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2,6-Diisopropylaniline

    • Product Name 2,6-Diisopropylaniline
    • Alias 2,6-DIPA
    • Einecs 221-032-2
    • 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
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    Specifications

    HS Code

    984828

    Chemical Name 2,6-Diisopropylaniline
    Cas Number 24544-04-5
    Molecular Formula C12H19N
    Molecular Weight 177.29 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 260-262 °C
    Melting Point 1-2 °C
    Density 0.934 g/mL at 25 °C
    Refractive Index 1.528-1.530
    Flash Point 120 °C
    Solubility In Water Insoluble
    Smiles CC(C)C1=C(C=CC=C1N)C(C)C
    Inchi InChI=1S/C12H19N/c1-8(2)10-7-11(9(3)4)12(13)6-5-10/h5-9H,13H2,1-4H3
    Synonyms 2,6-Bis(1-methylethyl)aniline
    Ec Number 246-675-6

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

    Packing & Storage
    Packing Amber glass bottle, 100 mL, with secure screw cap, chemical label listing “2,6-Diisopropylaniline,” hazard symbols, and handling instructions.
    Shipping **2,6-Diisopropylaniline** is shipped in tightly sealed containers, protected from light and moisture, and stored in a cool, well-ventilated area. It is classified as a chemical substance and may require hazard labeling. Shipping must comply with relevant transport regulations, ensuring safe handling to prevent leaks, spills, and exposure.
    Storage 2,6-Diisopropylaniline should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Protect it from moisture and incompatible substances such as strong oxidizers and acids. Proper labeling and secondary containment are recommended to prevent spills and accidental exposure. Always follow local safety regulations.
    Application of 2,6-Diisopropylaniline

    Applications of 2,6-Diisopropylaniline in Industrial Manufacturing

    2,6-Diisopropylaniline is a specialized aromatic amine raw material, produced through precise alkylation and amination routes. Its unique steric and electronic characteristics make it essential for downstream synthesis in high-performance chemicals, lubricants, advanced polymer units, and agrochemical bodies. As a direct manufacturer, we supply this compound to qualified industrial producers that require consistent quality for demanding end-use segments. Below, we outline verified downstream application fields, each matched to real industry protocols, manufacturing requirements, and actual finished goods from global production lines.

    1. Antioxidant Production for Lubricant Additives

    Industrial formulators utilize this material as a core intermediate in the production of hindered phenolic and diarylamine antioxidant systems developed for synthetic and mineral oil lubricants. The bulky diisopropyl groups enhance thermal stability and reduce volatility, enabling downstream processors to achieve stricter oxidative performance targets in high-temperature lubricant blends, including engine, gear, and compressor oils. Close control of impurity profile and amine content is necessary to meet lube-grade regulatory and performance specifications worldwide.

    Industry compliance standards

    • ASTM D6560 (Additive Component Purity for Lubricants)
    • REACH Regulation (EC) No 1907/2006 for additive registration and use
    • API Lubricant Service Categories (SN Plus, CK-4 standards)
    • SAE J183 (Chemical Additives Requirements)

    Typical usage ratio

    • Intermediate conversion to antioxidant: 10–25% by mole in additive batch, final additive dosage in lubricants typically 0.2–1.5% by weight depending on base oil and target lifespan

    Downstream process integration

    • Material enters oxidation step for diarylamine synthesis
    • Post-derivatization blending with hydrocarbon carriers or dispersants
    • Final product filtration and dilution to supply form
    • Quality monitoring by HPLC and amine content titration per batch

    Final product types

    • Diaryl amine antioxidants for crankcase oils
    • Hindered phenol-based anti-oxidants for synthetic lubricants
    • Multi-functional lubricant additive packages
    • Anti-oxidant masterbatches for transmission fluids

    2. Agrochemical Synthesis (Herbicide Intermediate)

    This precursor enables targeted synthesis of specific amide and urea-based herbicide actives, including selective chlorophenoxy acid herbicides. The ortho-substitution protects the aniline ring during condensation and coupling, ensuring batch-to-batch repeatability and reduced side reaction formation. Downstream producers depend on pharmaceutical-level control over amine content and trace impurities to comply with global agricultural chemical market authorizations.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides and Agrochemical Intermediates
    • ISO 17025 laboratory testing accreditation of identity and purity
    • US EPA 40 CFR Part 180 pesticide tolerance levels
    • China GB/T 1600 series for technical active ingredient

    Typical usage ratio

    • Use rate in final herbicide active ingredient synthesis: 1.0–1.1 mole equivalents; final technical material concentration adjusted to 92–98% active based on crop and target market

    Downstream process integration

    • Charge as nucleophile in condensation and coupling step for selective amide formation
    • Distillation-based purification immediately after coupling
    • Formulation into final suspension/dispersible concentrate or granule, if required
    • QC with GC-MS and chlorinated impurity screens

    Final product types

    • Active herbicidal agents (e.g., diarylureas and phenoxyamide herbicides)
    • Pre-emergent herbicide technical concentrates
    • Formulated bulk herbicides for large-scale agriculture
    • Intermediate building blocks for further agrochemical diversification

    3. Synthesis of Photostabilizer Additives for Polymers

    Major polymer processors use this material as a starting component in the synthesis of hindered amine light stabilizers (HALS), applied in engineering plastics, films, and coatings. Its particular steric demand limits reactivity to defined positions, critical for producing high-purity stabilizers with enhanced UV-absorption properties. Traceability and contaminant control are mandatory, with full documentation on suitability for contact with consumer plastics regulated across international supply chains.

    Industry compliance standards

    • EU Regulation (EC) No 10/2011 on plastic food contact materials
    • US FDA 21 CFR 177.1520 for olefin polymers additives
    • ISO 4582 (Polymer weathering resistance testing)
    • RoHS Directive 2011/65/EU (Heavy metals and amine impurity limits)

    Typical usage ratio

    • 5–20% by mole in HALS intermediate syntheses; applied at 0.05–0.7% stabilizer content in final resin formulations depending on plastic type, UV exposure, and processing requirements

    Downstream process integration

    • Direct input for Mannich or alkylation steps to form piperidinyl HALS core
    • Pilot plant purification and microfiltration for regulated markets
    • In-line blending with plasticizers and compounding agents
    • Online QC for migration and extractables via UV spectroscopy

    Final product types

    • Hindered amine light stabilizers (HALS) for polyethylene and polypropylene
    • Photostabilizer masterbatches for automotive trim and exterior plastics
    • UV-resistant agricultural film additives
    • Weathering-resistant technical polymer compounds

    4. Pharmaceutical Intermediate for Active API and Specialty Drug Synthesis

    API manufacturers employ this intermediate in patented or generic synthesis routes for biologically active molecules incorporating sterically hindered aniline motifs. The regioselectivity conferred by diisopropyl groups supports consistent yields in complex API scaffolds, especially for advanced intermediates used in anti-inflammatory and anti-neoplastic candidates. Control over residual solvents, trace heavy metals, and bioburden is strictly monitored for cGMP production environments according to international health authority expectations.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice Guidance
    • USP–NF monograph compliance for relevant intermediates and related compounds
    • EU GMP Guideline (EudraLex Vol 4)
    • US FDA 21 CFR Part 210/211 finished pharmaceutical standards

    Typical usage ratio

    • Intermediate loading: 1.0–1.05 molar equivalents per API batch; adjusted in multi-step synthesis for target molecular yield, with residual below 0.1% in finished API

    Downstream process integration

    • Stepwise coupling or cyclization with activated carboxylic acids or aldehydes
    • In-process HPLC and NMR method for intermediate quantification
    • Final purification by preparative chromatography and crystallization
    • QA documentation for traceable batch release

    Final product types

    • Key aniline-containing API intermediates
    • Active drug molecules for oncology and immunomodulation
    • Specialty fine chemical intermediates for biotech R&D
    • Custom synthesis pharmaceutical building blocks

    5. Dye and Pigment Intermediate for Specialty Colorants

    Colorant manufacturers use this material to synthesize sterically hindered azo and anthraquinone dye molecules that deliver superior lightfastness and chemical resistance for textile, ink, and high-temperature plastics processing. The introduction of diisopropyl groups restricts side reactions during diazotization and coupling, supporting reproducibility in chromophore construction. Producers require controlled particle size and purity to ensure consistent spectral behavior in end-use sectors—from polyester yarns to technical coatings.

    Industry compliance standards

    • Oeko-Tex Standard 100 (Textile dye safety)
    • GHS Labeling and Hazard Classification for industrial dyes
    • ISO 105-B02/B04 (Color fastness to light and weathering)
    • EN 71-3 (Migration of certain elements in toys for pigment safety)

    Typical usage ratio

    • Mole ratio: 1.0–1.2 equivalents in diazotization and coupling steps, final colorant content in formulated products ranges from 0.1–5% by weight based on fiber, polymer, or surface application

    Downstream process integration

    • Precursor stage in diazonium salt formation
    • High-temperature coupling to anthraquinone or azo cores
    • Wet milling and ultrafiltration
    • Particle size and hue control prior to paste or powder formulation

    Final product types

    • Lightfast azo dyes for polyester yarn
    • High-purity pigment dispersions for printing inks
    • Specialty textile and leather colorant pastes
    • Heat-resistant plastic color masterbatches
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    More Introduction

    2,6-Diisopropylaniline: Practical Insights from the Manufacturer’s Bench

    Understanding 2,6-Diisopropylaniline at Its Core

    When our team produces 2,6-Diisopropylaniline, we’re not simply working with a catalog entry — we’re engaged with a material that has proven itself vital in more than one segment of the specialty chemical world. We manufacture this compound, model number DIPA-261, in a modern facility focused on reliable purity and traceability, right from the raw materials to the finished drum. We commit each lot to a purity benchmark that consistently exceeds 99%, determined through in-house GC and NMR validation, because downstream performance always starts with what goes into the reactor.

    Distinct Chemical Personality

    Aromatic amines often share family similarities, but in our daily lab practice, 2,6-Diisopropylaniline stands apart for a couple of clear reasons. Its bulky isopropyl groups at the ortho positions fundamentally change reactions compared to regular anilines. We’ve observed that this makes the molecule much less prone to unwanted substitution at those positions, which has helped several of our custom synthesis clients achieve higher selectivity. Many of us remember cases where just swapping from aniline to 2,6-Diisopropylaniline eliminated headaches over poly-substituted byproducts, reducing labor at the purification step. For those designing ligands or working on catalytic applications, this steric shielding does more than just prevent over-reaction — it shapes the coordination geometry itself.

    Why Our Customers Come Back for This Chemical

    Over the years, industries from agrochemical research to materials science repeatedly choose our 2,6-Diisopropylaniline. It allows them to introduce specialized structural elements in complex molecules, where any compromise in purity or physical profile can ripple through a costly multi-step synthesis. Pharmaceutical researchers trust this molecule as a building block because the controlled isopropyl substitution brings the kind of selectivity their medicinal chemistry demands, especially in kinase inhibitor scaffold construction or in arylation protocols.

    From first-hand experience, we know that small deviations in the melting point (ours falls between 42-45°C, based on our production runs) can signal inconsistencies with raw feedstock, temperature control, or residual solvents. By focusing directly on these small but critical quality signals, we ensure consistent product form as granules or fine powder. We avoid issues that crop up with off-spec product: caking in the feed hopper, variable dissolution rates, or unpredictable crystallization in downstream chemistry.

    Real-World Handling on the Factory Floor

    Every batch of 2,6-Diisopropylaniline we make gets tested under the same conditions our customers use: weighed out into glassware, dissolved, and processed for scale-up. The first thing most chemists notice is the distinctive floral-amine odor, which demands proper ventilation but also immediately confirms the identity to anyone who has worked with it long enough. Oil content — when present — will instantly give itself away as streaks on the sampling rod, a sign of incomplete recrystallization that we make a point to eliminate. Such direct handling experience means we never overlook the operational realities our customers face in their own labs or pilot plants.

    Performance in Key Applications

    The strength of 2,6-Diisopropylaniline often comes through clearest when it’s used as a core fragment in ligand design for metal catalysts. Our regular feedback from collaborating R&D groups shows that this material’s unique steric profile helps tune selectivity on metal centers such as palladium or nickel, allowing reliable formation of the desired complex with less tendency for undesired side reactions. That translates into fewer purification cycles, less waste, and better catalyst lifetime.

    In the production of agrochemical intermediates, the same para-position reactivity — left open thanks to the ortho-blocking — allows scientists to introduce custom substitution patterns. We’ve seen repeated success in coupling and functionalization reactions where standard aniline or less-hindered derivatives fail to deliver the same yields or purity, particularly when high-throughput screening is involved. Our internal batch records and feedback from downstream users reinforce this performance; for those optimizing for scale, reducing even minor byproduct routes can affect timelines and margins.

    Comparing 2,6-Diisopropylaniline with Other Anilines

    Working with dozens of aromatic amines in our own facility, we’ve found there’s a practical spectrum of behavior between basic aniline, alkyl- and halogen-substituted analogues, and the more hindered derivatives like 2,6-Diisopropylaniline. Standard aniline, for instance, provides maximum reactivity for classical transformations (acylations, sulfonations, diazotizations) but suffers badly from overreaction. The mono-substituted products such as para-isopropylaniline bring a degree of control, yet cannot redirect the major kinetic preferences.

    2,6-Diisopropylaniline alters this dynamic almost completely on account of its steric profile. In Buchwald-Hartwig or Ullmann coupling conditions, our experience shows it yields higher mono-arylation selectivity, a pattern confirmed in our process scale-ups as well as by customers making advanced intermediates. The compound also possesses improved solubility in nonpolar organic media compared to some less-hindered amines, a property that proves useful in solvent selection for flow chemistry and continuous processing.

    We have handled requests for custom derivatives based on this motif, and repeatedly find customers circle back to 2,6-Diisopropylaniline because other anilines failed to provide the cleaner downstream transformations they require. This is not just lab theory — it has been demonstrated in practice both using manual batch records and in pilot automation runs.

    Physical Properties Matter — Here’s Why

    The physical integrity of any aromatic amine makes a real difference in plant handling. Our production team invests effort in achieving a free-flowing, crystalline form for 2,6-Diisopropylaniline, since sticky, semi-crystalline lumps slow down automated feeding and promote bridging in scales larger than 25kg. We consistently dry our product to below 0.1% moisture (Karl Fischer titration) to prevent both caking and risk of hydrolysis in sensitive catalytic environments. These are not just spec-sheet numbers: we check batches directly, sift and resample, and discard those that don’t meet these real-world standards.

    Reducing Downstream Risks

    As a manufacturer, we see firsthand how even a small impurity in a reagent like 2,6-Diisopropylaniline can propagate through multi-step syntheses with costly consequences. We have fielded calls from partners who learned this lesson through failed pilot batches using generic supply — questions about trace amides, halides, or oxidized byproducts almost always point to insufficient upstream control. Our facility uses both HPLC and mass spectrometry to run off-the-line checks, looking for off-specification peaks that tell us the process ran hot or ran longer than planned. The purity data are not hollow numbers, but a reflection of active engagement with the process — a feedback loop that grows tighter with every shipment.

    We document and retain full traceability for every batch, so if challenges arise in later synthesis or scale-up, we can review the record together with our customer, resolve the source, and find a practical fix. That responsiveness is built on experience, and it has reduced repeat issues significantly in cooperative projects.

    Handling and Storage: Lessons Learned

    Moisture and light both affect 2,6-Diisopropylaniline over time. We structure our packaging process to use airtight, opaque containers, minimizing degradation during shipment or warehousing. In hot or humid climates, we’ve seen degradation spots appear rapidly if containers are not kept dry and cool, resulting in yellowing and, in some cases, a drop in assay by as much as half a percent over only two weeks. Our warehousing team monitors environmental conditions and we provide full recommendations to customers on how to achieve the same protection on their site, based on both our internal tests and return data from customers storing this compound over extended periods.

    Odor containment is also no small matter. 2,6-Diisopropylaniline, like other alkylated anilines, carries a strong and persistent odor. We house production and packaging in isolated rooms vented by activated-carbon scrubbing towers, avoiding cross-contamination with neutral materials which are far more odor-sensitive. For laboratory users, using a well-maintained fume hood is a minimum; on a plant scale, we recommend local exhaust venting for all charge and discharge steps involving this material.

    Demand from Research, Pharmaceuticals, and Beyond

    We started making 2,6-Diisopropylaniline for the pharmaceutical sector, where demand for high-purity intermediates never wavers. Its use spans from custom ligand synthesis to active component development. In pharmaceuticals, this molecule contributes to building blocks with targeted bioactivity or as precursor units for specialty dyes and enzyme inhibitors. Agricultural science teams turn to our product for phenylurea herbicide synthesis, due to its capacity to provide site-directed amine chemistry with low byproduct load. Specialty material companies draw on it for new polymer designs and high-performance aromatic monomers, benefiting from the unique reactivity profile that comes from the isopropyl shielding.

    Over the last decade, as we have become more attuned to regulatory shifts affecting aromatic amine use in materials applications, we have made specific adjustments in our process to meet updated safety compliance rules, prioritizing low-residual solvent content and documenting each step. This approach helps researchers downstream qualify new compounds for more demanding markets, whether in electronics or advanced coatings.

    Supporting Innovation: Our Role as Chemical Manufacturer

    Watching our clients make novel discoveries, or streamline an existing synthesis with our material, brings home the value of mastering production details. Our technical support team has collaborated with startups scaling up their inventions, fine-tuning feedstocks and temperature endpoints based on feedback sent straight from their reactor logs. This back-and-forth improves our manufacturing process as much as it helps chemists in the field, and ensures the product not only meets but directly supports the innovation happening in today’s labs.

    We know from experience that every time a chemist calls us in during process troubleshooting, the insights gained turn into both manufacturing improvements on our end, and smoother trials or upscales on theirs. This dialogue reduces risk, saves days during plant ops, and accelerates product launches in tight timelines.

    Safe and Efficient Use: Advice from the Production Line

    Having handled hundreds of kilograms of 2,6-Diisopropylaniline over the years, we’ve gathered plenty of practical advice on safe handling and optimal use. Purging lines after transfer eliminates odor residue; cleaning feed systems with compatible solvents prevents cross-reaction with subsequent batches. Personal experience taught us to avoid storing this material near oxidizers or acids, as even slow exposure can lead to discoloration and reduction in long-term purity.

    While standard PPE covers gloves and goggles, our operators have found that using NBR (nitrile butadiene rubber) gloves lasts significantly longer than latex types, given the compound’s tendency to permeate less-tough polymers. Fume hoods or site exhaust should stay active during weighing or mixing. These lessons, accumulated from many years on the factory floor, get shared with every customer looking to optimize their own safe handling procedures.

    Helping Our Customers Get the Results They Need

    Routine matters as much as batch precision. Unlike resellers or traders, we have a direct stake in ensuring each drum or package meets requirements for purity, color, physical form, and performance every time it leaves our site. Direct feedback, not generic boilerplate, drives our ongoing improvements. We keep flexible lot sizes, with production shifts able to pivot between different customer needs, whether a five-kilo research order or a 500-kilo campaign for pilot plant work. Our technical documentation draws directly from real batch history, not recycled templates, offering tried-and-true insight into working with this chemistry.

    As technology evolves, research demands grow more complex, and regulatory scrutiny increases, our ongoing commitment to consistent, high-quality 2,6-Diisopropylaniline production remains firm. This material, with all its unique quirks and advantages, reflects decades of hands-on learning, direct customer engagement, and an unwavering focus on delivering materials that truly work where it matters: in your plant, your lab, and your product pipeline.