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1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose

    • Product Name 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose
    • Alias Solketal
    • Einecs 265-604-6
    • 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
    VTB
    Specifications

    HS Code

    331845

    Chemical Name 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose
    Molecular Formula C12H20O6
    Molar Mass 260.29 g/mol
    Appearance White to off-white solid
    Cas Number 4074-62-2
    Melting Point 92-94 °C
    Solubility Soluble in water and alcohol
    Optical Rotation [α]D +92° (c=1, H2O)
    Storage Conditions Store at 2-8 °C
    Iupac Name (1R,2R,3S,4R,5R)-1,2-O-cyclohexylidene-α-D-glucofuranose

    As an accredited 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 25g of 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose is supplied in a sealed amber glass bottle with a tamper-evident cap.
    Shipping 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose is shipped in tightly sealed containers, protected from moisture and direct sunlight. The chemical should be handled with care, following standard safety protocols. Shipping complies with relevant regulations, ensuring proper labeling and documentation. Store in a cool, dry location during transit to maintain product integrity and prevent contamination.
    Storage **1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose** should be stored in a tightly sealed container, protected from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Avoid exposure to strong acids, bases, and oxidizing agents. Ensure that the storage area is clearly labeled and follow standard laboratory safety protocols for chemical storage.
    Application of 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose

    Applications of 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose in Industrial Manufacturing

    As an established manufacturer of high-purity 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose, we support customers across multiple industries with precise quality and supply assurance. Our production integrates user feedback from global manufacturers, informing our unique understanding of this specialty carbohydrate’s functional behavior in key sectors. The following downstream scenarios reflect real adoption in industrial formulations, with supporting compliance, usage, process, and finished product information.

    1. Pharmaceutical Intermediates for Antiviral Nucleoside Synthesis

    1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose serves as a protected sugar intermediate in the multi-step synthesis of nucleoside analogues, particularly in laboratories and industrial settings where the compound’s cyclic acetal group maintains selectivity under controlled deprotection conditions. Chemical and biochemical manufacturers utilize it to build complex pharmaceutical scaffolds while avoiding interfering reactivity at specific hydroxyl positions. Its high purity supports consistent batch yields and structural fidelity, essential for regulatory submission and clinical evaluation of downstream molecules.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs (Active Pharmaceutical Ingredients)
    • USP/NF (United States Pharmacopeia / National Formulary) for intermediates
    • EDQM (Ph. Eur.) monographs for starting materials (where referenced in nucleoside drug processes)
    • FDA 21 CFR Part 210–211 for process controls

    Typical usage ratio

    • 0.8–2.5 molar equivalents relative to nucleobase backbone, adjusted per pathway design and batch reactor size

    Downstream process integration

    • Charged as a key reactant at the protected glycosylation stage in nucleoside analogue synthesis
    • Subjected to selective deprotection and further functionalization in multi-step organic synthesis
    • Isolated as an intermediate by downstream crystallization and refined for subsequent coupling

    Final product types

    • Active pharmaceutical ingredients (APIs) for antiviral and anticancer nucleoside drugs
    • Specialty protected sugars for R&D pilot batches

    2. Chiral Building Block for Specialty Fine Chemicals

    Chemical manufacturers incorporate 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose into enantioselective synthetic routes, where it provides a defined stereochemical template. This application finds demand in the production of advanced intermediates for chiral catalysts, agrochemical candidates, and polymer precursors, with the carbohydrate’s multi-functional group protection allowing chemoselective modifications and minimizing downstream byproducts.

    Industry compliance standards

    • ISO 9001:2015 for quality management systems in chemical manufacturing
    • REACH regulation (EC) No 1907/2006 for import/export and handling across Europe
    • Product-specific customer audits and technical agreements on enantiomeric purity

    Typical usage ratio

    • 0.5–1.2 wt% in target chiral synthesis batches, modified according to desired output and waste minimization strategies

    Downstream process integration

    • Integrated after initial raw material charging as a core chiral auxiliary or template
    • Serves as a precursor to downstream oxidations, reductions, or cross-coupling reactions
    • Removed after reaction by selective cleavage, leaving behind the chiral center in advanced intermediates

    Final product types

    • Chiral fine chemicals and advanced intermediates
    • Agrochemical synthetic precursors
    • Chiral catalysts and ligands for downstream asymmetric reactions

    3. Carbohydrate-Based Protecting Group Strategies in Custom Organic Synthesis

    Custom synthesis service providers use 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose as a selectivity-defining aldehyde or alcohol protecting agent within routes that involve carbohydrates, polyols, or other multi-hydroxyl substrates. Its steric and electronic properties yield site-specific modification and facilitate orthogonal deprotection when pursuing multi-stage molecule assembly, supporting reliable process transfer in CMO (Contract Manufacturing Organization) settings.

    Industry compliance standards

    • ISO 13485:2016 for medical-grade starting materials
    • Client-supplied validation protocols in pharmaceutical CMO/CDMO operations
    • SOPs for process validation and traceability in regulated industries

    Typical usage ratio

    • Equimolar to 1.5 molar equivalents versus total protected hydroxyl groups; adjusted per target compound complexity

    Downstream process integration

    • Employed in protecting group installation phases of stepwise organic synthesis
    • Removed by acidolysis or hydrolysis at specific process stages
    • Supports mid-to-late stage assembly lines requiring defined glycoside integrity

    Final product types

    • Tailor-made oligosaccharides for diagnostics
    • Sugar-modified peptides and small molecule conjugates
    • Therapeutically-relevant intermediates with protected glycosyl motifs

    4. Analytical Reagent in Carbohydrate Structure Elucidation

    Analytical and quality control laboratories employ 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose to derivatize carbohydrate standards for high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy. The resulting protection of specific hydroxyl groups stabilizes carbohydrate configuration, providing consistent retention times and accurate structure assignments during complex mixture analyses in research and release testing environments.

    Industry compliance standards

    • ISO/IEC 17025:2017 for accredited analytical laboratories
    • FDA Guidance for Industry: Q2(R1) Validation of Analytical Procedures
    • GLP (Good Laboratory Practice) for reference standard preparation

    Typical usage ratio

    • 0.5–2.0 mole equivalents relative to analytical carbohydrate substrate; determined by analyte concentration and instrument detection limits

    Downstream process integration

    • Applied as a derivatization reagent during sample work-up phases
    • Supports formation of protected monosaccharide and oligosaccharide standards
    • Analyzed post-derivatization by HPLC, GC-MS, or NMR for identification and quantification

    Final product types

    • Certified reference standards for carbohydrate analytics
    • Derivatized carbohydrate panels for quality control laboratories
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    Competitive 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose 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

    Quality-Driven Manufacturing of 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose

    Consistent Results Through Practical Experience

    On the manufacturing floor, precision builds trust. With 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose, consistency matters just as much as the chemical purity. Chemists and process engineers put in years refining reaction controls, isolations, and purifications to yield a crystalline compound that behaves predictably in both research and scale-up trials. We spend time where it counts: temperature control during protection, solvent recovery for sustainability, careful monitoring of isomer formation. Each batch reflects the hard-earned lessons of process optimization. Purity rarely exceeds raw numbers on an assay; it predicts how well the product integrates and performs in downstream applications.

    Understanding the True Value: The Role of Cyclohexylidene Blocking Groups

    It takes hands-on experience to recognize the difference that a cyclohexylidene group can make in carbohydrate chemistry. Compared to simpler protecting groups like acetals or benzylidene rings, the cyclohexylidene variant introduces a rigid, space-filling structure that better shields the 1,2-positions of D-glucofuranose. This structural bulk often provides greater selectivity in subsequent functionalization reactions, letting synthetic chemists target other available hydroxyls with higher confidence. Research teams report cleaner reaction profiles, less side-product formation, and improved yields in glycosylation studies. The workflow becomes leaner, because our cyclohexylidene-protected sugars don’t require as many purification steps or ad hoc troubleshooting. That reliability sums up the core reason why this variant sees repeated demand from academic and industrial carbohydrate groups alike.

    Production Parameters Shaped by Real Challenges

    Manufacturing never runs on theoretical ideals. Process chemists face trade-offs at every scale-up step: balancing reagents, controlling reaction stoichiometries, and troubleshooting equipment fluctuations. We use controlled hydrogenation, with palladium catalysts chosen for batch longevity, and always monitor for catalyst leaching to prevent unwanted trace metals. Filtration protocols get revisited each quarter—sometimes more frequently—following customer feedback or shifts in raw material quality. Operators check crystal morphology and particle size, and adjust cooling regimes to keep the product easy to handle and package. Physical handling deserves as much attention as analytical spec sheets, so shipping containers are selected to preserve crystal integrity during transport.

    Model, Grade, and Purity: Words That Match the Real World

    Laboratory context sets the expectation for chemical grade and specification. We classify 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose as pharma-intermediate grade. This means every lot gets full NMR analysis, Karl Fischer water content, and specific optical rotation. Labs don’t need to filter unknown particulates or troubleshoot ambiguous NMR signals; we catch off-spec batches before they leave the warehouse. The model designation links directly to chromatographic purity—by HPLC and GC-MS verification—so chemical structure, impurity profile, and trace elements are fully documented. A narrow melting range points to purity, not just the absence of obvious contaminants. Packaging typically spans from 25 g research vials to multi-kilogram drums, each sealed to prevent moisture uptake and solvent exchange.

    Device Integration and Downstream Use

    Chemists working with such a molecule expect seamless integration in multi-step syntheses. We’ve spent years collecting feedback from researchers who deploy this sugar building block in oligosaccharide assembly, glycosylation, and diagnostic reagent development. Alpha-D-glucofuranose protected with the cyclohexylidene group gives clear advantages: less ambiguity in downstream substitution, improved resistance to acid-catalyzed hydrolysis, and tighter selectivity during regioselective functionalizations. Researchers also appreciate a lower rate of decomposition during storage, thanks to the robust cyclohexylidene moiety. In automated synthesizer applications, this translates to fewer faults and improved reproducibility of batch results.

    Differences You Can See and Measure

    Some buyers ask how cyclohexylidene-protected glucofuranose compares to other blocking strategies. Experience shows the cyclohexylidene group forms a spatial barrier that limits undesired side reactions more than standard acetonides. For projects demanding orthogonality, cyclohexylidene gives process chemists a powerful way to shield and unmask specific hydroxyls with fewer steps. It doesn’t introduce aromatic residues, which can complicate mass spec interpretations or interfere with downstream bioassays. We have observed less transacetalization, even in conditions that sometimes challenge other acetal-type protecting groups. Such tangible advantages become clear once you scale up experiments: higher yields, purer fractions, and more predictable timeframes.

    Safety and Handling Refined by Experience

    Every chemical brings unique handling questions, and our plant personnel follow a set of protocols built on real accidents and near-misses, not just regulatory lists. 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose ships as a stable, free-flowing powder—no need for inert atmosphere packaging under normal storage. Our team found low static electricity risk compared to other crystalline sugars, reducing dust hazards in the packaging bay. We recommend cool, dry storage in sealed containers, away from high humidity to prevent slow hydrolysis or deliquescence. As the manufacturer, we pay for external stability studies and encourage customers to request accelerated aging data; that transparency helps labs and production teams plan storage and re-testing intervals according to real needs.

    Supporting Progress in Research and Industry

    We see the practical impact of this intermediate as it moves beyond our inventory system. In synthetic organic chemistry, its use in regioselective glycosylation opens new avenues for natural product development and modified carbohydrate synthesis. Biotech groups rely on its predictable reactivity to customize probes for diagnostics or vaccine development. Several partners have documented smoother conversion to target structures, thanks to the gentle deprotection profile unique to the cyclohexylidene protecting group. This saves time, chemical waste, and labor costs. Each partnership brings added real-world data to help us fine-tune batch consistency and offer better technical support.

    Process Improvements: Lessons From the Production Line

    Our process engineers do more than watch readouts—they strip out bottlenecks and push for safer, leaner, greener production. Solvent selection goes beyond cost and theoretical yield; we base every choice on recovery efficiency and actual waste streams. Reactor cleaning hinges on how the last batch responded at the workup stage, not just scheduler convenience. Over the years, small tweaks to the way we introduce starting materials and control cooling rates have trimmed by-products and maximized product purity. We track yields and impurity buildup at the pilot and full-scale reactor, not just on paper. Every cycle brings incremental improvement.

    Traceability and Documentation: Earning Trust, Not Just Meeting Regulations

    Clients value clear documentation. We ship every lot with a full Certificate of Analysis—batch-specific data, not recycled templates. Test results for critical parameters, including residual solvents and heavy metal content, go well beyond minimum requirements. Our analysts cross-check chromatographic fingerprints, not just spot check for common contaminants. When customers ask for details on trace impurity origins, we consult years of in-house batch logs and raw material audits. This data-driven feedback loop builds confidence—it doesn’t leave technical teams guessing about batch histories.

    Responding to Customer Needs

    No chemical process holds static forever, so we regularly invite customer feedback to refine our workflows. Some teams needed tighter control over particle size for automated dosing systems; our response involved adjusting crystallization cooling rates and upgrading sieving capacity. Other requests focused on limiting specific residual solvents to meet downstream regulatory filings. We changed extraction solvents and adopted new drying protocols, based on pilot trials and industry feedback. This dialogue makes us better manufacturers and gives our partners a sense of ownership in the ongoing process.

    The Competitive Edge: Reliability Over Hype

    On the open market, plenty of suppliers advertise generic sugar intermediates or cut-rate pricing. We know from experience that reliability commands more value in the long run: research delays from failed reactions, ambiguous product quality, or unexpected by-products cost labs time and money. Our focus on reproducibility starts in procurement and persists through shipping; every kilogram packaged gets tracked and supported through detailed lot histories. Because we produce in-house, we don’t gamble on spot-market intermediates or offload technical support onto third parties. Our brand is our commitment. Researchers come back for the surety that each batch will perform as the last.

    Partnering Beyond the Sale: Ongoing Technical Support

    Purchasing the batch isn’t the end—collaborating with researchers and production chemists builds a two-way street. We answer method development questions, give insight into purification tweaks, and help troubleshoot reaction anomalies. Our technical team feeds customer observations back into the process, building a learning loop that sharpens both manufacturing and R&D. Customers rely on our real-world problem solving when experiments move off the whiteboard and into production.

    Why Sourcing Directly From Manufacturers Matters

    Chemists value the direct line: they don’t wait for intermediaries to relay technical details or batch histories. As the producer, we keep direct records of every raw material, every process deviation, and every inspection, and technical questions get answered by the engineers who run the plant. These relationships help customers plan longer projects and accommodate custom batch sizes or documentation needs, all without translating requests through third parties. Traceability, transparency, and technical depth flow naturally from direct collaboration.

    Real Insights Into End-of-Life and Waste Management

    Our accountability does not end with product delivery. Many customers ask about waste disposal protocols and environmental impact. From our end, cyclohexylidene-protected glucofuranose generates few hazardous by-products under standard hydrolysis and recycling; the main breakdown products are naturally occurring sugars and cyclohexanone derivatives, which downstream operations can neutralize or recover. We supply process waste sheets on request, drawing from our firsthand experience running large-scale crystallizations and filtration setups. Customers pursuing green chemistry initiatives benefit from this partnership of information. Everyone upstream and down benefits when manufacturers own their environmental outputs.

    Looking Forward: Continuous Innovation

    The story of 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose doesn’t stop with current batch specs. Chemists and engineers in our team continually investigate better routes—greener reagents, less energy-intensive processes, and new analytical tools to catch critical impurities even earlier. Pilots run side by side with the main line, applying new catalysts or tweaking reactor geometries for greater throughput. These investments stem from our knowledge that customer needs shift: higher purity, lower cost, custom functional group modifications. We invest because manufacturing excellence grows from real use cases, not just marketing slides.

    Building Trust: Why Our Product Works for You

    Our experience flows into each batch shipped. From process development through to shipment and technical support, we’ve worked with chemists who challenge our standards, push for better specs, and test the limits of each intermediate’s performance. The result: a 1,2-O-Cyclohexylidene-Alpha-D-Glucofuranose supply built on a foundation of practical chemistry, real feedback, and honest engagement. Manufacture quality doesn’t land by luck—it’s the outcome of continuous scrutiny, clear documentation, and the give-and-take of partnership. We’re proud to deliver a sugar derivative that brings real, measurable performance to research and industry alike.