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HS Code |
467611 |
| Chemical Name | Cyclobutyl Chloroformate |
| Cas Number | 3193-11-1 |
| Molecular Formula | C5H7ClO2 |
| Molecular Weight | 134.56 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 170-172°C |
| Density | 1.208 g/mL at 25°C |
| Melting Point | -43°C |
| Refractive Index | 1.446 |
| Solubility | Reacts with water; soluble in most organic solvents |
| Flash Point | 68°C (closed cup) |
| Synonyms | Cyclobutanecarbonyl chloride, Cyclobutyl carbonochloridate |
As an accredited Cyclobutyl Chloroformate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Cyclobutyl Chloroformate, 25g, is supplied in a sealed amber glass bottle with a secure screw cap for light-sensitive chemicals. |
| Shipping | Cyclobutyl Chloroformate is shipped as a hazardous chemical, typically in tightly sealed containers or glass bottles, under protective packaging to prevent leaks. It should be transported in accordance with regulations for toxic and corrosive substances, avoiding heat, moisture, and incompatibles, and with appropriate hazard labeling to ensure safe handling during transit. |
| Storage | Cyclobutyl chloroformate should be stored in a cool, dry, and well-ventilated area, away from sources of moisture and incompatible substances such as strong bases, oxidizers, and acids. It must be kept in tightly sealed containers made of compatible materials, shielded from direct sunlight and heat sources. Proper labeling and secure storage to prevent accidental release or exposure are essential. |
Applications of Cyclobutyl Chloroformate in Industrial ManufacturingCyclobutyl chloroformate serves critical functions in multiple industrial sectors, particularly within specialized organic syntheses, pharmaceutical active ingredient preparation, and agrochemical development. As a direct manufacturer, we ensure strict quality controls, batch traceability, and supply chain transparency supporting regulated downstream integration. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediate SynthesisWithin pharmaceutical manufacturing, cyclobutyl chloroformate acts as a chlorocarbonylating agent for constructing protected amine and alcohol intermediates. Process chemists utilize it primarily during peptide coupling reactions where selectivity, reaction yield, and impurity profile control are critical. The material enters during side-chain or terminal functional group protection steps, facilitating downstream deprotection strategies in the later API stages. Lot documentation, impurity limits, and elemental impurity risk assessments form part of manufacturing best practices, ensuring traceability from starting raw materials through final API batches. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingAgrochemical formulators employ cyclobutyl chloroformate during the synthesis of urea or carbamate-based insecticide and herbicide intermediates. The reagent introduces carbamate groups via isocyanate formation with subsequent coupling, generating key building blocks for active pesticide ingredients. Trace metal testing and batch process registration with local authorities remain standard to comply with environmental and product safety requirements. Industry compliance standards
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3. Specialty Polymer FunctionalizationManufacturers of engineering polymers incorporate cyclobutyl chloroformate for post-polymerization functionalization, specifically to introduce pendant cyclobutyl carbonate moieties. Operators feed the material into reactive extrusion or solvent-phase modification tanks, typically under strict anhydrous conditions to prevent premature hydrolysis. Process controls target conversion yield, absence of unreacted chlorocarbonyl groups, and minimal formation of oligomers or crosslinked gels. Industry compliance standards
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4. Fine Chemical Custom SynthesisChemical synthesis service providers and custom manufacturers use cyclobutyl chloroformate for constructing protected derivatives needed for medicinal chemistry research and advanced building blocks. The reagent provides selectivity for specific functionalities in multistep syntheses, with tight documentation and analysis of trace impurities to support client-facing projects. Synthesis conditions—including solvent, temperature, and order of addition—are optimized case by case in project-specific batch documentation. Industry compliance standards
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Every specialty chemical brings its own challenges and opportunities. At our own facility, Cyclobutyl Chloroformate stands out both for its unique ring structure and the kind of custom work it enables for organic synthesis projects. The way this molecule handles itself in the reactor hall shows both the complexity and reliability that process chemists and formulators look for in today’s performance-driven environments.
Chemically, Cyclobutyl Chloroformate belongs to the family of chloroformate esters. Its structure typically appears as C5H7ClO2, where a cyclobutyl group attaches directly to the chloroformate functional unit. The cyclobutyl ring, compact but strained, offers certain synthetic advantages and opens new avenues for downstream chemistry. Those with first-hand experience using regular alkyl chloroformates will immediately recognize that the four-membered ring can change reactivity, offering a balance between stability in storage and reliability during transformation stages.
The main reason many teams prefer cyclobutyl derivatives often comes down to two factors: selectivity and unique ring strain. Once inside a synthesis campaign, the cyclobutyl chloroformate tends to give narrower side product profiles, an important aspect for fine chemicals and pharma intermediates. In our facility, technical staff noticed years ago that cyclobutyl chloroformate doesn’t bring the same handling hassles sometimes seen with smaller or larger chloroformate esters—particularly in scale-up. With regular methyl or ethyl chloroformate, it’s easy to see volatility issues create discrepancies in batch-to-batch yield or loss during transfer. Cyclobutyl’s boiling point and vapor pressure make it better to manage, limiting occupational exposure and tightening process control.
We keep a close watch on several specs with every run: assay by GC, moisture, acidity, and appearance. Material usually rolls off our lines as a colorless to pale yellow liquid, with typical assay levels above 98%. The odor gives a sharp, characteristic signal—nothing like the heavier carbonates or the smoke of aryl versions. From the plant manager’s perspective, storage comes straightforward with the right precautions: proper ventilation, sealed containers, shaded from direct sunlight, temperature below 30°C, and away from bases or moisture sources. No one wants decomposition, especially at this price point, so on-site protocols require periodic retesting by QC and keeping cycle times quick from plant to truck.
Cyclobutyl Chloroformate is not shipped or stored like typical solvents. The reactive chlorine atom in the molecule means every person handling it uses gloves, goggles, and fume hoods. Years ago, someone in our pilot area skipped checking a transfer line connection, and a tiny leak immediately gave off sharp fumes—a quick reminder that direct contact can cause burns and that safety briefing isn’t just paperwork. Each drum we fill passes both nitrogen purging and integrity validation, reducing hydrolysis risks and the possibility of HCl formation.
Most partners buying Cyclobutyl Chloroformate focus on synthesis of ureas, carbamates, and certain protected amino acids. The molecule’s performance in these transformations draws attention. If you compare carbamate synthesis with methyl, ethyl, or isopropyl chloroformate, the cyclobutyl version typically shows a shift in reaction rate, often yielding cleaner product and minimizing those nagging side-chain rearrangement reactions. For example, when scaling up carbamates destined for active pharmaceutical ingredients or advanced agro intermediates, the distinctive four-membered ring leaves less room for side processes, which simplifies purification downstream.
We’ve run both kilo-lab and commercial-scale kinetic studies on this molecule. Results consistently show that under mild basic conditions and moderate temperatures, cyclobutyl chloroformate reacts efficiently and lets chemists set up more predictable work-ups without the runaway exotherms you get with tert-butyl or benzyl analogues. Water- and air-sensitive substrates remain protected until the right trigger, giving process engineers tighter process windows and better reproducibility batch after batch.
What makes cyclobutyl different from its family relatives? From our standpoint, the cycle-ring structure gives three immediate payoffs: controlled volatility, manageable hydrolysis risk, and greater stability during extended storage. Methyl and ethyl chloroformates sit near the top of the volatility stack, so their fumes demand heavy-handed controls, and they slip into environmental monitoring logs far more often. Cyclobutyl’s higher boiling point means fewer headaches about loss or staff exposure during transfers, especially in summer.
Looking at reactivity, secondary and tertiary alkyl chloroformates show more resistance to nucleophilic attack, which can complicate low-temperature carbamoylation or other functional group transformations. Cyclobutyl sits between the extremes, offering predictable conversion rates and less risk of over-reaction. These features have helped customers who push toward greener chemistry goals, reducing reliance on heavy-duty acid scavengers or excess amine bases, and simplifying aqueous work-up stages. Down the line, these elements lower effluent burdens and waste handling charges for users, making their projects both cleaner and leaner.
Chlorination-triggered byproducts and overreaction—pain points for those with experience using benzyl and phenyl chloroformates—rarely show up in cyclobutyl campaigns. Our technical team has worked hand in hand with clients to replace old aryl chloroformates, and the drop in hazardous waste volumes is plain to see. Product labeling and downstream compliance headaches shrink at the same time. This isn’t a small shift in labs with strict emissions policies or high energy bills for solvent recovery.
We listen closely to feedback from technical managers, bench chemists, and operators at partner sites. A recurring comment concerns batch-to-batch reproducibility. Small-chain chloroformates sometimes lead to variable reaction outcomes, with inconsistent impurity profiles. We’ve seen cyclobutyl’s rigid structure dampen those risks, giving tighter assay and byproduct spread even when customers push to higher scales. It’s common for a project to start on propyl or isopropyl derivatives and migrate to cyclobutyl as teams try to improve yield or process safety.
An aspect we’ve watched in our own plant is shelf-life. Properly handled, cyclobutyl chloroformate sits stable for months. QA inspections rarely find meaningful decomposition when storage conditions follow the normal guidelines. That predictability lets procurement teams purchase in larger lots, cutting delivery and packaging costs, and gives engineers less frequent batch requalifications to juggle. Everyone on the plant team appreciates the reduced workload from not constantly replacing aged drums or reworking old material. This kind of reliability is a big part of why we’ve extended our output capacity for this product over the past five years.
From the manufacturing side, process safety experience shapes every action. Years of in-plant work taught us how even small departures from protocol with reactive compounds can trip up a health and safety record. Unlike some alkyl or aryl chloroformates, cyclobutyl versions release sharply irritating fumes only under strong heat or acid contamination; at normal temperatures under nitrogen, accidental release risks remain lower. Still, standard PPE and air monitoring never go out of practice. Decontamination drills and line purges get tested after every turnaround, so any residue from prior batches doesn’t trigger unwanted reactivity.
Waste neutralization protocols benefit too. The hydrolysis byproducts keep the same family risks as with other chloroformates—mainly acid, CO2, and alcohol production on exposure to moisture. Still, we see a smaller exotherm and less aggressive fuming in our neutralization tanks compared to methyl or ethyl chloroformate runs. This practically shortens the turnaround between campaigns, helping us support rush orders more reliably. Routine air sampling in and around our storage, pumping, and drum filling stations has shown fewer excursions above occupational exposure limits since shifting our larger specialty production over to cyclobutyl lines.
Many of the development projects using Cyclobutyl Chloroformate today aim for carbamate intermediates and specialty ureas. Pharmaceutical manufacturers favor it for side-chain protection in peptide synthesis and for building unique cyclic intermediates. Agrochemical researchers look to it for carbamate herbicides that demand tighter isomer control. Each application’s workflow has subtle differences, but the core appeal always comes down to improved yield, fewer purification steps, and steadier cost models.
By maintaining a consistent supply chain link for cyclobutyl chloroformate, we help process labs stick to their project timelines, whether they’re running gram-scale proof-of-concept or scale-up to multi-ton production. Crop protection and life science companies already report better downstream reproducibility and less deviation in API quality when shifting to this starting material. As synthetic demands get stricter on regulatory compliance and emission limits, reducing impurity generation and solvent waste with a reliable core building block can make all the difference.
Logistics links play a key role from our side, too. Truck to tank, and tank to plant, any slip in process control can cut into margins. Cyclobutyl Chloroformate holds up well in our field logistics tests, arriving at off-site warehouses with little to no drop in specification. Our shipping team seals every container under dry nitrogen before leaving the filling bay. No cargo passes the gate without corrosion-resistant packaging and clear date-coding, a step that’s reduced downstream complaints about product aging and container leaks.
For customers running multi-stage synthesis with high-purity needs, our analytical lab keeps every lot traceable by GC–MS, IR, and Karl Fischer. Technicians check for even low-level impurities, which a few ppm can disrupt in high-value advanced intermediates. During past root cause investigations on off-color batches, QA confirmed that minor upstream air leaks, not reagent degradation, were to blame—promptly corrected in the next cycle. Robust protocols for regular process audits keep these issues rare, and lessons filter back into every new run. In short, the real-world stability of cyclobutyl chloroformate in transport and storage has made it a favorite among procurement managers under pressure to meet fill rates and spec targets.
Chemicals like Cyclobutyl Chloroformate will never be “green” in the same sense as minerals or phosphorus compounds, but their role in process intensification remains valuable. Compared to earlier generations of chloroformate esters, this variant helps plants cut solvent use and batch losses during purification. Teams working to hit sustainability targets—wastewater volume cuts, carbon footprint reduction, tighter VOC limits—see tangible progress after switching over from more volatile chloroformate options. For sites balancing strict environmental permits, that shift can allow higher output per line or reduce the need for additional emission abatement equipment.
On our shop floor, new closed-loop nitrogen blanketing systems now surround drum filling and decanting areas to cut open-air vapor phase losses. We spent years refining these systems, and it paid off by reducing off-spec and aged material returns nearly to zero. Across the sector, further research into catalysts and process alternatives for cyclobutyl chloroformate remains lively. Green chemistry advocates look at heterogenous base or phase-transfer protocols, aiming to avoid using excess amine or acid scavengers. This pathway points toward both efficiency and safer, more sustainable workflows in the decades ahead.
Those who’ve worked long enough on the plant side rarely underrate the importance of minor chemical differences. Cyclobutyl Chloroformate’s blend of stability, selectivity, and process-safe behavior owes as much to its structure as to the everyday commitment of operators, engineers, and QC specialists on production lines. The lessons pulled from years of actual incidents, near misses, and successful campaigns shape every protocol update and inspire every improvement in plant engineering.
Today, rising demand from pharma, crop protection, and fine chemical sectors keeps the pace of innovation moving. Yet, in our experience, stability in the supply of chemicals like cyclobutyl chloroformate depends as much on plant operations as it does on regulatory changes or market demand spikes. No batch leaves our facility without full traceability and real-time production feedback. We encourage users—whether researchers, process engineers, or project leads—to pass back insights from their own campaigns, so future batches suit both shifting technical specs and evolving safety requirements.
In summary, Cyclobutyl Chloroformate has become a go-to intermediate not simply for its molecular features, but because hands-on teams see fewer process headaches, better yields, and more reliable project planning when using it. From first pilot lots to regular multi-ton shipments, each batch ties back to close process control, a safety-first culture, and ongoing dialogue between chemists at every stage. Whether used in innovation or routine manufacturing, these characteristics shape how specialty chemicals support progress in both industry and science.