teaches how a bargain powder can wipe out the value of a successful pilot campaign. As a producer, we keep a hands-on relationship with our chemical engineers and synthesis managers for this reason. Traceability means that if something goes wrong in your plant, you get answers fast—actual batch histories, full spectral data, and residue analysis at your fingertips. We leverage our tight production loop to serve as a real feedback channel, not a distant supplier with little practical concern.

    For newer users, we always suggest pilot-scale first, not just jumping straight to thousands of kilograms. Involving your analytical team early cuts the risk of expensive surprises. Our facility is set up to provide trial quantities that come from our regular production—no small-batch, “special” material that might not scale. This keeps your comparison meaningful and predictions trustworthy. It’s an attitude shaped by cleaning our own reactors between runs, not just sitting behind a desk.

    Comparing With Other Benzaldehydes

    Some ask why not use unsubstituted benzaldehyde, or another para-protected version like 4-methoxybenzaldehyde. The answer emerges at the reaction bench. The tert-butoxy group’s bulk provides steric shielding that methoxy or ethoxy substitutions can’t deliver, and the enhanced electron-donating effect shifts selectivity in nucleophilic aromatic substitution. In condensation or addition steps, we watch for cleaner reactions with tert-butoxy compared to the more reactive plain benzaldehyde, which tends to polymerize or oxidize rapidly under air.

    From experience, this difference pays off in every downstream transformation. Less byproduct means easier purification and more reproducible leads. For specialty polymer makers, uncontrolled benzaldehyde residues can introduce color or stability problems that tert-butoxy-protected products avoid. In laboratory hydrogenations and protected fragment formation, many see the value in the lower tendency to form hydrates during storage.

    Competition exists, of course: some suppliers offer imported, barrel-aged aldehyde at a price that looks attractive. Users who switched from resellers have reported a range of headaches, from lingering off-odors to high moisture and unexpected IR bands in their own QC checks. Our operation sees each drum from the day of synthesis to packaging, right through shipment, ensuring a clear chain of responsibility and—vital for sensitive scale-ups—a reliable supply history that’s not upended by mysterious substitutions or adulterated inputs.

    Meeting Changing Regulatory and Market Demands

    Changing environmental and safety regulations challenge every chemical producer. We continually update our procedures to keep both our workers and downstream users safe. Increased scrutiny on VOC limits has led us to invest in improved condensation control during synthesis, and automated vent scrubbing for emissions. This reduces the risk of workplace exposure and meets stricter air-quality standards for all our outgoing materials.

    Documentation and traceability sit at the center of our approach. Every batch ships with a full set of laboratory records and every customer—large or small—receives access to the details needed for both internal audits and regulatory needs, covering substances of very high concern and potential trace residues. We respond quickly to change because our production is agile and direct, not chained to distant third-party contractors or unreliable sources. What you order stays what you get from year to year, an advantage for those committed to long-term R&D or established product lines.

    Safe handling recommendations come from what we practice daily, not just what’s printed on a certificate. If new evidence emerges pointing to a safer way to handle or process our aldehydes, we adapt immediately—not just for regulatory compliance but to better protect teams like ours at every step in the supply chain.

    Continual Refinement in Quality and Service

    Producing high-quality 4-(tert-butoxy)benzaldehyde requires more than ticking off regulatory boxes. It takes a continuous willingness to learn alongside our customers. Each time someone finds an unexpected use—like an improved step in photoresist formation or a new synthetic intermediate for generics—we update our process, documentation, or analytical inspections as needed.

    Quality isn’t static in specialty chemistry. We refine testing as analytical standards evolve. Whenever a common impurity emerges in a customer’s own post-reaction QC, we investigate and, if necessary, amend not just our batch checks but upstream cleaning and storage as well. Our open approach to quality improvement meshes with real-world chemistry, not generic marketing promises.

    We invite regular site audits and technical visits and maintain a transparent record of any process changes so our users can keep their workflows uninterrupted. Every time a partner expands a pilot run into full-scale production, our team coordinates packaging, documentation, and support to prevent disruption or downtime. Longstanding customers testify to this collaborative approach, noting fewer surprise quality deviations and a smoother road to scaled-up manufacturing.

    Looking Forward

    The value of 4-(tert-butoxy)benzaldehyde grows alongside innovations in fine chemical synthesis, advanced material science, and pharmaceutical development. We remain committed to delivering a product built on genuine quality control, personal accountability, and technical support based on firsthand experience. Our success rides not just on the purity of an individual compound, but on the relationships forged with chemists, engineers, and researchers who transform rare building blocks into the functional products that shape everyday life.

    The landscape of specialty chemicals continues to evolve, shaped by emerging science, new regulations, and the need for cost controls. As seasoned producers, we’ve built our reputation on authenticity and reliability. Our team’s daily work—cleanroom maintenance, analytical testing, careful batching—ensures that every shipment enables downstream synthesis to proceed further, cleaner, and with greater confidence. We stand ready to support both established partners and the innovators at the frontier of chemical discovery with consistent, real-world-tested 4-(tert-butoxy)benzaldehyde that outperforms commodity-grade alternatives.