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2,4,6-Tri-Tert-Butylaniline

    • Product Name 2,4,6-Tri-Tert-Butylaniline
    • Alias TTBN
    • Einecs 253-057-0
    • 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

    414306

    Cas Number 728-61-4
    Molecular Formula C18H31N
    Molecular Weight 261.45 g/mol
    Iupac Name 2,4,6-tri(tert-butyl)aniline
    Appearance White to off-white solid
    Melting Point 152-156 °C
    Density 0.98 g/cm³ (25°C, approximate)
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in most organic solvents (e.g., ether, benzene)
    Purity Typically ≥98%
    Smiles CC(C)(C)c1cc(C(C)(C)C)cc(C(C)(C)C)c1N

    As an accredited 2,4,6-Tri-Tert-Butylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g brown glass bottle features a secure screw cap, clear labeling for 2,4,6-Tri-Tert-Butylaniline, hazard warnings, and batch details.
    Shipping 2,4,6-Tri-Tert-Butylaniline is typically shipped in sealed, chemical-resistant containers to prevent contamination and moisture exposure. It should be transported as a hazardous material according to regulatory guidelines, with appropriate labeling and documentation. Store and ship in a cool, dry place away from incompatible materials, ensuring proper handling and personal protective equipment usage.
    Storage 2,4,6-Tri-Tert-Butylaniline should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect it from light and moisture. Use appropriate personal protective equipment when handling, and ensure proper labeling to prevent accidental misuse. Store at room temperature and avoid prolonged exposure to air.
    Application of 2,4,6-Tri-Tert-Butylaniline

    Applications of 2,4,6-Tri-Tert-Butylaniline in Industrial Manufacturing

    As a producer specializing in high-purity 2,4,6-Tri-Tert-Butylaniline, we supply this advanced aromatic amine primarily to manufacturing partners in coatings, polymer stabilization, specialty rubber, and industrial lubricant additive fields. Our experience with global technical standards, regulatory needs, and downstream integration ensures robust support for customers’ proprietary formulations and compliance objectives. Below, we highlight principal application scenarios validated by major industrial users and supply chain audits.

    1. Antioxidant Intermediate for High-Performance Lubricant Additives

    Industrial lubricant formulators use our material as a key amine intermediate to synthesize hindered phenolic antioxidants and ashless dispersants, providing enhanced oxidative stability for turbine, compressor, and engine oils under rigorous thermal load. Incorporators prioritize consistency in purity and molecular structure to ensure reaction yields when producing finished additive blends requiring long-term oxidation resistance and low deposit formation in high-performance lubricating environments.

    Industry compliance standards

    • ASTM D4951 (Engine Oil Additive Content)
    • API Base Oil Categories (API Group II/III Lubricant Additive Approval)
    • REACH Registration for Industrial Chemicals (European Regulation EC 1907/2006)
    • OECD Guidelines on Industrial Additive Safety

    Typical usage ratio

    • Used at 0.5–3% by weight in additive package manufacture, adjusted based on base oil group and blending target for oxidation induction time. Formulators may increase proportion for severe service formulations as validated by bench tests (e.g., TOST, RPVOT).

    Downstream process integration

    • Introduced during alkylation and further condensation in batch or continuous reactors for antioxidant intermediate synthesis. Final incorporation as a reacted component in multifunctional additive packages (antioxidant, dispersant) before blending into lubricating oil base stocks via solvent and mechanical mixing.

    Final product types

    • Compressor oils for power generation
    • Heavy-duty diesel engine oils
    • Synthetic turbine lubricants
    • Hydraulic fluids subjected to extreme thermal conditions

    2. Polymer Stabilizer Synthesis in Polyolefin Manufacturing

    Specialty chemical manufacturers consume this compound as a starting material for the synthesis of non-staining phenolic antioxidants and UV stabilizers specifically designed for polyolefin applications. These stabilizers aim to prevent polymer degradation during extrusion, molding, and subsequent long-term service life, meeting critical color and tensile property retention in polypropylene and polyethylene films and molded goods.

    Industry compliance standards

    • EU Regulation (EU) No 10/2011 (Plastic Food Contact Materials)
    • US FDA 21 CFR 177.1520 (Olefin Polymers for Food Packaging)
    • ISO 11357 (Plastics DSC Testing Methods)
    • GB 9685 (China Hygienic Standards for Food Contact Additives)

    Typical usage ratio

    • Precursor used to synthesize finished antioxidant or UV stabilizer; the final stabilizer is typically dosed at 0.05–0.2% by resin weight, dependent on resin melt flow index and end-use stress environment (outdoor vs indoor film).

    Downstream process integration

    • Enters reaction step as primary amine for the synthesis of high molecular weight phenolic stabilizers. End users introduce finished stabilizer masterbatches during polymer compounding in twin-screw extrusion or direct resin blending before film blowing or injection molding.

    Final product types

    • BOPP (biaxially oriented polypropylene) packaging films
    • HDPE and LDPE molded containers
    • Polyolefin-based automotive trim components
    • Food contact grade plastic wraps

    3. Rubber Antioxidant Precursor for Tires and Technical Rubber Goods

    Producers of industrial rubbers employ this chemical as a precursor in the synthesis of selective aromatic amines for use as antioxidants in high-performance natural and synthetic elastomer compounds. Tire and technical rubber manufacturing utilize these precision stabilizers to counter heat-initiated and ozone-induced polymer degradation, which is crucial for tread and sidewall compounds with demanding service lifespans.

    Industry compliance standards

    • ISO 9001:2015 (Rubber Compound Quality Systems)
    • ISO 14001:2015 (Environmental Management Rubber Processing)
    • ASTM D3157 (Standard Test Method for Rubber Antioxidant Analysis)
    • EU REACH Annex XVII (Rubber Chemical Restrictions)

    Typical usage ratio

    • Utilized at precursor stage to synthesize finished amine antioxidants; typical antioxidant content in final rubber recipes ranges from 1–2 phr (parts per hundred rubber) but adjusted by compounder within 0.75–2.5 phr for required ozone and heat resistance profiles.

    Downstream process integration

    • Reacted with suitable alkylating agents during rubber antioxidant production. Compounders blend the finished antioxidant into rubber during Banbury mixing prior to vulcanization, ensuring homogeneous dispersion in masterbatch or final mix before forming and curing.

    Final product types

    • Radial and bias-ply tires (tread and sidewall)
    • Automotive hoses and belts
    • Vibration-damping rubber parts
    • Seals and gaskets for general industrial use

    4. Chemical Reagent for Electronic Grade Epoxy Hardener Production

    Adhesive and encapsulant manufacturers utilize our material within the synthesis pathway of substituted aniline-based epoxy hardeners, optimized for the demands of electronics assembly. These hardeners offer targeted curing profiles and low ionic impurities, essential to producing advanced printed circuit boards and microelectronic device packaging requiring clean, reliable, and stable performance in aggressive service conditions.

    Industry compliance standards

    • IEC 61249-2-7 (Materials for Printed Boards)
    • UL 94 (Flammability Standard for Plastics)
    • RoHS 3 (EU Directive 2015/863, Restriction on Hazardous Substances in Electronics)
    • JIS C 5010 (Japanese Standards for Epoxy Compounds in Electronics)

    Typical usage ratio

    • As reactant for specialty hardener production; finished hardener usage varies from 10–20% of overall epoxy formulation mass, modulated based on targeted mechanical properties and cure schedule.

    Downstream process integration

    • Charged to closed reactors with epichlorohydrin and other intermediates to build substituted aniline-based hardener structures. Downstream, electronics material companies blend the finished hardener with liquid epoxy oligomer precursors before thermal or UV curing during PCB lamination or device encapsulation lines.

    Final product types

    • High-Tg copper clad laminates for multilayer PCBs
    • Semiconductor encapsulants
    • Insulating adhesives for electronic components
    • Potting compounds for microcircuitry
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    Certification & Compliance
    More Introduction

    Introducing 2,4,6-Tri-Tert-Butylaniline: The Chemist’s Reliable Choice

    Over the last decade, 2,4,6-Tri-Tert-Butylaniline has changed the way we approach the development of specialized compounds in industrial chemistry. In our experience as manufacturers of high-purity 2,4,6-Tri-Tert-Butylaniline, we have seen the compound’s unique characteristics simplify both research and production for clients in diverse sectors. Dedicated to consistent quality, we maintain rigorous standards throughout synthesis, purification, and packaging, drawing from over twenty years in the field. We believe that a transparent introduction to both the unique aspects and practical applications of our product can offer value beyond a conventional product spotlight.

    Model and Specifications from the Factory Floor

    We manufacture our 2,4,6-Tri-Tert-Butylaniline in bulk according to industry benchmarks that reflect both purity and reproducibility. From our reactors, each batch is checked for chemical purity using gas chromatography and nuclear magnetic resonance analysis. Through each production cycle, we reach a purity level above 99%, with residual moisture and by-products kept far below conventional limits. The chemical formula—C18H31N—gives this material a robust molecular weight and distinct steric profile. Every lot leaves our plant as a fine crystalline solid, typically off-white, with a melting point close to 160°C.

    Storage always deserves attention. We recommend cool, dry, and sealed containment—preferably in inert-atmosphere drums lined with polyethylene. The compound demonstrates excellent shelf stability under these conditions, holding its structural integrity for months, even in demanding climates.

    Our clients may choose between standard 500-gram and 5-kilogram pails, but we also offer custom batch sizes. Each shipment comes with a batch analysis, reproducible under third-party lab scrutiny. We have invested in real-time lot tracking software, and the feedback loop with clients has pushed us to improve not only on compliance but also on ease of product handling across scales.

    The Real World Applications: From Laboratory to Industry

    There’s a reason 2,4,6-Tri-Tert-Butylaniline keeps popping up in new patent filings and technical disclosures: its versatility is not theoretical. In our own interactions with academic labs and chemical engineers, practical discussions always center on two core features: strong electron-donating properties and pronounced steric bulk that shields active sites.

    Synthetic chemists value its performance as an intermediate in custom ligand design. Many choose it to synthesize N-heterocyclic carbene (NHC) ligands, which have transformed homogeneous catalysis in pharmaceutical and materials development. The unusually bulky tert-butyl groups create a protective effect around the nitrogen atom, giving the ligands unique selectivity and stability.

    In electronics, 2,4,6-Tri-Tert-Butylaniline acts as a stable precursor for organic semiconductors. Its electron-rich environment and resistance to oxidation pay off in the manufacture of hole-transport materials and advanced polymers. Some of our biggest volume customers use the product as part of OLED research, noting cleaner reactions and higher yields for both small-scale synthesis and pilot plant runs.

    Apart from these high-profile roles, we have also witnessed demand surge in specialty polymer chemistry and surface science. The bulky structure disrupts polymer packing, often leading to improved mechanical properties or altered solubility profiles. It also sometimes serves a vital role in blocking or modifying surfaces, particularly for anti-corrosion coatings or anti-fouling formulations.

    How Our Product Differs from Common Alternatives

    A question that comes up frequently: “Why 2,4,6-Tri-Tert-Butylaniline, and not a related aniline derivative?” Our team answers this from a practical perspective, based on consistent client feedback and the direct experience of our onsite chemists.

    Other anilines—simple derivatives like aniline itself, or less hindered analogues like 2,6-diisopropylaniline—bring fewer bulk groups to the molecular structure. This difference is not cosmetic—it shapes reactivity, color stability, and even storage conditions. For instance, 2,4,6-Tri-Tert-Butylaniline’s heavy substitution makes it highly resistant to oxidative degradation, a problem that frustrates users of more basic analogues under routine synthetic conditions. The presence of three tert-butyl groups at the ortho and para positions shields the amine group, reducing susceptibility to unwanted side reactions or polymerization.

    Comparing the flow and solubility behavior, we have run head-to-head tests with both triisopropylaniline and triethyl-substituted analogues. 2,4,6-Tri-Tert-Butylaniline shows distinct advantages in both organic and mixed solvent systems. Its higher melting point and reduced volatility also simplify shipment and storage, particularly on intercontinental routes where temperature fluctuations and time in transit can lead to minor decomposition in less robust chemicals.

    On the cost side, our engineers have always worked to streamline the multistep manufacturing process. While the upfront synthetic cost of introducing large tert-butyl groups is higher than for simpler alkyl groups, many clients report that the savings in downstream purification and the improved lifetime of process catalysts more than compensate. Higher purity and more stable reactions often translate to fewer quality failures, less equipment fouling, and lower clean-up costs.

    Manufacturing Insights and Choices

    We approach manufacturing 2,4,6-Tri-Tert-Butylaniline as a fine balance between efficiency and uncompromising quality. The basic steps begin with commercially available tert-butyl chloride and aniline, following an alkylation pathway under strong Lewis acid catalysis. Temperature control and reaction workup prove crucial here — side reactions can generate unwanted oligomers if batch variables aren’t carefully managed. Our chemists closely monitor every batch using real-time analytics. In cases where we observe slight deviations, we adjust process parameters to recover optimal selectivity.

    We continuously re-examine the environmental impact of each synthesis step. The reagents and solvents in use carry their own safety profiles and disposal challenges. Our facility utilizes a closed-loop solvent recovery system, cutting waste volumes substantially. Hazard reduction does not stop at the gate; we coordinate with downstream partners for proper handling of spent by-products. In partnership with local regulatory authorities, our reporting and tracking meet the highest standards for transparency.

    The Technical Side: Challenges and Solutions

    Every product, no matter how thoroughly refined, faces certain hurdles. With 2,4,6-Tri-Tert-Butylaniline, the main issue engineers face often relates to solubility and compatibility in specific low-polarity or high-viscosity media. We collaborate on custom blending projects to modulate the compound’s dispersibility. In several cases, co-solvents or gentle heating have produced the intended solution. Overly vigorous heating or the use of highly reactive additives leads to degradation and should be avoided.

    We have also responded to concerns from clients about potential contamination during scale-up. To address this, we deploy a closed pilot reactor system for any new process exceeding five-kilogram output. Inline filtration and low-particulate-grade transfer keeps the risk of metallic or polymeric inclusions well below international standards. Our quality team doesn’t sign off on a batch until it passes environmental, health, and application-specific thresholds, all documented in a certificate that travels with the product.

    Safety in transport remains a daily concern. 2,4,6-Tri-Tert-Butylaniline is classified as a hazardous chemical in certain jurisdictions, particularly due to toxicity upon inhalation or skin contact of dust. Every drum and container is sealed against air and moisture ingress and clearly labeled with GHS-compliant hazards. Our logistics crew has undergone annual hazardous materials handling certification, and we regularly update our standard operating procedures as regulations change.

    From Customer Feedback to Process Refinement

    Direct conversations with our customers shape how we improve both product and service. As a manufacturer, we witness firsthand the day-to-day challenges and incremental wins that become visible only by working closely with those who use the compound in real applications.

    For example, early users in advanced materials development pointed out issues with static build-up during decanting and weighing. Our investigation led to an improved drum lining that virtually eliminates static discharge, reducing spillage and vastly improving worker safety. After several months, repeat clients reported smoother workflow and fewer lost batches.

    Other teams developing customized ligands for specialty catalysis expressed concern about micro-batch purity deviation and trace metal introduction. In response, we implemented new glassware cleaning protocols and switched to a new grade of reagent that cut potential contamination below the most stringent thresholds. For research-scale users, this step virtually eliminated unexplained catalytic inhibition.

    On the logistic front, global supply chain pain points became an open subject during the last few years. A combination of pandemic-related disruptions and shifting regulatory practices encouraged us to pre-position inventory and add redundancy in our supply channels. Our forwarders employ temperature- and humidity-controlled transport so the product arrives with the same chemical profile with which it left our plant—no surprises at the bench.

    Responsible Stewardship and Community Interface

    Long-term business in specialty chemicals depends on trust, transparency, and continual effort to reduce negative footprint. 2,4,6-Tri-Tert-Butylaniline does not present the same scale of environmental risk as heavy metals or halogenated aromatics, but responsible management starts in the lab and continues through the full supply chain. We invest in training for every worker, so that safe handling becomes second nature and proper disposal is a priority rather than an afterthought.

    Waste stream management is never left to chance. Excess solvents and minor by-products undergo neutralization and are sent to licensed waste management partners for full recycling or safe disposal. Each year we support outreach and workshops with technical schools to promote awareness of chemical safety and environmental best practices, including for compounds such as 2,4,6-Tri-Tert-Butylaniline. We see the next generation of chemists bringing both diligence and creativity to sustainable challenges, and we support their efforts however possible.

    Continuous Improvement and Where We Go Next

    We review the product lifecycle regularly. New science is always emerging in the world of bulky anilines. Academic and industrial groups keep discovering alternative methods with lower carbon impact and higher atom economy. Our team keeps up-to-date with catalytic routes or solventless methods to bring both financial and environmental value. The journey is ongoing—there are always ways to push performance margins higher, drive costs down, and streamline delivery.

    As demand for advanced materials continues to expand, with clients probing unexplored applications for 2,4,6-Tri-Tert-Butylaniline, we remain committed to both reliability and innovation. Each batch, each drum, and each customer query connects us to a wider network of ideas and challenges. By listening, refining, and responding, we believe that chemical manufacturing can lead the way in productivity, responsibility, and transparency. The evolution of 2,4,6-Tri-Tert-Butylaniline’s role in fine chemical manufacturing reflects the deeper story of progress and partnership across science and industry.