|
HS Code |
265342 |
| Chemical Name | 5-Iodo-2-Furancarboxaldehyde |
| Cas Number | 5919-86-6 |
| Molecular Formula | C5H3IO2 |
| Molecular Weight | 237.98 g/mol |
| Appearance | Light brown to beige solid |
| Melting Point | 86-88°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents like DMSO and ethanol |
| Smiles | C1=C(OC=C1I)C=O |
| Inchi | InChI=1S/C5H3IO2/c6-4-1-5(3-7)8-2-4/h1-3H |
| Synonyms | 5-Iodo-2-formylfuran |
| Storage Conditions | Store in a cool, dry place, protected from light |
As an accredited 5-Iodo-2-Furancarboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 5-Iodo-2-Furancarboxaldehyde, sealed with a screw cap and labeled with hazard information. |
| Shipping | 5-Iodo-2-Furancarboxaldehyde is shipped in tightly sealed, chemically compatible containers to prevent moisture and light exposure. Packaging complies with relevant hazardous material regulations. The product is handled by trained personnel and includes safety documentation. Temperature and transit times are controlled to maintain chemical integrity during shipping. |
| Storage | 5-Iodo-2-Furancarboxaldehyde should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Refrigeration is recommended for long-term storage. Proper labeling and handling procedures should be followed to ensure chemical stability and user safety. |
Applications of 5-Iodo-2-Furancarboxaldehyde in Industrial ManufacturingAs a specialized manufacturer of 5-Iodo-2-Furancarboxaldehyde, we supply this compound to a select range of downstream industrial sectors. The following section details its real-world integration into core chemical manufacturing workflows, with a focus on compliance, typical usage levels, process position, and the nature of finished products at each site of application. 1. Pharmaceutical Intermediate for Antiviral Drug SynthesisPharmaceutical formulators frequently use 5-Iodo-2-Furancarboxaldehyde as a key building block in synthesizing antiviral agents, particularly furan-based heterocycles. The material enters multi-step synthesis routes, where its iodo and aldehyde functionalities enable targeted substitutions and cyclizations critical for producing nucleotide analogs and other therapeutic molecules. Its exact role and inclusion level depend on active ingredient specifications and patent-protected processes governed by regulated GMP environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Fine Chemical Intermediate for Agrochemical SynthesisChemical companies incorporate 5-Iodo-2-Furancarboxaldehyde into custom synthesis schemes for crop protection APIs, leveraging the high reactivity of the iodinated furan ring. This intermediate enables site-selective couplings and the introduction of complex furan motifs into fungicide and herbicide scaffolds. Downstream manufacturers adjust input quantities based on target molecule yield, environmental regulations, and batch scale, with stringent oversight for residual iodine species. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Building Block for Specialty Organic Electronics MaterialsProducers of organic electronic materials employ 5-Iodo-2-Furancarboxaldehyde to fabricate advanced molecules with electron-donating and conjugation properties. Its integration allows for controlled substitution during the functionalization of furan-based monomers, supporting the development of materials for organic semiconductors and light-emitting diodes. Stringent control over purity and trace metallic impurities remains essential due to performance sensitivity in downstream electronic devices. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Synthesis Intermediate for Aroma and Fragrance Ingredients5-Iodo-2-Furancarboxaldehyde serves as a valued intermediate in the controlled synthesis of furan-derived aroma compounds for perfumery and flavor applications. Industrial fragrance manufacturers leverage its aldehyde function to perform selective reductions or condensations, enabling the generation of novel furanone derivatives with strong sensory impact. Batch processing must conform to food-grade or IFRA requirements when products enter regulated consumer markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 5-Iodo-2-Furancarboxaldehyde prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
At our chemical manufacturing facility, every batch of 5-Iodo-2-Furancarboxaldehyde takes shape under conditions we have refined through years of production experience. This compound, recognized by its CAS number 696-47-9 and molecular formula C5H3IO2, enters the world of fine chemicals where precision matters as much as purity. Working directly with its synthesis has shown us both the value and challenges that this highly functionalized furan aldehyde brings to complex organic transformations.
Chemists frequently search for reliable intermediates when their synthetic targets involve heterocyclic scaffolds, rearrangements, or unique group coupling. 5-Iodo-2-Furancarboxaldehyde offers a rare combination: the furan ring, which stands out due to its electron-rich aromaticity and versatile reactivity, and an iodine atom at the 5-position, which enables straightforward entry into a number of cross-coupling reactions, including Suzuki, Sonogashira, and Heck protocols. The aldehyde group at the 2-position opens further functionalization options, making this molecule something of a crossroads for modular synthesis.
Seeing customers use this building block in their own R&D or pilot projects, it’s clear the benefits become even more apparent. The iodo substituent isn’t just a leaving group in theory — in actual process chemistry, it delivers greater selectivity and operational simplicity than lighter halogen derivatives. Extraction, purification, and subsequent reaction steps can often shorten timelines and reduce solvent use compared with chlorinated or brominated analogs.
In our plant, the primary orders for 5-Iodo-2-Furancarboxaldehyde come from both academic and industrial users. Medicinal chemists turn to it for installing new substituents onto aromatic scaffolds when developing lead compounds. Agrochemical researchers deploy it in the quest for new active ingredients, selecting the molecule’s dual-reactive positions to create diversity-oriented libraries. Material scientists recently began leveraging its furan core for conjugated polymers and organic electronics, where the need for tightly specified starting materials is absolute.
Scalability remains a cornerstone of our operation. In practical terms, this means we routinely manufacture this material in quantities large enough to support pilot plant and early-stage production runs. Lessons learned during kilogram-scale production cycles — for example, managing the sensitive balance between reaction temperature, iodine supply, and the rate of aldehyde introduction — translate directly into reliable supply for our clients. Consistent output comes from maintaining hands-on control over batch conditions, not just from an automated setup.
Discussions of purity, melting point, and physical characteristics arise often, but from our perspective, specifications serve as benchmarks for performance in synthesis, not just checkboxes. Regular batches of 5-Iodo-2-Furancarboxaldehyde emerge from our reactors with purities exceeding 98% by HPLC, because customers in advanced synthesis regularly request trace-level control over contaminants. Physical appearance can tell its own story: while the compound can range from pale yellow to light brown crystalline solid, subtle shifts often result from residual solvent traces left during workup, which we eliminate through vacuum drying and crystallization steps.
Moisture sensitivity, a feature due to the aldehyde group, directly impacts storage and repeated sampling. Fresh production runs come sealed under inert atmosphere after batch homogenization; this greatly reduces decomposition or hydrolysis. For customers performing multi-step campaigns in-house, fresh-pack guarantees translate to fewer surprises and more predictable yields.
Operating as a manufacturer, real-world feedback sometimes challenges textbook assumptions. Early on, some users noted inconsistent reactivity during scale-up experiments. The problem traced to trace metal impurities picked up during crystallization — not something most literature methods bothered to control. Changing to all-glass production and adopting a proprietary filtration protocol cut those metals by more than 80%, which then stabilized coupling performance in downstream transformations.
Other specialists in pharmaceutical settings raised concerns about aldehyde polymerization during transport in humid months. Adjusting our packaging workflow — including secondary moisture-barrier liners and closer monitoring of batch shipment conditions — dramatically slowed degradation, cutting customer complaints. Subtle fixes like these carry weight for us, because anything that helps clients finish syntheses on time adds real value far beyond specification sheets.
Having worked hands-on with a range of halogenated furan derivatives, direct comparisons quickly reveal the practical reasons customers favor the iodo version. Its leaving group ability in Pd-catalyzed reactions proves distinct, offering higher conversion rates and cleaner outcomes than either the chloro or bromo analogs, especially under low-catalyst loading. From a process safety angle, avoiding the formation of persistent organic halides means fewer post-reaction treatment headaches — something every scale-up chemist appreciates.
We also process a variety of para- and ortho-formyl furans, but their lack of reactivity at the 5-position limits their synthetic reach. The fusion of iodine and aldehyde in this specific framework increases overall handle count, making this compound a springboard for analog development, natural product mimicry, or ligation chemistry not easily accessible by other means.
Attention to detail earns its place through repeated cycles on the production line. For 5-Iodo-2-Furancarboxaldehyde, this shows up in two core principles: maintaining a stable, repeatable reaction process, and using purification protocols that don’t trade off cost for impurity risk. We reject partially reacted or over-iodinated byproduct fractions and invest time in multi-stage washing. This extends run times compared to faster, more economical processes, but the stability and performance in subsequent chemistry justify the effort.
Buyers sometimes ask about homologous products — 5-bromo and 5-chloro-2-furancarboxaldehyde, for instance — but the differences in practical applications can be stark. The iodo variant accommodates a broader range of coupling catalysts and can proceed under milder conditions, preserving sensitive motifs in complex targets. Key intermediates take fewer steps, and overall efficiency rises in library and candidate development. With the bromo and chloro versions, suboptimal conversion and increased byproduct formation add unnecessary purification work.
Responsible sourcing and outbound logistics play a direct role in our operation. Iodine, a limited earth element, needs careful stewardship to avoid wastage. Solvent recycling and effluent treatment are not theoretical goals for us; we implemented closed-loop capture schemes over five years ago specifically for halogenated runs. Reducing iodine consumption has cut raw material costs and mitigated environmental load.
Several customers in Europe and North America now request documentation on batch traceability and lifecycle impacts, not just material safety data. Full traceability, down to raw iodine barcodes and intermediate tracking, comes standard with every release. Our internal database records batch history, testing protocols, and process deviations for at least five years, giving chemists confidence in both supply continuity and quality.
Long-term users have told us how interruptions in supply of 5-Iodo-2-Furancarboxaldehyde stall multi-year projects. Simple logistical problems, like customs clearance hold-ups or label damage, can set a process back by weeks. To avoid these bottlenecks, we pre-stage inventory in both domestic and bonded facilities and invest in regular staff training on compliant shipping. These steps, based on years of direct importing and exporting experience, head off downtime for researchers and pilot-plant teams.
Safety in halogenated compound synthesis is not an afterthought in a production-scale environment. In the early days, we dealt with several incidents related to iodine fume release and poor waste handling. Now, all reactor bays incorporate fume scrubbing systems, in-line leak detectors, and operator training on immediate containment. MSDS information guides our staff, but routine on-site skill refreshers ensure everyone is prepared for an upset scenario.
Hazard labelling and documentation travel with every batch. Global regulatory compliance can demand region-specific paperwork — for example, DOT-compatible drums for the United States, and REACH pre-registration for the European Union. Maintaining proactive relationships with compliance consultancies ensures our documentation supports smooth cross-border transit and risk mitigation.
Our plant carries ISO 9001 and environmental certifications, meaning every step reflects both quality assurance and environmental stewardship. While these standards sometimes add cost and complexity, we see them as necessary commitments for any responsible manufacturer — not only as boxes to tick, but as practical ways to safeguard people and communities near our plant.
The process chemistry around 5-Iodo-2-Furancarboxaldehyde remains under active refinement. We invest in pilot studies to cut energy needs for iodine introduction, trial new catalysts that reduce metal content, and pursue greener extraction solvents. Chemistry does not stand still, and our end users expect better every year.
In our view, staying competitive involves listening closely to the newest requirements from pharmaceutical, biotech, and agriscience labs. For example, one recurring request involves eco-friendly packaging — we are piloting biodegradable liner systems to replace conventional polymer films, especially for regular shipment to regions with strict disposal rules.
Demand for even higher aldehyde integrity has led us to explore production runs at cryogenic temperatures, limiting side reactions and delivering sharper product bands. Batch tracking and analytics improvements now allow us to identify and address micro-variations before they affect the final customer.
Direct dialogue with leading researchers is invaluable. On more than one occasion, process tweaks from a university or industrial partner allowed us to fine-tune our standard operation, resulting in both quality gains and improved throughput. This spirit of co-development yields long-term benefits for everyone who relies on 5-Iodo-2-Furancarboxaldehyde in high-stakes synthesis.
The experience gained over years of focus on furan derivative chemistry, particularly iodinated aldehydes, gives our team insight into what makes 5-Iodo-2-Furancarboxaldehyde genuinely useful for real-world applications. Rather than simply filling a catalog, we prioritize reliability and quality because the pressures of modern pharmaceutical, materials, or crop protection research leave little room for inconsistent performance.
As a direct manufacturer, responsibility goes well beyond batch production. Reliable access to high-purity intermediates unlocks innovation in fields from small-molecule therapeutics to new organic materials. Each improvement made in-house shapes better outcomes for chemists working at the forefront of discovery.
For those exploring new synthetic routes, 5-Iodo-2-Furancarboxaldehyde remains a preferred toolkit compound. Its dual-reactivity design, consistent purity, and adaptable supply all contribute to practical progress in laboratories and pilot plants worldwide. Our role, learned from years on the production floor and refined by customer collaboration, centers on delivering these tangible advantages to the end user — every time.