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4-Chloro-1-Butyne

    • Product Name 4-Chloro-1-Butyne
    • Alias 1-Chloro-4-butyne
    • Einecs 211-827-0
    • 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

    104164

    Cas Number 928-49-4
    Molecular Formula C4H5Cl
    Molecular Weight 88.54 g/mol
    Iupac Name 4-chlorobut-1-yne
    Appearance Colorless to light yellow liquid
    Boiling Point 107-109 °C
    Density 0.98 g/cm3 (at 20 °C)
    Flash Point 21 °C (closed cup)
    Refractive Index 1.448-1.450 (at 20 °C)
    Melting Point -83 °C
    Purity Typically >98%
    Solubility In Water Slightly soluble

    As an accredited 4-Chloro-1-Butyne factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mL amber glass bottle with a sealed cap, labeled "4-Chloro-1-Butyne," includes hazard warnings, supplier details, and lot number.
    Shipping 4-Chloro-1-Butyne must be shipped as a hazardous material according to DOT/IATA regulations. It should be packed in tightly sealed, chemical-resistant containers, placed within secondary containment. Proper labeling and documentation are required, including hazard class (flammable liquid), UN number, and emergency contact information. Avoid heat, sparks, and incompatible substances during transport.
    Storage 4-Chloro-1-Butyne should be stored in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and use corrosion-resistant materials. Store separately from oxidizers, acids, and bases. Properly label the container and ensure spill containment measures are in place to prevent leaks or accidental releases.
    Application of 4-Chloro-1-Butyne

    Applications of 4-Chloro-1-Butyne in Industrial Manufacturing

    As a direct manufacturer of 4-Chloro-1-Butyne, we support multiple specialty chemical synthesis routes across core industrial verticals. The following sections outline the principal commercial applications where industrial producers achieve efficient transformation of this raw material under stringent compliance systems. All application scenarios reflect actual downstream deployments substantiated by industry standards and process needs.

    1. Pharmaceutical Intermediate for API Synthesis

    Pharmaceutical intermediates leverage 4-Chloro-1-Butyne as a building block in heterocyclic compound synthesis, particularly for the production of certain antiviral and anticancer agents. Process chemists incorporate this alkyne in nucleophilic substitution and cyclization reactions, ensuring defined molecular architectures required by registered drug substances. The integration occurs at the early synthesis stages, dictating impurity profiles and yield efficiency for high-purity APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211: Current Good Manufacturing Practice in Manufacturing, Processing, Packaging, or Holding of Drugs
    • European Pharmacopoeia (Ph. Eur.) Monograph reference requirements
    • Chinese Pharmacopoeia standards for pharmaceutical intermediates

    Typical usage ratio

    • 0.2–2.5 molar equivalents, based on target molecular transformation and desired throughput; optimized via pilot trials

    Downstream process integration

    • Added to multi-step organic synthesis as a functionalized alkyne for coupling, cyclization, or further derivatization in controlled reactor systems

    Final product types

    • Small-molecule APIs (e.g., alkynyl-heterocycles, pyridines, and related frameworks)
    • Registered pharmaceutical intermediates for contract manufacturing organizations

    2. Agrochemical Synthesis (Herbicide and Fungicide Active Ingredient Production)

    Specialty agrochemical plants utilize this compound primarily as an alkynyl source for synthesizing highly-functionalized pesticide actives through transition metal-catalyzed coupling and alkylation reactions. Its unique reactivity supports selective introduction of carbon-carbon triple bonds in target molecules, which is crucial for biological activity of some modern herbicides and fungicides. Precise addition and handling protocols minimize operational hazards while maintaining product quality across batch and continuous production lines.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Principles of Good Laboratory Practice (GLP) for registration studies
    • ISO 9001:2015 Quality Management Systems in agrochemical production
    • REACH Regulation (EC) No 1907/2006 for raw material registration and safety documentation

    Typical usage ratio

    • 0.3–1.8 molar equivalents, depending on the specific synthetic route and catalyst loading defined by technical transfer documentation

    Downstream process integration

    • Introduced during the core synthesis phase for C–C coupling, usually under inert atmosphere, followed by extraction and final formulation of actives

    Final product types

    • Precursor molecules for selective herbicides (e.g. acetylenic heterocycles)
    • Fungicide active substances requiring terminal alkynyl substituents

    3. Electronic Chemical Intermediate for Functional Material Synthesis

    Electronic material manufacturers incorporate this alkyne-terminated building block in the synthesis of advanced functional materials with conductive, optoelectronic, or crosslinking properties. Precision chemical engineers employ it for introducing controlled unsaturation in specialty polymers and molecular frameworks used in electronic film coatings, OLED intermediates, and photoresist resins. Process lines prioritize consistent purity, trace metal removal, and tight stoichiometric control for downstream device reliability.

    Industry compliance standards

    • SEMATECH Technology Transfer Standards (for chemical purity)
    • IPC-5701: Cleanliness requirements and test methods for electronic chemicals
    • RoHS Directive 2011/65/EU: Restriction of hazardous substances in electronics
    • ISO 14001:2015 Environmental Management Systems for cleanroom production

    Typical usage ratio

    • 0.5–1.2 molar equivalents; adjusted according to final target polymer chain length and desired crosslinking properties

    Downstream process integration

    • Charged to organic synthesis reactors for pre-polymer functionalization or crosslinker addition prior to purification and conversion to electronic material intermediates

    Final product types

    • Conductive oligomers and polymers for flexible circuits
    • OLED precursor materials (alkynyl-aromatic building blocks)
    • Specialty photoresist resins for microelectronics fabrication

    4. Fine Chemical Intermediate for Fragrance and Flavor Synthesis

    Manufacturers in the aroma chemicals sector employ 4-Chloro-1-Butyne as a valuable synthon for constructing aldehydes, lactones, or other key notes used in fragrance and flavor compositions. The selective alkyne reactivity allows controlled transformation via hydroboration, oxidation, or carbonylation to introduce unique scent or taste profiles. Production lines operate under food-grade and cosmetic quality systems to maintain compliance and deliver high-purity intermediates for sensorial applications.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • FEMA (Flavor and Extract Manufacturers Association) GRAS regulations
    • EU Regulation (EC) No 1334/2008 on flavoring substances
    • ISO 9001:2015 Quality Management in aroma chemicals

    Typical usage ratio

    • 0.2–1.0 molar equivalents; chosen based on target transformation yield and downstream olfactory requirements

    Downstream process integration

    • Added to batch reactors as a precursor for key aroma units, followed by selective derivatization under controlled temperature and pH regimes

    Final product types

    • Aldehydic intermediates for fine fragrances
    • Lactones and alkyne-derived aroma ingredients
    • Flavor enhancers for food and beverage formulations
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    Certification & Compliance
    More Introduction

    Introducing 4-Chloro-1-Butyne: A Closer Look from the Manufacturer’s Perspective

    Proudly Producing 4-Chloro-1-Butyne for Reliable Performance

    As a direct producer of 4-Chloro-1-Butyne, we approach each batch with close attention and hands-on knowledge. This specialty chemical takes a unique spot among haloalkynes, both for its reactivity profile and for its select applications that benefit from its blend of triple bond and chlorine reactivity. Compared to more routine building blocks, you notice the fine line between versatility and handling care needed for this compound.

    Distinct Structure, Distinct Uses

    4-Chloro-1-Butyne isn’t an off-the-shelf commodity. It’s a clear, colorless to pale yellow liquid at room temperature, marked by a sharp, often pungent odor typical of alkynes with halogen atoms. With the formula C4H5Cl, the molecule includes a terminal alkyne and a chlorine atom separated by a flexible three-carbon chain. This structural combination unlocks value for a range of chemical transformations, setting it apart from more common compounds like propargyl chloride or 3-chloropropyne, where the alkyne or chlorine sits in different positions.

    Because the terminal position of the alkyne and the chlorine at the fourth carbon provide both access and control, 4-Chloro-1-Butyne fits reactions that need selective activation, chain extension, or coupling where positional isomerism matters to synthetic outcome. Synthetic chemists use this dual reactivity to drive processes in crop protection, active pharmaceutical ingredient (API) intermediates, and specialty materials. Its specific reactivity comes into play in Sonogashira couplings, nucleophilic substitutions, and alkyne functionalizations when a chlorine group in the gamma position is needed.

    Understanding Specifications Through Firsthand Production

    Producing 4-Chloro-1-Butyne at scale brings its own set of challenges that only direct experience can reveal. The process typically involves chlorination of 1-butyne or dehydrochlorination of precursors, each step requiring precise temperature management, careful control of exothermicity, and reliable in-line analysis. Our plants rely on continuous monitoring of purity, as small contaminant levels—moisture, peroxides, or related haloalkynes—can skew outcomes for downstream chemistry. With consistent GC or NMR testing, we measure actual purity (usually above 98%) for every outgoing drum or cylinder, not only for compliance, but because we see how tiny variations Cascade through scale-up reactions in customer labs.

    4-Chloro-1-Butyne has a boiling point just above 70°C, which demands proper classification, sealed storage conditions, and mindful tank cleaning cycles. Whether shipping large quantities in ISO tanks or smaller lots for research synthesis, we pay attention to packing material compatibility: Certain plastics may embrittle or discolor after repeated exposure, though fluoropolymers generally show resilience. Metal drums receive tested linings to hold off corrosive attack, which isn’t always obvious on day one but shows up in repeat business. From our own runs, repeated analysis confirmed that PTFE gaskets and valves stand up well where hydrocarbons sometimes leach additives.

    Real-World Usage: What Sets 4-Chloro-1-Butyne Apart

    On the laboratory bench and in pilot production campaigns, 4-Chloro-1-Butyne’s greatest strength lies in bridging reactivity not conveniently achieved by its isomers or analogues. Chemists value its clean performance in alkylation reactions, especially when linear, four-carbon skeletons matter for downstream ring-closure or cross-coupling. Peering into the data, you’ll see this haloalkyne pop up in patent filings for propargyl-based kinase inhibitors, advanced materials precursors, and as a linker in radiolabeled probes. Our customers regularly share feedback from screening campaigns: If chlorine sits on the terminal position, elimination becomes an unwanted side reaction; too close to the triple bond, stability suffers.

    Compared with 1-chloro-2-butyne or propargyl chloride, 4-Chloro-1-Butyne offers less volatility and a less aggressive tendency toward hydrolysis. The physical properties—density, vapor pressure, viscosity—give formulators and process chemists a bigger operating window. Surfaces in our purification columns recover quicker between batches, because the fewer byproduct chlorides condense out earlier. This clarity is one benefit of working the material ourselves: You get to solve the rough spots that arise from unknowns in third-party batches, with quick troubleshooting that feeds learning back into our next syntheses.

    Putting Safety and Handling Front and Center

    Every operator who works with haloalkynes knows the importance of careful containment. 4-Chloro-1-Butyne brings manageable risk, provided it’s kept out of open flames or spark-prone environments. As with most alkynes, the presence of a halogen raises the stakes, both for acute exposure and for longer-term chronic vapor build-up in drums. Factory procedures emphasize regular leak checking, real-time indoor air sampling, and solvent wash-downs after filling lines have run. Operators tell us that this hands-on vigilance cuts down on unwelcome surprises—any hydrolysis product can release HCl gas or create irritating fumes, which proper ventilation and good shelter-in-place protocols intercept before they become an issue.

    We notice the difference between sites that maintain best-practice PPE—full nitrile gloves, close-fitting goggles, splash-resistant coveralls—and those that skimp on routine. People expect chemical plants to run tight ships, but the temptation to shortcut vapor testing for “routine” batches can undermine progress rapidly. Through years of working with 4-Chloro-1-Butyne in all weather, we built our own checklists, sometimes exceeding published recommendations, because real experience teaches what paperwork overlooks. Small temperature changes have outsized impact on vapor pressure and loss, especially in summer months: real-world handling beats theory every time.

    Comparing to Other Haloalkynes and Unsubstituted Butynes

    Once you handle both 4-Chloro-1-Butyne and its close cousins—propargyl chloride, 1-chloro-2-butyne, and the unsubstituted 1-butyne—the differences can’t be missed. Propargyl chloride, with chlorine at the terminal position beside the triple bond, reacts harshly and degrades faster in damp air. 1-Chloro-2-butyne offers a tighter bond angle but tends to form side products in Suzuki and Heck reactions when downstream chemistry calls for cleaner coupling. 4-Chloro-1-Butyne fills a gap that neither alternative covers well. Its gamma chlorine opens up selective functionalization while holding onto the alkyne’s click chemistry appeal.

    Production batches for 4-Chloro-1-Butyne show improved shelf life under nitrogen or argon, with less waxy deposit in warehouse storage—a subtle but real difference for those managing changeovers in glass-lined or steel reactors. Compared with unsubstituted butynes, the addition of a chlorine atom lifts the compound into a class of modifiers, activating agents, and leaving groups suited to unique derivatizations. Its role grows in importance for complex molecule assembly, especially in industries pushing for new pipeline candidates in pharmaceuticals or higher-performance electronic materials.

    What Quality Means in Actual Practice

    Being a chemical manufacturer, product quality isn’t just numbers on a certificate; it’s a chain of actions and verifications from feedstock sourcing through to drum loading. We’ve witnessed firsthand how contaminated or off-spec feed—say, butynes coming with traces of water or leftover catalyst residues—spoils entire shifts, demands rework, and sets back deliveries. Real-world product assurance means on-the-floor presence. Our chemists and operators take samples from every batch, directly supervise loading, and run the numbers before a drum leaves the plant. This evolves from experience, when you’ve seen a failed coupling reaction in a pharma customer’s lab traced to a fractional percentage of a side isomer.

    Customers who buy from chemical traders often see wider variance in stability and color, sometimes noticing a slow yellowing or drifting GC profile. By contrast, running our own synthesis, we keep waste down and keep the chain of custody visible. By knowing each step from chlorination to distillation, issues such as off-odor or residue buildup draw quick realigning of plant settings. The market expects consistency because missed deadlines or out-of-spec intermediate costs downstream customers thousands.

    Why 4-Chloro-1-Butyne Matters in Modern Chemistry

    Decades in chemical production have shown us that certain compounds, though niche, unlock leaps in technical progress. 4-Chloro-1-Butyne falls in this category for emerging therapeutics, crop protection agents that depend on agile carbon frameworks, and battery research seeking resilient molecular backbones. Research groups trust this molecule for prototyping candidates that will never be visible in finished goods—the precision of this building block impacts the yield, performance, and safety of new innovations. Over the years, we’ve seen its influence grow, particularly as more processes demand regioselective activation without over-reactivity. As global requirements shift toward custom molecules and shorter development cycles, the importance of access to 4-Chloro-1-Butyne free from legacy impurities rises.

    Besides supporting R&D, larger volumes increasingly move toward full-scale operations—thus, the margin for error tightens. Quality-driven suppliers don’t just talk purity, they deliver on it because they work their own product lines all the way up from small-scale runs to multi-ton containers. Facilities adapted for haloalkyne containment, advanced drying systems, and field-tested transport procedures don’t spring up overnight. We’ve tailored equipment, trained staff, and refined standard operating procedures based on recurring lessons from each campaign. The result is a deeper, operational perspective that informs every batch.

    Challenges and Solutions in the Field

    Chemical manufacturing teaches resilience and adaptation. Every molecule comes with a story, and 4-Chloro-1-Butyne is no exception. We’ve navigated shutdowns caused by moisture incursions, process bottlenecks linked to outdated reflux systems, and sourcing hiccups for specialty catalyst that meets REACH or other regulatory frameworks. Each scenario forced on-the-ground troubleshooting, not just paperwork. Experience reveals that even small changes in catalyst purity or reaction agitation ripple through to physical properties of the final product. Long retention times in over-packed columns led to off-color drums, prompting us to reconfigure our distillation protocols. Investing in advanced in-line monitoring systems, while demanding upfront, paid off in rework avoidance and sustainability benchmarks.

    Not every challenge finds a textbook answer. Local utilities affect production consistency, where steam pressure fluctuations or water supply cleanliness tilt yields without warning. Building redundancy into critical systems—duplicate sensors, parallel feed lines—cuts downtime and keeps customer promises credible. For 4-Chloro-1-Butyne, microbial or chemical fouling of heat exchangers, even at trace levels, posed enough risk to justify more frequent maintenance than generic solvent lines.

    Looking Ahead: Sustainability and Changing Demands

    Increasing environmental scrutiny means processes involving volatile organic compounds and halogenated intermediates can’t stand still. We view regulatory adaptation as an ongoing responsibility. Our plant responded by closing loop solvent recovery, tightening landfill avoidance, and treating vent lines for trace chlorine or acetylenic emission. Not only does this safeguard licenses, but employees working 12-hour shifts see real differences in odor and air quality on the floor. Solvent minimization through reaction optimization cut both waste generation and process time. These are not abstract commitments, but rooted in lessons learned batch by batch, year by year.

    Future applications for 4-Chloro-1-Butyne span emerging fields—advanced battery electrolytes, cross-linked polymers with tailored reactivity, and agrochemical scaffolds with built-in triggers for targeted release. Feedback from downstream users paints a clear picture: performance depends as much on tight upstream quality as on application know-how. We plan for this by staying in close contact with users, not only on sales visits but through plant tours, live troubleshooting, and technical exchanges.

    The Manufacturer’s Commitment: Depth Over Volume

    Making 4-Chloro-1-Butyne at commercial scale doesn’t mean churning out undifferentiated barrels. It’s an ongoing partnership with chemists and industries depending on the reliable function of every molecule. By managing every step—from raw material vetting, through careful chlorination, to hands-on packaging—confidence in each shipment grows through shared effort. We stake our reputation not on trading volumes or after-the-fact documentation, but on the direct chain linking operator to reactor to customer lab bench.

    The full value of 4-Chloro-1-Butyne shines brightest where quality and reliability rule. Our experience, built across years and thousands of kilos shipped worldwide, grounds our belief in chemical manufacturing as a craft—one that honors both detail and innovation. In our world, this product isn’t anonymous: it’s an answer to evolving needs, trusted by those who measure progress in synthesis, not just in sales.