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3-Methyl-4-Nitrophenol

    • Product Name 3-Methyl-4-Nitrophenol
    • Alias m-nitro-p-cresol
    • Einecs 221-569-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    585551

    Chemicalname 3-Methyl-4-Nitrophenol
    Molecularformula C7H7NO3
    Molarmass 153.14 g/mol
    Casnumber 2581-34-2
    Appearance Yellow crystalline solid
    Meltingpoint 86-89°C
    Solubilityinwater Slightly soluble
    Density 1.336 g/cm³
    Purity Typically ≥98%
    Synonyms 4-Nitro-m-cresol
    Smiles CC1=CC(=C(C=C1)O)[N+](=O)[O-]
    Inchikey QYDPDJFDNWGHSN-UHFFFAOYSA-N

    As an accredited 3-Methyl-4-Nitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle of 3-Methyl-4-Nitrophenol comes in a tightly-sealed, amber glass container with hazard labels and safety information.
    Shipping 3-Methyl-4-Nitrophenol is shipped in tightly sealed containers, protected from light and moisture. It should be packed according to regulations for hazardous chemicals, with clear labeling. Transport must adhere to applicable local and international safety guidelines to prevent leaks or environmental release. Proper documentation and emergency instructions accompany each shipment.
    Storage **3-Methyl-4-Nitrophenol** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of heat, ignition, and incompatible substances such as strong oxidizers and acids. Store away from direct sunlight and moisture, and label containers clearly. Use chemical-resistant shelving and ensure secondary containment to prevent accidental spills or leaks.
    Application of 3-Methyl-4-Nitrophenol

    Applications of 3-Methyl-4-Nitrophenol in Industrial Manufacturing

    As a specialized manufacturer, we supply high-purity 3-Methyl-4-Nitrophenol directly to core industrial sectors where this intermediate drives unique value in key chemical synthesis routes. Our quality controls are designed for critical applications where consistency, traceability, and adherence to tight technical specifications are fundamental for downstream processing and market compliance.

    1. Agrochemical Active Ingredient Synthesis

    In pesticide formulation, 3-Methyl-4-Nitrophenol serves as an essential intermediate for synthesizing certain phenolic herbicides and insecticides, particularly within the organophosphate and carbamate classes. This compound enters the manufacturing flow at the nitration and methylation stages that precede functional group transformation into active moieties. Strict regulatory oversight governs traceability of all active substance intermediates within this sector, necessitating complete analytical documentation, including pathway yields and any by-product tracking. Downstream manufacturers incorporate this intermediate into core reaction vessels under controlled temperature and pH parameters to maximize conversion and minimize environmental residue load.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for chemical intermediates)
    • REACH Regulation (EC) 1907/2006 substance registration and downstream user obligations
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products Framework)
    • Chemical Facility Anti-Terrorism Standards (CFATS, USA), precursor chemicals list

    Typical usage ratio

    • Intermediary input at 12–26% w/w per batch of agrochemical precursor, adjusted according to target molecule and catalyst strategy

    Downstream process integration

    • Introducted post-methylation step into coupling or substitution reactions under inert atmosphere, often with temperature escalation above 70°C and solvent extraction steps

    Final product types

    • Selective phenoxy herbicides
    • Organophosphate insecticides (including downstream esterification derivatives)
    • Carbamate pesticide intermediates for further reduction or etherification

    2. Pharmaceutical Intermediate Manufacturing

    Strictly as a chemical intermediate, 3-Methyl-4-Nitrophenol factors into the synthesis of certain non-sterile pharmaceutical agents where the nitro-phenol moiety transforms into amino-phenol or heterocyclic end structures. Its defined reactivity profile allows process chemists to achieve high yields in one-pot reductions required for downstream API assembly. All active ingredient supply chains must adhere to stringent process validation and impurity profiling, as required by international pharmacopoeias and regulatory agencies. This material typically enters multi-step synthetic routes, advancing from protected nitrophenol into core substrates for additional coupling or acylation in GMP-compliant environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia 11.0 (relevant monographs for intermediates)
    • USP General Chapter <1086> for chemical intermediate qualification

    Typical usage ratio

    • Intermediate charge between 5–18% by mass, dependent on desired amino-phenol yield and scale; stoichiometry adjusted for impurity minimization

    Downstream process integration

    • Reduction stage: Catalytic hydrogenation employs this compound as feedstock, followed by purification and conversion to amine- or aniline-based API precursors

    Final product types

    • Paracetamol (acetaminophen) analogues
    • Heterocyclic ring pharmaceuticals where nitro group becomes amine
    • Secondary amine pharmaceutical building blocks

    3. Dye and Pigment Intermediate Production

    3-Methyl-4-Nitrophenol is routinely implemented in the synthesis of specialty azo and anthraquinone colorants, where its nitrophenolic functionality enables precise diazotization and subsequent coupling to yield pigments with tailored chromaticity and solvent resistance. Processing control over substitution patterns is essential for downstream manufacturers targeting high shade purity and durability in demanding textile and industrial coating sectors. This intermediate occupies a pivotal role in the monomer charge during continuous dye reactor operations, often under carefully monitored pH and pressure parameters.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for restricted substances in dyestuffs)
    • REACH Annex XVII (Listed Substances Regulation, EU)
    • ISO 9001:2015 (Dyestuff production quality systems)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, textile input chemical protocol)

    Typical usage ratio

    • Intermediate constituent for colorant synthesis at 10–22% capacity, balanced with diazonium donors and coupling agents specific to the pigment target

    Downstream process integration

    • Added to batch or continuous synthesis vessels during initial diazotization under acidic conditions, followed by direct coupling with appropriate aromatic systems to enhance product color stability and fastness

    Final product types

    • Azo pigments for plastics and textile printing
    • Aniline dye precursors for paper and ink
    • Color-stable coating pigments

    4. Specialty Resin and Polymer Modifiers

    Manufacturers in the advanced materials sector use 3-Methyl-4-Nitrophenol to impart specific reactivity in crosslinking agents and heat-resistant resin systems. The unique substitution on the aromatic ring supports functionalization during condensation polymerization or as a chain-stop inhibitor in select thermoset applications. Producers must maintain strict control over reaction kinetics and residual monomer content, reflecting polymer industry compliance, with performance attributes documented for each batch deployed into customer applications. Formulation chemists adjust input levels based on the targeted final molecular weight and crosslink density.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management—applicable to resin production)
    • GADSL (Global Automotive Declarable Substance List for plastics)
    • ASTM D256 (Statistical Quality for plastics/raw polymers)
    • REACH SVHC candidate list (screening for hazardous monomers)

    Typical usage ratio

    • Adoption between 0.5–4% by total monomer mass, regulated by resin end-use requirements and application-specific performance testing

    Downstream process integration

    • Charged at initial monomer blend stage in condensation or radical polymerization processes; subsequently monitored throughout cure profile to ensure complete incorporation or reactive conversion

    Final product types

    • Heat-resistant phenolic resins
    • Modified polyurethanes with improved thermal stability
    • Crosslinked epoxy coatings for industrial sector
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    Certification & Compliance
    More Introduction

    Introducing 3-Methyl-4-Nitrophenol: Insights from a Chemical Manufacturer

    Understanding 3-Methyl-4-Nitrophenol from a Production Perspective

    Walking through our production floor, I often see 3-Methyl-4-Nitrophenol running through various manufacturing steps, its pale yellow crystals gradually forming as our process flows from reaction, filtration, to purification. We take particular care with this compound, as it handles like a seasoned chemist in the lab—reliable and direct, but never forgiving of shortcuts or carelessness. Among the portfolio of nitrophenol derivatives, 3-Methyl-4-Nitrophenol stands out for its consistency, stability, and the distinct positions of its methyl and nitro groups.

    Looking at the chemical structure, the methyl group at the 3-position and the nitro group at the 4-position give this molecule a unique reactivity and performance profile. That means neither the 2-nitro nor 5-methyl alternatives can fill its role in a synthesis without significant changes to reaction pathways. Chemists value this specificity, since in organic synthesis, especially in agrochemicals and pharmaceutical intermediates, seemingly slight shifts on the aromatic ring can separate a successful target compound from a shelf full of failed experiments.

    From Reactor to Packed Drum: Maintaining Quality at Every Step

    Over years in this industry, I’ve found that the reliability of our 3-Methyl-4-Nitrophenol begins at the very first charge into the reactor. We use high-quality starting materials and monitor the exothermic nitration steps carefully to control byproduct formation. Here’s where manufacturer experience pays off: subtle adjustments in temperature and timing, guided by years watching reactions unfold, often mean the difference between pure yellow crystals and a brownish impurity-laden batch.

    Our plant specifications typically target a purity of no less than 99 percent by HPLC. Our customers run stringent analytics, and we match or surpass those requirements every cycle. Residual moisture, unreacted starting material, and traces of isomeric side products fall well under commercially relevant thresholds. Product is dried in a vacuum, passed through a particle sizer, and filled under inert atmosphere—the nature of nitro compounds makes this step just as important as the synthesis itself. We avoid cross-contamination with other phenolic intermediates through dedicated lines, equipment, and thorough cleaning validations.

    Applications: Function Shaped by Structure

    3-Methyl-4-Nitrophenol serves as more than just another aromatic intermediate. Our largest customers work in crop protection and specialty chemicals. They trust this compound for its ability to build complexity into their molecules through the nitro group, positioned para to the phenol. Many widely used fungicides, herbicides, and veterinary formulations require that exact arrangement, because either the electron-donating methyl or the withdrawing nitro group can activate specific transformations. Silently, this molecule props up modern agriculture by playing a crucial part in more advanced synthesis targets.

    Pharmaceutical producers source their intermediates from us with a keen eye for residual metals, sulfated ash, and low-level impurities that might spoil a final step years down the development pipeline. Every kilogram we ship matches the same analytical profiles, batch to batch. For those involved in pigment and dye chemistry, this compound brings controlled reactivity without introducing unpredictable side products or tints, valuable for any producer needing color consistency.

    What Differentiates 3-Methyl-4-Nitrophenol from Close Relatives

    Our technical team often receives questions about the distinctions between nitrophenol isomers and methyl positioning. In our experience, efforts to substitute 3-Methyl-4-Nitrophenol with, say, 2-Methyl-4-Nitrophenol or the unsubstituted 4-Nitrophenol fail due to regioselectivity and reactivity differences that run deeper than most realize. The methyl group changes the electronic field, affecting nucleophilic substitutions and even controlling the orientation for downstream functionalization. Manufacturers who switch intermediates may risk unwanted byproducts or weak yields in reactions designed around the 3,4-substitution pattern.

    The melting point, solubility, and thermal behavior of 3-Methyl-4-Nitrophenol separate it even further from its siblings. For us as manufacturers, these differences dictate storage design, solvent selection, and the safety envelope forming around the process. We see far better flowability and handling under plant conditions than with the more hygroscopic or unstable alternatives, so we rarely deal with clumping or caking, even in high humidity.

    Handling and Safety Considerations on the Production Line

    Anyone who has spent enough time with nitro aromatics knows to respect their sensitivity. Our protocols, honed over years of hands-on experience, demand close attention to environmental controls—temperature, pressure, and especially ignition sources. We never let organic dust accumulate. Our team keeps to practical, clear procedures: reactor charging under closed systems, round-the-clock dust collection in packing areas, and regular maintenance on inerting equipment. We keep product movement direct and minimize transfers.

    Our workers train specifically on nitroaromatic health hazards, with direct air sampling and monitoring as part of daily operations. We regularly sample the final product for trace explosives, even when not required by regulations, to ensure zero surprises for customers who relabel or package bulk quantities. Safety data, real-world incident reviews, and feedback from major end users feed into our process validations, keeping us responsible not only to our own team, but to everyone down the supply chain.

    Sustainable Sourcing and Environmental Responsibilities

    From inside the industry, we see environmental compliance not as a hoop to jump through but as a practical reality woven into everyday decisions. Our raw materials sourcing team seeks out suppliers who follow proper effluent treatment and document full supply chains. Waste streams, especially those carrying residual nitro compounds, pass through our own multi-step treatment facility. This effort keeps local waterways clean and complies with both local and global standards. Our neighbors, like us, count on good chemical stewardship.

    Reducing volatile organic compound emissions has become a point of pride among our operators. We invested in advanced condensers and scrubbers that let us re-capture and re-use process solvents rather than venting them. That makes economic sense, but it also means our product leaves a smaller footprint, an advantage that global buyers increasingly recognize. When a prospective partner runs a full lifecycle analysis—tracking emissions from raw material delivery through shipping—they find our approach lets them meet tough new standards in Europe, North America, and East Asia.

    Consistency and Traceability: Building Trust through Repeat Performance

    One comment we often hear from buyers who switched from traders or generic third-party suppliers is the relief they feel dealing with a single manufacturer throughout the entire batch release process. Our traceability starts with individual lots of raw materials coded by supply date, all the way to drummed or supersacked product ready for loading. There’s no ambiguity for clients chasing audit trails or updating a master file with changes in supply chain or processing parameters.

    Regular external audits, customer site visits, and internal proficiency checks keep us focused on zero-slippage quality standards. We maintain duplicate analytical routes—gas chromatography, HPLC, and advanced spectroscopic methods—to cross-check both bulk product and retained samples after shipping. Feedback and requests for tighter specifications from users in fine chemical and life science applications directly influence our ongoing process improvements, tightening reproducibility over time.

    Market Dynamics and the Role of a Direct Manufacturer

    Market trends in 3-Methyl-4-Nitrophenol change rapidly. As a manufacturer, we track raw material price swings and shifts in agrochemical demand, sometimes feeling the pinch, often passing stability on to those who depend on predictable supply. We believe in long contracts and clear communication over spot market volatility, because a missed shipment can derail an entire synthesis campaign at the customer’s plant. Our direct relationship with both local and global end users helps us forecast surges or downswings, keeping inventory lean but sufficient even through supply chain disruptions.

    We adapt our plant capacity quickly to accommodate larger or smaller batch runs depending on growing season, pharma project timelines, or regulatory reviews on the other side of the world. Our experience tells us flexibility matters far more than raw volume in this specialty chemical sector. Feedback flows both ways: our customers warn us about changing environmental rules or new contaminants flagged in downstream QC, so we plan upgrades well in advance, without last-minute scrambling.

    Shipping, Storage, and Packaging Values Shaped by Production Experience

    Packing and storing 3-Methyl-4-Nitrophenol calls for more than thick drum walls and tight seals. We consider real world transport risks, especially exposure to heat and moisture. Locked into our standard dry containers, the material holds color and stability for extended periods. Our drivers and warehouse staff understand the challenges of moving nitroaromatics on hot summer days, so they take direct responsibility for route planning, climate control during transit, and simple best practices that avoid clumsy handling accidents.

    Clients can specify packaging size—fiber drums, lined sacks, smaller plastic kegs—and we’ve had requests for bulk totes in dedicated sealed systems for particularly large customers. Experience has taught us to check every shipment’s batch data against client-specific protocols, because recall or cross-contamination events nearly always trace back to careless paperwork or generic packaging. Getting those details right, every shipment, keeps us in business year after year.

    Why an Experienced Manufacturer Makes a Measurable Difference

    There’s no substitute for hands-on practice producing specialty chemicals. Each batch of 3-Methyl-4-Nitrophenol we make runs through operators who understand the subtle cues of reaction and the narrow windows for optimal product draw-off. That depth of experience, built up over years and passed from shift leader to apprentice, creates product consistency laboratories appreciate and production engineers trust. Customers tell us that production hiccups—undissolved residues, stray isomers, unexpected hues—trouble them far less with our supply than from broader-spectrum resellers.

    Through direct technical support, we troubleshoot downstream processing issues, advise on handling persistent residues, help labs adjust purification steps, and alert clients to regulatory shifts affecting import or customs handling. Only a manufacturer with a clear window into both chemical behavior and supply realities can answer those calls. We prioritize these discussions, knowing from our own upstream struggles how minor process tweaks can unlock greater overall efficiency.

    Improving Through Ongoing Research and Feedback

    Our research and development team draws from both bench-scale experiments and full production batch reviews. We collaborate internally and with university partners on cleaner, safer routes for nitration and methylation, targeting reduced energy use, minimized byproducts, and greener solvents. Several process improvements have come directly from careful analysis of spent filter cakes or recycled wash waters, suggesting operational tweaks many would overlook. Sometimes, customer requests for tighter impurity profiles or sharper melting ranges guide our next round of improvements.

    Access to continuous feedback, both praise and complaint, drives our drive for better product quality. We treat outlier batches as case studies, digging through every parameter to uncover root causes, close the gap, and feed those lessons into the next run. It’s this blend of humility—a willingness to learn from mistakes—and technical confidence that lets us deliver the kind of product serious users expect.

    Real-World Problems and Practical Solutions

    Manufacturing 3-Methyl-4-Nitrophenol at commercial scale occasionally presents challenges: inconsistent raw material quality from outside suppliers, unexpected bottlenecks in plant throughput, stray contaminants showing up in final product. Our teams rely on redundant quality control checkpoints, requalification of suppliers, and a troubleshooting culture that avoids blame-shifting in favor of real corrective actions. If operator error slips through, we own it and fix it—immediately notifying clients if any product could fall outside spec, even if the problem’s unlikely to reach a downstream user.

    Inventory management often emerges as a sticky point. Too little means missed opportunities or emergency production runs at premium cost. Too much ties up working capital in stock at risk of expiry. Our solution combines demand forecasting—melding client communication, historical data, and gut feeling from decades of seasonal swing—with flexible batch lifecycles managed from procurement to delivery.

    The Broader Role of 3-Methyl-4-Nitrophenol in Industry

    Each time we load a batch for shipment, it’s easy to see 3-Methyl-4-Nitrophenol not as a commodity but as an enabler of technological progress across multiple sectors. It supports advances in protective chemistry for crops, pushes pharmaceutical research boundaries, and enables pigment and dye makers to elevate product quality. The history of this compound links decades of evolving science, shifting regulation, and changing business models. As manufacturers, we stand at the intersection—responsible not only for shipping a consistent product but for doing right by partners, employees, and communities.

    That responsibility shapes every investment in process safety, every partnership built with ethical suppliers, and every innovation we pass on to our customers. We measure success less by monthly tonnage and more by the trust we build, the technical advice we provide, and the sustainable practices we put in place. Every batch of 3-Methyl-4-Nitrophenol leaving our plant tells that story—one of chemistry balanced with real-world care, and of a product with deep roots in the continuous evolution of modern industry.