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HS Code |
349495 |
| Chemical Name | (R)-(-)-Methyl Mandelate |
| Cas Number | 611-71-2 |
| Molecular Formula | C9H10O3 |
| Molecular Weight | 166.18 |
| Appearance | Colorless to pale yellow liquid |
| Optical Rotation | [α]D20 = -129° (c=1, CHCl3) |
| Purity | Typically ≥98% |
| Boiling Point | 145-148°C (13 mmHg) |
| Density | 1.193 g/cm3 at 25°C |
| Refractive Index | n20/D 1.495 |
As an accredited (R)-(-)-Methyl Mandelate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g (R)-(-)-Methyl Mandelate comes in a sealed amber glass bottle with a white screw cap and detailed labeling. |
| Shipping | (R)-(-)-Methyl Mandelate is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Standard packaging ensures stability during transit. Appropriate hazard labeling is included, and all shipments comply with local and international regulations for transporting laboratory chemicals, ensuring safe and secure delivery to the destination. |
| Storage | (R)-(-)-Methyl Mandelate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from strong oxidizing agents and moisture. Store at room temperature, and ensure proper labeling. Handle with care using appropriate personal protective equipment to avoid inhalation, ingestion, or skin contact. |
Applications of (R)-(-)-Methyl Mandelate in Industrial Manufacturing(R)-(-)-Methyl Mandelate serves as a specialty intermediate in several advanced manufacturing sectors. Derived through asymmetric synthesis, its enantiomeric purity and reactivity enable precise downstream transformations, supporting high-value chemical production at the technical and commercial scale. 1. Chiral Pharmaceutical Intermediate SynthesisThis material functions primarily as a building block in the synthesis of chiral drug molecules, including antihypertensives and CNS agents. Pharmaceutical manufacturers use (R)-(-)-Methyl Mandelate for constructing complex architectures with strict enantiomeric purity. It enters the route during the early to mid-stage steps, where the asymmetric substrate sets the absolute configuration for subsequent chiral centers. This application demands tight traceability, validated purity profiles, and compliance with regulated quality frameworks. Industry compliance standards
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2. Agrochemical Enantioselective SynthesisMajor agrochemical players utilize (R)-(-)-Methyl Mandelate as a precursor for synthesizing chiral pesticides and herbicide actives. It ensures the final crop protection chemicals meet regulatory guidelines for enantiomeric purity, which influences biological activity and reduces environmental impact. Manufacturers select this intermediate for its predictable reactivity in forming ester or amide linkages, critical for selective toxophore construction. Industry compliance standards
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3. Aroma and Flavor Ingredient SynthesisFlavors and fragrances manufacturers incorporate this material as a key intermediate for producing specialty aroma chemicals, particularly those requiring a high level of enantiopurity to mimic natural stereoisomers. The chiral methyl mandelate contributes to building blocks for fruit, almond, and floral notes, where strict control of trace contaminants and authentic scent profile is demanded by FMCG and luxury brands. Facilities rigorously monitor enantiomeric excess and traceability from raw material intake through blending and packaging. Industry compliance standards
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4. Specialty Polymer Modifier SynthesisChemical manufacturers deploy this material for introducing chiral centers in advanced polymers and specialty plastics. Its use targets high-value applications, such as enantioselective membranes, medical devices, and sensors, where chiral recognition or separation capability is essential. Integration occurs during the functional monomer or additive preparation, ensuring control over stereo-regularity and uniformity within polymer chains. Quality teams validate the chiral input through instrumental testing prior to scale-up and downstream extrusion. Industry compliance standards
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Every batch of (R)-(-)-Methyl Mandelate that leaves the reactor represents thousands of hours of development, purification, and hands-on experience gained over years of producing fine chiral building blocks. We produce (R)-(-)-Methyl Mandelate in response to the rigorous demands of researchers and manufacturers who depend on precise stereochemistry. The compound carries the CAS number 611-71-2 and delivers a specific optical activity that meets the toughest standards imposed by the pharmaceutical and agrochemical industries. With reliable chiral purity above 99% and chemical purity above 99%, this molecule provides a crucial asymmetric center, meeting the exacting requirements of advanced synthesis.
The molecular formula, C9H10O3, tells only part of the story. Our (R)-enantiomer, recognized by its negative optical rotation, sets itself apart through strict control of the reaction temperature, enclosure environment, and meticulous fractional crystallization steps. Each shipment must pass in-house HPLC and GC analysis, along with NMR confirmation, to ensure the absence of the S-enantiomer contaminant. Typical physical specifications show a white to off-white crystalline powder, melting between 54–57°C, and its specific rotation settles within a narrow band, confirming authenticity and predictable reactivity. Our technical team maintains documentation for each lot, including spectral comparisons from previous production runs, so any variation is caught before it impacts customer applications.
As a dedicated chemical manufacturer, the value in (R)-(-)-Methyl Mandelate comes from our decades in producing chiral molecules on scales from a few kilos for R&D all the way up to multi-ton custom orders. Our reactors handle enantioselective synthesis with in-line sensors and continuous sampling. Field failures during the early years taught us the pitfalls—trace amounts of metal catalysts, solvent residues, or racemization quickly destroy value for our clients. We maintain strict batch records, monitor for chemical and optical purity at every stage, and provide full analytical dossiers with all shipments. The result: what leaves our facility mirrors the expectations set in the original project specifications with no last-minute surprises.
A wide range of current pharmaceuticals and specialty chemicals stems from high-quality chiral intermediates. (R)-(-)-Methyl Mandelate has earned its reputation for producing (R)-alpha-phenylglycine, (R)-alpha-phenylalanine, and other complex amino acids through further transformation via reduction or Grignard chemistry. Synthetic teams depend on the enantiopure methyl ester because racemic mixtures lead to regulatory headaches and clinical setbacks. Without a reliable enantiopure source, downstream purification costs escalate and waste multiplies. We have witnessed the consequences, both technical and economic, when corners are cut with starting materials.
(R)-(-)-Methyl Mandelate has several analogs on the market, including the S-enantiomer, the racemic form, and the corresponding free acid. Each one fits a unique synthetic approach. Through direct experience, the methyl ester form displays greater stability and lower hygroscopicity than mandelic acid, easing storage and weighing during scale-up or routine use. The methyl group also allows milder ester cleavage under neutral to slightly basic conditions, preserving sensitive downstream intermediates. Chiral purity in the (R)-form particularly underpins applications in synthesizing beta-lactam antibiotics and cardiovascular agents, where even a trace of the wrong enantiomer can trigger regulatory noncompliance.
Compared to the racemic methyl mandelate, the value of producing strictly the (R)-enantiomer becomes clear whenever chiral HPLC analysis is performed on customer final products. Racemates introduce costly separation steps or the risk of reduced pharmacological activity, especially as regulatory agencies enforce stricter guidelines on stereochemical purity. We see an uptick in demand for asymmetric precursors because clients realize downstream costs spiral out of control without single-enantiomer inputs.
Our product serves as the backbone for several large-scale syntheses. In the API sector, multiple manufacturing partnerships require (R)-(-)-Methyl Mandelate to deliver optically pure alpha-hydroxy acids through simple saponification and reduction protocols. Teams with timelines measured not in months but in weeks rely on our material to move their clinical candidates through to pilot plant stages. Drawing examples from our own logistics records, shipments to North America have supported the launch of new cardiovascular drugs, while deliveries to Europe provided critical material for agrochemical development. The advantage of beginning with enantiomerically pure starting materials manifests in reduced purification cycle times, higher overall yields, and higher confidence in regulatory compliance.
Beyond pharmaceuticals, specialty fragrance developers and fine chemical companies trust the methyl ester to yield (R)-mandelic acid in downstream processes. This flexibility helps diversify market segments and stabilizes production schedules against seasonal market flux. Formulation chemists appreciate the ester’s performance during scale-up; it resists hydrolysis in atmospheric moisture, handles well, and dissolves rapidly in common laboratory solvents—attributes we engineered into the process based on extensive feedback from multi-year clients.
As the manufacturer, we control every variable from raw material input through to finished lot release. Unlike resellers who consolidate from several unknown sources, our supply chain rests on vetted, traceable suppliers we audit regularly. This oversight matters most when new regulatory challenges or global shipping disruptions arise. Direct communication between our technical team and on-site QC means batch-specific documentation is never generalized or fractured among intermediaries. If any customer calls for a custom batch—be it a particular particle size or specialized impurity profile—we can often retool a production line or provide a scaled pilot in days, not weeks.
In preparation for major formulation campaigns, our lead chemists advise clients on the merits of the ester form over the free acid. Many downstream processes, like selective reductions or chiral resolution steps, benefit from the methyl ester’s predictable reactivity profile. For labs working with kilogram to multi-ton requirements, product consistency and purity are not luxuries—they are necessities that impact regulatory filings, patent defenses, and, ultimately, time-to-market.
Years of supporting large and small customers alike have taught us to anticipate and address recurring challenges. Moisture intrusion during transit can degrade sensitive chiral esters; we combat this with vacuum-sealed, inert-gas-packed drums. Experience shows that controlling the headspace atmosphere reduces hydrolysis risk, preserving both appearance and purity. For long-term storage, our advice springs from real handling data—maintain temperatures below 25°C, shield from direct sunlight, and choose amber glass only for multi-month laboratory storage.
Regulatory compliance weighs heavily on project leaders. Our in-house regulatory affairs team updates documentation as soon as new standards emerge, ensuring that every shipment of (R)-(-)-Methyl Mandelate includes relevant certificates and complies with the latest REACH, ICH Q7, and GMP guidelines as required by the project. We have helped clients resolve customs delays by providing real-time evidence of purity and chiral integrity. Both analytical chemists and procurement officers know that direct sourcing from the manufacturer simplifies the compliance chain and reduces risk.
Our strongest process improvements grow out of rigorous conversations with customers facing real-world bottlenecks. Early batches revealed subtle issues—trace solvent peaks or slow filtration steps due to unwanted particle morphologies. Chemists flagged clumping or static buildup on transfer. Our process crew responded by tightening drying cycles, modifying sieve mesh during packaging, and reducing dusting. These tweaks, driven entirely by client feedback, translate into material that not only meets but often exceeds purity specs and flows cleanly through automated dispensers.
Just as critically, we invest in pilot reactions to validate each process tweak. Any alteration in catalyst, solvent, or temperature triggers a new round of analytical validation. The result cascades directly to clients in the form of improved batch-to-batch consistency and speedier technical support if a question is raised about reactivity or handling. For high-stakes custom syntheses, such as for active pharmaceutical ingredients or crop-protection agents, even a small improvement in product performance shortens project timelines and supports competitive patents.
The environment for pharmaceutical and specialty chemical manufacturing continues to evolve rapidly. As manufacturing partners for emerging biotech and academic teams, we see cutting-edge research often hinges on reproducibility and sample provenance. Labs running asymmetric syntheses at small scales cannot afford to waste time chasing unexplained side reactions or inconsistent optical rotations. By supplying reference standards and test quantities of (R)-(-)-Methyl Mandelate with full traceability, we lower the barriers for smaller teams to pursue complex targets.
Our decades-long partnerships with larger manufacturers mean their scale-up operations benefit from technical insights gained at every production tier. Questions about solvent compatibility, alternate ester groups, or accelerated aging come directly to our technical team and lead to ongoing knowledge transfer. Our clients benefit from this high-touch interaction, ensuring that the product fits seamlessly into both academic syntheses and industrial-scale GMP processes.
Responsible production matters for us as much as it does for our clients. We have made substantial investments in solvent recovery, waste reduction, and energy efficiency. Separating mother liquors during crystallization allows for reuse and minimizes hazardous waste disposal. Internal audits of emissions and solvent use shape our future project planning. Safety procedures—regular air monitoring, comprehensive PPE, and on-demand material safety data sheets—reflect our lived daily responsibility as operators, not as remote managers.
As global interest in green chemistry grows, our on-site process engineers experiment with bio-derived benzaldehyde sources and alternative esterification catalysts. Trials that hold up to bench-scale scrutiny migrate into pilot reactors under close analytical control. While the methyl ester process consumes less energy than earlier, high-temperature alternatives, we continue to push for lower environmental footprints without giving up chiral selectivity or purity.
The story of (R)-(-)-Methyl Mandelate in our facility reflects more than a technical datasheet; it tracks the evolution of our practical understanding and commitment to chemical reliability. Critical lessons come not from abstract standards but from real batch issues and joint troubleshooting with customer labs. Whether it’s rerouting waste lines to capture more solvent for recovery, revising an SOP after an unplanned shutdown, or extending QA sampling checkpoints, every change has a concrete impact on the product reaching your workbench.
The close relationships with our buyers, many of whom send technical teams to observe or audit operations, drive deeper improvements. Their input, whether prompted by regulatory requirements or field observations, underpins operational refinements and reinforces our product’s strong standing.
At our facility, (R)-(-)-Methyl Mandelate stands as a symbol of what careful, informed manufacturing can achieve. Whether the demand is measured in grams for an early-stage research group or in tons for a multinational API provider, our guiding principle never wavers: precision, reliability, and openness in every gram shipped. Our process is flexible, our expertise is personal, and our focus always returns to supporting the next breakthrough—wherever it originates.