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1,2,3-Butanetriol

    • Product Name 1,2,3-Butanetriol
    • Alias 1,2,3-Trihydroxybutane
    • Einecs 203-468-7
    • 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
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    Specifications

    HS Code

    606797

    Cas Number 528-44-9
    Iupac Name Butane-1,2,3-triol
    Molecular Formula C4H10O3
    Molar Mass 106.12 g/mol
    Appearance Colorless viscous liquid
    Density 1.191 g/cm³ (at 20°C)
    Melting Point −50°C
    Boiling Point 285°C
    Solubility In Water Miscible
    Flash Point 157°C
    Refractive Index 1.478 (at 20°C)
    Pubchem Cid 31218

    As an accredited 1,2,3-Butanetriol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,2,3-Butanetriol is packaged in a 500 mL amber glass bottle with a secure screw cap and hazard labeling.
    Shipping **1,2,3-Butanetriol** is typically shipped in tightly sealed containers, such as drums or bottles, made from materials compatible with organic chemicals. It should be stored and transported in cool, dry, well-ventilated areas, away from heat and sources of ignition. Proper labeling and documentation in compliance with regulations are essential.
    Storage 1,2,3-Butanetriol should be stored in a tightly closed container in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizers. It should be protected from moisture and direct sunlight. Proper labeling is essential, and secondary containment is recommended to prevent spills or leaks. Use appropriate chemical storage cabinets if available.
    Application of 1,2,3-Butanetriol

    Purity 99%: 1,2,3-Butanetriol with purity 99% is used in energetic materials synthesis, where it ensures consistent reaction performance and minimizes impurities.

    Viscosity grade low: 1,2,3-Butanetriol with low viscosity grade is used in coatings formulation, where it allows superior spreading and uniform film formation.

    Molecular weight 92.09 g/mol: 1,2,3-Butanetriol with a molecular weight of 92.09 g/mol is used in pharmaceutical intermediates manufacturing, where it provides reliable molecular incorporation and batch-to-batch consistency.

    Melting point 18°C: 1,2,3-Butanetriol with a melting point of 18°C is used in polymer plasticizer applications, where it imparts flexibility and low-temperature processability.

    Stability temperature up to 200°C: 1,2,3-Butanetriol stable up to 200°C is used in resin production, where it maintains molecular integrity under high-temperature processing.

    Water content ≤0.1%: 1,2,3-Butanetriol with water content ≤0.1% is used in explosives formulation, where it reduces the risk of undesirable side reactions and improves product safety.

    Colorless liquid form: 1,2,3-Butanetriol in colorless liquid form is used in cosmetic ingredient blending, where it provides aesthetic clarity and minimizes discoloration in end products.

    Low aldehyde content: 1,2,3-Butanetriol with low aldehyde content is used in adhesives manufacturing, where it enhances shelf life and reduces off-odors.

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    Certification & Compliance
    More Introduction

    1,2,3-Butanetriol: Rethinking Versatility in Chemical Industry Applications

    A Closer Look at a Game-Changer Chemical

    Few chemicals draw such diverse interest as 1,2,3-Butanetriol. Over the years, this polyol has become more than a mere laboratory curiosity, turning up in a surprising range of industries. Produced with a formula of C4H10O3 and a CAS registry number of 528-44-9, its value rises from unique structural features. What makes it especially practical is the presence of three hydroxyl groups attached to a four-carbon backbone. As anyone who has spent time comparing polyols knows, that configuration brings out a set of properties hard to replicate with its more familiar cousin, glycerol, or other isomers like 1,2,4-butanetriol.

    My own path in industrial chemistry often led me into the world of functional intermediates. There, I kept stumbling on 1,2,3-Butanetriol at meeting tables and in chemical request sheets. It stands apart because the triol arrangement influences reactivity and solubility, driving demand in formulations from explosives to resins. Quite a shift from the days when only glycerol reigned.

    Key Specifications Worth Noting

    Not all 1,2,3-Butanetriol on the market is made alike. Purity levels can top 98%, minimizing side reactions for sensitive applications. In terms of physical properties, this triol generally appears as a colorless to slightly yellowish viscous liquid, with a slight sweet odor. The melting point hovers close to 16–17 °C, while boiling is around 285–290 °C at standard pressure. Water solubility comes easily, thanks to those three hydroxyls crowding together. Viscosity, higher than diols, serves as an indicator of its sticky consistency.

    Density usually checks in at about 1.17 g/cm3, giving clear handling expectations for process chemists. The real performance difference shines when you test thermal stability: compared to more fragile alcohols, this triol resists breakdown under moderate heat, supporting robust synthesis processes.

    Finding Its Place: Usage Across Industries

    As a nitration enthusiast might point out, the striking feature of 1,2,3-Butanetriol lies in its ability to produce butanetriol trinitrate (BTTN). This energetic material, popular as a propellant plasticizer, turned the triol from benchwork into mainstream explosives production. BTTN’s lower freezing point compared to nitroglycerin adds flexibility for military and aerospace needs. This single use already changed the chemical’s reputation for decades.

    Stepping back from explosives, performance in polymer synthesis also stands out. 1,2,3-Butanetriol acts as a monomer or building block in making polyesters, polyurethanes, and specialty resins. The result? Products with improved flexibility, solvent resistance, and lasting durability. From my own work, I have noticed formulators appreciate how this triol imparts a degree of plasticization or crosslinking unmatched by basic glycols.

    On the research frontier, there are early notes suggesting pharmaceutical opportunities. With careful synthetic tweaks, the molecule can serve as a chiral precursor, potentially spinning off active pharmaceutical ingredients—especially those where the triol backbone contributes to bioactivity or metabolic stability. The scale is still experimental, but the seed of industrial adoption is there.

    What Sets 1,2,3-Butanetriol Apart?

    Choosing which polyol to use depends on subtle differences in physical and chemical properties. In the case of 1,2,3-Butanetriol, those differences carry real impact. Unlike glycerol, which offers a three-carbon backbone, this four-carbon triol opens up new reactivity patterns. The extra carbon boosts thermal and chemical toughness and shifts solubility equations, often resulting in better compatibility with hydrophobic chains in complex polymer matrices.

    In contrast with isomeric partners like 1,2,4-butanetriol, 1,2,3-Butanetriol’s configuration alters the hydrogen bonding map. You see this in clearer, more distinct phase separation when mixing with various solvents or in enhanced stability for esters derived from it. Process chemists exploit these subtle differences every day, especially in fine-tuning coatings, adhesives, or plasticizer blends.

    Environmental and Human Safety Considerations

    Every responsible manufacturer and user must take stock of safety concerns. 1,2,3-Butanetriol, though less volatile than many alcohols, still calls for caution in storage and handling. Viscous liquids can be tempting to underestimate, but this polyol deserves the same respect as any lab-grade polyhydric alcohol. Its derivatives, especially explosive esters, require much stricter controls.

    Waste streams containing 1,2,3-Butanetriol, though biodegradable through aerobic pathways, must be managed thoughtfully. In my own site visits, wastewater with high organic loads always raises the specter of regulatory scrutiny and real community impact. Safe containment, reuse, or responsible incineration matter for any high-volume plant. I have seen the difference between well-managed drainage and the costly headaches that follow neglect.

    From a toxicity perspective, few acute health risks turn up in the literature, yet protocols from Europe, North America, and Asia all recommend gloves, eye protection, and proper ventilation. Accidents and chronic exposure can never be ruled out, so experience tells me it pays to keep safety sheets close and run regular hazard checks. In the right hands, this triol supports innovation instead of headaches.

    Why Engineers Reach for This Triol

    Deciding between 1,2,3-Butanetriol and alternatives like glycerol, ethylene glycol, or trimethylolpropane is rarely a question of habit. For specialty applications—like low-freezing explosive formulations, high-performance coatings, or resilient foams—this triol delivers combinations of reactivity and mechanical properties not found in other polyols. One example stands out from a project I observed: custom polyurethane foams, needed for extreme weather applications, required a non-glycerol triol to maintain performance. Here, 1,2,3-Butanetriol made the difference between success and design fatigue.

    Research supports this hands-on wisdom. Articles in journals from Applied Polymer Science to Journal of Energetic Materials highlight its ability to improve esterification yields, form better crosslinked networks, or provide safer alternatives for explosives plasticization. The literature echoes what I found firsthand—when a team needs a triol for advanced formulations, they look beyond generic solutions.

    Potential Drawbacks and Real-World Solutions

    No product offers perfection. Sourcing reliable and affordable supplies of 1,2,3-Butanetriol can be challenging. Production involves chemical routes like catalytic reduction of tartaric acid derivatives or microbial fermentation, each bringing different purity profiles and costs. In years of working with sourcing teams, I noticed batch-to-batch consistency mattered especially in high-precision fields. Investing in supplier relationships and regular quality audits goes a long way.

    Handling viscosity and storage are manageable but demand careful attention. Tanks and transfer lines clog more readily than with lighter polycols. It surprised some junior operators how fast a poorly heated transfer line could seize up during winter. Simple solutions—such as selecting robust pumping systems and insulating storage—ensure steady operation.

    Environmental compliance hits hard if chemical waste streams cross regulatory boundaries. Wastewater treatment technology now adapts to catch and break down organic loads efficiently. On a positive note, emerging bio-based production routes show signs of reducing unwanted byproducts, creating the basis for greener and more sustainable butanetriol in the near future.

    Innovation at the Crossroads

    The arrival of 1,2,3-Butanetriol on the specialty chemicals stage changed the sorts of problems chemists could solve. Flexible enough for energetic materials, resilient enough for polymers, and just quirky enough to encourage creative formulations, this triol brings value in both established and experimental sectors.

    In the pharmaceutical research community, the unique stereochemistry invites chemists to design next-generation chiral drugs, glycosylated compounds, and hydrophilic coatings. In coatings R&D, the alcohol’s branching enables novel crosslink densities, letting formulators push past old durability barriers.

    These innovation stories echo in internal company reports, new patents, and lab notes that rarely make it to the public. Even on a routine production line, the chance to tune formulation properties by swapping to this less-common triol meant sudden leaps in product quality. My own team celebrated when stubborn resin mixtures stopped separating in the can after an ingredient switch. Details like these build real trust and confidence over time.

    The Market Moves Forward

    Markets for 1,2,3-Butanetriol ebb and flow with broader trends in explosives, advanced composites, and green chemistry. Demand spikes when governments ramp up aerospace or defense spending. At the same time, consumer trends toward durable, flexible, and safer plastics in electronics and automotive parts propel quiet but steady demand.

    Sustainability arguments gain traction as well. Where older production methods relied on fossil-based starting materials, new biotechnological approaches are opening paths to renewably sourced butanetriol. Process engineers now keep an eye on fermentation yields, purification techniques, and downstream optimization, trying to improve green metrics while holding onto reliability and price point. In technical meetings, I often hear concern about cradle-to-grave profiles, especially when designing next-generation materials for regulated markets. A shift to green chemistry practices—like using engineered micro-organisms or biomass waste streams—ushers in a future where life cycle assessments become part of standard product evaluations.

    Room for Improvement and the Road Ahead

    Looking at the full picture, companies and regulators seek further studies on environmental fate, long-term toxicity, and safe scaling. There’s always a chance for improvement in process control and waste reduction. Close monitoring and partnership with academic labs can catch emerging risks early and help prevent the sorts of health and safety incidents that haunt industrial towns and headlines.

    In regulatory circles, cross-border standards slowly align. The industry works to stay ahead of performance and documentation curves, keeping in step with new environmental and consumer safety expectations. My advice to any new entrant in the market—build alliances with reputable producers, support transparent audits, and keep technical staff engaged with the latest regulatory updates. Long-term investments in safety and compliance pay dividends that one-off cost savings never match.

    Experiences from the Field

    As a consultant, walking through plants and labs across continents, I hear similar stories repeated in different accents and languages. Production teams who finally nailed a tricky polymer thanks to 1,2,3-Butanetriol’s unique reactivity. Explosive specialists who cut their accident rates after switching to lower-freezing plasticizers. Wastewater engineers grateful for a compound that breaks down more easily than older synthetic alcohols. These case studies point to the nuanced, sometimes unexpected advantages of this versatile triol.

    The common thread becomes clear—in each context, people make the most progress by connecting technical knowledge with hands-on experience. Data matters, regulations shape choices, but the stories that make a chemical indispensable usually come from those quiet troubleshooting moments on the factory floor. When that happens, a product like 1,2,3-Butanetriol proves its worth not just on paper, but in everyday results.

    Building on Trust and Science

    People sometimes underestimate the value of transparency in specialty chemicals. In an age where supply chain disruptions can halt production and public scrutiny drives decisions, each link in the chain matters. That includes not only purity and consistency, but ethical sourcing and accurate product information. Companies choosing to use 1,2,3-Butanetriol have good reason to favor suppliers who share testing data, audit results, and compliance certificates. It’s easier to solve problems, improve formulations, and win regulatory approval when facts are on the table from the start.

    Working closely with teams that prize open communication, I have seen smoother collaborations and fewer surprises. When a contaminant cropped up in a resin batch, early disclosure and fast traceability turned a potential recall into a learning moment, not a crisis.

    The Role of Professional Knowledge in Product Success

    Technical teams who master the handling and integration of 1,2,3-Butanetriol stand out in a marketplace crowded with alternatives. Practical training, from lab handling to full-scale manufacturing, makes the difference between routine operation and repeated troubleshooting. Regular investment in training and equipment calibration cuts down on rework and boosts innovation success rates.

    The industry is moving toward smarter, more connected production lines. Digital controls and real-time analysis tools now help monitor purity, viscosity, and batch yield, preventing many downstream headaches. Experience from integrating these systems reveals that even small improvements in monitoring have outsized effects on efficiency and quality.

    Connecting Value to Everyday Impact

    Chemicals like 1,2,3-Butanetriol often seem distant from daily life, but their influence stretches further than most realize. Performance gains in car interiors, safer propulsion in rockets, longer-lasting building materials—all flow from quiet advances in chemical options like this triol. I remain convinced that learning from real-world use, not just spreadsheets and supply lists, gives the most honest insight into value.

    For those charting the future, 1,2,3-Butanetriol isn’t just a product code or inventory item. It is a story of gradual improvement, persistence through technical setbacks, and the ability to adapt as new needs arise. After all these years, it is clear to me that its greatest asset comes from being just distinctive enough to keep surprising even seasoned engineers and chemists.