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1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose

    • Product Name 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose
    • Alias DXylo
    • Einecs 209-415-1
    • 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

    929192

    Name 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose
    Cas Number 2595-54-2
    Molecular Formula C11H18O5
    Molecular Weight 230.26
    Appearance White to off-white crystalline powder
    Melting Point 95-99 °C
    Solubility Soluble in chloroform, dichloromethane, and methanol
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protect from moisture
    Synonyms D-Xylofuranose, 1,2:3,5-di-O-(1-methylethylidene)-, 1,2:3,5-Di-O-isopropylidene-α-D-xylofuranose
    Inchi InChI=1S/C11H18O5/c1-7(2)15-5-9(13)11(16-8(3)4)10(6-12)14-7/h9-13H,5-6H2,1-4H3/t9-,10+,11+/m1/s1
    Smiles CC1OC(OCC2OC(CO)C(O2)C(C)C)(C)C1

    As an accredited 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle containing 25 grams of 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose, sealed with screw cap and labeled.
    Shipping The shipping of 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose requires secure, airtight packaging to prevent moisture and contamination. The compound should be shipped at room temperature, avoiding extreme heat or cold. Ensure compliance with local and international chemical transport regulations, including proper labeling and documentation for safe and legal delivery.
    Storage 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose should be stored in a tightly sealed container, protected from moisture and light, at room temperature or at 2–8°C. It should be kept in a dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Ensure proper labeling, and follow standard laboratory protocols for storing organic compounds.
    Application of 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose

    Applications of 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose in Industrial Manufacturing

    As a trusted chemical raw material producer, we support a range of specialized industrial segments utilizing 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose as a key intermediate or protecting agent within complex downstream processes. The following scenarios present targeted applications, compliance requirements, practical additive ratios, integration methods, and typical end product outputs based on established industry practices.

    1. Pharmaceutical Synthesis: Intermediates for Nucleoside Analogs

    In GMP-regulated pharmaceutical environments, this material functions as a protected sugar intermediate essential to the multi-step synthesis of a wide variety of nucleoside-based active ingredients, such as antiviral and anticancer drug molecules. Its isopropylidene protection groups enable specific regioselective reactions, preventing unwanted side reactions during glycosylation and subsequent transformations.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • US Pharmacopeia (USP) General Chapter <1079> for bulk pharmaceutical chemicals
    • European Pharmacopoeia (Ph. Eur.) standards for nucleoside intermediates
    • ICH Q3A/B for impurities and residual solvents

    Typical usage ratio

    • 0.95–1.10 molar equivalents in nucleoside sugar coupling, adjusted according to target molecule’s synthetic route

    Downstream process integration

    • Charged during initial sugar protection step, typically with acid catalysis, followed by utilization in selective glycosylation under controlled temperature and moisture conditions

    Final product types

    • Antiviral nucleoside active pharmaceutical ingredients (e.g., abacavir, lamivudine)
    • Cytostatic agents derived from modified sugars
    • Nucleotide analog intermediates for further phosphorylation

    2. Carbohydrate Chemistry: Protected Sugar Building Blocks

    Manufacturers of specialty oligosaccharides and rare sugar derivatives incorporate 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose as a vital building block in chemo-enzymatic synthesis. The isopropylidene groups mask specific hydroxyl functions, affording high regioselectivity in chain elongation and deprotection phases when producing advanced glycan structures for research and diagnostics.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for specialty chemical production
    • REACH registration for industrial chemicals in the EU
    • OECD Guidelines for Good Laboratory Practice (for research materials)

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to primer carbohydrate, with scale optimized for yield and protection efficiency

    Downstream process integration

    • Dosed at initial glycosyl donor preparation stage, maintained in protected state through sequential reactions, then deblocked under acidic or oxidative conditions to liberate target saccharide units

    Final product types

    • Custom oligosaccharide standards
    • Advanced glycan probes for bioanalytical assays
    • Rare sugar alcohol derivatives used in specialty applications

    3. Fine Chemical Manufacturing: Intermediates for Agrochemical Synthesis

    Producers of chiral agrochemical intermediates employ this compound for transient hydroxyl protection in the targeted assembly of sugar-based scaffolds, required for next-generation crop protection agent synthesis. It allows precise control of reactivity and stereochemistry in the functionalization of xylose-derived units, ensuring consistent batch-to-batch performance in the downstream manufacture of high-value actives.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems
    • Chinese National Standard GB/T 21903-2008 for fine chemicals
    • REACH substance registration for agrochemical intermediates

    Typical usage ratio

    • 0.9–1.3 molar equivalents, varied according to substrate reactivity and desired protection selectivity

    Downstream process integration

    • Introduced during the initial protection phase, prior to regioselective oxidation, substitution, or coupling reactions forming chiral centers; final deprotection realized by aqueous acid workup

    Final product types

    • Chiral intermediates for herbicidal and insecticidal actives
    • Sugar-derived ligands for agrochemical catalysts
    • Functionalized xylose derivatives for plant growth regulators

    4. Research Chemicals: Synthesis of Xylose-Based Reference Materials

    Analytical reagent and certified reference material suppliers rely on this protected sugar for precise synthesis of stable-standard materials, especially for chromatography and mass spectrometry calibration. The defined blocking groups minimize by-product formation and decomposition, crucial for purity assurance in certified, traceable analytical standards required by global testing laboratories.

    Industry compliance standards

    • ISO 17034:2016 General requirements for the competence of reference material producers
    • ISO/IEC 17025:2017 Laboratory competence for testing and calibration
    • OECD GLP (Good Laboratory Practice) for non-clinical safety testing

    Typical usage ratio

    • 1.00 molar equivalent, exact-to-stoichiometry to ensure full protection during batch synthesis of analytical standards

    Downstream process integration

    • Applied in batch-wise synthesis of monosaccharide reference material under inert atmosphere; final product purified using preparative chromatography to guarantee certification-grade purity

    Final product types

    • Xylose and arabinose standard solutions for HPLC and GC-MS calibration
    • Labeled isotopic sugar standards for bioanalytical quality control
    • Certified purity reagents for trace analysis in food, pharma, and environmental labs
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    Competitive 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose: Insights from a Chemical Manufacturer

    In chemical manufacturing, certain molecules keep showing up in the R&D requests and scale-up batches, because they solve challenges chemists face every day. One of these molecules is 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose. From our daily work on the production floor and in the analytical lab, it stands out as a key intermediate and building block in synthetic organic chemistry. Our facility has focused energy on optimizing its synthesis and purity, because this compound carries a unique structure that supports a variety of crucial downstream applications. When we prepare and ship it, we’re not dealing with vague consumer trends or repackaging; every gram tells a story of controlled reactions, purification, and practical, hands-on quality checks.

    The Foundation: Structure and Characteristics

    Let’s begin with what makes 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose different from similar molecules. The compound belongs to the family of acetonide-protected sugars, where isopropylidene groups shield the hydroxyls of xylofuranose at specific positions. This protection forms a rigid, crystalline structure, typically delivered as a white to off-white solid. In practice, the stability of these protecting groups changes how researchers can use it. The rigid framework handles both chemical reactions and mechanical handling on a plant floor—whether during large-scale filtration, drying, or milling. The work we put in at the manufacturing stage ensures consistent particle size and stable melting ranges, both of which help our downstream partners avoid surprises when transferring the material to their reactors.

    The model we produce comes in various lot sizes, with quality verification at every scale. Our baseline production aligns with commonly accepted standards for synthetic intermediates: chemical purity above 98 percent, low residual solvent, and HPLC/GC profile reproducibility from batch to batch. Analytical checks run beyond paperwork—our QC team regularly cross-checks melting point, specific optical rotation (reflecting its stereochemistry), and moisture content, all of which impact the yield and reliability of subsequent steps. We’ve directly seen how even slight deviations in these parameters can disrupt a customer’s downstream reaction, underscoring the need for careful and repeatable control throughout synthesis and recrystallization. Our longest-standing customers know these minute differences make or break a route, so we confront the fine details head-on.

    Application as a Protected Sugar: Real-World Utility

    Most partners come to us for 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose as a protected sugar intermediate. Here, the dual isopropylidene groups serve as more than just a chemical contrivance—they are a practical tool to block reactivity at select positions of the sugar ring. Whether for oligosaccharide synthesis, nucleoside drugs, or specialty glycosidic linkages, this compound offers an efficient handle to introduce further transformations while avoiding side reactions elsewhere on the molecule. We see it in the raw requests from pharmaceutical innovators, the formulation notes from carbohydrate chemists, and the custom-order queries from fine chemical teams. In each instance, users appreciate the selective reactivity that stable, well-prepared protecting groups bestow.

    Our involvement doesn’t stop at shipping; we field technical support questions about cleavage conditions, storage stability, and compatibility with downstream protecting groups. Having run hundreds of kilograms through the process, we know the interruptions caused by trace impurities. Some customers have reported byproduct formation due to improperly controlled residual acid, which can be a risk if synthesis shortcuts are taken. We’ve responded by tuning our work-up and washing steps, and constantly investing in analytical tools to spot these early. This approach has not only improved customer outcomes but has also shaped our internal training and troubleshooting, sparing partner labs from wasted time and effort on re-purification or lost yield.

    Why 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose Beats Alternatives

    The natural question arises: why pick this protected sugar over others? The answer lies in the balance between reactivity, selectivity, and cost. We’ve synthesized a wide variety of sugar derivatives—the trial runs and pilot scale work have made this clear. In practical application, the twin isopropylidene groups on the alpha-D-xylofuranose platform control both water solubility and chemical accessibility in ways other options can’t. Alternate protecting groups often add unnecessary steps, harsher deprotection conditions, or less predictable outcomes under common reaction conditions. We’ve seen researchers switch to this compound after struggling with yields or compatibility in multistep syntheses. Some alternatives, such as benzyl-protected sugars, linger in reaction mixtures, complicating purification. Acetyl-protected sugars, meanwhile, may fall apart under basic or nucleophilic conditions that our product easily tolerates.

    There’s a consistent feedback loop between manufacturer and customer in this field—our role is to translate these learnings into higher-performing material. By tuning crystallization solvents, refining drying conditions, and focusing on endpoint analytics (optical purity, residual metals, and trace organic byproducts), our facility has made this product both consistent and adaptable for a wide range of processes. Our data shows fewer rejected lots and smoother reaction set-ups for end users, which makes the whole supply chain more robust. The product absorbs less moisture and cakes less easily than some sugar derivatives, which customers tell us cuts time spent on powder handling and weighing as their production lines scale up.

    Production at Scale: Challenges and What We’ve Learned

    Scaling up 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose posed textbook challenges and a few unexpected ones. Simple lab methods using excess acetone and mineral acid don’t always transfer smoothly into multi-kilo reactors. The biggest struggles included keeping everything dry and managing byproducts when running at tonnage scales. Early on, we learned to adjust agitation rates and crystallization temperatures to avoid the formation of sticky, impure gums. Precise solvent recovery and waste minimization required new equipment and process maps—these investments paid off, both economically and environmentally.

    We refined our distillation and solvent exchange protocols to improve product isolation, pursued greener work-up sequences, and doubled routine monitoring for trace acid residues. Over time, we adapted venting and containment for certain volatile organic byproducts, driving improvements in plant safety and worker comfort. These aren’t just data points—they’re the product of regular production meetings, conversations with operators, and feedback from customer audits. That kind of direct communication feeds rapid troubleshooting and continuous process improvement, all aimed at reliable, efficient batching.

    Troubleshooting and Advisory: Standing Behind the Product

    No chemistry route is immune to problems, and even well-run batches may require hands-on troubleshooting or reformulation. Our technical team recently worked with a pharmaceutical partner whose process stalled due to incomplete deprotection after a large-scale glycosylation. Rapid analytical work suggested trace inorganic salts, originating from a poorly controlled aqueous work-up. We backtracked, shared batch logs, and isolated the source, leading both us and the customer to adopt a cleaner washing protocol. This wasn’t a one-time event—reliability grows when manufacturers are available for real technical exchanges, not just order fulfillment.

    Across many collaborations, this kind of practical advice—shared between manufacturing and research—saves time, money, and frustration. For complex downstream chemistry such as the introduction of further protecting groups, or the construction of rare glycoside linkages, the details matter enormously. Isopropylidene groups respond to deprotection using acid catalysis, but excess acidity or heat can threaten the sugar backbone. Clear communication about recommended conditions makes the whole chain of synthesis smoother, and users know they’re not just buying a product, but tapping into accumulated experience. We encourage open dialogue about storage, shelf-life, and moisture tightness, since the physical properties shape real performance in both bench and manufacturing settings. Each improvement comes from listening and adapting on both sides of the supplier-customer equation.

    Quality, Compliance, and Documentation: No Shortcuts with Intermediates

    From the manufacturing side, repeated audits and site visits have sharpened our perspective: customers want more than a spec sheet. They ask about site security, batch traceability, and regulatory compliance for import and downstream approval. The demand for analytical documentation grows as their own quality systems become stricter. Our experience has taught us the value of detailed batch records, chain of custody, and regular calibration of equipment—from balances to analytical columns. GMP and ISO audits are not abstract; they come with checklists, walk-throughs, and requests for samples from retained lots. We treat these as checkpoints for our own teams, not just boxes to tick for outside inspectors.

    Each batch report now reflects more than raw numbers: it logs operator notes, environmental conditions, and any deviation from standard procedure. This attention to process and record-keeping not only meets current compliance requirements, but helps catch small inconsistencies before they turn into larger quality issues downstream. Our own experience with product recalls in the past has left a mark—every scrap of detail in the process history makes root cause analysis faster and more accurate if unforeseen problems arise. Customers appreciate this transparency, and their confidence keeps our product moving across lab benches and plant floors both locally and internationally. Those who treat compliance as an afterthought quickly fall behind.

    Market Trends and The Push for Innovation

    We track upticks in demand for 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose as new drug development pipelines seek more complex sugar motifs and nucleoside analogues. Innovation in glycochemistry and oligosaccharide synthesis has led to more requests for tailored intermediates, often with tight impurity profiles or upgraded documentation requirements. Some projects require enantioselective variants or modified ring structures, which drives us to refine isomer control and impurity removal. We invest in process development teams who stay current with literature and customer needs, seeking new ways to improve both yield and risk management.

    Beyond pharmaceuticals, we see uses in specialty polymer synthesis, flavors, fragrances, and diagnostics—each with their own purity and certification criteria. As customers push for greener chemistry, we respond by reducing process solvents, recycling mother liquors, and even piloting bio-based raw materials for input sugar streams. These changes reflect ongoing partnerships, not short-term sales maneuvers. Our plant teams regularly meet with R&D counterparts to discuss how modifications in process can lead to downstream improvements for both cost and product performance.

    Direct Communication Beats Third-Party Sourcing

    In this industry, the difference between dealing with an actual manufacturer and a distributor or third-party reseller becomes clear during technical crises. Handling 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose has taught us that knowledge transfer, troubleshooting, and iterative improvements work best through direct communication. Some of the worst quality incidents reported by customers have come from repackagers or resellers unfamiliar with the synthesis or handling quirks of the compound. By maintaining end-to-end oversight, from raw input to dispatch, our team stays embedded in each part of the workflow, which means better technical guidance, faster responses, and a higher degree of accountability. This approach wins more loyalty over time than the most aggressive low-cost offers from intermediaries who lack the means or motivation to solve problems at the source.

    We run our own in-house logistics and packaging, so route-specific packaging and delivery preferences factor into every contract. Whether the need is for moisture-barrier drums, anti-static liners, or documentation packets for regulated shipping, these requests roll into our daily checklist. On more than one occasion, specialized packaging has turned a potential usability problem into an on-time delivery. Direct lines of feedback keep us informed about what truly helps customers, versus what looks good in a brochure.

    The Human Factor: Plant, Lab, and Customer Collaboration

    Years in chemical manufacturing have underscored one unsung truth: expertise is cumulative, hands-on, and always in progress. Making 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose at scale blends bench science, chemical engineering, and production pragmatism, and no one can anticipate every issue from the start. We pull insights from every batch, every plant challenge, and every analytical anomaly. That learning gets passed along, formally in SOPs and batch records, and informally through cross-shift mentorship. Seasoned operators notice texture changes that signal subtle differences in crystallization, lab teams detect impurity spikes that predict hard-to-filter fines, and engineers listen when those observations reach them. Each production cycle offers a chance to tighten our process for the next one.

    Downstream users—R&D chemists, production managers, procurement specialists—become both critics and collaborators. Their feedback finds its way into our adjustment logs, driving changes like shorter drying times, drip protection on bagging lines, or modified filling weights for easier handling during high-throughput operations. In many ways, the product’s decades of acceptance flow as much from this iterative, dialog-based improvement as from any single technical attribute.

    Looking Ahead: Continuous Improvement and Sustainable Chemistry

    The future of chemical manufacturing will keep pushing for safer, cleaner, and more efficient synthetic routes. Our focus remains on strengthening each step in the production of 1,2:3,5-Di-O-Isopropylidene-Alpha-D-Xylofuranose—from sourcing renewable inputs to minimizing process waste. Better reactor controls, analytical upgrades, and green chemistry initiatives are all active projects, built on real-world needs voiced by our partners and our teams. We review new catalyst systems that promise lower energy input, screen solvents for reduced environmental impact, and examine ways to improve operator safety during batch transitions and cleaning cycles. Each incremental change builds a stronger, more resilient product and company.

    Transparent partnerships, consistent improvement, and genuine expertise sharpen every batch we produce. The result: a protected sugar intermediate that performs at scale, supports advanced research, and stands up to both technical scrutiny and day-to-day challenges. In manufacturing, these concrete, lived details win contracts and keep customers coming back—more than any piece of flashy marketing ever could.