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(S)-(-)-1,2-Propanediol Di-P-Tosylate

    • Product Name (S)-(-)-1,2-Propanediol Di-P-Tosylate
    • Alias (S)-(-)-Propylene glycol ditosylate
    • Einecs 214-438-0
    • 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

    103172

    Product Name (S)-(-)-1,2-Propanediol Di-P-Tosylate
    Cas Number 68957-94-4
    Molecular Formula C17H20O6S2
    Molecular Weight 400.47 g/mol
    Appearance White to off-white solid
    Melting Point 74-78 °C
    Specific Rotation -17° to -19° (c=1, CHCl3)
    Solubility Soluble in organic solvents such as dichloromethane and chloroform
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C
    Smiles C[C@@H](OS(=O)(=O)c1ccc(cc1)C)OS(=O)(=O)c2ccc(cc2)C
    Synonyms (S)-(-)-Propanediol ditosylate

    As an accredited (S)-(-)-1,2-Propanediol Di-P-Tosylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing (S)-(-)-1,2-Propanediol Di-P-Tosylate is supplied in a 25g amber glass bottle with a tamper-evident screw cap, labeled accordingly.
    Shipping The chemical (S)-(-)-1,2-Propanediol Di-P-Tosylate is securely packaged in sealed, chemical-resistant containers to prevent leakage or contamination. It is shipped under ambient conditions with standard hazardous material labeling, complying with international transportation regulations for chemicals. Shipping includes required documentation for safe handling and material safety data.
    Storage (S)-(-)-1,2-Propanediol Di-P-Tosylate should be stored in a tightly sealed container, away from moisture, light, and incompatible substances such as strong bases and oxidizing agents. It should be kept in a cool, dry, and well-ventilated area—preferably at room temperature or below. Proper labeling and secondary containment are recommended to prevent accidental exposure or spills.
    Application of (S)-(-)-1,2-Propanediol Di-P-Tosylate

    Applications of (S)-(-)-1,2-Propanediol Di-P-Tosylate in Industrial Manufacturing

    As the direct manufacturer of (S)-(-)-1,2-Propanediol Di-P-Tosylate, we supply this chiral intermediate to specialized sectors requiring high stereochemical control in advanced synthesis. The following segments illustrate its established roles within fine chemicals, APIs, and high-purity intermediates production, with an emphasis on operational detail, key standards, formulation intelligence, and downstream product outputs.

    1. Asymmetric Synthesis of Chiral β-Amino Alcohols for Pharmaceutical APIs

    Pharmaceutical producers utilize this chiral di-tosylate to introduce protected intermediate moieties in the stepwise construction of β-amino alcohol frameworks, supporting the synthesis of enantiomerically enriched drug substances. The reagent enters amidation or substitution steps after initial chiral pool synthesis, ensuring stringent enantiopurity and regulatory conformance for GMP-controlled API routes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for chiral substances
    • U.S. FDA 21 CFR Part 210/211 cGMP requirements
    • USP General Chapter <823> for Radiopharmaceuticals (when applicable)

    Typical usage ratio

    • 0.9–1.2 molar equivalents per target chiral center in substrate, adjusted according to reactant stoichiometry and transformation yield requirements

    Downstream process integration

    • Added during the key protection or activation phase of amino alcohol synthesis within multi-step API manufacturing—typically after initial diol resolution and before nucleophilic substitution or reductive amination

    Final product types

    • Chiral intermediates for anti-hypertensive agents (e.g., β-blockers)
    • Active pharmaceutical ingredients such as certain anti-infective or anti-cancer agents featuring chiral β-amino alcohol structures
    • Specialty building blocks for CNS/antidepressant actives

    2. Enantioselective Synthesis of Chiral Epoxy Alcohols for Agrochemical Intermediates

    Manufacturers in the agrochemical sector incorporate our specialty material as a precursor for the controlled formation of chiral epoxy alcohols, integral to the downstream production of select herbicides and pesticides. The reagent’s dual tosylate groups provide a stable leaving function, facilitating stereospecific ring closure during oxide formation in pilot and commercial-scale batch processes.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides
    • ISO 9001:2015 certified quality management throughout synthesis
    • REACH Registration (EU) for intermediate use
    • OECD Good Laboratory Practice (for process and QC validation)

    Typical usage ratio

    • Typically 1.0–1.3 equivalents, optimized for each epoxy alcohol-forming reaction based on impurity profile and conversion efficiency

    Downstream process integration

    • Introduced during the activation and cyclization stages of chiral diol processing—specifically before basic-catalyzed intramolecular nucleophilic displacement and subsequent work-up

    Final product types

    • Precursor intermediates for broadleaf herbicide active ingredients
    • Stereochemically controlled pesticide intermediates
    • Agrochemical active ingredient scaffolds featuring epoxy-alcohol functional groups

    3. Building Block for Liquid Crystal Monomer Synthesis in Display Materials

    Chemical manufactures producing advanced display materials, including liquid crystal monomers, favor this compound for its defined chiral configuration and reliable leaving characteristics, ideal for preparing mono- or di-functionalized intermediates. It is processed through nucleophilic aromatic substitution or Williamson ether synthesis to generate liquid crystal precursors with consistent optical properties.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for display electronics
    • IEC 61249-2-21:2017 for halogen-free base materials
    • ISO 14001:2015 (environmental management) for specialty chemicals
    • SEMI S2/EHS guidelines for handling organic process chemicals

    Typical usage ratio

    • Used in a 1:1 to 1:1.1 molar proportion relative to the target alcohol or phenol group during etherification or coupling reactions; fine-tuned based on desired yield and downstream purity demands

    Downstream process integration

    • Introduced at the monomer capping or terminal group modification stage to prepare high-purity chiral building blocks for subsequent polymerization or mesogen synthesis in LC panel production lines

    Final product types

    • Chiral liquid crystal monomers for LCD, OLED, and photonic display substrates
    • Structure-specific mesogenic intermediates for temperature-stable displays
    • Optoelectronic materials with precise enantiomeric ratios

    4. Intermediate for Stereospecific Catalyst Ligands in Fine Chemical Synthesis

    Producers of high-performance catalyst ligands incorporate our di-tosylated intermediate as a precursor in the staged assembly of bidentate or multifunctional chiral ligands. These ligands are crucial for asymmetric hydrogenation and carbon-carbon bond formation in fine chemical and pharmaceutical processes, where reproducible enantioselectivity and ligand purity are essential quality drivers.

    Industry compliance standards

    • Responsible Care® management system (for industrial fine chemicals)
    • ISO 9001:2015 Quality Management System certification
    • Compliance with customer-specific GMP or QC protocols
    • Chemical hazard communication as per GHS (CLP Regulation - EC 1272/2008)

    Typical usage ratio

    • 0.95–1.15 equivalents according to molarity of starting backbones, optimally adjusted to maximize chiral transfer in ligand synthesis routes

    Downstream process integration

    • Enters at early or mid-stage functionalization steps of ligand construction, typically following chiral resolution and before metalation or further backbone derivatization

    Final product types

    • Chiral phosphine or diamine catalyst ligands for homogeneous catalysis
    • Enantioselective catalyst precursor salts for specialty synthesis
    • Advanced ligand scaffolds sold as fine chemical additives
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    Certification & Compliance
    More Introduction

    (S)-(-)-1,2-Propanediol Di-P-Tosylate: Reliable Performance Through Experience and Commitment to Quality

    Building Trust in Every Batch of (S)-(-)-1,2-Propanediol Di-P-Tosylate

    Manufacturing chiral intermediates calls for deep responsibility. Over the years, strict raw material screening and precision-control systems have proven essential when producing compounds like (S)-(-)-1,2-Propanediol Di-P-Tosylate. Familiarity with these sensitive molecules, which show up often in pharmaceutical synthesis and organic frameworks, means more than following protocols. It means taking real pride in the consistency, purity, and transparency offered to every research team and chemical plant that uses our product.

    Model and Chemical Profile

    (S)-(-)-1,2-Propanediol Di-P-Tosylate stands out as a chiral, di-functional tosylate. Our teams monitor the entire synthesis pathway from the moment raw chiral diols arrive. Each batch comes out as a crystalline solid, usually appearing off-white or pale with a faint aromatic odor from the p-toluenesulfonyl moieties that anchor its stability. Actual measurement—from melting point to NMR trace—never gets left to automated routines alone; lab personnel conduct hands-on checks with every lot, addressing even minor impurities or water content problems before anything leaves the floor. Purity regularly exceeds 99%, based not only on HPLC but verified with orthogonal methods, including GC and polarimetry.

    For technical users, having a compound with a defined stereochemistry changes outcomes downstream. Relying on this (S)-enantiomer translates into predictable results for enantioselective synthesis. Customers working on new catalysts, peptides, or complex natural products mention smoother workflows, less rework, and fewer contaminants after isolating products from reactions using our chiral di-tosylate. This confidence comes from our willingness to go beyond specification sheets and keep improving isolation steps so that side-by-side, our material generates higher yields with very few by-products.

    Usage: Practical Experience from Synthesis Floors

    The core role that (S)-(-)-1,2-Propanediol Di-P-Tosylate performs shows clearest in real-world synthesis. For example, as a building block during nucleophilic substitution, chemists regularly favor this di-tosylate over mesylates or mono-protected versions. It enables a highly controlled introduction of leaving groups, supporting both ring closures and selective alkylations. Experience across dozens of pharmaceutical scale-ups has shown that starting from impurity-checked, dry di-tosylate simplifies downstream workups. That low moisture content—confirmed batch by batch—means users rarely need to pre-dry or treat material, saving time and reducing the risk of hydrolysis during coupling steps.

    Even small fluctuations in starting material quality can throw entire syntheses off track. Over time, our staff learned how to avoid issues with exothermic runaways and incomplete conversions by using precisely milled crystals, not fine powders, and maintaining particle size suitable for smooth solution handling. Unlike less rigorously-produced alternatives, our di-tosylate dissolves completely and behaves predictably in polar aprotic solvents, giving chemists the reliability needed day-to-day.

    How This Product Distinguishes Itself

    Throughout our history in specialty chemicals, a major lesson stands out: not every (S)-(-)-1,2-Propanediol Di-P-Tosylate delivered on market meets the needs of advanced synthesis groups. Many so-called “equivalent” samples—often sourced from re-packagers or traders—arrived in customer labs with inconsistent color, detectable odors unrelated to tosyl groups, or uneven physical states. Every one of these issues can derail a sensitive reaction.

    Greater attention goes not just into reaction set-up, but on in-plant handling and packaging. Instead of shipping in general-purpose containers, we select packaging with proven compatibility for tosylates, protecting against moisture or unintended cross-contamination. Our logistics chain is short: everything stays under our direct supervision, so untouched product quality from reactor to customer bench becomes the rule, not the exception.

    Comparing (S)-(-)-1,2-Propanediol Di-P-Tosylate to similar derivatives reveals the real difference made by hands-on manufacturing experience. Mono-tosylated or mesylated variants may offer specific utility in certain transformations, but most lack the dual functionality and chiral purity controlled in our di-tosylate. Entries from secondary market sources often fail to match the exact melting range and spectral profile you’ll see from batches produced by a team whose primary focus is this segment of chiral intermediates, not just general reagents.

    Lessons From the Field: Preventing Downtime and Rework

    Repeated feedback confirms why time invested in process optimization pays off for end users. Several specialized chemistry groups have explained how switching to our direct-manufactured di-tosylate resolved bottlenecks tied to solubility or lot-to-lot purity variation. What’s rarely spelled out on data sheets—but shows up in daily lab life—is the link between impurity levels and extra purification steps. Less pure, variable material may seem cheaper, but the hours lost to multiple recrystallizations or failed runs nearly always outweigh any savings.

    For those working under tight project timelines—drug discovery, pilot runs, or time-sensitive R&D—predictable loading, repeatable crystallization, and true stereochemical control matter as much as headline purity. More than once, we’ve heard from scale-up chemists that being able to count on regular supply schedules and a proven handling protocol spared them delays that would have disrupted downstream projects.

    Supporting Innovation Through Collaboration

    Years of direct engagement with process chemists and formulators have shaped how (S)-(-)-1,2-Propanediol Di-P-Tosylate reaches market. Suggestions from customers generated real improvements: switching from certain solvent extraction steps to more advanced filtration schemes helped address concerns about trace metal presence and reduced unwanted by-products during bulk manufacture. Insights from spectral comparison with in-house standards steer continuous refinement in chromatographic validation—nailing down stereochemistry beyond just optical rotation numbers.

    We welcome any lab that wants input on reaction optimization, since new synthetic routes often draw on lived experience gained from hundreds of trial reactions. Every production cycle brings new data to the table, and feedback loops with R&D partners help us fine-tune purification methods and reduce unwanted volatility. Staying adaptable, based on practical user interaction, keeps our offerings current and trustworthy—traits impossible to guarantee with distant, hands-off suppliers.

    Environmental and Safety Priorities in Tosylate Handling

    Sustainable, safe practices form another cornerstone of our daily routine. Our in-house teams manage all intermediate and by-product streams following national and international standards, using closed systems and on-site neutralization rather than outsourcing basic safety checks. For (S)-(-)-1,2-Propanediol Di-P-Tosylate, hazard assessments do not exist just on paper; regular drills, up-to-date PPE guidelines, and continued staff training all contribute to both staff safety and confidence among our customers.

    Handling diagnostics, like real-time moisture readouts and end-point detection in refrigerant-controlled storage, guarantee that even the last-packed units protect against degradation in transit. By monitoring potential impurity formation not only in production but also in the supply stream, we strive to provide something that stands apart from what generic suppliers ship: a product engineered for minimum waste during use, safer long-term storage, and straightforward regulatory documentation.

    Facilitating Compliance and Audit Transparency

    It’s not enough to supply pure (S)-(-)-1,2-Propanediol Di-P-Tosylate: traceability stands as key for every user with documentation demands. Our approach to batch recording, test result archiving, and on-demand certificate access comes from being audited by customers and certification bodies many times over. Certification data and method transparency keep every transaction open for scrutiny, with direct technical support ready to clarify even minor quality concerns. We invite partners to look through our quality histories, and respond in detail to audit queries—not standard in today’s chemical market.

    Material from our facility consistently meets rigorous standards required by both domestic and overseas regulatory regimes. Procedures adapt with any major change in testing technology, and if discrepancies appear during user-side QC, we examine them side-by-side with the client until a mutual resolution emerges.

    Reducing Environmental Burden: Progress in Green Chemistry

    Beyond reaction reliability, we take steps to lower the environmental impact of (S)-(-)-1,2-Propanediol Di-P-Tosylate production. Modifications in process heating, solvent recovery, and energy consumption cut yearly emissions and water use—not a theoretical reduction, but one measured by process meters checked weekly. By reclaiming a higher fraction of input solvents and using closed-circuit water cooling, emissions from manufacturing this intermediate have dropped over the years, even as output has grown.

    Efforts to pursue alternative sulfonating agents, and more benign work-up procedures, grew out of our own practical difficulties with waste handling. Sharing these developments with user labs helps spark new green chemistry ideas at both ends of the value chain. Instead of being content with older, higher-emission processes, the team keeps refining—always with eyes open for raw material improvements and safer substrate handling practices that can further cut risk to people or the planet.

    Supporting Consistent Process Scale-Up

    Many customers start with grams, only to move up to multi-kilogram or even tonne quantities in a short window. Early on, we faced the same challenge. At small scale, careful hand-weighing and visual checks give confidence, but as demand increases, automation takes over more tasks—unless something goes wrong. Meeting unexpected scale jumps takes nimble, real-world-adjusted routines, from re-confirming supply lines for rare chiral precursors to upgrading temperature control at scale, since larger reactors react differently.

    Our facilities maintain uninterrupted batch-to-batch homogeneity while moving from pilot to large-batch mode because new production runs always reference archived master lots and retain input from technical staff who remember how each transition worked in practice. This institutional memory beats any outsourced, spreadsheet-driven plan when surprises show up midway through a project.

    Why Manufacturability Wins Over Paper Specifications

    Many labs receive samples that read well on specs yet trigger obstacles in the real world: increased filter blockage, off-odors, or slow dissolution that add hours to the most basic procedures. Over time, we’ve learned that even minor lapses—particles caked at the drum rim after transit, uneven moisture uptake, or surface flaws—can force users to re-think an entire process. Our focus always lands on delivering not just a chemical that checks all purity boxes, but a batch that behaves the same way every time.

    Chemists enduring unplanned reworks because of subtle lot shifts share stories that never make it to public feedback forums. Fixing these issues means going back to the fundamentals: fresh input chemicals, redundant QC checks before final packing, and careful documentation of physical form. Any trouble report that crosses our desk, no matter how rare, sparks a hands-on response from the shop floor, not just an email chain or a brush-off. Continuous improvement isn’t just a poster on the wall; it’s an honest reaction to what end-users tell us, time after time.

    Summary: Investing in Trust and Results

    Decades of experience underline the value of manufacturing (S)-(-)-1,2-Propanediol Di-P-Tosylate through deliberate, meticulous approaches. Rather than rushing to push out high volumes, teams focus day in and day out on keeping impurity levels in check, maintaining true chiral purity, and responding quickly both to customer emergencies and new technical requirements. This product matters as both a critical step in advanced synthesis and a trust point between our facility and every lab, pilot plant, and production hall that depends on reliable supply.

    The true worth of this compound lies in the thousands of unseen hours invested before a drum ever ships—real effort from procurement through delivery, backed by in-person experience at every turn. Users pursuing new molecular designs, aiming to scale pharmaceutical targets, or building custom catalyst libraries resemble our team: exacting, practical, and always searching for the best solution—not just on paper, but in actual practice. Expectations may be high, but so is our commitment to raising the bar, one batch at a time.