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(S)-(+)-1,3-Butanediol

    • Product Name (S)-(+)-1,3-Butanediol
    • Alias (S)-(+)-1,3-Butylene glycol
    • Einecs 225-453-0
    • 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

    955804

    Cas Number 6290-03-5
    Iupac Name (S)-butane-1,3-diol
    Molecular Formula C4H10O2
    Molecular Weight 90.12 g/mol
    Appearance Colorless liquid
    Boiling Point 197-198 °C
    Melting Point −50 °C
    Specific Rotation +21.5° (neat)
    Density 0.965 g/cm³ at 25 °C
    Solubility In Water Miscible
    Purity Typically ≥98%
    Chirality S-enantiomer
    Synonyms (S)-1,3-Butanediol, (S)-(+)-1,3-Butylene glycol
    Flash Point 93 °C
    Refractive Index 1.432 (20 °C)

    As an accredited (S)-(+)-1,3-Butanediol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mL clear glass bottle with a tightly sealed cap, labeled "(S)-(+)-1,3-Butanediol," including hazard symbols and lot number.
    Shipping (S)-(+)-1,3-Butanediol is shipped in tightly sealed containers to prevent contamination and moisture absorption. It should be handled in accordance with safety guidelines, protected from heat and direct sunlight, and clearly labeled as a chemical substance. Shipping complies with relevant regulations to ensure safe and secure transport.
    Storage (S)-(+)-1,3-Butanediol should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Protect from moisture, direct sunlight, and physical damage. Appropriate precautions should be taken to prevent spills and exposure, and storage should comply with local chemical safety regulations.
    Application of (S)-(+)-1,3-Butanediol

    Applications of (S)-(+)-1,3-Butanediol in Industrial Manufacturing

    As a direct manufacturer of (S)-(+)-1,3-Butanediol, we supply high-purity material to global producers involved in advanced chemical synthesis, specialty polymers, pharmaceutical intermediates, and cosmetics. The following application scenarios demonstrate the real-world incorporation of our material within highly regulated downstream industries, providing unique value at each stage of the production chain.

    1. Chiral Intermediate for Statin Synthesis in Active Pharmaceutical Ingredient (API) Manufacturing

    Pharmaceutical companies employ (S)-(+)-1,3-Butanediol as a key chiral building block in the asymmetric synthesis of intermediates for statin-type cholesterol-lowering drugs. This application requires stringent stereochemical integrity and traceability, necessitating close monitoring of each production batch. Producers integrate our raw material into multi-step synthetic routes involving selective oxidation, esterification, and subsequent functional group modifications to achieve high enantiomeric purity for regulatory drug submissions.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • United States Pharmacopeia (USP) API Quality requirements
    • European Pharmacopoeia (Ph.Eur.)
    • FDA Drug Master File (DMF) and regulatory filings

    Typical usage ratio

    • 0.5–1.8 molar equivalents per synthesis stage, calculated based on the specific statin intermediate; quantities adjusted according to enantioselective process needs and desired batch output

    Downstream process integration

    • Charged during initial or mid-stage chiral synthon assembly; handled under nitrogen atmosphere with in-process chromatographic monitoring for enantiopurity; further transformed through oxidation and coupling reactions

    Final product types

    • Statin active pharmaceutical ingredients (e.g., Atorvastatin, Rosuvastatin intermediates)
    • Other chiral pharmaceutical intermediates for APIs

    2. Hydrophilic Monomer for Biodegradable Polyesters in Medical Devices

    Producers in the biomedical sector utilize our material as a hydrophilic monomer for synthesizing specialty polyesters destined for use in absorbable medical implants and sutures. Its stereochemical configuration enables the polymerization processes to yield tailored mechanical flexibility and controlled degradation rates, supporting performance requirements for temporary in vivo applications such as tissue scaffolds and drug-eluting stents.

    Industry compliance standards

    • ISO 13485 (Quality management for medical devices)
    • US FDA 21 CFR 820
    • USP Class VI Biological Reactivity Test
    • ISO 10993-1 (Biocompatibility)

    Typical usage ratio

    • 5–25 wt% as co-monomer within copolymer formulations; ratio determined by desired hydrolysis behavior and implant strength

    Downstream process integration

    • Introduced into melt or ring-opening polymerization reactors alongside lactide, glycolide, or caprolactone; followed by pelletizing, extrusion, and medical-grade sterilization

    Final product types

    • Absorbable surgical sutures
    • Biodegradable tissue scaffolds
    • Drug-eluting stent coatings
    • Soft tissue regeneration membranes

    3. Solvent and Humectant for Personal Care and Skin Care Formulations

    Major personal care manufacturers employ (S)-(+)-1,3-Butanediol as both a humectant and co-solvent in high-performance skin care products targeting sensitive and premium segments. Its chiral purity ensures low irritation potential and stable integration with actives, preserving formulation clarity and enhancing skin-feel without altering fragrance profiles or viscosity. Formulators benefit from its compatibility with a broad spectrum of emulsion and gel technologies, supporting the trend toward minimalist and "free from" ingredient disclosures.

    Industry compliance standards

    • ISO 22716 (Cosmetic GMP)
    • EU Regulation (EC) No 1223/2009 (Cosmetics Regulation)
    • US FDA 21 CFR 700 Subpart B
    • Japanese Standards of Quasi-drug Ingredients

    Typical usage ratio

    • 2–7 wt% in finished formulations; concentration optimized to balance effective humectancy with viscosity and skin sensory requirements

    Downstream process integration

    • Added during the water phase blending step, processed under vacuum homogenization for emulsion stability; final product subjected to microbial challenge testing

    Final product types

    • Facial creams and serums
    • Moisturizing lotions for sensitive skin
    • Color cosmetics (liquid foundations, cushion compacts)
    • Dermatological ointments

    4. Precursor for Artificial Flavors & Food Additives Production

    Food additive and flavor houses utilize this raw material as a chiral precursor in the synthesis of natural-identical flavors, such as gamma-butyrolactone and chiral gamma-lactones. High purity and traceability enable downstream manufacturing processes to comply with strict regional regulations on food-contact substances and flavor ingredient purity. The ingredient also contributes to mild, sweet notes in flavor compositions for beverage, dairy, and bakery applications.

    Industry compliance standards

    • FCC (Food Chemicals Codex)
    • EU Regulation (EC) No. 1334/2008 (Flavorings and Food Ingredients)
    • GB 2760 (China National Food Safety Standard for Use of Food Additives)
    • US FDA 21 CFR 172.515 (Flavouring Agents and Related Substances)

    Typical usage ratio

    • 0.1–0.5% as feedstock input in flavor chemical synthesis; downstream flavor blending targets ppm levels in finished foods

    Downstream process integration

    • Fed into esterification, lactonization, or oxidizing reactors under food-grade controlled environments; batch protocols adhere to HAACP and allergen management plans

    Final product types

    • Natural-identical fruity flavor compounds (e.g., GBL, delta-octalactone)
    • Food-grade solvents for flavor carriers
    • Beverage and confectionery flavor bases
    • Bakery and dairy flavor ingredients

    5. Intermediate for Manufacture of Chiral Agrochemical Actives

    Leading agrochemical companies select our material as an enantiomerically pure intermediate in the synthesis of crop protection agents where chirality enhances biological selectivity and environmental degradability. Used in the construction of herbicide and fungicide molecules, this material supports process chemistries that require strict stereocontrol to ensure efficacy and regulatory acceptance. The raw material allows chemists to streamline multi-step synthesis while controlling byproduct profiles and minimizing racemization.

    Industry compliance standards

    • FAO/WHO Specification for Agrochemicals
    • OECD Principles of Good Laboratory Practice (GLP)
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • EPA Registration Requirements (US CFR Title 40, Part 158)

    Typical usage ratio

    • 0.7–1.6 molar equivalents according to specific synthetic needs for targeted pesticide intermediates; scale adjusted for pilot and commercial batches

    Downstream process integration

    • Incorporated in early-phase enantioselective reactions, followed by purification and coupling steps; enabled through closed-loop batch reactors with real-time chiral HPLC tracking

    Final product types

    • Chiral herbicide active ingredients
    • Fungicidal intermediates with tailored enantiomeric content
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    Certification & Compliance
    More Introduction

    (S)-(+)-1,3-Butanediol: A Manufacturer’s Perspective

    Real-World Chemistry Drives Our Process

    Our production environment brings us face to face with the strengths, limits, and quirks of every molecule we make. The (S)-(+)-1,3-Butanediol we manufacture stands out in our day-to-day work, not just by name, but by its hands-on value and consistent quality. Over years in the plant, handling raw materials and refining our methods, we've learned there’s more behind this ingredient than what a simple chemical datasheet reveals.

    Product Overview—Model and Specifications

    We produce (S)-(+)-1,3-Butanediol using a stereoselective catalytic hydrogenation of acetoacetic acid derivatives, ensuring an enantiomeric excess typically above 98 percent. Our batches meet high purity thresholds—verified by chiral HPLC and GC—resulting in a clear, colorless liquid with a slight, characteristic odor. It features a molecular weight of 90.12 g/mol, with the absolute configuration confirmed by polarimetry, where you’ll find an optical rotation between +18.5° and +19.5° (measured neat, 20°C). Each lot keeps water content below 0.1 percent and residual solvents well under control, factors critical for sensitive downstream syntheses.

    Our tanks, piping, and holding vessels serve only (S)-enantiomer batches. This strict segregation avoids racemization or contamination—a detail easy to underappreciate unless you’ve ever had a costly batch fail quality control due to a leaky gasket or shared pump.

    Why End Users Seek Out This Molecule

    Chiral building blocks like (S)-(+)-1,3-Butanediol play a silent but vital role across pharma, flavor, and cosmetic labs. From our conversations with leading R&D labs and production teams, the message is clear: reproducible chiral purity saves headaches and improves yields in later steps, especially during asymmetric synthesis of active pharmaceutical ingredients.

    Many rely on this compound to introduce hydroxyl groups with precise stereochemistry onto target molecules. Peptide modification, beta-lactam antibiotics, and even certain bioactive small molecules all start with a well-defined chiral diol. A few years back, a client working on a new antihypertensive agent needed a secure, uninterrupted supply—one impurity spike risked weeks of work. By keeping our process under tight in-line monitoring, we delivered consistent material batch after batch. These field stories underline why we go beyond minimum specs.

    Outside pharma, some high-end personal care formulators have turned to (S)-(+)-1,3-Butanediol for skin hydration systems, seeking a unique sensory profile and biocompatibility. Its stereospecific hydroxyl pattern offers different skin feel and humectancy than its racemic counterpart or common glycol-based options. This is the type of feedback only long-term partners tend to share with manufacturers directly; rarely does it appear on a spec sheet.

    Comparing to Other 1,3-Butanediol Stereoisomers

    Inside our plant, the challenge isn’t just making 1,3-butanediol—it’s delivering a single hand, not a mix of both. The structural formula doesn’t tell the full story; the (S)-enantiomer interacts differently with enzymes, receptors, and product matrices than the (R)-enantiomer or a racemic blend.

    In pharma synthesis, a racemic 1,3-butanediol can cause headaches during downstream chiral separations. A client once described how a racemic input forced them into multiple costly crystallizations. With our (S)-(+)-product, their synthetic step delivered cleaner conversions, letting them skip a time-consuming resolution phase. In formulations for flavors and cosmetics, subtle differences in smell, taste, and safety profiles emerge between enantiomers. Purified (S)-(+)-1,3-butanediol consistently provides the sensory and physiological responses these end markets aim for, reducing unwanted side effects or offtastes that can creep in from an uncontrolled mixture.

    No manufacturing shortcut can create a true replacement for the single-handed variant. Only the (S)-form performs specific biological functions and chiral recognition tasks in these environments. Troubleshooting failed reactions or sensory inconsistencies downstream often traces back to these molecular “handedness” mismatches. Years in the field have taught us how much difference a single stereocenter can make.

    Handling, Storage, And Downstream Performance

    From tanks to drums, every handling step shapes the quality of (S)-(+)-1,3-Butanediol. Incoming raw materials matter. Factory humidity levels and drum cleanliness matter. Even something as simple as temperature fluctuations in a storage room may shift purity and reactivity, so real experience—rather than idealized theory—guides our operations.

    We keep storage at a steady 15–25°C, away from acids or oxidizing agents. We prefer high-grade HDPE containers and vacuum transfer lines to avoid moisture pickup or aerobic degradation. Over time, adjusting these details reduced the risk of discoloration and maintained a consistent product profile even months after manufacture.

    Users often ask about shelf life and reactivity. In our practice, batches held under nitrogen show no measurable breakdown over 24 months, holding chiral purity and color just as the day of manufacture. This creates confidence for formulators planning scale-ups or longer R&D timelines. Suddenly, that added reliability lets teams focus on new developments rather than requalification or impurity troubleshooting.

    Regulatory and Safety Observations From the Plant Floor

    We follow strict documentation and regular audits to meet the standards our customers count on—these include periodic analysis of trace heavy metals, validation of chiral purity methods, and compliance with international chemical safety codes. In routine handling, spills or skin contact rarely cause concern at our exposure levels, but we train every technician to use gloves and goggles since repeated contact with diols dries out the skin. Our experience shows a drop in minor incidents after we phased in closed system transfers and instilled regular housekeeping habits. It’s these efforts, not just paperwork, that build real-world safety.

    Shipping regulations can shift quickly. Over the last decade, we’ve adapted as new labeling, hazard communication, and air transport rules have changed. International customers now ask for transparency not just on purity, but on the traceability of any potential by-products. Our labs retain samples from each batch and keep records for every lot so that questions—be they from customs or downstream QA—get answers grounded in evidence rather than educated guesses.

    Supply Chain Perspectives and Market Needs

    Demand for high-purity (S)-(+)-1,3-Butanediol fluctuates with the cycles of major pharmaceutical launches, new regulations, and cosmetics innovation. At the plant, these market shifts become tangible when purchase orders surge or drop with little warning. To support our customers, we keep safety stock and coordinate with logistics partners who understand how to handle temperature- and time-sensitive goods.

    Last year, global supply chains tightened due to geopolitical shifts. We faced delivery bottlenecks on hydrogen and precursor chemicals. Our technical team ran contingency scenarios, mapped new sourcing options, and adjusted batch sizes to hold customer commitments steady. Industry veterans will recognize how critical these crisis-preparedness steps become—no customer wants to hear about a missed shipment due to what amounts to poor planning or lack of backup equipment.

    Transparency in supply chain communications wins trust. We regularly bring customers on site to see not just brochures and certificates, but the actual shop floor, real reactors, and the staff behind every batch. That level of visibility lets users understand how molecules move from raw material intake to finished product and why consistent quality comes from process discipline, not luck.

    Innovation in Production and Analytical Control

    Continuous improvement never leaves our agenda. Our process engineers constantly monitor reaction parameters—pressure, temperature, solvent ratios—and integrate real-time analytics into production. By tying analytical HPLC and polarimeter readings into the batch release process, we spot deviations early, before product ships out the door.

    A few years back, we upgraded our hydrogenation catalysts to a more selective variant. This single step boosted our selectivity for the (S)-enantiomer, dropped energy requirements, and reduced undesired by-products by over 30 percent. Quality audits since have shown tighter purity ranges and a notable reduction in customer complaints about odor or reactivity outliers. These improvements didn’t come from management decrees or copying competitors—they came from operators, chemists, and lab analysts collaborating to fine-tune every input.

    Routine customer feedback also shapes our upgrades. A pilot plant operator once flagged higher-than-normal peroxide reactivity in a new batch. This sent us investigating storage procedures and prompted a change in tank venting protocols. The fix resulted in longer product stability, benefitting every downstream user. Open communication like this creates a loop that embeds quality across the production chain.

    Practical Usage—From Lab to Scaled Manufacture

    Chemists value (S)-(+)-1,3-Butanediol for its flexibility in synthetic design. Its two primary alcohol groups undergo high-yielding transformations with esters, ethers, and carbamates. Teams use it to open epoxides, generate chiral cyclobutanes, or build up protected derivatives for multistep organic synthesis. In our technical support dialogues, advanced users often probe for by-product profiles and kinetic data—details that make a real difference during scale-up, where side reactions multiply and small impurities can turn problematic.

    In flavor work, application chemists tap its faintly sweet, cooling note as a chiral building block or even as a functional humectant replacing propylene glycol. Cosmetic customers often experiment with its inclusion in lotions or serums that demand both stability and a gentle feel on the skin. Not all molecules offer this kind of crossover; most competitors in the glycol family lack both the stereo-defined structure and the low toxicity profile evidenced through repeated in vivo and in vitro safety testing.

    In our own pilot lab, we’ve collaborated with customers to build customized derivatives from the (S)-(+)-parent compound—ranging from acylated esters to oligoether chains. Because our teams control both the upstream and downstream chemistry, we help partners rapidly screen new modifications without lengthy qualification stages. This saves innovators significant lead time.

    Quality Challenges—Learning from Setbacks

    Not every batch has run flawlessly. Early on, unanticipated side reactions led to slightly yellow product. The fix was not a simple one—it emerged from a combination of better temperature control, catalyst screening, and tweaking our quenching protocols at the end of hydrogenation. Time spent on the production line, watching how small differences in stirring rate or heating uniformity impact quality, taught us that theory always meets its match in practice.

    On more than one occasion, incoming shipments of acetoacetic esters arrived out of spec—too much water, trace impurities, inconsistent container handling. Each event can cascade into headaches downstream. By working closely with our raw material suppliers—insisting on regular audits, conducting joint analyses, and even checking their storage environments—we raised our incoming material quality. For everyone downstream, these efforts mean product that performs batch after batch, reducing the odds of lost time or failed experiments.

    Internally, cross-training our team led to fewer production hiccups and more robust handoffs between shifts. Exposure to both equipment maintenance and analytical lab work helped everyone understand why every measurement—every small decision—impacts what finally arrives in our customers’ containers.

    What Reliability Looks Like in Practice

    Reliable manufacture means more than certificates. We see quality reflected in rapid customer support, transparent paperwork, and open invitations to audit both methods and facilities. Our best customers ask about process design, risk controls, and ongoing improvement efforts. As a direct maker, we’re accountable for every aspect—no outsourcing, no excuses. Factory leadership walks the floor daily, sitting in on pre-shipment tests and digging into every batch history before approving a lot for dispatch.

    Our lab teams support customer method development, providing not only standard purity and chiral content certificates but analytical spectra and impurity breakdowns tailored to specific project needs. By sharing this technical foundation, we empower end users to troubleshoot issues quickly or adapt our product to new applications.

    Environmental Choices—From Solvent Management to Emissions

    Efforts to reduce waste and emissions run through every aspect of our operation. Closed-loop solvent recycling programs now recapture and reuse over 85 percent of the THF and ethanol solvents involved in purification. Investments in energy-efficient reactors and real-time monitoring of vent emissions have helped trim overall greenhouse gas output year-on-year. Our on-site wastewater treatment plant scrubs outgoing water, keeping biological oxygen demand and chemical residues well within regulatory targets.

    Customers increasingly request data on our lifecycle impact. Supplying this information requires not only adherence to documentation, but also a willingness to adapt production scheduling, run pilots with greener raw materials, and report meaningful progress. In one recent upgrade, we replaced our high-energy distillation step with a fractionating column using low-pressure steam—reflecting both cost and resource savings.

    Looking Ahead—What Matters to Users

    The most important lesson from producing (S)-(+)-1,3-Butanediol is that consistency pays off—especially once research moves out of the lab and into scaled manufacturing. Every user wants predictability: in quality, delivery, and support. For years, we’ve prioritized face-to-face technical exchanges, responsiveness to challenging timelines, and continual investment in our plant and people. That experience, not just our certificates, forms the backbone of projects from first gram through multi-ton scale-up.

    As new chiral technologies and bio-based syntheses emerge, we’re prepared to adapt our processes to maintain both the purity and reliability chemists and formulators demand. Our team combines practical shop-floor know-how with the flexibility to address rapidly changing market and technical needs. The difference, as our customers often tell us, lies not only in the molecule, but in the hands and minds that make it. Through this lens, (S)-(+)-1,3-Butanediol isn't merely a chiral diol; for every innovation built on top of it, it's an opportunity to solve real-world problems side by side.