|
HS Code |
102716 |
| Cas Number | 4098-18-6 |
| Molecular Formula | C7H8N2O3 |
| Molecular Weight | 168.15 g/mol |
| Appearance | Yellow to orange crystalline powder |
| Melting Point | 193-197°C |
| Solubility In Water | Slightly soluble |
| Pka | Approximately 6.6 |
| Purity | Typically ≥98% |
| Synonyms | 2-Amino-4-methyl-6-nitro-phenol |
| Chemical Classification | Nitrophenol derivative |
| Storage Conditions | Store in a cool, dry place, protected from light |
As an accredited 2-Amino-4-Methyl-6-Nitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g package contains 2-Amino-4-Methyl-6-Nitrophenol in a sealed amber glass bottle with hazard labeling and product details. |
| Shipping | 2-Amino-4-Methyl-6-Nitrophenol should be shipped in tightly sealed containers, clearly labeled, and protected from moisture, heat, and direct sunlight. It must comply with local and international regulations for hazardous chemicals. Transport via ground or air should ensure secondary containment to prevent leaks, with appropriate documentation for safe handling and emergency procedures. |
| Storage | Store **2-Amino-4-Methyl-6-Nitrophenol** in a tightly sealed container, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep in a cool, dry, and well-ventilated area. Avoid exposure to moisture and heat. Ensure that storage areas are clearly labeled, and handle using appropriate personal protective equipment to minimize risk of inhalation or skin contact. |
Competitive 2-Amino-4-Methyl-6-Nitrophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Years of hands-on manufacture have taught us one universal lesson: each chemical reveals its character not only through structure, but through how it responds to human touch and process. Our experience with 2-Amino-4-Methyl-6-Nitrophenol stands as a strong example. The process that takes this molecule from precursor to packaged product pulls together problem-solving with chemistry know-how. The way our team works with this compound tells a story that runs deeper than a tidy specification sheet ever could.
What we produce as 2-Amino-4-Methyl-6-Nitrophenol breaks down to a distinct pale yellow solid with a chemical nature that combines an amino group at the two-position, a methyl group at four, and a nitro group at six on the phenol ring. From a manufacturer’s point of view, this arrangement brings both assets and quirks to our daily operations. During crystallization, even a small shift in temperature nudges solubility, so tight control in this stage becomes essential to get pure crystalline output and minimum byproduct. We usually see batch-to-batch consistency in color and melting properties, which our repeat customers depend on for their downstream production.
Many users look for 2-Amino-4-Methyl-6-Nitrophenol with very high purity, sometimes as much as 98% or above. We make this possible using tailored recrystallization steps and real-time impurity monitoring. The details here matter. Trace impurities, especially unwanted isomers or incomplete reduction byproducts, can cause color instability in applications—most often in cosmetic and hair dye industries, where a minor contaminant will show up as unexpected shade drift or inconsistent performance after shelf storage.
We learned through experience that even small shifts in the pH of the mother liquor during crystallization can ramp up impurity load, so in our facility, operators focus on rapid sampling and pH tracking. Our technical staff spares little tolerance for off-color crystals or stubborn fines; rework is easier at this point than fielding complaints from a customer six months later, after their end product fails in use.
Most orders for 2-Amino-4-Methyl-6-Nitrophenol head straight for formulation in oxidative hair dye products. We see customers who operate global retail brands as well as boutique formulators. The compound acts as a direct dye precursor, partnering with oxidizing agents and couplers in the coloring cream to produce shades ranging from deep reds to violets. This function demands tight control over both particle size and moisture content. Moisture, even at the half-percentage range, will drop shelf life—so we stress controlled drying and rigorous packaging with low permeability materials.
Another set of clients use 2-Amino-4-Methyl-6-Nitrophenol as an intermediate in specialty pigments. The reactivity of the amino group makes the compound a good substrate for further transformations. These customers often request custom packaging or larger batch sizes, and we support toll-manufacturing approaches for scale-up projects. That flexibility, rooted in the factory itself, lets us respond to precise synthetic needs, including requests for less common particle grades or extra quality certification.
Many buyers compare this compound with related aminophenols—typically 2-Amino-5-Nitrophenol or 4-Amino-2-Nitrophenol. The difference isn’t academic. For manufacturers, the methyl group at the four-position on our product brings more than a subtle shift in electron density; it tunes the compound’s redox behavior during formulation. In practice, that means dye outcomes with 2-Amino-4-Methyl-6-Nitrophenol show improved stability under oxidative conditions, especially during storage. The methyl group’s influence on solution pKa also lets formulation chemists design around baseline color tone and fades.
Other aminonitrophenols can show higher reactivity at unwanted sites during certain coupling reactions, leading to more off-shades or waste. Our specific product reduces this risk. Over years in the plant, we saw that the nitro group at the six-position resists reduction during end-use, meaning the color stays truer in hair dye or pigment applications even under challenging storage. Keeping a consistent end shade also cuts the need for excessive stabilizers or antioxidants, making things easier for our customer’s technical and regulatory teams.
Making this molecule isn’t about running a checklist of unit operations. Each step shapes downstream quality. Our synthesis begins with careful nitration of an upstream methylaminophenol, using conditions that minimize over-nitration and manage exotherm risk. Some commercial processes—especially quick-turn batch production—may race through this stage, compromising reproducibility. Over the years, we found that slow addition and staged temperature ramps lead to higher purity and fewer process interruptions.
Downstream, our crystallization process focuses on managing seed loading and solvent ratios. Operator experience with each reactor’s quirks becomes more valuable than automation: a new engineer might follow the numbers, but the seasoned hand runs their thumb along the glass and checks the cake’s wetness before making the call to decant. That kind of practiced touch keeps quality at the core of each batch.
From a chemistry textbook, 2-Amino-4-Methyl-6-Nitrophenol might look like a stable solid. Daily work with the product says otherwise. The compound’s phenol group and its exposed amino functionality can pick up ambient moisture and trace acetic acid vapors, especially in uncooled, high-humidity climates. We use high-barrier linings and keep warehouse temperatures low, not as a selling point, but because we learned from too many foot-thick cakes of caked-up powder in summer. Customers appreciate product that pours without clumps or hard spots; it’s an outcome of obsessive attention at the storage stage, not luck.
Shipments to humid coastal regions can arrive with minor surface oxidation or color change, even when packaged well. We share real batch history—storage time, conditions, and post-packing handling—with downstream clients, so they can adjust their process if needed. Troubleshooting is part of the manufacturer’s everyday reality.
As a specialty chemical with direct contact uses, 2-Amino-4-Methyl-6-Nitrophenol draws scrutiny from health and safety regulators. Hair dye end-uses mean every batch rolling out from our facility holds its own set of analytical documentation—purity, contaminants, residue solvents, and absence of restricted aromatic amines. These records come from actual assays done in our on-site lab, using validated methods, not from generic third-party certifications.
We update our analytical screens as regulations evolve. If the local agency tightens its nitrosamine monitoring, our QC team revalidates with the new detection limits before batches go to market. The cost is not trivial, but returns in fewer downstream disruptions—customers count on compliance, and so do we. On more than one occasion, a customer reported an unexpected impurity peak in their own test; by keeping thorough retention samples and lab results, we often re-analyze and help pinpoint the batch issue and its root.
Broader chemical industry trends push for more sustainable production, and that’s been a real conversation for us. The nitration process produces waste streams with acid residues and trace organic materials. Years ago, allowed practice involved simple neutralization and disposal, but now, we recover and treat effluent for minimal environmental load. We run audits on water usage and solvent recovery. In recent years, our process shift to more selective catalysts and recapture of wash solvents reduced both water demand and net emissions.
We keep an open line with customers developing “clean label” or “eco-preferred” product lines. For these clients, traceability and restricted substance dashboards are more than buzzwords. Here, our plant-level transparency goes beyond safety data sheets. We map out batch genealogy, origin of major raw materials, and make process modifications visible when asked. Not all features can be changed overnight, but incremental progress speaks to both regulatory needs and end-customer expectation. In the hair color sector especially, clarity about trace substance load, processing aids, and risk measures drives trust up and returns down.
Our work doesn’t end when a drum rolls off the dock. Questions come in regularly: “Why did this batch show a slightly darker hue?” “Can we get material ground to a finer fraction for our dispersion line?” “Any trace benzene detected during synthesis?” Our answer always comes back to what we control in the plant and the data underpinning each step. In many cases, we’ve rerun specific reactions to provide insight or to customize the physical form of the powder based on the customer’s processing needs. We keep technical staff available for direct client conversations, not just remote sales, because real partnership is built on access, not on terms buried in an email chain.
More than a few times, new users of 2-Amino-4-Methyl-6-Nitrophenol bring legacy procedures from older aminophenols or different nitro aromatics, only to see unexpected behavior in blending or reaction. Each time, practical process understanding helps bridge the gap—walking customers through the effect of the methyl group, water content, or purification method on their real-world outcomes. In cases where batch-to-batch consistency matters—such as for branded retail products—our direct lines of communication and archive sampling make difference. Field performance reports, collected from end users through our partners, feed back into the plant. That closed loop doesn’t exist when material comes from anonymous traders; it defines responsible manufacturing and customer care.
Every batch starts with stringent inspection of feedstocks, where we look for not just assay value but also trace inorganics and byproduct amines. Downstream, our batch controls record every process stage—temperature holds, agitation rates, solvent type, filtration time. These records aren’t just paper trails; they serve as troubleshooting tools and value markers for our partners. The ability to trace back a subtle impurity or quality drift means fewer recalls, less customer inconvenience, and a product reputation that stands up under scrutiny.
During batch release, we run final property checks beyond chemical analysis—flowability, bulk density, visual inspections for fines or caking. Sometimes it’s these “minor” features that make or break a client’s process flow. More than once, a customer has reported that smoother powder form yields better blending, faster wet-out during formulation, or reduced need for pre-processing. That kind of feedback loops directly into our future batch planning.
Plant work for 2-Amino-4-Methyl-6-Nitrophenol means facing down both expected and novel challenges. As markets expand and formulation chemistries shift, our manufacturing team regularly reviews routes for yield, waste, and complexity. Sometimes a small change—swap in a more robust condenser, tweak solvent polarity—turns up surprising gains in both purity and throughput. We share these process improvements with our repeat customers, especially when the change affects downstream application or our understanding of the compound.
Supply chain disruptions pushed us to qualify local raw material suppliers, with all the variability that entails. Our technical staff compares not just assay values, but behavior through the reaction train. Having backup sources, especially for critical precursors, fits into an overall strategy of resilience. Our commitment isn’t to being cheapest or fastest-to-market; it’s about giving each customer a clear, consistent, and transparent product history.
We see growing interest from academic and industrial researchers testing new applications for 2-Amino-4-Methyl-6-Nitrophenol—organic electronics, coordination chemistry, and sensor platforms all make appearances. Our plant responds with tailored support: small batch runs for R&D, support for custom grades, and sample-sharing programs for collaborative work. The idea is not to push bulk orders but to let researchers experience the real physical and chemical behavior of the product as made under industrial conditions. Sometimes, feedback from research groups points out stability issues under high-sensitivity conditions, which then leads us to process tweaks or extended analytical screens.
Some new applications lean on the precise reactivity offered by this compound. The combined electron-donating and withdrawing groups confer unique selectivity in further functionalizations. We help clients with process development insights, based on our own trials in reaction scalings and impurity management. Tracking patterns in reactivity and stability broadens application horizons and builds up a real-world knowledge base—the kind that marketing collateral alone rarely provides.
Chemical manufacturing means adapting to shifting application profiles, regulatory frameworks, and customer habits. For 2-Amino-4-Methyl-6-Nitrophenol, changing trends—from stricter contaminant controls to new shelf-life demands and expansion in analytical standards—demand ongoing adjustment. We rely on the collective experience of our team, from senior operators through to process engineers, to meet those needs head-on. The lessons we take from every batch, every customer request, and every production hiccup build up the expertise that supports safe, reliable, and effective supply.
Each lot heading out from our facilities represents the intersection of plant realism, scientific rigor, and communications built on demonstrated results, not generic claims. Our work with 2-Amino-4-Methyl-6-Nitrophenol forms a narrative—we shape quality in real time, one batch at a time, through a mix of known methods, hands-on checks, and unfiltered customer input. With this, both seasoned users and newcomers can count on a product that translates technical promise into everyday performance, batch after batch.