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(-)-Corey Aldehyde Benzoate

    • Product Name (-)-Corey Aldehyde Benzoate
    • Alias CAB
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    392880

    Product Name (-)-Corey Aldehyde Benzoate
    Cas Number 112093-23-5
    Molecular Formula C15H12O3
    Molecular Weight 240.26
    Appearance White to off-white solid
    Optical Rotation [α]D20 −95° (c=1, CHCl3)
    Melting Point 88-91°C
    Purity Typically >98%
    Solubility Soluble in chloroform, methanol, and dichloromethane
    Storage Temperature 2-8°C
    Synonyms (-)-Corey Lactone Aldehyde Benzoate
    Smiles O=CC1[C@@H](OC(=O)C2=CC=CC=C2)CC=CC1=O

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

    Packing & Storage
    Packing (-)-Corey Aldehyde Benzoate is supplied in a 1 g amber glass vial, tightly sealed, with hazard labeling and clear product identification.
    Shipping (-)-Corey Aldehyde Benzoate is shipped in compliance with chemical safety regulations. It is securely packaged in sealed, inert containers to prevent contamination and degradation. The shipment includes appropriate labeling and documentation. Temperature-sensitive handling and expedited delivery options may be applied to ensure product stability and integrity during transit.
    Storage **(-)-Corey Aldehyde Benzoate** should be stored in a tightly sealed container, protected from light and moisture, under an inert atmosphere such as nitrogen or argon. It is best kept at low temperatures, typically in a refrigerator or freezer (2–8 °C or below), to prevent decomposition. Avoid exposure to air, acids, and bases. Store in a well-ventilated, cool, and dry chemical storage area.
    Application of (-)-Corey Aldehyde Benzoate

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

    As a dedicated manufacturer of (-)-Corey Aldehyde Benzoate, we supply this chiral intermediate to high-value sectors with stringent process and quality requirements. Our material is involved in precise downstream syntheses across specialty pharmaceuticals, advanced agrochemicals, fragrance intermediates, and research reagents. Below are key application pathways that demonstrate real industrial use.

    1. Asymmetric Synthesis of Pharmaceutical APIs

    Pharmaceutical producers utilize (-)-Corey Aldehyde Benzoate as a key chiral building block during the multi-step synthesis of targeted active pharmaceutical ingredients. Its optical purity enables stereoselective reactions required for clinical candidates and commercial drugs. The material typically enters during the chiral pool phase or early intermediate construction, where enantioselectivity can’t be compromised. Batch records, traceability, and contamination control at this stage all meet the highest pharmaceutical standards, directly impacting final drug safety.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia—National Formulary) monograph specifications for starting materials
    • EU EMA Guidelines for starting materials (Directive 2001/83/EC and 2011/62/EU)
    • FDA 21 CFR Parts 210 and 211

    Typical usage ratio

    • Usage in the range of 1.0–5.0% molar equivalent in the chiral intermediate stage; exact ratio set by target API yield and reaction sequence

    Downstream process integration

    • Introduced in controlled enolate alkylation or aldol condensation steps
    • Used in enantioselective reduction or chiral auxiliary removal protocols
    • Feeds directly into protected amino alcohol, oxazolidinone, or β-amino acid synthesis routes
    • Requires validated analytical QC on input and output for stereochemical purity tracking

    Final product types

    • Chiral β-lactam antibiotics
    • Non-steroidal anti-inflammatory drugs (NSAID) precursors
    • Selective serotonin reuptake inhibitor (SSRI) intermediates
    • Enantiopure specialty pharmaceutical APIs

    2. Intermediate in Agrochemical Synthesis

    Major agrochemical producers use this compound in the assembly of optically active pesticide and herbicide molecules, where stereochemistry controls field efficacy and regulatory acceptance. It enters downstream flow after initial core structure construction, enabling site-selective transformations before final formulation. Suppliers must guarantee consistent specification per registration dossiers and maintain controlled impurity profiles for global market access.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for raw material supply
    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) technical specifications
    • REACH (EC 1907/2006) registration and safety verification for downstream supply
    • Relevant OECD harmonized templates for agrochemical ingredient reporting

    Typical usage ratio

    • Generally 2–6% of total reactant mass in enantioselective synthesis phases, modulated by crop-protection molecule stereoselectivity demands

    Downstream process integration

    • Supplied for use in chiral Grignard addition, Michael addition, and asymmetric hydrogenation protocols
    • Quality checked before and after key synthesis steps
    • Integrated into route steps leading to chiral acid or ester agri-active structures
    • Process scale and waste stream compliance tracked by in-plant audits

    Final product types

    • Enantiopure herbicide active ingredients
    • Optically active fungicide synthons
    • Pesticide intermediates for crop protection products
    • Stereochemically defined insecticide molecules

    3. Chiral Fragrance Intermediate Production

    Manufacturers in the fine fragrance industry select this compound to create high-value, optically pure intermediates for complex aroma chemicals. Here, batch records and GMP alignment are crucial due to direct use in formulations applied to consumer skin or inhaled products. Our material’s purity profile minimizes process corrections, allowing direct transformation in Diels–Alder chemistry or selective oxidations.

    Industry compliance standards

    • IFRA (International Fragrance Association) standards for raw material sourcing and traceability
    • ISO 22716:2007 Cosmetic Good Manufacturing Practices
    • European Union Cosmetics Regulation EC No. 1223/2009
    • REACH registration and notification for aromatic chemicals

    Typical usage ratio

    • Applied at 0.5–2.5% in intermediate batch makeup, determined by the stereochemistry target of final aroma component

    Downstream process integration

    • Processed by selective reduction or esterification steps following introduction
    • Maintained in closed-system reactors for odor-critical operations
    • Specification checked for residual benzoate content and chiral purity before transfer to blending
    • Fed into downstream compounding of luxury perfume bases or flavor encapsulants

    Final product types

    • Optically active musks
    • Chiral macrocyclic lactones
    • Complex aroma signatures for prestige perfumery
    • Natural-identical flavoring agents

    4. Stereoselective Synthesis for Research Reagents

    Specialty chemical and analytical reagent manufacturers leverage this material to synthesize reference standards, catalysts, and lab-scale compounds used in academic or applied R&D. Fully documented origin and enantiomeric excess data support informatics and reproducibility, allowing credible result publication and patent filings. The compound supports the production of advanced ligands and auxiliary agents for asymmetric transformation research worldwide.

    Industry compliance standards

    • ISO 17034:2016 Requirements for Reference Material Producers
    • GLP (Good Laboratory Practice) compliance per OECD series on testing of chemicals
    • Documentation for National Metrology Institute registration where applicable
    • Internal batch traceability systems for catalog and custom synthesis chemicals

    Typical usage ratio

    • Formulated at 0.1–1.5% of total reaction mixture during model compound synthesis, with scale adjusted to research or validation test batch size

    Downstream process integration

    • Added during ligand design or chiral standard production runs
    • Handled under inert atmosphere in dry-box facilities for sensitive chemistry
    • Batch-specific certificates of analysis issued for enantiomeric and chemical purity
    • Supports scale-up or transfer to pilot synthesis upon customer request

    Final product types

    • Certified chiral reference standards
    • Advanced research ligands for asymmetric catalysis
    • Stereochemically pure small molecule libraries
    • Chemical tools for R&D and process development laboratories
    Free Quote

    Competitive (-)-Corey Aldehyde Benzoate prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Bringing Reliability and Precision: Introducing (-)-Corey Aldehyde Benzoate from the Manufacturer’s Bench

    Our Journey to a Trusted Chiral Building Block

    In the world of synthetic chemistry, few compounds offer as much utility and reliability as (-)-Corey Aldehyde Benzoate. Through years at the lab bench and in scaled manufacturing, we have seen demand for this compound climb alongside advances in drug discovery and complex molecule construction. Originally described by E.J. Corey in one of his major breakthroughs, this molecule stands apart for its ability to transfer absolute stereochemistry into challenging architectures. Scientists relying on enantioselective control need materials that won’t introduce irregularities, especially as projects ramp from milligrams to kilograms. Every batch we produce goes through hands-on evaluation, drawing on both automated equipment and experienced eyes. We have worked through countless production runs, investigating solvents, crystallization conditions, and isolation protocols. Problems in bench-scale synthesis can snowball in a plant environment and we believe true manufacturing skill comes from smoothing out those rough edges and ensuring batch after batch runs with minimal surprises.

    Our (-)-Corey Aldehyde Benzoate stands as more than a reagent — it is a benchmark in our product portfolio representing what chemical manufacturing looks like at its best: rigorous proof of enantiomeric purity, clear traceability to starting materials, and adaptation to the ongoing changes in synthetic routes favored by academic and industrial groups. Researchers run recurring projects in asymmetric synthesis and often face unexpected complications with new suppliers. The difference that direct-from-the-manufacturer material brings is consistency, support for custom scale-ups and, above all, technical guidance rooted in firsthand production experience.

    Model, Purity, and Technical Specifications Borne of Manufacturing Experience

    Typically, our operation maintains (-)-Corey Aldehyde Benzoate as both a standard analytical grade (HPLC >98%) and a preparative grade exceeding 99% enantiomeric excess, supported by chiral HPLC and NMR verification. Older procedures used basic column chromatography or even manual extractions, which often left behind organic impurities, particularly benzoic acid, methylbenzoate, or traces from downstream derivatization. We have re-engineered purification with a focus on simple, repeatable crystallization techniques. Modernization eliminated batch-to-batch drift in color, melting point, and rotating optical values. Each lot ships with a full chromatogram and certificate validated by chemists who work the actual reactors — not distant analysts or generic paperwork. The quantities we provide range from gram-scale vials for method development to multi-kilo drums for pilot plants or commercial production, each filled and sealed onsite.

    Environmental criteria also frame manufacturing: solvent recovery, waste minimization, and thorough containment of benzoic acid vapor ensure we exceed regional workplace standards. Production lines change quickly depending on customer priorities and we have spent years perfecting switch-over steps to eliminate contamination from previous reactions. All this supports a level of controllability often hard to achieve in outsourced or trading-based models. We understand firsthand the impact that even small process deviations can have downstream, not just on the active molecule but on every intermediate and side product that develops along the way.

    Distinctive Features and Application Advantages

    Racemic aldehyde benzoate is widespread and, for simple oxidations or open-label reductions, it works well enough. Research programs pursuing enantioselective synthesis pathways see pronounced advantages with the optically active compound. In our facility, chiral purity arrives from carefully maintained resolution methods — either enantioselective synthesis using chiral catalysts or high-efficiency separations. Unlike some lower-grade offerings, where repeated handling and repacking introduce moisture or potential racemization, our production cycle minimizes exposure every step, as we’ve learned how oxygen and humidity can quickly alter sensitive aldehydes. Each worker on the line trains to handle the entire series of manipulations, not just isolated steps, and stores fresh product under strict moisture exclusion.

    Our direct customers often need supplies that remain stable during shipment and storage, holding their stereochemistry over weeks or even months. This means we rely on temperature control and custom-designed packaging built for aldehyde stability — solutions developed only after multiple disappointing experiences with generic containers leading to polymerization or off-odors. Time spent in real production illuminates so many weak points invisible at a distributor’s level. We strengthen those points, and the result emerges as a reagent that delivers not just high standards at the moment of shipping but lasting value when used in sensitive transformations or long synthesis campaigns.

    Comparison with Other Chiral Auxiliaries

    Chemists have access to dozens of chiral auxiliaries and resolved aldehydes, each with its own benefits or tradeoffs. Many are derived from amino acids, menthol, or tartaric acid cores. Our (-)-Corey Aldehyde Benzoate owes special status to its bench-proven performance in constructing complex oxygen heterocycles, particularly in iterative asymmetric additions or Diels-Alder reactions. Where standard aldehydes falter due to ambiguous enantiopurity or unknown byproduct profiles, customers tell us our material unlocks consistent yields and clean hand-offs to the next synthetic step. In high-stakes pharmaceutical R&D, having complete spectral documentation and a loyal product history reduces project risk and avoids regulatory uncertainty.

    Other auxiliaries often require lengthy deprotection or introduce groups that complicate downstream purification. By design, the (-)-Corey variant attaches and detaches predictably, minimizing byproduct formation. With experience, we recognized key subtleties: some users want higher throughput and less solvent load — so we integrated continuous flow crystallization and filtered solid transfers. Others request heightened attention to trace oxidants, so we double-vacuum pack and include desiccant monitors in every drum. All these tweaks grew from seeing real customers hit roadblocks and reflecting on our own trial-and-error. Rather than settling for a ‘sufficient’ product, we strive for results that earn repeat orders from chemists serious about time and accuracy.

    End-Use Applications: Impact in Real Projects

    Many stories surface from our conversations with end-users. Process chemists designing natural product syntheses often rely on (-)-Corey Aldehyde Benzoate to initiate chiral pool strategies. The benzoate group, in their hands, offers clean introductions of stereochemistry then removal under mild conditions, preserving delicate intermediates. Medicinal chemistry teams have cited our batches for enantioselective reductions in preclinical library generation and scale-up. In these cases, speed is vital — pharma must move lead candidates to toxicology fast, so the wrong auxiliary creates unacceptable delays.

    Certain customers develop customized ligands or organocatalysts that demand a core aldehyde with tight purity and matching enantiomeric excess across lots. Here, having access to a reliable manufacturing source cuts down on validation work, and they value being able to call on our technical team for insight if crystallization or resolution behaviors shift. Over several years, our product made its mark as the chiral handle of choice for challenging aldol reactions, allowing researchers to tune selectivity for diverse side chains. They avoid costly reruns when their starting material tracks tightly to specification, a benefit that looks small on paper but proves huge project after project.

    The Manufacturing Difference: How Involvement at Every Step Translates to Quality

    From the outside, chemical manufacturing can look like a set recipe. Experience tells us each stage brings unique hurdles — temperature swings, ambient humidity, the quirks of scale. Early batches years ago underscored how even a change in stirring speed or minor bottle aging affects the outcome. These lessons taught us not to chase minimum standards, but to invest in repeat pilot runs and verify new suppliers for every critical input. The value of hands-on oversight can’t be overstated.

    Some intermediates in the Corey series are known to decompose if not handled with fresh reagents or prompt downstream conversion. This means our team regularly reviews protocols not just for the aldehyde itself but for everything upstream and downstream in the chain, dialing in the quality parameters most likely to influence the customer’s yields. Adapting reactor cleaning cycles, monitoring bin storage times, and even the way the material is dispensed into containers can make or break a project for cGMP clients. From kilo labs to multi-ton facilities, we invest in in-house verification so customers get what our own lab crew would use for complex, high-value syntheses.

    Supporting the Scientific Community: Knowledge Sharing and Real-Time Adaptation

    We do more than ship out parcels. Our technical team keeps pace with current literature on asymmetric methodology, contributing when possible and always open to feedback from new applications. Several times a year, we’re contacted by researchers who ran into yield plateaus or mysterious byproducts when using generics, only to find our batch gave them the consistency to publish or patent a new scaffold.

    Our participation extends to troubleshooting through synthetic route changes, providing insight on isolation and workup, and exchanging best practices learned in commercial production. The give-and-take with creative chemists keeps us improving old processes and investing in new purification or resolution setups. We learn which improvements matter most only after reflective dialogue and problem-solving over real-world challenges. This continuous engagement allows us to react rapidly — if a researcher reports a trace impurity or handling difficulty, we run pilot batches to reoptimize those steps.

    Logistical Considerations: Ensuring an End-to-End Solution

    Customs, export paperwork, temperature controls — all these details become trouble spots for sensitive materials. We keep tightly monitored cold-chain shipping for users in demanding climates and take special care to comply with regional transportation rules. Each drum or vial leaves the factory with immediate track-and-trace numbers, shielding research groups from delays or uncertainty about product origin.

    Over the years, we’ve learned to watch for the small details: vented stoppers to manage pressure, amber vials to protect from UV, and just-in-time inventory to meet labs faced with shifting deadlines. We know that a well-packed container doesn’t just preserve a chemical’s integrity, it also gives the user confidence to press on with high-value experiments without second-guessing their starting point.

    Evolving with Research: Flexibility in Quantities and Customization

    As the landscape for chiral synthesis shifts, so too do the ways our compound is used. What started out as a specialty reagent popular in academic total synthesis has grown into something demanded by discovery chemistry, process development, and now even advanced materials. We field regular requests for different enantiomer ratios, ultra-low moisture lots, or tight residual solvent controls. Our technical liaison meets these adjustments by translating real-world requirements back into process tweaks: modifying drying steps, adjusting atmosphere controls, and altering packaging lines for specialty runs.

    Scientists working at the frontiers of new molecular frameworks often approach us with specialized queries: can we adapt the crystal form? Could we refine the benzoate cleavage conditions for a particularly sensitive molecule? By remaining adaptable instead of locking ourselves into rigid catalog definitions, we find ourselves supporting project timelines that shift or scale rapidly, knowing that the right product at the right moment makes all the difference.

    Facing Today’s Challenges: Quality, Security, and Supply Resilience

    Chemical supply chains today face unpredictability — global shocks, shifting regulatory regimes, and changing sustainability demands. We have absorbed many disruptions over the past years and used each as a driver for strengthening operations and communications. Direct manufacturing control means we don’t wait for someone else to correct process errors, and that sense of responsibility filters down to even the smallest staff decision. As companies evaluate their partners, the difference between a trading label and a manufacturer-runship becomes plain: continuity, direct support, and the ability to course-correct mid-project.

    Sustainability grows ever more critical, and we have invested in solvent recovery and low-emission technologies not just for regulatory compliance, but because those choices keep production robust and shield our customers from future shortages or quality swings. The resource-intensive nature of chiral auxiliaries demands this kind of attention, so we build redundancy into raw material sourcing and always stock backup supplies to avoid delays. Resilience comes not from luck, but from deliberate hardening of supply lines and operational know-how.

    Learning From Setbacks and Building Toward Future Innovation

    Not every project runs perfectly — we have faced unsatisfactory lots, challenges in isolation, and even unexpected customer returns. Each event spurs process improvement, not blame-shifting. If a chromatographic signal hinted at potential instability, our R&D set to work modifying the quench step. When a scale-up led to unsightly color, production re-examined filtration. This relentless drive to adapt and perfect underpins the integrity of our finished product, season after season and across expansion into new markets.

    In recent years, more innovation emerged from partnerships than from isolated working. We support contract manufacturing projects with hands-on training for customer staff using our (-)-Corey Aldehyde Benzoate in novel organocatalytic transformations. As sharing real-world trial results becomes commonplace, customers and colleagues push us to explore bolder solvent systems, greener operations, and even new benzoate derivatives tuned for application-specific advantages.

    Why Direct Manufacturer Engagement Matters

    Decades making and shipping (-)-Corey Aldehyde Benzoate have taught us the many ways direct communication builds better outcomes. Projects run smoother, risks drop, and the scientific community moves more efficiently from concept to conclusion. Our doors stay open to feedback, to new synthesis ideas, and to rigorous critique — all to ensure our core product line does more than meet minimum specifications. The real differentiator is the deep, technical partnership with every lab that trusts us to deliver this key chiral building block.

    Real-world chemistry calls for materials you grow to trust through every stage: the order form, the vial in your hand, the analytical results on your screen, and the reproducible output in your notebook. As direct manufacturers, we commit to that journey, investing in quality at each level from raw material to finished reagent. This commitment brings not just product, but continuity and peace of mind, so every research program using (-)-Corey Aldehyde Benzoate can build on a rock-solid chemical foundation.