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HS Code |
848601 |
| Iupac Name | methyl 2-(acetyloxy)benzoate |
| Cas Number | 119-36-8 |
| Molecular Formula | C10H10O4 |
| Molecular Weight | 194.18 g/mol |
| Appearance | colorless to pale yellow liquid |
| Boiling Point | 220 °C |
| Melting Point | -8 °C |
| Density | 1.18 g/cm3 |
| Solubility In Water | slightly soluble |
| Smiles | COC(=O)C1=CC=CC=C1OC(C)=O |
As an accredited Acetylsalicylic Acid Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Acetylsalicylic Acid Methyl Ester, 25g, supplied in a sealed amber glass bottle with tamper-evident cap and detailed labeling. |
| Shipping | **Shipping description for Acetylsalicylic Acid Methyl Ester:** Acetylsalicylic Acid Methyl Ester should be shipped in tightly sealed containers, protected from light, heat, and moisture. Transport in compliance with local, national, and international regulations. Ensure proper labeling, documentation, and handling as a potentially hazardous chemical. Avoid contact with oxidizing agents and keep away from incompatible substances. |
| Storage | Acetylsalicylic Acid Methyl Ester should be stored in a tightly sealed container, away from light, humid conditions, and sources of heat. Store at room temperature, ideally between 15–25°C (59–77°F), in a well-ventilated, dry area. Keep away from incompatible substances such as strong oxidizers. Ensure proper labeling, and store in compliance with local chemical storage regulations. |
Applications of Acetylsalicylic Acid Methyl Ester in Industrial ManufacturingAcetylsalicylic Acid Methyl Ester provides functional value in specialty chemical manufacturing and intermediate processing across select downstream industries. Our facility delivers production-grade material conforming to end-use specifications, focusing on four core segments with established market adoption. 1. Active Pharmaceutical Ingredient SynthesisPharmaceutical manufacturers adopt Acetylsalicylic Acid Methyl Ester as a methylating agent and a key synthon within multi-step organic synthesis for selective active pharmaceutical ingredients. It enters the API pipeline during late-stage amidation and esterification, contributing to the structure of targeted analgesic and antipyretic intermediates. Utilization requires precise control of purity, trace residues, and consistent batch-to-batch supply. Customers adjust ratio dependent on pathway reactivity, impurity formation, and regulatory batch declarations. Industry compliance standards
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2. Fine Chemical Building Blocks ManufacturingAcetylsalicylic Acid Methyl Ester serves chemical manufacturers as a platform building block in the production of high-purity assignment esters and functionalized specialty intermediates. It enters as a feedstock for further transformation, supporting synthesis routes of targeted ether, ester, and amide molecules. Quality requirements center on residual solvents and stable methyl ester content. Operators control dosage based on stoichiometry and desired conversion yield to final derivative. Industry compliance standards
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3. Industrial Analytical Standards FormulationLaboratories and certified analytical manufacturers employ Acetylsalicylic Acid Methyl Ester for preparation of calibration standards and reference solutions essential for chromatographic quantitation. Material characterization relies on strict control of assay, moisture content, and absence of interfering impurities to meet trace analysis methods for pharmaceutical and food quality labs. Producers formulate at specific concentrations to match end-user method requirements, shipping under sealed inert conditions. Industry compliance standards
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4. Polymer Additives and Modification AgentsSelect polymer producers incorporate Acetylsalicylic Acid Methyl Ester as a functional additive for precise surface modification and branching during copolymer or specialty resin fabrication. Material input focuses on utility in engineering plastics where controlled ester linkages impart modified solubility or processability. Application requires close monitoring under extrusion or reactive blending environments to achieve targeted polymer architecture, with dosage calculated relative to polymerization feedstock. Industry compliance standards
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Not every chemical in our catalog sparks the same curiosity as the one derived from the backbone of aspirin—Acetylsalicylic Acid Methyl Ester (commonly known by chemists as Methyl 2-acetoxybenzoate). Manufactured for precision applications, this ester offers a distinct profile that sets it apart from standard acetylsalicylic acid derivatives. We craft our batches under tight conditions, working directly with pharmaceutical and chemical research clients who challenge us to deliver high-purity products for delicate reactions, new product development, or specific analytical needs.
Chemically, Acetylsalicylic Acid Methyl Ester brings a methylated twist to acetylsalicylic acid’s functional structure; the addition of a methyl group changes both the molecule’s reactivity and solubility. A closer interaction between our chemists and end-users often reveals how this property can mean better control in targeted esterification or transesterification reactions, reduced side products, or an improved profile when exploring new synthetic routes.
As a factory rooted in decades of organic synthesis work, our approach always begins with the sourcing and handling of raw materials. We never lose sight of how minor impurities can amplify downstream—each step is measured, tracked, and optimized. Synthesis of this compound involves careful control during methylation to avoid byproducts that would compromise assay or stability. Every drum, wide-mouth jar, or bottle leaving our plant comes with a complete batch history. Typical purity for Acetylsalicylic Acid Methyl Ester hovers well beyond 99%, with HPLC, NMR, and GC documentation available for every lot.
Customers in the pharmaceutical sector often remind us that specifications aren’t just numbers—they’re the fine line between research success and failure. That explains our investment in in-house equipment upgrades: routine calibration of spectral equipment, cross-validation of results between methods, and a renewed commitment to training our senior chemists in method development. If a customer requests a customized assay or impurity profile, our lab team dives deeper to run problem-solving experiments rather than stick to the minimums.
Rather than toss out a string of catalog numbers, let’s focus on qualities that matter most in everyday use. We produce Acetylsalicylic Acid Methyl Ester as a white to off-white crystalline powder, formulated for easy measurement and integration into various workflows. Melting range reliably hits in the 58–62°C window, which ensures a predictable physical state for storage and handling. We guarantee low moisture content to prevent hydrolysis and an impurity profile verified by state-of-the-art chromatographic methods. Packaging is adapted for scales from early-stage research to pilot plant operations, with size flexibility that comes from operating our own filling and sealing lines. Safety information, COAs, and analytical printouts travel with each shipment.
As experienced chemists, we know how different specifications matter to different buyers—whether for recrystallization studies, advanced intermediate synthesis, or formulation trials. Bulk orders benefit from production runs tailored around tight turnaround times and customer batch reservation, which comes from our direct manufacturer-to-client relationship.
On the application front, we see the demand for Acetylsalicylic Acid Methyl Ester growing steadily among custom synthesis companies, pharmaceutical research institutes, and academic labs. The molecule becomes a trusted building block in the quest for new analgesics, anti-inflammatory agents, and even for synthetic analogs targeting specific therapeutic indications. Researchers use its methyl ester function for selective protection in stepwise organic synthesis, creating functionality that pure acetylsalicylic acid cannot deliver in the same context.
In manufacturing, our clients count on this compound to streamline workups. Its improved solubility in non-polar solvents compared to standard acetylsalicylic acid can edge reaction yields higher or help in separating intermediates by extraction. We’ve seen feedback where switching to the methyl ester during key synthetic steps cut hours off processing times, reduced the need for additional purification, and simplified isolation of the final product. Those time and resource savings mean more than numbers—they support cost competitiveness and workflow reliability, which become critical at scale.
Another notable trend involves analytical laboratories using Acetylsalicylic Acid Methyl Ester as a reference or calibration standard. Its sharp chromatographic behavior and predictable NMR spectra provide reliable benchmarks for method development. We provide technical support and run inter-laboratory comparisons when needed to help resolve unexpected analytical questions or to troubleshoot anomalous data.
Acetylsalicylic Acid Methyl Ester draws clear lines of distinction against its parent acid and against other esters like the ethyl or propyl variants. The underlying methyl group influences not just volatility, but also metabolite pathways and synthetic flexibility. In workup and purification, this can mean avoiding the need for repeated chromatographic runs or eliminating stubborn side products that would appear with a bulkier ester moiety.
When our factory’s research team runs comparative tests, we monitor for hydrolytic stability, solvent compatibility, and temperature resilience. Some clients whose methods stalled using acetylsalicylic acid have pivoted to the methyl ester and cleared synthetic hurdles with better results. The industry's push to streamline multi-step synthesis for APIs (active pharmaceutical ingredients) draws a hard line—the easier a protecting group can be introduced and then cleaved, the better. The methyl ester provides a smart balance, serving as a protecting group that resists mild base and acid exposure but surrenders under more forceful hydrolysis, giving chemists one more lever to pull in complex sequence designs.
This ester also carries a lower tendency to crystallize prematurely during cooling, compared with the ethyl or propyl esters. That allows for more manageable solvent evaporation and a smoother transition through intermediate handling. We’ve adjusted our packaging protocols in response to customer plant feedback, adding extra anti-static liners to prevent cohesion issues common with fine crystal powders.
One advantage of being a direct manufacturer is flexibility in meeting both high-volume and customized research needs. Production-scale clients expect reliable, repeatable quality and complaint-free handling, which only comes from hands-on control over the synthesis and packaging process. That means regular maintenance on reactors, more frequent quality checkpoints, and direct feedback channels with production chemists. Research-focused customers often need highly detailed documentation, include mass spectral data, and sometimes additional studies on byproduct identification—services we provide with the same intensity as our large contract lots.
During scale-ups, subtle physical and reactivity differences become significant. A batch too prone to caking or carrying trace moisture can cause downstream issues. Our teams learned this through years spent troubleshooting plant floor errors and working with process engineers to redesign reactor temperature profiles or agitation speeds. We often run small-scale pilot batches to iron out unseen issues before committing to metric-ton production runs. Our goal has always been aligning plant realities to the expectations of downstream users.
With repeated large-scale synthesis, we face challenges of solvent recovery, waste management, and meeting ever-stricter environmental standards. Tight controls on emissions and rigorous post-reaction neutralizations keep waste below legal thresholds. Solvent systems are re-evaluated and swapped out where safer alternatives exist, and effluent testing is routine. Our clients benefit from this, as sustainability steps upstream mean fewer headaches during audits and downstream processing.
Feedback from our partners keeps us alert to new pain points. Sometimes customers find unpredictable behavior when switching between ester types from different sources. We respond by running parallel analyses to highlight deviations in crystallinity or ease of dissolution and looking deeper into how our process impacts the product’s performance. Several clients have approached us looking for improvements over generic supply chain solutions, and our tailored formulation adjustments have helped them avoid delays, optimize yields, or reduce lab downtimes.
Consistency drives so much of what research and manufacturing customers need. Whether talking about melting points, color, flowability, or impurity levels, tight control is key. Failures in these areas quickly become evident in inconsistent analytical data or during upscaling—lessons we’ve collected both from our own mistakes and from the candid stories customers share with us. By responding directly with adjusted drying cycles, changed storage recommendations, or tailored batch splits, we help keep projects on track.
Reformulation requests push us to tweak reaction times, catalyst loading, or purification steps. In some cases, requests for higher purity grades for trace analysis move us outside our routine comfort zone. Our setup allows us to respond quickly—testing new approaches internally and cross-checking any new impurity patterns or trace residual solvents. Only when our technical and QA leaders sign off on the repeatability do we move the revised grade into regular production.
The shift towards green chemistry principles also shapes our manufacturing philosophy. Our teams regularly assess production flows to cut back on solvent use, lower reaction temperatures, or select less hazardous reagents. Any change that reduces handling risk or environmental impact adds value—not just for our company, but for every downstream user who has to account for these factors in their compliance frameworks.
Years of manufacturing this compound reveal insights the textbooks sometimes overlook. While product catalogs often focus heavily on technical parameters, in real world use the story is shaped by actual handling, reproducibility, and process fit. Chemists in our plant continue to field questions about reaction setups, post-synthesis purification, and unexpected impurities. They build this experience into each production campaign, making small but meaningful adjustments each season as regulations and analytical standards evolve.
Significant time and resources are spent annually on keeping our assays and documentation aligned to the latest pharmacopoeial or internal customer standards. A robust feedback loop connects plant operators, analytical specialists, and corporate QA, ensuring nothing gets missed between production and delivery. By the time our Acetylsalicylic Acid Methyl Ester reaches a customer’s bench, it carries both the technical assurance and practical know-how that marks every good chemical manufacturer’s output.
Pharmaceutical companies pursuing new aspirin analogs, specialty chemicals firms building bespoke intermediates, and academic labs probing new methodologies all rely on the reliability of this ingredient. Their success, in turn, drives our commitment to producing Acetylsalicylic Acid Methyl Ester that meets not just the letter, but also the spirit, of their research goals.
As industry shifts in response to regulatory tightening, environmental priorities, and the demand for even cleaner starting materials, our processes will continue to evolve. Automation and process analytics increasingly support quality objectives—so we invest in training and updating our methods. In practice, this means more in-line monitoring, quicker response times for process deviations, and the ability to trace every kilogram’s journey from raw material to final shipment.
The demand for transparent traceability, especially in regulated industries, has shaped our investment in batch tracking, data integrity, and digital archiving. Our teams respond to audits with a spirit of openness and continual improvement. We push for process updates that help keep analytical data robust and documentation seamless, anticipating needs before they grow into operational bottlenecks.
As the chemical sector emphasizes safety and sustainability, we look for chances to transition legacy processes to greener alternatives. Staff are encouraged to spot waste, raise safety concerns, and propose alternative ways to achieve equal or better results. The push toward less hazardous reagents and safer plant practices now shapes process development more than ever, reflecting our responsibility not only to immediate customers, but to the wider community.
The story behind each bottle or drum of Acetylsalicylic Acid Methyl Ester involves a close partnership among plant floor workers, analytical chemists, compliance auditors, and, perhaps most importantly, our customers themselves. Every formulation improvement, packaging innovation, or upgraded instrument stems from feedback or a new regulatory shift. Real-world needs—whether for a tweaked impurity threshold, superior solubility, or robust supply—inform our everyday practices.
As we look ahead, staying close to the pulse of both research and industry standards ensures that our future batches of Acetylsalicylic Acid Methyl Ester will continue to raise the bar for quality, reliability, and service. Rather than chasing the lowest price, responsible manufacturers invest in know-how, adaptability, and direct customer engagement. The result: products that fit the needs of today’s synthetic chemists and remain reliable, safe, and efficient building blocks for the innovations yet to come.