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(+)-2,3-O-Isopropylidene-L-Threitol

    • Product Name (+)-2,3-O-Isopropylidene-L-Threitol
    • Alias L-(-)-DIPT
    • Einecs 256-974-4
    • 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

    748088

    Productname (+)-2,3-O-Isopropylidene-L-Threitol
    Casnumber 22918-66-7
    Molecularformula C7H16O4
    Molecularweight 164.20
    Appearance White to off-white crystalline solid
    Meltingpoint 62-65°C
    Purity Typically ≥98%
    Solubility Soluble in water, methanol, ethanol
    Opticalrotation [α]D20 +12° (c=1, H2O)
    Smiles CC(C)(O)OC[C@@H](O)[C@H](O)CO
    Storagetemperature 2-8°C
    Synonyms L-Threitol 2,3-acetonide; L-Threitol acetonide
    Shelflife Stable under recommended storage conditions

    As an accredited (+)-2,3-O-Isopropylidene-L-Threitol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical `(+)-2,3-O-Isopropylidene-L-Threitol`, 5g, is packaged in a sealed amber glass vial with a secure screw cap.
    Shipping (+)-2,3-O-Isopropylidene-L-Threitol is shipped in tightly sealed containers to prevent moisture exposure and contamination. It is typically transported at room temperature, unless specified otherwise, and packaged according to chemical safety regulations. Proper labeling, documentation, and handling guidelines are followed to ensure safe and compliant delivery.
    Storage (+)-2,3-O-Isopropylidene-L-Threitol should be stored in a tightly sealed container in a cool, dry place, protected from moisture and light. It should be kept at room temperature or lower, away from incompatible substances such as strong oxidizers. Proper labeling and storage in a well-ventilated area are recommended to maintain chemical stability and prevent degradation.
    Application of (+)-2,3-O-Isopropylidene-L-Threitol

    Applications of (+)-2,3-O-Isopropylidene-L-Threitol in Industrial Manufacturing

    As a focused manufacturer of (+)-2,3-O-Isopropylidene-L-Threitol, we supply this chiral building block to specialized downstream sectors where high enantiomeric purity and reliable sourcing drive both advanced materials innovation and consistent batch production. Below, we outline several established application scenarios from our commercial client base and technical support cases, demonstrating where this material actively contributes to next-step formulations, synthetic routes, and final product development.

    1. Chiral Ligand Synthesis for Asymmetric Catalysis

    Producers of chiral ligands in homogeneous catalysis protocols integrate this intermediate due to its defined stereochemistry, which directly impacts the selectivity of downstream metal-catalyzed transformations. Fine chemical manufacturers use it to construct custom ligands that enable efficient enantioselective hydrogenation or addition processes, targeting high-value APIs and specialty intermediates where asymmetric induction precision is critical to end-product performance.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical registration
    • IUPAC guidelines for chiral purity in catalyst production
    • ISO 9001:2015 for quality management systems
    • Specific internal SOP compliance for trace metal and enantiomeric excess testing

    Typical usage ratio

    • 10–20 mol% relative to transition metal precursor, depending on desired selectivity and conversion; quantity adjusted based on optimization screening and production scale

    Downstream process integration

    • Ligand assembly step, before complexation with palladium, rhodium, or iridium salts
    • Further derivatization to support ligand backbones
    • Integrated into iterative scale-up for catalytic batch campaigns

    Final product types

    • Chiral diphosphine or diamine ligands for pharmaceutical catalysis
    • Specialized ligands for agrochemical or fragrance intermediate synthesis
    • Tailor-made catalyst systems for academic and contract research organizations

    2. Precursor in Nucleoside Analog and Oligonucleotide Manufacturing

    Oligonucleotide and nucleoside analog manufacturers incorporate this protected threitol derivative during the synthesis of non-natural sugar backbones, particularly in the assembly of locked nucleic acids (LNAs) and other modified nucleosides. The defined stereocenters and protecting groups facilitate stepwise phosphorylation and glycosylation, allowing precise control over sugar modifications that modulate the binding affinity and metabolic stability of the final therapeutic oligonucleotides.

    Industry compliance standards

    • USP-NF (United States Pharmacopeia – National Formulary) for pharmaceutical oligonucleotides
    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • WHO Guidance on Nucleic Acid Therapeutics
    • ISO 13485:2016 for medical device-grade reagents, when used in diagnostic kit manufacturing

    Typical usage ratio

    • 1.0–1.2 equivalents per sugar residue in backbone construction; precise ratio varies with coupling efficiency and target sequence length

    Downstream process integration

    • Protection step for L-threitol backbone prior to phosphoramidite or phosphotriester synthesis
    • Participates as a sugar moiety in solid-phase oligonucleotide synthesis
    • Incorporation during multi-step convergent assembly of modified nucleoside monomers

    Final product types

    • Locked nucleic acid (LNA) and bridged nucleic acid (BNA) oligos for antisense therapies
    • Non-natural nucleoside analogs for antiviral or oncology drug research
    • Molecular probes and qPCR primers/probes for diagnostics

    3. Chiral Auxiliary Sourcing in Fine Chemical Synthesis

    Manufacturers in the specialty chemicals sector use (+)-2,3-O-Isopropylidene-L-Threitol as a core source for preparing chiral auxiliaries. The defined stereochemical configuration allows selective installation onto target substrates, promoting desired stereoselectivity in enolate alkylation, aldol reactions, or cyclizations. This application underpins the preparation of single-enantiomer building blocks required for fragrance, flavor, and advanced material manufacturing.

    Industry compliance standards

    • REACH Annex VII–X for specialty intermediate registration
    • ISO 14001:2015 for environmental and safety process management
    • Internal standards for stereopurity (>99% ee) and trace impurities control
    • Chemical Weapons Convention (CWC) screening for specialty chemicals

    Typical usage ratio

    • 0.8–1.5 equivalents relative to targeted substrate; adjusted for auxiliary recovery strategies and process cost

    Downstream process integration

    • Auxiliary attachment via esterification or carbonate formation before stereocontrolled reaction
    • Removal and recovery step post-reaction using mild hydrolysis or alcoholysis
    • Recyclable auxiliary workflows for continuous operation

    Final product types

    • Single-enantiomer intermediates for specialty perfumery
    • Chiral alcohols for high-end flavor compounds
    • Advanced materials monomers for optoelectronic polymers and resins

    4. Protecting Group Intermediate in Carbohydrate Synthesis

    In advanced carbohydrate chemistry, this compound serves as a starting point for assembling selectively protected polyols. Research and industrial carbohydrate labs rely on the isopropylidene acetal functionality to temporally shield vicinal diols, enabling regioselective opening or further modification. This controlled protection is vital when producing complex oligosaccharides and glycoconjugates for pharmaceutical and vaccine R&D as well as for high-purity food ingredient formulations.

    Industry compliance standards

    • ICH Q11 (Development and Manufacture of Drug Substances) for carbohydrate APIs
    • Food Chemicals Codex (FCC) if used in food-grade ingredient intermediates
    • USP <1043> for quality attributes of bulk chemical intermediates
    • GMP Part II for starting materials supplied to regulated markets

    Typical usage ratio

    • 1.0 equivalent per protected diol unit, with excess (up to 10%) occasionally applied to drive complete protection during initial charge

    Downstream process integration

    • Protection step in synthesis of custom glycosyl donors and acceptors
    • Applied in regioselective derivatization protocols for complex sugar mapping
    • Included in semi-automated oligosaccharide assembly systems

    Final product types

    • Pharmaceutical grade oligosaccharides for therapeutic and vaccine development
    • Food-grade rare sugar derivatives
    • Glycosylated polymers for biomedical research applications

    5. Starting Material in Chiral Polyol and Polyester Development

    Polymer and advanced materials companies depend on this stereochemically pure intermediate when developing specialty polyols, polyesters, and resin systems with customized backbone architectures. The consistent configuration of its four-carbon skeleton directly introduces chirality into polymer chains used in high-performance thermoplastics, adhesive formulations, and biodegradable plasticizer matrices.

    Industry compliance standards

    • ISO 9001:2015 for quality management in materials manufacturing
    • RoHS 3 Directive 2015/863 for restricted substances in electronics-compatible plastics
    • EN 13432 for compostable/biodegradable plastics when targeting environmental applications
    • Internal RM specifications for optical purity and trace solvent content

    Typical usage ratio

    • 10–30% by weight for polyol-based thermoplastics; the precise level set by required mechanical and thermoplastic properties of target resin

    Downstream process integration

    • Polycondensation step as a diol unit with diacid or diisocyanate partners
    • Chain-extension via functionalized polyol derivatives
    • Incorporation in compounding with additives and co-monomers

    Final product types

    • Biodegradable thermoplastic polyesters
    • Optically active polyurethane adhesives
    • High-refractive index resins for electronics and optical coatings
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    Certification & Compliance
    More Introduction

    (+)-2,3-O-Isopropylidene-L-Threitol: A Closer Look from the Manufacturer’s Bench

    Walking through our production line, the distinctive crystalline quality of (+)-2,3-O-Isopropylidene-L-threitol always grabs my attention. This chiral diol, sometimes called L-Threitol Acetonide, isn’t just another specialty chemical on our catalog. To our team, it’s the result of a focused commitment to consistent process development, careful purification, and solid working relationships with leading researchers. Over years in this business, we’ve seen customer priorities evolve, but requests for purity, reliable supply, and batch-to-batch consistency never shift. Like so many staple intermediates, the true value of this compound comes to light in the way it quietly underpins innovation across pharmaceutical, analytical, and synthetic chemistry labs.

    Model, Purity, and Consistency: Why Specifications Matter

    Our team pays attention to small details at every stage of production. The standard product offering carries the CAS number 136030-28-7 and is supplied as a high-purity white crystalline solid. During QC, we typically target a purity of >99% by HPLC or GC, with residual solvents far below threshold levels set by major pharmacopoeias. Moisture content tests are routine, and the NMR spectra always match authenticated reference materials. These steps speak directly to what matters in real-world synthesis and lab method development. Lab staff don’t want to stop their flow to troubleshoot strange side peaks or sub-par yield. Every extra decimal of purity brings peace of mind down the line, and that ultimately protects ambitious projects from expensive delays.

    Sometimes we receive requests for alternate grades—larger particle size for easier filtration, solutions in methanol, or material packed under inert gas. Having a production system designed for chiral compounds lets us respond without compromising quality. Most of our output is in 25-gram to 1-kilogram packs for process R&D or pilot scale, but we can readily expand that to larger runs if the need arises. Packing and labeling remain straightforward—our goal is to remove potential confusion before product ever leaves our dock.

    Applications and End Uses: Why Customers Keep Asking for This Compound

    It’s always rewarding to talk with a customer who’s scaling up a promising asymmetric synthesis, and (+)-2,3-O-Isopropylidene-L-threitol frequently finds its way into those conversations. Its acetonide group offers protective functionality for the vicinal diol system, letting chemists manipulate one end of the molecule while keeping the other end locked. That impacts total synthesis routes for chiral drugs, agricultural active ingredients, and complex natural products. In our own discussions with process chemists or analytical method specialists, we often hear how this molecule’s diastereomeric purity saves effort on downstream steps.

    This molecule isn’t just for capricious or delicate reactions, though. Materials researchers come to us asking for high-purity chiral building blocks for enantioselective recognition studies, custom sensor development, or polymer backbone modifications. Instrument calibration specialists sometimes source this material as a reference for chiral column performance. We’ve shipped it to customers developing pilot processes for specialty flavors and fragrances, and to labs conducting environmental biomarker analysis. In each application, the molecule’s specific arrangement of stereocenters and robust protecting group make it easy to “plug in” to a wide variety of custom synthetic plans—a rare trait in the chiral intermediate world.

    How This Product Differs From Other Chiral Diols

    Having worked closely with a wide catalog of chiral diols, I know not all intermediates are created equal. Many have inherent stability concerns or finicky crystallization behavior that can frustrate both chemists and production staff. (+)-2,3-O-Isopropylidene-L-threitol offers a sturdy alternative, thanks to its acetonide protection. The protecting group resists acid and base under typical work-up and isolation conditions, granting end users flexibility in developing their own synthetic approaches. Compared to L-threitol without the acetonide, the protected form stays solid under ambient storage and ships reliably worldwide, even in humid or variable climates.

    We get plenty of requests to substitute other regioisomers or epimers, but our customer feedback makes clear why this material is considered a gold standard for applications needing predictable stereochemistry. When process teams compare cost and quality, they find cutting corners on chiral purity eventually triggers more headaches than savings. Our product’s NMR and chiral HPLC traceability, combined with detailed impurity profiles, takes the guesswork out of quality control. The consistent melting point and clean crystallization response during isolation means this product fits seamlessly into scaling studies, in contrast with other, less robust chiral diol derivatives that can turn sticky, oily, or unstable during handling.

    Direct alternatives like 1,4:3,6-dianhydro-D-sorbitol or unprotected D-threitol exist, but those lack either the selectivity or the chemical “handle” needed for more demanding library builds. We have seen clients attempt in-house protection of L-threitol with acetone, only to run into variable acetonide incorporation, and headaches sourcing reliable acetone-drying protocols. Consistency matters, and smaller research-scale batches won’t always survive scale-up blips the way well-established commercial grades do.

    Lessons Learned Through Collaboration and Production

    Making this compound in bulk, as a chiral manufacturer and not just a niche supplier, teaches patience and humility. The starting materials don’t always look the same from batch to batch, and minor trace impurities in acetone or catalyst can have real consequences for downstream processing. Our technical team keeps detailed process logs that flag any batch irregularities for review. Lab-scale preparation feels very different from full-scale lot production, and it’s easy to miss small process steps that turn crucial once you’re purifying kilograms of product. Most of the improvements in our process came from working hand-in-hand with both experienced chemists and determined junior staff, troubleshooting everything from glassware contamination to vacuum pump stability. The robustness of our systems now extends well beyond GMP expectations, thanks to hundreds of small institutional lessons collected over years.

    Adhering to green chemistry principles plays a practical role. By optimizing the isopropylidene protection reaction and recycling solvents wherever possible, our plant reduces both cost and impact. It’s not just for regulatory reporting; it keeps our raw material costs competitive, and gives us tools to pivot more quickly to new orders. By monitoring byproducts and minimizing toxic waste, we keep our people and the community safer—a responsibility every chemical manufacturer feels every day.

    Supporting Researchers and Production Chemists: Firsthand Impact

    As a producer, seeing how (+)-2,3-O-Isopropylidene-L-threitol fits into so many workflows—sometimes far beyond what any one lab can imagine—reminds us that most successful chemistry rests on basics done well. Several years ago, a university customer shared how reliable supply of this material helped them secure a grant for a new asymmetric catalysis project. Their letter was simple: “On-time shipments, no spikes in impurity profile, easy to handle.” To a large trading company, statements like these might get buried under pricing memos. To our staff, it’s a badge of honor. There’s real satisfaction in sending out each drum, knowing it will spark new discoveries, or clear a bottleneck for a drug synthesis group already under timeline pressure.

    We put time into documentation and technical data sharing—NMR traces, full COAs for every lot, and focused safety discussions for new users. Over the years, several customers have visited our plant for audits. They ask questions most distributors can’t answer: details on reactor cleaning, off-gas capture, or how small-lot samples relate to the main batch. Discussing those details directly connects us to the end-user, builds trust, and sparks honest feedback that helps us improve future runs.

    Meeting Demand: Reliability During Volatile Markets

    Every chemical maker faces market twists that can stretch inventories or stress supply chains. Our management team learned this lesson during the pandemic. Even with tight global logistics, our steady supplier relationships for chiral starting materials—and a willingness to keep larger buffer stock in-house—meant we rarely faced stock-outs for core products like (+)-2,3-O-Isopropylidene-L-threitol. During several months of surging orders from both academic and pharmaceutical customers, our staff put in extra hours to make sure no request fell through the cracks. Many buyers reached out, noting that other suppliers either couldn’t fill their needs, or delivered erratic quality.

    Reliable supply isn’t just about manufacturing capacity. It comes from knowing the rhythm of customer projects and seasonality, keeping channels of communication open, and solving problems before they escalate. Tracking performance allows us to spot trends—a series of requests for lower-impurity lots from European customers, a few more calls for kilogram quantities from developers of green agrochemicals. From here, we can adjust capacity, order critical raw materials, or tweak purification sequences in anticipation. This close relationship with the chemists and project managers actually using our products keeps us anchored in the real needs of those doing the science.

    Transparency, Traceability, and User Confidence

    One area where experience as a manufacturer pays off is traceability. Each batch receives a full set of analytical data, including NMR, IR, GC/HPLC, and, if needed, chiral purity checks. These aren’t just checkboxes—they represent hundreds of accumulated lessons about what can go wrong when a production campaign gets off track. Customers receive the same data we review internally, and our in-house chemists are never more than a phone call away to clarify points or walk through specific spectra. This isn’t something most resellers can provide, as they lack access to production-side records or live lab staff.

    Failures happen sometimes in chemical manufacturing, but our approach is to catch them early and keep the documentation honest. That might mean a frank call to a client about an off-spec batch, or flagging a shipment for expedited retesting. Any mistakes go onto our process logs, where they can inform corrective actions or refinements to SOPs. Customers have rewarded this candor with continued business; several large accounts have actually expanded their portfolios to cover multiple complex chiral intermediates, reflecting trust built on handling sensitive information and supporting tight project timelines.

    Sustainability and Responsible Manufacturing

    The chemical world faces growing expectations for greener production and sustainable supply chains. Our plant invested in energy-efficient reaction systems and closed-loop solvent recovery—not because it was trendy, but because it cuts recurring costs and improves margin stability long-term. More importantly, our customers increasingly ask about the traceability of raw material sources, worker safety, and environmental standards before placing even a small order. For (+)-2,3-O-Isopropylidene-L-threitol, we publish sustainability summaries and welcome detailed audits. Real transparency means acknowledging difficult trade-offs—sometimes greener alternatives cost more, or require a longer lead time. We lay out options for customers, and find most teams appreciate being treated as partners, rather than just end-points in a price chain.

    On the day-to-day shop floor, we see the difference this approach makes. Workers stay safer when solvents are reused effectively and spills get contained before entering drains. New team members pick up on the importance of monitoring, maintenance, and continual improvement culture. Departments talk openly about yield targets and the pressure points that can lead to waste. External certifications and audits keep us on track, but it’s the internal pride of ownership—knowing each batch reflects a shared effort—that sustains progress.

    Anticipating the Evolving Roles of Chiral Building Blocks

    Product demand doesn’t always track with headline research news. Some weeks we’ll have a flood of requests from pharma process teams pushing a new intermediate. Other months, it’s the fine chemicals sector hunting for kilogram lots for catalyst studies or next-generation monomers. Recently, green chemistry and flow synthesis teams have started exploring this compound’s reactivity in continuous operations. As more customers pursue rapid screening and scalable asymmetric reactions, the push for reproducibility intensifies. The presence of a reliable acetonide-protected chiral diol gives these developers a familiar “anchor”—an intermediate with performance and outcomes they can map to other studies.

    We keep a close watch on published reaction pathways, new patent filings, and market innovations. These signals help us anticipate requirements, whether it’s finer material for column packing, or custom purifications to sub-ppm impurity levels. Every new use case gives us an opportunity to support customer science, share what we’ve learned, and nudge forward the standards for what chemical manufacturing can achieve at scale.

    Final Thoughts: Perspective from the Chemical Manufacturer's Plant Floor

    Being the original maker of (+)-2,3-O-Isopropylidene-L-threitol changes a manufacturer’s mindset. We measure success not just in sales, but by customer projects that succeed because their materials perform as promised. Every process improvement, every carefully documented batch, and every quality test sends a signal—there’s skilled people behind this molecule, tracking its journey from raw materials to reaction flask. Across industries, the real backbone of innovative chemistry comes from reliable, thoughtful manufacturing practice. It’s a perspective earned over years, and each container we ship contains not just a chemical product, but the collective effort and commitment of an experienced team dedicated to scientific advancement.