|
HS Code |
686298 |
| Cas Number | 603-99-4 |
| Molecular Formula | C7H7NO3 |
| Molecular Weight | 153.14 g/mol |
| Iupac Name | 3-methyl-2-nitrophenol |
| Appearance | Yellow crystalline solid |
| Melting Point | 67-71 °C |
| Boiling Point | No data available (decomposes) |
| Solubility In Water | Slightly soluble |
| Density | 1.33 g/cm³ (approximate) |
| Pubchem Cid | 10003 |
| Smiles | CC1=C(C(=CC=C1)[N+](=O)[O-])O |
| Flash Point | 170.6 °C |
| Refractive Index | No data available |
| Storage Temperature | Store at room temperature |
| Hazard Statements | May cause eye, skin, and respiratory irritation |
As an accredited 3-Methyl-2-Nitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 3-Methyl-2-Nitrophenol, with tamper-evident cap and hazard labeling for chemical safety. |
| Shipping | 3-Methyl-2-Nitrophenol is shipped in tightly sealed, chemically resistant containers to prevent leaks and contamination. It is packed with proper hazard labeling and documentation in accordance with local and international regulations for transport of hazardous chemicals. Shipping may require temperature control and is restricted to certified carriers. |
| Storage | 3-Methyl-2-Nitrophenol should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizers and strong bases. Keep it protected from light, heat, and moisture. Label the container clearly and store it in a designated chemical storage cabinet, following all applicable safety regulations and guidelines. |
Competitive 3-Methyl-2-Nitrophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615380400285
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Every batch of 3-Methyl-2-Nitrophenol we produce reflects a hands-on commitment to both precision and reliability. As a chemical manufacturer with deep roots in phenolic intermediates, we’ve witnessed the way slight differences in nitrophenol isomers can make or break a synthesis, especially in pharmaceuticals, agricultural chemistry, and dye intermediates. Our teams work each day with an acute awareness that this isn’t just a stock compound—our customers build new molecules on the foundation we provide. We understand how important it is to recognize not just the specifications, but the practical pressures and goals of the industries we serve.
The product 3-Methyl-2-Nitrophenol, with CAS number 603-99-2, comes to you after a carefully controlled process that balances purity, yield, and consistency. Our current model features a tightly specified purity threshold (not less than 99%), as determined by HPLC and supported by GC trace analysis. The compound typically appears as a yellowish crystalline powder. Melting points for our standard batches range from 94°C to 98°C, and we keep moisture and ash content well below industry norms with in-line NIR monitoring.
It’s easy to overlook details like color and melt consistency, but for manufacturers downstream of us, those issues surface fast when processing hundreds of kilograms at commercial scale. The appearance and solubility profile in polar and semi-polar solvents is especially critical in dye and pigment sectors, where even minor contamination leads to unpredictability in color development and final product appearance. We test regularly for trace iron, copper, and other transition metals since these cause downstream problems for many of our long-term clients in agrochemical synthesis.
We’ve supplied 3-Methyl-2-Nitrophenol to a wide variety of customers, but most requests cluster around three application types: specialty dye manufacture, selective pharmaceutical intermediate synthesis, and as a critical step in certain crop protection actives. This specific nitro derivative, with its methyl group at the 3-position, delivers selectivity advantages in electrophilic aromatic substitution—allowing for greater control in multi-step organic syntheses and less need for purification steps later in the chain.
Our long-term partners in the pigment field often comment that switching even a small portion of their feedstock to lower-purity product leads to batch-to-batch differences in shade strength. Few things create more headaches than a client calling about color drift in a key batch. Over the years, we’ve supported these customers by implementing routine spectral fingerprinting—using both UV-vis and FTIR—which assures reproducibility that holds up to third-party QC scrutiny.
In the pharmaceutical field, 3-Methyl-2-Nitrophenol has drawn particular notice as a building block for fine chemicals and active pharmaceutical ingredients (APIs). The ortho-nitro group preserves the aromatic ring stability during further transformations, while the methyl substituent tunes reactivity. This translates to higher yields and lower waste, which matters both financially and from a process safety point of view. One of our long-standing projects involved collaborating with a generics manufacturer aiming to remove a downstream chromatographic purification step—by supplying better input quality, we enabled real production savings and reduced solvent use.
There’s often confusion between 3-Methyl-2-Nitrophenol and its structural relatives, such as 4-Methyl-2-Nitrophenol or 2-Methyl-4-Nitrophenol. As the actual producer, we’ve characterized these differences through repeated pilot-scale runs and close work with R&D teams. The substitution pattern matters greatly—both for physical properties like solubility, and for downstream reactivity. For example, the mononitro substituted at the ortho position creates unique steric and electronic effects, which in some pharmaceutical syntheses cuts unwanted side reactions by as much as 20%.
Other grades and sources—often coming from contract tolling operations—can show broader impurity profiles, including traces of dinitro compounds or unreacted toluidine. These become problematic in many high-precision applications, especially in pharmaceuticals and specialty colorants. Our plant runs a continuous batch system with in-line GC monitoring specifically to control for these side reactions. The feedback loop helps us keep by-products under strict control, and routine comparison with competitor samples demonstrates clear differences in both impurity levels and the uniformity of physical characteristics.
Several times we’ve dealt with customers facing problems after switching from lab-scale purchases to bulk industrial lots from resellers. These complaints usually center on off-odors, unexpected coloration after heating, or gradual precipitation in otherwise stable solutions. We routinely address these by sharing comprehensive batch histories, traceability data, and contaminant reports, helping our customers troubleshoot not just the symptom but the underlying cause. From our experience, direct dialogue between manufacturer and end-user consistently leads to fewer unexpected failures on the line, compared to buying from trading houses or distributors.
Feedback from users drives our production philosophy. For example, our agricultural chemistry clients require rapid wetting and dissolution in both methanol and acetone. The standard grind and particle size can affect slurry preparation rates at scale. In our facility, we adjust mill settings between runs destined for different industry sectors. Over time, we’ve learned that even a slight change in crystal habit can shift handling characteristics in both automated and manual feed systems. We work with customers to match product form to their needs, whether that’s a finer crystalline powder or a coarser, free-flowing grade.
The effort pays off on both sides. Our sharper focus on customer process constraints—realities like dusting issues, caking, or equipment fouling—allows us to recommend variants with less risk of problems down the road. Dye manufacturers, for example, have pushed us toward greater tightness in iron and copper controls, while API producers request more rigorous ash-content monitoring. By openly sharing our analysis protocols and results, we’ve built trust that goes beyond the typical number-driven spec sheets.
From the warehouse floor to the reaction vessel, practical storage advice often stands apart from the technical literature. 3-Methyl-2-Nitrophenol requires protection from moisture and light, as the nitro group can degrade slowly, especially under alkaline conditions. We ship in double-lined drums and recommend transfer in low-humidity environments. Our technical support team works with facilities managers to set up humidity controls and proper PPE procedures, minimizing operator exposure and maximizing product shelf stability. By staying involved after delivery, we help maintain consistency from our storage to your production line.
We also update our recommendations as we learn more from customers’ day-to-day handling. For bulk end users running high-throughput blending or reaction steps, we stress the importance of staged material acclimatization—avoiding thermal shock or condensation risk, which can create localized caking or loss of flowability. By focusing on these nitty-gritty details, our product remains reliable not merely on paper, but in real, working plants.
Chemical manufacturing faces new expectations in every sector, and phenolic compound production is no exception. Environmental and safety standards are rising, and our approach continues to evolve. We recover by-products like sodium nitrate from our synthesis streams, aiming to minimize overall environmental load; these practices developed from the cumulative experience of decades in the field, not quick regulatory fixes.
Low-waste processes and green chemistry initiatives now shape our daily production routines. Our technical staff test alternate nitrating agents and greener workup procedures in collaboration with sourcing teams and external researchers. These changes take time to perfect, especially since small adjustments can ripple downstream, affecting product characteristics. In parallel, we’re engaging with our longtime clients to pilot closed-loop packaging systems. By reducing drum turnover and supporting reconditioning, we help tackle both cost and waste issues.
Partnering with academic groups, our R&D team explores new catalyst technologies to further cut solvent use and improve reaction selectivity. The focus remains not just on regulatory compliance, but on building a product lifecycle that sits well with future generations of chemicals policy and customer expectations.
3-Methyl-2-Nitrophenol serves different sectors in unique ways, but across dye, agriculture, and pharma, the real test of quality comes after delivery. As a manufacturer, we stand behind every lot—ready to support customers with data, advice, and direct technical input. Our investment in better analytical controls, customer-driven specification tweaks, and open feedback ensures that both quality and trust remain high.
Years in this business have shown us that even a well-characterized molecule like 3-Methyl-2-Nitrophenol benefits from straightforward, human communication. Our team keeps learning from each partnership, feeding real-world insight into every new batch. Whether troubleshooting a process hiccup or exploring greener production options, we’re always keen to share what works, what doesn’t, and why. In today’s rapidly changing chemical landscape, honest, evidence-driven relationships between manufacturers and users make the difference that routine specifications can’t capture.