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3,4-O-Isopropylidene-D-Mannitol

    • Product Name 3,4-O-Isopropylidene-D-Mannitol
    • Alias DIM
    • Einecs 213-059-4
    • 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

    903247

    Product Name 3,4-O-Isopropylidene-D-Mannitol
    Cas Number 2420-63-3
    Molecular Formula C8H18O6
    Molecular Weight 210.22 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 142-144°C
    Boiling Point Decomposes
    Solubility In Water Soluble
    Storage Temperature Room temperature
    Purity Typically ≥98%
    Synonyms 3,4-Isopropylidenemannitol, Mannitol Isopropylidene Acetal
    Smiles CC(C)(O)OC[C@@H](O)[C@H](O)CO
    Uses Intermediate in organic synthesis

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

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 3,4-O-Isopropylidene-D-Mannitol, sealed with a screw cap and labeled for laboratory use.
    Shipping 3,4-O-Isopropylidene-D-Mannitol is securely packed in air-tight, chemical-resistant containers to prevent moisture absorption and degradation. The shipment follows standard chemical transport regulations, with clear labeling and documentation. Upon transit, temperature and handling conditions are monitored to ensure product integrity and safety compliance during delivery to the recipient.
    Storage 3,4-O-Isopropylidene-D-Mannitol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from moisture and direct sunlight. Avoid exposure to strong oxidizing agents. Store at room temperature, typically between 15–25°C (59–77°F). Ensure proper labeling and keep away from incompatible substances to maintain chemical stability and safety.
    Application of 3,4-O-Isopropylidene-D-Mannitol

    Applications of 3,4-O-Isopropylidene-D-Mannitol in Industrial Manufacturing

    As a direct manufacturer of 3,4-O-Isopropylidene-D-Mannitol, we supply this specialty polyol to diverse industrial sectors with established downstream demand. Its molecular structure and functional properties support critical roles in advanced synthesis, formulation, and finishing steps across several regulated fields. The following sections detail actual downstream uses, compliance factors, and integration methods.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical producers use 3,4-O-Isopropylidene-D-Mannitol as a protected sugar intermediate in the multi-step synthesis of nucleotide analogues, HIV inhibitors, and advanced carbohydrate-based APIs. The material’s acetonide group provides the necessary steric protection during selective oxidation, glycosylation, and subsequent functional group modifications, which ensures critical regioselectivity and preserves chirality throughout synthesis. End-dose control manufacturers specify this intermediate during scale-up for pilot and full GMP manufacturing routes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and Ph. Eur. guidelines for drug substance starting materials
    • FDA 21 CFR Part 210/211 cGMP for Finished Pharmaceuticals
    • Custom documentation per DMF and COS/CEP submissions

    Typical usage ratio

    • 20–40 mol% of total sugar intermediates, with precise input calculated from target API batch scale and stoichiometry
    • Ratio adjusted by route specificity, often in excess over downstream reactants to achieve full protection

    Downstream process integration

    • Introduced during early-stage API intermediate formation post-carbohydrate activation step
    • Used in batch reactors or continuous flow synthesis lines in GMP-validated cleanrooms
    • Purified by crystallization or preparative HPLC prior to further chain extension or deprotection steps

    Final product types

    • Antiviral nucleotide analogues (e.g., tenofovir prodrugs)
    • Nucleoside reverse transcriptase inhibitors
    • Carbohydrate-derived specialty APIs
    • Intermediates for diagnostic agents

    2. Chiral Building Block for Specialty Organic Synthesis

    Specialty fine chemicals and contract synthesis companies frequently employ 3,4-O-Isopropylidene-D-Mannitol as a source of predefined chirality in stereoselective transformations. Chemists take advantage of its diol-protected scaffold for creating non-racemic ligands and catalysts, as well as for asymmetric synthesis of pharmaceutically active small molecules. The compound’s stability under various anhydrous and basic conditions makes it suitable for multi-step, high-yield production runs.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for chemical manufacturing
    • REACH Annex VII-XII for registration and safe use of intermediates in the EU
    • Specific customer-driven impurity and trace metal specifications
    • Company-defined analytical release protocols (chiral HPLC, NMR, purity by GC-MS)

    Typical usage ratio

    • 10–50 mol% depending on downstream product structure and the number of chiral centers required
    • Batch size and input mass optimized for desired ligand or final chiral compound output

    Downstream process integration

    • Added at the initial protection step of polyhydroxy compounds
    • Serves as the precursor in enantioselective alkylations, reductions, or additions
    • Subsequent deprotection and purification permit isolation of chiral end-products

    Final product types

    • Chiral auxiliaries and ligands for asymmetric catalysis
    • Stereopure organic intermediates
    • Complex fine chemicals for electronic materials
    • Chiral alcohols and amines for contract synthesis orders

    3. Protecting Agent in Oligosaccharide and Glycoside Synthesis

    Producers of specialty oligosaccharides and glycosides incorporate 3,4-O-Isopropylidene-D-Mannitol as a temporary protecting agent to control regioselectivity during monosaccharide coupling and chain extension steps. The protection of vicinal diol groups prevents unwanted side reactions, allowing sequential glycosylation to yield well-defined polymers and derivatives for advanced food ingredients, diagnostic kits, or plant protection actives.

    Industry compliance standards

    • ISO 22000:2018 Food Safety Management System for food additive precursors
    • FAO/WHO Codex Alimentarius for food-grade carbohydrate derivatives
    • ISO 13485:2016 for manufacture of diagnostic raw materials
    • Batch traceability under HACCP for food and agricultural applications

    Typical usage ratio

    • 5–25 mole equivalents relative to target diol groups, depending on chain length and branching requirements
    • Input ratio fine-tuned for multistep protection/deprotection strategies

    Downstream process integration

    • Protecting agent added at the initial activation phase before glycosyl donor or acceptor assembly
    • Removal performed after oligosaccharide elongation, typically via mild acid hydrolysis
    • Purified intermediate isolated for downstream derivatization or conjugation

    Final product types

    • Functional oligosaccharide additives (prebiotics, food fiber blends)
    • Glycoconjugates for diagnostic reagent kits
    • Plant-derived bioactive glycosides
    • Custom carbohydrate standards for research and quality control

    4. Precursor for Modified Sugar Alcohol Derivatives in Food and Cosmetics

    Manufacturers of low-calorie foods, sugar-free confectionery, and specialty personal care bases employ 3,4-O-Isopropylidene-D-Mannitol as a precursor for customized sugar alcohol derivatives. Through catalytic hydrogenation and selective deprotection, downstream plants generate functional polyols offering sensory and textural enhancements, improved stability, and modified solubility compared with conventional mannitol. Strict input and release controls support compliance with food additive and cosmetics regulations.

    Industry compliance standards

    • Food Chemicals Codex (FCC) for polyol ingredients
    • Regulation (EC) No 1333/2008 for food additives in the European Union
    • ISO 22716:2007 for Good Manufacturing Practices in cosmetic raw materials
    • FSMA (FDA Food Safety Modernization Act) for U.S. food and beverage producers

    Typical usage ratio

    • 15–30% of total carbohydrate input for food sugar alcohols
    • 5–20% w/w in cosmetic base formulations depending on target skin-feel and osmotic properties
    • Usage level determined by final product performance and regulatory maximums

    Downstream process integration

    • Hydrogenation of the acetonide derivative under controlled pH and catalytic conditions
    • Deprotection and neutralization prior to blending with carrier sugars or emollients
    • QC analysis for purity, residual solvents, and contaminants per batch specification

    Final product types

    • Sugar-free candies, chewing gum, and baked goods
    • Low-calorie beverage sweetener blends
    • Moisturizing cream and gel bases for cosmetics
    • Specialty toothpastes and oral care preparations
    Free Quote

    Competitive 3,4-O-Isopropylidene-D-Mannitol prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    Introducing 3,4-O-Isopropylidene-D-Mannitol: A Closer Look from the Factory Floor

    From Raw Material to Reliable Ingredient: Our Experience with 3,4-O-Isopropylidene-D-Mannitol

    Working in the business of specialty chemical manufacturing, every new compound represents a story shaped by process know-how, raw material purity, and unbroken attention to detail. 3,4-O-Isopropylidene-D-Mannitol is a material that brings together lessons from handling polyols and building molecules with exacting care, getting used in a range of applications that call for more than just another commodity. For years, we’ve met requests from pharmaceutical teams, research chemists, and process engineers by producing this compound with strict quality controls baked into every batch.

    Getting to Know the Material: Model and Specifications Reflected in Real-World Work

    Each lot of 3,4-O-Isopropylidene-D-Mannitol we turn out matches specifications that come not only from documents, but from what clients actually use in labs and production lines. Having started production after years of experience with mannitol derivatives, we now stick to the crystalline, white solid standard with purity levels above 98% as determined by HPLC and NMR analysis. Our batches usually present a melting point range from 108 to 112°C, although careful drying and handling allow us to maintain lot-to-lot consistency, which labs notice right away.

    People who order from us want clarity on moisture content since this can affect yield in follow-on steps—so Karl Fischer titration results usually sit well below 0.3%. Impurities impact reaction predictability, and our quality team screens for traces of starting material, byproducts, and possible inorganic residues, reporting these figures transparently with shipped product.

    Manufacturing Insights: What Sets Our Process Apart

    Folks sometimes ask what it takes to get a batch of 3,4-O-Isopropylidene-D-Mannitol right the first time. Much comes down to dryness of starting mannitol, choice of ketone (acetone in our setup), and careful acid catalysis under controlled conditions. Neutralization, phase separation, and distillation steps cut down residual acidity and sulfate. Filtration at the right temperature avoids forming softer product that tends to clump or cake.

    Automation handles repetition, but experienced operators still oversee every critical step—especially during final crystallization, where agitation speed, temperature ramp, and solvent removal rates make or break crystal habit. We let each batch settle for at least 12 hours to ensure conversion is complete and keep each vessel isolated to avoid cross-contamination, even if it means smaller lot sizes. That’s the only way we’ve found to make sure every kilogram meets the mark for customers who need consistent yield during downstream chemistry.

    Comparing 3,4-O-Isopropylidene-D-Mannitol to Related Compounds

    As a producer, we get a first-hand look at how end uses and performance shift between members of the mannitol acetonide family. 3,4-O-Isopropylidene-D-Mannitol stands out from unprotected mannitol because its acetonide group locks down the central diols, improving stability under mild acid conditions and supporting selective transformations. Our customers tell us they see fewer side-products when building heterocycles or protecting other sugar-based materials.

    Some users try alternatives like 1,2:5,6-di-O-isopropylidene-D-mannitol for more rigid protection, but this increases cost and synthetic steps. 3,4-O-Isopropylidene-D-Mannitol instead delivers targeted protection and easier removal at a better price, so academic and industrial labs often settle on this model for preparative routes that need robust protection without excess processing.

    From the factory, we see different physical behavior between these compounds: 3,4-O-Isopropylidene-D-Mannitol offers fine, free-flowing crystals under our standard drying protocol, with low tendency toward agglomeration. Some alternative mannitol derivatives hold on to solvent or oil out after storage, which risks clogs and measurement issues on sensitive scales. Direct feedback tells us our batches are easy to weigh and dissolve, reducing handling errors in fast-moving labs.

    Looking at Usage: Real-World Purposes and Feedback from the Field

    In pharmaceutical synthesis, the need for orthogonal protection matters more than just theoretical selectivity. Time and again, project chemists ask for 3,4-O-Isopropylidene-D-Mannitol to protect diol functions, enabling stepwise glycosylation or phosphorylation, essential in nucleotide chemistry. Over the years, our batches have supported the synthesis of rare sugars and nucleoside analogues. The isopropylidene mask handles mild acid deprotection, helping teams avoid harsh reagents and minimize degradation in multistep campaigns.

    Materials scientists pick this molecule due to its ability to adjust the hydrophilicity of matrices. We see this trend growing with the expansion of bio-based plastics, coatings, and film-forming agents. Customers crafting customized hydrogels often report clean removal of the acetonide groups post-polymerization, yielding products with exactly the swelling and mechanical properties they expect from their early-stage designs.

    Several R&D users work with 3,4-O-Isopropylidene-D-Mannitol thanks to its consistent reactivity profile. In our support log, requests for technical guidance often focus on solubility, choice of deprotection method, or minimal presence of by-products in analytical HPLC runs. Our product has seen reliable use in chiral resolution, asymmetric reduction, and the development of dendritic molecules in academic research.

    Why Consistency Matters More Than Ever

    Anyone who runs the same chemistry week after week recognizes that inconsistent input materials create headaches no testing team needs. Each new production run in our plant involves full retention samples, purity confirmation by HPLC, and moisture checks. While some specs appear fine on paper, field users can run into trouble if batches fluctuate between runs. As a chemical manufacturer, we cut out variables wherever possible. We stick to the same lot sizes, fixed parameters, and triple-cleaned reactors, so a kilo ordered today matches what went out last quarter. Customers sending precise feedback let us tune profiles further, so the product supports rare or especially demanding transformations.

    We have dealt with operations where a single change in drying cycle or a drop in yield from off-spec starting raw material caused a headache for an entire project. Our priority has always been to keep the cycle flawless from reception to testing, which preserves both supply timing and batch quality. That attention means less downtime and less reworking for contract research clients and in-house teams alike.

    Sourcing, Traceability, and Clean Supply Chains

    Decades of specialty manufacturing have shown us that traceability protects both quality and customers. We buy raw mannitol from established, audited suppliers and keep full trace records for every barrel and drum. Each modification to our production protocol gets logged, not just for compliance, but because small variations in temperature or solvent composition can result in measurable shifts in product appearance, solubility, and thermal stability.

    Shipping always matters, especially when customers need guaranteed shelf life and stable product in changing climates. Our plants use sealed, moisture-resistant packaging straight from drying, and finished product lots get run through stability trials over extended periods. Direct experience shows that shipped material at ambient preserves melting point and recognizable crystal habit over months in controlled warehouse storage. In wet climates, double-bagging and desiccant packs come as standard to cut down risk.

    Talking About Problems and Solutions

    Variability in starting mannitol—density, moisture, and trace organics—introduces batch risks that don’t reveal themselves until downstream. We run additional tests on incoming raw material using NMR and mass spectrometry, something we learned after a batch from a new supplier failed to fully convert in our standard run. This extra layer tacks on cost but dodges expensive lost time and off-grade product in the hands of clients who can’t afford schedule delays.

    Users sometimes report slow dissolution or haze after long storage. Our experience points to trace moisture and static buildup during filling as culprits, so we use stainless equipment earthed to prevent clinging fines and keep transfer lines short from reactor to blend, lowering the chance of picking up water from ambient air. If a customer reports product that clumps, we ask for storage conditions and offer to run additional drying at their request—often at no charge, since a happy customer repeats orders and keeps lines running.

    Some early customers wanted faster removal of the acetonide group. Based on shared feedback, we wrote up a protocol library for acid-catalyzed and enzymatic deprotection, along with solvent screening tips. If project chemists get stuck, they call us directly and walk through the problem, which helps us flag subtle impurities, fix drying issues, or give solvent recommendations that cut deprotection time. More than once, we’ve adjusted our own process after hearing about problems with deprotection lag or odd HPLC peaks, which led us to add a final recrystallization step and tweak our mother liquor removal protocol.

    Supporting Demand Across Markets While Keeping Quality Intact

    Demand shifts often come fast, whether from new synthetic routes or regulatory pressure to use defined protecting groups. We run our batches in production plants that emphasize flexibility. Each year brings more orders but also pushes us to scale without sacrificing the hands-on checks that make specialty production reliable. Our operators maintain records of every run, and our test lab issues certificates based on real analysis performed on the actual outgoing lot—never a previous batch. That’s the only way industrial and academic teams can keep projects on track, since a change in input material mid-campaign means lost time and budget.

    We make adjustments on the fly when research groups want kilogram-scale lots for pilot runs or larger orders for scale-up, but refuse to cut corners that could send impure or off-moisture material. Over-automation can sometimes hide small slips in process, so, as batch producers, we keep skilled technicians involved all the way through shipment. Regular communication with customers, direct troubleshooting, and willingness to discuss what worked or what failed in their labs help keep our own operation sharp and our batches aligned with evolving needs in the field.

    Building Trust by Sharing What We See Day to Day

    We engage with clients throughout the research, sampling, and scaling process. If shipping large lots, we recommend sampling across bags or drums for the most accurate take on moisture and homogeneity, based on what we’ve seen can happen after long ocean or air transit. We’ve built up a bank of applications, test data, and incident logs that we use to answer technical questions or help a customer identify whether a result points to product, solvent, handling, or equipment issues.

    Trust isn’t just about paperwork. It’s built by getting orders right, clearly labeling batch numbers, and delivering what the certificate states—the actual tested product and not a generic average over time. For the few cases where an off-spec batch does land, we jump in with replacement material, extra technical input, or a new batch prepared under heightened controls.

    The Future: Evolving Expectations and Ongoing Refinement

    Newer applications of 3,4-O-Isopropylidene-D-Mannitol keep appearing, especially as interest grows in modified sugar chemistry, novel biomaterials, and advanced pharmaceutical intermediates. As a manufacturer, we take this as a sign that the product meets a real need but also as a push to keep raising the bar on purity, stability, and responsiveness. Over time, customers request green process changes, higher documentation standards, or express interest in traceability from renewable feedstocks. We discuss openly which upgrades are realistic in current processes and which ones demand R&D investment.

    We see questions increasing around regulatory compliance, environmental impact, and documentation for international shipment. Staying ahead means routine audits, supply chain mapping, and prepping quality documents in a form that stands up to local and overseas inspections. Small changes in regulation often drive shifts in request, so we work closely with trade groups and industry bodies to make sure our batches meet both today’s needs and likely changes in definition or safety protocol.

    A strong cycle of customer-dialogue, open data, and hands-on batch records builds the trust that lets us keep producing innovative intermediates like 3,4-O-Isopropylidene-D-Mannitol in a busy and demanding marketplace. Each run gives us new feedback to upgrade process, fine-tune drying, or add another process check. Over time, that experience stacks up, so each kilo out the door is ready for immediate use—helping teams get more from every reaction and keeping their supply lines simple and predictable.

    Conclusion: A Commitment That Runs More Than Skin Deep

    Dedicated production of 3,4-O-Isopropylidene-D-Mannitol connects decades of chemical experience with the needs of today’s scientists and engineers. We invest in reliable supply, thorough analysis, and a process fine-tuned by feedback from customers using the material in cutting-edge synthesis. Over time, users see the difference in batch reliability, clear documentation, and the open dialogue that keeps shipment, storage, and application simple.

    From our view as direct producers—not brokers or marketers—3,4-O-Isopropylidene-D-Mannitol stands out as more than another intermediate on a spreadsheet. It represents a promise that starts with pure incoming raw material and ends with well-documented, dependable product where users know exactly what’s in every lot. That sort of reliability still comes from people who know their process, watch every run, and share in the work of every finished batch.