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HS Code |
907763 |
| Cas Number | 21340-23-2 |
| Molecular Formula | C8H8N2O3 |
| Molecular Weight | 180.16 g/mol |
| Iupac Name | 4-Methyl-3-nitrobenzamide |
| Appearance | Yellow solid |
| Melting Point | 186-190 °C |
| Synonyms | 4-Methyl-m-nitrobenzamide |
| Solubility | Slightly soluble in water |
| Smiles | CC1=CC(=CC(=C1)N(=O)=O)C(=O)N |
| Inchi | InChI=1S/C8H8N2O3/c1-5-2-3-6(8(9)11)7(4-5)10(12)13/h2-4H,1H3,(H2,9,11) |
| Pubchem Cid | 224803 |
As an accredited 4-Methyl-3-Nitrobenzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Methyl-3-Nitrobenzamide is packaged in a sealed amber glass bottle, labeled 25 grams, with hazard and handling instructions. |
| Shipping | 4-Methyl-3-Nitrobenzamide is shipped in tightly sealed containers under dry, cool conditions to prevent degradation and ensure safety. Packaging complies with chemical transportation regulations, including proper labeling and documentation. Handling precautions are observed during shipping to avoid exposure, spills, or environmental contamination, ensuring safe and compliant delivery to the destination. |
| Storage | 4-Methyl-3-Nitrobenzamide should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep it at room temperature and protect from moisture. Clearly label the container and follow appropriate safety protocols to prevent accidental exposure or contamination. |
Applications of 4-Methyl-3-Nitrobenzamide in Industrial Manufacturing4-Methyl-3-Nitrobenzamide serves as a key intermediate in advanced chemical synthesis for regulated industrial segments. Below are focused application scenarios with explicit compliance, ratio, process, and end product details applied by manufacturers in the actual downstream supply chain. 1. Pharmaceutical Synthesis: Active Pharmaceutical Ingredient (API) IntermediatePharmaceutical manufacturers use 4-Methyl-3-Nitrobenzamide as a core building block in the synthesis of specific heterocyclic compounds, which are then converted to therapeutic agents such as anti-inflammatory and central nervous system drugs. The compound enters the multistep organic synthesis stage after initial condensation, assisting in the selective introduction of nitro and amide functionalities. Process chemists adjust the loading of 4-Methyl-3-Nitrobenzamide depending on the specific route and targeted yield, ensuring strict traceability and impurity profiling throughout scale-up. Industry compliance standards
Typical usage ratio
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2. Agrochemical Production: Herbicide and Fungicide IntermediateIndustrial agrochemical formulators introduce 4-Methyl-3-Nitrobenzamide in the multi-step route to substituted anilines and benzamide-based herbicides or fungicides. Its functional group arrangement offers unique reactivity for selective functionalization, which supports the development of bioactive molecules for crop protection. Manufacturers rely on targeted dosing and containment protocols due to regulatory thresholds for active residue. Industry compliance standards
Typical usage ratio
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3. Dye and Pigment Synthesis: Aromatic Amine IntermediateCommercial dye and pigment manufacturers employ 4-Methyl-3-Nitrobenzamide during the creation of specialty aromatic amines. The compound serves in controlled reduction stages, generating amine intermediates for azo or anthraquinone dye molecules. Operators calibrate the reaction scale to maximize chromophore purity and consistency, aligning with textile and plastics application demands. Industry compliance standards
Typical usage ratio
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4. Specialty Polymers: Reactive Monomer PrecursorProducers of engineered polymers utilize 4-Methyl-3-Nitrobenzamide in synthesis chains where benzamide moieties impart enhanced thermal resistance and mechanical stability. Its controlled reactivity allows for customization in backbone integration, primarily in high-value sectors requiring robust molecular design such as electronic materials and specialty coatings. Industry compliance standards
Typical usage ratio
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In the dynamic world of organic chemistry, 4-Methyl-3-Nitrobenzamide stands out with its unique chemical structure and broad applications. Having spent over a decade dedicated to small-to-medium batch production of specialty chemicals, we’ve seen demand for this compound grow beyond expectations. Direct feedback from synthetic chemists, R&D groups, and our own pilot plant colleagues has shaped the way we approach its manufacture and delivery.
The chemical, known among our peers as 4-MNBA or sometimes by its CAS identifier 6306-26-3, belongs to the substituted benzamide family. It features a methyl group attached at the fourth position and a nitro group at the third on the aromatic benzene ring, giving it distinct physical and chemical properties. Over the years, we have optimized our synthesis to ensure high purity and batch-to-batch consistency, supporting both laboratory research and semi-commercial scale-up.
Reliability in this compound comes down to purity control and robust process monitoring. Minor variations in starting materials or narrower temperature windows during nitration steps can introduce side-products. It took us hundreds of pilot batches and repeated QA sampling to learn that the smallest shortcuts in purification influence downstream application results. Vigilance in process control allows us to ship 4-Methyl-3-Nitrobenzamide tested for organic and inorganic impurities through techniques like NMR, HPLC, and Karl Fischer titration. Our product specification reflects hard lessons from returns and unhappy emails—small oversights echo all the way to client labs.
Some of the largest gains for our clients come from our willingness to reformulate or respecify. A pharmaceutical team, for example, needed the compound as an intermediate for a kinase inhibitor project. Early on, they highlighted issues with residual solvents. We responded by modifying the recrystallization protocol and extending vacuum drying. That transparency in communicating batch data and matching their HPLC standards ensured they could run reproducible reactions and GMP documentation processes.
On the agrochemical side, one customer working on novel herbicide scaffolds shared that small quantities of residual metallic impurities—like iron from corroded reactors—led to side reactions during chlorination steps. They worked closely with our analytical lab staff to nail down acceptable ppm levels for metals, prompting us to update our vessel maintenance and storage materials protocols. Long after shipping, our technical managers kept open lines with their team to troubleshoot unexpected color formation or solubility hiccups during later stages.
Unlike many simple aromatic amides, 4-Methyl-3-Nitrobenzamide displays a moderate solubility profile in polar organic solvents. Based on our experience, users achieve clear solutions in DMF, DMSO, and acetone at moderate heating. Methanol and ethanol work well for recrystallization if gentle cooling is applied. Many standard nitrated aromatics release dust or fine powder during transfer—ours, thanks to precise crystallization and drying, pours smoothly and shows low static cling, making manual and automated handling straightforward during lab and pilot-plant transfers.
Storage discussions often crop up with transportation teams. Our compound maintains its integrity under ambient conditions, but for prolonged storage, we advise keeping packaging tightly closed and protected from light and humidity. Shelf-life studies in our own facilities confirm stability for well over a year under these measures. We use sealed polyethylene or lined metal drums for shipments beyond several kilograms, based on several incidents with older, card-paper barrels leading to unwanted absorption of ambient moisture.
Compared with similar nitrobenzamide derivatives, the combination of a para-methyl and meta-nitro group represents a sweet spot for reactivity and selectivity in synthetic sequences. For example, chemists synthesizing heterocyclic scaffolds find that the electronic push-pull between methyl and nitro groups leads to unique site-selectivity during further functionalization. We see reports that other isomers, such as 2-methyl-4-nitrobenzamide, lack this stability under strong basic or acidic aqueous conditions.
A handful of customers attempt to swap in 3-methoxy or unsubstituted benzamide analogues but report lower yields or issues with regioselectivity. Our technical service fielded a request from a peptide synthesis group attempting to use 4-nitrobenzamide as a coupling intermediate. They encountered partial reduction or color changes incompatible with their solid-phase resin. After consultation about electron-donating effects, our R&D partners recommended 4-MNBA, which solved purity and compatibility issues without changes to their workup steps.
Our catalogue doesn’t flood customers with a confusing array of variants. Over the years, two principal models have proven to satisfy almost every downstream use-case—standard research grade (99% minimum purity, white to faint yellow crystalline solid) and enhanced purity for pharmaceutical development (≥99.5% by HPLC, with certificate of analysis for trace metals, residual solvents, and water content <0.5%).
Our research grade version dominates sales to university labs, small molecule discovery groups, and analytical reference teams. The enhanced pharmaceutical grade emerged because a partner in drug development reported GC/MS-detectable phthalate traces, likely picked up during earlier plastic packaging production years. That single episode drove us to source medical-grade packaging and adopt rigorous testing protocols. Few clients need the enhanced purity, but those who do see tangible benefits in seamless regulatory filings and batch-release documentation.
No manufacturing operation is immune to setbacks. In early days, a batch of 4-Methyl-3-Nitrobenzamide failed to meet purity requirements due to a nitration step deviation—a transfer pump in a semi-continuous reactor leaked trace lubricants into the intermediate. Analytical staff flagged unexpected baseline drift on the HPLC, leading to stoppage and deep-dive root cause analysis. Rather than hiding the problem and blending the failed lot, our team reviewed—and then rebuilt—our preventive maintenance schedules. We shared incident documentation with our client, who appreciated the open communication and adopted similar safeguards in their pilot reactor trains.
Lessons like these underline the difference between a contract trader and manufacturers who truly own the process. Our operators know the quirks of every reactor, from gasket quality to historical pressure readings during exotherms. They keep logs of subtle color or viscosity changes during purification. Experience with thousands of well-characterized batches gives us a database of outcomes that helps predict and prevent future issues—skills impossible without hands-on stewardship.
Our involvement rarely ends at shipment. Many clients approach us for technical input, whether it’s troubleshooting a stalled reaction or interpreting unusual spectral data. Our in-house team includes chemists who have run these same reactions in reactors next to process engineers able to adjust for real-world plant-scale constraints. One drug discovery group struggled with an unanticipated side product during amide coupling. We traced the issue to minor solvent residues in their prep, traced against our own batch results, and co-developed a solution plan involving simple pre-drying steps.
Academic researchers sometimes need sub-gram samples with ultra-high purity for NMR or X-ray crystallography studies. In these cases, we offer controlled crystallization techniques and tailor the production to match single-crystal selection. Feedback from these projects translates into ongoing product improvements even for industrial scale batches. These nuanced tweaks wouldn’t be possible without direct access to our own equipment and a culture of open technical dialogue.
Substituted benzamide derivatives each bring subtle strengths and limitations. Through our own testing, 4-MNBA displays easier scale-up kinetics than 2-methyl or 4-chloro derivatives, thanks to the resonance stability imparted by the para-methyl group. Customers working under tight batch-cooling regimes report smoother temperature profiles during nitration steps, leading to more efficient yield and lower incidence of uncontrolled side reactions.
Advantages extend to downstream purification. Colleagues running flash chromatography for closely related isomers often report more complex separation and higher solvent consumption. With our 4-MNBA, tighter elution profiles cut prep time by up to 20 percent, saving labor and solvent costs. Compared to simple benzamide or 3-nitrobenzamide, our compound’s physical form allows automated powder handling with less airborne loss, reducing operator exposure and increasing batch reproducibility.
We find that not all differences show on certificates of analysis. Manufacturing at scale exposes hidden variables—particle morphology, moisture uptake rate, grinding compatibility, and cross-contamination risk from shared production trains. By owning every production step, we address these subtle quality markers head-on.
Stakeholder expectations around sustainability continue to rise. In response, our procurement team shifted toward regionally sourced aromatics where possible, reducing shipping emissions and supply delays. Technical staff optimized the main nitration reaction to reduce by-product formation, not only boosting desired yield but also cutting acidic waste streams by 15 percent over the last three years.
Solvent selection for crystallization and washing balanced process safety, operator health, and environmental regulations. We replaced some higher-VOC solvents with more benign alternatives after internal pilot runs showed comparable product quality. Daily practice from our staff—from training on chemical hygiene to routine residue collection—keeps us ahead of many regulatory audits and fosters a culture of accountability.
Encountering new client applications means pushing boundaries in both analytical predictiveness and scale flexibility. Some biotech customers have started exploring 4-Methyl-3-Nitrobenzamide as a scaffold in material science and dye chemistry, each introducing parameters outside traditional pharma or agrochemical requirements. Our technical staff continually updates analytical methods—NMR pulse programs, advanced LC/MS calibrations—to meet specialty tests.
Scaling batch sizes remains a running challenge. Clients running high-throughput screening want faster lead times on kilogram lots, while others need consistent gram-scale vials for ongoing exploration. Our investment in modular reactor systems and rapid-drying technologies came from seeing such fluctuations firsthand. Coordinating trials, documentation, and shipments demands genuine teamwork—logistics, technical, and operations groups keeping customer priorities at the forefront.
Compliance doesn’t end at GHS labels or customs paperwork. For pharmaceutical use, regulatory teams need full traceability—batch production records, analytical data, and material origins. Our team has built data management protocols around this need, linking raw material lot numbers to finished product through every production step. Audits and client site visits helped train staff on data integrity, bridging the gap between plant and laboratory.
Our document control team participates in project startup meetings, ensuring they understand each customer’s regulatory context. Experiences from FDA, EMA, and other agency audits have fed directly into how we compile and archive test results, change control logs, and material certifications.
Developing a product like 4-Methyl-3-Nitrobenzamide isn’t a solitary exercise. Our facility stands as part of a network—customers, raw material suppliers, R&D partners, and regulatory advisors all contribute to improvements large and small. By staying hands-on with every batch and open to ongoing feedback, we keep evolving. Our daily work—process monitoring, pilot-scale troubleshooting, and operator education—drives the incremental gains that make our version of 4-MNBA dependable.
End users gain the most from our willingness to share direct, unscripted insights, born of real plant-floor experience and honest feedback. Owning the chemistry, listening to customer feedback, and taking accountability for results define our approach and shape the path for future partnerships.