|
HS Code |
124126 |
| Chemicalname | 3-Hydroxy-4-Iodobenzaldehyde |
| Casnumber | 3743-13-9 |
| Molecularformula | C7H5IO2 |
| Molecularweight | 264.02 g/mol |
| Appearance | Light yellow to beige solid |
| Meltingpoint | 155-157°C |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=C(C=C1I)O)C=O |
| Inchikey | RQNBKBVZFAQJKZ-UHFFFAOYSA-N |
| Synonyms | 3-Hydroxy-4-iodobenzaldehyde; 4-Iodo-3-hydroxybenzaldehyde |
| Storageconditions | Store at 2-8°C, protected from light and moisture |
As an accredited 3-Hydroxy-4-Iodobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Hydroxy-4-Iodobenzaldehyde, 5g, is supplied in a sealed amber glass bottle with tamper-evident cap and detailed safety labeling. |
| Shipping | `3-Hydroxy-4-Iodobenzaldehyde` is securely packaged in airtight, chemical-resistant containers to prevent contamination and degradation. During shipping, it is protected from moisture, light, and extreme temperatures. All shipments comply with relevant chemical safety regulations, including proper labeling and documentation, ensuring safe domestic and international transport. |
| Storage | 3-Hydroxy-4-iodobenzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. The storage area should be free from sources of ignition. Proper labeling and chemical safety protocols must be followed to prevent contamination and ensure safe handling. |
Applications of 3-Hydroxy-4-Iodobenzaldehyde in Industrial Manufacturing3-Hydroxy-4-iodobenzaldehyde serves as a strategic intermediate across selected advanced manufacturing fields. As a direct chemical producer, we support industrial formulators needing highly controlled input materials for high-value downstream synthesis in regulated sectors. Below we provide detailed application insights for the material within recognized commercial arenas. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient SynthesisThis specialty benzaldehyde acts as a core building block in the multistep synthesis of targeted pharmaceutical compounds. Downstream formulators employ its iodine-functionalized aromatic structure for nucleophilic substitution and palladium-catalyzed cross-coupling reactions while adhering strictly to regulatory requirements at every process stage. High-purity grade is specified to avoid downstream impurity accumulation, and material traceability must be maintained in accordance with batch protocols. Integration occurs at defined intermediate stages for antioxidant agents, antitumor scaffolds, and fine APIs requiring halogenated aromatic cores. Industry compliance standards
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2. Agrochemical Synthesis – Advanced Pesticide IntermediatesAs a precision halogenated aromatic aldehyde, this compound enters agrochemical synthesis lines to form iodinated phenolic cores in high-performance crop protection agents. Bulk manufacturers require defined impurity control and batch-to-batch consistency to meet agrochemical registration protocols. Its reactivity allows efficient incorporation into multi-step processes for the synthesis of fungicidal and herbicidal active molecules. Quality audits frequently check source documentation and allergenic profile per supply contract terms. Industry compliance standards
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3. Dye and Pigment Intermediate for Specialty ColorantsThe benzaldehyde's halogenated structure provides important raw material functionality for downstream producers of advanced colorant molecules. Under controlled oxidative conditions, downstream converters exploit its 3-hydroxy group to ensure targeted chromophore formation. Process engineers must optimize protocol to avoid iodine loss and byproduct darkening. Compliance documentation for heavy metal and aromatic aldehyde limits, as required in textiles or food-adjacent printing applications, is mandatory. Industry compliance standards
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4. Fine Chemical Intermediate in Electronic Material SynthesisThe controlled introduction of iodine onto the aromatic ring within this material is essential for the electronic materials sector. Circuit board and liquid crystal display (LCD) developers require this intermediate for constructing advanced functionalized monomers and oligomers, impacting film performance and stability. Application specialists document traceability as per product stewardship guidelines, while usage depends on circuit architecture and polymerization parameters. Inspection routines routinely verify purity, moisture, and halogen content at incoming QA. Industry compliance standards
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On the factory floor, nothing matters more than reliability and reproducibility. Those of us handling transformations daily see firsthand what separates a high-value building block from an average intermediate. 3-Hydroxy-4-Iodobenzaldehyde has become essential at this intersection of practical need and technical performance. Its molecular structure, featuring a hydroxy group ortho to an aldehyde and an iodine at the para position, forms the basis for why it’s seen increasing use in complex syntheses.
As the people making this compound rather than merely packaging or selling, we observe the recurring problems that arise with inconsistent raw materials. Purity shifts, especially in sensitive aromatic aldehydes, sabotage entire reaction sequences. Through systematic investments in reaction control, our 3-Hydroxy-4-Iodobenzaldehyde achieves reliable batch-to-batch purity—HPLC figures consistently exceed 98%. We maintain low moisture content to protect the function of the aldehyde group. Titration reports confirm the targeted range, but what matters more is how this reduces side-product build-up in subsequent steps, from Grignard additions to Suzuki couplings.
Experienced chemists understand the subtle impact that molecular orientation brings. The iodine atom on the benzene ring, as seen in this compound, opens versatile avenues, especially for processes like palladium-catalyzed cross-couplings. The hydroxy group brings added reactivity, facilitating etherification, esterification, and nucleophilic aromatic substitutions. The close proximity of the aldehyde gives routes to further derivatizations—a feature valued in the pharma sector, where targeted modifications drive structure-activity relationships.
Unlike generic aryl halides or simple salicylaldehydes, this compound’s distinct substitution allows for selective activation. We’ve noted that research labs using this product frequently pursue advanced heterocyclic frameworks, including benzofurans and complex ligands, as well as the synthesis of potential imaging agents and small-molecule therapeutics. Our own direct feedback from customers in med-chem departments shows that its use reduces the need for elaborate protection or deprotection of functional groups, which cuts both reaction time and solvent load.
Sourcing this compound from a manufacturer, not a trader, brings a different perspective. Production starts with raw iodophenol processed under controlled conditions; temperature, pH, and solvent composition are tightly regulated. We work with small production volumes at critical quality points to limit the risk of ortho/para isomer formation. The resulting product carries minimal heavy metal residues and residual solvents are carefully monitored by GC, not simply assumed negligible.
Sub-standard product from third-party channels often suffers from elevated water content. This decomposes the aldehyde on storage or leads to unknown side products. We invest in proper anhydrous packaging and rapid bottling to preserve product integrity. If a researcher needs to carry out an Ullmann-type etherification or pursue halogen-metal exchange for further large-scale runs, diminished quality in this step can derail even well-planned sequences.
We aren’t theorizing from a distance. Partner companies in contract research and specialty chemicals production have detailed how critical this intermediate becomes in actual working conditions. 3-Hydroxy-4-Iodobenzaldehyde frequently anchors the synthesis of ligands for cross-coupling catalyst frameworks, facilitating substitutions that simpler halobenzenes can’t manage with comparable selectivity or yield. In medicinal chemistry, scaffold modifications that require orthogonal functionalization benefit from the protected yet accessible aldehyde and hydroxy handle.
One domestic biotech company reported that by switching to our product, they reduced the number of chromatographic purifications in a complex, seven-step synthesis. The hydroxy group’s ortho position, kept free from phenolic impurities thanks to our purification process, allowed a key cyclization to proceed above 80% yield with no rework needed. These incremental advances—from slightly improved yields to reliable handling—translate into millions in larger-scale projects, especially when a single impurity, such as iodinated biphenyls, can disrupt regulatory filings.
Even chemical manufacturers can fall prey to a “commodity mindset.” Not all substituted aromatic aldehydes play the same role. Many labs deal with 3-hydroxybenzaldehyde, lacking the iodine leaving group. While still useful in certain transformations, this compound can’t substitute in cross-coupling routes requiring transition-metal catalysis. Substituted aryl iodides without functional hydroxy or aldehyde groups work in some routes but eliminate key retrosynthetic shortcuts.
The significance doesn’t stop with reaction feasibility. Cost per kilogram takes a back seat to downstream impact. If a competing intermediate results in higher impurity profiles or threatens to generate persistent contaminants, the losses mount quickly. The failure of a scale-up due to unanticipated byproduct formation or a single hazardous impurity can jeopardize the entire supply chain. It’s not only about high purity; the position and integrity of functional groups set apart true high-value intermediates from their generic relatives.
On a practical level, 3-Hydroxy-4-Iodobenzaldehyde requires careful storage. Even minor oxidation transforms the aldehyde group, leading to unwanted carboxylic acid formation. From manufacturing tanks to final containers, we use nitrogen blankets and moisture barriers. Packaging in amber bottles slows photolytic degradation. For large batches intended for multi-step syntheses, product moves directly from final reactor into inert-lined drums without unnecessary exposure. These details emerge from decades of failures and improvements, not textbook theory.
In day-to-day lab routines, chemists appreciate solids that dissolve predictably and handle without excessive static or caking. We measure bulk density and checklist flow properties to ensure practicality in weighing and dispensing. Users on pilot lines report no issues with dust generation, reducing worker exposure risk compared to some finely milled competitors. There’s no substitute for routine, hands-on handling data to inform continuous process tweaks.
Demand from the life sciences and electronics sectors brings escalating quality requirements, not just in terms of purity but trace element profiles and traceability. Throughout our process, trace iodine recovery sits under rigorous scrutiny, as does compliance with REACH and, in select markets, the Recording and Reporting Requirements for controlled substances. Documentation and batch records are maintained in-house. Samples are retained for cross-checking by clients, eliminating delays in troubleshooting or scale-up queries.
Regular audits by pharmaceutical partners prompt continued refinement. We conduct parallel syntheses for each production run to compare the impact of minor process tweaks, reviewing results under real-world reaction conditions. It’s clear that meeting these standards isn’t about obtaining a certificate but about protecting investment downstream. Failure to do so risks hold-ups for regulatory audits or the need for burdensome reprocessing.
As capacity scales from kilogram to multi-ton, unexpected bottlenecks appear. For this aromatic intermediate, maintaining purity and color—even at high volumes—becomes challenging. Trace metal leaching from equipment, especially after repeated cycles, or subtle solvent breakdown products can undermine shelf life.
Continuous investment in cleaning validation, process automation, and analytical monitoring underpins our ability to supply research and commercial volumes without quality drift. Shifts in raw material suppliers, reactor downtime, and seasonal ambient humidity swings all feed into final product performance. Instead of running batch after batch on autopilot, each lot receives a final in-process quality verification, tested under the typical downstream conditions reported by our biggest clients.
Direct feedback from academic and industrial users has shaped our approach. Many synthetic routes still rely on legacy aldehyde and phenol chemistry, incurring avoidable waste and poor atom economy. The specific substitution pattern of 3-Hydroxy-4-Iodobenzaldehyde allows stoichiometric reductions in halide or oxidant excess. We work collaboratively on greener process alternatives, introducing catalytic oxidizers and solvent recovery systems. These incremental gains, refined over each development cycle, gradually drive down cost and environmental load while supporting clients’ sustainability goals.
Looking to the future, customers request ever-more specialized analogs—fluorinated, methoxylated, or deuterated derivatives—where the lessons learned from this compound’s synthesis provide a template for tackling new manufacturing challenges. Dedicated R&D lines evaluate the impact of small functional changes on everything from solubility to downstream reactivity. Manufacturability, not just technical curiosity, governs the compounds we bring to larger scale—direct learning from real-world trials rather than theoretical promise.
No textbook defines service as closely as hands-on troubleshooting does. Researchers who call us aren’t met with generic responses; they reach the chemists responsible for making the batch in question. It’s not unusual for a custom run to require adjustments in the post-synthesis purification based on a single client’s solvent sensitivities or purification needs. Real working relationships develop, based on mutual problem-solving rather than price-led transactions. Documented process change controls and historical analytical data are shared openly—confidence is built on openness, not bluster.
Delays can happen when a unique impurity profile emerges or a new analytical method is deployed. Our standard is straightforward: solve the problem, explain the process change, ship only when fully resolved. This approach has built long-standing partnerships with customers in fine chemicals, specialty pharmaceuticals, and academic research sectors. What starts with a kilogram order can grow to monthly multi-ton shipments when people trust that each lot will perform as expected.
The attitude on the production line matters as much as the equipment. Operators and chemists stationed at every step of the synthesis don’t see the work as a commodity process but as an evolving handiwork. Years spent studying the intricacies of column chromatography or drying oven temperatures translate into smoother workflows. After each run, teams meet to debrief on issues—yield fluctuations, minor off-colors, even anecdotal feedback from a customer’s synthetic campaign. These insights feed directly into revised standard operating procedures.
External audit feedback, response to processing bottlenecks, and frequent technology upgrades all contribute to an evolving best practice. There’s no “final word” on method—only a relentless drive for higher reliability and lower risk. Even small changes, such as adjusting filtration speed or redesigning reagent addition protocols, result from cumulative knowledge shared within the team. The benefit is clear: chemists who receive our 3-Hydroxy-4-Iodobenzaldehyde know it’s the product of experience, not a rushed commodity packed in a box.
Real-world examples tell the story better than claims. A university lab developing photoreactive probes faced repeated issues with byproduct contamination using a lower-grade intermediate. Direct consultation identified that the issue stemmed from poor hydroxy group protection in raw materials. After switching to carefully characterized product—verified by our in-house NMR and elemental analysis—their probe synthesis succeeded with only minor purification, accelerating their time to publication by several months.
In pharmaceutical scale-up, process engineers struggle with lot variability when intermediates change hands too often between traders. One team in Asia reported a 15% yield boost in their final API synthesis by sourcing directly from us; our control of upstream raw material selection negated the need for recursive batch reworking. In a field where missed schedules equal major costs, shaving days off the purification process raises efficiency and confidence in frontline project management.
Beyond operational efficiency, we embed environmental care at all stages. The production of iodinated aromatics generates byproduct streams that, if unmanaged, impact both the environment and worker safety. We continually invest in comprehensive waste minimization strategies: sequential solvent reuse, iodine recovery units, and advanced scrubbers on vent streams. Operators and technical leads monitor personal and area exposures, documenting compliance with evolving local and international guidelines.
Incoming questions about packaging and shipment drive our shift towards using recyclable containers where feasible, and batch transport follows a tracked, sealed-chain protocol to eliminate cross-contamination or accidental release. This practical, real-world approach to stewardship supports not just regulatory compliance but genuine safety and environmental improvement. It is not about slogans but direct, measured process changes year on year.
Every day, hands-on experience and honest evaluation drive our approach to 3-Hydroxy-4-Iodobenzaldehyde. Detailed knowledge of how it performs, how even subtle changes affect chemistry, and how it fits into broader synthetic efforts—the result is not just a chemical, but a platform for research and manufacturing progress. Our engineers and chemists take pride in going the extra mile, building a reputation not on claims, but on proven reliability and open conversation. For those in demanding technical environments—where every variable counts—direct connection to expertise makes all the difference. Change comes not through generic shortcuts, but on the foundation of real knowledge, accumulated and applied where it matters most.