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(-)-Corey Lactone Benzoate

    • Product Name (-)-Corey Lactone Benzoate
    • Alias C3961181
    • Einecs 871-500-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    897503

    Product Name (-)-Corey Lactone Benzoate
    Cas Number 112022-75-4
    Molecular Formula C15H14O4
    Molecular Weight 258.27
    Appearance White to off-white solid
    Optical Rotation [α]D20 -195° (c=1, CHCl3)
    Melting Point 112-114 °C
    Purity ≥98%
    Storage Temperature 2-8°C
    Solubility Soluble in chloroform, dichloromethane

    As an accredited (-)-Corey Lactone Benzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5g (-)-Corey Lactone Benzoate is packaged in a sealed amber glass vial, labeled with product details and safety information.
    Shipping (-)-Corey Lactone Benzoate is shipped in secure, airtight containers to ensure stability and prevent contamination. Packages are labeled according to regulatory requirements and transported under controlled temperatures. All relevant safety documentation is included, and shipping complies with hazardous materials guidelines for prompt and safe delivery.
    Storage (-)-Corey Lactone Benzoate should be stored in a tightly sealed container, under an inert atmosphere such as nitrogen or argon, and kept in a cool, dry place away from light and moisture. Ideally, it should be refrigerated at 2–8 °C. It must be protected from strong acids, bases, and oxidizing agents. Proper labeling and handling according to safety guidelines are essential.
    Application of (-)-Corey Lactone Benzoate

    Applications of (-)-Corey Lactone Benzoate in Industrial Manufacturing

    As the original manufacturer of (-)-Corey Lactone Benzoate, we support multiple specialized sectors with verified large-scale applications. Our chemical delivers precise performance in synthesis and product development for advanced molecules. Explore dedicated use cases demonstrating controlled process parameters, regulatory fit, and output quality.

    1. Chiral Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers utilize (-)-Corey Lactone Benzoate as a key chiral building block in enzymatic and stereoselective synthesis routes for complex APIs, such as statins and macrolide antibiotics. The material’s enantiopurity and reactivity support asymmetric synthesis and resolution steps, especially in early-phase and scale-up development, ensuring traceable audit trails from input to final drug substance batch. Comprehensive documentation and batch records enable clearance for post-synthesis QC and regulatory filings.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia Monograph 5.2.1
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • GMP Annex 13 (API Impurity Control)

    Typical usage ratio

    • Standard chiral step: 2% – 8% molar ratio relative to primary precursor
    • Varies with target molecule’s complexity and desired stereoselectivity
    • Lower ratios during pilot trials before scale-up
    • Ratio refined per batch documentation and target yield

    Downstream process integration

    • Charged at the enantioselective coupling or cascade reaction stage
    • Included in automated reactor charging lists
    • Removed via established workup and purification (HPLC or crystallization)
    • Parallel release of isolated intermediates to next synthesis phase

    Final product types

    • Statin API intermediates (e.g., Atorvastatin precursor)
    • Macrolide core units for antibiotic development
    • Synthetic prostaglandin analogues
    • Advanced research molecules for clinical candidates

    2. Agrochemical Stereoselective Compound Synthesis

    Agrochemical producers incorporate our raw material in the enantioselective synthesis of select herbicides and insecticides, targeting compounds that require strict isomeric purity for safe environmental profile and field efficacy. The compound enables downstream manufacturers to meet both yield and regulatory review for export and domestic use, with traceable lot control throughout pilot, validation, and commercial runs.

    Industry compliance standards

    • ISO 9001:2015 (Agrochemical Quality Management)
    • OECD Principles of Good Laboratory Practice (GLP)
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • Chemical Control Law (REACH, USA EPA regulations)

    Typical usage ratio

    • Usually 1.5%–5% by mol, depending on stereoisomer targets
    • Customized per downstream crop protection formulation
    • Adjusted for active ingredient purity testing pre-registration
    • Modified to minimize by-products before crystallization

    Downstream process integration

    • Added at the asymmetric coupling stage for chiral pyrethroids
    • Used in scale-up cell for pilot to commercial validation
    • Monitored for residue in post-processing by trace GC-MS
    • Residue removal completed post-crystallization for regulatory compliance

    Final product types

    • Chiral pyrethroid insecticides
    • Strobilurin class fungicides
    • Phenoxy acid herbicide intermediates
    • Other enantiopure agrochemical active ingredients

    3. Fine Chemical Synthesis for Flavors & Fragrances

    Leading flavor and fragrance producers employ (-)-Corey Lactone Benzoate for precision synthesis of enantiopure aroma and flavor molecules, where olfactory properties depend on strict stereochemistry. The controlled use of this intermediate enables complex lactone and ester construction for formulations sold into regulated consumer markets, with full traceability and supported by certificates of origin and analysis.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • EU Regulation (EC) No 1334/2008 (Food Flavorings)
    • Good Manufacturing Practice for Food Additives (21 CFR 110)
    • JECFA (Joint FAO/WHO Expert Committee on Food Additives) guidance

    Typical usage ratio

    • Usage level generally 0.5%–3% in reference to final aroma compound batch
    • Precisely determined by GC purity analysis and end-use composite requirements
    • Adjusted as per targeted enantioselective yield in multi-step synthesis
    • Minimized to control costs on kilogram-output batches

    Downstream process integration

    • Introduced in chiral lactone and ester-forming steps
    • Quality confirmation prior to formulation blending
    • Blending into finished aroma or flavor as soon as intermediate validated
    • Residual control assures odor threshold limits in end products

    Final product types

    • Fruit lactone fragrances (e.g., peach, coconut notes)
    • Chiral musk aroma materials
    • Custom flavor ingredients for beverage and dairy industries
    • Lactone-based perfumery bases

    4. Specialty Polymer Building Block for Medical Devices

    Producers of advanced medical-grade polymers integrate (-)-Corey Lactone Benzoate to develop precisely engineered lactone copolymers. These specialty materials provide biocompatibility, controlled degradation rates, and defined molecular weights needed for use in implants, suture materials, and controlled drug delivery systems. Technical documentation and validation support are provided to meet all downstream quality system requirements.

    Industry compliance standards

    • ISO 13485:2016 (Medical Devices Quality Management Systems)
    • USP Class VI (Plastics for Medical Applications)
    • EU Regulation 2017/745 (Medical Device Regulation – MDR)
    • ISO 10993-1 (Biological Evaluation of Medical Devices)

    Typical usage ratio

    • Typically 0.2%–2.5% by total monomer weight for copolymer synthesis
    • Ratio optimized for targeted molecular weight distribution
    • Adjusted following lab-scale hydrolysis or degradation studies
    • Varies with end-use segment (e.g., fast vs. slow resorbable devices)

    Downstream process integration

    • Dosed at solution polymerization or copolymerization step
    • Monitoring via in-process NMR or GPC for chain-length accuracy
    • Up-scaled after validation batches meet degradation and purity specifications
    • Material transition controlled under closed-system blending

    Final product types

    • Bioresorbable suture threads
    • Drug delivery microparticles
    • Polymer coatings for medical devices
    • Temporary implantable scaffolds

    5. Research & Development of Custom Chiral Ligands

    Advanced research laboratories and pilot plants apply (-)-Corey Lactone Benzoate as a precursor for synthesizing custom chiral ligand libraries. These ligands are critical for catalytic asymmetric reactions in pharmaceutical and specialty material discovery. Robust documentation and analytic support ensure confidence during complex multi-step synthesis and subsequent scale-up to semi-works or commercial scale.

    Industry compliance standards

    • OECD GLP for laboratory chemicals
    • ISO 17025 for laboratory competence
    • Company-specific SOPs for analytical and synthesis protocols
    • Local hazardous chemical use registration where applicable

    Typical usage ratio

    • Ranges from 0.1 mmol to 2 mmol per chiral ligand batch in research scale
    • Flexible for exploratory synthesis and SAR (structure–activity research)
    • Higher loads may be evaluated for catalyst optimization studies
    • Scaled down for cost and reagent optimization in screening stages

    Downstream process integration

    • Loaded at ligand skeleton construction in multi-step organic synthesis
    • Verified via NMR and LCMS before combinatorial expansion
    • Ligands used directly in catalytic assays or crystallographic studies
    • Batch archive maintained for subsequent upscaling assessments

    Final product types

    • Chiral phosphine ligands
    • Chiral diol and diamine derivatives
    • Custom screening libraries for pharmaceutical development
    • Asymmetric catalyst toolkits for academic and industrial labs
    Free Quote

    Competitive (-)-Corey Lactone Benzoate 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.

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    Certification & Compliance
    More Introduction

    Introducing Our (-)-Corey Lactone Benzoate: Precision Chemistry Starts Here

    A Chemist’s Solution: From Synthesis to Scale-Up

    In today’s synthetic organic laboratories, demand for reliable, optically pure intermediates continues to press upward each season. Over the last decade, we’ve seen (-)-Corey lactone benzoate emerge as a benchmark chiral building block, thanks to its central role in the asymmetric synthesis of natural products and advanced pharmaceuticals. As the manufacturers who produce this compound from raw precursors, our focus never strays from purity, reproducibility, and practical utility in process chemistry.

    Real-World Chemistry: The Backbone of Chiral Synthesis

    For many synthetic routes aimed at preparing complex molecules, the need for enantiomerically enriched lactones has become undeniable. Our (-)-Corey lactone benzoate, with an enantiomeric excess routinely greater than 98%, offers chemists an edge during multi-step preparations. Few chiral starting materials have the supporting literature or track records to match — this lactone benzoate has found its place in top-tier university labs and pharmaceutical pilot plants alike. Its utility in constructing polyoxygenated frameworks makes it a mainstay in total synthesis methodology. Every batch we manufacture must withstand scrutiny in terms of rotation value, residue profile, and stability — not just at shipment but on the shelf months down the line.

    Model and Specifications: No Trade-Offs With Consistency

    We produce (-)-Corey lactone benzoate in several scales, from select research-grade vials to multi-kilogram drums for plant operation. Our manufacturing model prioritizes thorough traceability, so each lot ships with a complete certificate of analysis including chiral HPLC and NMR verification. Typical specifications include enantiomeric excess above 98%, chemical purity above 99%, and water content below 0.5%. Each parameter receives its own spot check to ensure no shortcuts. No batch leaves our facility without confirmation of physical properties — melting point, optical rotation, spectral data — sitting squarely within supporting literature ranges. Purity means very little if a sample degrades in months, so we run ongoing stability studies to follow each lot over time.

    From Lab Bench to Plant Floor: Flexible Quantities, Real Support

    Chemistry rarely respects arbitrary scales. A group investigating a novel reaction might call for only a few grams, while process teams optimizing a route for late-stage intermediates will order in kilos. Our systems let us serve both, without cutting corners on QA. When we prepare your order, real people check and pack every sample — not just a shipping robot. Customers can reach out to discuss particle size or storage concerns directly with someone who has produced the material, not a call center that just relays messages. This small touch translates into smoother transfers, higher yield, and less troubleshooting on the customer’s side. We have seen how delays or subpar batches impact project timelines and research grants, so we plan every run with contingencies to keep lead times steady even during peak demand.

    Supporting R&D: Customization and Application Experience

    Projects evolve, and research goals shift often. Whether a group is pioneering a new synthetic pathway or scaling an established protocol, unexpected hurdles crop up. Our experience with (-)-Corey lactone benzoate extends beyond simple production. We help customers evaluate which protecting groups, solvents, or storage temperatures really deliver on yield and stereocontrol. By collaborating directly with bench chemists, we’ve learned to anticipate issues such as unforeseen hydrolysis during extended reaction times or racemization under unbuffered conditions. Typical protocol advice comes straight from what has succeeded on the shop floor, not just from academic tables. We see repeated interest in the benzoate derivative for its added stability compared to the parent corey lactone, especially when intermediates will be isolated or stored before further use.

    Why Choose the Benzoate? Insights from Manufacturing Practice

    The benzoate form of (-)-Corey lactone has distinct advantages over unprotected lactones or alternate esters. Benzoate protection shields the lactone from transient nucleophiles or acids that could otherwise cause ring-opening. From a process standpoint, this saves time spent re-purifying and analyzing samples that degrade or isomerize. We keep close records of process yields, and the benzoate consistently helps teams push reactions forward with cleaner isolation steps and fewer surprises. Shelf-life extends, and waste diminishes. In contrast, the methyl ester variant tends to hydrolyze more easily when subjected to basic conditions, undermining reproducibility for downstream reactions. The p-methoxybenzoate offers a compromise but often adds cost or diminished ruggedness during purification. Over years of feedback, the benzoate stands as the most robust protection for labs under pressure to publish or ship product within tight timelines.

    Specific Uses: Unlocking Advanced Synthesis

    Our customers use (-)-Corey lactone benzoate to install chiral centers in sterically congested targets, synthesize macrolides, or assemble polyhydroxylated scaffolds in stepwise fashion. The optically pure backbone derives from landmark Corey lactone chemistry, named for Elias James Corey’s pioneering work. During partial reduction, the compound enables regioselective additions, and the benzoate protection allows for selective deprotection later using mild reagents. In medicinal chemistry, researchers use this intermediate to achieve non-racemic, functionally dense fragments in lead candidate synthesis. Years of aggregate customer feedback highlight its value in controlling stereochemistry when constructing natural product cores, especially polyketide and carbohydrate analogs. We continue to update protocols based on real-world feedback, closing the loop from plant to publication.

    Distinctiveness: What Sets Our Material Apart

    Others sell (-)-Corey lactone benzoate, but far fewer control every step from starting acid to finished, purified material. We optimize our purification through multi-stage crystallization and high-resolution chromatography, eliminating minor impurities, benzoylated side-products, or trace metals. This kind of oversight matters less at milligram scale but proves critical when a kilogram batch has to run through expensive, multi-step couplings or hydrogenations. The confidence to take our material straight into a vital step instead of running additional pre-purification or quality checks can reduce the number of reactions stalled mid-process. It’s not just theory; we’ve seen multi-million-dollar projects run smoother because their lactone intermediate performed as expected, batch after batch.

    Safety and Handling: Practical Knowledge, Not Just Paperwork

    Having run hundreds of batches in our own facility, we’ve learned what warnings matter in the real world and which are only theoretical. The benzoate derivative compacts well and resists airborne dust, so we rarely see issues of inhalation hazard outside of major spills. Bulk samples store best chilled and dry, out of direct light. We include silica packets and double-sealed jars for every shipment; these touches have cut the number of customer complaints about caking or clumping by over half. Users should avoid unnecessary exposure to strong acids or bases, as the benzoate group provides some protection but not absolute barring to hydrolysis or transesterification. Standard laboratory gloves and splash goggles remain the order of the day, and our team reviews any reported incidents to prevent repeat issues. Any time a property shifts batch-to-batch, we track it, record it, and work to eliminate the root cause in subsequent runs.

    Environmental Concerns: Commitment Beyond Compliance

    Manufacturing chiral building blocks like (-)-Corey lactone benzoate brings a responsibility to minimize waste streams, especially when benzoyl groups or lactone byproducts enter the effluent. We engineered our synthesis route to favor recovery of leftover reagents and solvents wherever possible, cutting our total organic load by 20% over the last cycle. Where others might dump aqueous waste or avoid recycling, our staff developed a real-time monitoring setup to track organic carbon, ensuring every batch limits chemical discharge well below legal thresholds. Solvent tanks and columns run on a closed-loop to reclaim as much as possible for future runs, saving costs but more importantly keeping downstream ecosystems cleaner. We never view compliance with international regulations or local requirements as a checkbox; each process modification follows from the same instinct that drives us to improve our finished product.

    Collaborative Quality: Responding to Problems and Feedback

    Problems never disappear entirely; even the best manufacturing runs face the occasional interruption, faulty pump, or solvent contamination. We log every customer report on a weekly dashboard — not for show, but to push toward a zero-complaint reality. Lessons learned from a missed delivery window or a purity drop fire changes to scheduling, storage, or training for everyone in the plant. Our closest relationships have grown through helping resolve synthesis snags, not just selling material; whether the problem stems from an obscure side-reaction or upscaling a previously flawless route, our team prioritizes transparency and technical resolution. Having walked the process from weighing starting material to boxing finished vials, we approach troubleshooting with empathy and focus, recognizing that one delayed shipment can stall months of research.

    Comparison With Comparable Reagents: Listening to Years of Bench Science

    Other chiral lactones or benzoate-protected intermediates exist. Yet most alternatives either lack robust optical purity, lose stability in humid conditions, or show more batch-to-batch variability as measured by chiral HPLC. In a typical project cycle, we observe yield drags when non-Corey-based lactones swap into published routes — often leading to a return for the original material. Process chemists report that alternative esters may improve transient solubility but compromise separation or risk increased hydrolysis, especially at scale. Even among Corey-derived options, the benzoate group hits the sweet spot for inertness and practicality: sufficiently tough for long-term storage, yet easy to remove under base-catalyzed or reductive conditions.

    Traceability and Documentation: Confidence Supported by Data

    We build every batch history with intensive documentation, not just to create a trail for regulators but to give practical assurance if a batch ever comes up for review. Chromatograms, spectra, and inventory controls stand ready to resolve even arcane queries. Our laboratory ERP system tracks raw materials, intermediates, inspection points, and final packaging by barcoded lots. Samples sit in reference libraries for years, giving us the confidence to stand behind a shipment long after a competitor would lose paperwork. We recognize that mistakes or defects — rare as they have become — cast a long shadow. Each record builds confidence in both the product and the processes that create it.

    Staying Ahead: Ongoing Improvement Driven by Direct Practice

    New researchers entering the field and veterans alike press us for continual upgrades: tighter assays, faster shipments, better packaging, and new derivatives. We learn from every complaint, every delayed timeline, and every glowing email about a clean reaction or fast isolation. Production shifts over time, as does chemistry — we track changes in academic methodology just as closely as regulatory or market shifts. Helping a customer shave 4 steps from a process or boost chiral purity by a percent gives satisfaction few other industries can match. As green chemistry initiatives reshape operational goals, we adapt more closed-cycle systems and recover more solvents and reagents with each annual upgrade.

    Building Relationships, Not Just Transactions

    Every flask of (-)-Corey lactone benzoate we ship carries months or years of planning behind it — not as an anonymous shipment but as the end result of conversations with real scientists and manufacturing staff. We value every return call, protocol update, or troubleshooting session that follows from a shipment. Beyond supplying a reagent, we aim to become partners embedded in the experimental process, sharing responsibility for breakthroughs and setbacks alike. Through this collaborative spirit, and by keeping craft at the center of our manufacturing, we strive to advance the future of organic synthesis, one batch at a time.