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2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose

    • Product Name 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose
    • Alias Tetra-O-benzyl galactose
    • Einecs 623-018-3
    • 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

    749141

    Chemical Name 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose
    Molecular Formula C34H36O6
    Molecular Weight 540.65 g/mol
    Cas Number 18599-88-5
    Appearance White to off-white solid
    Melting Point 95-100°C
    Solubility Soluble in organic solvents (e.g., dichloromethane, chloroform, methanol)
    Purity Typically >97%
    Storage Conditions Store at 2-8°C, protect from light and moisture
    Iupac Name 2,3,4,6-tetrakis(phenylmethoxy)-D-galactopyranose
    Smiles OC1C(OCc2ccccc2)OC(OCc3ccccc3)C(OCc4ccccc4)OC1Cc5ccccc5
    Optical Rotation [α]D20 +30 to +36 (c=1, CHCl3)
    Synonyms Tetra-O-benzyl-D-galactopyranose, Tetra-O-benzylgalactose

    As an accredited 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5g quantity of 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose is supplied in a sealed amber glass bottle with tamper-evident cap.
    Shipping 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose will be shipped in a sealed glass vial, securely packaged with cushioning material to prevent breakage. It will be transported at ambient temperature unless otherwise specified. All shipments comply with applicable chemical transport regulations and include appropriate labeling and documentation for safe handling and identification.
    Storage 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose should be stored in a tightly closed container, protected from light and moisture, under an inert atmosphere such as nitrogen or argon if possible. Store at room temperature or as directed on the supplier’s label, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers.
    Application of 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose

    Applications of 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose in Industrial Manufacturing

    2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose serves as a crucial carbohydrate intermediate for advanced synthesis processes in several specialized downstream industrial sectors. Our manufacturing expertise supports B2B partners who require high-purity, consistently supplied raw materials for their regulated, high-value production lines. Below, we outline major industrial application fields, focusing on practical integration details, compliance regimes, technical formulation data, and real end-use products.

    1. Active Pharmaceutical Ingredient (API) Synthesis – Glycosylation Intermediates

    Leading pharmaceutical companies apply this protected galactose derivative as a key glycosyl donor in the stepwise chemical synthesis of oligosaccharide API precursors, where precise stereochemistry and high reactivity are essential for structure-defined drugs and prodrugs. The raw material is typically introduced during multi-stage glycosylation reactions, especially in procedures that require orthogonal protection and late-stage deprotection cycles, supporting cGMP batch records and full regulatory traceability.

    Industry compliance standards

    • ICH Q7 for Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • EU EudraLex Volume 4, Part II
    • USP–NF or EP mono­graph guidance for API starting materials (as applicable for specific drug synthesis plans)

    Typical usage ratio

    • 10–30 mol% relative to core aglycone or acceptor, depending on oligosaccharide chain length and batch size; higher ratios address scale-up purification yield losses and multistep requirements.

    Downstream process integration

    • Direct introduction during the stepwise protection/glycosylation cycle; subsequent purification by column chromatography or preparative HPLC; benzyl group removal at late stage by hydrogenolysis as part of cGMP protocols.

    Final product types

    • Oligosaccharide APIs for antiviral and anticancer agents
    • Glycopeptide antibiotics
    • Glycosylated enzyme inhibitors and synthetic vaccine candidates

    2. Carbohydrate-Based Diagnostic Reagent Production

    Manufacturers of analytical reagents and diagnostic kits use this compound as a protected galactose building block during the synthesis of complex glycan structures. These glycans often serve as immobilized molecular recognition elements for immunoassays or biosensor arrays. Selection of this intermediate enables the assembly of structurally defined oligosaccharides, ensuring reliable assay performance and minimal batch-to-batch variation through tightly controlled functionalization and purification steps.

    Industry compliance standards

    • ISO 13485:2016 (Quality Management for Medical Devices including IVDs)
    • FDA 21 CFR Part 820 (Quality System Regulation for diagnostics and medical devices)
    • CLSI guidelines for diagnostic reagent materials (for clinical laboratories)

    Typical usage ratio

    • Approximately 15–40 mol% per target glycan unit; varies based on glycan size requirements and immobilization method; proportion refined to minimize unreacted species in functionalization.

    Downstream process integration

    • Incorporated during chemical or enzymatic glycan elongation steps; after glycosylation, benzyl groups are removed by hydrogenation prior to surface immobilization or bioconjugation; quality monitored by HPAEC-PAD and MALDI-TOF MS.

    Final product types

    • ELISA and chemiluminescent immunoassay plates coated with synthetic carbohydrates
    • Biosensor chips for pathogen or lectin detection
    • Glycan microarrays for biomedical research and screening

    3. Specialty Polymer Modification – Galactose-Functionalized Polymers

    Producers of specialty materials incorporate this protected galactose into their polymer backbones to create biofunctional materials for targeted applications, such as affinity media, chromatography resins, and biocompatible coatings. The unique protection pattern of this material enables selective introduction of glycan motifs without unwanted side-reactions, ensuring consistent polymer modification and high end-use product performance.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for Materials Manufacturing)
    • FDA 21 CFR 177 (Indirect Food Additives: Polymers) if resins interact with biologics or food contact
    • REACH Registration for chemicals in the EU

    Typical usage ratio

    • 5–20 wt% relative to backbone polymer mass, depending on targeted density of galactose units; optimization guided by binding capacity measurements and functional testing.

    Downstream process integration

    • Grafted onto activated synthetic polymer scaffolds through controlled coupling reactions in organic solvents; benzyl deprotection executed post-attachment using catalytic hydrogenation to expose free galactose functionalities for final product performance.

    Final product types

    • Affinity chromatography resins for protein purification
    • Biocompatible hydrogels for cell adhesion studies
    • Galactose-terminated nanoparticles for targeted delivery research

    4. Glycosylated Natural Product Synthesis

    Advanced fine chemical manufacturers utilize this intermediate in the total synthesis of glycosylated natural products, such as saponins and cerebrosides, where tightly controlled stereochemistry is mandatory. Its robust benzyl protection system permits multistep reactions under diverse conditions, ensuring site-specific glycosyltransfer without premature deprotection or compromise of core molecular scaffolds.

    Industry compliance standards

    • ISO 22716:2007 (Good Manufacturing Practices for Cosmetics) for natural actives in cosmetic applications
    • GMP EU 2015/983 Annex 2 for active substances for non-medicinal use (cosmetic grade)
    • REACH compliance for specialty chemicals produced or imported into the EU

    Typical usage ratio

    • Variable: typically 1.2–1.8 equivalents per natural product core; adjusted based on acceptor molecule reactivity and number of required glycosylations per product molecule.

    Downstream process integration

    • Introduced during chemical glycosylation step after full protection of aglycone or core scaffold; after coupling, benzyl group removal performed under anhydrous conditions to minimize byproduct formation; finished glycoside isolated by preparative chromatography.

    Final product types

    • Synthetic saponins for cosmetic and research markets
    • Glycosylated ceramide analogues
    • Reference standards for complex natural products in analytical labs

    5. Precursor for Homogeneous Glycan Vaccine Development

    Biotechnology and pharmaceutical R&D firms deploy this compound as a controlled carbohydrate unit in synthesis routes for homogeneous glycan antigens used in conjugate vaccine trials. Its fully protected status permits stepwise elongation and precise branching control over immunogenic oligosaccharide structures vital for preclinical vaccine candidate pipelines.

    Industry compliance standards

    • ICH Q11 Guidelines for Drug Substance Development and Manufacture
    • WHO Technical Report Series 1010 Annex 2 for Vaccine Substance Manufacture
    • USP–NF for reference material and QMS assessment

    Typical usage ratio

    • 5–25 mol% per glycan branch point; ratio set per target epitope density and scale (laboratory, pilot, or clinical trial supply); tracked via in-process sugar analysis and batch control.

    Downstream process integration

    • Incorporation in automated or manual glycan chain assembly during solid-phase and solution-phase synthesis; benzyl group cleavage conducted post-assembly prior to conjugation to carrier proteins such as CRM197 or TT; finalized conjugates purified and QC’d via HPSEC and NMR.

    Final product types

    • Homogeneous glycan-protein conjugate vaccines for bacterial and viral preclinical R&D
    • Well-defined glycan antigens for immunogenicity studies
    • Analytical standards for glycovaccine characterization
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    Competitive 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose: A Practical Backbone in Complex Synthesis

    Understanding the Product From a Manufacturer’s Perspective

    In the world of carbohydrate chemistry, routine and precision blend to create building blocks that drive advanced research forward. 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose stands out for those looking to work with well-protected galactose derivatives. Unlike generic supplies, every batch we produce comes from in-house synthesis using locally sourced, quality raw sugar feedstock. Astute chemists know that protecting group chemistry reshapes the way you approach glycosylation tasks, and our team has spent years refining both the consistency and utility of this specific protected galactose.

    Features That Translate Into Day-to-Day Lab Value

    The foundation for every successful oligosaccharide lies in the purity and selectivity of your starting material. This compound, fully benzylated on the 2,3,4, and 6 positions, offers strong protection during demanding steps that often degrade less robustly protected sugars. From our own lab benches, the clarity and persistence of its crystalline form save time in purification — which those managing tight research timelines recognize immediately.

    Years of direct feedback from university and industry partners have shown how the solubility profile makes this material a favorite in solution-phase strategies. Benzyl groups on all four of the non-anomeric oxygens not only ensure selectivity when building complex structures but also resist migration and hydrolytic loss. There’s a certain confidence in reaching for a compound that doesn’t leave you guessing what fraction remains after a tricky coupling or wash step.

    Production Insight: Doing More Than Just Meeting a Spec Sheet

    Our manufacturing line doesn’t just produce a “standard” 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose. Every run begins with careful attention to temperature ramping, solvent control, and reagent stoichiometry—details that turn into subtle, but real, performance differences in your hands. By handling the hydrogenolysis and benzylation steps in-house, purity stays high and batch-to-batch reproducibility remains steady year after year. In a market where the quality of derivatives can swing on minor process variances, our approach means fewer surprises at the bottleneck of a project.

    Usage in Synthesis and Research: Value at Every Step

    2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose isn’t just a specialty sugar—it’s a strategic reagent for laboratories focusing on glycochemistry, structural biology, and cell-surface engineering. In our own R&D, it serves as both a precursor and intermediate for assembling oligosaccharides. Its high level of protection guards against base- or acid-catalyzed degradation common with less robust sugars. The selective exposure of the anomeric position supports glycosyl donor or acceptor generation with minimal side-reactions.

    Protection with benzyl groups isn’t purely for stability. During hydrogenolysis, the same groups are conveniently removed under mild conditions, freeing up sites for downstream modification or conjugation to other bioactive compounds. Customers often share that they pick this compound when native stereochemistry or linkage control is critical. There’s no guesswork in downstream functionalization steps — which prevents wasted effort and unnecessary costs.

    For anyone planning multi-step carbohydrate syntheses, this specific derivative reduces the risk of partial deprotection, rearrangement, or unwanted branching. Time and again, scientists doing glycan synthesis tell us this single material cut weeks from their project timelines simply because it “behaves” under both bench and pilot-scale runs.

    Specifications That Matter in Practice

    While the chemical formula and CAS number headline every data sheet, from a production chemist’s perspective, it’s the repeatable melting point, crystal habit, and spectral clarity that matter more in a real workflow. Each lot passes our own chromatographic and NMR fingerprint, which means customers skip a lot of troubleshooting right out of the gate.

    We guarantee a minimum purity above 98 percent, a figure reflecting the limits of careful, hands-on production rather than the overstatements sometimes seen from traders who never see real material. Optical rotation stays within expectation, confirming stereochemical integrity. Most end-users tell us that product received is ready to use, with little or no additional workup, sparing valuable time in fast-moving research groups.

    We’ve tested solubility across numerous organic solvents to suit a range of synthetic strategies, and our internal reference samples show consistently strong dissolution in dichloromethane, toluene, and chloroform. This material will not clump or separate, maintaining uniform mixing and accurate reagent dosing — advantages frequently cited in positive customer reports.

    How This Product Compares to Alternative Protected Sugars

    Choices abound in protected carbohydrate chemistry, from acetylated and benzoylated analogs to mixed protection schemes. Through our own direct experience, we’ve observed that tetra-O-benzyl derivatives like this one trump acetylated galactopyranoses for both chemical and mechanical robustness. Acetyl groups, while easy to install, hydrolyze readily under both acidic and basic conditions, leading to byproducts and waste material. Benzoyl groups handle some conditions better but are tough to remove cleanly without harsher reagents — complicating downstream recovery and purity.

    Our product keeps the anomeric center open, giving more precise control for selective glycoside formation or for installing linkers. We’ve received lab requests for more mixed-protection sugars, but ultimately find that full benzyl protection cuts down on side reactions, limits contamination, and offers a straightforward hydrogenolysis to remove protecting groups: no need for aggressive deprotecting steps that introduce new impurities or damage sensitive appendages. During repeated chromatography sessions at our site, tetra-O-benzyl products generate sharper, cleaner separations than their acetyl or mixed analogs.

    In troubleshooting collaborations with several synthetic groups, we’ve tracked the lower frequency of failed couplings and impurity build-up when benzyl-protected galactopyranoses are used as starting points. Especially in automation or high-throughput systems, where robustness trumps incremental cost, this specific material wins out again and again.

    Real-World Applications: From Basic Research to Industrial Programs

    New toolkits in glycomics, immunology, and antiviral drug research all lean heavily on easily functionalized sugars, and this compound finds steady demand in linking glycans or assembling partial structures for vaccine research. Our collaborations with academic groups working on tumor-associated carbohydrate antigens have confirmed how crucial both purity and reliable deprotection profiles are when transitioning from pilot reactions to larger scales.

    Many antigen conjugation projects see successful results using this product as an intermediate. Its chemical durability under a range of coupling conditions gives more freedom to pursue divergent synthetic strategies. In one in-house project, we used our own tetra-O-benzyl galactose to assemble a complex glycosyl donor in a route that cut total steps compared to the prior acetyl-protected scheme. Consistent feedback shows researchers benefit by having fewer byproducts and higher yields through all stages.

    Pharmaceutical companies and diagnostic manufacturers turn to this compound when needing high-fidelity substrates for enzyme testing or surface immobilization. The mechanically stable, crystalline powder flows freely, scoops out of storage without clumping, and doesn’t retain excess solvent. Even simple storage at ambient or low refrigeration ensures long shelf life, with no signs of degradation or discoloration after multi-month monitoring.

    Manufacturing Practices Shaped by Years in the Field

    Our facility doesn’t operate as a generic outsourcing hub — we continually tune and refine equipment and workflows to respond to feedback and internal analytical data. Benchtop work informs plant improvements, closing the loop between research, pilot, and scale-up synthesis so setbacks are caught before field delivery. Real-world synthesis doesn’t forgive errors, and our chemists have faced every side reaction, precipitation, and assay failure that shows up with ill-prepared materials.

    High performance in the field reflects the work done during batching. Detailed temperature control, solvent recovery, and careful exclusion of moisture form the cornerstones of our process, locking in reliability before product leaves the site. Technicians monitor crystallization and drying under nitrogen, minimizing oxidation and particulate load. Over the years, iterative process tweaks have made our production more efficient and environmentally conscious.

    Quality, Safety, and Traceability

    Ensuring every recipient can count on a safe and reproducible experience drives us to monitor, trace, and document every lot down to the kilogram. All staff spend time in the lab weekly, so there’s no gap between knowledge and practice. By maintaining direct oversight of every production and packaging stage, we avoid pitfalls common among bulk handlers and brokers who never interact directly with the molecule.

    From delivery to disposal, we’re committed to educating end users on safe handling — based in the reality of bench workflows, from avoiding cross-contamination to disposing of benzylated byproducts. Overexposure to benzyl compounds means no open evaporation outside fume extraction, and every lot includes dependable MSDS support and batch analysis data. Years of working with customers on scaling, troubleshooting, and documentation means we avoid blind spots that show up with traders who have never touched the actual chemistry.

    Troubleshooting and Ongoing Support: A Real Partnership

    A large portion of our interaction with clients doesn’t stop at the invoice; it starts with questions about solvent selection, order-of-addition concerns, or cycling between automated and manual reaction conditions. We’ve pilot-tested scores of coupling, deprotection, and isolation steps just to answer these questions directly. Using this protected galactopyranose, troubleshooting a failed step often means checking minor solvent impurities or temperature drifts — not worrying about protection group lability or random decomposition.

    Feedback loops from customers let us update bulk storage and packing protocols for better product flow and easier dispensing. In our own automated synthesis equipment, the handling properties of our material deliver fast, dust-free dispensing and simple line clearing, whether you’re working with grams or multi-kilogram batches. Even workflow documentation has evolved based on shared lessons from end users looking for accelerated processes and fewer hands-on corrections.

    Future Directions and Continuous Improvement

    Chemical manufacturing operates in a shifting landscape of demands, regulatory changes, and technical advances. By keeping a line open to synthetic groups worldwide, our team regularly updates analytical routines and invests in emerging detection and purification techniques. The rise of rapid oligosaccharide assembly, custom glycan arrays, and precision bioconjugation shows that what was once a niche specialty now sits center stage.

    Bench chemists, research managers, and students all count on predictable supply chains, approachable product experts, and a willingness to adjust specifications as new breakthroughs arrive. Our hands-on approach to both routine and custom synthesis goes beyond just making a molecule. Past experience has taught us that what matters most are the materials that work seamlessly through every stage, removing friction and guesswork from ambitious synthesis tasks.

    Summary: What Truly Sets 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose Apart

    Years in the business have shown that shortcuts in protecting group chemistry ripple across every stage that follows. 2,3,4,6-Tetra-O-Benzyl-D-Galactopyranose offers a blend of resilience against demanding synthetic transformations, reliability batch after batch, and support for high-yield carbohydrate assembly. Whether you’re linking intricate oligosaccharides, building enzyme substrates, or charting new routes to glyco-conjugates, the material in your hands should advance your project, not limit it.

    Behind every successful lot stands a real team with direct experience facing the same hurdles as our customers. We believe honest feedback, continuous learning, and open support keep both our production line and your research moving forward — with products that outperform, not just meet, expectations.