|
HS Code |
727176 |
| Cas Number | 527-69-5 |
| Molecular Formula | C5H3ClO2 |
| Molecular Weight | 130.53 g/mol |
| Iupac Name | furan-2-carbonyl chloride |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 85-87°C at 18 mmHg |
| Melting Point | -14°C |
| Density | 1.32 g/cm³ |
| Solubility | Reacts with water, soluble in organic solvents |
| Refractive Index | n20/D 1.541 |
| Flash Point | 65°C (closed cup) |
| Purity | Typically ≥98% |
As an accredited Furoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Furoyl Chloride is packaged in a 500 mL amber glass bottle with a secure blue screw cap and a warning label. |
| Shipping | Furoyl Chloride should be shipped in tightly sealed containers, protected from moisture and incompatible substances, such as strong bases and oxidizers. It must be labeled as a corrosive and transported according to local, national, and international regulations for hazardous chemicals. Appropriate personal protective equipment (PPE) is required during handling and transport. |
| Storage | Furoyl chloride should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from moisture and incompatible substances such as strong bases and oxidizers. It must be kept away from direct sunlight and sources of ignition. Containers should be labeled properly and checked regularly for leaks or corrosion. Use appropriate personal protective equipment when handling. |
Applications of Furoyl Chloride in Industrial ManufacturingAs a dedicated manufacturer of furoyl chloride, we support a select set of downstream industries where this specialty intermediate plays a significant role in value-added production. Our consistently high-purity batches meet stringent demands across sectors that require assurances on traceability, compliance, and process compatibility with their advanced synthesis operations. 1. Active Pharmaceutical Ingredient (API) SynthesisLeading pharmaceutical plants employ furoyl chloride in the acylation of advanced intermediates, particularly during the synthesis of drug molecules with a furoyl moiety. This step often defines the pharmacokinetic performance and stability profile of targeted APIs. Quality-driven integration requires careful monitoring of residual chloride and related impurities, with compliance traceability extending from incoming raw material through validated downstream operations, including reaction, purification, and documentation for final regulatory submission. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis (Herbicides and Fungicides)Agrochemical plants use furoyl chloride to introduce furan-derived moieties during the construction of active ingredients, particularly those requiring selectivity in complex weed or fungal control scenarios. Careful formulation guides its integration to control hydrolysis and maintain the targeted activity spectra. All operations must align with regional and international regulatory frameworks, both for raw material sourcing and completed active ingredients, ensuring traceability for country-specific residue and registration protocols. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Pharmaceutical Intermediate ManufacturingProducers of specialty pharmaceutical intermediates utilize furoyl chloride for selective acylation of advanced building blocks, often forming protected intermediates for further transformation or strategic deprotection. This application demands a precise feed of material, with full adherence to customer audit trails and stringent process controls to prevent unwanted side reactions, particularly in substrates sensitive to acid chlorides. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Advanced Material Science: Electronic ChemicalsManufacturers of fine electronic chemicals integrate furoyl chloride during the precision synthesis of specialty polymers and organic semiconductors where a furanyl substituent benefits dielectric or charge transport characteristics. The process, reliant on batch reproducibility and online purity verification, requires heightened environmental compliance and control of by-products, as even trace contaminants can compromise downstream material performance in semiconductor fabrication. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive Furoyl Chloride prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.
We will respond to you as soon as possible.
Tel: +8615365186327
Email: admin@ascent-chem.com
Flexible payment, competitive price, premium service - Inquire now!
In our day-to-day work producing specialty intermediates, Furoyl Chloride stands out as both a technically interesting compound and a pivotal building block for several industries. Chemists recognize it as an acid chloride derived from furoic acid, molecular formula C5H3O2Cl, CAS Number 527-67-1. Transparent to pale yellow in appearance, it carries a sharp, penetrating odor and demands careful handling. Over the decades, continuous feedback from researchers and process engineers has influenced the way we synthesize and purify Furoyl Chloride, driven by the demand for tighter analytical specifications and higher regulatory scrutiny.
We rely on practical, tested methods to produce material with high purity — reaching levels above 98% in our best technical grades, as measured by gas chromatography. The product’s melting point lies around -9°C, with a boiling point near 195°C, and remains stable under standard storage if moisture is excluded. The presence of free acid or unconjugated bases affects downstream reactions, so residual acidity and colorless clarity have become key parameters in our internal batch release. Many laboratories and manufacturers look closely at free acid values below 0.1% and color indices nearly matching distilled reference grades. From extensive experience, we have found that maintaining water content under 0.5% by Karl Fischer titration prevents hydrolytic degradation, keeping reactive chloride intact for further synthesis.
Our production process begins with furoic acid, usually sourced from well-characterized agricultural by-products, which allows us to trace back potential impurities. The acid reacts with thionyl chloride under controlled conditions, producing Furoyl Chloride and liberating sulfur dioxide and hydrogen chloride. Strict ventilation prevents vapor buildup, both to avoid contamination and ensure worker safety. We employ glass-lined reactors for superior corrosion resistance; stainless steel lines would rapidly deteriorate from the evolved gases. Attention to cleaning cycles and gasket materials further distinguishes reliable batches from inconsistent ones on the market.
Pharmaceutical companies and research institutions prioritize Furoyl Chloride for its role in acylation reactions, especially where the furan ring’s electronic properties introduce new behavior in active pharmaceutical ingredients. Medicinal chemists rely on its ability to acylate amines and alcohols, creating furoyl-substituted anilides, amides, and esters. Our direct partnerships with R&D groups have highlighted its use in drug discovery pipelines, where small-molecule inventors are eager for both purity and repeatable batch performance. Generics facilities see it as a must-have intermediate for drugs that require furan rings for bioactivity—antibacterial, antifungal, and anti-inflammatory agents all trace some development roots to this compound.
Outside pharmaceuticals, agrochemical innovators use Furoyl Chloride to create herbicides and fungicides by integrating the furoyl motif. Materials science groups working on specialty polymers experiment with this material for functionalization steps, aiming to incorporate furyl units for improved thermal behavior or reactivity. Textile auxiliaries and dyes, fragrance intermediates, and specialty fine chemicals draw on its robust reactivity and moderate handling requirements—if one has the right infrastructure for acid chlorides, workflow adjustments are minimal.
Many chemists ask how Furoyl Chloride compares to more common acid chlorides like benzoyl chloride or acetyl chloride. The answer always comes back to the furan ring. Unlike aromatic benzoyl chloride, Furoyl Chloride’s oxygenated heterocycle impacts both stability and reactivity. While handling still requires dry and inert conditions, the lower boiling point and greater sensitivity to bases make Furoyl Chloride more reactive—a feature sought after by chemists hoping to push reactions toward completion under milder conditions. The furan ring’s electron distribution affects acylation selectivity; in peptide coupling, it contributes to unique by-product profiles and sometimes faster reaction rates. This makes it less interchangeable with more conventional acyl donors in combinatorial libraries or pilot plants.
Odor and volatility differ as well. Furoyl Chloride’s volatility sits between low-molecular-weight acid chlorides like acetyl chloride and heavier aromatic types. The odor is distinctly sharper, without the sweet chlorinated perfume of benzoyl or the acrid punch of acetyl chloride. Plant operators new to the material soon notice the difference.
Disposal and handling routines set further distinctions. The presence of the furan ring drives slightly different waste treatment protocols, as hydrolyzed residues and their breakdown products follow somewhat different environmental fates than plain alkyl or aryl chlorides. We work with environmental chemists to ensure run-off water and air emissions never exceed regulatory guidance. As regulations tighten, especially in Europe and Japan, the industry adapts disposal processes to fit the requirements for heteroatomic organics, and we keep clients updated on these changes.
Customers entering the world of furan chemistry often ask about packaging and storage. From experience, the main rule stays constant: keep Furoyl Chloride away from moisture. Even a small amount of water initiates rapid hydrolysis, creating furoic acid and generating heat and hydrochloric gas. This underscores the need for dry, airtight glass containers or lined metal drums with desiccant packs. Standard steel barrels, even with linings, offer insufficient resistance over time, so we use glass bottle inserts or Teflon-lined closures.
Transport presents logistical challenges, especially in hot climates. Reaction to sunlight or excessive temperatures can cause pressure buildup inside containers, so temperature-controlled freight becomes a worthwhile investment—not just for product quality but for safe handling at each step. For projects requiring kilogram to tonne-scale deliveries, we ship only under UN-approved transportation guidelines, and offer advice to receive and store product well before any scheduled process date. This practice stops project delays from poor material quality.
Producing Furoyl Chloride regularly puts plant equipment through its paces. Highly reactive chlorides can attack weld seams, gaskets, and even instrumentation. Adding that the furan ring brings unusual reactivity, facilities engineers often find themselves swapping out parts or upgrading sensors sooner than with other acid chlorides. Small leaks can create localized corrosion, emitting strong fumes and risking workplace irritation. For this reason, plant managers pay close attention to regular maintenance, choosing elastomers and coatings after thorough testing for chemical compatibility.
Workplace exposure controls require constant vigilance. Even trace vapors can irritate eyes and the respiratory tract. Proper PPE, including goggles and fitted respirators, coupled with air extraction and monitors, limit worker risk. During drum filling or sampling, operators work in flow hoods or local exhaust systems, and undergo regular health checks. In the rare event of a spill, our safety teams deploy neutralizing agents such as sodium bicarbonate or specialized sorbents, and we’ve learned over time how to minimize secondary contamination.
We’ve spent years perfecting quality assurance—analysts perform titrations, measure color, GC purity, and water content with every lot. Materials destined for pharmaceutical synthesis undergo further tests looking for potentially genotoxic impurities and unusual by-products. By building data sets for each batch, we spot trends early, flagging if process modifications have altered impurity profiles or yields. This investment in analytics reduces customer complaints and increases confidence for both established and novel applications.
Chemical manufacturing always faces unexpected hitches. Sometimes supply interruptions in base furoic acid slow production. Harvest seasons, transportation restrictions, or changes in agricultural by-product output impact our operations line. We build stock and work with long-term suppliers who can certify cultivation and processing standards. Collaboration helps us keep pricing and deliveries steady, even as raw material volatility continues to affect specialty chemicals.
We occasionally see batch-to-batch differences in color or odor intensity. Slight shifts in reaction temperature, gas stripping rates, or feedstock composition translate into variation—especially for highly reactive materials like Furoyl Chloride. Our teams document these variables, fine-tuning each step for repeatability. If our own tests spot an unexplained outlier, we recall the batch immediately, even if it meets customer specs, and communicate proactively. Long-term relationships in fine chemical supply survive through honest exchange and openness about potential risks and rewards.
Another ongoing challenge comes from regulatory changes. Environmental protection agencies steadily expand reporting and emission control rules for acid chlorides and furan derivatives. We routinely review emission streams, revise waste disposal procedures, and invest in scrubber upgrades to meet new targets. Clients in highly regulated pharmaceutical and agrochemical sectors receive regular updates and revised safety documentation. These efforts provide confidence, allowing users to scale up new products and match internal safety guidelines with supplier assurances.
Applications for Furoyl Chloride are evolving. Researchers now explore new classes of furoyl-linked compounds, expanding from legacy pharmaceuticals to specialty catalysts and green chemistry solutions. Since the furan ring offers unique electronic attributes, organocatalysis groups have started using Furoyl Chloride to prepare new ligand systems. Collaborations with university groups spur technical support requests for custom purities, strict control of metal or organochlorine impurities, or new, less hazardous derivatives. Our technical service chemists spend more time than ever discussing reaction optimization, scale-up troubleshooting, and custom packaging.
Growth in the Asian R&D sector has encouraged us to plan capacity expansions and refine local distribution. Laboratory equipment quality and local regulatory requirements differ from North American or European standards; we’ve adapted our packaging, documentation, and validation reports to help these labs adopt Furoyl Chloride more easily. Training on acid chloride handling, waste neutralization, and contamination prevention is part of our supply chain support for these growing labs.
We also continue to investigate alternatives for traditional reagents like thionyl chloride, both from a safety and environmental perspective. Green chemistry initiatives and pressure from multinationals spur us to experiment with less hazardous chlorinating agents, direct electrochemical chlorination, and continuous flow reactors to reduce operator exposure and cut down on waste. Innovations in gas abatement and solvent recovery help us further minimize our environmental footprint, meeting the demands of a more responsible supply chain.
Buyers choosing among several suppliers for Furoyl Chloride frequently discover large disparities in quality, shelf stability, and analytical support. Sourcing directly from a committed, active manufacturer brings practical benefits. We honor agreements by keeping precise release records, offering retained samples with every order, and responding quickly should process issues arise downstream. By working hands-on in production, we understand how small changes—during synthesis, purification, or packaging—impact end user outcomes. Instead of relying solely on certificates of analysis, our partners gain direct access to technical support, trend analytics, and discussion of process improvements.
Over years of production, we’ve confronted every challenge: unstable supply chains, regulatory changes, evolving product applications, and the inevitable surprises from highly reactive chemistries. Each success and setback shapes better controls and smarter process investments. Sourcing Furoyl Chloride from a manufacturer invested in its own methods—one who tracks each lot from raw material to finished drum—delivers more than just supply, but a partnership that improves both safety and long-term innovation.
We’ve worked closely with site chemists and plant staff through all sorts of process incidents. The stories behind each drum of Furoyl Chloride carry many hours of hands-on effort, train-the-trainer sessions, and late-night troubleshooting when a pilot batch refuses to behave. Sitting down with users, hearing what works and what doesn’t, offers lessons no technical data sheet could capture. Many process improvements and new ideas start with these real-world discussions, not from top-down management.
Whether project teams need analytical advice, help with waste minimization, or troubleshooting for failed reactions, our approach remains to treat each challenge as a chance to learn and build trust. In the specialty chemical space, relationships matter as much as batch release tests—and with Furoyl Chloride, the stakes reach every area of operation, from reaction yield to safety, waste disposal, and intellectual property. Remaining actively engaged in the actual manufacturing process grounds our team in the details that drive both daily decisions and broader innovation.
In the end, manufacturing Furoyl Chloride represents a blend of science, logistics, engineering, and a commitment to practical chemistry. The world’s demand for reliable intermediates keeps pace with advances in medicinal chemistry, green technology, and specialty materials. Working directly with end users, investing in plant equipment and analytics, and never losing sight of the regulatory horizon ensures both present dependability and future innovation in this demanding market.