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4-Pentyn-1-ol

    • Product Name 4-Pentyn-1-ol
    • Alias 4-Pentynol
    • Einecs 203-942-2
    • 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

    502387

    Name 4-Pentyn-1-ol
    Iupac Name Pent-4-yn-1-ol
    Cas Number 5390-04-5
    Molecular Formula C5H8O
    Molecular Weight 84.12 g/mol
    Appearance Colorless liquid
    Boiling Point 133-135 °C
    Melting Point -56 °C
    Density 0.912 g/mL at 25 °C
    Flash Point 38 °C
    Refractive Index 1.432
    Solubility In Water Miscible
    Pubchem Cid 11953

    As an accredited 4-Pentyn-1-ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 4-Pentyn-1-ol, 100 mL, features an amber glass bottle with a secure screw cap and clear labeling.
    Shipping 4-Pentyn-1-ol is typically shipped in tightly sealed containers to prevent leaks or evaporation. It should be stored in a cool, well-ventilated area, away from incompatible substances. During transport, classified as a hazardous material, it requires compliant labeling and documentation in accordance with relevant regulations for flammable liquids.
    Storage 4-Pentyn-1-ol should be stored in a tightly closed, clearly labeled container, in a cool, dry, and well-ventilated area away from sources of ignition. Keep it away from oxidizing agents, acids, and bases. Protect from direct sunlight and moisture. Ensure proper grounding and use non-sparking tools when handling. Store according to local, state, and federal regulations for flammable liquids.
    Application of 4-Pentyn-1-ol

    Applications of 4-Pentyn-1-ol in Industrial Manufacturing

    As a direct manufacturer, we supply high-purity 4-Pentyn-1-ol for crucial use in specialty chemical synthesis, pharmaceutical intermediates, advanced materials, and electronics. We maintain strict quality control and consistency in specifications to support downstream partners in regulated process environments.

    1. Pharmaceutical Intermediate for API Synthesis

    Major pharmaceutical producers use 4-Pentyn-1-ol as a key building block for synthesizing propargylic intermediates in active pharmaceutical ingredient (API) development. The compound supports selective functional group transformations, including click chemistry reactions and Sonogashira couplings, facilitating the production of antiviral, anticancer, and central nervous system (CNS) drug candidates. In this application, material purity and traceability remain critical due to the direct impact on pharmacological safety and regulatory submissions. Dedicated lines ensure compliance with trace impurities and batch reproducibility from lab scale to full cGMP production.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • EU GMP Directive 2003/94/EC
    • USP/NF Monograph-based specifications (where applicable)

    Typical usage ratio

    • Commonly 1–10 mol% relative to target intermediate in multi-step syntheses
    • Ratio adjusted via process optimization according to API yield and impurity control requirements

    Downstream process integration

    • Introduced during first- or second-stage condensation or alkylation reactions in custom synthesis pipelines
    • Fed into closed reactor systems for batch or fed-batch manufacturing strategies

    Final product types

    • Small molecule API intermediates
    • Finished bulk pharmaceutical compounds for oral or injectable formulations
    • Research-grade reference standards
    • Preclinical compound libraries

    2. Electronic Chemical Manufacturing (OLED and Semiconductor Fabrication)

    Electronics material manufacturers incorporate 4-Pentyn-1-ol into synthesis routes for small-molecule precursors used in OLED emitters and advanced photoresists. Its terminal alkyne group supports high-efficiency coupling in fine patterning agents and modifies polymer backbones to impart photoactive and charge-transporting properties. Control of moisture, trace metals, and batch uniformity is essential for electronics-grade applications, given the sensitivity of device fabrication to impurities. Standard operating procedures support integration into both pilot and commercial production of optoelectronic chemicals.

    Industry compliance standards

    • SEMI C3 Standard for Process Chemicals
    • IECQ QC 080000 HSPM (Hazardous Substance Process Management)
    • ISO 9001:2015 Quality Management Systems
    • IMDS (International Material Data System) declaration for electronics materials

    Typical usage ratio

    • Ranges from 0.5–5 wt% in functionalized polymer or small-molecule synthesis
    • Dosage specified per target emitter or photoresist class through R&D customization

    Downstream process integration

    • Used in pre-polymer modification and crosslinking reactions in cleanrooms
    • Added during solution preparation for spin-coating, inkjet printing, or photolithographic fabrication

    Final product types

    • OLED light-emitting layer precursors
    • Photoresists for advanced semiconductor patterning
    • Organic TFT material stock
    • Charge transport and blocking additives in display manufacturing

    3. Agrochemical Synthesis (Herbicide and Pesticide Active Ingredients)

    Leading agrochemical formulators utilize 4-Pentyn-1-ol for the synthesis of propargylic intermediates used in selective herbicides and insecticides. The molecule’s reactivity supports high-yield, low-byproduct conversion paths for actives that are crucial in crop protection mixes. Our supply features lot traceability and consistent GC-MS profile control, which helps downstream integration into multi-step organic syntheses and minimizes off-spec batches in regulated environments.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • REACH (EC) No 1907/2006 Registration
    • ISO 9001/14001 Certification (Quality & Environmental Management)
    • EPA Pesticide Production Regulations (40 CFR Part 167)

    Typical usage ratio

    • 1–7 mol% as a coupling/alcohol source in propargylation and other modification steps
    • Ratio determined by desired final active and product formulation matrix

    Downstream process integration

    • Introduced post-chlorination or halogenation as a nucleophilic reagent
    • Used in continuous or semi-batch mode for agrochemical actives synthesis

    Final product types

    • Herbicidal propargyl compounds (e.g., dinitroaniline herbicides)
    • Specific contact insecticides and plant growth regulators
    • Agro-chemical intermediates for soil and foliar application products
    • Pre-emergence and post-emergence pesticide formulations

    4. Fine Chemical Synthesis for Perfume and Fragrance Intermediates

    Leading fragrance houses incorporate 4-Pentyn-1-ol in the manufacture of high-impact aldehydic and alcohol intermediates for finished perfume bases. Its molecular structure enables propargylic rearrangements, yielding precursors with enhanced volatility and olfactory character. Tight control on residual solvents and color index supports consistency for olfactory evaluation and regulatory export, especially to the US, EU, and Japan.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • REACH compliance for non-hazardous REACH-registered substances
    • ISO 9001:2015 for batch traceability in fine chemicals
    • RIFM (Research Institute for Fragrance Materials) guidelines on purity and toxicity

    Typical usage ratio

    • 0.2–3 wt% relative to total reactant mass in key rearrangement or functionalization reactions
    • Ratio determined by the olfactory concentrate and downstream dilution standards

    Downstream process integration

    • Fed into controlled propargyl rearrangement or reduction steps under inert-atmosphere synthesis lines
    • Subsequently combined with natural extracts and aroma chemicals during perfume base compounding

    Final product types

    • Functionalized aldehydes for luxury perfumery
    • High-purity aroma alcohols
    • Fine fragrance intermediates exported to regulated markets
    • Signature aroma blends for branded consumer goods

    5. Reactive Diluents in High-Performance Coatings and Adhesives

    Industrial coating manufacturers introduce 4-Pentyn-1-ol as a reactive diluent and crosslinker in the formulation of specialty epoxy and polyurethane systems. Its terminal alkyne group allows covalent bonding during curing, contributing to improved chemical resistance, abrasion properties, and adhesion to composite substrates. Quality protocols cover VOC content, viscosity index, and shelf-life stability to support both in-house and contract manufacturing lines serving the automotive, aerospace, and electronics sectors.

    Industry compliance standards

    • ASTM D5402 (Solvent Content of Organic Coatings)
    • ISO 12944 (Corrosion Protection of Steel Structures by Coatings)
    • RoHS 2 Directive (2011/65/EU) for electronics-bound coatings
    • OECD SIDS for environmental impact assessment (where required)

    Typical usage ratio

    • 1–6 phr (parts per hundred resin) depending on target hardness and cure rate balance
    • Dosage refined through coating thickness and final film characteristic requirements

    Downstream process integration

    • Blended during pre-polymer dispersion prior to primary or secondary cure steps
    • Added into batch mixing tanks with controlled addition rates for large-scale application

    Final product types

    • Two-component epoxy floor coatings for automotive and aerospace hangars
    • Moisture-curable electronic encapsulation resins
    • UV-cured acrylic-epoxy hybrid adhesives
    • Specialty varnishes for high-durability requirements

    6. Laboratory Reagent for Click Chemistry and Materials Research

    Research institutions and contract R&D labs purchase 4-Pentyn-1-ol as a precision reagent for copper-catalyzed azide-alkyne cycloaddition (CuAAC, “click chemistry”), supporting the development of new macromolecules, bioconjugates, and functionalized surfaces. The material’s stability and well-defined end groups enable advanced material prototype and bioactive compound screening. Analytical-grade specification and full documentation of assay and moisture content provide R&D departments with the reproducibility needed for patent filings and tech transfer.

    Industry compliance standards

    • ACS Reagent Chemicals Purity Standards
    • ISO/IEC 17025 Laboratory Accreditation (analytical certification)
    • OECD GLP (Good Laboratory Practice) for research records
    • Material Safety Data Sheet (MSDS) compliance with GHS labeling

    Typical usage ratio

    • 0.1–2 molar equivalents in azide-alkyne conjugation trials
    • Adjusted per target molecular weight or degree of functionalization required

    Downstream process integration

    • Dosed manually or with auto-dispensing systems in microscale to kilogram R&D batches
    • Used in one-pot, stepwise, or sequential addition reactions for rapid screening studies

    Final product types

    • Novel triazole-linked peptides and oligonucleotides
    • Functionalized polymers for medical device coatings
    • Advanced dendrimer branches and star-shaped polymer prototypes
    • Surface-modified nanoparticles for material testing
    Free Quote

    Competitive 4-Pentyn-1-ol prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    4-Pentyn-1-ol: A Chemist’s Take on a Unique Building Block

    Understanding 4-Pentyn-1-ol in Modern Synthesis

    Every year, thousands of kilograms of specialty alcohols move through our manufacturing lines. Among them, 4-Pentyn-1-ol stands out for its role as both a basic and intermediate chemical in countless synthetic pathways. Chemists know this material as a five-carbon alkyne with a primary alcohol group. Structurally, it’s C5H8O, with the triple bond at one end and the alcohol at the other, and that simple arrangement is exactly what makes it valuable for diverse applications.

    Drawing on years spent scaling up and refining this product, I’ve learned that there’s always something new to say about this molecule. Factors like triple-bond functionality, clean end-group reactivity, and manageable handling set it apart from many saturated alcohols and make it an anchor in both R&D and industrial production schemes.

    Our Manufacturing Experience

    I’ve seen every step of our process, right from substrate sourcing to final bottling. Each stage is engineered to minimize contaminants, starting from careful handling of acetylenic starting materials. For example, acetylene-based routes often invite impurities that compromise both yield and subsequent reactions. Purity matters, and we’ve put in the work to reach levels above 98%, thanks to a close watch on distillation temperature and acid-wash treatments. This focus directly translates into repeatable, high-yield performance in customer labs.

    We deliver 4-Pentyn-1-ol in clear, odorless form, typically as a colorless to slightly yellowish liquid. With a boiling point near 142-143°C and a density around 0.88 g/cm³, the product ships easily in common polyethylene or glass containers, offering stability during both short- and long-distance transport. Our QC team checks water and peroxide content regularly because trace oxidation can limit shelf life and, in rare cases, lead to safety concerns.

    The Value in Alkynyl Alcohols

    It’s easy to overlook why a simple molecule like 4-Pentyn-1-ol still lands on the hotlist for synthetic chemists. We watch laboratories choose this compound for Sonogashira and Cadiot-Chodkiewicz coupling reactions, where the terminal alkyne launches cross-coupling with aryl or vinyl halides. This backbone builds complex molecules that drive pharmaceutical, material, or agrochemical development.

    From our vantage point, the presence of a terminal triple bond means robust reactivity—you almost never see this kind of handle in saturated alcohols like 1-Pentanol or even unsaturated ones like 1-Penten-3-ol. 4-Pentyn-1-ol allows regioselective additions and cyclization protocols that don’t always succeed with saturated or internal alkynes. The product’s straight carbon chain also enables it to participate cleanly in elongation and homologation reactions, something branched analogs often compromise.

    From Synthesis to Application

    Watching our product go from a barrel in the plant to a key ingredient in some of the most intricate molecular designs has driven home the industrial importance of reliable intermediates. 4-Pentyn-1-ol doesn’t sit on shelves for long. We supply it to researchers preparing propargyl ethers, halogenated derivatives or complex macrocycles. Our supply chain partners regularly call for assured quality, as minor contaminants derail platinum- and palladium-catalyzed processes. A little extra moisture or residue from previous distillation runs can ruin an entire week's worth of combinatorial chemistry.

    We also observe the alcohol group’s versatility. It opens the door for selective protection and deprotection strategies. Trityl, silyl, or benzyl groups go on or off smoothly. In one recent batch, a client reported building an azide derivative for click chemistry in less than a day, saving a project previously held up by low-yielding alcohol-to-azide conversions using less pure reagents.

    Comparing 4-Pentyn-1-ol to Other Alcohols

    No matter how deep your catalog runs, simple side-by-side comparisons reveal what makes 4-Pentyn-1-ol unique among C5 alcohols. Versus 1-Pentanol, it introduces a triple bond, making it almost twice as reactive in elective pathways. Saturated alcohols offer few options for constructing bis-aryl frameworks or adding new functional groups through click reactions. Compared to allylic alcohols, the extra unsaturation means you get different regioselectivity in epoxidation and oxidation steps.

    We’ve compared purification processes for 4-Pentyn-1-ol and its closest analogs. While internal alkynes such as 2-Pentyne-1-ol avoid acetylene-based reactivity, they trade away the simplicity of terminal functionalization. Chemists seeking selective acylation gravitate toward our material for cleaner yields, especially in the context of complex molecule construction. Gone are the work-ups where you have to fish out minor by-products at every turn.

    Real-World Use Cases

    We’ve worked directly with both pharmaceutical and application laboratories developing next-generation anti-cancer and anti-inflammatory agents. In one typical synthesis route for a key heterocycle, the triple bond of 4-Pentyn-1-ol served as the keystone for ring-closure; alternate alcohols couldn’t deliver the required reactivity. That same batch went on to underpin a pilot run that cleared regulatory milestones. In many pilot programs, finding a batch of material with off-specification purity led to chain reactions of failed reactions and months of lost work—solving this means a lot on our end.

    Material scientists in our network use 4-Pentyn-1-ol as an anchoring point for functional polymers. The terminal alkyne polymerizes with azides, while the alcohol group permits further derivatization with acrylates or epoxy groups. These functionalized polymers show up in everything from adhesives to hydrogels. We’ve scaled up customized orders where bespoke length and purity enabled researchers to develop new photonic materials.

    Production Considerations and Quality Control

    Our process does not just focus on basic output. In routine scale-up, the exothermic nature of some coupling reactions forces strict thermal control, or you risk runaway scenarios. Our technicians monitor temperature and pressure at every stage, tracking bottlenecks. Fractional distillation apparatus is calibrated regularly to avoid cross-contamination from other alcohols or alkynes. We don’t just depend on standard titrations for alcohol content: our lab runs gas chromatography on each batch, flagging trace impurities down to parts-per-million.

    Managing shelf life is a real concern. The alkyne group makes 4-Pentyn-1-ol more susceptible to unwanted polymerization or oxidative changes than a plain alcohol. Storing bulk drums under inert gas reduces risk and lets our clients store inventory longer without worrying about subtle breakdowns. The client feedback loop is important—early training and in-plant demonstrations have given customers peace of mind around both handling and disposal.

    Regulatory and Safety Insights

    Making and moving 4-Pentyn-1-ol isn’t only about synthesis and shipping. Safety regulations vary across markets. We follow REACH and GHS requirements for labeling and transport, tying every container’s serial to batch analysis. Our staff completes annual safety training so end-users receive material along with current MSDS sheets—a practical need, since the alkyne can sensitize organic peroxides and, under rare circumstances, combust in poorly ventilated labs. Training and clear labeling reduce risk without slowing down downstream R&D timelines.

    Since 4-Pentyn-1-ol is not classified as a controlled precursor in most regions, researchers enjoy relatively streamlined ordering. We still work with local regulatory consultants whenever we see a customer scaling up to pilot or commercial use cases, a lesson learned after an early client faced customs delays from missing documentation. This close connection between manufacturing and regulatory compliance often makes the difference between seamless supply and missed project deadlines.

    Trends in Downstream Chemistry

    The demand profile for 4-Pentyn-1-ol evolves year by year. I’ve seen a surge in orders from contract research organizations supporting combinatorial chemistry. The flexibility of the molecule shows up in its many offspring—propargylated sugars, functionalized aromatics, and next-generation surfactants. More than a specialty product, it acts as an unlocking tool, making otherwise complex transformations possible using simple transition-metal-catalyzed protocols.

    Recently, sustainable and green chemistry trends have driven demand for higher atom-efficiency processes. Our technical team has been working with third-party labs to validate routes using less solvent and fewer hazardous reagents, all made possible by the reliable triple-bond and alcohol functionality. Since 4-Pentyn-1-ol often participates in one-pot reactions, researchers looking to reduce waste and simplify purification cycles lean on its clean conversion properties.

    Feedback and Technical Service

    Clients often invite our technical staff to consult on reaction troubleshooting and process optimization. In one memorable case, a customer experienced side-product formation in a copper-catalyzed coupling due to residual base in the alcohol. Our team traced the problem to a subtle shift in neutralization pH during the final wash step. By adjusting the quenching protocol and tweaking distillation pressure, we returned to reliable, high-yield runs within two production cycles. Sharing that kind of in-field know-how sets manufacturers apart from resellers or global traders offering only a COA and a pallet tag.

    We meet regularly with research teams to discuss the changing needs of emerging fields. Opportunities to supply high-purity bulk for a specialty ink producer, or micro-scale lots for an academic group developing molecular sensors, remind us that every batch matters. The flexibility to scale up or down—without introducing time-wasting paperwork or arbitrary minimums—means more projects move from theoretical to practical at a pace that suits research, not bureaucracy.

    Addressing Supply Challenges

    Back in early pandemic days, disruptions in raw acetylene supply forced tighter prioritization across product lines. We adapted by validating additional suppliers and lengthening process buffers. This adaptability has stuck, even as global logistics improved. Customers relying on 4-Pentyn-1-ol for life sciences work see us as a consistent source in an industry where three-week delays can shutter entire workflows. Our on-site storage and continuous process monitoring have insulated both lab-scale and industrial users from common out-of-stock headaches.

    International expansion has required sharper logistics. Moving 4-Pentyn-1-ol across borders needs clear paperwork and Real-time tracking. Our shipping and compliance teams swapped static batch reporting for digital lot tracking, integrating each shipment’s route to customer facilities. This accountability builds relationships. Clients don’t just check a delivery date; they see analytics on lead times and shelf life, offering real control over their project timelines.

    Commitment to Consistency and Reliability

    After all the specialization and technical documentation, the measure of a manufacturer’s value comes down to consistency. Every chemist who orders 4-Pentyn-1-ol—whether for a groundbreaking macrocycle or a repetitive isolation—expects the same quality, time after time. Our lab staff understand that even the smallest shift in feedstock or process conditions shows up in reaction outcomes. They calibrate instruments daily and keep detailed session logs tracking each run. This routine work forms the backbone of reliable, reproducible product.

    In one instance, a unique odor variant triggered a round of process validation. Instead of delivering product with an unexpected sensory profile, we treated and re-analyzed batches until every lot matched spec. This hands-on approach isn’t just about meeting a number; it’s about maintaining trust with researchers who depend on fast, trouble-free experimentation.

    Looking to the Future of 4-Pentyn-1-ol Utilization

    The future of 4-Pentyn-1-ol will continue to be shaped by innovation in both method and material. New transition metal catalysts and late-stage functionalization strategies keep researchers searching for more reliable starting materials. In the past year, advances in click chemistry and bioconjugation have positioned terminal alkynes even more squarely in the spotlight.

    Our R&D team already collaborates with partners to develop next-generation derivatives—from fluorinated analogs used in PET imaging, to isotopically labeled variants for metabolic tracing. Each modification builds on our base product, using the same synthesis standards and batch monitoring to ensure nothing slips through unseen. The flexibility of 4-Pentyn-1-ol means it continues to anchor not only industrial syntheses, but also the most demanding scientific applications on the market.

    Summary: Why 4-Pentyn-1-ol Has Enduring Value

    Over years of work and countless production runs, I’ve seen first-hand how much reliability and reactivity matter in specialty chemicals. 4-Pentyn-1-ol’s triple bond and primary alcohol group deliver a level of chemical flexibility that raises it well above its straight-chain or fully saturated peers. Our unique production insight and commitment to both process control and application support ensure that researchers and manufacturers working at the sharp edge of chemistry can count on every drop. The work isn’t always glamorous, but the results are clear: pure, reliable, and ready for whatever transformation comes next.