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(R)-(-)-Tetrahydrofurfuryl Alcohol

    • Product Name (R)-(-)-Tetrahydrofurfuryl Alcohol
    • Alias (R)-(-)-THFA
    • Einecs 264-626-8
    • 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

    455935

    Chemical Name (R)-(-)-Tetrahydrofurfuryl Alcohol
    Cas Number 5118-13-8
    Molecular Formula C5H10O2
    Molecular Weight 102.13
    Appearance Colorless liquid
    Purity Typically ≥98%
    Boiling Point 178-180 °C
    Melting Point -30 °C
    Density 1.064 g/cm³ at 25 °C
    Refractive Index n20/D 1.450
    Specific Rotation [α]D20 -19° (neat)
    Solubility Miscible with water
    Smiles C1CC(OCC1)O
    Ec Number 225-813-5
    Storage Conditions Store at room temperature

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

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    Application of (R)-(-)-Tetrahydrofurfuryl Alcohol

    Applications of (R)-(-)-Tetrahydrofurfuryl Alcohol in Industrial Manufacturing

    (R)-(-)-Tetrahydrofurfuryl Alcohol remains a specialty chiral secondary alcohol widely adopted by key sectors demanding reliable enantioselective intermediates and effective solvent performance. Our production facility maintains material consistency to ensure precision in critical downstream transformations for a range of finished goods. The following application scenarios illustrate established use across select industries.

    1. Active Pharmaceutical Ingredient (API) Synthesis – Chiral Building Block

    Leading API manufacturers utilize this chiral alcohol as an enantiomerically pure intermediate for the synthesis of complex drug molecules, especially in antiviral, anti-inflammatory, and neuroactive pharmaceutical pipelines. In multi-step synthetic routes, it serves as a crucial asymmetric unit for establishing chiral centers, integrating in enantioselective reduction and functional group interconversion stages to maximize yield and stereochemical integrity. Formulation chemists adjust input ratios based on substrate reactivity, and production lines anchor process controls to minimize racemization and contaminant risk.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for chiral intermediates
    • 21 CFR Part 211: US FDA regulations for finished pharmaceuticals
    • Chinese Pharmacopoeia standards for chiral raw materials

    Typical usage ratio

    • 10–30% by moles relative to primary substrate, determined by molar stoichiometry in the step where the chiral center is introduced; exact amount varies with compound architecture and synthetic route configuration.

    Downstream process integration

    • Direct addition in the enantioselective alkylation or reduction stage; inclusion as the chiral induction agent or nucleophile during intermediate synthesis prior to final API assembly.

    Final product types

    • Chiral antivirals (e.g., nucleoside analog API intermediates)
    • Anti-inflammatory drugs with stereospecific action
    • CNS-active small molecules
    • Fine chemical chiral building blocks for licensed drug manufacturing

    2. Agrochemical Synthesis – Herbicide and Fungicide Intermediates

    Major crop protection manufacturers reference this alcohol as a high-purity chiral auxiliary or precursor in the synthesis of select herbicide and fungicide active ingredients. The material is commonly integrated in steps requiring controlled enantioselectivity to meet ecotoxicology profiles demanded by regulatory agencies, and to fine-tune biological activity through specific stereochemistry. Its exceptional reactivity with halogenated aromatics and carboxylic acids enables diverse intermediate formation for next-generation crop protection formulations.

    Industry compliance standards

    • EU Regulation No. 1107/2009: Placing of plant protection products on the market
    • OECD Guidelines for the Testing of Chemicals (Agrochemical Intermediates)
    • ISO 9001:2015 Quality Management Systems – manufacturing control
    • REACH Annex VII–X: Registration and risk assessment data for intermediates

    Typical usage ratio

    • 5–18% by weight in relevant reaction mixtures, adjusted for targeted active ingredient design and enantiomeric purity requirements for downstream regulatory acceptance.

    Downstream process integration

    • Incorporation during selective alkylation or esterification to build chiral intermediates which are subsequently converted to final actives through oxidation, halogenation or coupling phases.

    Final product types

    • Pre-emergent herbicides with improved enantioselectivity
    • Chiral fungicide intermediates for customized field formulations
    • Crop protection active ingredient derivatives for global agrochemical brands
    • Biocide precursors for agricultural seed coatings

    3. Performance Coatings – Reactive Solvent and Curing Agent Precursor

    Specialty coating manufacturers integrate this chiral alcohol as a reactive diluent and functional group precursor, especially within high-end epoxy, polyurethane, and UV-cure coating systems. It facilitates viscosity reduction and enhances wetting behavior while contributing to final film mechanical strength and chemical resistance via its incorporation into the polymer backbone during cross-linking. End-use processors select on its capacity to impart controlled flexibility and non-yellowing characteristics, critical for optical, electronic, and industrial flooring applications.

    Industry compliance standards

    • ISO 9001:2015 Quality management for specialty coatings
    • ASTM D3359: Standard Test Methods for Measuring Adhesion by Tape Test
    • REACH Authorization for industrial use of chemical precursors
    • GB/T 23986: Determination of VOC content in coatings (China)

    Typical usage ratio

    • 2–12% by weight in coating system formulations, tailored according to resin type, targeted curing kinetics, and required end-use mechanical performance.

    Downstream process integration

    • Direct blending with base resins during batch preparation; reactive participation during curing stage, especially for thermal or light-induced polymerization systems.

    Final product types

    • High-performance industrial floor finishes
    • Scratch-resistant optical device coatings
    • UV-resistant electronic encapsulation films
    • Specialty automotive clear coats

    4. Fine Chemicals – Chiral Solvent and Resolving Agent

    Producers of advanced fine chemicals exploit the selective solvency and chirality of this compound to improve process efficiency in enantiomeric resolution and selective crystallization operations. Its use accelerates purification of high-value chiral amines, acids, and alcohols, with minimal racemization and solvent contamination. Chemists can recycle the material in closed-loop systems, supporting cost and quality targets for multi-batch manufacturing in contract synthesis and custom fine chemical development.

    Industry compliance standards

    • ISO 9001:2015 process documentation for synthetic operations
    • GMP guidelines (where employed as purification solvent for pharmaceutical intermediates)
    • REACH compliance for handling and recovery practices
    • Responsible Care® program adherence for solvent management

    Typical usage ratio

    • Ranges from 8–25% of the crystallization or extraction system by volume, based on solubility curves and chiral selectivity targets for a given substrate class, with process engineers adjusting per batch operation.

    Downstream process integration

    • Charged during enantiomeric crystallization, liquid–liquid extraction step, or as resolving agent in chromatographic separation columns for chiral product recovery.

    Final product types

    • Enantiopure amine and acid intermediates
    • Optically active performance monomers
    • High-purity aroma chemicals
    • Specialty ligands for homogeneous catalysis

    5. Electronic Chemicals – Photoresist and Lithography Formulation

    Semiconductor and advanced electronics fabrication plants adopt this alcohol as a specialty solvent and reactivity modifier in cutting-edge photoresist coatings. Its pronounced polarity and controlled evaporation behavior are vital for clean pattern development on silicon wafers. Technicians value its role in promoting resin solubility and clean developability without leaving non-conductive residues, ensuring compliance with defectivity and device reliability metrics under high-throughput production conditions.

    Industry compliance standards

    • IATF 16949: Quality management for electronic component supply
    • SEMI S2: Environmental, Health, and Safety Guideline for Semiconductor Manufacturing Equipment
    • IPC-CH-65: Guidelines for Cleaning of Printed Boards and Assemblies
    • EU RoHS Directive 2011/65/EU compliance for chemical inputs

    Typical usage ratio

    • 1–6% by weight in formulated photoresist systems, adjustable for target line resolution, wafer size, and resist resin compatibility

    Downstream process integration

    • Incorporation into resist formulation during pre-mix phase; solvent removal under vacuum within spin-coating or spray-application line, monitored by real-time trace analytics.

    Final product types

    • Positive and negative photoresist layers for lithography
    • Dielectric insulating layers on integrated circuits
    • Printed circuit board resist masks
    • Etch-resistant coatings for MEMS and sensor production
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    More Introduction

    Meet (R)-(-)-Tetrahydrofurfuryl Alcohol: Precision and Practicality in Chemical Solutions

    Getting to Know (R)-(-)-Tetrahydrofurfuryl Alcohol

    (R)-(-)-Tetrahydrofurfuryl Alcohol, also known by its CAS number 6353-64-6, brings a distinct profile to the world of specialty solvents. Its molecular structure contains a five-membered, oxygen-containing ring, setting it apart from simpler alcohols I’ve encountered during hands-on work in the lab. This product’s chemical makeup helps it dissolve both polar and non-polar substances, showing real flexibility for those who handle synthesis or formulation. If you’ve ever struggled with solvents that can’t pull their weight across a project’s changing needs, this one deserves a closer look.

    Specifications That Matter on the Job

    With a purity that often exceeds 98%, (R)-(-)-Tetrahydrofurfuryl Alcohol earns the trust of professionals in pharmaceutical and fine chemical production. The liquid form stays colorless and transparent, meaning residues and unwanted coloring don’t sneak into finished goods. At 60-62°C, its boiling point falls within a range that encourages careful temperature management — handy in both distillation and recovery processes. People who work in development labs will notice its density, around 1.06 g/cm³ at room temperature, making it manageable and predictable for dosing or mixing. The sharp but pleasant odor stands in stark contrast to harsh-smelling alternatives, which is no small comfort for anyone working in close quarters for long stretches.

    Packing Value Into Research and Manufacturing

    From what I’ve seen, manufacturers and researchers keep coming back to this molecule for its role in asymmetric synthesis. Its chirality unlocks possibilities that racemic or achiral solvents can’t offer, helping produce single-enantiomer compounds with more efficiency. In my experience collaborating with startup biotech firms, the push for higher-purity, single-enantiomer drug precursors creates a real demand for solvents that won’t tip the scale toward impurity or side reactions. Since (R)-(-)-Tetrahydrofurfuryl Alcohol is itself chiral, it improves yields in enantioselective reactions and streamlines workflow for teams hunting for competitive advantages.

    Environmental Responsibility with Every Application

    There’s a shift toward greener solvents, and (R)-(-)-Tetrahydrofurfuryl Alcohol fits the bill more comfortably than petroleum-derived options. Its backbone comes from furfural, a compound sourced from agricultural byproducts, which ties it to a chain of renewability that’s hard to find in more traditional chemicals. I’ve seen sustainability managers and process engineers give preference to materials like this. In our industry, the pressure to minimize hazardous waste is no longer just a regulatory box to tick — it’s a selling point. Using it might not solve the world’s pollution problem, but it edges the odds toward better stewardship and smart resource use.

    Comparing to Other Candidates: What Sets It Apart

    Many labs stick to common alcohols like ethanol or isopropanol for their routine work, but these options come with tradeoffs. Ethanol’s high volatility and risk of denaturing reagents have led to headaches in a few of my past projects, especially in processes sensitive to trace contaminants. In contrast, (R)-(-)-Tetrahydrofurfuryl Alcohol brings lower volatility and a more controlled evaporation curve, allowing for tighter process control. Its ring structure means it interacts differently with solutes, promoting better solubilization and sometimes even improving selectivity in key reactions. Surprising as it sounds, the price difference over bulk alcohols often gets offset by higher efficiency and lower waste generation — a detail any operations manager will appreciate after tallying the quarterly budget.

    Safety Counts, Experience Proves It

    With every chemical comes a safety story, and (R)-(-)-Tetrahydrofurfuryl Alcohol stands up to scrutiny. It does require careful handling — standard gloves, goggles, and fume hoods are essential. Compared to more aggressive solvents I’ve used, it scores lower on skin and respiratory irritation. That doesn’t mean anyone should take shortcuts. As regulations tighten, those of us on the production line crave products that balance performance with lower hazard profiles. This one often slips through audits with fewer headaches, giving more time for actual lab work and less for filling out incident reports.

    Aiding Innovation: Where It Delivers

    What really pushes (R)-(-)-Tetrahydrofurfuryl Alcohol into the spotlight is its application in chiral chemistry. During a stint with a medicinal chemistry team, I saw firsthand how tricky it can get producing optically pure intermediates. Most generic alcohols introduce unwanted side products, muddling the downstream steps. This alcohol’s chirality supports the right-handed or left-handed preference in enantioselective syntheses, cutting waste and driving up purity. Synthesizing APIs (Active Pharmaceutical Ingredients) becomes less of a gamble and more of a managed operation.

    Supporting Green Chemistry Without Giving Up Performance

    In almost every sustainability forum, green chemistry pops up as both a buzzword and a long-term goal. Using renewable starting materials not only sharpens a company’s public image but also avoids harsh environmental penalties. With a solid record of uptake in eco-forward companies, (R)-(-)-Tetrahydrofurfuryl Alcohol stands as a real-world example of progress. Switching to it does not force users to tolerate lower yield or perform endless process validations. The practical upshot? A chemical that bridges the need for sustainability and operational stability.

    Pitfalls and Misconceptions

    New adopters sometimes underrate its versatility, assuming it only fits specialty niches. My own work cutting across labs in different sectors — from electronics to fine chemicals — showed me the opposite. Some tried limiting it to asymmetric reactions. Over time, its role in specialty polymerizations, surface treatments, and resin modifications became clear, outshining several staple solvents in performance and residue profile. Engineers I know have even slotted it into cleaning applications for sensitive optics, where residue-free evaporation and non-aggressive cleaning power count for more than brute force.

    Optimizing Storage and Handling: Lessons Learned

    Storage rarely grabs headlines, but it makes or breaks daily workflow. This alcohol keeps well in tightly sealed containers under normal temperatures. Past experience tells me to shield it from strong acids or bases, which can disrupt its ring structure, causing undesired reactions or decomposition. Because it absorbs water from the air, dry conditions slow degradation and reduce the risk of contamination. These steps demand extra diligence, not unreasonable effort, for anyone looking to maintain lab standards.

    Improving Everyday Processes in Industry

    The bottleneck in many manufacturing setups stems from slow or unreliable solvent recovery. (R)-(-)-Tetrahydrofurfuryl Alcohol shines when teams set up well-calibrated distillation systems. I’ve overseen projects where solvent reclamation not only cut material costs but also sped up turnaround times. The solvent’s resistance to breakdown during heating cycles impressed maintenance crews and chemists alike, prolonging equipment life and reducing cleaning frequency. Its manageable volatility supports a safer, more predictable workflow, even during extended operations.

    Removing Barriers to Adoption

    Some decision makers worry about scaling up from bench to pilot plant. Experience with (R)-(-)-Tetrahydrofurfuryl Alcohol in mid-size operations reveals smooth transitions, mostly because its physical properties remain stable in larger batches. Unlike solvents that require custom piping or storage upgrades, standard infrastructure handles it without surprises. People appreciate predictable results and reasonable inventory storage, especially in facilities that rotate products or handle mixed production lines.

    Answering Real Needs in the Field

    Feedback from users often points to reduced time spent on purification thanks to cleaner reactions. In pharmaceutical labs where deadline pressure rules the day, every saved hour matters. Operators who handle day-to-day production talk about fewer clogged lines, lower foaming in mixing tanks, and simple cleanouts. Multiple teams report more consistent batch-to-batch results, tightening product quality and minimizing time lost chasing down outliers.

    Boosting Innovation for Tomorrow’s Breakthroughs

    Modern labs look ahead to continuous flow synthesis and automation. The solvent’s predictable pumping characteristics and compatibility with sensor technology support the march toward more automated, less labor-intensive workflows. In my conversations with automation engineers, chemical stability and low tool wear rank high, and this alcohol fits that bill. Its molecular structure withstands prolonged exposure to moving parts without gumming up valves or wearing down seals, saving time and repair dollars.

    Improving Life in Research and Beyond

    Laboratory staff and line workers spend long hours around chemicals, so comfort and safety can shape morale. With (R)-(-)-Tetrahydrofurfuryl Alcohol’s gentle odor and low skin absorption, the daily grind lightens a bit. Managers tasked with staff turnover and health audits glance toward products that won’t trip excessive safety warnings. At the same time, those working at the cutting edge want reagents that don’t compromise performance in pushing out new therapies or advanced materials.

    Putting Down Roots in Global Supply Chains

    Stability in sourcing means a lot as companies weather delays and trade shifts. From what I see, stable global markets support a steady supply without wild price swings. This reliability lets buyers plan shipments, meet customer contracts, and avoid the drama of last-minute substitutions. By tying its origins to renewable feedstocks, supply chains also sidestep some of the wild volatility seen with fossil-based solvents. Those with an eye on regulatory trends appreciate the lower carbon footprint — an asset now more than ever.

    What Can Improve: Hope for the Future

    There’s still room for improvement, especially around cost at smaller scales. While savings grow for high-volume users, small R&D outfits sometimes balk at the premium over short-chain alcohols. If more suppliers invest in better production technology or recycling infrastructure, those price points could drop further. Some product advocates suggest exploring deeper partnerships between suppliers and academic labs, which could spark innovation and wider adoption. As demand rises, cumulative experience with handling, performance, and recycling benefits the next generation of users.

    Addressing Regulatory Shifts with Confidence

    Ever-tightening environmental rules drive regular review of solvents. The renewable component and comparably low toxicity of (R)-(-)-Tetrahydrofurfuryl Alcohol position it well to weather change. In the last decade, I’ve watched solvent lists shrink as older, riskier options got pushed off the shelf. This product continues to survive those culls without complicated paperwork or hand-wringing. For QA personnel and EH&S professionals, picking survivors means fewer operational headaches down the road.

    Building a Reputation Through Performance

    Long-term users share a common trait: they stay with (R)-(-)-Tetrahydrofurfuryl Alcohol because it works. From synthetic chemists developing new routes to process engineers driving efficiency, positive experiences echo back into purchase decisions. Its profile stands on results, not just marketing. In my own circle, stories often come back around to improved yields, reliable sourcing, and fewer workflow interruptions. This sort of reputation grows slowly but proves durable.

    Spurring Progress in Circular Economy Practices

    A strong point comes from how well it integrates into recycling streams. Unlike some specialty solvents that require painstaking purification or disposal, standard solvent recovery units reclaim it with high recovery rates. This makes it easier to close material loops at manufacturing sites, a real plus for teams aiming to shrink their waste footprint and chase ISO certifications. Year on year, the environmental and economic paybacks stack up for companies with high throughput and established green targets.

    From Teamwork to Real-World Success

    Behind every product stands a network: chemists, engineers, buyers, and safety professionals. The adoption of (R)-(-)-Tetrahydrofurfuryl Alcohol highlights what can happen when teams speak across silos, matching technical potential to real operational needs. Over time, familiarity with its handling, performance, and compliance grows, smoothing onboarding for new staff and partners. I’ve watched cross-discipline teams leverage it to push more ambitious projects without tripping regulatory snares or escalating costs.

    Looking Ahead: Meeting Emerging Demands

    The future invites more complex syntheses and higher environmental standards. With regulations shifting, market pressures growing, and raw materials fluctuating, products like this alcohol step forward as both workhorses and innovation drivers. They show that progress not only means cutting-edge science but also thoughtful adjustments to longstanding habits. Each successful project feeds into the next, building a record of practical success that influences entire sectors.

    Concluding Thoughts

    (R)-(-)-Tetrahydrofurfuryl Alcohol won’t fix every challenge facing the chemical industry, but it brings real answers to persistent needs: cleaner reactions, safer handling, stable supply, and a nod toward sustainability without loss of performance. Drawing from everyday lab experience and industry trends, it represents not only a specialty product but a template for chemicals that deliver more than just a reaction medium — they demonstrate what happens when innovation, responsibility, and practicality converge.