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3-Aminophenylacetylene

    • Product Name 3-Aminophenylacetylene
    • Alias m-APA
    • Einecs EINECS 229-246-8
    • 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

    418243

    Product Name 3-Aminophenylacetylene
    Cas Number 64326-35-2
    Molecular Formula C8H7N
    Molecular Weight 117.15
    Appearance Light yellow to brown solid
    Boiling Point 284-286°C at 760 mmHg
    Melting Point 52-56°C
    Density 1.08 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms m-Aminophenylacetylene
    Smiles C#CC1=CC(=CC=C1)N
    Refractive Index 1.630 (predicted)
    Storage Conditions Store at 2-8°C, tightly sealed

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with a tightly sealed cap, labeled with "3-Aminophenylacetylene" and relevant safety and handling information.
    Shipping 3-Aminophenylacetylene is shipped in tightly sealed containers, protected from moisture and light, and labeled according to hazardous material regulations. It should be transported at ambient temperature, handled by trained personnel, and accompanied by appropriate safety documentation, including a Safety Data Sheet (SDS), due to its flammable and potentially harmful nature.
    Storage 3-Aminophenylacetylene should be stored in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers and acids. Keep the container tightly closed and protected from light and moisture. Use appropriate chemical-resistant containers and ensure proper labeling. Store at room temperature unless otherwise specified by the manufacturer or safety data sheet.
    Application of 3-Aminophenylacetylene

    Applications of 3-Aminophenylacetylene in Industrial Manufacturing

    3-Aminophenylacetylene serves as a precision intermediate across several specialized chemical industries. As the manufacturer, we supply this material directly to formulators and processors integrating it into value-added products in pharmaceuticals, specialty polymers, OLED materials, and advanced organic synthesis. Below we detail distinctive downstream application areas, compliance requirements, processing integrations, and typical final product outcomes.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    API producers use 3-Aminophenylacetylene for the construction of key heterocyclic scaffolds, specifically in targeted kinase inhibitors and oncology drug candidates. This intermediate enters Suzuki-Miyaura and Sonogashira coupling reactions, providing an essential handle for the installation of functional acetylene motifs on aromatic cores. Formulators control impurity levels according to regulatory pharmacopoeias, achieving consistent batch quality for clinical-grade manufacturing. The downstream use influences synthetic routes for integrating aromatic amine acetylene fragments into advanced pharmaceutical molecules, particularly where metabolic stability or bioisosteric replacement is needed in small-molecule drugs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP General Chapter <941> Identification of Organic Compounds
    • Ph. Eur. 5.4 Residual Solvents
    • FDA cGMP 21 CFR Part 211

    Typical usage ratio

    • 0.2–1.6 molar equivalents per coupling step, adjusted for yield optimization and route-specific stoichiometry; QC determines residual levels below 0.5% in the final API

    Downstream process integration

    • Direct charge into reactor during palladium-catalyzed cross-coupling step; solvent selection (e.g., DMF, DMSO) based on solubility; purification via preparative HPLC or crystallization before downstream derivatization

    Final product types

    • Targeted cancer therapeutics
    • Kinase inhibitor APIs
    • Pharmaceutical intermediates for nervous system agents
    • Precursor blocks for library synthesis in drug discovery

    2. High-Performance Polyimide Monomer Preparation

    Specialty polymer manufacturers employ this aromatic amine-acetylene in the step-growth polymerization of high-strength polyimides. Its combination of amino and acetylenic functionalities allows connection into rigid-rod backbones, enhancing thermal stability and mechanical strength. Careful raw material metering ensures the preservation of target stoichiometry for molecular weight control. The integration step often uses a two-stage imidization process: prepolymerization at moderate temperature, followed by cyclodehydration at higher temperatures under inert gas. Site audits and internal batch tracing maintain adherence to rigorous electronic or aerospace quality requirements.

    Industry compliance standards

    • ASTM D5213 Standard Specification for Polyimide Resins
    • ISO 9001:2015 Quality Management Systems for specialty chemicals
    • RoHS Directive 2011/65/EU Annex II (for electronics applications)
    • UL 94 Flammability Testing (where applicable)

    Typical usage ratio

    • 20–30% molar ratio (compared to total dianhydride/diamine charge); adjusted based on chain rigidity targets and end-use application (flex circuit substrates vs. molded components)

    Downstream process integration

    • Monomer charged into polycondensation reactor with dianhydride; controlled feed to achieve targeted imide/acetylene composition; solution casting or melt processing prior to imidization

    Final product types

    • Flexible printed circuit base films
    • High-temperature electrical insulation tapes
    • Aerospace-grade molded polyimide components
    • Powder coatings for microelectronics

    3. Organic Light-Emitting Diode (OLED) Material Synthesis

    Producers of advanced OLED materials apply 3-aminophenylacetylene as an intermediate for synthesizing electron transport and host molecules, especially where conjugation extension and amino group reactivity are critical for tuning photophysical properties. Formulators rely on precise molar ratios to align synthetic batches for consistent emission spectra and charge mobility. GMP-compliant cleanrooms and trace metal analysis protocols back the synthesis to meet the stricter standards of electronic display manufacturers. The component enters the process through selective functionalization reactions, such as Sonogashira couplings, followed by purification and blending into final device formulations.

    Industry compliance standards

    • ISO 9001:2015 for electronic chemical manufacturing
    • IEC 62321 for hazardous substance analysis in electrical/electronic products
    • IPC-4552 Halogen-Free Materials Standard (if applicable)
    • REACH (EC 1907/2006) Registration, Evaluation, Authorisation and Restriction of Chemicals

    Typical usage ratio

    • 5–15% molar percentage in host matrix monomer mixtures; adjusted in proportion to target electron transport/hole blocking balance in OLED stack

    Downstream process integration

    • Introduced in ligand synthesis stage; purified and isolated as building block before final coupling to OLED functional layers; final compound typically vacuum sublimed for thin-film device fabrication

    Final product types

    • Blue and green emitter hosts
    • Electron transport layer molecules
    • Charge injection improvement additives
    • High-end OLED display device materials

    4. Dual-Functional Ligand Synthesis for Catalysis

    Catalyst makers use this material to develop ligands featuring both acetylenic and aromatic amine sites, supporting metal complex formation for homogeneous catalysis in pharmaceuticals, fine chemicals, and specialty polymerizations. The dual reactivity enables custom tuning of electronic and steric effects for metal-ligand coordination environments, boosting selectivity and kinetics in cross-coupling and polymerization reactions. Batch documentation includes full traceability for GLP or industrial catalyst system certifications, with regular heavy metal/organic impurity profiling.

    Industry compliance standards

    • ISO 17025 Laboratory Accreditation (for analytical services)
    • OECD Principles of Good Laboratory Practice
    • REACH (EC 1907/2006) safety data for raw material handling
    • Company internal QC protocols for metal catalyst precursors

    Typical usage ratio

    • 2–10 mol% loading relative to metal precursor; further adjusted based on catalytic cycle turnover and specific substrate requirements

    Downstream process integration

    • Reacted in ligand formation step (e.g., formation of Schiff base or acetylene-metal complex); intermediate purified and coordinated to metal salt under inert atmosphere; final catalyst introduced to reaction media as preformed solution or solid

    Final product types

    • Cross-coupling reaction catalysts
    • Polymerization initiator systems
    • Fine-chemical synthesis catalyst kits
    • Chemoselective transfer hydrogenation catalysts
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    Certification & Compliance
    More Introduction

    3-Aminophenylacetylene: Practical Notes from the Production Floor

    What Sets 3-Aminophenylacetylene Apart?

    Working hands-on with 3-aminophenylacetylene, its personality in the plant stands clear compared to most phenylacetylenes or substituted anilines. Chemically, it carries an acetylene group attached to the phenyl ring, with the distinct position of an amino group at the 3-spot. In practice, the product we ship hits a purity benchmark above 98%, with a pale-brown to light-yellow appearance that often signals its authenticity to our loading crew well before the paperwork comes through. We pack it tightly on drums or in custom glass bottles based on freight logistics and the sensitivity of each batch.

    In our facility, the process starts with scrutinizing incoming raw materials on the dock and verifying by NMR and GC-MS, not just for paperwork’s sake but to prevent headaches when the reactors come online. The acetylene bond brings some reactivity — experienced operators handle it carefully, understanding its tendency to polymerize under heavy catalyst loads if the temperature ramp goes out of spec. We keep reaction times short and limit exposure to atmospheric moisture, not because standard guidelines insist but because we have seen batch quality suffer otherwise.

    The Role It Plays Across Industries

    Customers working in pharmaceuticals and specialty materials rely on this intermediate for building more complex frameworks. We know several medicinal chemistry groups use our 3-aminophenylacetylene in small-scale routes to kinase inhibitors. Teams focusing on liquid crystals or OLEDs tend to prefer the electron-donating amino paired with sp-hybrid acetylene for tuning optical behavior. In our experience, R&D labs often come calling for as little as 25 grams, while production projects demand batches tipping over several kilograms, often in a rush when a project milestone moves up.

    Applications have shifted through the years. At one point, requests came mostly from academic chemists screening novel coupling reactions. More recently, commercial outfits in Japan and parts of Europe ask for large lots, running Suzuki or Sonogashira cross-couplings and reaching out for detailed impurity profiles before onboarding a new supplier. Only about one in ten customers ask for certifications for use in regulated drug synthesis. The rest care most about batch-to-batch reproducibility and stability during transit, especially over long sea freight.

    Addressing the Technical Limitations

    Some newcomers expect 3-aminophenylacetylene to behave like simple acetylenes: easily stirred, robust to storage, and forgiving in air. Practical experience with production and long-term storage tells a different story. The amino group increases polarity, so the compound absorbs atmospheric moisture much more readily, especially in our coastal facility. Over time, if containers are not tightly sealed or held under nitrogen, product color deepens and trace decomposition begins. Our team runs stability checks monthly, extending shelf life not by elaborate nitrogen blanketing, but by moving inventory quickly and repacking any lot showing visual change.

    Shipping brings its own headaches. The acetylene group falls under “reactive” in many regulatory lists. We’ve had shipments held up over minor label wording, so our logistics office pre-clears exports with customs and forwards MSDS updates to repeat customers. Inside the warehouse, flammable liquid storage is the norm, though the actual flash point is higher than expected—something that comes up again and again in customer audits.

    Why Our Approach Is Different

    Long-time technicians in our plant have found shortcuts and pain points few outside the industry ever see. For example, most commercial suppliers avoid metal catalysts like copper during synthesis, worried about trace contamination. We experimented for months with base-free coupling variants to cut down on heavy metal carryover, hitting high purity by refining isolation and not just by adding more purification steps. It keeps our downstream customers from reprocessing, especially in pharmaceutical routes where copper or palladium have to be controlled.

    Given how sensitive the amino and acetylene functions are, we monitor residual solvents using GC every time. Tetrahydrofuran and acetonitrile are easy to purge, but traces persist if the drying step gets rushed. Customer feedback after a poor batch five years ago led us to switch solvent systems. Since then, complaints about color changes or unstable storage have dropped by more than half, saving both sides added work.

    How It Differs From the Alternatives

    Other phenylacetylenes lack the amino group’s influence on electronic structure. In the lab, this matters. It changes reactivity in coupling reactions and lets end-users add other functional groups down the line, making 3-aminophenylacetylene more versatile for building complex molecules. Analysts in purchasing departments sometimes compare it to 4-aminophenylacetylene or even unsubstituted phenylacetylene. We walk them through the unique reaction pathways—meta substitution versus para or none at all—because experience shows that switching between them mid-synthesis eats up time and resources as reaction conditions need new optimization.

    Practical substitution means more than what’s on paper. Handling-wise, 3-aminophenylacetylene stays more sensitive to light, showing color shifts in clear containers. We use amber glass or steel drums not out of tradition, but because history in production shows less decomposition with those choices. Dry, cool storage keeps shelf life respectable, but we encourage repeat customers to use up stocks within six months for best results, which reflects what we have learned from our own QC logs and returned product reviews.

    Quality From Experience, Not Just From Testing

    Behind each drum of 3-aminophenylacetylene is a hard-earned lesson in plant operations. We built our process flows not from standard literature but by running small batches under different reaction scales. Early years saw washing steps that failed to remove colored byproducts, leaving product with mild but unacceptable scent and tinge. Over time, team members adjusted pH in the wash cycles, shortened reaction times, and reworked purification columns until only minute traces of side products remained. The learning stuck, and we codify each adjustment, no matter how minor, into the plant’s process manual.

    Feedback from customers working on energy storage or advanced electronic materials triggered another round of process reviews. Their needs for ultra-low metal content outranked even the requirements from pharma groups. To meet that, we started batch-testing for iron, copper, and chromium even when those numbers didn’t show up on audit lists. It cost more upfront, but sales and reputation both improved as a direct result.

    Supporting Innovation While Managing Supply Chain Risks

    Research-driven industries depend on regular, reliable access to specialty intermediates. COVID-era disruptions exposed weaknesses, with raw materials arriving late or suppliers unable to fill crucial orders due to border issues. We coped by localizing as much sourcing as possible, leveraging relationships with regional chemical producers for starting materials. For some competitive products, other manufacturers respond by cutting quality to fill backorders. We chose to limit sales, costing us a few accounts, but avoiding rushed, subpar production and product recalls.

    Using in-house synthesis keeps us close to every process variable. If a solvent shortage looms, our lab pivots to alternatives with minimal downtime. In several instances, competitor-supplied intermediates failed to meet functional testing in OLED device fabrication or medicinal synthetic steps. Customers returned for our material after product failures, typically pointing to missing QC oversight elsewhere. From that, we've learned the value of transparency—regularly uploading batch purity data and analytical spectra for established customers to audit on their own timelines.

    Adapting to Regulatory Pressure and Safety Audits

    3-Aminophenylacetylene’s reactive character attracts regulatory attention. Before large-scale production kicks off, we pre-screen operational steps against environmental and workplace safety rules. Staff complete refresher training on acetylene management and review secondary containment plans, not just box-ticking but to bring new hires up to speed based on accident reports from other plants—stories that passed down through the crew, not posted on public safety boards.

    Auditors sometimes raise questions about our continuous monitoring for off-gassing or storage at the interface of refrigerated and ambient storage zones. Hearing the same questions, year after year, led us to add secondary containment for all products with an acetylene feature. Slowly, these changes decrease incident reports and speed up insurance clearance during annual site reviews. We see direct benefits in fewer lost days to minor incidents and improved morale on the floor.

    With environmental standards growing stricter, we proactively monitor waste streams for residual solvents or reaction byproducts, especially amines and trace heavy metals. Waste handling shifted from centralized pooling to on-site neutralization and solvent recovery wherever reasonable. Not every change appeared cost-friendly initially, but after problems in neighboring industries led to fines and production pauses, our team’s early moves paid off. Steady business and customer confidence count for more than saving pennies on waste disposal.

    Improving Consistency with Technology and Teamwork

    Earlier process years depended on batch notes scrawled by shift supervisors. That old system led to slow learning, repeated mistakes, and wasted materials. Now each run gets logged electronically—temperatures, raw material batch numbers, output color, observed side-reactions, and post-reaction handling. Reviewing those logs monthly, we spot trends before they turn into production problems. New employees receive hands-on training with senior operators, not just protocols on paper.

    For a compound like 3-aminophenylacetylene, where sensitive groups and possible impurities can disrupt a customer’s entire synthesis, consistent teamwork and process documentation matter more than just hitting numerical specifications. Teams in quality assurance work closely with line operators, sharing fast feedback about observed deviations, dialing back adjustments before major issues arise. This information flow—faster than any outside audit—keeps our rejection rates low and customer return rate high.

    Partnering with Customers for Better Applications

    3-Aminophenylacetylene rarely ships to end-users without back-and-forth with technical staff. Chemists from customer companies often call about catalyst compatibility, optimal storage, and reactivity in their newest routes. Our technical support comes straight from production and lab workers, delivering practical advice rather than generic service answers. If solvent choice for cross-coupling changes, teams run pilot reactions using customer conditions in our bench lab, reporting back with problems and possible work-arounds.

    We take pride in following the product’s journey as it transforms in the hands of our customers—seeing it adopted into advanced materials, new drugs, and high-performance coatings. Some breakthroughs occurred after our teams provided feedback on side reactions or helped customize purification. This collaboration builds long-term trust, as each party wins from shared troubleshooting and transparency.

    Outlook for the Future

    Markets for specialty intermediates like 3-aminophenylacetylene continue to push us for more analytical depth, lower impurity thresholds, and improved documentation. Investments in new purification technology, improved waste handling, and better training sharpen our competitive edge. Yet the real advantage comes from keeping chemists deeply involved in every step, not just running automated production. That approach ensures each lot we send matches quality, utility, and safety benchmarks, learned from years in the business and hundreds of feedback calls.

    As regulatory and application fields evolve, so do customer expectations. Our job remains steady—maintaining open lines for input, adjusting to technical changes, and following through when issues turn up. Production of 3-aminophenylacetylene reflects these ongoing lessons, not just as a collection of facts but as the record of a living, learning process that puts safe, reliable chemicals in the hands of those who need them most.