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Phenylpropiolic Acid

    • Product Name Phenylpropiolic Acid
    • Alias 3-Phenyl-2-propynoic acid
    • Einecs 207-014-3
    • 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

    940123

    Name Phenylpropiolic Acid
    Cas Number 614-74-2
    Molecular Formula C9H6O2
    Molecular Weight 146.14
    Appearance White to off-white crystalline powder
    Melting Point 137-141°C
    Solubility In Water Slightly soluble
    Density 1.242 g/cm3
    Pka 2.3 (carboxylic acid group)
    Smiles C#CC(=O)Oc1ccccc1
    Inchi InChI=1S/C9H6O2/c10-9(11)7-8-5-3-1-2-4-6-8/h1-6H,(H,10,11)

    As an accredited Phenylpropiolic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for Phenylpropiolic Acid is a 100g amber glass bottle, securely sealed, labeled with hazard warnings and product information.
    Shipping Phenylpropiolic acid should be shipped in tightly sealed containers, protected from light, moisture, and physical damage. It should be kept at ambient temperature and handled as a potentially hazardous material according to local regulations. Include appropriate labeling and safety documentation. Avoid shipping with incompatible substances, such as strong oxidizing agents.
    Storage Phenylpropiolic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it at a cool, dry place, away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Adequate ventilation is necessary in the storage area. Always label containers clearly and handle with appropriate personal protective equipment to ensure safety.
    Application of Phenylpropiolic Acid

    Applications of Phenylpropiolic Acid in Industrial Manufacturing

    Phenylpropiolic acid serves as a high-purity specialty intermediate in selected chemical sectors, consistently supporting downstream innovation in pharmaceutical synthesis, agrochemical development, organic electronics, and advanced fine chemical manufacturing. Leveraging our vertically integrated production, we provide traceable origin, batch-specific documentation, and technical advice directly linked to each key industrial usage.

    1. Synthesis of Active Pharmaceutical Ingredients (APIs)

    Manufacturers incorporate phenylpropiolic acid as a critical synthon in the construction of molecular frameworks for nonsteroidal anti-inflammatory drugs (NSAIDs) and select central nervous system (CNS) agents. It enters stepwise multi-stage synthetic routes, typically as an alkyne donor for ring closure or substitution reactions, where strict trace residue profiles and consistent lot analysis are mandatory. Production lines adjust charge ratios according to targeted reaction yields and downstream impurity control protocols.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) standards for API intermediates
    • European Pharmacopoeia (Ph. Eur.) monographs, Section 5.10 related substances
    • 21 CFR Part 210/211 (FDA cGMP for pharmaceuticals)

    Typical usage ratio

    • Formulation input ranges from 0.5 to 2.0 molar equivalents, modified by specific API route requirements and desired yield versus byproduct minimization.

    Downstream process integration

    • Charged at the initial reaction stage for alkynylation or condensation sequences.
    • Subject to intermediate purification (crystallization, extraction) before the next transformation step.
    • Residual monitoring via HPLC/GC as required by API impurity profiles.

    Final product types

    • Pharmaceutical intermediates for anti-inflammatory medicines
    • Precursors for CNS drug candidates
    • Reference compounds for analytical standards in medicinal chemistry

    2. Crop Protection Compound Synthesis

    Leading agrochemical R&D groups utilize phenylpropiolic acid as a fundamental building block in constructing aryl-substituted acetylenic herbicides and fungicide actives. The compound offers precise alkyne connectivity critical for patent-unique variants, and quality audits regularly demand origin traceability and impurity mapping for both R&D validation and upscaling phases. Processing technicians tailor reagent ratios according to batch size, target conversion, and process safety limits.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • FAO/WHO JMPR specification benchmarks for pesticide raw materials
    • REACH (EC 1907/2006) registration for European market supply
    • GLP (Good Laboratory Practice) for field trial qualification lots

    Typical usage ratio

    • Addition rates range from 1.0 to 2.5 equivalents per downstream elected synthetic target, variation set by agrochemical product structure and scale-up reproducibility.

    Downstream process integration

    • Loaded in the initial carbon-carbon coupling step for heterocycle or aryl-acetylenic assembly.
    • Undergoes controlled temperature and pH regimes for selective activation.
    • Subject to extraction or vacuum distillation for downstream concentration.

    Final product types

    • Technical active ingredients for selective herbicides
    • Intermediate scaffolds for systemic fungicides
    • Batch samples for regulatory field residue analysis

    3. Advanced Organic Electronic Materials Manufacturing

    Producers of organic semiconductors and advanced materials deploy phenylpropiolic acid in the precursor synthesis of π-conjugated compounds and optoelectronic small molecules. Its precise triple-bonded structure enables the assembly of functionalized arylacetylenes used in organic field-effect transistors (OFETs), OLEDs, and photonic polymers. Strict control of impurity levels, trace metals, and photo-stability parameters shape lot release and integration protocols in electronics manufacturing.

    Industry compliance standards

    • JEITA standards for organic semiconductor purity
    • IPC-4101 for base materials qualification
    • RoHS Directive 2011/65/EU for hazardous substance control
    • ISO 14001 for materials environmental management systems

    Typical usage ratio

    • Charge ratios from 0.8 to 1.2 equivalents relative to co-reactants, optimized by targeted conjugation length and process yield during arylation or cyclization.

    Downstream process integration

    • Introduced during the core backbone-forming reaction (e.g., Sonogashira or Glaser coupling).
    • Followed by chromatographic purification for monomer isolation.
    • Feeds into final polymerization or device ink formulation phases.

    Final product types

    • Organic electronic small molecule precursors
    • Conjugated polymers for flexible displays
    • Photoactive layers for OLEDs and OFETs

    4. Synthesis of Fine Chemical Building Blocks and Specialty Reagents

    Custom fine chemical producers integrate phenylpropiolic acid as a precursor in the manufacture of halogenated alkynes, aryl-substituted carboxylic acids, and specialty ligands for coordination chemistry. This material supports high-complexity downstream conversions, where traceability and microimpurity documentation play critical roles in maintaining production batch quality. Usage scales in these settings are governed by target molecule complexity, regulatory submission batches, and tailored conversion rates.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical production management
    • REACH registration for manufactured intermediates
    • Safety Data Sheet (SDS) requirements per GHS/CLP
    • Custom client quality agreements specifying impurity thresholds

    Typical usage ratio

    • Applied from 1.0 up to 3.0 equivalents per reaction, matched to specific synthetic methodologies and functional group transformations.

    Downstream process integration

    • Employed in halogenation, carboxylation, or transition-metal-catalyzed functionalization stages.
    • Treated with controlled addition rates to manage exothermic reactions.
    • Purified by distillation or crystallization based on end-use purity requirements.

    Final product types

    • Halogenated alkynes for synthetic chemistry
    • Aryl carboxylic acids used in flavors, fragrances, or lab research
    • Custom ligands for organometallic catalyst systems
    Free Quote

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