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HS Code |
482710 |
| Iupac Name | (4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-dicarboxylic acid dimethyl ester |
| Molecular Formula | C9H12O6 |
| Molar Mass | 216.19 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 98-102 °C |
| Density | 1.31 g/cm³ (estimated) |
| Cas Number | 70968-95-3 |
| Optical Rotation | [α]D20 +166° (c=1, CHCl3) |
| Smiles | COC(=O)C1C(OC(=O)OC)OC(C)(C)O1 |
| Inchi | InChI=1S/C9H12O6/c1-9(2)12-6(7(10)13-3)5(4)15-8(14-9)11 |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., dichloromethane, methanol) |
| Storage Conditions | Store at 2-8 °C, protected from light and moisture |
As an accredited (4R,5R)-2,2-Dimethyl-1,3-Dioxolane-4,5-Dicarboxylic Acid Dimethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of (4R,5R)-2,2-Dimethyl-1,3-Dioxolane-4,5-Dicarboxylic Acid Dimethyl Ester in a sealed amber glass bottle, labeled with safety information. |
| Shipping | The chemical `(4R,5R)-2,2-Dimethyl-1,3-Dioxolane-4,5-Dicarboxylic Acid Dimethyl Ester` requires shipping in tightly sealed containers, protected from moisture and direct sunlight. It should be handled as a chemical substance, compliant with all local and international transport regulations, and shipped at ambient temperature unless otherwise specified by the manufacturer’s guidelines. |
| Storage | Store (4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-dicarboxylic acid dimethyl ester in a tightly sealed container, protected from light and moisture. Keep at room temperature (15–25°C), away from heat sources and incompatible substances such as strong acids, bases, and oxidizers. Ensure good ventilation in storage areas, and label the container clearly to avoid accidental misuse or contamination. |
Applications of (4R,5R)-2,2-Dimethyl-1,3-Dioxolane-4,5-Dicarboxylic Acid Dimethyl Ester in Industrial ManufacturingAs an experienced manufacturer, we supply (4R,5R)-2,2-Dimethyl-1,3-Dioxolane-4,5-Dicarboxylic Acid Dimethyl Ester to multiple advanced downstream sectors where it functions as a key chiral intermediate, protecting group, and building block. The following application fields reflect real, compliant industry use cases, each presenting unique process and formulation details for end-product manufacturers. 1. Chiral Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers use this compound in asymmetric synthesis to introduce chiral centers, particularly for β-lactam antibiotic development and other APIs that demand high enantiopurity. Its stereochemical fidelity ensures batch consistency during critical carbon backbone construction. Downstream operators implement stringent impurity control, referencing ICH Q7 and local pharmacopeial guidance, to support both laboratory-scale R&D and full-scale bulk API production. Industry compliance standards
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2. Custom Peptide and Peptidomimetic ManufacturingSpecialty peptide producers apply this material as a diester protecting group for amino acid derivatives, supporting the production of high-purity peptide APIs and complex bioactive compounds. Its rigidity and bulkiness enable orthogonal protection during multistep solid-phase or solution-phase peptide assembly, enhancing selectivity during coupling and deprotection cycles. Industry compliance standards
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3. Advanced Polymeric Material SynthesisThe diester finds use in specialty polymer research and manufacturing, especially in producing polyesters, polycarbonates, and biodegradable materials with defined stereochemistry. Industrial formulators favor its ability to impart stereoregularity, enabling precise mechanical and degradation properties in bioresorbable medical polymers and high-value specialty plastics. Industry compliance standards
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4. Fine Chemical Asymmetric SynthesisManufacturers of aroma chemicals and advanced agrochemical actives select this compound as a chiral auxiliary or protecting agent in multi-step synthesis of structurally complex fine chemicals. Its stereoselectivity facilitates construction of key intermediates for downstream cross-coupling, cyclization, and oxidative functionalization, crucial to the quality of aroma and crop-protection molecules. Industry compliance standards
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5. API Impurity Standard and Reference ProductionAnalytical labs and reference substance producers utilize this dioxolane-based compound for preparing certified reference materials (CRMs) and labeled impurity standards, critical for API batch release and stability testing. Its well-characterized stereochemistry and high purity support traceable analytical benchmark creation in regulated environments. Industry compliance standards
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6. Enzyme Substrate in Biocatalytic Process DevelopmentEnzyme engineering and industrial bioprocess research groups apply this dioxolane diester as a defined chiral substrate to screen and optimize novel biocatalysts. The rigid, sterically hindered structure yields high sensitivity in assays for enantioselective hydrolysis and transesterification, supporting enzyme selection and kinetic profiling under controlled reaction conditions. Industry compliance standards
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Producing (4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-dicarboxylic acid dimethyl ester takes more than careful lab work. From firsthand experience, every stage of the process matters. This compound’s weight and structure spring directly from the steps of stereoselective protection and methylation. Attention to each batch and every variable decides the outcome. Chemists at the bench see, in real-time, how humidity, temperature, and even the grade of acetone drive purity and yield. In our facility, process controls evolve from repetition and hands-on adjustments rather than software routines. Our product comes off the line after rigorous monitoring of each transformation, checked by eyes that have seen a thousand crystallizations before. NMR spectra and HPLC traces confirm quality, but years of practice get us there. The push for both yield and stereochemical integrity keeps the challenge alive.
Building chirality into intermediates is no sideline. It carries through to the very heart of end products—anyone who’s spent a morning tuning reaction conditions for an asymmetric synthesis knows this. (4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-dicarboxylic acid dimethyl ester sits inside the toolkit of serious medicinal and fine chemical manufacturers because it locks in chiral information with remarkable reliability. Small missteps during manufacture risk racemization, jeopardizing downstream performance. In practice, this ester outperforms many achiral alternatives when syntheses call for exacting control over enantiomeric excess—so crucial in pharmaceutical lead construction. We’ve exchanged enough notes with customers running scale-ups to know that one slip in stereoselectivity undoes months of planning, turning kilo-scale into clean-up. That’s why our process never takes enantiopurity for granted. Maintaining stereochemistry begins at raw material selection and runs through every purification step until the final flask.
Specification for this compound comes out of pragmatism, not just theory. Over the years, we found that melting point isn’t the best yardstick for every batch. Moisture, trace acid, color—we’ve seen them all affect reactivity. Specs stem directly from downstream chemistry. The real benchmark, at least for our regulars, comes with customer reactions: does their resolution work, do their intermediates crystallize cleanly, does the downstream protection step click without surprises? In our line, purity isn’t an afterthought. We designed our final work-up and filtration steps with the experience that a stray 0.5 percent impurity—sometimes even less—can cascade into full-blown process failures for customers developing chiral active ingredients. Final product leaves our plant only after chromatographic and optical rotation checks confirm what chemists working at scale expect.
Many years in this field show one simple thing—customers find the most value when a compound earns its place on the bench. We designed this ester for chemists targeting high-value chiral building blocks. Labs reaching for it tend to be preparing protected tartaric acid derivatives, asymmetric auxiliaries, or key intermediates for drug synthesis. Experienced researchers prefer it to less-defined mixes or in-house solutions because it brings repeatability. Unlike generic acid esters, this compound stands out when reactions need precise chiral induction. In practical terms, it comes into play during ligand design, catalyst development, and synthesis of chiral functional groups. Labs scaling up medicinal chemistry always want to limit surprises—a lesson we’ve taken deeply to heart—so we’ve worked to bottle up reliability in every shipment.
Chemists have never shied away from alternatives, so we see firsthand how competitors stack up. The experience of running reactions in parallel demonstrates the contrast between our product and lower-purity, racemic, or differently protected esters. The distinguishing factor always roots itself in stereochemical purity. Many generic dioxolane esters bring along a mix of isomers or hidden side-products that subtly disrupt sensitive reactions. Discussions with process chemists confirm this again and again: side-products alter yield, selectivity, and purity. What truly separates our material is not just higher purity but consistent chiral ratios, borne out by near-identical performance from batch to batch. For pilot plant runs and scale-ups, that edge means shorter cycle times and less troubleshooting. It’s seldom glamorous work, but hard-earned consistency isn’t something you fake.
Scaling this molecule from lab glassware to reactors uncovers the small cracks in a manufacturing plan. Early on, we faced solvent incompatibilities that threatened optical purity; a few batches taught us not every filtration medium behaves the same when you scale to drums. In production, we learned how a standard rotary evaporator can cause subtle hydrolysis if the pressure curve isn’t just right. No two sites are quite the same, either. Water quality in the plant changed the drying curves unexpectedly before our experienced hands figured out the fix. Each hiccup built our institutional memory and prompted tweaks to the workflow. These aren’t issues likely to show up on a data sheet, but long-term users will notice the difference in product handled by people who have solved problems over hundreds of runs.
Anybody who has handled moisture-sensitive intermediates knows just how finicky shipping and storage can become. We settled on packaging that really keeps this ester stable through climate shifts and long-haul transit. Some customers favor glass; others, high-density polyethylene containers. Product integrity matters more than packaging fads, so over time our operations team tried and tested real-world conditions, from southeast Asia’s rainy season to dry northern winters. We learned that simple desiccants and careful sealing make all the difference during transit, keeping material crisp and free-flowing upon arrival. Stubbornly resisting shortcuts, we seal each order for a tight, dry finish, confirming that experience with the material drives out guesswork from our logistics.
Sustainability isn’t a checklist here—it’s a series of adjustments, each shaped by the realities of our plant’s daily flow. Tracing solvent recovery, we adapted our work-up to minimize waste while preserving product purity. Vendors supplying us with key reagents participate in regular audits; we prefer partners who share our approach to environmental stewardship. On the plant floor, recycling programs for spent solvents and judicious energy management emerged not from flashy targets but from technical teams wrestling with actual throughput and emissions charts. Those efforts aren’t a marketing flourish but the result of years untangling production challenges through practical, science-led tweaks. We know the chain of custody for raw materials and constantly track how byproducts are handled to meet not only regulations but our own standards.
Our experience shows that knowledge rarely moves in one direction. Some of the toughest challenges in manufacturing this ester got solved only after input from trusted collaborators and customers wrestling with their own bottlenecks. Joint troubleshooting led to better impurity control on one line, and a tip from a customer running an unusual derivatization let us tweak crystallization temperatures for better yields. Analytical support flows both ways. Researchers at pharmaceutical companies have sent back feedback on assay conditions and alternative trace analysis methods that led us to finetune our batch control. Having spent more than a few nights in the plant to meet a sudden surge in orders, the value of direct feedback from real-world chemistry becomes obvious. Curiosity and perseverance, not a top-down mandate, have enriched every aspect of the product’s manufacturing cycle.
Years in the field lead to the realization that a certificate of analysis spells out only half the story. Quality comes from the discipline built into every run: training operators to spot process drift, insisting on fresh reagents for each batch, and refusing to cut corners when timelines tighten. We’ve seen, over time, how seemingly minor lapses—underrated reagents, a skipped drying step—can knock product performance off kilter. It’s direct conversations with users, plus batch records thick from handwritten notes, that force continuous improvement. We cross-check lots for not only expected impurities, but also for those below regulatory radar, relying on old school methods like TLC alongside modern LC-MS verification. Shipments going out of our facility are tagged not just by number but by pride in what arrives at the other end and the care behind it.
It’s easy to find cheaper or seemingly equivalent dioxolane esters or tartaric acid derivatives. Decades of comparison trials have taught our team the ugly truth: what sometimes works in the hands of an experienced academic chemist falls apart in scale-dependent operations. Too many suppliers push “meets minimum” purity, leading to a host of headaches downstream—overruns, failed resolutions, or mystery byproducts. Repeatedly, our longest-standing clients send feedback that their key projects only move forward with batches performing to exacting standards. Cutting corners—whether on raw material prep, reaction time, or final QA—ends up damaging more than reputation; it costs in rework, lost time, and failed submissions. Our product’s track record in large-scale syntheses, published process chemistry, and systematic comparisons stands as a testament to what careful manufacturing adds to every kilo.
No training manual replaces what the shop floor teaches. Staff turnover, new equipment, and shifting supply chains push us to adapt systems—to ensure not just reproducibility, but to keep the accumulated knowledge alive. Every time a new operator joins, senior team members walk them through the history behind each run—where to watch for foaming, how to spot color changes signaling side reactions, the best way to pack a column for this specific ester. Written procedures back up this oral tradition but never replace the intuition built over years. And new challenges keep arriving: a new solvent supplier once sent drums with a subtle contaminant, caught just because a technician stuck to the habit of checking every shipment by hand. That storytelling, passed from batch-to-batch and shift-to-shift, keeps quality consistent.
Working with academic and industrial labs means staying ahead of evolving synthetic strategies. A few years ago, demand spiked for enantiopure diesters in asymmetric catalysis and new ligand frameworks. We expanded our pilot line and tweaked route optimizations to answer those needs. Whether it’s a shift toward greener reaction conditions or requests for tailor-made esters with different protecting groups, our R&D team works in real time with external researchers. Trials often begin small—grams at a time—before moving up to scale. Adapting means finding not just new chemistry but better analytical tools and smarter logistics. The interplay of field results and in-plant innovation keeps our process current and our product portfolio relevant—driven by the practical needs of teams outside our walls.
Outlook for (4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-dicarboxylic acid dimethyl ester stems from both market reality and what chemists on the ground are pursuing. More companies dive into chiral drug synthesis, crop protection, and advanced material science, pushing us to refine both process safety and flexibility. Automation and digital analytics shape batch tracking, but the last line of defense always circles back to hands-on oversight. Continuous improvement, real-time feedback, and keeping the right people in decision-making roles ensure we move forward without losing sight of what built our business. Sustainable choices, reliability, careful stewardship of each batch, and an open dialogue with both seasoned and new customers give our product both its legacy and its edge.
In this line of work, long-term trust means more than a slick brochure or a standardized spec sheet. Chemists, managers, and procurement teams tell us directly that the defining feature lies in the reliability of every shipment—crystals that dissolve as expected, reactivity that doesn’t waver, and documentation that matches the real-world performance of the material. That trust forms not from one-time wins, but the quiet accumulation of hundreds of batches done right, each improved by lessons gleaned from the last. We meet setbacks head-on, solve problems where they arise, and translate technical expertise directly into better product. Working from the bench up, we keep an open door to feedback, welcome tough questions, and stand behind the compound we make—every time, without exception.