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(R)-(+)-2-Tetrahydrofuroic Acid

    • Product Name (R)-(+)-2-Tetrahydrofuroic Acid
    • Alias (R)-(+)-Tetrahydro-2-furoic acid
    • Einecs 689-545-4
    • 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

    612487

    Product Name (R)-(+)-2-Tetrahydrofuroic Acid
    Cas Number 17668-48-5
    Molecular Formula C5H8O3
    Molecular Weight 116.12
    Appearance White to off-white solid
    Optical Rotation +24.0° to +28.0° (c=1, H2O)
    Melting Point 41-44°C
    Purity ≥98%
    Boiling Point 247-249°C at 760 mmHg
    Solubility Soluble in water, methanol, and ethanol

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

    Packing & Storage
    Packing White, sealed plastic bottle containing 25 grams of (R)-(+)-2-Tetrahydrofuroic Acid, labeled with product details, safety, and handling instructions.
    Shipping (R)-(+)-2-Tetrahydrofuroic Acid is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is packaged according to standard chemical safety regulations, with appropriate labeling and cushioning. Ensure storage in a cool, dry place during transit. Handle with care as per Material Safety Data Sheet (MSDS) recommendations.
    Storage (R)-(+)-2-Tetrahydrofuroic Acid should be stored in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use. Store at room temperature and protect from excessive heat and moisture. Ensure proper labeling and avoid prolonged exposure to air to prevent degradation or contamination.
    Application of (R)-(+)-2-Tetrahydrofuroic Acid

    Applications of (R)-(+)-2-Tetrahydrofuroic Acid in Industrial Manufacturing

    (R)-(+)-2-Tetrahydrofuroic Acid serves as a valuable enantiomerically pure intermediate for a range of advanced industrial production streams, supporting processes that demand precision stereochemistry. As the manufacturer, we supply this material with specific control on enantiomeric excess to ensure consistency and traceability in every downstream application. Our product integrates into specialty synthesis for pharmaceuticals and fine chemicals, agrochemical intermediates, peptide modification, and high performance polymer production, each requiring clear process controls and compliance with industry standards. The following sections detail real-world use cases across key segments.

    1. Chiral Building Block for Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical manufacturers employ (R)-(+)-2-Tetrahydrofuroic Acid as a core chiral fragment during the synthesis of stereospecific drug substances, particularly for beta-lactam and furan-based scaffold molecules. The requirement for absolute configuration mandates precise input at established stages of total synthesis, with extensive tracking under regulated environments.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice (GMP) for APIs
    • USP/NF: United States Pharmacopeia
    • EP: European Pharmacopoeia
    • FDA 21 CFR Part 210/211 (for US markets)

    Typical usage ratio

    • 0.05–0.25 molar equivalents relative to core scaffold precursors, adjusted based on desired final product yield and stereochemical control

    Downstream process integration

    • Introduced during chiral auxiliary assembly or in asymmetric catalytic reactions within multi-step API synthesis
    • Monitored via in-process chiral HPLC analysis to verify enantiomeric purity

    Final product types

    • Chiral beta-lactam antibiotics
    • Pyrrolidine and tetrahydrofuran-based pharmaceutical actives
    • Enantiopure building blocks for clinical candidate libraries

    2. Intermediate in Agrochemical Synthesis

    Producers of selective crop protection agents use this acid to construct molecular frameworks with specific spatial orientation, supporting the assembly of enantioselective fungicides and insecticides. Its inclusion at key synthetic steps assures the correct three-dimensional geometry essential for biological activity and regulatory authorization in food crop applications.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice
    • FAO/WHO Specifications for Pesticides
    • EPA 40 CFR Parts 150–189: Pesticide Programs
    • ISO 17025: Quality management for testing and calibration labs

    Typical usage ratio

    • 10–30% w/w relative to target intermediate mass in the chiral coupling step; modified as per crop application toxicological dossier

    Downstream process integration

    • Undergoes direct coupling or cyclization, typically after halogenation or protection/deprotection steps, with analytical confirmation of residual chiral impurity below regulatory thresholds

    Final product types

    • Stereospecific fungicides
    • Enantio-enriched insecticidal actives
    • Chiral intermediates used in herbicide synthesis pipelines

    3. Monomer Precursor for Chiral Polyesters and Polyamides

    Polymer manufacturers turn to (R)-(+)-2-Tetrahydrofuroic Acid as a monomer precursor for engineering specialty plastics with designed chiral properties. The acid's configuration impacts polymer tacticity, delivering materials with improved optical activity or enantioselective separation functions in downstream membrane or fiber applications.

    Industry compliance standards

    • ISO 9001: Quality management systems for polymer production
    • REACH Regulation (EC) No 1907/2006 for registration and safe use
    • FDA 21 CFR 177 (for food contact polymers, where relevant)
    • ASTM D4603 & D5336 for polymer characterization and resin properties

    Typical usage ratio

    • 8–15 mol% as a comonomer unit, with optimization based on targeted chiral property in the finished polymer

    Downstream process integration

    • Condensation polymerization or ring-opening polymerization after activation (e.g., conversion to acid chloride or ester derivative)
    • Batch QC validation for enantiomeric distribution in polymer matrix

    Final product types

    • Chiral selective membranes
    • Functional polyesters for biomedical applications
    • Advanced polyamides for enantioselective chromatography

    4. Custom Amino Acid and Peptide Synthesis

    Providers of synthetic peptides for pharmaceuticals and biochemical research deploy (R)-(+)-2-Tetrahydrofuroic Acid to install chiral motifs at side chains or terminal ends, enhancing peptide stability or biological activity. The acid functions as the point of introduction for furan-based chirality under tightly controlled peptide assembly protocols.

    Industry compliance standards

    • GMP for Peptide APIs: ICH Q11/Q7, EudraLex Volume 4
    • USP General Chapter <1047> for peptide characterization
    • ISO 13485 (for custom peptides with medical device use)
    • FDA 21 CFR 210/211/820 based on application

    Typical usage ratio

    • 1–5 mol% per amino acid coupling, varied by peptide sequence and desired modification density

    Downstream process integration

    • Integrated into solid-phase or solution-phase peptide synthesis after conventional amino acid assembly
    • Subject to final product purification via preparative HPLC to achieve regulatory-grade enantiopurity

    Final product types

    • Custom-modified peptides for preclinical research
    • Pharmaceutical peptide leads featuring furan rings
    • Chiral peptide reference standards for analytical method development

    5. Synthesis of Fine Chemicals for Flavors and Fragrances

    Manufacturers specializing in fine flavor and fragrance intermediates incorporate this acid to introduce controlled stereochemistry into high-value aroma compounds where the sensory profile depends on chiral purity. Careful process control governs input ratios and ensures compliance with international food and fragrance standards.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • FEMA GRAS status guidelines (Flavor and Extract Manufacturers Association)
    • ISO 9235 for definition and QC of natural flavor materials
    • Regulation (EC) No 1334/2008: EU food flavorings

    Typical usage ratio

    • 0.1–2.5% w/w in the total formulation, tailored to target aroma intensity and process batch size

    Downstream process integration

    • Enters after precursor aldehyde or ketone coupling, in esterification or reductive transformation steps
    • Chiral content confirmed via GC-MS and sensory panel to meet client specification

    Final product types

    • Stereospecific flavor intermediates for beverages and confectionery
    • Enantiopure fragrance ingredients for fragrance oil blending
    • Chiral modifiers for specialty aroma compositions
    Free Quote

    Competitive (R)-(+)-2-Tetrahydrofuroic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    (R)-(+)-2-Tetrahydrofuroic Acid: Precision for Advanced Applications

    Decades of Experience at the Production Source

    In the chemical industry, minute differences in structure often shape the direction of entire sectors. At our manufacturing facility, we have invested years refining the synthesis of (R)-(+)-2-Tetrahydrofuroic Acid, building expertise with a close attention to every detail of our process. Authentic (R)-enantiomer production draws on precise control of temperature, feed ratios, and reaction progress. Skipping steps, rushing reactions, or overlooking purification always shows up in the finished material—mistakes we've learned through real production experience, not just theory or literature.

    The Model of (R)-(+)-2-Tetrahydrofuroic Acid You Receive

    Our (R)-(+)-2-Tetrahydrofuroic Acid—Chemical Abstracts number 78644-54-3—arrives straight from our reactor lines. This material features high enantiomeric purity, as verified by chiral HPLC and optical rotation measurements. We do not rely on third-party convertible intermediates, nor do we modify racemic mixtures post-synthesis to isolate the desired form; our standard operating approach starts with chiral induction and results in a high-yield, single-enantiomer product before it enters the final purification train.

    We supply this material in solid crystalline form, with particle size controlled within a narrow window for reliable reproducibility. Analytical data, including melting point and residue-on-ignition values, connect to every lot for traceability and customer transparency. Each batch is backed by our in-house process records—proof that we are the original producer, not just a packager or re-seller.

    Demands in Research and Industry

    (R)-(+)-2-Tetrahydrofuroic Acid has become more important in synthetic organic chemistry, especially in pharmaceutical and agrochemical research programs searching for bioactive heterocycles and chiral building blocks. Our direct customers often use this acid as a precursor for complex ligand scaffolds or as a resolving agent for chiral amines and alcohols. One distinct application has been in the synthesis of β-lactam antibiotics, where the (R)-configuration provides a specific stereochemical foundation. Other customers apply it as a synthon in the construction of furan-derived peptidomimetics or as a monomer in polymer research targeting advanced material properties.

    Teams in academia and industry trust the material straight from the manufacturer for consistent performance. Early-stage scale-up and medicinal chemistry campaigns both suffer when enantiomeric impurities or residual solvents creep above trace levels. Our team understands these constraints: Orders ship with supporting certificates generated not from third-party labs, but from our on-site analytical team experienced in validating stereochemistry and purity.

    Differentiation: Purity, Enantiomeric Excess, and Reliable Supply

    Many confuse (R)-(+)-2-Tetrahydrofuroic Acid with its racemate or its (S)-enantiomer counterpart. A simple glance at the container label is never enough. The difference becomes obvious in reactivity and selectivity during downstream synthesis. We guarantee through direct experience that only the (R)-form consistently directs stereoselective reactions necessary for several key pharmaceutical candidates. Even a small fraction of the wrong enantiomer can jeopardize an entire batch by introducing unwanted side-products or by failing to match reference standards.

    Our process minimizes by-products and keeps heavy metal residue far below typical limits. Years of calibration on our glass-lined reactors and filtration lines allow us to hit target enantiomeric excess levels above 99 percent. This high selectivity comes from careful catalyst selection and post-reaction workup that avoids contamination from external sources. Technical staff document every critical control parameter, and samples from each batch pass through both wet chemistry analysis and advanced NMR before approval.

    Why Manufacturer-Direct Sourcing Matters

    Unlike traders, we can provide answers about the origins of every kilogram, recount issues from previous syntheses, and discuss process changes openly—because we are the source. Downstream users planning multistep syntheses count on that traceability when defending their data to regulators or patent reviewers. Direct feedback from customers cycles into our process improvements: adjustments made to optimize solubility or prevent agglomerates in humid climates often originated from shared challenges in formulation labs or pilot plant settings.

    Supply disruptions, force majeure events, and regulatory changes all weigh heavily on chemical programs dependent on rare chiral building blocks. Our commitment as a manufacturer has been to keep a reserve inventory ready for critical orders, rather than stretch thin across too many SKUs. We help de-risk customer planning by offering long-term scheduling, batch reservations, and real-time data on production capacity. Our plant protocols have evolved through nearly two decades’ worth of audits and batch records, not just through paperwork.

    Safety and Environmental Responsibility in (R)-(+)-2-Tetrahydrofuroic Acid Production

    Real-world manufacturing brings unique challenges. Furan-based compounds can pose fire hazards if solvents are mismanaged, and chiral catalyst residues, even at parts-per-million, can cause downstream reactivity issues. Our facility standards require closed-system handling and solvent recovery on each run. Engineering controls, including vapor recovery and thermal monitoring, form the core of our plant’s commitment to in-plant safety. By reclaiming spent solvents and purifying wash streams, we actively cut down environmental impact and occupational exposure.

    Handling organocatalysts and temperature-sensitive reactants over long campaigns forced our team to design reinforced vessel liners and in-line analytical monitoring. Staff receive ongoing safety training, not just boilerplate hazard reviews, but sessions built on actual near-miss case studies from our own operations. This culture of accountability extends through every step, from raw material qualification to packaged product release.

    Adaptability and Collaborative Problem-Solving

    Every customer process is different. Some requests have challenged us with questions about non-standard impurity profiles, or about performance under scale-up to several hundred kilograms. Others need documentation for regulatory filings across different jurisdictions. Direct manufacturing experience means we offer not only technical paperwork but nuanced guidance on handling, storage, and specific reaction compatibility beyond the written specifications.

    Our teams often run trial lots in collaboration with clients’ chemists before full-scale orders. This hands-on approach shortens troubleshooting cycles. If a customer flags impurity carryover or instability under certain storage conditions, we draw on archived plant data or previous batches to propose process changes backed by direct operational evidence.

    We share process control charts, real-time deviation logs, and batch summary sheets if the project requires them. If a research team needs a modified solvent system or altered crystal habit, we bring together plant chemists, analytical staff, and sometimes even client partners to solve process puzzles as a team—not as vendor and buyer, but as colleagues with a shared stake in success.

    (R)-(+)-2-Tetrahydrofuroic Acid versus Racemic and (S)-Counterparts

    Working with small-molecule chiral acids, the real challenge lies in getting one configuration, not a mix. Racemic tetrahydrofuroic acid contains both enantiomers in equal measure, doubling the purification work and opening the door to unpredictable by-products. Some synthetic routes cannot tolerate the racemate at all; just a few percent wrong-handed material shifts reaction trajectories. The (S) form, serving different markets and applications, often lacks the exact biological or catalytic profile required by our core clients. This points to an important boundary—one detailed enough to matter in docking studies or in the final synthetic yield, but not always obvious in paperwork or spec sheets.

    We see demand fluctuate based on patent lifecycles and emerging reaction technologies, but reliable, high-purity (R)-acid maintains steady importance for stereoselective synthesis. Direct users—those running catalytic asymmetric synthesis or precise kinetic resolutions—cannot risk guessing or hoping through a middleman. Our plant’s strict demarcation between production lines guarantees that cross-contamination never impacts the chiral integrity of the acid. Separate inventory, equipment, and final QA checks help maintain this segregation, which ends up protecting our downstream partners from regulatory and scientific headaches.

    Lessons from Real-World Use and Process Feedback

    Laboratory and pilot plant chemists face the consequences of impurity drift, solvent residues, and subtle stability issues not immediately apparent during short-term storage. Over the years, feedback loops with both multinational and startup R&D teams have highlighted common failure points—incorrect jar labeling from bulk repackaging, unexpected phase separation in high-humidity storage, or even minor pH drifts affecting resuspension in buffered systems.

    There have been instances where even well-meaning traders supplied “R-enriched” material that failed strict downstream chiral purity tests. These events re-emphasize why manufacturer-level production, with end-to-end testing and direct sign-off, carries measurable value. We provide reference spectra and impurity-cutoff logs with every batch, shaped not to impress buyers, but to solve the problems that chemists repeatedly flag. In collaborative pilot campaigns, minor process tweaks—like adjusting recrystallization rates, or pre-drying finished product under vacuum—often made the difference between a workable and an unworkable batch.

    Enhancing Trust and Reducing Uncertainties

    New users often approach (R)-(+)-2-Tetrahydrofuroic Acid through project-driven urgency. They want to know not just the COA and general specs, but the full pedigree of the material—every relevant processing variable and lot-specific anomaly. Direct dialogue with manufacturer production teams sidesteps the long game of troubleshooting through middle layers.

    Our documentation tracks handling temperature, cooling rate, and final packaging, so if a customer needs to trace a stability deviation, every record stands ready for review. Production logs include every shift’s intervention, manual notes on blending or sieving, and the complete analytical trail attached to each shipment.

    We believe trust grows when partners share both successful outcomes and lessons from troubleshooting. In cases where a project ran into solubility or stability trouble, honest discussions about recovered and reject batches led to practical changes in process protocol the next time. This degree of accountability, impossible to achieve through distant sources, gives project managers the confidence to build timelines around assured supply.

    Supporting Global Research, Scale-Up, and Material Innovation

    (R)-(+)-2-Tetrahydrofuroic Acid supports many experimental designs—anywhere chemists demand a well-defined chiral building block for asymmetric catalysis, ligand synthesis, or advanced polymer science. Some of the world’s leading research programs credit their progress to direct support from manufacturers who treat process transparency seriously. Time pressure and resource limitations push teams to seek not just the lowest price or the first available jar, but a reliable technical partnership.

    Our own process development stories often begin with customer problems: the need for a specific counterion, a request for a unique packing density, or a desire to use greener solvents. Addressing these requires more than re-labelling or spec compliance; they require willingness to rethink, test and record new preparation strategies. In each case, the solution emerges from the deep process familiarity unique to genuine manufacturers.

    Real Risk Management in the Supply Chain

    Processed intermediates like (R)-(+)-2-Tetrahydrofuroic Acid play outsize roles in risk calculations for pharmaceutical and specialty chemical makers. Any batch anomaly—be it a minor deviation in optical rotation or a rounding error in assay—wastes resources and sets back launch schedules. Our focus lies in making the supply chain as predictable as possible through robust, long-proven methods. Customers receive full-run batch records, deviation logs, and pre-shipment stability data because we want every user, from benchtop to pilot plant, building on a foundation that’s secure and fully known.

    Where we have detected challenges—seasonal variation in raw material quality, unexpected downtime in a reactor’s agitator, or fluctuations in water purity—we document and relate these factors to any observable variation in product output. Many clients have used this transparency to defend regulatory filings or patent challenges, showing that their supply source lives up to the standards outlined in global compliance frameworks.

    Looking Forward: Customer-Driven Solutions, Not Spec-Driven Compromise

    Our team’s commitment to (R)-(+)-2-Tetrahydrofuroic Acid production springs from the reality that every kilogram reflects real work, hard-won expertise, and a willingness to adapt. We have watched competitors struggle with imported racemates that never quite clear the chiral purity test, or with supply chains that falter under shipping bottlenecks or customs delays. As regulatory scrutiny on chiral specialty chemicals rises, we expect more end-users to demand records and process transparency with every purchase.

    Future developments may push us to refine our methods—maybe with non-toxic catalysts, cleaner solvent systems, or automated purification. The thread running through all this is a deep-rooted belief that chemistry remains a partnership. Our technology grows alongside our customers’ challenges and ambitions. Improved analytical methods, expanded reactor lines, and flexible process routes all come from requests and lessons learned from those actually using the material, not from chasing paper-thin differentiators.

    Putting the Product to Work

    Every process and batch of (R)-(+)-2-Tetrahydrofuroic Acid we release responds to a user need—a demand for purity, traceability, and technical engagement that the open market cannot always deliver. The difference between material from the true source and stock labeled by resellers rests not in the off-the-shelf numbers, but in the confidence that technical setbacks will meet options for real corrective action. Our team stands ready to share, explain, or adapt every aspect of the production journey that impacts your project’s success.

    Over years of hands-on experience and customer collaboration, we have proven that genuine manufacturing—supported by open process data, responsive technical support, and willingness to confront unexpected problems—delivers not just product, but peace of mind. For teams pushing the boundaries in research or building scalable commercial synthesis, this partnership with the producer marks the difference between progress and delay. Our role remains providing the material foundation for those next steps.