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HS Code |
161879 |
| Chemical Name | 2-Amino-4,6-Dichloro-5-Methylphenol |
| Cas Number | 700-38-9 |
| Molecular Formula | C7H7Cl2NO |
| Molecular Weight | 192.05 g/mol |
| Appearance | Solid (usually crystalline or powder) |
| Melting Point | 132-135 °C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% (commercial) |
| Synonyms | 2-Amino-4,6-dichloro-5-methyl-1-hydroxybenzene |
| Structure Type | Aromatic compound with amino, hydroxyl, methyl, and dichloro substituents |
| Storage Conditions | Store in a cool, dry place, tightly closed container |
| Hazard Statements | May cause skin or eye irritation |
As an accredited 2-Amino-4,6-Dichloro-5-Methylphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 g of 2-Amino-4,6-Dichloro-5-Methylphenol is supplied in a sealed amber glass bottle with a tamper-evident cap. |
| Shipping | Shipping of 2-Amino-4,6-Dichloro-5-Methylphenol should comply with regulations for hazardous chemicals. Package in appropriate, tightly sealed containers, clearly labeled with hazard information. Handle with care, avoiding exposure to heat and moisture. Ship via authorized carriers with required documentation, ensuring protection against spills, leaks, and environmental contamination during transit. |
| Storage | **2-Amino-4,6-Dichloro-5-Methylphenol** should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep separate from oxidizing agents, acids, and incompatible substances. Label containers clearly and avoid exposure to extreme temperatures. Always follow local regulations and use appropriate personal protective equipment when handling and storing this chemical. |
Applications of 2-Amino-4,6-Dichloro-5-Methylphenol in Industrial Manufacturing2-Amino-4,6-Dichloro-5-Methylphenol serves as a specialized intermediate and functional additive in several finely categorized downstream sectors. As the direct manufacturer, we highlight its established industrial applications where regulatory compliance, controlled formula dosing, and specific processing steps are mandatory for producing consistently high-quality finished goods. 1. Synthesis of Antibacterial Agents for Personal Care FormulationsThis compound provides a key building block for the in-situ synthesis of antibacterial ingredients in personal care manufacturing. Its aromatic structure with halogen substitution is leveraged by formulators seeking targeted microbial inhibition, particularly in high-performance soaps, hand washes, and hygiene wipes. Manufacturers optimize incorporation during the active blend compounding step to ensure long-term preservative reliability under large-batch production runs, requiring strict raw material QC and precise batch tracking. Industry compliance standards
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2. Intermediate in Pharmaceutical Active Ingredient Synthesis (API Manufacturing)2-Amino-4,6-Dichloro-5-Methylphenol acts as a critical phenolic precursor in the multi-step synthesis of select antibacterial and antifungal pharmaceutical APIs. Downstream integrators in API plants rely on its reactivity for controlled substitution reactions under cGMP conditions, supporting production of final actives destined for regulated human and veterinary medicinal markets. This role demands rigorous raw material traceability, analytical verification, and consistent performance in scale-up. Industry compliance standards
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3. Active Component in Polymer-Based Antimicrobial CoatingsWithin industrial polymer coatings, this phenolic compound is actively incorporated to impart durable, broad-spectrum antimicrobial properties. Coating formulators select it for its halogenated aromatic structure, which interacts strongly with polymer matrices, ensuring long-term release and environmental stability, especially in high-traffic building surfaces and equipment. Quality assurance measures emphasize homogeneity and leachable residue control throughout the compounding and cure stages. Industry compliance standards
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4. Preservative Precursor in Industrial Water Treatment ProductsIn specialty water treatment chemical production, this compound serves as a precursor for synthesizing advanced phenolic biocides. Downstream formulators exploit its molecular structure to generate agents targeting microbial fouling in closed-loop water circuits and cooling towers. This application involves precise batch synthesis with oversight for disinfection efficiency, biodegradability, and regulatory discharge limits, demanding validation of both starting material purity and final blend performance. Industry compliance standards
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5. Chemical Intermediate for Agrochemical SynthesisAs a functional intermediate, this material forms part of the synthetic routes to produce specific halogenated phenol-based agrochemicals. Agrochemical producers value its controlled reactivity profile for building active moieties required in advanced crop protection chemistries. The bulk production process typically incorporates this intermediate at a precisely controlled step to ensure target activity and compatibility, aligned with regulatory residue and safety limits on final formulations. Industry compliance standards
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In our workshops, everything comes down to what works in real life. We produce chemicals not for theoretical catalogs but for hands-on researchers, industrial formulators, and synthesis engineers who rely on reliability and quality batch after batch. 2-Amino-4,6-dichloro-5-methylphenol stands as a specialty intermediate born out of decades experimenting with phenolic derivatives and their industrial applications. Creating a product like this draws on real-world insight, not just standard practices.
Looking at the structure, each functional group in 2-amino-4,6-dichloro-5-methylphenol shapes its behavior across various end-uses. The methyl group on the ring brings hydrophobic character, which affects solubility in polar and nonpolar systems. Adding chlorines at the 4 and 6 positions does more than increase molecular weight; it toughens the core of the molecule against oxidative degradation and shapes the interaction with enzymes or catalysts later in a downstream process. The amino and phenolic hydroxyl groups don’t just offer hydrogen bonding sites for molecular recognition, they allow for unique transformation routes in pharmaceutical, photographic chemical, and materials synthesis.
We have worked side by side with development chemists looking for intermediates strong enough to hold up in rigorous multi-step reactions yet flexible enough for essential downstream modifications. In our experience, this balance is not easy to strike. The dual chloro substitution distinguishes this compound from less reactive phenols, increasing both electron withdrawing effects and halogen reactivity in nucleophilic aromatic substitution. The methyl and amino groups are key donor sites—once you have run reactions with less functionalized phenols or monohalogenated analogs, the difference in both conversion and selectivity is clear.
Sourcing from actual manufacturing lines brings nuances that spec sheets usually don’t capture. Our typical production run for 2-amino-4,6-dichloro-5-methylphenol maintains a purity greater than 98%, but attention focuses as much on impurity patterns as on numbers alone. By tracking the source of every precursor, temperature sequence, and byproduct handling method, we tailor the output for the kinds of reactions clients expect to perform—chlorination, amination, methylation, and exhaustive downstream conversions.
Batch after batch, we’ve noticed that trace byproducts of the methylation step can poison catalytic cycles or introduce color bodies downstream, a lesson learned only through tight feedback with our users and years of running pilot reactors. In this sense, the difference between buying from a manufacturer and pulling random batches from brokers isn’t abstract: it means better reproducibility, lower downstream purification costs, and confidence that behavior doesn’t vary from drum to drum.
2-amino-4,6-dichloro-5-methylphenol presents as an off-white to pale-yellow crystalline solid, easily handled under standard lab or plant conditions. The melting point, typically seen around 145–148°C, keeps it stable in storage and enables precision in controlled reactions. We designed our standard filtration and drying process to avoid thermal darkening and limit exposure to trace atmospheric moisture. Chemists working with this product know the value of a consistent material—crystals of the right size, known polymorphic tendencies, and tightly controlled residual solvents, especially in syntheses meant for regulatory approval or scale-up.
Over the years, 2-amino-4,6-dichloro-5-methylphenol has found its place in several industries. Many resin formulators select this intermediate when they seek enhanced chemical resistance and thermal performance in specialty polymers. The dual chloro pattern resists both UV degradation and microbial attack, often extending the usable life of coatings in outdoor or high-humidity environments. In colorant chemistry, this compound yields versatile azo and azomethine derivatives, unlocking shades and fastness unattainable with simpler phenols. Through feedback from pigment chemists, we fine-tuned the product to ensure every kilogram meets expectations for both shade development and dispersibility.
A growing share of our output goes toward pharmaceutical research. The molecule serves as a unique scaffold, bridging aromatic and heterocyclic chemistry in several promising drug candidates. Medicinal chemists engage with us repeatedly not just for purity but for reproducible impurity profiles, as regulatory pathways for these intermediates get ever stricter.
Some clients targeting photographic chemicals prefer 2-amino-4,6-dichloro-5-methylphenol for its capability to generate stable image-forming compounds. The fine details of freeze-thaw stability, solution clarity, and photoreactivity only emerged by iterating real manufacturing practices, taking feedback from clients running multi-week process trials. The product’s high photostability and minimal background coloration drew these users in—not something one discerns from a catalog, but a product of direct engagement and iterative process refinement.
Many industrial users begin with 2,4-dichlorophenol, 2,6-dichlorophenol, or 4-amino-2-chlorophenol, but these lack the balanced electronic and steric profile of 2-amino-4,6-dichloro-5-methylphenol. Once the methyl group enters the ring, reactivity changes in real and practical ways: Electrophilic aromatic substitution rates drop, desired selectivities appear, and thermal stability rises. When side-by-side batch experiments pit this product against 2-amino-4-chlorophenol in high-temperature alkylation or condensation reactions, outcome differences are not subtle. The final conversion, color, and mechanical properties of resins or chemicals clearly trace back to these structural features.
Downstream purification can make or break a process; our customers found that by starting with a highly functionalized, pre-chlorinated and methylated phenol, they reduce numbers of process steps. This keeps waste lower and sustainability targets within reach, a practical benefit as regulatory and environmental pressures mount in every sector. Products lacking either the dichloro or the methyl group often lead to side reactions in heterocycle synthesis—our focus has been to give a consistent, predictable tool for cleaner, more straightforward chemistry.
Across all product grades—whether destined for pilot plant or kilogram-scale pharma work—consistency roots itself in hands-on attention. Batch records for 2-amino-4,6-dichloro-5-methylphenol track not only purity and melting point, but also color, particle size, and impurity spectrum, as each of these affects subsequent use. Our technicians frequently run additional quality checks overlooked by standard monographs, recognizing that two batches with identical numbers can behave differently if overlooked traces slip by.
Supplier variability has sparked more headaches in real-world manufacturing than any textbook will admit. Over years, clients shifting to our direct-from-factory shipments reported increases in batch yields, less downtime for recalibration, and improved ease of regulatory submission. Our familiarity with every production step—from amination reagent ratios to filtration and drying parameters—lets us collaborate on custom material as R&D needs evolve.
Manufacturing specialty aromatic compounds brings sustainability and safety into sharper focus each year. The methods leading to 2-amino-4,6-dichloro-5-methylphenol often present environmental management challenges: byproducts of chlorination, mineralized residues from amination, and drying cycle emissions. We have focused on process optimization to minimize these loads, incorporating recovery and recycle of chlorinating agents and tight effluent control in plant design. Over time, as regulatory scrutiny increased, these measures paid off—not only by earning compliance certifications but also by providing reliable, long-term cost stability for our clients counting on dependable supply.
Safety in handling matters for manufacturers and end-users alike. Our experienced staff handle bulk material transfers, drum packaging, and sampling with eyes open for both acute and chronic hazards unique to chlorinated aromatics. From experience, users come to trust packaging that seals well, labels that clearly state content and precautions, and supporting documentation that reflects real findings, not generic language.
Each market sector brings fresh requirements. Never do we see a “one size fits all” approach succeed. Over the last decade, we’ve worked alongside advanced materials developers working on conductive polymers, pharmaceutical chemists developing anti-infectives, and pigment labs fine-tuning new hues. In each case, formulation or synthesis teams send feedback about transitions, stability, or unexpected side reactions that demand a shift in how we approach both production and QC.
We’ve acted on suggestions such as narrowing the melting range, drying to below 0.1% water content, or refining packaging to reduce static buildup, improving both user safety and product integrity. Sometimes, a client’s discovery in scale-up revealed a trace impurity catalyzing an undesired reaction; our tight process control allowed us to suppress that pathway, returning them reliable, improved batches. These stories pair proof and accountability to claims, embodying the experience both sides build up over time.
Pharma and specialty chemicals need more than clean batch sheets—they demand insight into traceability, residual solvents, and robust analytical methods. We routinely supply supporting GC, HPLC, and NMR data on request, having found that open dialogue with user labs streamlines audits and relieves onboarding delays. Our analytical chemists maintain validated protocols for quantifying known impurities and solvents, frequently updating them in sync with evolving standards.
Truckload or small drum, each lot moves through the same mapping process—date and time of synthesis, operators involved, in-process control yields, and lot-specific test results. By providing these details up front, chemists at the receiving end avoid surprises, and project leads have what they need for regulatory filings from day one. We learned this from years sputtering through audits triggered by incomplete paperwork from others—once you go through enough, you learn what real compliance means.
Aromatic intermediates rarely act in a vacuum. Our relationships with large and small users have taught us that minor lot-to-lot variation in flowability, reactivity, or dissolution rate has outsized effects on process economics and capacity planning. Routine calls come in—one batch clumping under humid conditions, another showing delayed color change in diazotization, or a new user reporting higher reactor shearing energy. Instead of treating these as minor complaints, we integrate feedback into future cycles by fine-tuning particle treatments and optimizing drying time.
Real engagement goes beyond batch releases. Our team provides technical data gleaned from hands-on work—filter cake handling, bulk transfer, long-term storage best practices, and solution stability under different lighting or humidity conditions. These lessons accumulate not just as theoretical recommendations but as practical bullet points that save time, reduce waste, and avoid process restarts. This perspective comes from a genuine manufacturer’s role—living with the consequences of every batch over years, not single sales.
Every kilogram of 2-amino-4,6-dichloro-5-methylphenol rolling out our plant reflects shared purpose between skilled production teams, QC chemists, and users innovating in their fields. Having lived through the full journey—process scale-up, client troubleshooting, regulatory paperwork, and industrial feedback—we build more than just a commodity. This molecule stands as a reliable tool for those aiming at precise, high-value chemistry, differentiated by quality, hands-on experience, and flexibility earned over years practicing the trade.
Chemical manufacturing isn’t about impersonal shipments or tick-box compliance; it’s about supporting ever-higher targets for purity, process reliability, and sustainability. That only happens when real production expertise and user dialogue drive the process—a lesson we see playing out every day with compounds like 2-amino-4,6-dichloro-5-methylphenol.