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HS Code |
146770 |
| Chemical Name | 1,2-O-Isopropylidene-D-Glucofuranose |
| Molecular Formula | C9H16O6 |
| Molecular Weight | 220.22 g/mol |
| Cas Number | 35893-57-3 |
| Appearance | White to off-white solid |
| Melting Point | 94-98 °C |
| Solubility | Soluble in water and polar organic solvents |
| Synonyms | 1,2:5,6-Di-O-isopropylidene-α-D-glucofuranose, 1,2-O-Isopropylidene-α-D-glucofuranose |
| Optical Rotation | [α]D20 +112° (c=1, H2O) |
| Storage Temperature | Store at 2-8°C |
As an accredited 1,2-O-Isopropylidene-D-Glucofuranose factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,2-O-Isopropylidene-D-Glucofuranose is supplied in a 25g amber glass bottle with tamper-evident seal, labeled for laboratory use. |
| Shipping | 1,2-O-Isopropylidene-D-Glucofuranose is shipped in tightly sealed containers under dry, cool conditions to prevent moisture absorption and degradation. The packaging complies with chemical safety regulations, and material safety data sheets (MSDS) are included. Standard transportation is via ground or air, following all relevant local and international shipping guidelines for laboratory chemicals. |
| Storage | 1,2-O-Isopropylidene-D-Glucofuranose should be stored in a tightly sealed container, protected from moisture and direct sunlight. Keep it in a cool, dry, well-ventilated area, preferably at room temperature or below. Ensure the storage location is free from incompatible substances such as strong oxidizing agents. Proper labeling and adherence to safety data sheet (SDS) recommendations are essential. |
Applications of 1,2-O-Isopropylidene-D-Glucofuranose in Industrial ManufacturingAs the origin manufacturer, we supply high-purity 1,2-O-Isopropylidene-D-Glucofuranose to global sectors in fine chemicals and specialty synthesis. Our material supports key synthetic reactions in pharmaceutical, food additive, cosmetic, diagnostic, and specialty intermediate manufacturing. The following applications reflect actual downstream use in dedicated process environments. 1. Pharmaceutical Intermediates for Nucleoside Analog Synthesis1,2-O-Isopropylidene-D-Glucofuranose serves as a protected sugar moiety in the multi-step synthesis of nucleoside analogues. Its acetonide group protects diol positions, maintaining stability during glycosylation. Process chemists integrate it in precise ratios during the construction of the sugar backbone for active pharmaceutical ingredients (APIs) targeting antiviral, antifungal, or anticancer indications. Batch processes require tight control over impurity profile and downstream protection/deprotection cycles. Industry compliance standards
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2. Chiral Building Block for Food Flavour Ingredient SynthesisIn specialty food ingredient manufacturing, 1,2-O-Isopropylidene-D-Glucofuranose acts as a chiral starting material for flavor molecules such as lactones and rare sugars. Flavor chemists use this intermediate to construct natural-identical compounds, promoting consistent enantiomeric purity and traceability as required for high-quality consumables. Its protected structure prevents oxidation and undesired ring opening during process steps. Industry compliance standards
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3. Specialty Cosmetic Ingredient IntermediateFormulators in cosmetic ingredient manufacturing use 1,2-O-Isopropylidene-D-Glucofuranose as an intermediate for polyol-derived humectants and sugar acid compounds. The acetonide function allows selective chemical derivatization, creating mild and biodegradable substances for skin care matrices. This input enables fine-tuning of the hydrophilic-lipophilic balance in advanced cosmetic actives. Industry compliance standards
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4. Diagnostic Enzyme Substrate Synthesis1,2-O-Isopropylidene-D-Glucofuranose is a reliable intermediate for the synthesis of diagnostic-grade enzyme substrates and blockers. R&D and manufacturing labs use its protected form to prepare chromogenic and fluorogenic substrates for glycosidase assays. Strict control over side reactions ensures batch consistency essential for reproducible assay outcomes in clinical biochemistry and research diagnostics. Industry compliance standards
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5. Fine Chemical Intermediate for Carbohydrate-Based MonomersProcess engineers use 1,2-O-Isopropylidene-D-Glucofuranose during the synthesis of carbohydrate-based monomers for specialty polymer production. The acetonide-protected furanose enables selective modification at positions 3, 4, and 5, offering defined reactivity needed in stepwise monomer construction for advanced materials, adhesives, or degradable plastics. Reliability at scale is crucial to support downstream continuous or batch polymerization. Industry compliance standards
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Over the years in the chemical manufacturing industry, certain fine chemicals stand out for their reliability in both synthesis and customer results. 1,2-O-Isopropylidene-D-Glucofuranose has proven itself as a solid building block across pharmaceutical, biotech, and specialty chemical sectors. Our team has worked with this acetal-protected sugar derivative for decades, learning its behaviors, optimizing batch sizes, and listening to researchers and process chemists about what they need out of each kilogram.
Our chemists work with carbohydrates every day, and selectivity poses one of the recurring challenges. Unprotected sugars often give reactions that are hard to control, leading to mixtures that waste time and solvents. 1,2-O-Isopropylidene-D-Glucofuranose solves this by shielding crucial hydroxyl positions at C1 and C2, making subsequent modification of the remaining hydroxyls at C3, C4, and C5 far easier. That precision is what drove our steady investment in this compound over newer, less-characterized intermediates.
The isopropylidene group doesn’t just offer reactivity advantages. Products downstream demand a predictable starting point. As we walk the fine line between protecting groups with reliable deprotection chemistry and those resistant to unwanted hydrolysis, this molecule lands right in the Goldilocks zone. Customers developing N-glycosides, glycosylamines, and other specialty derivatives have repeatedly told us about improved impurity profiles and less need for repeated column chromatography when starting from our product.
After pouring countless batches in our reaction vessels, the physical profile of 1,2-O-Isopropylidene-D-Glucofuranose is thoroughly familiar. We produce material that consistently crystallizes as a white solid with stable handling at room temperature, which helps in planning large scale runs or just routine lab work. In our experience, fine particulate formation varies with humidity, but the core characteristics—melting range, solubility profile—will match reference standards.
Our chemists pay close attention to stereochemistry and purity, as any slip there can derail downstream syntheses. We routinely run NMR and rotation checks after every crystallization to confirm the D-configuration and precise acetal formation. End-user feedback tends to focus on sample homogeneity and ease of weighing, small details that actually make work easier on a busy bench.
Anyone sourcing sugar derivatives from the open market knows consistency isn’t a given. A run of material from a trader or poorly controlled supply chain might behave unpredictably: excess moisture content leads to caking, or subtle impurities can tank a key glycosylation. At our facility, we calibrate each run for lot-to-lot integrity, sampling at every crucial process point and archiving reference spectra. Every certificate of analysis we send follows after in-house QC verification, informed by years of experience in how this molecule responds on both GC and HPLC.
For projects that demand an extra level of scrutiny—think scale-up for new drug candidates or diagnostic probes—we custom-tailor purification to user specs. In these batches, we reduce minor positional isomers and tighten UV-absorbance thresholds. Our clients regularly comment on the difference between bulk commodity grades and the fine intermediates they receive here, saying the latter gives them tighter control and less troubleshooting.
Customers sometimes ask for model numbers or index values, but our team talks more about what users experience in the flask. For us, keeping water content low and verifying the acetal’s selectivity through routine NMR checks has proven more meaningful than any document number could be. In our workflow, small impurities or partial deprotection can disguise themselves, showing up as confusing signals in downstream reactions; that’s why we test every kilogram personally, extending the same care to gram-scale and hundred-kilogram scale alike.
Over time, we’ve learned metrics like specific rotation, melting range, and TLC mobility serve as an early warning for subtle problems. Unusual batches get flagged for rework onsite, not pushed forward. Our technical staff knows from experience that catching an outlier at the source saves everyone headaches far down the line, leading to a smoother process—not just for us, but for every scientist along the chain.
Many chemists new to carbohydrate work wonder whether it matters which acetal-protected sugar they choose for their route. Experience shows that 1,2-O-Isopropylidene-D-Glucofuranose compares favorably against other D-glucose derivatives, especially outside strictly academic settings. For one thing, its selectivity profile dramatically lowers the rate of byproduct formation in nucleophilic substitution or phosphorylation reactions. We have seen lower drag in solvent washes and less need for silver oxide or other scavengers for unwanted ion impurities.
Other common protecting groups, such as benzyl or acetyl, can give rise to side reactions or demand harsher removal conditions later in the synthesis. In contrast, the 1,2-O-isopropylidene group fares better under moderate acid hydrolysis, minimizing the chances of glycosidic bond cleavage elsewhere in the molecule. Customers focusing on biodegradable active ingredients appreciate this, as they can streamline purification steps and get cleaner release of the parent sugar.
Decisions on scale go beyond simple cost per kilo. Over the years, we have worked hand in hand with technical teams scaling from bench to pilot to manufacture, and our own plant has had to adapt production blocks accordingly. The lessons here inform our choices: crystalline batches package better for international shipping, but flake or powder may benefit customers looking for rapid dissolution. Our packaging team regularly adjusts drum liners and anti-static measures in response to customer input, drawing on decades of logistics knowledge.
Process engineers have commented that the relatively mild conditions needed for 1,2-O-isopropylidene group introduction and removal result in lower amounts of hazardous waste. We track solvent usage tightly, sending distillation residues for recovery instead of landfill. Over the years, even small tweaks in our procedures—swapping minutes at reaction endpoint, or changing crystallization temperatures—have shown measurable reductions in both chlorinated solvent dependency and overall process effluent.
Chemists working in glycoside chemistry, oligosaccharide synthesis, or even specialty cosmetic actives frequently send us questions about customizing grade or blending batches. As the manufacturer, our doors are open for technical dialogue—regular phone calls or on-site visits often bring about a tweak in drying parameters or an upgrade to analytical checks. These relationships don’t just help us improve product quality, they result in genuine advances for customers using this compound at the cutting edge of research.
Our technical partnerships run deep. We have supported teams troubleshooting glycosylation failure by reviewing batch history and even sending researchers batches from different production dates to sort out whether storage, handling, or subtle process variation was at play. This level of manufacturer support has sent positive ripples throughout the community, as reliability in intermediate supply can mean the difference between another month of troubleshooting and a published paper.
A sugar intermediate like 1,2-O-Isopropylidene-D-Glucofuranose sees a variety of users. In our workflows, academic groups working in carbohydrate mechanism studies might order small multi-gram batches, seeking max purity for sensitive reactions. Meanwhile, pilot plant chemists want assured supply when costs, material purity, and regulatory tracking come into play. Our experience in running every step of the process—from crystallization to analytical approval—means we can predict and adapt for special requirements as projects grow.
For scale-up, we work with engineering colleagues to optimize the isolation and drying stages so their team doesn’t lose time tackling persistent residual solvent or batch-to-batch texture changes. Our goal all along has been to supply more than a material specification; we serve as partners in delivering a compound that behaves reliably every time. Customers relay back that shortcuts on buying decisions in early phases can bite later—nothing replaces a chemistry partner who stands behind their own product, with batch documentation stretching back for decades.
In today’s climate, researchers and process leads increasingly ask for analytical documentation beyond basic test results. From our viewpoint, transparency is essential. Beyond the usual spectral checks for carbohydrate functional groups, we offer customers the option of high-resolution mass spectral documentation and full traceability from each production stage. Frequent customer requests include lower endotoxin requirements for biotech work and the documentation of process solvent history for those writing up regulatory filings.
Our quality system makes material traceable long after the original order. When a customer needs to check the granularity of a five-year-old batch, we can pull up production notes, spectral archives, and storage detail. This level of recordkeeping isn’t a luxury, it's a necessity for those pushing compounds toward IND submissions or specialty food applications.
Anyone in manufacturing sees the temptation to substitute cheaper, synthesized furanose derivatives or blended sugar mixtures. Over time, the downstream setbacks—hard-to-separate impurity clusters, inconsistent results—catch up. Our production approach has focused on clean, high-selectivity runs, using solvents that minimize racemization or the formation of epimeric byproducts. Through targeted washing and filtration steps, we keep the tracked impurity profile narrow, which translates into fewer surprises for users.
Less carefully prepared grades, especially those distributed by third-party brokers, may include significant amounts of moisture or unravel in harsher reactions, resulting in lower conversion rates. Working entirely in-house from raw input through finished packaging means we control each step. If a researcher flags a rare issue, we can reconstruct every variable; this level of responsiveness simply doesn’t exist with unknown third-party channels.
Customers engaged in synthesizing C-glycosides, developing enzyme substrates, or preparing carbohydrate-based probes often describe bottlenecks associated with material quality. From our side, experience shows that 1,2-O-Isopropylidene-D-Glucofuranose brings tangible benefits. With this derivative, our clients get improved control during glycosyl halide preparation, less formation of overacylation, and faster progress through reaction monitoring. For scale-up jobs, the crystalline form packs easily into reactors and dissolves quickly without excessive dust generation, which improves both operator safety and batch reproducibility.
In the field of diagnostics and emerging therapeutic development, knowing that every round of material will match the last is non-negotiable. Demand for stable, high-purity intermediates serves as a benchmark not just of technical output but of organizational rigor. Having supported research projects on several continents, our technical staff brings firsthand experience in adapting storage, temperature control, and documentation to meet the most demanding site-specific needs.
As a manufacturer accountable for everything from solvent intake to shipping waste, every decision about 1,2-O-Isopropylidene-D-Glucofuranose reflects lessons about process safety and sustainability. Over the last decade, our shift away from hazardous extraction agents brought both environmental wins and safer working conditions. Waste handling, previously a messy afterthought, now draws on proven solvent recycling and neutralization protocols, which reduce both regulatory burden and environmental impact.
Customers increasingly expect to see green chemistry principles applied to even intermediate production—our own journey has led us to spotlight this compound’s relatively low hazardous waste output, compared with more exotic sugar derivatives. As regulations and customer priorities evolve, we continue improving both upstream sourcing and downstream disposal protocols.
Customers often say that easy claims or spec sheets do little to assure them when deadlines loom and synthesis runs need to succeed the first time. The experiences of everyone from technical operators handling 50-liter reactors to process engineers troubleshooting unexpected byproducts shape how we approach not just 1,2-O-Isopropylidene-D-Glucofuranose, but our broader line of carbohydrate building blocks. We maintain direct channels for both standard questions and deep technical dives, always drawing from thousands of cases where chemistry either went smoothly or hit a bump.
Ultimately, behind each batch delivered stands a core team of chemists and production engineers who take pride in personal accountability. Our regular internal reviews, driven by feedback from the world’s top research and manufacturing teams, keep us iterating on everything from filtration speed to package design. For any project reliant on a tightly defined, selectively protected sugar, experience amounts to more than paperwork or online promises—it’s a guarantee sewn into each stage of production, batch after batch, year after year.