|
HS Code |
173238 |
| CAS_Number | 95-68-1 |
| Molecular_Formula | C8H11N |
| Molecular_Weight | 121.18 g/mol |
| IUPAC_Name | 2,4-Dimethylaniline |
| Synonyms | 2,4-Xylidine |
| Appearance | Colorless to pale yellow liquid |
| Melting_Point | 22-23 °C |
| Boiling_Point | 216-217 °C |
| Density | 0.98 g/cm³ at 20 °C |
| Solubility_in_Water | Slightly soluble |
| Flash_Point | 101 °C |
| Vapor_Pressure | 0.13 mmHg at 25 °C |
| Refractive_Index | 1.556 at 20 °C |
| PubChem_CID | 7385 |
| UN_Number | 2261 |
As an accredited 2,4-Dimethylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 500 mL amber glass bottle, tightly sealed, labeled “2,4-Dimethylaniline,” with hazard warnings and detailed chemical information. |
| Shipping | 2,4-Dimethylaniline is shipped as a hazardous material. It should be packed in tightly sealed containers, protected from light, moisture, and incompatible substances. Follow all relevant regulations for transport, including labeling and documentation (UN Number 2431, Class 6.1, Packing Group III), and handle with appropriate personal protective equipment to ensure safety. |
| Storage | 2,4-Dimethylaniline should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizing agents and acids. It should be kept away from direct sunlight and heat. Store in a chemical storage cabinet designed for flammable and toxic substances, and clearly label containers to prevent accidental misuse. |
Applications of 2,4-Dimethylaniline in Industrial ManufacturingAs a dedicated manufacturer of 2,4-Dimethylaniline, we serve core chemical sectors by supporting specialized downstream synthesis. This material is crucial for targeted organic synthesis in colorants, agrochemicals, pharmaceuticals, and polymer intermediates. Below, we detail distinct industrial application routes, relevant compliance, integrated usage levels, and true final product classes based on direct feedback from global plant operators and formulation specialists. 1. Intermediate for Azo Dye ProductionThe downstream dye industry uses 2,4-Dimethylaniline as a key intermediate for the synthesis of specialized azo dye molecules, including C.I. Solvent Yellow 33 and C.I. Disperse Yellow 42. Its methylating effect on the aromatic ring offers distinct shade intensity and improved dye stability in textile, leather, and plastics coloration. Production facilities dose this compound during the early diazotization stage, requiring batch quality monitored by sector-specific colorimetric control. Compliance with effluent control and exposure thresholds remains critical in large-scale operations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Synthesis of Agrochemical Active IngredientsCrop protection manufacturers rely on 2,4-Dimethylaniline to construct aromatic ring systems essential in certain selective herbicides and plant growth regulators. It undergoes targeted halogenation, alkylation, or nitration to create active amide, carbamate, or urea derivatives. Strict traceability from raw material input to technical-grade active ensures regulatory acceptance for use in agricultural zones subject to pesticide residue audits. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. API Intermediate for Pharmaceutical Synthesis2,4-Dimethylaniline supports pharmaceutical sector needs as a building block for certain APIs and their intermediates, notably in antipyretic, analgesic, and antimicrobial agent production. It acts as an aromatic amine donor in multi-step syntheses requiring documented purity, residual solvent minimization, and full batch traceability to meet regulatory submissions in both advanced and emerging markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Precursor for Polymerization Inhibitors and AntioxidantsPolymer and rubber compounders use 2,4-Dimethylaniline in the controlled synthesis of specialty inhibitors and stabilizers, especially for unsaturated polymer resins and synthetic rubbers. It is converted to N-substituted derivatives optimized to protect monomers from premature polymerization during storage and processing. The finished additives also suppress oxidation pathways in hot-melt or high-shear applications, meeting industry-mandated residuals and performance tests. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2,4-Dimethylaniline prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Producing 2,4-Dimethylaniline in our chemical facility gives a clear and practical vantage point on what actually matters to end users in the specialty chemicals industry. This compound, sometimes listed by its CAS number 95-68-1, appears as a light yellow to brownish liquid at common handling conditions. We keep close tabs on each batch’s purity, water content, and byproduct traces, as even minor inconsistencies can frustrate downstream developers. Our standard release runs between 99% and 99.5% purity, using GC to verify analysis. Water by KF titration regularly sits below 0.1%. With close attention to these aspects, we build a reputation with customers who work in fields like dyes, pharmaceuticals, and agrochemicals, where the smallest deviation can halt a synthesis or ruin a full production run.
Making 2,4-dimethylaniline isn’t just about throwing raw materials together. We start with select grades of toluene, ensuring low sulfur and minimal halide contaminants, since off-grade toluene brings side products or discolored output. The nitration process that produces 2,4-dinitrotoluene relies on precise temperature control. For years, we used jacketed reactors with manual oversight. Now, PLC integration keeps exotherms in check and alerts us if response time drifts. Reductive steps require our operators to monitor hydrogen flow and catalyst quality. We run our reactions in such batches that impurities, especially nitro byproducts, stay below our own threshold limits, which are more rigorous than what many buyers stipulate in their contract specifications.
It is routine for us to check retention times and impurity profiles by gas chromatography on each lot, and to keep a retained sample on file per ISO requirements. Unstable batches risk red oil separation or slow polymerization, especially if stored beyond recommended periods. Storage tanks, valves, and feed lines require weekly inspection, a lesson taught by hard experience after early years of unscheduled shutdowns due to minor leaks or carbon build-up.
Customers in dye synthesis and intermediates repeatedly tell us that ease of coupling and clean reaction pathways are non-negotiable for them. 2,4-Dimethylaniline’s two methyl groups, placed at the ortho and para positions on the aniline ring, produce significant reactivity differences compared to simple aniline or its other methylated analogues, such as 2,6-dimethylaniline or toluidine isomers. Dyes made with this compound show vivid color and sharp band visibility on textile or polymer matrices. We have seen direct feedback from partners in textile dye manufacturing, noting that substitution at both 2 and 4 positions brings out different hue stability and colorfastness.
Pharmaceuticals manufacturers harness 2,4-dimethylaniline as a precursor for targeted APIs. In these cases, the cleanliness of our product directly impacts their yield and impurity removal workload. Trace metals, for example, have a measurable impact on hydrogenation steps in active ingredient synthesis. With several years’ worth of supply chain audits and root cause investigations, we find that consistent purity trumps raw cost per kilo for those in regulated markets.
On paper, 2,4-dimethylaniline sourced from different global markets can look almost identical. Customers tell a different story. After fielding complaints about sticky residues and colored deposits in earlier years, we overhauled our drying and filtration system. Now, forced nitrogen sparging pulls dissolved oxygen out, minimizing oxidative byproducts and discoloration. As we scale, a key improvement comes from repeat feedback cycles—not from recipe books but from customers whose lines clog or whose end products discolor.
Shipping also shapes what arrives at a customer’s site. Bulk users sometimes face issues with tank car deposits or browning after transit in summer. We’ve trialed several stabilizer blends and packaging protocols to reduce problems. Since storage temperature swings and trace amounts of acid can drive polymerization, tank linings need regular passivation and customers benefit from insulated or UV-protected containers with small headspace. These practical refinements turn risk management into daily standard operating procedure, not marketing copy.
Chemically speaking, 2,4-dimethylaniline stands beside a family of similar aromatic amines. The most common comparisons our operations team fields include aniline (the parent compound), toluidine (with a single methyl group in three possible ring positions), and 2,6-dimethylaniline. Each substitution alters both the physical properties and the synthetic applications.
Aniline itself is more volatile and generally more reactive towards certain coupling agents, but lacks the steric influences found in the dimethylated forms. The presence of two methyl groups on our product pushes the boiling point up and gives a higher flashpoint, which affects storage requirements, especially in bulk drums. 2,4-dimethylaniline resists oxidation better than simple toluidines, as experienced during extended heat exposure tests in lagged tanks.
Yields in azo-dye synthesis run higher with our product than with monomethylated amines. For certain pigment manufacturers, our compound helps avoid side reactions that introduce muted or brown shades, keeping colors pure and shelf-stable. For developers experimenting with new intermediates, the steric bulk of the 2 and 4 methyl groups changes selectivity during downstream modifications—tools that help create specialty pharmaceuticals or custom pigments not feasible with other methylated or halogenated analogues.
Through years of bulk supply, we know that packaging makes or breaks product consistency. Drums used for 2,4-dimethylaniline require tight closures; exposed product absorbs water and picks up trace oxygen, which sets off a yellowing process visible within weeks. We employ coated or lined containers for critical-use clients, reducing contamination chances and extending shelf life. Tankers destined for large-scale customers follow a cleaning and drying regime that’s unique to this product’s storage risks, based on years of tracking returned containers and troubleshooting shipment issues.
Logistics during temperature swings also impact performance. During cold seasons, the compound’s viscosity rises, making pumping and transfer slower and increasing line pressures. Heat waves shift the equilibrium, making vapor pressure management essential in vented systems. Facility managers and transport planners work together to pre-load shipments and avoid peak temperature fluctuations that can produce off-odors or “drum sweating.” Our response teams draw on site-specific incident history to set decision rules—rarely shared on data sheets but fixed into our internal logistics code.
Producing and handling aromatic amines carries risk. We cannot understate the importance of occupational hygiene controls and environmental safeguards in real factory settings. 2,4-Dimethylaniline presents inhalation, skin absorption, and handling risks familiar to all who work in specialty chemical plants. Over years of running plants, we have incrementally improved our PPE standards, using positive-pressure respirators for open-drum operations and introducing mandatory skin coverage for cleaning tasks. These investments have a clear payback measured in lost-time incidents, not just regulatory box-checking.
Wastewater management needs real-world attention. Even minor spills lead to detectable contaminants; downstream biological plant loads respond to trace aromatic amines with swings in oxygen demand and toxicity. Our plant effluent undergoes multi-stage neutralization and advanced oxidation to reduce aromatic content before discharge. Inspector audits taught us that documentation isn’t just a legal matter but a source of innovation. Collaboration with downstream users reduces off-site waste issues as many solvents and reaction byproducts, previously considered waste, now return as feedstocks in lower-purity applications.
Incidents with aromatic amines have shaped stricter standards in bulk storage and site zoning. We use continuous gas detection sensors and tight drum quarantine routines. Operators see the benefit not just from regulatory audits but from real risk avoidance, after learning the lessons of early missteps and near-misses which data sheets alone don’t reveal.
Through years of production, we observe the widest application of 2,4-dimethylaniline lies in dyes, pigments, pharmaceuticals, and agrochemical intermediate synthesis. The compound acts as a direct precursor to azo dyes and as a key step in triphenylmethane and phthalocyanine dye production. Feedback both from process-critical colorant plants and from research labs shows our attention to consistency and byproduct control pays off in higher dye yield, as well as less reprocessing or purification.
Specialty pigment makers often adopt our batches due to narrow impurity spread. Synthesis for color-fast polymer coatings, especially on polyester or synthetic blends, benefits from the stability of methyl substituents which shelter the amino group from unwanted side reactions. In the pharmaceutical field, 2,4-dimethylaniline provides a methylated aromatic building block, enabling targeted modifications on the ring not possible with base aniline or its ortho/para mono-derivatives.
Crop protection chemistry, a major user of aromatic amines, builds on this product to produce fungicides, herbicides, and insecticides. Each application presents different tolerances for side products, color bodies, and water load. Production planners often call us directly with test feedback, requesting tweaks in distillation cut or drying stage to support their process windows. These calls produce better product outcomes than any standardized technical document.
Unlike trading firms or off-shore consolidators, manufacturing teaches us to prioritize end-use realities. We’re not optimizing only for lowest cost, but for predictable process behavior over hundreds or thousands of kilograms. Before a material reaches shipping, our staff interacts with technical teams at customer sites to cross-check application needs: from pigment residue tolerances to reactor fouling tendencies. We tweak distillation curves, adjust anti-polymerization dosing, and pilot filtration upgrades based on how real production chemists and engineers run their equipment.
It’s a cycle of improvement chained to actual hands-on work. For some high-activity applications, we reduce trace nitro compound carryover; for bulk pigment segments, we manage costs by producing broader specification ranges, but still within margins that safeguard downstream processing. Comparison with generic or reclaimed sources typically reveals less predictable impurity loads, which have hampered continuous flow reactors or sensitive enzymatic synthesis “on the ground.” Building decades of batch records, we spot patterns and preempt issues, a perspective unique to those who make—not just sell—their products.
Staying ahead in a specialty market like 2,4-dimethylaniline requires both attention to detail and willingness to learn from mistakes. We put resources into process mapping, batch traceability, and digital monitoring—upgrading from time-booked paper logs to networked quality stations with every vessel tied into a centralized database. Our experiences with unexpected impurity spikes, changing supplier qualities, and new regulatory rounds drive constant refinements; nothing replaces seeing how a gallon of product moves through a continuous run versus a pilot batch.
Leading customer projects allows us to experiment beyond legacy batch processes. One partner’s need for ultra-dry feedstocks prompted us to invest in new vacuum-drying hardware. Another, developing next-generation organic semiconductors, asked for chromatographic purity verification previously out of scope for bulk shipments. Such requests elevate baseline expectations, leading to broader quality improvements that later benefit the majority of clients across the textile, pharma, and pigments sector.
No two factories process aromatic amines in exactly the same way. Bridging lab development to commercial scale means putting experienced eyes on each transfer, filtration, and storage step. Training teams to recognize batch-to-batch variation and to manage potential hazards shapes safer, more reliable operations. For pipeline customers scaling from bench synthesis to tonnage, our technical teams walk through every phase, connecting manufacturing reality with application goals.
After years of close work with R&D heads and plant managers worldwide, trust in product comes less from spec sheets and more from results on real lines: reproducible performance in dyeing kettles, clean runs through synthesis reactors, and less waste-water reprocessing. Continuous feedback—not just annual surveys but daily calls and shared test reports—lets us adapt batches, shipment plans, and even reactant procurement in a way that builds durable value between manufacturer and developer.
Behind every kilogram of 2,4-dimethylaniline stands a network of operators, logistics planners, process chemists, and quality controllers who recognize the impact of their attention to detail on the people using the compound far downstream. The most meaningful praise comes not from appearance in global product registries but from the users whose critical processes succeed batch after batch. Real-world experience—solving the unexpected, learning from setbacks, and building capability—gives confidence to take on more demanding applications and longer-term R&D challenges.
We welcome direct engagement with new partners, ready to share our on-the-ground experience and to meet the requirements as they actually exist—at the intersection of chemical know-how and real industry need.