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3-Phenyl-2-Propyn-1-ol

    • Product Name 3-Phenyl-2-Propyn-1-ol
    • Alias Phenylpropargyl alcohol
    • Einecs 203-937-5
    • 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

    103594

    Chemical Name 3-Phenyl-2-Propyn-1-ol
    Cas Number 933-97-1
    Molecular Formula C9H8O
    Molecular Weight 132.16 g/mol
    Appearance Colorless to light yellow liquid
    Boiling Point 137-139 °C (12 mmHg)
    Density 1.086 g/cm3 (at 25 °C)
    Refractive Index 1.574-1.577
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C#CC(O)C1=CC=CC=C1
    Inchi InChI=1S/C9H8O/c1-2-8(10)9-6-4-3-5-7-9/h1,3-8,10H
    Synonyms Phenylpropargyl alcohol; 2-Propyn-1-ol, 3-phenyl-
    Flash Point 106 °C

    As an accredited 3-Phenyl-2-Propyn-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 is a 100g amber glass bottle with a secure screw cap, labeled "3-Phenyl-2-Propyn-1-ol, 99% purity."
    Shipping 3-Phenyl-2-Propyn-1-ol is typically shipped in tightly sealed, chemical-resistant containers to prevent leaks and exposure. It should be transported in accordance with local regulations for hazardous chemicals. Avoid extreme temperatures, ignition sources, and physical damage. Shipping documentation must include proper labeling and safety data sheets for safe handling and compliance.
    Storage 3-Phenyl-2-Propyn-1-ol should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Store in a cool, dry, and well-ventilated area, segregated from oxidizing agents and strong acids. Clearly label the container and keep it in a dedicated flammables cabinet for added safety. Avoid prolonged exposure to air or moisture.
    Application of 3-Phenyl-2-Propyn-1-ol

    Applications of 3-Phenyl-2-Propyn-1-ol in Industrial Manufacturing

    As a specialized manufacturer, we supply 3-Phenyl-2-Propyn-1-ol for production processes across the fine chemicals and specialized material sectors. Our expertise supports downstream industrial users in strictly regulated, high-value applications, maximizing the raw material’s reactivity and performance within demanding formulation protocols.

    1. Pharmaceutical Intermediate Synthesis

    3-Phenyl-2-Propyn-1-ol enables key transformations in the synthesis of APIs, particularly within central nervous system (CNS) and anti-inflammatory small molecule pipelines. Its propargylic alcohol group serves as a building block for coupling and cyclization steps in pyridine, indole, and phenylacetylene derivative frameworks. Its purity profile matches rigorous pharmaceutical manufacturing standards, supporting consistent API yields and low impurity thresholds throughout multistep organic syntheses.

    Industry compliance standards

    • Good Manufacturing Practice (ICH Q7, EU GMP, US FDA cGMP)
    • USP, EP, JP monograph reference compliance in final API synthesis stages
    • REACH registration for pharmaceutical chemical intermediates
    • Certificate of Analysis aligned with customer-specific QC protocols

    Typical usage ratio

    • 0.5–2.5 molar equivalents per batch, varying based on targeted synthetic route and desired throughput; adjusted for direct coupling or Grignard addition steps.

    Downstream process integration

    • Added during intermediate assembly (e.g., Sonogashira, C–C bond formation, or nucleophilic addition stages) prior to core API cyclization or functionalization.

    Final product types

    • Active Pharmaceutical Ingredients for CNS indications
    • Non-steroidal anti-inflammatory drug intermediates
    • Pyridine derivative API scaffolds
    • Finished small molecule APIs incorporating propargylic moieties

    2. Agrochemical Active Ingredient Manufacturing

    Many crop protection product synthesis pathways leverage the unique reactivity of 3-Phenyl-2-Propyn-1-ol for producing pyrrole, imidazole, and phenylacetylene based active ingredients. Its triple bond position enables regioselective halogenation and direct heterocycle construction, allowing downstream formulators to tune the resulting molecules for target-specific efficacy in herbicides and fungicides. Process safety and batch homogeneity are monitored in line with increasing global environmental scrutiny on agrochemical production chains.

    Industry compliance standards

    • ISO 9001 and ISO 14001 for agrochemical manufacturing
    • FAO/WHO specification for technical active ingredients
    • EU Regulation (EC) No 1107/2009 for pesticide approval
    • China GB 2763-2021 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 0.2–1.2 molar equivalents incorporated relative to the main starting reagent, depending on batch scale and final molecular architecture.

    Downstream process integration

    • Utilized in controlled-batch reactors as a propargylic coupling partner, commonly preceding heterocycle ring closure or halogen functionalization stages.

    Final product types

    • Fungicide active ingredients based on propargyl aryl skeletons
    • Herbicide intermediates featuring terminal alkynes
    • Crop protection agents (technical-grade solids and concentrated liquids)
    • Finished pesticide actives for further formulation

    3. Specialty Fragrance and Aroma Compound Production

    The aromatic and propargylic structure of 3-Phenyl-2-Propyn-1-ol makes it valued for high-purity aromatic intermediate formulations in the fine fragrance and industrial aroma compound sector. Its controlled addition in synthetic perfume bases yields novel aroma chemicals for floral, spicy, and woody notes, often via subsequent esterification or acetylene coupling. Stringent impurity and allergen content control are maintained to suit IFRA and regulatory requirements for direct and indirect skin contact fragrances.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • EU Cosmetics Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 9235:2013 for aromatic raw materials
    • REACH SVHC criteria and allergen content disclosure compliance

    Typical usage ratio

    • 0.01–0.25% by weight in the concentrated fragrance or aroma compound blend, fine-tuned based on target aroma intensity and safety exposure risk evaluation.

    Downstream process integration

    • Dosed at the alcohol or essential oil blending stage; proceeds to downstream esterification, acetylene coupling, or direct compounding for aroma profile enhancement.

    Final product types

    • Fine fragrance concentrates
    • Industrial aroma blends for personal care
    • Aromatic intermediates for candle and home care products
    • Synthetic musks incorporating phenylpropargylic structure

    4. Polymerization and High-Performance Resin Modification

    In engineered resin manufacturing, 3-Phenyl-2-Propyn-1-ol functions as a specialty monomer or chain modifier. Its incorporation confers improved rigidity, thermal endurance, and chemical resistance when grafted or copolymerized into epoxy, polyurethane, or acrylic resin matrices. The material’s precise dosage and reactivity require strict lot traceability and compatibility assessment with base resin protocols, aligning with industry quality systems demanded by electronic encapsulants and specialty coating producers.

    Industry compliance standards

    • ISO 9001 for specialty resin manufacturing
    • UL 94 and IEC 60695-11-10 flammability assessment (final electronics encapsulation materials)
    • RoHS 2011/65/EU and REACH Annex XVII restrictions for electronic-grade polymers
    • ASTM D638, D790 performance standards for thermoset resins

    Typical usage ratio

    • 0.05–0.8% by weight of precursor resin; specific incorporation rates adjusted based on targeted modification of glass transition temperature and solvent resistance.

    Downstream process integration

    • Introduced at resin prepolymer or modifier addition stage, followed by in-situ polymerization, chain extension, or end-group capping within the reactor.

    Final product types

    • High-performance epoxy molding compounds
    • PCB encapsulation resins for electronics
    • Thermal resistant industrial coatings
    • Modified polyurethane adhesives

    5. Analytical Derivatization Reagent Production

    High-purity grades of 3-Phenyl-2-Propyn-1-ol are utilized to manufacture derivatization agents for use in quantitative analytical testing, particularly for GC/MS and HPLC workflows requiring selectivity for carbonyl and active hydrogen compounds. Its integration allows chemical analytical laboratories and reagent suppliers to provide enhanced chromatographic discrimination and improved sample detection limits, supporting pharmaceutical, food safety, and environmental quality control sectors.

    Industry compliance standards

    • ISO/IEC 17025 for accredited analytical reagent production
    • Pharmacopeial methods (USP, EP, JP, ChP) reference for laboratory-use reagents
    • OECD GLP (Good Laboratory Practice) guidelines
    • 21 CFR Part 211 for laboratory chemical manufacturing quality

    Typical usage ratio

    • 5–150 μg per sample reaction for analytical-scale derivatization; process scaled proportionally for bulk reagent manufacture.

    Downstream process integration

    • Used during synthesis of bespoke derivatization agents, typically through acylation or alkylation to functionalize primary amines, carbonyls, or thiols prior to instrument analysis.

    Final product types

    • GC/HPLC derivatization kits
    • Laboratory reference standards
    • Test sample preparation reagents
    • Calibration kits for environmental analysis
    Free Quote

    Competitive 3-Phenyl-2-Propyn-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.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

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    Certification & Compliance
    More Introduction

    3-Phenyl-2-Propyn-1-ol – A Practical View from the Manufacturer

    Understanding 3-Phenyl-2-Propyn-1-ol: Product Overview

    In the chemical manufacturing business, we sometimes meet molecules that punch well above their weight, and 3-Phenyl-2-Propyn-1-ol is one of them. With the chemical formula C9H8O and CAS number 538-48-9, this alkyne alcohol stands out because of its reactive triple bond paired with a benzene ring and primary alcohol group. Our production batch currently offers a purity level above 99%, measured by standard gas chromatography, and we keep the water content below 0.2%. For those using 3-Phenyl-2-Propyn-1-ol in organic synthesis, stability and impurity control mean everything. Long before this product leaves the factory, we scrutinize every drum for color, clarity, and residual solvents. Our goal is not just to meet your immediate chemical requirements but also to keep the product reliable for your downstream work.

    Features that Matter in Daily Production

    As manufacturers, we value the fine balance between reactivity and storage stability. 3-Phenyl-2-Propyn-1-ol, with its boiling point around 265°C and a melting point near 40°C, falls into a range that allows for straightforward handling without the headaches of volatile losses or crystalline blockages in pipes under standard conditions. Every time we package this material—usually in dark glass containers lined for moisture resistance—we think about the user’s need to avoid contamination or air contact that could jeopardize sensitive reactions down the line. Whether a customer needs 10 kg or a metric ton, our filling lines are calibrated to reduce oxygen pickup and dust, supported by nitrogen blanketing before each drum is sealed.

    Applications: Real-World Utility and Outcomes

    From our vantage point, the actual value of 3-Phenyl-2-Propyn-1-ol shows up in its practical use in synthesis labs and process plants. Its triple bond and benzyl alcohol group serve as handles for building more elaborate molecules. Contract manufacturers frequently give us feedback on how the propargyl alcohol group provides a useful starting point for Sonogashira or click-type coupling reactions. The aromatic ring brings stability and electronic richness that let research chemists push towards designer pharmaceuticals, fine chemicals, or targeted ligands. Research and scale-up teams seek out our product not only for its purity but for its consistency from drum to drum. Here, we stick to strict production cycles using verified starting materials—not all suppliers make the effort to track and log their raw materials as closely as we do.

    More than a few established pharmaceutical routes rely on this compound to introduce alkyne motifs, and agrochemical companies use it to create stable, active ingredients with the help of our batch-tested material. As a manufacturer, we know that a few tenths of a percent impurity in such multifunctional intermediates can kill whole product lines—especially when these defects pass unnoticed into the next stage of synthesis. So we maintain a hands-on approach to production: analytical chemists walk the floor, looking for shifts in physical properties or any color changes, even after the formal tests.

    What Sets Our 3-Phenyl-2-Propyn-1-ol Apart?

    Working inside the plant gives you a unique perspective on what goes wrong in this business, and the details matter. Customers sometimes approach us after dealing with unreliable batches from smaller suppliers: yellowed product, poor yield in their final reaction, or unexplained byproducts. Often, these problems stem from poor temperature control during distillation, incomplete removal of reactant residues, or even issues with storage during shipping. We have worked out an all-season process to correct these, including precise temperature ramping and post-production holding periods to catch any tendency to oxidize or darken over time.

    Many producers on the market cut corners with less thorough in-process monitoring, but we track parameters like residual moisture and specific gravity in real time, pushing the analytics beyond the minimum required. We’ve learned—sometimes the hard way—that consistent product doesn’t come from a generic protocol. Every modification in upstream feedstocks, catalyst batches, or even supply-chain delays can change the chemistry downstream. Our feedback loops work because plant operators, QC chemists, and engineers all see the data and talk through any deviations. This attention to detail results in a 3-Phenyl-2-Propyn-1-ol grade with sharp, reproducible melting and boiling points, clear transparency, and zero off-odors.

    Comparative Realities: How It Differs from Similar Chemicals

    We often field calls asking how 3-Phenyl-2-Propyn-1-ol compares with other common alkyne alcohols, like propargyl alcohol or 3-butyn-1-ol. Here’s what we’ve seen: the phenyl ring in our compound brings a level of aromatic stability and modulates reactivity. While parent propargyl alcohol reacts aggressively, especially with strong bases or transition metal catalysts, 3-Phenyl-2-Propyn-1-ol shows steadier, more predictable reactivity thanks to the electron-withdrawing and resonance participation from the benzene ring. That gives formulation chemists more wiggle room on process conditions and reduces unwanted side reactions in scale-up.

    Some users tell us they tried running reactions designed for propargyl alcohol but switched to the phenyl-derivative because downstream purification becomes easier; byproducts tend to separate cleanly, and the main product elutes with higher selectivity on standard chromatography columns. Solubility profiles also shift noticeably—our product dissolves seamlessly in common organic solvents like dichloromethane or toluene, but remains easily extractable without phase transfer headaches.

    Physically, the higher molecular mass and aromatic core mean stronger odor and a tendency to form crystalline solids at room temperature. We embrace this, as the crystalline form often signals lower volatility and a longer shelf life during transit. The melting point, a degree or two above room temperature, lets us keep the product stable but easy to handle with minimal heating in all but the coldest shop floors. Technicians have commented that they appreciate not having the compound seep out or evaporate unnoticed, which happens with lighter, more volatile alkynes.

    Use Case Experiences From the Shop Floor and Lab Bench

    Years of direct feedback have shaped how we prepare and recommend 3-Phenyl-2-Propyn-1-ol for users across the spectrum. In pilot plants, we notice reactions involving this molecule often scale more readily than those starting from plain propargyl alcohol. The added bulk from the phenyl ring lets operators tune reaction rates and control exotherms—never just an academic concern when making multi-kilogram lots. Teams report lower batch-to-batch variation in yields and easier separation of side-products.

    Business partners in the pharmaceutical sector use our material as a direct intermediate in the synthesis of kinase inhibitors or other small molecule drugs. They appreciate that our batch control eliminates the need for additional drying and filtration steps, saving time and raw materials. Some of our agricultural clients feed 3-Phenyl-2-Propyn-1-ol into multi-step processes to create pest control compounds that need both alkyne reactivity and aromatic robustness. Their buyers have come back for repeat lots, citing not just purity but consistent physical handling behavior—no sticky residues, uniform color, and storage stability for months at a time.

    In our R&D corner, we keep a supply of 3-Phenyl-2-Propyn-1-ol on hand for small molecule library synthesis and test it regularly against incoming lots. Over time, we’ve honed our cleaning protocols for reactors and transfer lines to avoid cross-contamination and have shared these insights openly with select partner labs and customers. By documenting every step and collecting user data about unexpected side reactions, we refine our process and ensure smooth handover from our plant to your facility.

    Quality Control Rooted in Experience

    Many bulk producers tout their big volumes, but the real question lies in how well they catch problems before they reach buyers. In our facility, QC staff dedicate time to cross-check physical and chemical purity with each new production cycle. Each lot goes through a gauntlet of tests: chromatographic verification, spectroscopic fingerprinting, moisture measurement, and a thermal stability screen. On top of conventional purity checks, our team investigates possible breakdown pathways, especially during prolonged storage or after transport over long distances.

    Years ago, we noticed certain packaging formats let trace air enter during heat cycles in transit. Those lessons led us to shift entirely to nitrogen-flushed bottles with tamper-evident closures. That single change cut opening complaints by over 80%. Through ongoing collaboration with transport partners, we cut down on temperature spikes and pressure shifts, further improving lot stability. Even small tweaks—like adjusting drum liner materials or switching to higher-barrier seals—translate directly to fewer field failures for our customers.

    We also believe in transparency: every shipment includes a formal certificate of analysis, but we maintain archived retention samples for up to three years per batch. Users with unique requirements—for example, ultra-dry or specifically particle-sized material—can receive special production runs with detailed documentation. Our process engineers stand ready to adjust cycles if feedback indicates a need; that’s how we have kept defect rates well below the industry average.

    Downstream Impact and Environmental Responsibility

    Our responsibility stretches beyond just making a pure product. Safe use and environmentally sound disposal count as much to us as any product spec. 3-Phenyl-2-Propyn-1-ol carries moderate toxicity, so we stress best handling practices for those working with kilo quantities. Our SDS sheets are updated promptly after every regulatory adjustment, and our staff responds directly to questions about containment or accidental release. Plant operators have undergone workplace training tailored to alcohol alkynes, ensuring spills or off-gassing events are minimized and documented.

    On the production side, our team recycles solvents through in-house distillation and reuses wash solvents whenever possible. Process waste containing 3-Phenyl-2-Propyn-1-ol undergoes neutralization and is routed through aerobic treatment to break down reactive intermediates before disposal. We report regularly on material outputs and emissions and follow all local and international protocols. Our plant engineering team has helped us reduce residual solvent loss by over 20% in the last five years, using closed-loop systems developed after an internal audit revealed unnecessary open-transfer steps.

    For downstream users, we offer ongoing guidance on both regulatory reporting and practical environmental controls. We know—because we've helped design them—that many customers have improved their own solvent capture and waste handling based on our feedback and monitoring data.

    Looking Ahead: Product Versatility and Custom Manufacturing

    Modern synthesis asks for ever-more specialized building blocks, and as manufacturers, we receive requests for modifications of 3-Phenyl-2-Propyn-1-ol to build in new utility. Our technical team regularly evaluates custom derivatives or tweaks to the supporting chemical infrastructure. Whether it’s adjusting the water content, particle size, or stabilizing agents, we balance customer desires with process realities. Some applications—such as advanced material synthesis or the creation of designer ligands for catalysis—often rely on exceptional purity, or tolerance to specific solvents or temperatures.

    Thanks to our long-track record, we can provide small-scale pilot lots or full production runs without compromising documentation integrity or process repeatability. Each request for a change sparks a review within our process R&D group, setting up quick tests and pilot-scale demonstrations before upgrading to plant scale.

    We also keep our ear to the regulatory ground. Each year brings subtle changes to the status or recommended levels for certain chemical families. Our compliance staff is proactive in updating batch testing requirements and labeling, ensuring downstream users don't face compliance surprises.

    Collaborating for Continuous Improvement

    Our relationships don't end at the loading bay. Many clients keep us in the loop about their successes and challenges, providing detailed reports on yields, product quality, and unexpected hurdles they face. This open communication has influenced several rounds of process improvement and allowed rapid resolution of issues. For example, reports of slight color shifts or off odors led to refining our distillation end-points and post-filling venting times. We believe these back-and-forths make our product better and lower the risk of unexpected batch failures for users.

    We invest in ongoing training for our production and QC teams. Everyone—from the line operator to the analytical chemist—receives regular updates about reaction mechanisms, troubleshooting strategies, and case studies involving both success and failure. Rather than leaving improvement solely to management, suggestions percolate up from all levels and result in new SOPs shared company-wide.

    These internal steps feed directly into our production quality. Each successful process tweak, each carefully documented investigation, translates into a more dependable supply of 3-Phenyl-2-Propyn-1-ol for every customer, whether for small academic labs or major industrial users.

    Final Words from the Factory Floor

    Working directly with 3-Phenyl-2-Propyn-1-ol day after day, we recognize that solid manufacturing means more than hitting a spec sheet. It means understanding the true needs and challenges of users, refusing to compromise on quality, and learning from both good and bad outcomes. Every improvement in our workflow, every tweak to packaging or process, stems from real experience and hands-on troubleshooting.

    For anyone working in organic synthesis, pharmaceuticals, or specialty chemicals, reliable intermediates like 3-Phenyl-2-Propyn-1-ol can make the difference between project success and weeks of frustration. As actual chemical manufacturers, we stand by our track record and the lessons learned from years in the field, and we invite ongoing dialogue to keep improving. Reach out to our technical staff with your real-world problems: there’s no substitute for direct collaboration and honest feedback.