|
HS Code |
800414 |
| Chemical Name | (S)-(-)-Methylsuccinic Acid Dimethyl Ester |
| Cas Number | 85753-45-1 |
| Molecular Formula | C6H10O4 |
| Molecular Weight | 146.14 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 87-88 °C at 9 mmHg |
| Density | 1.15 g/cm3 |
| Optical Rotation | -20° (c=1, CHCl3) |
| Purity | Typically ≥98% |
| Smiles | COC(=O)C(C)C(C)=O |
| Inchi | InChI=1S/C6H10O4/c1-4(5(7)9-2)6(8)10-3/h4H,1-3H3/t4-/m0/s1 |
| Solubility | Soluble in organic solvents |
As an accredited (S)-(-)-Methylsuccinic Acid Dimethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | (S)-(-)-Methylsuccinic Acid Dimethyl Ester is supplied in a 25g amber glass bottle with a tamper-evident screw cap and labeling. |
| Shipping | (S)-(-)-Methylsuccinic Acid Dimethyl Ester is shipped in tightly sealed containers under cool, dry conditions to prevent contamination and degradation. The package is clearly labeled, complies with chemical transport regulations, and is cushioned to avoid breakage. Hazard documentation and safety data sheets accompany the shipment for proper handling upon arrival. |
| Storage | (S)-(-)-Methylsuccinic Acid Dimethyl Ester should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protect it from moisture and direct sunlight. Store at room temperature or as specified by the manufacturer, and follow all safety regulations for chemical storage. |
Applications of (S)-(-)-Methylsuccinic Acid Dimethyl Ester in Industrial ManufacturingAs a dedicated producer of (S)-(-)-Methylsuccinic Acid Dimethyl Ester, we supply this chiral building block to major chemical sectors requiring consistent quality and strict adherence to process control. The following industries utilize our compound as a key intermediate or functional additive in specialized downstream production flows recognized under international regulatory frameworks. 1. Pharmaceutical Chiral SynthesisLeading pharmaceutical manufacturers incorporate this compound as a stereoselective intermediate for constructing active pharmaceutical ingredient (API) frameworks, such as β-lactam antibiotics and anticonvulsants. Its enantiopure nature aligns with regulatory demands for chiral purity in precision drug synthesis, entering the chemical route at early-stage condensation and coupling. Downstream processors reference validated quality control methods throughout multistep synthesis and purification, which ensures regulatory submission for global markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediates ManufacturingProducers of advanced agricultural actives use this dimethyl ester as a precursor for the synthesis of chiral herbicide and fungicide intermediates. Intake occurs at a key step where selectivity influences biological activity and environmental persistence profiles. Strict quality standards demand full traceability from each batch to ensure product stewardship throughout the crop protection compound’s lifecycle; this includes the adaptation of enantioselective ester hydrolysis and subsequent modification. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Polymeric MaterialsHigh-performance polymer manufacturers add (S)-(-)-Methylsuccinic Acid Dimethyl Ester during the synthesis of biodegradable polyesters and polyamides. Its chiral methyl branch introduces asymmetry tailored for specialty engineering plastics, targeting specific mechanical and degradation profiles. The compound enters melt polycondensation reactors under controlled temperatures, where feedstock purity ensures reproducible polymer characteristics demanded by international standards for food-contact and medical-grade resins. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Flavors and Fragrances SynthesisSpecialty aroma chemical firms utilize this chiral diester as a precursor molecule for constructing high-value fragrance intermediates and complex esters intended for food and personal care applications. Its stereochemistry enables the synthesis of nature-identical components essential for authenticity claims in natural-compliant formulations. Processing occurs under food-grade conditions, with batch traceability and allergen avoidance monitored to international food ingredient standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Fine Chemicals for Specialty SurfactantsManufacturers of high-performance surfactants employ this compound as a structurally defined diacid ester in the stepwise synthesis of enantioselective surface-active agents for industrial cleaning and microemulsion formulations. Chiral configuration enhances emulsion stability and substrate compatibility, directly affecting product functional properties. Production facilities conduct synthesis under closed, validated systems to meet stringent customer and regulatory audit trails. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive (S)-(-)-Methylsuccinic Acid Dimethyl Ester 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!
Long before a batch of (S)-(-)-Methylsuccinic Acid Dimethyl Ester leaves the plant, the process begins with understanding chemistries from the bench-top upwards. Our work draws deeply on years of hands-on experience handling stereoselective syntheses and esterification routes. Decisions at the synthesis stage—choice of raw materials, purification, esterification catalysts—directly affect finished purity, stability during storage, and suitability for use in chiral chemistry or pharmaceutical intermediates. Consistency grows out of careful control at every checkpoint, not from standard protocols but from paying attention to how real reagents react, even batch to batch.
In our manufacturing lines, the model for (S)-(-)-Methylsuccinic Acid Dimethyl Ester reflects that commitment. We choose glass-lined reactors for esterification because they resist corrosion, especially in acid chloride and methanol conditions. Temperatures and residence times receive daily review based on actual yield and color, not just set points handed down by a consultant. Isolation of the target compound relies on distillation techniques dialed in through experience—getting the product free from methylsuccinic monoesters or residual acid rarely happens on the first attempt. Seasoned operators have learned by trial and error where small changes in water content or methanol purity impact the methyl ester output.
Specifications for (S)-(-)-Methylsuccinic Acid Dimethyl Ester come about through genuine demand. In the real world, a fine chiral building block rarely needs to meet textbook '99.9% purity' figures, but it must minimize optical impurity and chemical side products below levels that interfere with downstream chiral catalysis or pharmaceutical synthesis. Our batches regularly achieve optical purities that have satisfied demanding pharmaceutical firms and research institutes, but purity, as any chemist on a prep scale knows, also means not bringing in potential headaches like high-boiling methyl esters or water-insoluble oligomers.
Many customers ask about the typical appearance or solubility of the methylsuccinic acid dimethyl ester. From our blending drums, fresh product runs clear, colorless to very pale yellow, with a mild, sweet ester scent. Viscosity remains low—so factory staff fill containers rapidly, and lab users never struggle to measure aliquots. Our trust in the material's consistency stems not from bureaucratic checklists but from years spent in the blending room and along loading docks, looking out for anomalies before they reach you.
Chemists talk a great deal about stereochemistry on paper. Putting this into industrial practice means walking a tightrope between downstream utility and manufacturing cost. The (S)-(-) enantiomer sets itself apart through its fit in enzyme-catalyzed reactions, chiral reductions, and as a precursor in active pharmaceutical ingredient syntheses that demand defined chirality. Each container carries a chiral GC or HPLC certificate proved out by our lab team—whose technicians have faced countless learning moments eking out signal separations barely apparent in messy raw mixtures.
In handling both (S)-(-) and racemic versions, practical differences show themselves in real reactions. The (S)-(-)-isomer offers improved selectivity in many organocatalytic steps and lower threshold for regulatory compliance in the pharma sector. Users of racemic product often face extra separation burdens at their own site; those burdens soak up time and budget. Over the years, our R&D chemists collected feedback directly from pilot customers who either reached for our resolved product, or struggled to split mixtures on their own and circled back for cleaner input materials. Those stories shape how tightly we monitor each batch and guide our ongoing investments in advanced resolution and purification methods.
Many datasheets describe a product’s flash point or recommended PPE but say little about what factory teams learn through daily use. Our plant’s experience with (S)-(-)-Methylsuccinic Acid Dimethyl Ester proves its storage demands less fuss than many active chemicals. It resists light-induced decomposition and does not polymerize under ambient conditions, so warehouse staff face fewer dramas moving bottles between cold and controlled ambient rooms. Still, the low viscosity does increase risk of spillage, especially during drum transfers on colder days. In our team’s experience, using the right gaskets and slow-fill techniques pays off more than simply reposting the MSDS on walls.
Over the years, our operators developed a keen nose for the material’s natural scent as a quick index of batch health. A sweet ester smell might signal a good batch, but a hint of burnt or chemical tang leads our QA crew to investigate before shipping anything downstream. Those subtle cues, learned from decades in the plant, keep waste low and customer rejections at rare levels.
Deploying (S)-(-)-Methylsuccinic Acid Dimethyl Ester outside the lab puts each batch to the test in complex organic syntheses. Our colleagues in the field report the methyl ester group’s behavior during hydrogenation or transesterification proves robust; incidental hydrolysis forms the expected methylsuccinic acid without unwanted byproducts clogging downstream filtration or chromatography. When paired with base-catalyzed steps, this ester resists saponification long enough for high conversion in many industrial process cycles.
Pharmaceutical end-users typically request background on impurity profiles, since any side-product can complicate API registration. In our work serving process development partners, we've found that delivering a consistently clean GC profile takes blending know-how—sometimes it’s more about timing and order of addition than raw analytical numbers. Getting feedback on scale-up performance—such as how esters hold up during multi-kilo reactions or whether storage stability meets the mark—has spurred us to tighten control points in both raw material purchase and final line-off.
These practical lessons, drawn from hard-won trial and error, matter more on factory floors than tidy technical data. We design production around not just purity but also process robustness—because in pharma and specialty chemicals, reliability over time means more than chasing a notional yield percentage.
We often field questions about how our methylsuccinic acid dimethyl ester matches up to its diethyl or racemic cousins. Side-by-side in the reaction flask, the dimethyl ester regularly shows quicker participation in some condensation reactions and better purification by simple distillation—a direct result of its lower molecular weight and higher volatility. In storage, our experience shows the dimethyl variant absorbs less atmospheric moisture than higher alkyl esters, which reduces hydrolysis during transit and lengthens shelf life, especially in humid climates or long-haul shipping.
Chiral selectivity stands apart, too. Many customers working in asymmetric synthesis prefer our (S)-(-)-isomer over the racemate not only for regulatory reasons but because it removes a major variable from pilot-scale optimization. Diethyl or isopropyl esters, for all their utility, require higher activation energy for the same transformation and often leave behind more persistent byproducts due to bulkier leaving groups. These nuances surface directly in our continuous dialogue with formulation chemists and bench researchers—people who report their real outcomes, not just wish-list specifications.
Maintaining supply quality stands as a daily challenge, not a slogan. In real business, the headaches show up in the form of late railcars, equipment downtime, weather that clogs up shipping lanes. Our staff has lived through chemical shortages, working not just as process chemists but as logistics planners, batch adjusters, and midnight troubleshooters. Delivering (S)-(-)-Methylsuccinic Acid Dimethyl Ester batch after batch under variable conditions takes honest communication both up and down the chain.
Our crew stays directly connected with technical queries, whether a researcher needs milligram samples or a process manager requires drums for a continuous flow plant. The conversations that leave the biggest impression aren’t about technical tables but whether the ester arrives within the window someone crucially needs for a clinical batch or pilot run. We’ve learned to predict bottlenecks based on the seasonal swings in raw material supply and the super-short windows our customers face, particularly in the leadup to regulatory filings or time-sensitive projects.
Over the last decade, our shop has steadily moved toward greener processes in methyl ester production. Reducing process waste, energy use, and risk of exposure for operators began as a cost-saving effort and became part of how managers and floor staff think about daily tasks. The (S)-(-)-isomer now comes from resolution techniques that minimize organic solvent waste, and distillation setups are continually tweaked for lower environmental footprint. Every modification in procedure comes out of group discussions: what worked, what held up scale-up, where solvents could be swapped or reused safely.
Our process chemists have found key opportunities to minimize byproduct formation through in-line analytics and reduce the frequency of cleaning campaigns with better heat-exchanger maintenance. Safety rounds include real walkthroughs, not box-ticking exercises, with every incident or near-miss providing fuel for system redesigns. These daily habits make a difference not only in economics but in the carbon footprint of each finished drum leaving the gates.
Every week, someone on our team talks with chemists, formulators, or project buyers who have frontline experience with the material. Our feedback loop involves not just sending out a quality survey but understanding whether a batch did the job in actual trials. If a researcher reports a purification snag or changes in solubility, we backtrack to investigate any upstream tweak we made, no matter how minor.
We’ve seen that trust comes not from perfect paperwork but from genuinely helping a partner solve a formulation snag, rerouting a shipment, or reanalyzing a batch that didn’t meet a specific application need. These calls take time but provide insights that drive our improvement efforts far more than reading regulatory circulars or chasing arbitrary targets. Chemists at our site share not only stock answers but war stories—how a particular batch handled on Friday compared to one made mid-week, or why a specific drum survived an ocean crossing better than predicted.
Over the years, not every batch runs without a hitch. We recall times a methylsuccinic acid dimethyl ester crystallized unexpectedly during winter shipment, gumming up drum pumps on arrival. Each incident presses us to rethink container specs, winterize storage, and, crucially, coach distributors on best handling during cold snaps. On the flip side, improvements in batch scheduling and resin selection for gaskets came about only through hard experience and persistence, not wishful thinking.
Our product’s journey—as a chiral building block, a specialty intermediate, or a reference sample—runs parallel to the demands of a global market that prizes transparency and speed. We often share technical briefs showing how a specific lot fared over time, whether the ester retained its clarity, whether the chiral GC spots lined up batch after batch, and what factors might have played a role if results shifted. Chemistry moves fast; so do the expectations of the labs and plants that depend on us.
It’s one thing to talk about top-end purity and packaging. The greater value arises when repeated orders show no surprises—no sudden color change, no new contaminant peaks, no shipping delays. We follow changes in global compliance regulations, making sure that our methylsuccinic acid dimethyl ester’s certificate matches up with the shifting requirements for chiral intermediates in pharma pipelines and specialty materials. Batch after batch, the job is delivering the right material at the right time. In the real world, that matters far more than theoretical maxima.
On a practical level, our R&D team holds quarterly reviews of customer field reports, solubility tests against shifting solvent specs, and close analysis of chromatographic retention times. Each review shapes the next production run, not in isolation but by building on real-world feedback. If a problem crops up—incompatibility in a new solvent blend, a change in crystalline form, or a dropout in optical rotation—our crew responds quickly with follow-up batches and, if needed, line-by-line process reviews. Chemistry production, as we see it, responds directly to the actual tables and reactions our partners work through, not just numbers on a sales flyer.
Our future in (S)-(-)-Methylsuccinic Acid Dimethyl Ester production sits where practical chemistry and hands-on troubleshooting meet. The road ahead asks us to keep learning from the ground up—using better sensors, training up the next crew of plant chemists, and keeping quality controls fluent and flexible as needs evolve. Every year brings a fresh round of innovations from our team, like running continuous flow trials, working with university partners on greener catalysts, or investing in smart packaging to reduce waste.
Whether you’re looking for kilogram lots for scaling up or carefully controlled small batches for discovery projects, our team brings all this experience to the table. We work as much with the people down the hall as with customers around the world. The work never feels finished. This product, from its earliest syntheses to its latest refinements, reflects thousands of choices made by chemists and operators in dialogue with real users. The bar for quality keeps rising, and so do we.