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2-Sec-Butyl-4,6-Dinitrophenol

    • Product Name 2-Sec-Butyl-4,6-Dinitrophenol
    • Alias Dinoseb
    • Einecs 209-118-2
    • 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

    483857

    Cas Number 88-25-5
    Molecular Formula C10H12N2O5
    Molecular Weight 240.21 g/mol
    Iupac Name 2-(Sec-butyl)-4,6-dinitrophenol
    Appearance Yellow crystalline solid
    Melting Point 75-77 °C
    Solubility In Water Slightly soluble
    Density 1.34 g/cm³
    Pubchem Cid 6798

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

    Packing & Storage
    Packing Sealed amber glass bottle containing 100 grams of 2-Sec-Butyl-4,6-Dinitrophenol, labeled with hazard warnings and handling instructions.
    Shipping 2-Sec-Butyl-4,6-Dinitrophenol is shipped as a hazardous material due to its toxic and potentially explosive nature. It must be packaged in tightly sealed, chemical-resistant containers, clearly labeled, and transported in compliance with local, national, and international regulations. Protective measures must be taken to prevent exposure, leakage, or accidental ignition during transit.
    Storage 2-Sec-Butyl-4,6-dinitrophenol should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from direct sunlight and sources of ignition. Keep it separated from incompatible substances such as strong oxidizers and reducing agents. Handle with care, using proper personal protective equipment, and store in a labeled, designated chemical storage cabinet. Avoid moisture and physical damage.
    Application of 2-Sec-Butyl-4,6-Dinitrophenol

    Applications of 2-Sec-Butyl-4,6-Dinitrophenol in Industrial Manufacturing

    2-Sec-Butyl-4,6-Dinitrophenol stands as a specialty intermediate for selected segments of industrial synthesis. Its performance profile supports defined chemical transformations in advanced sectors, where stability and specific reactivity are important for downstream production yields and regulatory acceptance. Below, we detail principal application areas in which international manufacturing partners integrate this compound at scale.

    1. Synthesis of Commercial Dinitrophenol-Based Dyes

    Textile and specialty dye manufacturers incorporate 2-Sec-Butyl-4,6-Dinitrophenol as a core intermediate, particularly in the development of azo and nitro dye series for synthetic fiber coloration. The controlled introduction of the molecule after diazotization steps enhances target chromophore construction, contributing to color fastness and thermal stability. Process engineers adjust the additive load to balance reactivity with safety requirements in high-throughput reactors. Inline quality control verifies residual impurity levels, in accordance with sector-specific colorant regulations, before final dye formulations head to application in continuous fiber or fabric finishing lines.

    Industry compliance standards

    • REACH (EU Regulation No 1907/2006)
    • ZDHC Roadmap to Zero MRSL for Colorants
    • Oeko-Tex Standard 100 (Class III for Dyes)
    • ISO 9001:2015 Quality Management in Dye Production

    Typical usage ratio

    • 3%–12% by weight relative to the target dye batch; adjusted for molar equivalents in downstream coupling reactions

    Downstream process integration

    • Dosing during diazotization or azo coupling operations in batch or flow reactors, following the initial amine activation step

    Final product types

    • Disperse dyes for polyester and acetate fibers
    • Azo dyes for acrylic coloration
    • Direct dyes for cellulosics (under special formulations)
    • Reactive dye intermediates for blended yarn dyeing

    2. Manufacture of Advanced Agrochemical Synthesis Intermediates

    Within the agrochemical sector, formulators utilize the dinitrophenol derivative in the multi-step synthesis of phenolic herbicide and pesticide intermediates. This building block reacts with alkylating agents under controlled alkaline conditions, directing regioselectivity for downstream active ingredient production. Precise material handling and metered addition ensure that all final agrochemical products comply with national and international residue regulations and environmental standards before release into active ingredient conversion plants.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 17065 Certification for Crop Protection Chemicals
    • US EPA 40 CFR Part 180 (Tolerances for Residues)
    • China GB 2763: National Food Safety Standard for Maximum Residue Limits

    Typical usage ratio

    • 5%–15% of total precursor molar mass, proportionate to final herbicide or insecticide variant; precise loading set based on targeted conversion yield in lab screening

    Downstream process integration

    • Feedstock for nitration and etherification stages in controlled closed-system reactors; post-reactor purification with solvent recovery included

    Final product types

    • Butyl/dinitro-phenol herbicide active ingredients
    • Intermediate compounds for contact fungicide synthesis
    • Precursor to dinitrophenol-based insecticide molecules
    • Pesticide formulation blocks for granulated and liquid products

    3. Industrial Polymer Cross-Linking Additive

    Producers of specialty resins and high-performance polymers use this material as a cross-linking facilitator, especially in nitro-aromatic or phenolic resin chains for enhanced mechanical resistance. Its carefully monitored introduction during polymerization ensures bonding density aligns with specified tensile properties. On-line viscometric and spectroscopic monitoring govern the addition rate to avoid over-crosslinking, especially for use in industrial laminates and advanced composite structures.

    Industry compliance standards

    • ISO 14001 Environmental Management for Polymer Facilities
    • EU Regulation (EC) 1272/2008 (CLP) Hazard Classification for Additives
    • RoHS 3 Directive 2015/863/EU (if used in electrical component composites)
    • ASTM D1653-13 for Polymer Film Permeability Testing

    Typical usage ratio

    • 0.8%–4% relative to total resin batch weight; ratio selected based on target cross-link density in application end-use requirements

    Downstream process integration

    • Introduced at pre-polymer mixing stage or during chain-extension in batch reactors; homogenization facilitated by pre-dilution in compatible solvent systems

    Final product types

    • Phenolic-based laminating resins
    • Specialty thermoset composites for industrial use
    • High-resilience coatings for machinery parts
    • Electrical insulation resins (pending RoHS compliance)

    4. Intermediate for Explosives and Detonator Compound Synthesis

    The energetic materials industry relies on selected dinitrophenol isomers as intermediates for synthesizing specialty explosives and detonator cores. Our material is integrated during nitration and salt-formation processes under stringent temperature and pressure control. Safety, traceability, and batch segregation are prioritized, with regulatory inspections confirming compliance to national security standards, and with full hazardous materials documentation maintained throughout handling and secure transportation to licensed ordnance manufacturing facilities.

    Industry compliance standards

    • UN Recommendations on the Transport of Dangerous Goods (UN Model Regulations, Orange Book)
    • US Bureau of Alcohol, Tobacco, Firearms and Explosives (ATF) Title 27 CFR, Part 555 for Explosive Materials
    • EU Directive 2014/28/EU on Explosives for Civil Uses
    • ISO 17025: Lab Competence for Energetic Compounds

    Typical usage ratio

    • 6%–18% by mass, set according to the desired sensitivity and brisance of the finished composition; final ratio refined after pilot production scale-up data

    Downstream process integration

    • Admitted during aqueous or solvent-phase nitration; transferred hot-filtration to subsequent salt or energetic matrix blending line with full QC sampling

    Final product types

    • Initiating explosives (primary detonators)
    • Secondary explosives for mining and construction (formulated blends with nitrate and nitramine)
    • Pyrotechnic assemblies for industrial blasting
    • Detonating cords and boosters

    5. Precursor in Pharmaceutical Intermediate Synthesis (Non-Drug Endpoints)

    Certain pharmaceutical process routes, especially legacy synthesis tracks for industrial-scale phenol-derived intermediates, use this dinitrophenol as a blocking group or reactive intermediate. Process chemists monitor stoichiometry and quenching conditions to avoid formation of regulated impurities, and all output faces strict documentation for traceability per international standards. Final intermediates serve as feedstocks for further modification in regulated but non-API (active pharmaceutical ingredient) steps, such as imaging agents and specialty biochemistry reagents.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients (applied for intermediates)
    • EU GMP Volume 4 for Intermediates Management
    • Pharmacopoeial monographs (USP, Ph. Eur.) as technical references for impurity controls
    • ISO 9001:2015 for pharmaceutical raw material manufacturing

    Typical usage ratio

    • 2%–10% of process mass, adjusted for multi-step synthesis scale and route-specific yields; tuned via in-process control analytics

    Downstream process integration

    • Blended post-activation in stepwise chemical transformations; followed by work-up and chromatographic purification before transit to fine chemical conversion lines

    Final product types

    • Phenolic aldehyde intermediates for radiolabelled tracer synthesis
    • Monomers for specialty medical polymer coatings
    • Diagnostic imaging chemical precursors
    • Tech-grade pharmaceutical synthesis intermediates (non-API usage)
    Free Quote

    Competitive 2-Sec-Butyl-4,6-Dinitrophenol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2-Sec-Butyl-4,6-Dinitrophenol: A Manufacturer’s Perspective on a Powerful Intermediary

    Years on the Line with 2-Sec-Butyl-4,6-Dinitrophenol

    The production of 2-Sec-Butyl-4,6-Dinitrophenol feels like a conversation between chemistry and industry. Each batch tells a story of precision, experience, and meticulous control. In our factory, this compound isn’t just another name on a list—it plays a real role in several high-stakes industrial processes, and it is shaped by the real-world grit of handling strong nitro-organics day in, day out. The compound’s structure, with a sec-butyl group on a dinitrophenol backbone, gives it a distinctive set of chemical properties that not only affect its own stability but also its effectiveness as an intermediate.

    Getting the Product Right: Purity and Features

    Any manufacturer worth their salt knows this compound is unforgiving in the hands of those who cut corners. In our operations, we carry out nitration with an eye fixed as much on precision as on safety, keeping temperatures and reaction times under tight control. Most of what comes off our line shows a purity above 98 percent—checked by experienced technicians, not just instruments. This attention helps keep trace contaminants like lower alkyl dinitrophenols and residual acid at minimum, qualities that matter far more once the product goes into further chemical processes, especially in the agrochemical and dye markets.

    How 2-Sec-Butyl-4,6-Dinitrophenol Carries Its Weight in Industry

    Our experience shipping kilos and tons of 2-Sec-Butyl-4,6-Dinitrophenol to large synthesis plants tells us what makes it indispensable. For companies crafting specialty dyes or advanced crop protection agents, this compound becomes a foundation layer, enabling reactions that simply won’t work with alternative phenol nitration products. Some users in the plant protection space remark on its ability to offer cleaner end-reactions compared to similar dinitrophenols, leading to sharper activity in the final active ingredient. We hear from clients who experience fewer side-reactions when switching from generic dinitrophenols, so there’s less loss of yield and less need for expensive purification steps later.

    Model of Consistency: Why the Chemical Form Matters

    The demand doesn’t disappear for granular or crystalline product, but most users reach out for the fine pale-yellow powder. Grinding and sieving matter—not just for smooth blending, but because clumped material in a reaction doesn’t dissolve on pace with instructions, complicating the operator’s job. The work starts well before packaging. Controlling the particle size lets us guarantee quicker, more uniform reaction onset in downstream usage, whether in large stirred reactors or more controlled semi-batch processes. Besides, the aromatic nitro-compounds pack a punch on volatility and safety, so a consistent powder saves headaches all the way from weighing to final dissolution.

    Understanding Its Genuine Differences from Common Dinitrophenols

    Not all dinitrophenols hold the same value in synthesis. The addition of a sec-butyl group to the 2-position isn’t a trivial design. That specific alkyl substitution impacts both lipophilicity and solubility parameters in solvents like methanol, acetone, and even in certain glycols. Over decades of working with both 2,4-dinitrophenol and its butylated variants, we’ve seen sharper selectivity in downstream reactions using 2-Sec-Butyl-4,6-Dinitrophenol. Take azo-dye chemistry, for example: the electron effects from the butyl group allow for more controlled coupling, limiting the formation of unwanted tars.

    Field reports from formulation chemists show the compound absorbs and interacts at slightly different rates compared to the straight-chain butyl or ethyl dinitrophenols, which can change the game for specialty pigment makers looking for repeat performance. There’s also a subtle improvement in resistance to hydrolysis under basic conditions, owing to the branched alkyl chain, so the product holds up longer in storage and remains more reliable after long hauls in less than ideal warehouse environments.

    Stability and Storage Lessons Learned in Practice

    Anyone who works with nitro-aromatics learns quickly that dry, cool storage is more of a directive than a suggestion. We built our facility to handle both temperature management and humidity, so product on its way to the customer holds up—or at minimum, doesn’t pose extra risk during transit. Experience has shown us that stacking containers even two-high in summer heat leads to caking and minor decomposition, so we store in single rows with sufficient airstream between drums.

    Moisture uptake remains an enemy, even though the product seems robust in dry powder form. Seals and liners received as much attention as our process steps, and we discourage users from cutting corners here. The compound can slowly yellow further if exposed, with a hint of odor developing only under truly poor storage. But in real use, these problems rarely develop if standard warehouse discipline is followed.

    Safety and Environment in Real Operations

    The days of handling dinitrophenols without personal protection belong in the past. Our crew tightens procedures with every passing year, not just per box-ticking, but out of lived experience. Early missteps in the field—spills, mistaken use of incompatible gloves—sent a clear message. 2-Sec-Butyl-4,6-Dinitrophenol acts as a skin and respiratory sensitizer, which calls for sealed systems and prompted investment in negative-pressure blending rooms.

    On the environmental side, we took early cues from evolving regulations. Our scrubber installations didn’t just slash nitrous off-gassing, but also improved operator morale, since they see real results. The concern stays with us: accidental release remains a risk, so every drum that leaves carries traceability right back to synthesis date, reactor line, and QA sign-off. Not all facilities go this far, but in major chemical zones, oversight and inspections drive us to keep raising standards—so downstream users aren’t left holding the liability.

    Supporting R&D and Custom Requirements: More Than “One Size Fits All”

    Every year, we support specialty clients who tweak the product spec. Even though most usage settles on the standard assay and particle-size range, some labs push for tighter limits on water content or request a certain bulk density for pilot plant optimization. Our own people have spent hours in process labs slugging out otherwise “minor” production tweaks—because when scale-up comes, those edge cases become critical.

    For one crop chemical manufacturer, small shifts in moisture pick-up led to differences in end-formulation stability. Working together over several campaigns, we engineered an air-drying step before final packaging, eliminating an entire blending issue. In other cases, dye manufacturers called on our technical team to help field process failures—such as batch-to-batch issues in their reactors that ultimately linked to handling or minor variants in our shipment. It all circles back to dialogue; quick feed-back loops between plant floor and end-user lab prevent expensive downtime.

    Supply Chain Perspective: Why Manufacturer Origin Matters

    Speaking from our factory vantage point, care and responsibility can’t be faked by relabelers down the chain. The biggest difference turns up in transparency: when questions come up about a batch, only the originator retains the records needed to help a customer retrace steps. Tighter integration with bulk solvent suppliers, nitrating acid producers, and local inspectors only comes from those who produce from start to finish.

    We’ve seen traders buy misrepresented product in good faith, only to find out mid-reaction that critical specs were missed. The time, energy, and goodwill lost in chasing solutions could be avoided by keeping lines of communication short and direct with the source. As capacity in the market waxes and wanes, traceable production underpins not just confidence but continuity.

    Product Identity and Confidence at Scale

    The chemistry community knows the landmines of mislabelled or subpar dinitrophenols. Our customers—companies pushing for new colorants or higher-activity crop solutions—count on being able to verify the material, batch after batch. Each drum stands as proof that chemical identity and purity aren’t marketing lines but product realities. The way a batch is traced through every point of its journey sets real manufacturers apart from mere repackagers.

    People who work with nitrophenols know the odor, the texture, the reaction profile. They spot the difference between a powder that flows and one that clumps. Our own teams rely on these cues, and those lived details inform everything, from the raw acid procurement to the controls used during sulfonation quenching. This lived knowledge is what we pass on with every shipment, and it’s a product of years, not mere automation.

    Innovation and Future Outlook: Chemical Makers Setting the Pace

    The toolkit of intermediates keeps evolving, but some compounds like 2-Sec-Butyl-4,6-Dinitrophenol still anchor progress in areas where reliability beats novelty. Environmental scrutiny and demand for ever-tighter specs only push true manufacturers further. There’s no silver bullet for every issue—each new batch or customer use case brings lessons in flexibility, whether it means tweaking crystallization temperatures or troubleshooting a downstream polymerization.

    We work side-by-side with academic collaborators or custom synthesis groups, running test reactions on fresh lots and sharing those results with customers who want data, not just promises. Most progress comes in small steps—a blend that won’t quite react as cleanly, a discharge color that hints at a contaminant, a safety tweak that tightens process time by ten percent. Innovations in this field don’t arrive via marketing bluster but out of gritty adjustment, trial, and plenty of communication up and down the supply chain.

    Cost, Capacity, and Global Sourcing Realities

    Over time, costs shift, raw material prices swing, and regulatory hurdles fluctuate. Our focus remains simple: build capacity that matches real, verifiable demand, and keep channels to users open. That means anticipating surges in agrochemical pre-season or supporting colorant makers facing shifts in trends. By keeping close tabs on our reactor schedules and storage, we have the agility to handle sudden changes, like a new regulatory clampdown in a major market or unplanned maintenance causing downtime.

    Outside our plant, global events can upend assumptions. Political or shipping disruptions expose the value in reliable, domestic production. Many users recall times when a promised load from overseas failed to arrive, and only localized producers could bridge the gap. Production line investments pay off not just in quantity, but in the assurance they offer industrial partners who value continuity, not just price.

    Closing Thoughts from the Manufacturing Floor

    Every shipment of 2-Sec-Butyl-4,6-Dinitrophenol reflects not only chemical expertise, but a hard-won commitment to those who use the product in everything from plant growth solutions to the next generation of bright, lasting dyes. Out on the line, our people respect what’s at stake. Experience in manufacturing this compound—and distributing it responsibly—matters more than the numbers on a certificate. Every customer inquiry, every story of a batch performing or failing in real-world conditions, shapes tomorrow’s process steps. This feedback loop is both challenge and reward of making challenging chemicals in today’s world, a reality lived anew with every drum filled, sealed, and shipped.