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(R)-(-)-2-Pentanol

    • Product Name (R)-(-)-2-Pentanol
    • Alias (R)-(-)-2-Amyl alcohol
    • Einecs 214-115-7
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    485307

    Iupac Name (R)-(-)-pentan-2-ol
    Cas Number 4265-56-1
    Molecular Formula C5H12O
    Molar Mass 88.15 g/mol
    Appearance Colorless liquid
    Boiling Point 119-120 °C
    Melting Point -95 °C
    Density 0.808 g/mL at 25 °C
    Specific Rotation -16.3° (neat, 20 °C)
    Refractive Index 1.418-1.420 (20 °C)
    Flash Point 30 °C (closed cup)
    Solubility In Water Moderate (16 g/L at 20 °C)

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

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled "(R)-(-)-2-Pentanol, 25 mL," including hazard warnings, supplier, and purity details.
    Shipping (R)-(-)-2-Pentanol is shipped in tightly sealed containers, protected from light, moisture, and sources of ignition. During transport, it must be labeled as a flammable liquid and handled according to relevant hazardous material regulations to ensure safe delivery. Ensure compliance with local, national, and international shipping requirements.
    Storage (R)-(-)-2-Pentanol 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. The storage area should be labeled and protected from heat and direct sunlight. Proper chemical storage protocols should be followed to prevent leaks, spills, or contamination.
    Application of (R)-(-)-2-Pentanol

    Applications of (R)-(-)-2-Pentanol in Industrial Manufacturing

    (R)-(-)-2-Pentanol serves as a chiral building block and functional intermediate in several downstream industries. Our manufacturing processes ensure high purity and consistent optical activity for precise industrial integration. Below, we present verified downstream applications across different sectors from an industrial raw material producer's perspective.

    1. Chiral Intermediate for Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical manufacturers rely on (R)-(-)-2-Pentanol as an essential chiral auxiliary and intermediate in the synthesis of enantiomerically pure APIs. The alcohol group and specific (R)-enantiomer configuration allow stereoselective formation of active pharmaceutical compounds, particularly in beta-adrenergic blockers and antifungal agents. Chiral purity at each batch run directly impacts the downstream drug approval process and clinical performance.

    Industry compliance standards

    • USP (United States Pharmacopeia) for chiral raw materials
    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • European Pharmacopoeia (Ph. Eur.) purity requirements
    • FDA cGMP quality management for pharmaceutical ingredients

    Typical usage ratio

    • 5–15% of the total reaction volume for chiral intermediate stages; ratio adjusted by target synthetic route and required optical yield

    Downstream process integration

    • Introduced during asymmetric synthesis steps, chiefly through Grignard or reduction reactions, and involved in esterification or acylation for final API molecule assembly

    Final product types

    • Beta-blocker APIs including Propranolol
    • Chiral antifungal drugs
    • Enantiopure building blocks for further pharmaceutical derivatization
    • Specialty peptide intermediates

    2. Synthesis of Flavors and Fragrances

    Our (R)-(-)-2-Pentanol supports aroma compound manufacturers in producing chiral esters and alcohol derivatives used in fine fragrances and food flavorings. The specific enantiomer imparts unique, intense olfactory notes necessary for consistency in high-end perfumery and certified food flavors. Downstream formulators choose this material for applications where regulatory and sensory standards require tight enantiomeric excess control.

    Industry compliance standards

    • FEMA GRAS (Flavor and Extract Manufacturers Association’s Generally Recognized as Safe) listings
    • IFRA (International Fragrance Association) standards for essential chemicals
    • EU Regulation (EC) No 1334/2008 on flavorings and certain food ingredients
    • ISO 9235 requirements for aroma raw materials

    Typical usage ratio

    • 0.1–5% in fragrance synthetic blends; typically 0.01–0.5% in finished food flavorings based on intensity and target regulatory thresholds

    Downstream process integration

    • Reacted under esterification or acylation to yield chiral esters used as flavor or fragrance keynotes; also deployed as a chiral solvent or modifier in complex blend formulations

    Final product types

    • High-impact flavor esters for beverages and confectionery
    • Luxury perfume bases
    • Food-grade natural-identical aroma chemicals
    • Specialty aroma concentrates for fine cosmetics

    3. Agrochemical Synthesis (Herbicides and Fungicides)

    Chemical producers in the agrochemicals sector introduce this raw material as a chiral auxiliary or starting material during the manufacturing of selective herbicides and fungicides. The (R)-(-) form increases the enantioselectivity and biological activity profile of the downstream actives, required for both efficacy and regulatory compliance in crop protection compounds.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • EU Regulation (EC) No 1107/2009 concerning plant protection products
    • EPA 40 CFR Part 158 for pesticide registration (USA)
    • ISO 17025 accreditation for analytical batch release

    Typical usage ratio

    • 1–10% in reaction feed for chiral agrochemical synthesis, controlled by enantiopurity requirements of the target pesticide

    Downstream process integration

    • Incorporated during the active ingredient synthesis step, especially in compounding stages where molecular chirality ensures selectivity and environmental stability

    Final product types

    • Chiral phenoxyalkanoic acid herbicides
    • Enantioselective triazole fungicides
    • Custom agricultural intermediates
    • Pre-formulation concentrates for downstream registration and field trials

    4. Chiral Auxiliary for Asymmetric Catalysis in Fine Chemical Production

    Specialty chemical manufacturers employ (R)-(-)-2-Pentanol as a chiral auxiliary in asymmetric synthesis workflows, especially for producing custom ligands, performance monomers, and specialty intermediates. Its controlled optical purity enables the downstream formation of new compounds with strict stereochemical requirements, supporting precision catalysis and advanced material innovation.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 registration for intermediates
    • ISO 9001:2015 for chemical manufacturing and QC
    • Chemical Manufacturing Control (CMC) guidelines for specialty materials
    • EHS (environment, health, safety) protocols for handling chiral organics

    Typical usage ratio

    • 2–12% relative to total monomer or ligand synthesis batch, with specific ratio depending on reaction scale and target stereochemistry

    Downstream process integration

    • Added to catalytic reaction vessels prior to substrate introduction, forming chiral complexes or supporting stereoselective polymerization and ligand assembly

    Final product types

    • Enantiomerically enriched catalysts and ligands
    • Performance specialty monomers
    • Chiral fine chemical intermediates
    • Advanced material additives for electronics and coatings

    5. Analytical Chemistry Reference and Calibration Standards

    Reference standard producers and analytical testing laboratories include this enantiopure alcohol as a calibration material to validate analytical instruments and enantiomeric excess measurements for chiral analysis. Excellent purity profile and tightly specified enantiomeric ratio make it suitable for critical comparators in HPLC, GC, and NMR workflows across pharmaceutical, environmental, and chemical QA applications.

    Industry compliance standards

    • ISO 17034 General requirements for the competence of reference material producers
    • Ph.Eur. and USP compendia for reference substances
    • ISO/IEC 17025 for testing and calibration laboratories
    • GLP (Good Laboratory Practice) protocols in analytical control

    Typical usage ratio

    • 0.5–10 mg per calibration run; adjusted depending on detection method and calibration curve linearity

    Downstream process integration

    • Dosed as a chiral reference standard during instrument calibration, method validation, or routine analytical batch quality checks

    Final product types

    • Pharmaceutical-certified reference materials
    • Analytical-grade calibration kits for chromatography
    • Standard solutions for QC laboratories
    • Enantiomeric excess test standards

    6. Fine Chemical Synthesis of Specialty Solvents

    Producers of custom solvents and performance fluids rely on the high-purity and enantiomeric control offered by our material for blending specialty solvent systems. The pronounced chiral structure delivers unique solvation properties, especially in applications requiring optical activity or selective interaction with other chiral molecules in downstream fine chemical processes.

    Industry compliance standards

    • REACH pre-registration dossier for non-commodity solvents
    • ISO 14001 for environmental management
    • Local workplace safety regulations for chemical handling
    • Industry customer-specific specifications for solvent quality

    Typical usage ratio

    • 3–20% in functional solvent blends, balanced to achieve target optical rotation and miscibility characteristics required by end-formulator

    Downstream process integration

    • Added directly in solvent compounding lines or during solvent extraction steps to modulate chiral selectivity or physical properties of final blend

    Final product types

    • Chiral solvent formulations for laboratory R&D
    • Performance fluids in separation technology
    • Reactant-specific extractants
    • Solvent blends with defined enantiomeric activity
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    Certification & Compliance
    More Introduction

    (R)-(-)-2-Pentanol: Hands-On Insights into a Crucial Chiral Building Block

    Understanding (R)-(-)-2-Pentanol from a Manufacturer’s Perspective

    Years in chemical production have shown me that some molecules never achieve wide recognition, yet quietly shape entire markets. (R)-(-)-2-Pentanol—known chemically as (R)-2-Pentanol, CAS 4265-06-9—belongs to this group. This alcohol, with its clear, colorless, and faintly aromatic liquid form, delivers chirality with purity that seasoned chemists demand and innovative teams rely on.

    Through direct synthesis, my team maintains control over enantiomeric excess and residue profiles. This attention to detail distinguishes material brought directly from reactors and distillation columns, avoiding the uncertainties that come when chiral alcohols have passed through multiple traders before reaching the hands of a researcher or process engineer. The stereo-specific configuration of (R)-(-)-2-Pentanol remains intact, giving repeatable results in everything from pharmaceutical intermediates to specialty flavors.

    About Manufacturing Quality

    Making chiral alcohols is a game of precision and persistence. We rely on asymmetric reduction, not mere resolution, because time spent improving selectivity at the catalyst level pays off through fewer purification steps and more reliable batches. A typical batch exits with enantiomeric excess often upwards of 98%, but measurement is only half the story. In downstream reactions, we track how even slight shifts in optical purity change the yield or selectivity of the final product—whether that's for a high-value active pharmaceutical ingredient or a fragrance compound.

    (R)-(-)-2-Pentanol production is never a set-and-forget process. Our team trains on trace analysis to spot even sub-ppm byproducts, understanding that overlooked impurities spoil weeks of downstream work. By keeping the lab and production lines under tight temperature and pressure controls, contamination gets shut out before it starts. A bottle labeled with our batch code carries with it years of investment in analytical technique and practical knowledge about how small variations create big consequences.

    The Significance of Optical Purity

    There's a straightforward reason (R)-(-)-2-Pentanol lands on order sheets for fine chemicals: chirality changes everything. Pharmaceutical teams know minor stereochemical impurities can introduce unwanted activity or even toxicity in target molecules. We see the ripple effect up close—resolving a racemic mixture doubles the workload and discards half the precious material, wasting effort and raising costs.

    Our process, refined to favor (R)-enantiomer formation, returns better yields and more reproducible performance. In regional markets with strict regulatory oversight, we find that providing certificates of analysis for every lot matters less than providing predictable, reliable chemistry that performs identically batch after batch. The stories from formulators stuck trouble-shooting inconsistent intermediate supplies convinced us to keep the entire production on one site, so line-to-line and tank-to-tank differences disappear from the chain.

    Using (R)-(-)-2-Pentanol in Practice

    The typical user of this alcohol is far from a novice. Medicinal chemists and flavor developers discuss not just chemical names but optical angles and impurity fingerprints. (R)-(-)-2-Pentanol feeds into asymmetric synthesis pathways, where its stereochemistry controls the outcome of esterification, acylation, and further transformations. Teams developing beta-blockers, anti-infectives, or agrochemicals treat this molecule not as a simple reagent but as a logic gate, channeling the direction of molecular assembly and locking selectivity into the next synthetic step.

    In flavors and fragrances, the nuanced difference between (R)- and (S)- forms stands out. This chiral alcohol imparts a unique, subtly fresh note that the (S)-isomer never matches, and the wrong one can throw off the target aroma entirely. Beverage and food scientists searching for a trace 'lift' in a profile choose lots where the optical rotation confirms identity and quality.

    Comparing with Other Chiral Alcohols

    (R)-(-)-2-Pentanol sits beside other straight-chain alcohols like 1-pentanol or racemic 2-pentanol. The differences may look small in the chemical formula, but their impact unfolds across applications. Take 1-pentanol: it lacks chirality, offers bulk solvation and volatility, but can’t direct asymmetric synthesis or flavor profiles. Racemic 2-pentanol, which mixes R- and S-, splits activity and wastes efficiency in select reactions.

    For process chemists, using the wrong isomer translates to lower yield or more complicated separations downstream. Enantioselective reductions in the pharmaceutical pipeline fail to deliver high specific activity unless fed enantiopure (R)-(-)-2-Pentanol. I have seen teams switch suppliers or even revise protocols after problems trace back to batch-to-batch racemization in their reagent supply.

    The differences play out in real time. A flavorist once described the S-isomer as muddying a liquor’s bouquet, while the R-isomer sharpened and extended it. Our quality team uses gas chromatography with chiral columns, cross-validated by polarimetry, to give clear distinction between the isomers, closing the case for the product’s utility over widely available mixtures or achiral analogs.

    Addressing Challenges in Stereoselective Chemistry Supply

    In the field, requests for enantiopure (R)-(-)-2-Pentanol never stop. The usual reason: lower grade or racemic material ruins months of R&D work in seconds. Teams recount frustration when even reputable suppliers deliver bottles with hidden byproducts, mistaken labeling, or diminished optical purity after months in warehouse environments that don’t respect the volatility and sensitivity of small chiral alcohols.

    We've dealt with the logistics ourselves. Light, temperature, and atmosphere exposure gradually erode optical rotation, especially when containers breathe during storage or shipping. We package in light-blocking, nitrogen-purged containers, and ship quickly so that what leaves the facility assures every customer that optical purity remains intact. It’s common to hear about ‘mystery yield loss’ in pilot scale reactions until the batch provenance is checked and compromised racemization is found in the raw material.

    Clients frequently ask why costs fluctuate, especially compared to the more common non-chiral alcohols. We share our production methods and stability profiles openly; purification and quality assurance are resource-intensive at this scale, but this investment prevents costly setbacks further down the supply chain. The expense makes sense when you compare the long-term waste from failed synthesis or rejected product batches.

    Health, Safety, and Handling: Practicalities Over Protocols

    Production-scale (R)-(-)-2-Pentanol lives in a regulated world. Teams on the floor know its volatility isn’t just a technical detail: a dropped drum or leaking line transforms an ordinary hour into a scramble for containment and ventilation. Years of in-house experience told us to avoid shortcuts. Open handling elevates exposure risk and drives off the very optical purity that the market seeks. Strict protocols for trained personnel—not formulaic compliance routines—make a bigger difference than any label on a bottle.

    Despite its wide use, this molecule poses distinctive flammability and inhalation hazards. Repeated incidents at poorly equipped facilities illustrate how neglecting these realities ends up damaging both reputation and research. We build redundancy into fire safety and use closed transfer systems for all bulk storage and decanting steps. On the research bench, small-scale users appreciate sealed ampoules and easy-to-verify batch identity.

    Traceability and Documentation: Lessons Learned in the Field

    Through years of troubleshooting with customers, our teams realized that paper trails don’t assure performance unless batch documentation includes rigorous in-lab verification. We log full chromatograms, not just certificate of analysis checkboxes, for each output drum. Researchers and pilot teams regularly call on us for historical batch data when tracking a fouled reaction pathway, and a fast answer means we provide not only a product but a partnership based in lived experience. Every time we see a customer’s protocol improved by our trace analytics, we gain confidence not by documentation, but by real-world results.

    Demanding End Use: Pharmaceuticals, Flavors, Agrochemicals

    Every sector using (R)-(-)-2-Pentanol expects something different. In pharma, downstream hydrogenation depends on getting the right isomer at the right time. The process routes used for statin intermediates or chiral amines demand fast turnarounds, so lead times and batch variability become serious performance indicators. Several clients return to direct-from-manufacturer sourcing after problems with secondary suppliers. They recognize the difference after seeing compromised yield or unwanted byproducts from racemized or degraded raw material.

    Other users find less obvious bottlenecks. Food and beverage formulators need subtle hints of freshness or fruitiness, where tiny impurities or racemization destroy the signature aroma of premium spirits or soft drinks. Our flavor industry partners send back detailed sensory reports, drawing direct relationships between minute stereochemical differences in raw alcohol and their finished goods’ market impact. The relationship grows over time as each new application presses for ever-lower detection thresholds.

    Agrochemical research similarly presses the limits. Developing new-growth regulators or selective herbicides, R&D teams push for absolute selectivity. Even small racemic drifts can sabotage biological studies or regulatory filings. Having seen material disqualified after expensive field trials, research users have joined us in developing tighter analytical techniques, always with a view to preventing the long delays and cost overruns that ripple from upstream inconsistency.

    Improvements in Chiral Synthesis: Stories from the Lab

    Several years back, we faced stubborn issues with catalyst performance during scale-up. Chasing a clean reduction pathway while holding down byproduct alcohols pushed process chemists to rethink batch composition and reaction times. By shifting to a custom ligand system in the reduction step, and tuning solvent conditions based on ongoing NMR monitoring, we reached higher selectivity and lower byproduct levels. Small tweaks—like pre-drying the feedstock pentanone to below 100 ppm moisture—cut down on nasty side reactions, smoothing both yield and downstream purification.

    On another occasion, one of our partners discovered an unexpected contaminant profile during pilot scale optimization in a fragrance synthesis. Gas phase impurities traced back to drum seals on transport containers supplied by a well-known distributor. Switching exclusively to our own in-plant filled containers, with scheduled QC on each seal, stabilized their blends and ended the batch-to-batch headaches. That experience pushed us to invest in tamper-evident cap technology across all sales lines.

    Looking ahead, we work on continuous process improvement, implementing feedback from end users who need longer shelf life and broader temperature stability. Developing single-use transfer lines and modular micro-reactors has enabled us to respond rapidly to orders without sacrificing optical purity or identity. The close relationship with application scientists drives ongoing upgrades in purification, packaging, and analytical capabilities.

    Transparency and the Role of Direct Sourcing

    Direct contact with development chemists, production engineers, and flavor scientists has shaped our methods. Delivering (R)-(-)-2-Pentanol straight from our reactors to application labs closes the communication loop. Details often missed in trading layers—like cold chain breakdowns, seal selection, or shelf-life drift—come to light. Both producer and user get a clearer picture of what influences batch quality and supply dependability.

    Success means giving more than expected. Our team shares not just a certificate and a bottle but process harmonization advice, analytical tools, and troubleshooting insights. It isn’t about chasing minimum spec compliance or the lowest price—it's about offering a molecule that acts predictably and safely in the hands of people who turn it into medicines, flavors, fragrances, or agrochemical solutions.

    Discussing the Market: Global Trends and User Needs

    Global demand for chiral alcohols, especially optical pure (R)-(-)-2-Pentanol, continues to rise. The move toward greener asymmetric synthesis keeps pushing for higher selectivity, lower waste, and fewer purification steps. Regulations in pharmaceuticals and food have grown stricter, penalizing off-spec or adulterated lots. The supply chain pressures faced during recent disruptions highlighted the value of working with manufacturers who hold inventory and manage logistics in-house.

    End users stream feedback to us about shifting needs: some want tighter moisture controls, others look for expanded documentation support for cross-border regulatory submissions. Developments in green chemistry, including bio-based reduction processes, have attracted attention, and our team follows biocatalyst advances to keep the production route adaptable in the future. We stay ready to retool based on new customer criteria—sometimes shifting upstream steps, sometimes opening projects for tailor-made blends.

    Looking Ahead: Lessons for Technical and Research Users

    (R)-(-)-2-Pentanol acts as both a staple and a specialty. For new research applications, we recommend open discussions—involving both technical and procurement sides—on batch-specific needs: precise optical rotation, impurity profiles, stability data, and logistical expectations. Doing so closes the gap between what’s ordered and what actually works at scale.

    Decades of hands-on production and feedback have given us a perspective grounded in real-world use, not just in theoretical specifications. The stories, challenges, and solutions shared with customers continue to shape our approach, driving improvements that go beyond simple compliance or transaction. Whether incorporated in a new medicine, a fragrance, or an agrochemical formulation, dependable (R)-(-)-2-Pentanol production stays rooted in lived experience at every step.