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HS Code |
115202 |
| Product Name | L-(-)-Dibenzoyl Tartaric Acid (Anhydrous) |
| Cas Number | 14726-36-4 |
| Molecular Formula | C18H14O6 |
| Molecular Weight | 326.30 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 192-195°C |
| Optical Rotation | [α]D20 -146° to -153° (c=1, EtOH) |
| Solubility | Slightly soluble in water, soluble in alcohols and ethers |
| Purity | Typically ≥98% |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store in a cool, dry place, tightly closed container |
| Ec Number | 238-995-1 |
As an accredited L- (-) - Dibenzoyl Tartaric Acid (Anhydrous) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging contains 25 grams of L-(-)-Dibenzoyl Tartaric Acid (Anhydrous) in a sealed, amber glass bottle with detailed labeling. |
| Shipping | L-(-)-Dibenzoyl Tartaric Acid (Anhydrous) should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Store and transport at ambient temperature. Ensure packaging prevents damage and complies with chemical handling regulations. Include appropriate labeling and documentation as required for safe chemical transport. Handle with suitable personal protective equipment. |
| Storage | L-(-)-Dibenzoyl Tartaric Acid (Anhydrous) should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong oxidizers and bases. Protect from direct sunlight and heat. Ensure the storage area is equipped with appropriate containment to prevent environmental contamination in case of spillage. |
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Purity 99%: L- (-) - Dibenzoyl Tartaric Acid (Anhydrous) with a purity of 99% is used in chiral resolution processes, where it enables high enantiomeric excess in target compound isolation. Melting Point 193-195°C: L- (-) - Dibenzoyl Tartaric Acid (Anhydrous) with a melting point of 193-195°C is used in pharmaceutical synthesis, where stable thermal properties support efficient recrystallization operations. Optical Rotation -146° (c=1, ethanol): L- (-) - Dibenzoyl Tartaric Acid (Anhydrous) with optical rotation -146° (c=1, ethanol) is used in analytical laboratories, where it ensures precise chiral performance in enantiomer differentiation. Particle Size ≤ 50 μm: L- (-) - Dibenzoyl Tartaric Acid (Anhydrous) with particle size ≤ 50 μm is used in chromatography column packing, where fine granularity improves separation resolution. Stability Temperature up to 80°C: L- (-) - Dibenzoyl Tartaric Acid (Anhydrous) with stability temperature up to 80°C is used in preparative chromatography, where thermal reliability maintains product integrity during processing. Water Content ≤ 0.5%: L- (-) - Dibenzoyl Tartaric Acid (Anhydrous) with water content ≤ 0.5% is used in organic synthesis reactions, where low moisture content prevents undesired hydrolysis and ensures reproducibility. |
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Every shift in our plant feels a little like rolling up sleeves for a critical job in precision. We manufacture L-(-)-Dibenzoyl Tartaric Acid (Anhydrous), watching closely as raw tartaric acid leaps, step by step, toward a final product that speaks for itself in crystal form. The molecular formula C18H14O8 and CAS number 14721-48-7 serve as our checkpoint IDs, but beyond shorthand lies a product built for the real needs of labs, pharma, and research environments.
Over years on the production line, we've refined our synthesis route to bring purity above 99%. Labs count on this level for the kind of optical resolution chemistry that doesn’t forgive missteps. The anhydrous form offers an edge: it stays crisp, without the unpredictable moisture baggage of hydrates, and that makes it a repeat favorite for industrial processes seeking unclouded results.
Our experience has shown that the L-(-) version separates itself from racemic or D-(+)-dibenzoyl tartaric acid, not only for its left-handed chirality. We’ve stood side by side with chemists running chiral HPLC columns and have seen how the L-form delivers clean splits, where alternative versions muddle the peaks. Anyone purifying bases like alkaloids, or resolving amines enantiomerically, benefits from a product that behaves predictably in both batch and continuous processes.
Removing water cleanly during drying—so the finished crystals meet the demands of the anhydrous label—takes more than tweaking oven knobs. This step demands experienced hands, rigorous monitoring, and the right vacuum and temperature settings. Inconsistencies in residual moisture can blunt performance in both chromatography and synthesis, so we monitor each lot with Karl Fischer titration and address defects as they arise, not after complaints land.
Back in our early production, batches sometimes emerged with uneven color or sticky residues—a red flag we no longer see. The road from small flask to stainless steel reactor taught us lessons in temperature ramps, mixing dynamics, and filtering speed. We’ve fielded calls from clients whose own bench-scale experiments floundered with material from third parties; working through these problem lots drove home the importance of a tightly controlled process at every scale.
A customer once shared test results where our L-(-)-dibenzoyl tartaric acid outperformed a competitor by shaving hours off a batch resolution time for a prized chiral amine. High purity matters here; by cutting impurities, the separation sharpens and side reactions never have a chance to take root. Labs running resolutions on deadline trust us to keep up with demand, batch after batch, without surprises hiding in the melting range or IR scan.
It’s easy to get tunnel vision about staples like melting point—typically 194-198°C for our lots. But we see those numbers as signposts by which we judge the process itself. Bulk density, particle size distribution, and appearance all get tracked for every production run. Oversized crystals might look impressive, yet they slow down dissolution and impact batch kinetics. By dialing in the recrystallization and solvent stripping, we keep morphology and particle behavior in line with what synthetic chemists want.
“Anhydrous” often gets tossed around loosely in catalog copy. That can lead to a rude surprise if a product’s been stored carelessly or packed without a proper moisture barrier. Because we go from vacuum drying straight to nitrogen-purged bottles, we know the water content at the point of dispatch. Fielding questions from R&D chemists who see variable yields in their resolutions, we always return to this tight control of water—every milligram can matter in asymmetric catalysis or chiral pool syntheses.
We’ve shipped this material to university labs using it as a resolving agent for racemic amines, and to pharmaceutical plants aiming for kilogram-scale purifications. The L-(-) form plays a silent but critical role in separating mirror-image molecules—processes that underpin countless APIs and bioactive intermediates. Its use goes deeper than routine eluent additives: seasoned practitioners use it to form diastereomeric salts, extracting the target isomer with a precision that nothing else substitutes.
There’s no shortcut in handling sensitive acids. We emphasize moisture protection, both at our facility and in recommended storage. After a few misadventures with condensation-laden shipments some years ago, we overhauled our workflow. Every order ships fast, sealed, and with clear expectations for how users should keep it in the lab. In our own stockrooms, periodic checks keep tabs on caking or color change—early warnings that a batch isn’t as fresh as it should be.
Chemists sometimes ask why go with this tartaric acid derivative instead of classical options—like mandelic acid, camphorsulfonic acid, or parent tartaric acid. Our answer reflects what we’ve seen play out in practice. L-(-)-dibenzoyl tartaric acid offers robust solubility in organic solvents, which liberates users from tedious protocol tweaks. Where mandelic acid struggles in hydrophobic solvents or camphorsulfonic acid leaves behind sulfonate residues, dibenzoyl tartaric acid offers a clean slate for downstream recovery. Recovery and recycling of this chiral resolving agent also beat out other candidates, trimming material costs where every dollar and gram matter.
We once reviewed a returned shipment flagged for off-spec melting point. Though the initial lot barely missed the target by one degree, it started us down a line-by-line audit that caught a slip in recrystallization temperature. Adjusting the process fixed not just the symptom but also tightened overall control in subsequent runs. We keep every analytical trace and quality record on hand—if a user picks up a subtle IR outlier on a fresh lot, we look both backward and forward in our archive to resolve it. Lessons learned from detective work translate into fewer surprises, both for us and our customers.
Keeping each batch matched as closely as possible to the last goes beyond simple scale-up tricks. Years ago, we struggled with seasonal variance in raw tartaric acid supply, which affected not just cost but also impurity profiles. By locking down reliable raw material partners and running incoming tests that match the same scrutiny as finished goods, we stabilized our manufacturing chain. We don’t wait for customer complaints to trigger quality reviews; our operators check key parameters at the drum and kilogram level—no batch ever ships before cross-verification.
Sometimes a lab calls in, reporting incomplete resolution in a method that previously worked. More than once, we’ve walked through whole workflows, checking for changes in solvent, temperature, even the rotation speed of a phase separator. These conversations usually uncover factors that aren’t visible in a typical certificate of analysis, proving how application insight helps bridge the gap between technical specifications and real results.
One of the reasons we see repeat business is not just technical performance but a willingness to be transparent. We’ve had researchers ask for full impurity profiles after a single questionable result. Rather than stonewall, we scan and send the data, along with a batch sample if needed. By acting early to investigate any deviation—color, melting point, or yield hiccup—we build trust that doesn’t fade with the next PO.
Even with years of optimization, we keep refining. Early on, we switched from single to multiple recrystallizations. We recently invested in in-line moisture monitoring to spot drift even in automated zones. Upgrades in filtration and solvent recovery have not just kept the environment cleaner but brought down turnaround times. Collaborating directly with downstream formulators allows us to tweak crystal size or solvent residue specifications as applications evolve.
Managing organic solvent streams and minimizing residuals in finished goods rests at the core of our daily operations. With stricter regulations and shifting environmental targets, we adopt closed-loop systems, recycle solvents where possible, and invest in process upgrades. Commitment to minimizing byproduct formation doesn’t just lower waste—it cuts hidden production costs and reassures our customers that their endpoints meet evolving green chemistry expectations.
Chemical supply chains haven’t been immune to shocks—pandemics, raw material price swings, or logistic bottlenecks. From time to time, we’ve faced slowdowns that could have hamstrung clients on deadline. Building partnerships with alternate suppliers means we don’t rely on a single source, and transparent dialogue with shipping and warehousing partners keeps delivery windows predictable. We hold buffer stocks, not just to ride out crisis years but to support scaling demand.
Every call we field from a lab encountering a new challenge with this compound feeds back into our R&D loop. As the demands in enantioselective synthesis get sharper, we look for ways to push purity up, moisture even lower, and supply reliability higher. We’ve begun joint development projects with researchers working at the front edge of pharmaceutical and materials chemistry, so improvements flow directly from use cases on the bench.
Making L-(-)-dibenzoyl tartaric acid isn’t just a process—each drum we ship out represents the sum of what we’ve learned and the care with which we treat every step. We’ve realized that openness, rigorous analysis, and a willingness to innovate form the foundation of real value in specialty chemistry. The future rests on deepening that trust—batch by batch, challenge by challenge, solution by solution.