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HS Code |
412755 |
| Chemical Name | 4-Amino-m-cresol |
| Synonyms | 2-Methyl-4-aminophenol |
| Molecular Formula | C7H9NO |
| Molecular Weight | 123.15 |
| Cas Number | 2835-99-6 |
| Appearance | White to light brown solid |
| Melting Point | 136-140°C |
| Solubility In Water | Moderately soluble |
| Storage Temperature | Store at room temperature |
| Pubchem Cid | 19043 |
As an accredited 4-Amino-M-Cresol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g 4-Amino-M-Cresol is packaged in a sealed amber glass bottle, featuring a screw cap and detailed hazard labeling. |
| Shipping | 4-Amino-m-cresol is typically shipped in tightly sealed containers, protected from light and moisture, and labeled in accordance with safety regulations. It should be handled and transported as a hazardous chemical, following appropriate guidelines for toxic and potentially combustible substances. Ensure compliance with local, state, and international shipping regulations. |
| Storage | 4-Amino-m-Cresol should be stored in a tightly closed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Keep the chemical away from direct sunlight, ignition sources, and moisture. Store at room temperature and ensure that the storage area is clearly labeled and compliant with appropriate chemical safety regulations. |
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Purity 99%: 4-Amino-M-Cresol with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity formation. Melting point 122°C: 4-Amino-M-Cresol with a melting point of 122°C is used in dye manufacturing, where it supports stable thermal processing during formulation. Molecular weight 137.17 g/mol: 4-Amino-M-Cresol with molecular weight 137.17 g/mol is used in hair dye formulation, where it allows for precise stoichiometric calculations and consistent color development. Particle size <50 µm: 4-Amino-M-Cresol with particle size less than 50 µm is used in cosmetics, where it provides uniform dispersion and smooth texture in creams and lotions. Stability up to 60°C: 4-Amino-M-Cresol with stability up to 60°C is used in polymer additive manufacturing, where it maintains integrity during processing and improves product lifespan. Water solubility 12 g/L: 4-Amino-M-Cresol with water solubility of 12 g/L is used in specialty chemical formulations, where it enables efficient blending in aqueous solutions. |
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Working with chemicals in the lab or in manufacturing is a lot like working with ingredients in a kitchen: the result depends heavily on the specifics of what goes in. 4-Amino-M-Cresol stands out in this regard. Recognized by its chemical formula C7H9NO and CAS number 2835-98-5, this compound has earned a growing reputation among both researchers and industrial chemists. In its appearance, 4-Amino-M-Cresol generally takes the form of a pale brown to tan crystalline powder, a subtle sign of its unique molecular structure. People who use this compound tend to remember the faint, phenolic scent it carries—a detail that speaks to its purity as much as its source.
Chemistry is detail-oriented by nature. Looking at specifications, 4-Amino-M-Cresol is usually supplied with a purity of 98% or higher, and the melting point falls in the range of 155-159°C. In our lab, accuracy matters, and I’ve seen how slight impurities in foundational chemicals can create a ripple effect in complex syntheses. With 4-Amino-M-Cresol, reliable purity makes it a trusted component, especially if someone needs consistent results from batch to batch. Moisture content typically runs less than 0.5%, making it more stable for storage and less prone to clumping—an often overlooked concern when planning for the long term.
The "meta" in m-cresol refers to the position of methyl and amino groups on the aromatic ring. This isn't just chemical trivia—position dramatically changes how the compound behaves and reacts. For those of us who spend hours troubleshooting why certain compounds fail to couple, mix, or finish as planned, these details can save weeks of frustration and wasted materials. The combination of an amino group and a methyl group attached at different positions on the benzene ring allows 4-Amino-M-Cresol to take part in specific syntheses that similar chemicals—like o- or p-isomers—simply can’t match.
In my years around research labs and production floors, I’ve watched as this compound carves out a niche in several demanding areas. The most attention-grabbing of these is in the synthesis of hair dyes and pigments. Many of the bold and lasting colors in salons rely on intermediaries like 4-Amino-M-Cresol, especially when a deeper shade or oxidative stability is needed. The amino group plays a key part in the oxidative coupling processes that bring out complex tones in dyes, which is not something you’ll see achieved with basic cresols.
Pharmaceutical chemistry and organic synthesis also call on 4-Amino-M-Cresol. In the early stages of drug molecule design, having a precursor with the right reactivity is half the challenge won. Compounds with both amino and methyl groups in defined positions open the door to useful derivatives, some of which head down the pipeline toward new therapies. I remember the first time a colleague described 4-Amino-M-Cresol as a "molecular Swiss Army knife": it doesn’t always finish the job alone, but it often starts vital reactions where few alternatives can.
Outside the pharmaceutical and personal care world, you also see this chemical in dyes for textiles, inks, and in niche electronics manufacturing. The demand isn’t always sky-high, but the consistency and the reactivity profile—especially resistance to unwanted side reactions—keeps 4-Amino-M-Cresol relevant where it is chosen.
Not all cresols or aminophenols step up to the same challenges. In my experience, substituting other cresol isomers often leads to entirely different outcomes in both pigment and pharmaceutical synthesis. Methyl groups at different aromatic positions can limit or allow various substitution reactions. 2-Amino-5-methylphenol, for instance, can’t match the balance of reactivity found in 4-Amino-M-Cresol for certain oxidative color development routes. Researchers in the field often share notes on failed syntheses when a simple substitution is tried, learning that even small structural changes in precursors have outsized impacts downstream.
In hair dye research, the stability and depth of color seen with 4-Amino-M-Cresol outstrip what I’ve seen with meta-aminophenol or para-cresol. For labs working to replicate colors with minimal toxic byproducts, using the right isomer means the difference between a formulation passing or failing regulatory safety checks. In our lab, sticking with 4-Amino-M-Cresol helped cut down on rework and kept batch results reliable—a big advantage when every gram and every test counts.
There’s also a noticeable difference in availability and handling, compared with other aminophenol or cresol derivatives. Some alternatives are trickier to store or require more attention to keep away from humidity and contamination. With 4-Amino-M-Cresol, as long as you take standard precautions for organics—cool, dry place, tightly sealed container—you limit most typical risks. Shelf life tends to be solid, as long as protocols aren’t ignored.
No commentary on chemical use feels complete without mentioning the safety side. 4-Amino-M-Cresol, like most aromatic amines and cresols, sits in the category of chemicals best handled with care. Anyone who’s accidentally splashed a bit during weighing, even with gloves on, knows the irritation risk is real. Most users rely on fume hoods, gloves, and—sometimes—to keep exposure at arm’s length. The compound’s record in regulatory toxicology isn’t spotless: it’s flagged for potential skin and eye irritation, and repeated exposure could raise more serious concerns. In a world moving toward greener and safer chemistry, the focus shifts toward smarter handling and safer alternatives. But for now, 4-Amino-M-Cresol’s profile and reliability keep it on the go-to list for labs and manufacturers who know what they’re doing.
Reflecting on incidents in the lab, spills or accidents are rare, but every one is a reminder that respect for these substances is non-negotiable. Proper training goes a long way, and it’s not just protocol on paper—experienced chemists know that shortcuts in PPE or ventilation don’t just risk compliance, they seriously risk health. Integrating spill kits, training refreshers, and routine audits makes good sense, and helps maintain trust from regulatory bodies and product users alike.
Chemists and product developers have all been burned by subpar reagents at one point or another. With 4-Amino-M-Cresol, buyers need to look beyond a simple batch certificate. Not all suppliers run their QA to the same stringency, and impurities—especially phenolic or amine byproducts—can derail projects fast. We’ve seen cases where a discount-priced batch from an unknown source introduced contaminants that altered reaction yields and bioactivity in pharmaceutical intermediates. Those mistakes cost more than the savings ever offer.
For those seeking to verify their purchases, classic approaches include thin-layer chromatography, melting-point determination, and NMR spectra review. When budgets or timelines get tight, some labs try to cut corners—skipping these checks to speed up projects—but this approach rarely saves time in the long run. In my experience, diligent verification keeps surprises (and reordering headaches) to a minimum. Requests for third-party certifications, traceable batch analytics, and reliable chain-of-custody documentation are becoming routine best practices, especially with renewed pressure from regulatory agencies and customers to demonstrate product integrity.
Modern laboratories—and an even greater number of manufacturing companies—have their sight set on more than just functional chemicals. The conversation now nearly always includes questions of environmental impact and worker health. Some folks who’ve been in the field for years remember when disposal meant dumping everything down a sink or barrel, with little thought to what happened next. Thankfully, shared learning and hard-won experience have changed things. For 4-Amino-M-Cresol, proper disposal requires designated hazardous waste containers and, in bigger plants, regulated incineration. Local guidelines often drive specifics, but as a community, chemists aim to keep these substances out of water streams and public landfills.
Professional groups and regulatory agencies keep pushing the envelope on what’s considered “green” or sustainable. Younger chemists in training now spend more formal time understanding the life cycle of these chemicals—tracking emissions, waste, and potential secondary impacts at every stage. Personally, I see this trend bringing more accountability and also sparking innovation. Some labs experiment with enzyme-based alternatives or new processes that reduce the need for aromatic amines altogether. Of course, tradeoffs remain. Certain properties—like chemical reactivity or pigment stability—aren’t so easy to replicate with greener substitutes, which means ongoing research and a willingness to adjust as new data comes in.
What really stands out in the story of 4-Amino-M-Cresol is how it keeps evolving along with advances in both research and industry. In cosmetics, consumer demand for reliable, lasting coloration that doesn’t compromise safety has led to more rigorous control of precursors and contaminants. Market leaders invest in cleaner synthesis routes and improved purification techniques. This creates a feedback loop: as the bar rises for both product safety and performance, buyers become more discerning, and manufacturers respond with better quality controls.
I’ve seen, through shifts big and small, how customer feedback and market trends become drivers for improvement upstream in the supply chain. People now want transparency, traceability, and data to back up purity claims. Some companies are even putting blockchain tags on raw materials to track every handoff. This level of granularity isn’t just for show. It prevents fraud, protects intellectual property, and gives researchers the confidence they need to invest time and money into novel uses for established chemicals like 4-Amino-M-Cresol.
Education and professional exchange push things forward too. The online communities of chemists, industrial hygienists, and process engineers have become powerful tools for crowdsourcing best practices and sharing troubleshooting advice. I remember times in the past when weeks would go by without a good answer to an unexpected side reaction. Today, a quick consult in a closed forum or virtual seminar can unlock solutions in hours. This interconnected knowledge helps prevent waste, lowers costs, and improves outcomes across the board.
Not all trends favor easy wins for chemical users. Enough concern exists about possible toxicity and environmental persistence that 4-Amino-M-Cresol has come under the microscope in some regions. In Europe, for example, personal care formulation rules have gotten stricter, especially for ingredients that may cause skin sensitization over time. Some companies have shifted toward multi-stage safety evaluations and more comprehensive end-use tracking, preparing for the possibility of future restrictions.
Researchers and manufacturers are exploring safer analogues or trying to develop combination formulations that lessen exposure risks. For those who handle 4-Amino-M-Cresol on a regular basis, this means constant vigilance. Health surveillance, better local exhaust systems, real-time air monitoring, and continual employee training form the backbone of modern safety culture. For many smaller labs, these steps may feel expensive or overdone, but the cost of skipping them often runs far higher in fines, downtime, or reputational risk.
Importantly, a balanced outlook offers the clearest path forward. A stubborn focus on minimizing chemical hazards—paired with a respect for established lab techniques—ensures that 4-Amino-M-Cresol and its cousins remain available where they are needed, but only as long as the benefits clearly outweigh the risks. There’s no magic bullet: incremental improvements in process, oversight, and substitution are the steady ways progress happens.
As markets, regulations, and technologies evolve, so too do expectations for the products that drive innovation. 4-Amino-M-Cresol occupies a special place here. Its reliability and defined reactivity have enabled big advances in dye chemistry, pigment formulation, and specialty organic synthesis. At the same time, its challenges—safety, sourcing, sustainability—create ongoing demand for vigilance and improvement.
Through my years talking with scientists, quality specialists, and industry watchdogs, I’ve learned the most costly mistakes come not from what a chemical can do, but from what gets overlooked in preparation or follow-up. Trusted sources, verified lots, robust safety programs, and willingness to revisit standard practice form a toolkit that protects people and projects alike. The E-E-A-T principles—experience, expertise, authoritativeness, and trustworthiness—offer a wise framework not just for describing chemicals, but for making daily decisions about how to source, store, use, and ultimately retire them.
Solutions don’t always look like breakthroughs. Slow, steady progress—one improved guideline, one safer process, one better sourced lot at a time—creates the future most people in this field want to see. As the needs for pigments, intermediates, and specialty organics grow ever more sophisticated, keeping a handle on both upside and risk makes sure chemicals like 4-Amino-M-Cresol serve as tools for good. There’s pride in getting each detail right, and even greater satisfaction in knowing the next person to use these compounds will benefit from lessons already learned.