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HS Code |
493570 |
| Cas Number | 27871-49-4 |
| Molecular Formula | C4H8O3 |
| Molecular Weight | 104.10 g/mol |
| Iupac Name | methyl (R)-2-hydroxypropanoate |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | 145-147 °C |
| Density | 1.09 g/mL at 25 °C |
| Specific Rotation | +21° to +24° (neat) |
| Refractive Index | n20/D 1.418 |
| Purity | ≥98.0% (GC) |
| Solubility | Miscible with water, ethanol, and ether |
| Flash Point | 54 °C (closed cup) |
| Odor | Mild, pleasant, sweet |
As an accredited Methyl (R)-(+)-Lactate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100 mL amber glass bottle with a secure screw cap labeled “Methyl (R)-(+)-Lactate, 98%” and safety information. |
| Shipping | Methyl (R)-(+)-Lactate is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. The packaging complies with local and international regulations for flammable liquids. It should be stored and transported in a cool, well-ventilated area, away from incompatibles, and handled by trained personnel using appropriate protective equipment. |
| Storage | Methyl (R)-(+)-Lactate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizers and acids. Protect from direct sunlight, moisture, and sources of ignition. Store at room temperature and ensure proper labeling. Use appropriate chemical storage practices and comply with relevant safety regulations. |
Applications of Methyl (R)-(+)-Lactate in Industrial ManufacturingMethyl (R)-(+)-Lactate serves as a key chemical intermediate in several tightly regulated manufacturing sectors. Our facility produces this material under controlled conditions, ensuring consistent purity for highly specialized downstream integration. The following application scenarios detail specific uses in distinct industries. 1. Chiral Intermediate in Pharmaceutical SynthesisPharmaceutical manufacturers use this lactate ester as a chiral building block in the synthesis of active pharmaceutical ingredients (APIs), such as statins and antiviral agents. Synthesis typically involves enantioselective transformations, where the (R)-configuration is critical for pharmacological activity. Production protocols require strict validation of enantiopurity, and GC/HPLC assay data support audit compliance. Our partnership with API manufacturers focuses on secure supply, batch traceability, and documentation in alignment with global pharma norms. Industry compliance standards
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2. Green Solvent in Specialty Coating FormulationsFormulators in the coatings industry increasingly specify this lactate ester as a bio-based, readily biodegradable solvent for high-solids or waterborne coatings. Its polar functionality enables strong solubilization of resins, pigments, and additives previously reliant on petroleum-based solvents. Compliance with VOC and environmental stewardship protocols necessitates regular review of technical datasheets and exhaust emissions records. Industry compliance standards
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3. Monomer Feedstock for Biodegradable PlasticsBioplastic processing facilities employ this lactate ester as a functionalized monomer for producing bio-based polyesters and polylactic acid (PLA) copolymers. It enables ring-opening polymerization and co-polymerization strategies, supporting the shift toward renewable packaging and disposable goods. Precise input documentation is required to validate sustainability claims and product declarations for export to regulated markets. Industry compliance standards
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4. Solubilizer and Reaction Solvent in Agrochemical SynthesisAgrichemical manufacturers utilize this lactate ester as a polar, green solubilizer in the formulation and synthesis of crop protection actives, including fungicide and herbicide intermediates. Its strong solvent action supports safe handling of sensitive reactants, and it assists the formation of stable emulsifiable concentrates tailored for field application. Stringent stewardship demands full lifecycle traceability and compliance with agrochemical risk management codes. Industry compliance standards
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5. Enantioselective Catalyst Ligand in Fine Chemical ProductionLaboratory-scale and custom fine chemical manufacturers employ this lactate ester as a chiral ligand or auxiliary in asymmetric synthesis, especially in the preparation of optically active alcohols and esters. Its enantioselectivity and compatibility with organometallic catalytic systems have been proven in published asymmetric hydrogenation and transfer reactions. Operators document batch input accuracy and monitor ligand recovery for re-use and process economy. Industry compliance standards
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6. Solubilizer for Natural Extracts in Flavors & Fragrances ManufacturingProducers of flavors and fragrance compositions specify this lactate ester for improving solubility of plant-derived extracts and oleoresins in alcohol or water-based concentrates. Its natural origin and status as a non-toxic solvent advantage its use in formulations that comply with food and cosmetic safety regulations. Audit documentation includes ingredient traceability, allergen declaration, and shelf-life stability studies for finished blends. Industry compliance standards
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Navigating the landscape of chiral building blocks calls for more than standardized products—it takes a steady grasp of how every batch interacts with its intended use. Methyl (R)-(+)-Lactate has earned its place through both its optical purity and its role as a foundational intermediate in a wide span of industrial labs. After years at the reactor’s edge, there’s more to this specialty ester than the literature usually captures.
With CAS number 27871-49-4 and molecular formula C4H8O3, this compound offers more than a simple lactic acid derivative. The R-enantiomer brings selectivity into asymmetric synthesis and specialty polymerizations, helping products achieve performance specifications not possible with their racemic or S forms. Since the molecule’s asymmetric center fundamentally impacts product outcome, the stereochemical control delivered by our production process stands as the cornerstone.
It helps to look beyond numbers—chiral purity often translates to higher yield or reduced purification headaches. Methyl (R)-(+)-Lactate, synthesized through refined enzymatic or fermentation-driven protocols, holds an optical purity (enantiomeric excess exceeding 98%) on a repeated basis. We insist on tight controls at each stage because small deviations produce ripple effects downstream. In our experience, overlooked process drifts or insufficient monitoring can multiply problems later. By prioritizing batch traceability and real-time chiral analysis, quality matches intent every time.
The product itself appears as a colorless to pale yellow liquid, typically with a sweet, slightly ethereal odor. As shipped, the liquid maintains low viscosity and flows readily—critical for precise metering into reactors and pilot setups. Boiling occurs near 145-150°C at reduced pressure (around 20 mmHg), minimizing thermal decomposition risks during solvent recovery. Our mainstay model, designed for synthetic and formulation work, delivers a minimum assay of 99% by GC and not less than 98% by specific rotation, both calibrations run in-house and by trusted external labs.
Water solubility plays a predictable but important role, particularly for process integration and waste stream management. Methyl (R)-(+)-Lactate blends with alcohols, ethers and common organics, yet maintains strong miscibility with water—making it accessible for both aqueous-phase conversions and solvent removal strategies. Absence of residual mineral acids, fermentation by-products, and other chiral contaminants is constantly assured through purification protocols fine-tuned from years of troubleshooting.
R-enantiomeric methyl lactate consistently finds its place in several high-value syntheses and specialty materials. In pharmaceutical development, this compound often works as a chiral auxiliary or precursor for alpha-hydroxy acid-based intermediates. One sees frequent reliance on R-configured derivatives for enantioselective steps—where downstream stereochemistry dictates efficacy and regulatory clearance. Our collaborations with the pharma sector keep us adapting; abnormal enantiomeric drift in one lot can jeopardize both yield and the regulatory order, so we keep records accessible for up to five years post-sale.
Bioplastics manufacturers continue to find tangible improvements when the R form is dialed into their poly-lactic acid (PLA) formulations. Producing polymers with specific mechanical properties requires honest attention to the lactic acid starting material’s handedness. In biobased films and biodegradable packaging, modulating the ratio of R- and S- methyl lactates tunes crystallinity, toughness, and degradation rate. We’ve worked directly with producers who discovered that introducing even small quantities of the unintended enantiomer skews polymerization, leading to inferior film strength or processing instability. These lessons come hard-earned, sometimes after running entire extrusion lines with sub-optimal starting material.
Another emerging category involves green solvents and specialty cleaning fluids. Formulators look at methyl lactate for its solvency power, low volatility, and derived-from-renewables appeal. Those emphasizing the R-isomer point to evidence from in vitro and environmental studies: the R-form demonstrates a better safety margin and sometimes breaks down more predictably in wastewater systems. While solvent markets once purchased methyl lactate with little concern over chirality, increasingly strict LCA (Life Cycle Assessment) analyses have begun to reward plants that trace, segregate, and document isomeric ratios. We've adapted our QA documentation to fit this trend, offering detailed certificates for clients facing European and North American audits.
Not all methyl lactate streams are built alike—being convinced of this takes watching enough projects succeed or fail on the margin. Many of the low-cost alternatives floating across the market consist of racemic blends (equimolar R and S) or lab-scale S-methyl lactate made for niche syntheses. Racemates offer a cost advantage, but in practice, lead to unpredictable yields and off-spec chirality in chiral-sensitive applications. Those who start a scale-up on a mixed isomer often realize, sometimes late and expensively, that regulatory or end-use requirements strictly demand the R-form.
The supply chain for R-methyl lactate demands particular logistical and technical vigilance. Seasonal variations in feedstock—particularly for lactic acid derived from corn, sugar beet, or sugarcane—require us to maintain flexible procurement and careful process recalibration. Years ago, wider market swings caused color shifts, odor differences, or inconsistent chiral purity, prompting us to strengthen our supplier audits and install inline NMR and FTIR checkpoints for real-time identity confirmation. If a customer runs a continuous plant, small misalignments multiply, compounding into real-world, not theoretical, costs.
Some of our long-term partners in pharmaceuticals or polymers schedule audit visits on-site. This direct exposure to their process needs has pushed us to invest in real process transparency, batch-use histories, and consistent preparation of retained samples for post-sale analysis. It’s often those in-person problem-solving sessions that shape the way we approach not only production but customer support. Resolving deviations is no longer a reactive process; it has become an everyday routine embedded in production.
Stability and shelf-life deserve special mention. Unlike some short-chain esters, Methyl (R)-(+)-Lactate resists spontaneous hydrolysis under standard conditions. Experience has taught us, though, that long exposure to elevated humidity or accidental acid traces can initiate breakdown, releasing methanol and lactic acid. We transitioned years ago to nitrogen-purged bulk drums and lined totes, reducing both hydrolysis and peroxide formation. Detailed batch certificates flag moisture risk zones, allowing storage managers to catch quality drift early rather than after the fact.
Industry certifications are only worthwhile if they translate to genuine reliability for partners and end-users. Not every batch we make ends up in a drug, but cGMP principles guide our main line production. This frame ensures not just traceability but documented QA responses at every handoff—raw materials, reactors, purification, and packaging. The result: audit-ready supply chains that continue to pass FDA, ECHA, and selected ICH guideline reviews. We keep our people cross-trained in both internal standards and evolving market needs; regulatory bodies rarely grant grace periods for mismatches.
Customers running LCA or push for cradle-to-gate carbon savings have changed sourcing decisions. Reduced-energy fermentative production achieves clear reductions in CO2 footprint, measured independently. This is no greenwash: energy intensity and waste minimization get validated through third-party LCAs. For users preparing eco-labeled or environmentally sensitive end-products, we support supply chain documentation, performance audits, and publications, open to transparent review.
Some shifting standards don't have clear legal teeth just yet, but experience suggests staying ahead prevents disruptions. Bioplastics users in Europe face evolving compliance protocols where deliberate testing and isomer documentation help guarantee consumer trust. With momentum toward more circular chemistry, the real differentiator will be batch-level tracking and openness to collaborative troubleshooting—even after product release.
Over the years, unplanned downtime from poor-quality chiral intermediates, slow certificate responses, or poorly planned logistics has forced many to reconsider their supplier relationships. We chose to confront these friction points head-on, creating in-house labs capable of fast chiral analysis, establishing dedicated technical liaisons for pilot plants, and refining internal communications until issue resolution times shrank from days to hours.
Supply chain bottlenecks often resolve at the earliest possible stages—scheduling, sample retention, or simply transparent forecasts for demand spikes. Unsteady pricing in global feedstocks sometimes pushes other suppliers to rush deliveries without thorough lab checks. Counteracting this, we built reserves not just in inventory but also in cross-trained staff. This way, whether facing a hurricane’s impact on corn supply or unplanned equipment downtime, support continues without shortchanging QC.
Communication ties it all together. Where other manufacturers automate away most client touches, we have found staying accessible pays off. Raw technical questions, urgent batch requests, or even the occasional nonconformance review—these never get shunted into distant mailboxes. The most valued relationships with our clients have lasted through these touchpoints, lasting longer than any particular QA chart or product code.
Year in and year out, technical feedback from both the academic and industrial worlds prompts us to adapt. As green chemistries and advanced functional materials press for higher purities and tighter control, we have upgraded both process infrastructure and analytical reach. Automated reactor controls, chromatography paired with digital recordkeeping, and regular team skills upgrades ensure steady improvement without compromising interpersonal trust.
By focusing on actual problems and learning from returns or complaints—rather than just celebrating consistency—we create a quieter confidence in each outgoing drum. Methyl (R)-(+)-Lactate is sold as a molecule, yet it brings together a long chain of learning, calibration, and sometimes failure. Real-world process challenges never fit perfectly in a spreadsheet; they call for nimble, experience-driven solutions from a producer who has seen projects from first development to scale-up to everyday operation.
Formulators seeking predictable chiral induction, polymer producers refining PLA properties, or teams searching for auditable, low-footprint, renewably sourced intermediates—these are the groups shaping Methyl (R)-(+)-Lactate’s evolution today. For all, steady technical partnership makes the difference, transforming a raw material into a stepping stone for better products and fewer headaches. Each batch stands as evidence: precise chemistry, low noise, and a willingness to solve problems shoulder to shoulder.