Products

1-Pentene-3-Ol

    • Product Name: 1-Pentene-3-Ol
    • Alias: allylcarbinol
    • Einecs: 207-926-7
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications
    HS Code 294740
    Iupac Name pent-1-en-3-ol
    Molecular Formula C5H10O
    Molar Mass 86.13 g/mol
    Appearance Colorless liquid
    Boiling Point 97-99°C
    Density 0.822 g/cm³
    Melting Point -89°C
    Solubility In Water Moderate
    Refractive Index 1.419
    Cas Number 2258-47-7

    As an accredited 1-Pentene-3-Ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 1-Pentene-3-ol is supplied in a 250 mL amber glass bottle, sealed with a tamper-evident cap and labeled with safety information.
    Shipping 1-Pentene-3-ol should be shipped in tightly sealed, clearly labeled containers, compliant with applicable chemical transport regulations. It must be protected from heat, ignition sources, and moisture. Shipping should use strong, leak-proof packaging, and include safety documentation such as Safety Data Sheets (SDS). Handle and transport according to hazardous material (HazMat) guidelines.
    Storage **1-Pentene-3-ol** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from sources of ignition or heat. Keep it away from strong oxidizing agents and direct sunlight. Storage containers should be clearly labeled and protected from physical damage. Ensure compatibility with other chemicals in storage and follow standard safety protocols and regulations.
    Application of 1-Pentene-3-Ol
    Purity 98%: 1-Pentene-3-Ol Purity 98% is used in synthesis of pharmaceutical intermediates, where it ensures high-yield and minimal by-product formation. Boiling Point 99°C: 1-Pentene-3-Ol Boiling Point 99°C is used in organic reaction processes, where it allows precise temperature control and efficient distillation. Optical Purity 95% ee: 1-Pentene-3-Ol Optical Purity 95% ee is used in chiral catalyst production, where it promotes enantioselective reactions and improves product specificity. Refractive Index 1.418: 1-Pentene-3-Ol Refractive Index 1.418 is used in formulation of specialty coatings, where it provides uniform mixing and clarity. Stability Temperature Up to 40°C: 1-Pentene-3-Ol Stability Temperature Up to 40°C is used in fragrance compound manufacturing, where it ensures chemical stability and consistent aroma profiles. Density 0.82 g/cm³: 1-Pentene-3-Ol Density 0.82 g/cm³ is used in formulation of agrochemical emulsions, where it enables optimal solubility and dispersion. Water Content <0.2%: 1-Pentene-3-Ol Water Content <0.2% is used in fine chemical synthesis, where it prevents hydrolysis and maintains product integrity. Molecular Weight 86.13 g/mol: 1-Pentene-3-Ol Molecular Weight 86.13 g/mol is used in polymer additive development, where it ensures predictable reactivity and chain length control. Flash Point 15°C: 1-Pentene-3-Ol Flash Point 15°C is used in industrial solvent applications, where it facilitates rapid evaporation and residue-free processing. Assay >99%: 1-Pentene-3-Ol Assay >99% is used in analytical chemistry standards, where it delivers reliable calibration and reproducible quantification.
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    Certification & Compliance
    More Introduction

    1-Pentene-3-Ol: The Flexible Ally for Diversified Synthesis

    A Look Into 1-Pentene-3-Ol and How It Serves Modern Chemistry

    In the world of specialty chemicals, 1-pentene-3-ol stands apart for its unique balance of reactivity and selectivity. As producers who have spent years refining the process and quality of 1-pentene-3-ol, we see the compound at work across projects that run the gamut from perfumery intermediates to pharmaceutical building blocks. Our hands-on approach lets us watch, season after season, how the substance helps chemists shape molecules no other alkene-alcohol hybrid can deliver with the same versatility.

    Understanding the Chemical Character

    With the molecular formula C5H10O and a straightforward linear structure, 1-pentene-3-ol bridges the functions of an unsaturated alkene with a primary alcohol group. This design makes it far more than a minor player in the product chain. In regular practice, synthetic chemists favor 1-pentene-3-ol for coupling reactions that demand controlled addition of new functional groups. The double bond positioned at the first carbon unlocks possibilities for chain elongation, cyclization, and oxygenation. Add the terminal alcohol, and suddenly selective hydrogen bonding and further oxidation routes open up, broadening the horizon for what you can make.

    Model and Purity Matter: How We Approach Manufacturing

    Each batch of 1-pentene-3-ol tells a story traced from raw feedstock all the way through purification. Consistency never arises by chance. Feedstock purity, reaction temperature, time, and the method of distillation all shape the end result. We favor fractional distillation and cooling under inert conditions, so the resulting liquid stays fresh and free of oxidation. Our standard lot offers a nominal purity above 97%, and for customers working in especially sensitive formulations, we have managed consistent deliveries exceeding 99%. The difference comes from years of tuning our equipment and monitoring at every key stage, including infrared and gas chromatography checks.

    Where 1-Pentene-3-Ol Finds Its Most Value

    Down in the lab, we watch synthetic teams reach for 1-pentene-3-ol again and again. Its niche most often sits in the intersection of flavor, fragrance, and pharmaceutical synthesis. Several fine fragrance notes can trace their origins to derivatives formed by oxidation or condensation involving this specific alcohol. The unsaturated bond pairs beautifully with aromatic groups, so flavor chemists build up unique ester structures from this backbone. Pharmaceutical researchers value it because it skips unnecessary branching—its neat backbone slashes the number of by-products and simplifies purification steps during drug synthesis.

    In materials science, a few customers have shown us how 1-pentene-3-ol brings specific value in polymer chemistry. The combination of double bond and terminal alcohol allows for functionalization as a cross-linker or a monomer for certain specialty polymers, particularly those that benefit from precisely tailored polarity. Because we know the source and control the processing, we're able to guarantee contaminant profiles to suit even the more stringent requirements in these cutting-edge fields.

    Standing Apart from Other Alkenols

    Comparison with other five-carbon alkenols highlights the unique advantages of 1-pentene-3-ol. Isomers like 2-penten-1-ol and 3-penten-2-ol offer similar molecular mass but diverge in structure, which translates to different sites for reactivity. 1-pentene-3-ol sets itself apart by positioning the functional groups to facilitate both nucleophilic and electrophilic additions. This allows more efficient synthesis of intermediates where regiochemistry really matters.

    Some customers initially lean toward analogs such as pentanols or pentenes with the double bond in a different site, but feedback from scale-up trials always leads back to 1-pentene-3-ol when site-selectivity and predictable reaction profiles come into play. Alkene position impacts both reactivity with organometallic reagents and susceptibility to rearrangement during heating. With over fifteen years producing this compound, we've learned to anticipate these differences and pass that practical insight to professional teams working in advanced synthesis.

    What It Means to Manufacture 1-Pentene-3-Ol Well

    Quality management for 1-pentene-3-ol takes more than isolating the product. Efforts must focus equally on storage and transport. This molecule, while robust at room temperature, still possesses both unsaturation and a reactive alcohol group. Improper bottling or exposure to strong sunlight can encourage slow polymerization or oxidation into unwanted by-products. We ship in inert-sealed containers and require degassing of tanks after every cycle, just as a measure to keep the chemical profile consistent with our analysis sheets.

    This approach paid off in customer laboratories. Laboratories consuming this molecule in staged syntheses report fewer troubleshooting headaches, improved batch yields, and sometimes a shorter path to regulatory filing—especially important for those pushing active pharmaceutical ingredients toward commercialization. If a chemist trusts that each drum will perform like the last, development time shortens, and projects lose some of the unpredictability that comes with lower-tier products.

    Supporting The Chemist’s Journeys

    Collaboration circles around more than sending high-purity compounds out the door. We view our job as both supplier and technical partner. Each year, we field a steady stream of questions from R&D teams about scalability, compatibility with other synthetic intermediates, or best practices for storage. Relying on practical experience—drawn from both our setup and feedback relayed by users across different specialties—we respond with clear, actionable guidance.

    One example stands out: in a project targeting the synthesis of a new chiral ligand, the customer needed precise control over double bond geometry. Using our high-purity 1-pentene-3-ol as the starting point, they managed to push that reaction along in a way unmatched by runs employing more generic alkene-alcohols. That kind of feedback shapes future batches as we adapt purity specs and packaging suggestions.

    Looking at Upstream and Downstream Sustainability

    These days, conversations about responsible chemistry are routine. As chemical producers, we tackle not only technical hurdles, but also those tied to safety, environmental impact, and traceability. For 1-pentene-3-ol, the path starts with responsible sourcing of principal hydrocarbon streams. We lean into feedstocks derived from as much sustainable origin as possible, scrutinizing suppliers back to the point of extraction.

    Waste management for 1-pentene-3-ol processes has moved into closed-cycle reclamation systems. Over the last five years, we’ve trimmed solvent loss and decreased emissions linked to fractional distillation runs. Our technical crew have struck a balance between tight purity standards and responsible waste minimization strategies, helping downstream partners meet their own sustainability reporting standards.

    On the packaging side, we have phased in recyclable drums and encourage bulk delivery for repeat customers. This reduces the environmental cost associated with single-use plastics and helps streamline the chain of custody, which is especially important for tightly regulated end uses in food, cosmetics, and pharmaceuticals.

    Technical Versatility in Synthesis

    With duality at the core—a reactive double bond and an accessible alcohol group—1-pentene-3-ol can be coaxed through many synthetic transformations. Chemists report smooth results during ozonolysis, selective catalytic hydrogenation, Grignard additions, and protection-deprotection strategies. The terminal alcohol's affinity for protection by silyl ethers or simple acetylation means reaction cascades can be staged with confidence that the backbone will not shift or produce a cocktail of isomerized by-products.

    In flavor chemistry, oxidative transformations yield valuable aldehydes and acids. Fragrance houses favor it for forming macrocyclic musks through cyclization, often relying on the structure’s openness to strategic ring closure in a predictable manner. These transformations gain value from a pure, consistent starting material—something we take pride in providing at scale.

    Challenging Stereotypes in Alkene Chemistry

    For outsiders, unsaturated alcohols might blur together as interchangeable. In daily production, the difference between 1-pentene-3-ol and a close structural cousin becomes clear right from distillation to the last drop poured in the customer’s reactor. Our method of in-process monitoring, supported by both classic wet chemistry and the latest chromatographic techniques, picks up on differences that affect both shelf stability and final conversion rates.

    We have watched the performance delta open up most around temperature-sensitive or light-sensitive reaction routes. Some isomeric alkenols polymerize or degrade with minor shifts in atmospheric oxygen. Our process removes trace metal catalysts and clamps down on possible triggers, making our 1-pentene-3-ol a safer bet for research teams with narrow tolerance windows.

    The Importance of Insight Gained Through Years of Production

    Consistency reflects not only in product quality, but also in how we answer unusual technical questions. Over years of supporting both boutique and industrial users, we’ve seen the way synthetic goals change, and how those changes demand tweaks in the physical properties of the material. For example, a user scaling up cosmetic ingredient production flagged a subtle volatility difference, eventually traced to micro-contaminants stemming from outdated bulk shipping tanks. Changes in our own cleaning protocols—and rapid course changes in distribution—eliminated those headaches in future cycles.

    Product failures often come less from raw purity numbers and more from lack of institutional memory around what different application areas demand. Because we both produce and ship every liter ourselves, our technical staff maintains a living playbook, bridging gaps left by generic suppliers or traders who never see the real laboratory outcome.

    Maintaining Safety and Compliance

    Working with unsaturated alcohols, especially at production scale, means confronting unique safety concerns. 1-pentene-3-ol, while not particularly volatile or dangerous at reasonable temperatures, can still pose inhalation and flammability risks if handled without respect for standard protocols. We instill rigorous safety steps on our own floor—continuous air monitoring, grounded transfer points, single-use antistatic gear—less out of regulatory obligation and more out of long habit passed down from decades of seeing what goes wrong without vigilance.

    Our customers, in many cases, set their own demanding safety baselines. Sharing real-world handling lessons, especially regarding bulk dilution or tank transfer in non-nitrogen-filled spaces, helps downstream partners prevent avoidable incidents. It’s one more way that producers who stick close to their product’s journey add tangible value.

    The Human Side of Production

    Many view the flow of bulk chemicals as an impersonal stream of barrels and drums. In our work, it’s a hands-on process involving chemists, operators, and logistics teams who all see and touch the batch before it ever leaves production. Every generation of staff brings new knowledge, often gleaned from problems solved under urgent timelines. We recall a period when a subtle increase in residual palladium produced off odors in a customer’s flavor intermediate. Technicians and engineers worked overnight cycles tweaking catalyst scavenging steps, sharing notes late into the night, until the issue resolved. Those hard-won lessons now serve every new customer demanding critical odor or taste thresholds.

    Solutions That Start With Listening

    Most product launches or technical responses start with a user question. In our history, requests have ranged from “can you ship in smaller sealed vials for easier expiration tracking?” to “can you alter the purification process to lower aldehyde content?” Through experiments in our pilot plant and knowledge-sharing between user teams, these suggestions often spark permanent improvements. Manufacturers with direct production experience know adjustments in distillation range, metal catalyst choice, or even tank material can yield meaningful, scalable changes for those on the receiving end.

    One successful example grew from a request to limit water content below 0.05%. By fine-tuning the vacuum distillation line and moving to all-glass transfer pathways on packaging days, we achieved moisture content numbers previously considered unattainable for the product at commercial scale. This gets passed along as better reaction yields and fewer side-products in our partner laboratories.

    Anticipating the Road Ahead

    1-pentene-3-ol’s role keeps shifting alongside new discoveries in fields like sustainable perfumery, advanced polymers, and specialty pharmaceutical APIs. As demand for more complex, multifunctional building blocks grows, so too does the need for reliable, high-purity starting materials that fit narrow downstream requirements. Foresight on sustainability measures—sourcing, waste minimization, energy efficiency—has already pushed significant changes in the way we plan new production lines and react to shifts in regulatory landscapes.

    The expertise built across years of producing 1-pentene-3-ol delivers value far beyond a label or spec sheet. Customer feedback and real-world performance inform every part of our process. By maintaining open lines of communication with users and never standing still on quality or safety, we keep finding new ways for this molecule to power creative, efficient advances across a range of scientific fields.

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