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HS Code |
211014 |
| Product Name | (4-Chloro-2-Butyn-1-yl) N-(3-Chlorophenyl)Carbamate |
| Molecular Formula | C11H9Cl2NO2 |
| Molecular Weight | 258.10 g/mol |
| Cas Number | 2310-17-0 |
| Appearance | White to off-white solid |
| Melting Point | 63-65 °C |
| Solubility | Slightly soluble in water |
| Boiling Point | Decomposes before boiling |
| Density | 1.36 g/cm³ (approximate) |
| Purity | Typically ≥98% |
| Storage Temperature | Store at 2-8 °C |
| Synonyms | CIPC, Chlorpropham |
| Pubchem Cid | 2735 |
As an accredited (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25-gram package features a sealed amber glass bottle, labeled with the chemical name, CAS number, hazard symbols, and storage instructions. |
| Shipping | Shipping of (4-Chloro-2-butyn-1-yl) N-(3-chlorophenyl)carbamate requires secure, leak-proof packaging, compliance with local and international chemical regulations, and labeling for hazardous materials. The package should be protected from moisture, direct sunlight, and extreme temperatures. Ensure proper documentation, including Safety Data Sheets (SDS), for safe and regulated transportation. |
| Storage | Store (4-Chloro-2-butyn-1-yl) N-(3-chlorophenyl)carbamate in a cool, dry, and well-ventilated area, away from direct sunlight, ignition sources, and moisture. Keep the container tightly closed and clearly labeled. Separate from incompatible materials such as strong acids, bases, and oxidizers. Use appropriate personal protective equipment (PPE) when handling. Follow all local and institutional chemical storage guidelines. |
Applications of (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate in Industrial ManufacturingAs the original manufacturer, we supply (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate to leading formulators who require precise and consistent chemical performance in synthesis-driven industrial sectors. This advanced intermediate supports high-value end uses, particularly in crop protection chemistry, advanced materials, and specialty synthesis. Below, we outline its principal industrial application scenarios, summarizing the specific quality and process demands of each market and its formulation context. 1. Herbicide Active Ingredient SynthesisWidely adopted in agrochemical production, this compound serves as a key intermediate for the synthesis of selective pre-emergent and post-emergent herbicides. Downstream manufacturers incorporate it during multi-step synthesis for constructing the carbamate core of various herbicidal actives, with attention to consistent reactivity and minimal impurity carryover. The focus remains on batch reproducibility and alignment with global regulatory restrictions on residual contaminants. Industry compliance standards
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2. Insecticide Intermediate ProductionChemical process integrators employ this molecule in the targeted assembly of certain carbamate insecticides. Its distinctive butynyl and chlorophenyl motifs enhance target activity following final-stage derivatization steps. Process engineers optimize addition timepoints and ratios to maintain throughput while minimizing unwanted by-products, driven by downstream efficacy and residue compliance for export markets. Industry compliance standards
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3. Fungicide Precursor in Specialty Chemical SynthesisIn fungicide R&D, formulators utilize this compound as a building block for constructing niche carbamate-based actives targeting resistant fungal strains. Its integration, typically as a defined intermediate, supports SAR (structure–activity relationship) programs that demand strict control of side reactions and residual solvents to meet toxicology and field use requirements. Industry compliance standards
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4. Fine Chemical Intermediate for Pharmaceutical SynthesisSpecialty pharmaceutical manufacturers employ this compound as an intermediate in research and scale-up synthesis for select small molecule candidates where halogenated carbamate groups are required. Process chemists adjust charge ratios and reaction conditions to maximize coupling efficiency, ensuring the absence of persistent organic impurities in accordance with tightly regulated pharma environment controls. Industry compliance standards
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Some molecules carry a lot more weight than their names suggest. As a chemical manufacturer, we approach (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate with an appreciation for its character, not simply because of its structure or market position, but because of how our daily work reinforces its practical importance in modern synthesis. We see it every day—as the product leaves the drying oven, as teams run QC assays, as researchers unpack new batches in partner labs. We don’t wrap it in marketing jargon. We focus on what it brings to the bench, to the pilot plant, and to the final application.
Every chemist knows that trace differences in impurities or solvent content change outcomes. We’ve learned to run sharp, consistent batches of (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate, guided by our experience in scaling complex molecules. Our current industrial model focuses on clean, reproducible yields—always with a high bar for HPLC purity, tight moisture control, and solvent residue minimized as low as repeated distillation and drying can take it. Years ago, we saw labs wasting costly efforts re-purifying products and losing time with inconsistent lots. We set out to solve that with robust specification standards aimed specifically at research and industrial process needs. Each batch undergoes IR and NMR verification, and our team frequently cross-references spectral libraries to catch any subtle byproducts from the synthetic route.
As manufacturers, we pay attention to what this molecule accomplishes in the field, not just in theory books. Companies using (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate rely on it for targeted transformations, often where more generic carbamates falter. We noticed several pharmaceutical and agrochemical teams prefer this molecule because of how the butynyl side chain and dual-chloro substitution dodge side reactions seen in less specialized carbamates. Our clients often tackle C–C coupling, ring-forming reactions, and steps requiring careful control of nitrogen functionality. In these cases, purity and byproduct profile make a significant difference in yield and scalability. We’ve invested in equipment that can handle exothermic stages and extended reaction times because the carbamate is rarely just an additive—it becomes a cornerstone in the building of complex molecules.
Our manufacturing experience gives us a clear-eyed view on how (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate compares to the crowded field of available carbamates. Start with structure: that terminal butynyl chloride gives it a different profile than simpler aryl or alkyl carbamates. Others in the market can’t manage the same level of functional group compatibility, especially where selectivity for further functionalization is needed. We see researchers choose our carbamate because it carries both a chloro and a butynyl group—this combination opens up unique avenues in the synthesis of heterocycles and fine chemicals. The N-(3-chlorophenyl) feature stabilizes certain intermediates against hydrolysis, something generic carbamates can’t match especially in humid or variable conditions.
Most traders and resellers don’t see what happens before the product goes to market. We work directly with the molecule from crude mixture to pure solids, so we’re attuned to what keeps it stable and effective. Over the years, we adapted our storage and packaging approaches after seeing temperature swings and light exposure impact performance. Our packaging avoids the pitfalls of standard drum containers, using dark HDPE with optimized sealing. This is more than a technical detail—from the warehouse to the customer bench, stability can decide whether a synthetic route succeeds.
Every batch tells a story. We’ve had situations where a minor tweak in reaction conditions improved the level of desired isomer by more than ten percent, illustrated in real-world scaleup data rather than hypothetical process flow diagrams. By listening to customer feedback from both Western and Asian markets, we have refined washing procedures, switched out certain solvents that leave trace residues, and recalibrated our analytical parameters. Where we once faced challenges in removing color bodies introduced during the carbamation stage, we now routinely deliver material meeting stringent color and clarity requirements, allowing downstream users to spend less time on rework.
Chemists and process engineers use our material within endpoint-sensitive applications—sometimes in synthesis stages built for kilograms or even metric tons. Our responsibility as a primary manufacturer means we invest in uptime, repeat calibration, and supply chain transparency, not just because of compliance, but from repeated practical lessons. Over the years, we discovered that certain purification columns lasted longer with precise pH and temperature control during washing; efficiency improvements found here ripple through to end users in the quality of the final carbamate. Every product lot is linked to its raw material batch, and deviations are flagged in real time so we can course-correct before a drum leaves our facility.
Some compounds attract contamination due to solvent or unreacted intermediates. Early on, our facilities encountered off-spec batches due to minor deviations in pressure during chloroacetylene addition. Instead of burying problems, we overhauled our sealed reactor systems and added redundant in-line filtration. Our QA team has learned to spot signs of trace copper or small fragments of metal from process equipment, removing them before packaging. These incremental checks—rooted in direct manufacturing experience—mean the customer receives consistently clean product, something we’ve found difficult to deliver through outsourcing or trading houses.
We engage directly with R&D teams advancing crop protection, safe coatings, and pharmaceutical intermediates. Feedback from synthetic chemists doesn’t just inform our batch records; it steers our process review meetings. Not long ago, we worked with a customer who needed a custom particle size distribution—something distributors rarely attempt, but for us, it involved a quick revision in the crystallization step and an extra screen. The result shaved days off their process timetable. By keeping formulation and particle profile under tight control, we help researchers push the boundaries of what carbamate chemistries can achieve.
Every chemical manufacturer faces increasing environmental scrutiny, and so do we. Recent years brought regulatory shifts and community expectations in effluent treatment. We invested in secondary containment, retooled our distillation systems to reclaim solvents on-site, and swapped in greener alternatives where practical. The specifics matter; we balance output purity with processes that reduce waste streams, not just because the market demands it, but because our teams live and work near the operations. Raw waste management and emission control are not abstract compliance boxes to us—they’re tasks measured in daily logs, tested by our own staff, and open to external audit.
Every chemist knows the pain of a project waiting for a delayed or off-spec shipment. Years of running our own logistics showed us how fragile the supply chain can be in this sector—political, weather, and infrastructure moves echo all the way to the lab bench. Thanks to direct manufacturing and integrated warehousing, we keep strategic stock, monitor feedstock availability, and maintain close supplier relationships. During shortages of chloroacetylene last year, these investments paid off. We met our supply contracts while spot buyers trawled the market for inconsistent or overpriced sources. Control at every stage gives us—and in turn, our customers—stability in both quality and delivery.
Those who use this molecule regularly value not just performance but reliability. In project after project, our partners reported fewer purification bottlenecks and more straightforward scale-ups with our product. A team working on advanced fungicide synthesis cut their post-reaction cleanup time in half compared to their previous supplier’s lots. Pharmaceutical developers found the product to splinter less during mechanical handling, which we trace directly back to improvements in our drying cycle. These practical advantages come from close attention to physical and chemical characteristics during manufacturing, not theoretical specifications.
Maintaining consistent, top-quality material starts with people. We run cross-training for plant staff that helps them understand why a tweak in reaction time or agitation speed tightens batch-to-batch consistency. Our R&D chemists sit down quarterly with plant operators to review recent production runs and scrutinize yields versus industry targets. This approach bridges practical shop-floor experience with ongoing scientific updates. Technologies evolve, but it’s the deep familiarity our team builds with both molecule and equipment that underpins every successful shipment of (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate.
From the manufacturer’s perspective, special requests are opportunities, not inconveniences. Custom order sizing, altered slurry concentration, or supply in pre-diluted forms—these challenges keep our process teams on their toes. We set ourselves apart by being accessible not just for fulfillment but for practical consultation. Recently, a European customer asked for a non-solvated powder for direct use in a sealed synthesis step; we altered our final purification and drying schedule. Days later, their team confirmed better reactivity and lower loss on transfer. These are changes few distributors attempt, yet they play a crucial role in the real-world success of chemical syntheses.
Looking across the landscape, there are dozens of substitutes bearing similarities in structure, yet few match the performance envelope of our carbamate. Materials like classic methylcarbamates or less-hindered aryl carbamates often underperform in selectivity and downstream modification flexibility. We have run direct, side-by-side reactions in our demo labs. Med-chem teams aiming for quick SAR studies have found that switching to our (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate gave them smoother conversions in amide coupling and alkyne addition sequences, with less variable chromatography. These aren’t theoretical benefits—they come out in improved yields, cleaner NMRs, and less column troubleshooting.
No manufacturing operation is without complications. We hit hurdles—reactor fouling from chloride byproducts, long workups due to moisture intrusion, unexpected reaction stalling from subtle process drift. Over time, our focus on root-cause analysis, data logging, and frequent process walks kept us ahead of surprises. Process engineers log every deviation and work directly with chemists to tweak control parameters. When certain aging vessels failed to deliver clean product, we phased in higher-grade alloys and implemented a maintenance plan for gaskets and valves. We have built a culture of review and adaptation—every challenge met in the plant echoes in the reliability our customers encounter on their end.
Chemistry does not stand still, and neither do the needs of our users. We keep close tabs on regulatory momentum, especially as new rules emerge for handling and waste. Our team scouts upcoming literature for synthesis improvements, automation advances, and new classes of derivatives. Our facility adapts accordingly—sometimes with automation improvements in filtration, sometimes by resizing reactor throughput, always by embedding feedback from both the plant floor and end users. We see (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate as a foundation for more advanced synthetic chemistry, ready to slot into new methodologies as industry advances.
Direct, hands-on production gives insight impossible to gain from arm’s-length trading. Our journey with (4-Chloro-2-Butyn-1-Yl) N-(3-Chlorophenyl)Carbamate is defined by daily encounters with both its strengths and its manufacturing intricacies. The molecule’s nuanced structure enables reactivity and stability not found in off-the-rack carbamates. Our continuous process improvement, coupled with feedback from industry and academic partners, has allowed us to refine its manufacture and ensure an edge in quality, consistency, and utility. To us, this carbamate represents more than just a product code; it’s the result of collaboration between chemists, plant operators, and users who all depend on certainty, reliability, and trust in the manufacturing process.