|
HS Code |
721634 |
| Product Name | Methyl 4-(Butyrylamino)-3-Methyl-5-Nitrobenzoate |
| Molecular Formula | C13H16N2O5 |
| Molecular Weight | 280.28 g/mol |
| Appearance | Yellow solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in common organic solvents (e.g., DMSO, methanol) |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited Methyl 4-(Butyrylamino)-3-Methyl-5-Nitrobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle with secure screw cap, labeled “Methyl 4-(Butyrylamino)-3-Methyl-5-Nitrobenzoate, 25g,” hazard and storage information included. |
| Shipping | Methyl 4-(Butyrylamino)-3-Methyl-5-Nitrobenzoate is shipped in tightly sealed containers, protected from moisture, light, and extreme temperatures. Compliant with applicable chemical regulations, it is packed with appropriate labeling and documentation. Shipment is typically in small quantities via certified carriers, ensuring safe handling, and may require special hazard declarations depending on regional guidelines. |
| Storage | Store **Methyl 4-(Butyrylamino)-3-Methyl-5-Nitrobenzoate** in a tightly sealed container, protected from moisture and direct sunlight. Keep in a cool, dry, and well-ventilated place, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Clearly label the container and restrict access to trained personnel. Handle with appropriate personal protective equipment. |
Applications of Methyl 4-(Butyrylamino)-3-Methyl-5-Nitrobenzoate in Industrial ManufacturingMethyl 4-(Butyrylamino)-3-Methyl-5-Nitrobenzoate finds multiple applications as an advanced chemical raw material across specialized downstream industries. As an original manufacturer, we support bulk processing requirements, strict quality management, and regulatory compliance in high-value segments. Below, you will find detailed breakdowns of key industrial application fields with precise usage insights. 1. Pharmaceutical Intermediate for API SynthesisThis compound serves as an essential intermediate in the multi-step synthesis of selective antibacterial and anti-inflammatory active pharmaceutical ingredients, particularly within heterocyclic and nitroaromatic series. Process chemists rely on its nitrobenzoate framework to introduce targeted functional groups in the core stages of API route design. Operators use it during amidation, esterification, and subsequent reduction steps under controlled environments to avoid degradation, supporting batch or continuous production at scale. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Fine Chemical Building Block for Agrochemical SynthesisThis compound acts as a key structural intermediate for synthesizing substituted benzoyl derivatives used in crop protection actives. Agrochemical manufacturers employ it during the preparation of selective herbicidal and fungicidal esters, favoring its stable nitroarene core for further chlorination, acylation, and amination modifications. Batch reactors or continuous flow systems utilize this compound for high-yield coupling, targeting downstream registrations in regulated agricultural markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Key Intermediate for Specialty Dyes and PigmentsMethyl 4-(Butyrylamino)-3-Methyl-5-Nitrobenzoate provides a functionalized precursor in the synthesis of high-performance nitroaromatic and amino-benzene dyes. Industrial pigment producers incorporate its unique backbone for azo-coupling reactions, enabling deeply colored and lightfast organic pigments. Carefully controlled diazotization and subsequent coupling maximize chromophore yield for use in printing inks, textile coloration, and engineered plastics. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Intermediate in Functional Polymer Additive ManufacturingThe nitrobenzoate structure enables advanced performance in synthesis of polymer stabilizers and UV absorbers. Additive producers integrate the compound during high-shear mixing and co-polymerization for development of UV-resistant and anti-degradation agents in plastics. Its reactive moieties allow for covalent bonding with macromolecular chains, supporting enhanced weatherability and long-term color retention in molded and extruded goods. Large-scale compounding operations value precise feed rates to achieve regulatory compliance and cost efficiency. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive Methyl 4-(Butyrylamino)-3-Methyl-5-Nitrobenzoate prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Manufacturing a specialty compound like methyl 4-(butyrylamino)-3-methyl-5-nitrobenzoate demands more than precision and chemistry. Each decision involved in scale-up work, purification, and final quality checks rests on direct industry experience and the consistent challenge of repeatable results. In our labs and plant, our technicians don't just monitor parameters—they know how those numbers correlate with reaction health, impurity risks, and downstream stability. Over the years, this product has shown a set of strengths that make it stand out, especially for research, development, and scale-up partners demanding a clear audit trail and tight analytical control.
The structure of methyl 4-(butyrylamino)-3-methyl-5-nitrobenzoate is not unique in having bioactive potential, but the triple substitution pattern—nitro, methyl, and butyrylamino—expands options for further derivatization when compared with simple benzoates or single-substitution analogs. Through repeated synthesis, we have observed that the butyrylamino group, positioned para to the ester, brings improved solubility in polar aprotic solvents. This makes the material easier to integrate in multistep synthesis or for use as an intermediate in pharmaceutical and agrochemical research. Lab results and feedback from several formulation teams point toward smoother downstream purification and increased recovery over structurally similar esters that lack the nitro or methyl ring substitutions.
We notice a surge in requests for samples targeting pharmaceutical lead discovery and crop-protection R&D. Research investigators value this product most when they run parallel reactions and want to see how multiple substitutions on a benzenoid core affect the outcome. Linked with our own experience, the unique substitution arrangement reduces issues tied to isomerization or byproduct formation that can emerge in less densely substituted benzoates. Even skilled teams, we find, experience fewer chromatographic headaches and cleaner NMR integrations when running our batches through their workflows.
Our standard model offers methyl 4-(butyrylamino)-3-methyl-5-nitrobenzoate in a fine, pale yellow crystalline form. Over multiple campaigns, we refined the drying protocol to achieve consistently low residual solvent levels without thermal decomposition—a problem that can hit yields and shelf life if ignored. Every batch draws samples for melting point analysis and HPLC purity. Over the last year, typical purity tracks above 99%, with tightly controlled limits on single impurity classes. This didn’t happen overnight: maintaining crystal morphology that helps users dose precisely, while also meeting particle-size specifications for easy transfer, required iterative reworking of filtration and milling setups on our shop floor.
From the feedback we gather, product consistency means fewer surprises during method transfer or scale-up steps. Users who need larger lots for pilot-scale runs do not see lot-to-lot variability in their critical reactions or in subsequent analysis, which used to be a routine headache in earlier years when we depended on less precise controls and bulk purification steps. In a world where missing a project milestone by a week means losing the confidence of a research sponsor, those details matter greatly. Our laboratory teams understand that chasing tiny traces of byproduct, optimizing every degree of crystallization, and building traceability into each order separates a routine supplier from a reliable partner.
Chemists often need to tweak activity or absorption by modifying aryl esters in their discovery pipelines. Methyl 4-(butyrylamino)-3-methyl-5-nitrobenzoate serves as a valuable intermediate in several synthetic routes leading to heterocyclic frameworks, peptide mimics, and novel small molecules. The butyrylamino modification expands the usable chemistry, introducing flexible options for subsequent linkage to amines, alcohols, or active heterocycles. In agricultural research, structural analogs have shown value against certain fungal and herbicidal targets, prompting increased interest from field study teams. Direct communication with R&D groups confirms that access to reliable, scale-ready portions of this compound reduces bottlenecks and enables more meaningful structure–activity relationship (SAR) mapping over a broad series of targets.
We track usage trends and see that customers are applying this material to template new derivatives with potential anti-inflammatory, antibacterial, and enzyme modulation properties—not only as a simple scaffold, but as a versatile building block. By offering specialized particle size control or further processing such as conversion to the sodium salt, we help bridge the gap from concept chemistry to workable formulations. Developers then move more rapidly to preclinical screening or formulation optimization, significantly narrowing the gap between lab-scale discovery and real-world application.
This compound is distinguished by both the chemistry and the manufacturing journey. Many suppliers propose standard methyl benzoates, often with no more than a single functional group exchange. These simpler variants usually cannot offer the same reactivity spectrum or processability. In daily practice, this means that scientists mixing and matching building blocks do not see the broad window for property tuning a more complex molecule like ours delivers. We charted the number of side reactions and purification difficulties encountered with less substituted benzoates and found that users spent up to 40% more time recovering pure product or verifying quality when dealing with simpler structures. This product’s stability under various conditions offers clear differentiation: researchers pushing into higher temperature or longer duration chemistry report less breakdown and better mass spectra recovery, which ties back to the synthesis and crystallization controls we established after repeated pilot runs.
Our team knows the difficulty of cleaning up after sub-par feedstocks. Repeat customers often mention how switching to our methyl 4-(butyrylamino)-3-methyl-5-nitrobenzoate helped widen the process window and open up routes that weren’t viable with direct market analogs. These differences originate in the manufacturing cycle: employing advanced moisture and impurity removal techniques, verifying every lot through a combination of TLC, HPLC, and NMR, and rapidly troubleshooting any deviation from prior batch history. Years working directly with process engineers and research users shaped our decision-making for solvent selection, work-up protocols, and packaging choices, which all contribute to a better experience downstream. We remember the frustration of a fouled process or delayed shipment and use that institutional memory to anticipate how things can go wrong so buyers aren’t left cleaning up after another supplier’s shortcuts.
Success in this business means more than order fulfillment. It comes from a long-term perspective—knowing that lab staff, process engineers, and formulation scientists need something more than a certificate of analysis. We dig into every shipment, pulling samples, cross-checking all analytical runs, and creating a transparent chain of data behind every lot. This helps teams who must meet external compliance, especially in regulated environments, but the discipline spills over to industrial and academic users as well. In recently completed customer audits, all questions on trace contamination and consistency found answers in our records—a benefit to teams developing clinical candidates, scale-up runs, or patent-protected formulations.
The way the plant is set up integrates control of every step from raw material intake to packaging, ensuring low risk of cross-contamination. By running closed-system drying and crystallization cycles, we keep environmental loads down and reduce worker exposure. A few years ago, a strategic decision led us to restructure packaging flows, using multilayer barrier containers to combat the slow hydrolysis that can degrade ester-containing intermediates during international shipping. Several partners reached out to thank us after noticing improved stability over six-month storage, even after repeated opening in humid climates. These practical, ground-level decisions give users confidence to allocate resources to product development rather than product trouble-shooting.
Market requirements change rapidly. Trends come and go, but the need for trustworthy, well-characterized specialty chemicals remains steady. In our experience, scaling up new batches of methyl 4-(butyrylamino)-3-methyl-5-nitrobenzoate highlights the value of real-time process feedback. Teams monitor all critical reaction stages, logging deviations to a central repository. Cross-functional reviews spotted patterns—such as how minor variations in base addition linked to product stability and purity. This led to strict refinement in reagent delivery and mixing times, reducing process variations from one batch to the next. Quality teams independently verify all process documentation and analytical runs, following validation models shaped by years of customer audits and market regulations.
This learning extends into waste management and sustainability. Handling nitro-aromatic intermediates can generate specific safety and environmental questions. Drawing from our direct process experience, the plant standardized effluent separation procedures and updated scrubber capacity to meet tighter local standards. This represents more than compliance—it shapes material choices and encourages teams to minimize waste generation at every point, whether planning pilot runs or large-scale output. Some scientists on our team remember the painstaking cleanups of earlier years. The improvements reflect lessons learned, not mere policy shifts.
Just as much as we focus on product quality, we value close industry relationships. Early-stage innovators and full-scale production houses alike count on more than a material spec—they seek out collaborative troubleshooting and access to chemical know-how. We watch where our product is heading, supporting partners who need custom analytical support or process tweaks. Sometimes this involves tailored crystallization batches to minimize solvent inclusion; other times, customers ask for special documentation or shipment packaging to support international filings. We draw on crew members who remember ‘war stories’ of difficult projects and build that insight into every project proposal. These stories ground us—every unexpected delay, every unplanned filtration issue, every analytical deviation—they all shape a more responsive supply chain, benefiting everyone who counts on reliable methyl 4-(butyrylamino)-3-methyl-5-nitrobenzoate for demanding research or industrial milestones.
Batch after batch, product shelf-life stands out as a point of buyer concern, especially when coordinating delivery schedules across continents or managing inventory during uncertain demand cycles. Stability data, both on the bench and from stored product, bear out the effectiveness of our revised packaging and moisture control. Chemists notify us directly if packaging damage, anomalous color change, or odor occur during storage or transit. We rapidly follow up with root cause investigations and replacement as needed; experience tells us that trace package punctures or microleakage, if left unchecked, impact thousands of dollars in project costs and days of lost productivity. We built protocols that minimize packaging failures and empower users to store the compound under typical R&D or manufacturing conditions without fitting special climate controls.
Through repeated case-by-case follow-up, it became clear that the difference between a quarter-hearted generic and our purpose-focused specialty offering hinges on predicting issues before they matter. Knowledge gained by troubleshooting crystallization hiccups, understanding solvent compatibility for users blending in unusual matrices, and coaching teams in specialty applications all guide product handling improvements. In recent years, several firms rerouted their project plans after confirming rapid, consistent delivery of large-volume orders—something only possible through disciplined on-floor coordination and a network that learns from setbacks and keeps promises.
What separates manufacturing from trading is responsibility. Each kilogram of methyl 4-(butyrylamino)-3-methyl-5-nitrobenzoate reflects not just a lab protocol, but years of hands-on process trials, critical evaluation, and a continuous cycle of field-driven adjustment. We take pride knowing our customers rely on a team that owns every process detail, stands behind every shipment, and ultimately builds its name on the quiet successes playing out in labs and manufacturing suites around the world. For every project deadline kept, for every experiment that runs as planned, we hear from teams who remember disruptions caused by unpredictable product sources in the past. Those stories drive our focus—delivering a specialty chemical made with care, consistency, and a view toward every user’s success.
As applications for methyl 4-(butyrylamino)-3-methyl-5-nitrobenzoate continue to diversify, so do the expectations of research chemists and industrial engineers working at the edge of innovation. Recent collaborations explore not only novel pharmaceutical syntheses but also new applications in advanced materials and catalysis. We listen to the feedback from users conducting green chemistry, and wherever possible adapt synthetic strategies to reduce hazardous byproducts and streamline work-up steps. By integrating feedback loops between plant, analytical, and R&D partners, our teams keep improving not just the product, but the process as a whole.
Long-term reliability and real transparency form the backbone of this effort. We remain responsive to the shifts in regulatory environments, adopting stronger documentation, and maintaining a nimble supply infrastructure that supports sudden scale-ups or new project milestones. Every customer brings unique application needs—what remains constant is our commitment to clear communication, deep process understanding, and relentless pursuit of better outcomes for those relying on methyl 4-(butyrylamino)-3-methyl-5-nitrobenzoate in their next breakthrough.