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(R)-(+)-1,2,4-Butanetriol

    • Product Name (R)-(+)-1,2,4-Butanetriol
    • Alias (R)-(+)-1,2,4-Butanetriol; (R)-Butane-1,2,4-triol
    • Einecs 214-490-0
    • 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
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    Specifications

    HS Code

    695128

    Product Name (R)-(+)-1,2,4-Butanetriol
    Cas Number 52907-81-6
    Molecular Formula C4H10O3
    Molecular Weight 106.12 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥98%
    Specific Rotation +18° to +22° (c=1, H2O)
    Boiling Point 285 °C (lit.)
    Melting Point 17-19 °C (lit.)
    Density 1.176 g/cm³ at 20 °C
    Solubility In Water Miscible
    Flash Point 154 °C
    Chirality R-enantiomer
    Synonyms (R)-1,2,4-Butanetriol; (R)-Butane-1,2,4-triol

    As an accredited (R)-(+)-1,2,4-Butanetriol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g amber glass bottle with secure cap, labeled “(R)-(+)-1,2,4-Butanetriol”, includes hazard symbols and CAS number.
    Shipping (R)-(+)-1,2,4-Butanetriol is shipped in securely sealed containers to prevent moisture and contamination. It should be handled as a chemical reagent and stored at room temperature away from strong oxidizing agents. Shipping complies with standard chemical transport regulations, ensuring proper labeling, documentation, and packaging for safe transit.
    Storage (R)-(+)-1,2,4-Butanetriol should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature or lower, and ensure that containers are properly labeled. Avoid prolonged exposure to air to prevent degradation.
    Application of (R)-(+)-1,2,4-Butanetriol

    Applications of (R)-(+)-1,2,4-Butanetriol in Industrial Manufacturing

    (R)-(+)-1,2,4-Butanetriol serves as an essential chiral building block in diverse chemical manufacturing sectors, supporting high-value synthesis pathways and precise quality standards across pharmaceutical, agrochemical, and specialty chemical industries. As a direct manufacturer, we ensure rigorous quality control and supply chain transparency to enable efficient downstream processing and compliance with demanding regulatory requirements.

    1. Antiretroviral Pharmaceutical Intermediate Synthesis

    Manufacturers of antiretroviral active pharmaceutical ingredients (APIs), including Efavirenz and other non-nucleoside reverse transcriptase inhibitors (NNRTIs), rely on (R)-(+)-1,2,4-Butanetriol as a key chiral precursor. This intermediate enables the construction of complex molecular backbones and improved enantiomeric purity for final APIs. Downstream API producers introduce the raw material at the asymmetric synthesis stage, controlling enantiomer ratios and meeting global pharmacopoeia specifications throughout multistep synthesis campaigns.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP): FDA 21 CFR Part 210/211
    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.), United States Pharmacopeia (USP)
    • DMF (Drug Master File) referencing and traceability requirements for intermediates

    Typical usage ratio

    • 10–25% w/w relative to chiral API precursor batch mass; adjusted based on target yield, route-specific stoichiometry, and required optical purity

    Downstream process integration

    • Charged during the enantioselective synthesis step preceding API core assembly
    • Direct input to C–C and C–N bond-forming reactions for high-value intermediate formation
    • Purity and stereochemistry validated at the reaction step before final crystallization and formulation

    Final product types

    • Efavirenz tablets/capsules
    • Chiral non-nucleoside antiretroviral API bulk substances
    • Second-generation NNRTI intermediates and clinical trial materials

    2. Statin API Chiral Starter Material

    In cholesterol-lowering statin drug synthesis, butanetriol provides a specialized enantiomeric fragment for constructing side chains with high stereochemical purity. Manufacturers incorporate this material at the chiral pool stage, especially in the assembly of intermediates for Atorvastatin and Rosuvastatin, meeting compendial and excipient residue guidelines and facilitating process optimization for multi-ton batch processing.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP): US FDA, EMA, and CFDA harmonized guidance
    • USP-NF/Ph. Eur. monograph standards for API intermediates
    • ICH Q3A/B: Impurity and residual solvent limits
    • Synthetic process residue directives set by each pharma client’s quality agreement

    Typical usage ratio

    • 15–28% of total input mass at the chiral building block stage, fine-tuned according to final statin type and process yield requirements

    Downstream process integration

    • Used in early functionalization and chiral side chain formation (e.g., pre-lactonization)
    • Enters amidation or alkylation reactions specific to target statin APIs
    • Batch QC measures at intermediate and endpoint per cGMP

    Final product types

    • Atorvastatin calcium API
    • Rosuvastatin calcium API
    • Intermediates for other patent-expired statins targeting regulated markets

    3. Agrochemical Selective Herbicide Synthesis

    Producers of specific chiral herbicides leverage (R)-(+)-1,2,4-Butanetriol during the synthesis of pyridinecarboxylic acid derivatives and related products where enantioselectivity critically affects field efficacy and regulatory acceptance. Integration focuses on reduced byproduct formation and process scalability for later-stage oxidative coupling and esterification reactions.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015-certified production environments
    • REACH (EC) No 1907/2006: Registration, Evaluation, Authorization and Restriction of Chemicals
    • Local Ministry of Agriculture approvals (e.g., US EPA PRIA, Chinese MOA)

    Typical usage ratio

    • 8–18% by weight of precursors in the chiral forming step; altered per process efficiency and crop spectrum target

    Downstream process integration

    • Input at asymmetric synthesis phase to obtain the required herbicide enantiomer
    • Directly linked to yield and selectivity during main active ingredient construction
    • Process optimization to minimize racemization and maximize active isomer ratio

    Final product types

    • Pyridine-based selective herbicides
    • Enantio-enriched post-emergence weed control agents
    • Pre-mixed or single formulation herbicidal concentrates

    4. Energetic Materials Synthesis

    Specialty explosives manufacturers employ this compound as a precursor for the synthesis of 1,2,4-butanetriol trinitrate (BTTN), an advanced energetic plasticizer and propellant component. Introduced in tightly controlled environments, precise usage ensures compatibility with downstream nitration steps and compliance with worldwide energetics handling regulations for civil and defense applications.

    Industry compliance standards

    • UN Recommendations on the Transport of Dangerous Goods (Model Regulations, Orange Book)
    • US ATF explosives manufacturing and storage codes (ATF Ruling 2007-1)
    • Military production standards (e.g., MIL-DTL-46745A for plasticizers)
    • ISO 9001:2015 for quality management in explosives production

    Typical usage ratio

    • Used at 25–40% of batch mass in the pre-nitration phase, determined by targeted BTTN yield and nitrate content

    Downstream process integration

    • Entry point at the controlled reaction vessel for nitric/sulfuric acid nitration
    • Batchwise addition to manage exothermicity and maximize product conversion to BTTN
    • Purity and low moisture critical for safe integration into propellant paste

    Final product types

    • BTTN energetic plasticizer
    • Composite artillery propellants
    • Rocket and missile solid propellant blends

    5. Advanced Polymer Synthesis for Medical Devices

    Suppliers of biomedical-grade biodegradable polyesters use butanetriol as a triol monomer for initiating ring-opening polymerizations. By incorporating the triol at controlled ratios, polymers such as poly(butylene succinate-co-butylene triol) and derivatives achieve specific degradation profiles and mechanical strength, enabling use in surgical sutures, scaffolds, and controlled drug-release matrices. All integration aligns with medical device regulations and end-use sterilization pathways.

    Industry compliance standards

    • ISO 13485: Medical devices – Quality management systems
    • USP Class VI Biocompatibility Testing
    • European Medical Device Regulation (MDR) 2017/745
    • ISO 10993: Biological evaluation of medical devices

    Typical usage ratio

    • 5–15% triol content in catalyst-initiated polyester polymerizations, varied per required hydrolysis rate and polymer architecture

    Downstream process integration

    • Direct introduction during polyester chain initiation step
    • Monomer pre-conditioning, followed by batch or continuous ring-opening polymerization
    • In-process molecular weight control via triol input adjustment

    Final product types

    • Biodegradable surgical sutures
    • Implantable drug delivery matrices
    • Bioresorbable tissue scaffolding materials
    Free Quote

    Competitive (R)-(+)-1,2,4-Butanetriol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing (R)-(+)-1,2,4-Butanetriol: Production Insight and Practical Guidance

    Our Perspective on (R)-(+)-1,2,4-Butanetriol

    We have been producing (R)-(+)-1,2,4-Butanetriol at our chemical facility for years, refining both the process and the final product to meet strict performance and quality expectations from our partners in fine chemicals, pharma, and specialty intermediates. This compound, recognized for its chirality and selectivity, stands out not only because of its molecular design but for the consistency and care required in its synthesis.

    Product Overview and Manufacturing Realities

    The (R) enantiomer of 1,2,4-Butanetriol, with its three hydroxyl groups, takes precision to prepare. Our process follows a multi-step synthetic pathway that includes careful protection and deprotection phases—steps we fine-tune to maintain optical purity and yield. Our equipment runs under controlled temperature and atmosphere, not only to secure high conversion rates but also to limit by-product formation. Each batch passes through chromatography and advanced analytical confirmation, usually HPLC with a chiral stationary phase, as we aim to deliver a material that reliably meets over 99% enantiomeric excess.

    In our years as manufacturers, we have seen the challenges in making optically pure products, especially at industrial scale. Side reactions threaten selectivity. Interim products need tight handling and monitoring. Purity margins remain slim, which explains why many companies struggle to scale chiral processes from kilo to tonne levels without sacrificing quality. Our facility’s investment in quality management and practical training for operators make a difference in delivering a reproducible material.

    Typical Specifications from Real Plant Lots

    Commercial (R)-(+)-1,2,4-Butanetriol emerges as a clear to slightly yellow viscous liquid. Moisture content, absence of residual solvents, and color are points of concern in actual plant operation, much more than is often acknowledged. Left unmanaged, even slight contamination from process water or atmospheric oxygen lowers stability. Our logistics crew works in tandem with production to monitor every drum—you will not find unexplained haze, crystallization, or odor when using our product fresh from shipment.

    Standard output keeps impurity levels—by GC and chiral HPLC—far below 0.5%. Those using this chemical for high-value active pharmaceutical intermediates rely on these practices. Since specification is not simply a number but a result attained by strict cleaning, filtration, and in-process control, we know firsthand that specification needs to be earned batch after batch.

    End Uses: Applied Knowledge

    (R)-(+)-1,2,4-Butanetriol serves as a starting material in chiral pharmaceutical synthesis, specialty polymer modifiers, and some selective herbicide building blocks. Most demand comes from companies engaged in fine synthesis—where a single stereocenter in a precursor determines efficacy in the final active molecule. One such use: synthesizing chiral amino alcohol intermediates—where optical configuration directly influences pharmacological profile.

    Raw (R)-(+)-1,2,4-Butanetriol often goes into ring-forming reactions for lactones and oxetane derivatives. In our experience, users working on these routes focus on batch-to-batch consistency and the impurity profile. Any fluctuation in water or minor diol content impacts further steps. Synthetic flexibility—whether the butanetriol goes into Mitsunobu-type substitutions, selective oxidations, or resolution schemes—often stands or falls based not only on chemical structure but on real batch history and the presence or absence of micro-level contaminants.

    Some customers in the advanced materials field claim improved flexibility and resistance properties when incorporating this enantiomer into their polymer structure. Chemists seek our input about processing conditions, anticipating that hydroxy group protection or downstream acylation may be sensitive to slight variations in starting quality. Knowledge of what works rests not in technical sheets, but experience accumulated over hundreds of syntheses.

    What Sets (R)-(+)-1,2,4-Butanetriol Apart

    Comparing (R)-(+)-1,2,4-Butanetriol with its racemic version or the (S) enantiomer reveals how much stereochemistry shapes chemical behavior. Racemic butanetriol comes from a simpler process—for example by reduction of succinonitrile. This makes racemate much less costly, but it lacks the required chiral purity for use in advanced APIs or custom chiral ligands.

    Some companies pursue the (S) configuration for specific end molecules, which necessitates another catalytic or biocatalytic approach. In contrast, our (R)-(+)-1,2,4-butanetriol results from an enantioselective process based on asymmetric reduction and chiral auxiliaries. The supply chain runs longer and the chemistry needs closer attention, which leads to a measurable difference in batch reproducibility and performance in downstream reactions.

    In laboratory tests, (R)-(+)-1,2,4-Butanetriol delivers different results in optical rotation, enantioselective transformations, and biological evaluation compared to the racemate or (S)-enantiomer. We have tracked different impurity carryover and solubility in polar and nonpolar solvents, leading to better yields in epoxidation and select hydrogenation steps.

    Market Realities: Sourcing and Cost Pressures

    Sourcing any enantiopure polyol at commercial volumes always poses trade-offs between cost control and supply security. We have observed that spot purchases of racemic butanetriol usually satisfy commodity requirements, such as for bulk intermediates in industrial production. For enantioselective pharmaceutical or research work, end-users cannot trust generic, uncharacterized product. The risk of cross-contamination, inconsistent chiral purity, or trace metal impurities leads customers to source from proven manufacturers running validated, GMP-aligned processes.

    Customers often mention long lead times and tight logistics with (R)-(+)-1,2,4-Butanetriol. As a direct producer, we manage production runs with inventory scheduling, buffer stocks, and direct communications between our plant logistics and buyers’ planning teams. By holding intermediate inventories and reacting fast to demand changes, we reduce stockouts and minimize disruptions—especially during global raw material shortages or transportation bottlenecks.

    Quality Factors from the Factory Floor

    Some users underestimate the influence of micro-impurities and residual solvents found in commercial butanetriol. We have learned—sometimes the hard way—that a single substandard batch can derail a customer’s development or create rework waste downstream. Analytical monitoring must start with every batch, not just final product: careful in-process sampling, chiral HPLC for enantiomeric purity, GC-MS for volatile components, water determination by Karl Fischer, and trace metals screening. Customers putting this molecule into GMP-regulated facilities or injectable intermediates may even request additional TGA, DSC, or microbiological assays, which our site can produce when required.

    Maintaining high selectivity in the primary asymmetric reduction step remains technically demanding, especially at higher input volumes. Catalyst fouling, temperature swings, and atmospheric leaks hurt selectivity. Each reactor run needs skill—team members with deep process memory note anomalies others miss. We logged one summer where minor changes in local water pH started showing up as shifts in product water content and affected the shelf-life of stored material. Real production knowledge means picking up on these details.

    Handling and Storage Experience

    Storing (R)-(+)-1,2,4-Butanetriol successfully requires both clean container systems and careful environmental control. Tanks, drums, and IBCs used at our site are flushed and dried vigorously to avoid contamination. Product contact surfaces—from reactors to hoses—are validated for compatibility. Temperature control during shipping preserves low volatility and color stability, especially for international orders subject to variable climates. Our logistics staff treat storage as an extension of process control: no shortcuts in cleaning, labeling, or container sealing.

    Downstream users always find better results with freshly opened, quality-sealed samples. Our technical advice for those storing partial drums: purge air headspace with inert gas, keep containers tightly sealed, and transfer under dry conditions. Failing to do so speeds up oxidation and causes a build-up of colored or foul-smelling degradation products, particularly if the product is left unrefrigerated for extended periods—results we have observed directly in returned drums stored in uncontrolled conditions.

    Addressing Application Challenges and Offering Solutions

    Feedback from our application support team helped us understand where (R)-(+)-1,2,4-Butanetriol fits—or fails—in customer projects. Pure physical properties are often just a starting point. Downstream synthetic transformations—such as acetal formation, selective tosylation, or enzymatic resolution—respond to both the chemical profile and the remaining impurity load. Problems typically show up as incomplete conversion, loss of optical activity, or unexpected side-reactions.

    Our technical group helps users troubleshoot: product not reacting as it should often points to minor process contamination rather than an outright structural fault. Recent improvements include tailored packaging and extra drying steps for projects requiring maximum hydrolytic stability. We also collaborate on pilot lots to match custom process needs—adjusting storage, filtration, or even reprocessing batches to maintain tight specifications.

    Users developing next-generation drugs place high value on consistent, traceable supply. Many projects begin with gram-scale evaluations and grow into pilot or commercial campaigns. We foster stability by offering batch reserves, repeat-sample authentication, and full traceability from starting material source through to final packaging. By holding to the same validated process between lots, we help customers maintain reproducibility through the full scale-up journey.

    Environment, Safety, and Compliance Knowledge

    We carry direct experience with the environmental and safety implications of producing and transporting (R)-(+)-1,2,4-Butanetriol. Waste minimization starts on the plant floor. Side-stream handling, solvent recovery, and filtration byproducts get tight control to comply with evolving local and international waste norms—with robust documentation for customer audits.

    Safety regarding butanetriol centers on proper handling of polyol residues, avoiding inadvertent mixing with oxidizers, and maintaining clean workspace environments. Our team trains operators on the specifics of hot-stage cleaning, spill response, and periodic equipment checks. Emergency planning—run through frequent drills—goes beyond compliance to practical readiness, as real incidents stem from daily process operations much more often than extraordinary events.

    Our commitment toward compliance extends to documentation. Full batch records, analytical data files, and shipment traceability allow fast incident review and continuous improvement. We offer technical files tailored for customer regulatory submissions, including impurity profiles, shelf life support, and methods validation. Input from real regulatory audits guides our internal upgrades; we find that customer trust builds fastest when our onsite procedures stand up to independent scrutiny.

    Transparency and Building Long-Term Partnerships

    Supplying (R)-(+)-1,2,4-Butanetriol goes beyond a single transaction. Long-term buyers value communication, production transparency, and practical support. Being an actual producer means sharing detailed knowledge of batch histories, analytical support, and process changes. We regularly host site visits for trusted clients, opening our labs and production areas for firsthand inspection.

    Our experience shows that close partnerships—built on regular dialogue about forecasts, asset utilization, and technical issues—reduce risk for both supplier and end-user. We help customers plan inventory levels and process adjustments, and we have built priority reserve systems for those facing critical project timelines. In crisis periods—such as raw material shortages or urgent recalls—we work shoulder to shoulder with buyers, troubleshooting new supply routes or process workarounds. That spirit of cooperation, not just process capability, lies behind our success in keeping quality chiral building blocks available where and when they matter most.

    Continuous Improvement and Future Directions

    For those producing fine chemicals, every product presents opportunities for improvement. We constantly review process performance and feedback from real-world use of (R)-(+)-1,2,4-Butanetriol to find new ways to enhance quality and reliability. This spans from sourcing more consistent raw material substrates, optimizing purification steps, or further training our plant operators based on observed issues and changing regulations.

    Recent internal process tweaks—such as improved catalyst reactivation cycles and tighter moisture control—cut down on production waste and further raise the bar for product purity. We openly incorporate suggestions from experienced synthetic chemists using our product in complex multi-step syntheses, adapting our process to meet those evolving needs. Our regular technology upgrades sustain high repeatability, keeping us at the forefront of chiral intermediate production, year after year.

    As the world’s demand for complex chirally pure materials pushes higher, our responsibility grows along with it. Through close adherence to good manufacturing practices, ongoing site investment, and direct client experience, we expect to keep (R)-(+)-1,2,4-Butanetriol available at quality levels required for tomorrow’s advanced applications.

    Final Reflections from a Manufacturer’s View

    We see every lot of (R)-(+)-1,2,4-Butanetriol not as a mere commodity, but as the result of thousands of critical process choices—from raw material selection through storage and final shipment. As a chemical manufacturer, we have learned to treat each production run as a living project with real stakes for our partners in the market. Our role remains to deliver trusted, high-quality material, backed by transparency, cooperation, and a commitment to continual learning.