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HS Code |
146829 |
| Chemical Name | 4-Fluorophenylacetylene |
| Molecular Formula | C8H5F |
| Cas Number | 371-40-4 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 134-136°C |
| Melting Point | -22°C |
| Density | 1.087 g/cm3 |
| Refractive Index | 1.543 |
| Flash Point | 40°C |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water; soluble in organic solvents |
| Smiles | C#CC1=CC=C(F)C=C1 |
| Inchi | InChI=1S/C8H5F/c1-2-7-3-5-8(9)6-4-7/h1,3-6H |
As an accredited 4-Fluorophenylacetylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle labeled "4-Fluorophenylacetylene," featuring chemical structure, hazard symbols, and manufacturer details. |
| Shipping | 4-Fluorophenylacetylene is shipped in tightly sealed containers, protected from light and moisture. It is packaged according to regulations for hazardous chemicals, typically in bottles with cushioning material inside UN-approved cartons. Appropriate hazard labeling, including flammable liquid warnings, is applied, and shipments require proper documentation and, when necessary, temperature control. |
| Storage | 4-Fluorophenylacetylene should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon, to prevent degradation. Keep it in a cool, well-ventilated area away from sources of ignition, heat, and strong oxidizing agents. Avoid exposure to moisture and direct sunlight. Proper chemical storage protocols and personal protective equipment are recommended during handling. |
Applications of 4-Fluorophenylacetylene in Industrial ManufacturingAs an established producer of 4-Fluorophenylacetylene, we supply this intermediate to advanced manufacturing sectors. The unique electronic and steric properties of the fluorinated alkyne core enable direct integration into high-value molecules across several specialty industries. Below we present in-depth application details for major downstream pathways using our material. 1. Pharmaceutical API Synthesis4-Fluorophenylacetylene is routinely used by pharmaceutical manufacturers to introduce a fluorine-containing aromatic alkyne motif into target active pharmaceutical ingredients (APIs). The compound enters Sonogashira or C–H activation couplings under cGMP conditions, facilitating rapid library development of kinase inhibitors and CNS drugs. Process chemists value the selectivity and clean transformation profile, especially when building small-molecule APIs that demand exact fluorine substitution on the final structure. Industry compliance standards
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2. Advanced Liquid Crystal Monomer PrecursorAs a key monomer building block, 4-Fluorophenylacetylene enables manufacturers to tailor the mesogenic cores in specialty liquid crystals. Its rigid linear scaffold and electron-rich fluorine substituent tune the birefringence and viscosity in the final LC material. Actual production integrates our material into coupling steps for constructing oligomeric or dimeric LC monomers, used for high-resolution display and optical switching units. Rigorous QA and trace metals control are necessary to maintain LC-grade performance targets. Industry compliance standards
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3. Agrochemical Active Ingredient DevelopmentCrop protection R&D groups employ 4-Fluorophenylacetylene as a core structure modifier to enhance bioactivity and metabolic stability in heterocyclic agrochemicals. The material enters controlled cyclization and Sonogashira coupling steps under ISO-compliant batch production, allowing synthesis of candidate herbicides, pesticides, or fungicides with improved efficacy. Strict handling practices ensure safe incorporation into QC-controlled labs and pilot lines. Industry compliance standards
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4. Organic Electronic Material FabricationIn the organic electronics market, 4-Fluorophenylacetylene serves as a high-purity monomer enabling precise engineering of π-conjugated systems for semiconductors and photonic devices. Manufacturers use our grade material in the controlled polymerization steps, tailoring the electronic properties critical for device efficiency. Stringent trace metal and impurity limits are achieved through multi-stage purification. All batches include batch-traceable QC data to support device reliability claims. Industry compliance standards
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5. Fine Chemical Intermediates for Dyestuff ProductionSpecialty dyestuff manufacturers utilize 4-Fluorophenylacetylene as a building block for synthesizing high-performance azo and anthraquinone dyes. The fluorinated alkyne group enables colorists to produce pigments with enhanced lightfastness and adjusted absorption spectra, suitable for demanding textile or technical ink applications. Our product quality ensures consistency in chromophore assembly reactions and downstream environmental compliance. Industry compliance standards
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As a chemical producer dedicated to aromatic and alkyne intermediates, 4-Fluorophenylacetylene stands out as one of the most reliable building blocks on the bench. Decades of hands-on process experience in fluorinated organics tell us why chemists continue turning to this compound. With a molecular formula of C8H5F and a firmly defined CAS number—371-41-5—this material serves as a cornerstone for organic synthesis especially when seeking diversification in molecular scaffolds.
A single fluorine on the para position of the phenyl ring gives this molecule unique properties not shared by simple phenylacetylenes or other halo-derivatives. That single atom can influence reactivity, electron distribution, and the resulting physicochemical behaviors in final products. We've witnessed this real-world effect again and again in customer pilot trials and research applications.
Years of factory-scale runs allow for exacting standards. Typical product offers consistently clock in with a purity higher than 98%, usually surpassing that for more demanding downstream transformations. Trace moisture and side-products stay below actionable limits, tracked by spectroscopic and chromatographic methods our plant developed alongside academic partners. That gives chemists security—impurities like dibenzyl, unreacted halides, or ring-opened residues go undetected in most batches because of the process controls built from years’ feedback.
Particle size, melting point, and volatility don’t vary much between lots. That’s by design. Chemical research doesn’t pause for inconsistent intermediates, and dozens of teams in pharma, agrochemicals, and new materials rely on our predictability. Bottling and packaging can adapt to order size, but you see the same white-to-off-white crystals in research drums or kilo-scale containers.
This acetylene derivative finds its way into a range of synthetic applications. In our observation, most calls come from groups developing pharmaceutical lead candidates. The fluorine atom’s impact on bioactivity, metabolic stability, and even solubility, means subtle substitution often separates a promising hit from an abandoned project. Medicinal chemists use this intermediate to insert a fluorinated arylacetylene into core scaffolds—sometimes by Sonogashira cross-coupling, sometimes by alternative palladium-catalyzed routes. The clean, reproducible nature of our product keeps side reaction risks to a minimum, which cuts down wasted hours during scale-up.
Polymer chemists reach for 4-Fluorophenylacetylene during high-performance material design. Its introduction into polyphenylene matrices or as functional group spacers leads to new materials with improved mechanical endurance and chemical resistance. Those results came not by abstract modeling but by real compounds in advanced electronics and membranes. Whenever someone wants to tune their backbone with a para-fluorine, this alkyne plays a role.
There’s also frequent collaboration with agrochemical innovators. Modifying the electronic environment of pesticide fragments can block unwanted breakdown channels or redirect biological activity. Growers notice the practical effect in the field only months or years after innovation, but at the molecular starting line, 4-Fluorophenylacetylene often enters reaction schemes. Here, downstream yield and environmental control depend heavily on the reproducibility of each starting component.
Being the manufacturer, we see every coil, jacket, and vessel that carries this compound from reaction to purification. We know firsthand how raw material quality, reaction temperature, and work-up protocols influence final product properties. When specifications shift, it’s not just a line in a certificate—it’s a question of whether subsequent synthesis succeeds or fails in someone’s lab. By producing on an industrial site with multiple redundancies, supply remains stable even if one line undergoes maintenance.
Direct feedback from pilot plants and process chemists drives our improvements. One customer flagged an uptick in trace acetophenone byproducts; tracing root causes, we found a heating variance in a single reactor. After correcting thermal flux and adjusting timing, purity returned to previous levels—demonstrating the feedback loop between customer usage and manufacturing practice. That’s the unseen work behind the stability you see in each drum or flask.
For chemists weighing between different arylacetylenes, the question of para-fluorine substitution becomes about more than electronics. Many arylacetylenes look similar on paper, but their performance in real experiments can diverge sharply. Only through direct handling and years of customer dialogue can we share this: para-fluorine consistently provides both steric and electronic influence without destabilizing the aromatic system. Unlike ortho- or meta-fluorinated analogues, para position avoids introducing strain or complicating purification.
Side-by-side, non-fluorinated phenylacetylene remains a more basic toolkit item. Its price is lower, its behavior more established, but you lose the chance to tailor final product performance by manipulating hydrophobicity, electronic density, or metabolic stability. Other halogenated versions—like bromo or chloro—bring reactivity, but often at the cost of byproducts, increased hazard, or less nuanced electronic effects.
Over years, both major firms and small development teams order this compound in quantities ranging from grams to scores of kilograms. Internal batch tracking uses both spectral signatures and traditional wet chemical tests to double-verify identity and purity. No two research groups use exactly the same recipes, but keeping the starting intermediate at reliably high quality means the downstream results stay within expectations.
Solubility and storage show another advantage. 4-Fluorophenylacetylene resists unwanted polymerization and doesn’t readily degrade when stored cool and dry. This means a well-sealed bottle on a chemical shelf stays usable for extended periods. Some competitors ship similar compounds with excessive stabilizers; our control over chemical integrity eliminates that need, offering a cleaner compound for sensitive downstream work.
Innovation cycles demand flexibility. Research groups will call with unique requests, from semi-bulk orders for new process validation to micro-scale aliquots for high-throughput screening. Our facility adapts by scaling runs with minimal changeover time, leveraging modular reactors and targeted purification setups. This responsiveness comes from decades of dialogue with those at the forefront of discovery—hearing not just what’s possible, but what is actually practical under modern regulatory and operational conditions.
Experience handling this compound informs advice given to both new and established clients. During the pandemic, we saw a spike in inquiries from teams evaluating new pharmaceutical scaffolds aimed at antiviral action. Quick adaptation to shifting demand enabled us to keep lines open and stocks available, reflecting the agility required from a manufacturer—not just a stock-keeper or middleman.
Producing halogenated intermediates obliges special attention to environmental responsibility. Factory teams receive ongoing training in containment, spill response, and safe waste handling. More than regulatory box-ticking, this mindset stems from lived experience. Early in our production scale-up, occasional odor events prompted a redesign of tank venting and scrubber calibration; today’s plant rarely flags for emissions or off-spec air quality. Disposal streams pass through rigorous capture and neutralization steps, so workers and surrounding communities remain safe.
Shipping also follows best practice. Sealed, inert, and clear of potential cross-contamination, finished product containers come labeled with lot-traceable identifiers. Warehouse teams don’t cut corners—knowing from years of practice how a lax seal could impact both customer results and workplace safety. While bulk movement remains routine, custom projects demanding extra-low metal content or other specific exclusions draw extra scrutiny in filling and dispatch.
Customers return not because the molecule is unique but because our controls and transparency translate to less downtime and more certainty in their processes. Inevitably, someone faces a critical reaction that goes sideways. Access to the synthesis team and archived plant data sometimes reveals contributing factors not found in textbooks—a smart move during patent filings or production troubleshooting.
Yearly reviews analyze upstream raw material sourcing, validated against benchmarks from both supplier audits and our own in-house QC. There’s nothing theoretical about tracking incoming fluorobenzene and acetylene quality, nor about adjusting catalyst loads to match shifting impurity profiles. The plant has witnessed the difference a few ppm of residual solvent can make, so our standard work instructions grew out of those stories, not just regulatory guidance.
Expectation for chemical traceability and transparency grows annually. End-users—not just direct clients but their own stakeholders—now ask for data on origin, resource stewardship, and environmental impact. Long before it became widespread, we adopted full traceability on 4-Fluorophenylacetylene batches, including tracking raw material source, energy use, and yield optimization. That upfront commitment minimizes both supply-chain surprises and regulatory hiccups.
Sustainability pressures haven’t left chemical makers untouched. Route design now factors in atom efficiency, solvent recyclability, and energy intensity. The move to greener pathways reduced hazardous waste, with several process steps now leveraging continuously recycled solvents and heat integration. Process engineers constantly evaluate byproduct management not simply for local compliance but for practical impact further down the chemical value chain.
Technological trends indicate an expanding role for fluorinated intermediates, especially as molecular designs in medicine and electronics evolve. The rise of targeted delivery systems, next-generation OLEDs, and environmentally resilient crop protection compounds each rely on new classes of functionalized building blocks. Our technical team partners on a diverse array of development projects, sharing both raw materials and insight from process optimization.
We constantly receive new inquiries about custom derivatives—ortho- or meta-fluorinated variants, deuterated forms, and halogen combinations. Some require modified synthesis routes; others become part of combinatorial libraries for mass screening. Our ability to quickly adapt and scale toward these changes grows from long-term investments in both people and equipment.
What has never changed: customer needs for certainty, transparency, and a partnership attitude. The product’s role depends on trust in its reliability. Manufacturers carry the weight of not just making the molecule but ensuring it performs in the diverse labs and plants where new ideas become reality.
Labs and process teams regularly drop us follow-ups on product behavior under different conditions: questions about solvent compatibility, reaction byproducts, or purification tweaks. We believe that the accumulated knowledge on real process outcomes beats any single spec sheet. Feedback—positive or constructive—comes directly to the production, QC, or R&D team, not filtered through layers of sales or brokers. That's how adjustments happen promptly, and issues rarely linger between orders.
Even as order sizes change or regulatory demands shift, a reliable point of contact remains available to offer both historic and current batch data. Our continuous improvement approach keeps lines open for suggestions, troubleshooting, or even just discussing new synthetic routes.
Each batch of 4-Fluorophenylacetylene reflects not just raw material conversion but the practiced eyes and hands of operators, chemists, and engineers. Production isn’t a faceless, push-button task but a day-to-day discipline in getting the details right. Many staff spent years learning how atmospheric changes, small raw material shifts, or new equipment calibrations subtly affect final output.
Supporting both innovation and reliability requires balancing precise protocols with on-the-ground experience. Interns and new chemists quickly realize that production-scale chemistry rewards both vigilance and adaptability—adapting not just recipes, but procedures and equipment in response to the real world, not just a plan on paper.
Manufacturing 4-Fluorophenylacetylene teaches us every season that reliability and open communication matter more than theoretical potential. End users succeed or stumble based on the dependability of their building blocks, and every member of our team carries the practical stories behind the numbers on the latest spec report. With eyes on future requirements and hands invested in every stage from sourcing to final QC, we work to stay ahead of changing needs while sticking to those fundamentals—consistency, openness, and unflagging support for practical science.