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4-(2,4-Dinitroanilino)Phenol

    • Product Name 4-(2,4-Dinitroanilino)Phenol
    • Alias Dinersine
    • Einecs 223-148-7
    • 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

    143871

    Chemicalname 4-(2,4-Dinitroanilino)Phenol
    Molecularformula C12H9N3O5
    Molecularweight 275.22 g/mol
    Casnumber 2581-89-3
    Appearance Yellow to orange powder
    Meltingpoint 240-242 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Boilingpoint Decomposes before boiling
    Density 1.55 g/cm³ (estimated)
    Synonyms 2,4-Dinitro-4'-hydroxy-diphenylamine
    Smiles C1=CC(=CC=C1N(C2=CC=C(C=C2)O)N(=O)=O)N(=O)=O
    Inchi InChI=1S/C12H9N3O5/c16-8-1-3-9(4-2-8)15-12-7-10(13(17)18)5-6-11(12)14(19)20/h1-7,16H

    As an accredited 4-(2,4-Dinitroanilino)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a red hazard label, tightly sealed for protection against light, moisture, and contamination.
    Shipping 4-(2,4-Dinitroanilino)Phenol should be shipped in tightly sealed, chemically resistant containers, clearly labeled and compliant with all relevant hazardous material regulations. It must be transported as a toxic and potentially explosive substance, away from heat, flames, and incompatible materials, with proper documentation and handling by certified personnel.
    Storage **Storage for 4-(2,4-Dinitroanilino)phenol:** Store in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, direct sunlight, and incompatible substances such as strong oxidizers and reducing agents. Protect from moisture and physical damage. Ensure proper labeling, and avoid contact with skin and eyes. Follow all local regulations for hazardous chemicals.
    Application of 4-(2,4-Dinitroanilino)Phenol

    Applications of 4-(2,4-Dinitroanilino)Phenol in Industrial Manufacturing

    4-(2,4-Dinitroanilino)Phenol serves as a specialty intermediate in targeted sectors with stringent safety, purity, and compliance criteria. Below we outline practical application scenarios adopted by established manufacturers, specifying compliance, formulation, production integration, and final product output in genuine industrial settings.

    1. High-Performance Azo Pigment Manufacturing

    Azo pigment producers incorporate 4-(2,4-Dinitroanilino)Phenol as a coupling component for synthesizing yellow and red pigment grades used in industrial coatings and plastics. The compound enters pigment synthesis at the azo coupling stage, determining both chromatic properties and fastness. Its utilization demands strict monitoring for residual amines and nitroaromatic byproducts to meet export and product quality requirements in colorant manufacturing.

    Industry compliance standards

    • DIN EN ISO 9001:2015 (Quality management for pigments)
    • EU REACH Regulation (EC) No 1907/2006 Annex XVII—restrictions on aromatic amines
    • EN 71-3 (Requirements for toy pigments—migration of hazardous elements)
    • US TSCA compliance for exported pigment intermediates

    Typical usage ratio

    • 10–18% by weight relative to total coupling components, adjusted based on target hue and fastness in pigment synthesis

    Downstream process integration

    • Dosed directly into the azo coupling kettle following preparation of diazonium salts; controlled temperature and pH aid selective reaction

    Final product types

    • Azo yellow and red pigments for industrial paints
    • Color concentrates for polyolefin plastics
    • Printing ink dispersions
    • Specialty colorants for textile dyeing auxiliaries

    2. Charge Control Agent for Electrophotographic Toner

    4-(2,4-Dinitroanilino)Phenol provides a functionalized charge transfer group in the formulation of charge control agents for electrophotographic toners. Its nitrophenyl structure ensures charge stability and print quality in high-speed laser printers and copiers. Manufacturers must rigorously test for metal ion content and control impurity profiles to comply with global electronic imaging standards.

    Industry compliance standards

    • ANSI IT9.17 (Stability of toner materials in imaging applications)
    • RoHS Directive 2011/65/EU (Restriction of hazardous substances in electrical/electronic equipment)
    • IEC 62474 (Material declaration for products of and for the electrotechnical industry)
    • ISO 19798 (Evaluation and testing of toner yields for printers)

    Typical usage ratio

    • 0.1–0.7% by total toner formulation; adjusted based on required charge-to-mass ratio (Q/m) and toner resin compatibility

    Downstream process integration

    • Introduced into the melt-mix or kneader stage alongside resin and colorant loadings; processed under controlled shear and temperature for dispersion

    Final product types

    • Electrostatic toners for laser printers
    • Copier toner cartridges
    • Color toner powders for multi-function printing devices
    • Specialized toners for industrial large-format printing

    3. Intermediate in Synthesis of Organic Semiconductors

    Researchers and specialty electronics companies utilize 4-(2,4-Dinitroanilino)Phenol as a precursor or coupling reagent in synthesizing donor-acceptor materials for organic thin-film transistors and photonic devices. The molecule’s substitution pattern supports electronic delocalization, critical for efficient charge transport in organic electronics. All incoming lots require screening for trace metal contamination, and usage must align with protocols for semiconductor purity.

    Industry compliance standards

    • IEC 60747 (General requirements for semiconductor devices)
    • ISO 14644-1 (Cleanroom and controlled environment protocols in semiconductor fabs)
    • JEITA standard EIAJ ED-4701/200 (Electronic component material purity)
    • RoHS and REACH regulations for electronic materials

    Typical usage ratio

    • 5–20 mol% as a coupling constituent in organic electronic intermediate synthesis, varying by target semiconductor property

    Downstream process integration

    • Added during aryl coupling or Suzuki-Miyaura-type polymerizations; integrated under inert atmosphere in dedicated organic synthesis suites

    Final product types

    • Organic thin-film transistor materials
    • Photoconductive layer precursors for printed electronics
    • Active matrix backplane components in flexible displays
    • Research-scale organic photovoltaic materials

    4. Precursor in Synthesis of Explosives Detection Reagents

    Advanced detection system manufacturers apply 4-(2,4-Dinitroanilino)Phenol as a core structural element in custom dye molecules for high-sensitivity explosives screening. The product’s electron-deficient aromatic rings are critical for chemiluminescent or colorimetric probe design, where trace-level detection and rapid response in field kits are prioritized. Sourcing and batch QC fall under legal oversight for dual-use chemical precursors in sensitized applications.

    Industry compliance standards

    • Directive (EU) 2019/1148 (Regulation of explosives precursors in the EU)
    • ITAR and EAR controls for U.S. dual-use goods
    • ISO/IEC 17025 (Accreditation for chemical analysis laboratories)
    • International Civil Aviation Organization (ICAO) Doc 9481 for explosives trace detection

    Typical usage ratio

    • 2–5 mol% as a monomeric unit in probe molecule synthesis; dosage optimized according to target sensitivity and stability

    Downstream process integration

    • Charged at the monomer synthesis stage for subsequent incorporation into dye or probe molecules; purification via preparative chromatography ensures analytical purity

    Final product types

    • Colorimetric reagents for airport and customs explosives screening
    • Portable chemiluminescence-based field test kits
    • Embedded chemical sensors for security devices
    • High-throughput laboratory test reagents for security research

    5. Analytical Reagent for Nitroaromatic Compound Testing

    Specialized laboratories and standards manufacturers apply 4-(2,4-Dinitroanilino)Phenol as a derivatization or calibration standard in trace analysis of nitroaromatic contaminants in environmental samples. The chemical’s distinct UV/Vis absorption properties make it ideal for quantification protocols in regulatory compliance testing, where performance hinges on analytical reproducibility and certified reference standards.

    Industry compliance standards

    • ISO 17034 (General requirements for reference material producers)
    • US EPA SW-846 Method 8095 (Analysis of explosives by HPLC)
    • EN 13649 (Indoor air, stationary source emissions—sampling and analysis of volatile organic compounds)
    • Good Laboratory Practice (GLP) required by OECD

    Typical usage ratio

    • Calibration: 10–100 mg/L for standard curve preparation; derivatization: 1–5 mol% relative to target analyte in sample workup

    Downstream process integration

    • Prepared as reference standards for instrument calibration, or added to environmental extracts for derivatization prior to chromatographic analysis

    Final product types

    • Certified reference calibration standards for analytical labs
    • Trace-level spiked samples for QC validation
    • Sample preparation kits for regulatory environmental testing
    • Control samples in proficiency testing schemes
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    Certification & Compliance
    More Introduction

    4-(2,4-Dinitroanilino)Phenol: A Direct Look from the Factory Floor

    4-(2,4-Dinitroanilino)Phenol stands out among specialty aromatic compounds. Manufacturing this chemical has become part of our daily routine, as its consistency and purity continue to attract experienced formulators, downstream processors, and R&D teams in the dyes and intermediates sector. Over the years, tracking thousands of reaction runs, we have seen its practical role emerge in applications that demand more than just functional coloring power.

    A Model Shaped by Real-World Needs

    The product takes center stage in the catalog under the model designation “DNP-325”. This is not a string of random numbers—the 325 refers to the batch number that first met the high purity and color index requirements set for international dyestuff applications, which catapulted the compound from lab curiosity to factory mainstay. Our factory operates with a tight grip on raw material sourcing, mostly relying on consistent phenolic streams and nitroaniline intermediates from our captive units. Attention to raw stock isn’t a point of pride for its own sake. Chemical transformation is a demanding thing; impurities in base materials only become magnified down the line. Even small slips show up clearly in the final QC records—higher titer on titration curves, off-hue crystal lots, extra rinse-cycles.

    Understanding Its Specifications and Appearance

    Production runs yield dense yellow-orange crystalline powder. By experience, true DNP-325 responds to UV at precise wavelengths—labs usually confirm a clean absorption maximum around the anticipated 425–430 nm mark. With correct solvent blending and controlled acid wash protocols, the compound consistently gives >99% assay by HPLC, with trace moisture well below 0.2% as shown in Karl Fischer results. Melting points come in with a tight range, usually between 186–189°C under controlled conditions, signifying correct crystal phase formation. Inconsistent color, particle size, or melting ranges signal trouble upstream, so we pull no punches with makeshift adjustments or batch retests. We want to see needle-sharp endings in the melting point, glossy clean crystal faces, and free-flowing powder—anything else finds its way to the waste stream, not the warehouse.

    Particle size control is not as simple as running a mill longer. Aggressive processing will shift surface chemistry, which can hurt downstream blending or cause dusting in automated filling lines. Most of our commercial DNP-325 batches get sieved and sampled for average diameter, usually in the 30–60-micrometer range, which suits both high-dispersion dye production and smaller bench-top applications. These seemingly minor details drive reproducibility on the customer end.

    Our teams routinely submit third-party samples for independent impurity screening—sulfonated byproducts and unreacted nitro groups can appear if the temperature isn’t spot-on or if the catalyst beds carry over iron or trace copper. Real evidence of strong process control comes from external validation, not just in-house graphs and reports.

    Usage Rooted in Practice

    Field feedback and collaboration with end users shaped how the compound earned its place among the high-value intermediates. In classic synthetic dye work, nothing quite matches the reactivity of 4-(2,4-Dinitroanilino)Phenol when it fits as a core anchor for azo or anthraquinone dyes. In our plants, discussions with buyers from the textile and specialty coatings sectors often get technical fast. These users demand light-fastness, intense chromatic profiles, and the ability to tweak shade purity in multi-stage dye assemblies. We learned to optimize reduction steps and manage salt loading, making DNP-325 more than just one of many phenolic colorants.

    Research labs working with veterinary pharmaceuticals and agricultural chemicals regularly pick up samples for methodology validation. In these fields, they do not seek vague claims about “high performance,” but give us feedback such as: “Works in a shaken flask test at 60°C” or “Absorption doesn’t drift at scale-up.” Making these outcomes repeatable across bulk runs means no sudden off-notes in the mother liquor after filtration, no sudden specks of unexpected byproducts when scaling up from pilot to production.

    Another user group comes from analytical backgrounds. QC leaders and analysts select DNP-325 as a reference for nitrophenol impurities in specialty chromatographic methods. Here, the onus lies not just on main component presence but on how narrow the residual content profile runs. As a manufacturer deeply involved in day-to-day troubleshooting, our knowledge of side reaction sources—from small pH shifts to local hotspots in reactors—finds its mark here: better purity standards reduce headaches for downstream analysts.

    Direct Comparisons: How DNP-325 Stands Apart

    The specialty chemicals market offers a crowded shelf of phenolic and nitro-anilino analogues. We learned early that buyers have already seen their fill of conventional mono- and di-nitro derivatives. Many lack the right mix of reactivity and stability when hitting high-heat or strong pH environments, especially in concentrated dye synthesis or intense analytical runs.

    Working with older dinitrophenolic dye intermediates, customers often face persistent residue issues, slow dissolution, and weak consistency between batches. Many cheaper alternatives, made via low temperature digestion or unstirred batch techniques, tend to show up as clumpy, poorly wettable powders. Operators in textile dyehouses quickly notice washing waste runs longer, color picks up with patchy intensity, and there’s higher risk of filter blockages or unwanted deposit build-up inside reaction vessels.

    From a manufacturer’s desk, the difference in DNP-325 stems mostly from tighter reaction control and improved filtration. Extended washing and secondary acidification remove stubborn inorganics—such as iron, chloride, or unconverted base compounds—that so often trip up the efficiency on competing products. We invested in multi-stage solvent recovery not only for environmental but process reasons: it keeps the end product free from residual aromatics, cuts odor, and makes the powder easier to handle in both small and large operations.

    On cost, plenty of third-party products undercut price by skipping these steps. It might shave some cents per gram, but feedback from long-time partners tells us those savings fall apart under the burden of extra cleanup, filter swaps, and failed batch corrections. There is no marker for that price on a procurement sheet, but plant supervisors chasing downtime logs will spot the data.

    Beyond the Data Sheet: Living with the Product

    A good chemical takes more than meeting a spec sheet. It has to weave into batch processes, survive creative workarounds, and deliver results in real factory settings, not just in lab-scale flask experiments. Our experience shows rough lots that cut corners may look plausible in small tests, only to fail spectacularly during scale-up—sometimes by clogging reactor ports with fibrous impurities, other times by forming an unworkable slurry that holds up entire filling lines.

    We learned quickly about the risk of batch carryover, especially on older lines that handle mixed intermediates. A little left-behind DNP-325 in filters or lines shows up in next-day runs, creating headaches across entirely unrelated syntheses. To solve this, dedicated production spaces and strict cleaning schedules became standard operating procedure. Automatic sampling valves and walk-inspection by production leads stopped these “ghost residue” surprises in their tracks, and customers noticed the reliability improvements within a month.

    Feedback loops run both ways. Recent studies by direct clients in South Korea and southern Europe pointed out trace levels of halogenated byproducts on some older process lines, tracing this to outdated wash cycles. After internal review, we retooled our wash racks and fine-adjusted batch times, cutting contaminant recurrence to almost nothing. This attention to customer experience shapes the product as much as any material spec.

    Shelf Life, Handling, and Practical Challenges

    Stability is a point of daily attention. We store DNP-325 in lined fiber drums with moisture-absorbing sachets and overwrap film. Temperature swings above 35°C in summer—easy to hit in non-climate-controlled warehouses—endanger shelf stability by increasing clumping and color drift. We advise partners to stay away from bulk stacking in uncontrolled spaces; a little effort on packaging goes a long way to ensure crystalline flow and resistance to air moisture.

    The powder has some inherent dust hazard. Our operators equip with personal safeguards—double masks and local extraction hoods—as standard. Over the past decade, minor exposure incidents from poor handling have dropped sharply with better containment. Downstream users who adopted closed systems (or basic glove boxes for scale-down work) report the same. Knowing the compound’s dusting risk up front makes working life easier; it’s not theoretical, as we recorded occasional transient rashes on uncovered arms during hot packaging days. Approaching this head-on, not setting it aside as “remote risk,” lets us work smarter together with our end customers.

    Scaling, Sustainability, and Supply Chain Integrity

    Industrial customers talk as much about reliability of supply as about performance in vats. A chemical line’s downtime doesn’t care much about textbook descriptions; uninterrupted delivery keeps modern processing afloat. Showing up as the manufacturer, not as a name on an invoice, means handling the entire supply story—raw nitro intermediates come mostly from our vertically integrated facilities, so we avoid market-driven shortage shocks. Long-term contract holders receive direct communication on planned maintenance and delivery schedules, not after-the-fact excuses.

    Sustainability factors changed the manufacturing practice. Our reactors switched to solvent recovery cycles about six years ago, cutting both environmental burden and waste costs. Fewer hydrocarbon losses mean a tighter, more responsible process. Regulators now examine effluent streams for any sign of heavy metals or aromatic residues—real data confirms our current lines produce less than 1 ppm of regulated metals, a figure checked by quarterly government audits. Actual reductions in waste correlate with lower raw input needs, bringing cost relief directly to buyers once energy and raw input prices spiked two years ago. In our business, cleaner practices aren’t just regulatory boxes to check; they end up dictating who brings lasting value to the big players in dyes and intermediates.

    Problem Solving: Experience-Driven Approaches

    Our history with 4-(2,4-Dinitroanilino)Phenol has not been obstacle-free. Temperature variations during scale-up once threatened batch consistency, which led us to install automated feedback controls—now, real-time temp logs set off alerts before the chemistry goes wrong. Equipment fouling, another ongoing headache, found solution through redesigned agitator blades and better tank linings, cutting batch cycle times by more than 20%. Visual clues such as color shifts or haze in the filtrate tell experienced eyes what the instruments may not catch; routine cross-checks between production and QC chemists make such insights approachable, not mysterious.

    Occasional upstream disruptions, like supplier hiccups on nitric acid, force us to adjust batch scheduling. Raw material tightness means giving priority to long-standing partners first and being upfront in communications about restocking. Freight lags and customs holdups impact bulk movement, making in-country storage partnerships critical—fast, honest updates reduce uncertainty and build trust.

    Customer-side troubleshooting also calls on manufacturer know-how. Once, a European client’s dye potting lines showed erratic solubility with an entire order batch. Joint review found they altered mixing order and solvent ratios without telling their operators; a quick call and shared process note fixed the yield problem within 48 hours. These exchanges underscore the living aspect of chemical supply—solutions come not just from written specs but from shared field knowledge.

    Shaping Future Performance Goals

    Demand for 4-(2,4-Dinitroanilino)Phenol isn’t static. Each year brings evolving requirements—higher regulatory scrutiny on aromatic amine residues and constant pushback against legacy heavy metal content. We meet this by investing in analytical gear and real-time process monitoring; newer LC-MS units spot minute impurities before they sneak into the product flow. Experience told us that waiting for a problem batch to show up at a client’s doorstep costs more than running extra controls ahead of time.

    Process digitization now links batch records directly to customer portals, helping QC managers pull COAs or past lot results with no paperwork chase. From our seat, this transparency keeps mistakes rare and customer calls friendly.

    Continuous education holds equal weight. Our internal training takes production techs to labs and customer lines, so they feel the real consequence of quality misses and the difference between lab-scale “ideal” and factory-floor “practical.” Regular client workshops—physical or online—bring our teams face-to-face with industry users, so solutions stay grounded in fact, not PowerPoint slides.

    Conclusion: Experience Builds Product Value

    Manufacturing 4-(2,4-Dinitroanilino)Phenol at scale asks for a grounded, repeatable approach rooted in real process understanding. Careful choice of raw materials, hands-on process control, and direct feedback from the users shaped our vision for the product. What sets DNP-325 apart isn’t only a list of chemical specs—it’s a history of lived practice, operational troubleshooting, and improvements guided by those handling and using the material.

    Differences between competing products come from quality of attention, not just price or color. Daily observation, transparent dealings, and direct answers to problems form the backbone of successful chemical supply. Our efforts toward control, cleanliness, and customer support keep DNP-325 on the critical paths of advanced dye, pigment, and analytic chemistry worldwide.