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3,3-Dimethylbutyraldehyde

    • Product Name 3,3-Dimethylbutyraldehyde
    • Alias Pivalaldehyde
    • Einecs 211-012-2
    • 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

    716680

    Name 3,3-Dimethylbutyraldehyde
    Cas Number 595-83-1
    Molecular Formula C6H12O
    Molar Mass 100.16 g/mol
    Appearance Colorless liquid
    Density 0.801 g/mL at 25°C
    Boiling Point 107-109°C
    Melting Point -72°C
    Refractive Index 1.394-1.396 at 20°C
    Flash Point 8°C (closed cup)
    Solubility In Water Slightly soluble
    Pubchem Cid 11514

    As an accredited 3,3-Dimethylbutyraldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3,3-Dimethylbutyraldehyde is packaged in a 100 mL amber glass bottle, sealed with a screw cap, labeled with hazard warnings.
    Shipping **3,3-Dimethylbutyraldehyde** is shipped in tightly sealed containers, typically made of glass or chemically resistant plastic, to prevent leakage and volatilization. It is transported as a flammable liquid, with all necessary hazard labeling, and kept away from heat, sparks, or open flames. Proper ventilation and secondary containment are recommended during shipping.
    Storage 3,3-Dimethylbutyraldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Protect from direct sunlight, moisture, and incompatible materials such as strong oxidizing agents. Store under inert atmosphere if possible. Ensure proper labeling, and keep out of reach of unauthorized personnel. Handle under fume hood if available.
    Application of 3,3-Dimethylbutyraldehyde

    Applications of 3,3-Dimethylbutyraldehyde in Industrial Manufacturing

    3,3-Dimethylbutyraldehyde serves as a key intermediate in multiple specialized industrial segments, contributing distinct functional properties and unique molecular structure for high-value downstream production processes. Explore detailed application scenarios where our direct manufacturing expertise ensures strict quality control and traceability from raw material sourcing through final use.

    1. Synthesis of Aroma and Flavor Aldehydes for Food Ingredients

    Major flavor and fragrance manufacturers utilize 3,3-Dimethylbutyraldehyde in custom synthesis of aliphatic aldehyde aroma compounds, particularly in formulations aimed at imparting fresh, fruity, and green note profiles in processed foods and beverages. Its branched structure allows targeted derivatization to meet strictly regulated profiles demanded by global food ingredient standards. Ingredient technologists integrate this intermediate via scheduled additions during multi-step aroma compounds synthesis, controlling the reactivity with downstream amines and alcohols to produce food-safe flavors.

    Industry compliance standards

    • FCC (Food Chemicals Codex) purity requirements
    • EU Commission Regulation No 1334/2008 for flavorings
    • US FDA 21 CFR Part 172.515 (Synthetic flavoring substances and adjuvants)
    • ISO 22000 food safety management systems

    Typical usage ratio

    • Standard batch scale: 0.5–3.0% of total precursor mass, adjusted based on target tonal profile and process batch yield

    Downstream process integration

    • Introduced as core intermediate at the aldehyde condensation or reductive amination stage of aroma compound synthesis

    Final product types

    • Natural-identical flavor aldehydes (e.g., hexanal derivatives)
    • Beverage and confectionery flavorings
    • Compound food essences for bakery and snack industry

    2. Agrochemical Intermediate for Herbicide and Pesticide Synthesis

    Leading crop protection chemical producers select 3,3-Dimethylbutyraldehyde in the multi-step laboratory and industrial-scale synthesis pathways for select herbicidal and pesticidal active ingredient molecules. Its structural branching enhances steric and chemical stability in the finished actives. Our product is integrated at defined condensation reaction steps with organophosphorus, carbamate, or substituted aryl groups, followed by purification and formulation under controlled conditions.

    Industry compliance standards

    • FAO/WHO pesticide specifications
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • China GB/T 1604-2018 General Rules for Agro-chemical Pesticide Production

    Typical usage ratio

    • 1.0–4.5% relative to total active intermediate load, tuning based on molecular yield and desired crop selectivity profile

    Downstream process integration

    • Added at the nucleophilic addition or oxidation steps during the core structure assembly stage of active ingredient synthesis

    Final product types

    • Selective herbicidal active ingredients
    • Systemic pesticide precursors
    • Agrochemical technical concentrates

    3. Pharmaceutical Intermediate for API Synthesis

    Research-based pharmaceutical manufacturing sites deploy our 3,3-Dimethylbutyraldehyde as a controlled intermediate during critical steps in the preparation of certain drug substances, including those for central nervous system and metabolic disorder APIs. The aldehyde’s defined branching pattern enables medicinal chemists to construct substitution-sensitive scaffolds under strict cGMP conditions. It enters custom synthesis campaigns where reactivity, traceability, and purity directly influence product registration success globally.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • China Pharmacopoeia (ChP)

    Typical usage ratio

    • 0.7–2.0 molar equivalents per API scaffold unit; adjusted for stepwise conversion efficiency and downstream impurity control

    Downstream process integration

    • Utilized in the carbonyl addition or cyclization step for API skeleton construction and side-chain modification

    Final product types

    • Central nervous system (CNS) drug intermediates
    • Metabolic disorder active pharmaceutical ingredients
    • Specialty bulk pharmaceutical chemicals

    4. Fine Chemical Synthesis for Plasticizer and Polymer Modifier Production

    Producers of specialty plasticizers and polymer flow modifiers select 3,3-Dimethylbutyraldehyde in the targeted creation of branched ester and acetal compounds. The aldehyde undergoes precise condensation and esterification with alcohols or glycols, giving the resulting additives improved migration resistance and reactivity profiles for use in flexible PVC and engineering plastics. Industrial QC teams confirm strict batch purity and molecular weight distributions before downstream blending.

    Industry compliance standards

    • EU Regulation (EC) No 10/2011 for plastic materials and articles intended to come into contact with food
    • ASTM D7086 Standard for plasticizer performance
    • ISO 9001:2015 quality management
    • FDA 21 CFR 177.2600 (Identification of polymers in food contact)

    Typical usage ratio

    • 2.0–7.0% by weight in plasticizer modifier synthesis, dependent on polymer compatibility and targeted migration level

    Downstream process integration

    • Entered via initial feedstock charging prior to acetalization or esterification with base alcohols/polyols

    Final product types

    • Branched plasticizer esters for PVC and flexible vinyl compounds
    • Aldehyde-derived polymer flow modifiers
    • Specialty co-monomer additives for plastics manufacturing
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    Certification & Compliance
    More Introduction

    3,3-Dimethylbutyraldehyde: Reliable Building Block for Specialty Synthesis

    Direct from the Manufacturer: Our Experience with 3,3-Dimethylbutyraldehyde

    Every day in our production facility, we work with a range of aldehydes that serve essential roles across chemical synthesis. Among these, 3,3-Dimethylbutyraldehyde stands out—not because it’s the most famous aldehyde, but because its structure and performance keep it indispensable in targeted applications. Our teams strive for precision at every batch, checking the quality by GC and using hands-on experience to spot subtle variations that could affect downstream chemistry. What we deliver starts with a clear, colorless liquid, sharp and characteristic in odor, and—critically—stable under controlled storage.

    This compound, with the formula C6H12O, shows up again and again at the start of synthetic routes, particularly within fragrance intermediates and pharmaceutical precursors. Thanks to the two methyl groups on the alpha carbon, it resists unwanted side reactions that tend to derail more active, less hindered aldehydes. Chemists keep returning to 3,3-Dimethylbutyraldehyde for isobutyric structures where bulkier branches prevent excessive oxidation or condensation. Out on our factory floor, production campaigns run year-round, guided by careful temperature control and inerting—this protects both the product yield and the consistency our partners expect.

    Why Structure and Purity Make the Difference

    Not all aldehydes behave the same, even if their formulas look similar on paper. We see this in everyday operation. 3,3-Dimethylbutyraldehyde is substantially less prone to polymerization than straight-chain cousins—mainly because the bulky side groups slow down unwanted reactivity. Operators in the plant notice the difference. Pumps and storage lines stay cleaner, with less need to flush free aldehyde from polymeric residue. In formulations for flavors and fragrances, chemists rely on this stability to avoid discoloration and flavor profile drift. Some other aldehydes oxidize quickly, picking up off-notes or yellowing under warehouse lights; batches of 3,3-Dimethylbutyraldehyde, correctly packed and sealed, keep their integrity for extended periods.

    From our experience, meeting high purity specifications—typically above 98% by GC—is not just about numbers on a certificate. A pure batch holds onto its volatility, the functional group delivers what the formulator expects, and byproducts don’t show up in analytics or nose panels during customer evaluation. Achieving this involves more than automated packaging or software checks. Our technicians sample from every pack lot, checking for possible isomeric impurities or traces of alcohols that might have formed under mild hydrolysis. The difference in real-world outcomes—cleaner syntheses downstream, lower off-target yields in pharma, and predictable performance in R&D—justifies the continual investment in precise purification and monitoring.

    Working with End Users: Use Cases and Real-World Demands

    Having spent years supplying bulk 3,3-Dimethylbutyraldehyde to customers in Europe, North America, and Asia, we understand the diversity of end-markets. In fragrances, the manufacturing teams often look for tiny variations in raw material purity that change the final scent profile, especially where the aldehyde forms the backbone of musky, fresh compositions. Our specialists sometimes work alongside perfumers, exchanging insights on how even sub-ppm residuals affect the olfactory top notes. Meanwhile, our pharmaceutical clients tune batch sizes and delivery times around multi-step syntheses, using this aldehyde as a precursor for advanced building blocks—often requiring stringent trace metal analysis.

    The hands-on reality at our plant means we work closely with organic chemists and process engineers. Our product isn’t just a bottle or drum—it’s the starting point for months-long synthesis chains, during which a missed impurity or inconsistent batch profile can derail scale-up or regulatory submission. We constantly refine our distillation and drying steps, investing in continuous feedback loops with lab-scale and pilot plant teams, keeping the pathway as smooth as possible for downstream transformations. The value in what we do lies in the trust that customers place after years of open communication through technical support and post-delivery review.

    What Makes Our Approach Different

    Anyone can order 3,3-Dimethylbutyraldehyde from a catalog, but chemically speaking, not all samples perform equally. Over the decades, we’ve learned that strict attention to contaminant removal and control of aldehyde-water equilibria makes all the difference in high-value uses. Synthetic routes involving Grignard reactions, for instance, don’t tolerate residual water or small-chain alcohols. Each campaign run in our reactor trains involves multiple fractional distillation passes under nitrogen to protect the aldehyde function and remove volatile contaminants.

    For high-throughput customers operating on just-in-time models, the difference shows up as fewer rejections at quality control and less downtime for rework. Smaller R&D labs can scale new reactions with fewer surprises, leveraging the batch certification and traceability that our internal records provide. Having visited customer sites to troubleshoot synthetic hiccups, we know stabilizers and packaging controls influence real outcomes. Temperature logs during shipping, drum sealing systems, and vapor-barrier packaging all play their part in delivering an aldehyde that arrives ready to use, not sitting in darkened storage forming peroxides or oxidation products.

    Comparing 3,3-Dimethylbutyraldehyde with Related Chemicals

    The tendency in specialty markets is to compare aldehydes within families—think isobutyraldehyde, n-butyraldehyde, valeraldehyde, and their branched cousins. Some users assume that one will substitute smoothly for another, because prices and specs look close. Time and again, we have watched clients swap in 3,3-Dimethylbutyraldehyde for bulkier or linear aldehydes, seeking better shelf-life and outcome predictability.

    Laboratory trials highlight some big differences. With 3,3-Dimethylbutyraldehyde, the presence of two methyl groups shields the reactive carbonyl, making the molecule much less susceptible to unwanted oxidation. When compared to unbranched butyraldehyde in cross-aldol or Henry reactions, yields stay higher and product streams run clearer. Our QC team compares this in real time by lined-up comparative TLC plates and GC runs—evidence that subtle differences in molecular shape prevent many common side paths. Technicians working in polymer modification projects have shown us time and again that downstream chain-length and sterics change the outcomes in copolymerization, affecting end-use material properties.

    Other aldehydes can feel more aggressive, evaporating faster or yellowing storage drums after only a few months. Where customers need longer storage profiles or ship raw material across continents, 3,3-Dimethylbutyraldehyde keeps performance consistent. Our shipping containers undergo periodic review in collaboration with logistics partners; oxygen-scavenger liners and responsive inventory management cut down incident reports. Fragmented supplier networks sometimes lose track of handling protocols, but our site maintains single-batch integrity from synthesis to delivery, ensuring that what leaves our plant matches what we promised.

    Meeting Regulatory and Sustainability Challenges

    Environmental and process safety standards grow tougher every year, in every region where our products travel. We’ve adapted process steps to minimize waste and solvent use. Closed-system capturing of off-gas and aldehyde-rich vapors—paired with modern scrubber technologies—keeps emissions below legal thresholds, and we review output charts with our plant managers regularly. Customers ask about REACH, TSCA, and the compliance path for downstream applications; our specialists prepare not just documentation, but ongoing audits of material traceability. Raw materials come from vetted supply chains, and each intake is logged against our batch records, supporting an unbroken chain to the original synthesis.

    Some downstream partners demand customized statements around residual solvents and trace elements. Our team runs ICP and GC/MS panels on critical batches, ensuring that intermediates forwarded to cosmetic and pharmaceutical fields can clear internal requirements. Technical support remains a two-way street—engineers invite candid feedback, highlight possible process optimizations, and respond openly when regulatory changes affect probable impurity profiles or usage patterns.

    As public attitudes shift and sustainability targets grow more demanding, we continue updating our processes. Multiple teams spearhead closed-loop recycling of solvents, and we reinvest in safer oxidizing agents to handle routine cleaning or maintenance shutdowns. The blend of chemistry and responsibility means partnerships extend beyond a transactional exchange—every batch shipped draws on years of commitment to both consistent quality and environmental stewardship.

    The Real-World Side: Handling, Storage, and End-Use Performance

    Feedback from long-term partners shows how storage conditions and packaging directly influence downstream performance. Years ago, we learned to move away from unlined steel drums for 3,3-Dimethylbutyraldehyde due to trace metal catalysis leading to slow decomposition. Today, our packaging uses lined containers or HDPE drums, sealed under nitrogen or argon blankets depending on client specs. Regular review of supply chain incidents reinforces the need for consistent labeling, routine sampling, and temperature-mapped warehousing, especially for bulk shipments leaving the continent.

    Every production campaign closes with team walk-throughs and review sessions—operators talk through in-process measurements, maintenance logs, and even the subtle color shifts of incoming samples. A single off-spec drum triggers a full analysis, tying back to both on-site records and global best practices. Experience shows that by building real understanding—not just SOP compliance—we head off most delivery or application problems before they reach customers.

    Seeking Performance, Supporting Progress

    The future of specialty aldehydes lies with those able to innovate through technical expertise and operational honesty. As a manufacturer, we have to work shoulder-to-shoulder with every client, understanding not only their synthetic routes, but the practical issues faced inside their R&D or scale-up labs. Our work with 3,3-Dimethylbutyraldehyde has highlighted the importance of hands-on skills: daily calibration of distillation cut points, cleanup of line residues, and tracking subtle impurity markers. Years of experience allow our teams to recommend best-in-class use protocols—from adding small aliquots under inert gas, to switching between glass and polymer-lined reactors, depending on batch requirements.

    Direct dialogues with chemists reveal unexpected success stories. Several multinational fragrance developers have shared how they pivoted to 3,3-Dimethylbutyraldehyde as a stable backbone, constructing more complex scent molecules with greater repeatability. Polymer scientists find they can tweak chain branching and molecular weight by shifting which aldehyde they feed into the process, citing our product’s lot-to-lot reliability. It’s not about a single molecule, but the ecosystem of expertise, openness, and fine-tuned process engineering that brings real value to the user.

    Investment in new plant technologies, tighter process parameters, and ongoing customer hands-on support all shape our offering. Every shipment benefits from decades of continuous improvement, informed by trial-and-error, regulatory developments, and honest discussions with our partners. We maintain technical archives, learn from each campaign, and build flexibility into plant scheduling—allowing us to meet both large seasonal orders and one-time bulk requests with the same attention to quality.

    The Ongoing Journey: Building Trust and Reliability

    In any industry built on specialty chemicals, reliability is as much about follow-through as it is about molecular structure. Our ongoing commitment as a manufacturer means adapting processes in response to client feedback, regulatory demands, and evolving marketplace requirements. For those seeking a balance between performance and security of supply, direct partnerships and clear communication mark the difference between a commodity and a collaborative solution.

    As working chemists and engineers, we know 3,3-Dimethylbutyraldehyde only achieves its potential when handled with careful attention at every stage. Whether in fragrance R&D, pharmaceutical intermediates, or advanced polymer formulation, this molecule succeeds through the intersection of precise chemistry and hard-earned operational wisdom. We remain ready to share what we’ve learned, troubleshoot issues side-by-side, and continue improving how 3,3-Dimethylbutyraldehyde supports your innovation.