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HS Code |
858370 |
| Chemical Name | 3-Iodobenzyl Alcohol |
| Cas Number | 870-50-0 |
| Molecular Formula | C7H7IO |
| Molecular Weight | 234.04 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 39-43 °C |
| Boiling Point | 290.2 °C at 760 mmHg |
| Density | 1.837 g/cm³ |
| Smiles | C1=CC(=CC(=C1)I)CO |
| Inchi | InChI=1S/C7H7IO/c8-7-3-1-2-6(4-7)5-9/h1-4,9H,5H2 |
| Solubility Water | Slightly soluble |
| Synonyms | m-Iodobenzyl alcohol |
| Pubchem Cid | 21530 |
As an accredited 3-Iodobenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Iodobenzyl Alcohol is supplied in a 25g amber glass bottle with a secure screw cap, labeled with safety and identification details. |
| Shipping | 3-Iodobenzyl alcohol is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a hazardous chemical, and labeled according to relevant regulations. Shipments typically require cushioning and secondary containment, and are transported under ambient conditions with proper documentation, in compliance with local and international chemical shipping guidelines. |
| Storage | Store 3-Iodobenzyl Alcohol in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition, strong oxidizers, acids, and bases. Clearly label the container and ensure appropriate safety measures are in place to prevent accidental release or exposure. Follow all relevant chemical storage regulations and guidelines. |
Applications of 3-Iodobenzyl Alcohol in Industrial ManufacturingAs a direct manufacturer of 3-Iodobenzyl Alcohol, we supply to specialized sectors requiring controlled reactivity, precise substitution patterns, and reliable raw material provenance. The following industrial applications outline its downstream integration, regulatory conditions, and material handling approaches as used by compliant OEMs worldwide. 1. Pharmaceutical Intermediate for Antihypertensive APIsPharmaceutical companies use 3-Iodobenzyl Alcohol primarily as a building block in the synthesis of specific antihypertensive drug molecules, particularly those structurally based on benzyl or aryl iodide motifs. Manufacturers incorporate this intermediate during early-stage coupling reactions, where its benzylic alcohol group facilitates conversion to protected intermediates prior to fermionic or palladium-catalyzed cross-coupling. Quality assurance conducts comprehensive GC-MS analysis to confirm residual solvent and heavy metal levels before further processing, ensuring compliance with key regulatory frameworks. Industry compliance standards
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2. Advanced Material Synthesis for Liquid Crystal MonomersThe display and optical material sector employs the benzyl alcohol derivative for introducing bulky, electron-rich aromatic groups into specialty monomers for liquid crystal materials. Processing specialists leverage its iodine substituent to enable site-specific functionalization via nucleophilic substitution or Sonogashira coupling, forming rigid rod-like or asymmetric LC monomers for advanced displays and smart glass applications. Stringent trace impurity profiling is required to meet Japanese and Korean panel manufacturer QC standards. Industry compliance standards
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3. Agrochemical Active Ingredient PreparationIn the agrochemical sector, large producers use this iodinated benzyl alcohol as an intermediate in the synthesis of benzylic and heterocyclic pesticides and growth regulators, taking advantage of its functional handle for alkylation and halogen exchange processes. In process synthesis, engineers introduce this intermediate at the step prior to cyclization or heteroatom incorporation to retain iodine atom integrity until the last conversion step, aiding overall process yield and selectivity. Industry compliance standards
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4. Specialty Dye and Pigment ManufacturingManufacturers of advanced dyes and photoactive pigments select this compound for constructing complex aromatic cores where halogenated intermediates improve lightfastness and chromatic properties. Synthetic chemists leverage the high reactivity of the iodo substituent in step-growth polymerization or for introducing protected functional groups during dye molecule assembly for industrial textile or imaging applications. Stringent control of trace heavy metal and color purity is required for integration with REACH-compliant pigment supply. Industry compliance standards
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5. Custom Synthesis for Chemical Research ReagentsChemical research organizations and custom synthesis service providers order this high-purity compound for building libraries of benzyl-based molecular scaffolds and designing new aryl iodide-based reagents. Chemists select for its benzylic alcohol function and ortho-iodo activation, which permit modular functionalization in advanced organic synthesis — especially for pharmaceutical analog research and structure-activity optimization programs where unique halogenated scaffolds expand available SAR space. Documentation includes full NMR, HPLC, and COA traceability. Industry compliance standards
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Production of 3-iodobenzyl alcohol means a lot more than following a synthesis route. It calls for precision, safety, and commitment from the first raw material delivery to the moment the bottle leaves the plant. Our plant has delivered halogenated benzyl alcohols to global pharmaceutical and specialty chemical producers for years, and we’ve responded to feedback from countless chemists along the way. With 3-iodobenzyl alcohol, chemists get material that consistently reacts as expected. Whether for complex coupling reactions or as a key intermediate, this compound delivers not just iodine content but reliability in yield and downstream conversion.
CAS: 619-58-9. Molecular formula: C7H7IO. The molecule offers the chemist an aromatic ring complete with a benzyl alcohol at the para position relative to iodine. The compound arrives as a clear to pale yellow liquid or low-melting solid, depending on storage temperature. The purity checks consistently exceed 98%, with trace impurity control monitored to a handful of ppm—because unmeasured side-products at the start of a synthesis can snowball into headaches after scale-up.
Comparing this product to alternatives like bromobenzyl or chlorobenzyl alcohol, the unique reactivity of the aryl iodide group stands out. The carbon–iodine bond allows for milder activation in palladium-catalyzed cross-coupling, such as Suzuki or Sonogashira reactions, reducing demands on base and temperature. Synthetic chemists regularly note higher yields and cleaner product profiles when working from aryl iodides. There’s also improved selectivity in side-chain functionalization, thanks to the combination of accessible benzyl alcohol and the powerful leaving group effect of the iodine atom.
Many in the chemical industry know that commercial 3-iodobenzyl alcohol often has color or odor issues; unchecked hydrolysis or oxidation makes a difference. From first-hand experience, process engineers have learned that using only high-purity starting materials, keeping the reactor and transfer lines dry, and adopting hydrogenation conditions that avoid over-reduction ensures a clean product. The intermediate benzyl iodide, notorious for decomposition, needs careful handling under inert atmosphere. Equipment reliability—especially in cooling and vacuum systems—cannot be overstated, as uncontrolled temperature causes by-product formation that is tough to purge downstream.
Routine in-house analytics like GC and NMR back up quality claims. Years of international shipping experience taught us that fluctuations in temperature and exposure to sunlight during transit can affect product quality, so packaging incorporates amber glass and airtight seals. On arrival, customers receive material within agreed purity and moisture bounds, and remote video batch-release is available for critical applications.
Screening commercial samples from a dozen international sources, customers noticed certain tell-tale odors and colorations, especially in older lots. Freshly manufactured 3-iodobenzyl alcohol from a controlled, domestic supply line shows virtually none of these batch-to-batch inconsistencies. The plant’s production team tracks every drum, running aging studies on retained samples and sharing these results with customers looking for long-term stability assurance.
Our technical support has worked side-by-side with process chemists on late-stage pharmaceutical API development and with materials scientists tuning new specialty polymers. 3-iodobenzyl alcohol often enters as a growth point for larger aryl ethers, aliphatic-aryl hybrids, or custom heterocycle synthesis. The manufacturer’s team doesn’t just ship drums; we handle documentation in multiple languages, clear customs, and help troubleshoot reactivity hiccups in the customer’s own facility.
Regulatory confidence matters. Batch release comes with full traceability on the supply chain, heavy metal or residual gas analysis options, and SDS in the format best suited to the site’s EHS needs. Our site operates under ISO-certified processes and is familiar with REACH registration and EPA scrutiny for import.
Those working the production floor know that 3-iodobenzyl alcohol responds best to basic process care. Benzyl alcohols can sometimes absorb air moisture and show a slight cloudiness. Our staff practices low-humidity filling during bottling. Simple measures, like keeping containers closed between uses and using dry syringes for withdrawals, keep product on-spec through repeated handling. Chemists appreciate these details when running multi-step syntheses.
Sometimes, labs scale up fast and need reliable resupply. We routinely answer calls for same-day expedited shipment, helping teams keep pilot plant campaigns on schedule. Logistics professionals select carriers based on local routing reliability and import rules for aryl iodides, staying attuned to regulatory changes that affect cross-border deliveries.
Waste minimization efforts at the plant include drum return services, streamlined tech sheets with digital distribution, and on-call hazardous waste guidance. Long-term customer relationships developed because we returned calls during off hours and solved issues caused by documentation confusion, missed courier pickups, or packaging breakage.
Not all halogenated benzyl alcohols deserve the same attention. Tolerances on moisture, trace solvents, and stabilizers set specialty-grade material apart from low-cost bulk product. Chlorinated and brominated analogs are more widely available, and sometimes cheaper per kilogram. In use, though, chemists comment on lower conversion rates in cross-coupling or tough purification hurdles during downstream workups. Iodinated intermediates like 3-iodobenzyl alcohol shorten synthetic sequences, support softer conditions, and frequently translate into higher overall yield in target molecules.
Large customers often press for COAs with detailed impurity profiles and willingness to run extra in-process checks. For academic groups developing new ligands, trace impurities can make or break results. Rather than treating every customer the same, our technical teams openly share methods, reveal batch histories, and tailor delivery formats when it helps on the bench or in the pilot reactor.
Making aryl iodides demands responsible waste handling. We actively recover excess iodine from spent solutions, regenerating it for internal use or sale as a raw material—keeping overall iodine usage down and landfill footprint low. Air emission controls meet or exceed local standards. Production schedules optimize batch size to match actual demand, not a sales forecast, preventing waste at both ends of the supply chain.
The technical team tracks regulations on hazardous chemicals, toxicology updates, and storage law. Customer feedback led to secondary containment for export containers, upgraded MSDS translation, and better labeling. Operators on the packing line receive regular health checks and ongoing safety training. Any hint of instability in a batch triggers full material review and, if needed, disposal instead of release.
Academics, process chemists, and industrial technologists increasingly use 3-iodobenzyl alcohol as a building block for complex pharmaceuticals, radiolabeling, imaging agent precursors, and specialty polymers. Its place in C–C or C–N coupling, and as a methylene fragment source, sets it apart from simpler ring-substituted alcohols.
Experience at the manufacturing site shows that demand for 3-iodobenzyl alcohol aligns with growth in green and automated synthesis. Automated platforms, such as flow chemistry skids, benefit from the compound’s high reactivity and predictable performance, allowing for faster optimization cycles. Feedback from contract manufacturing organizations revealed that the right grade of aryl iodide makes the difference between single-pass and repeated rework in large-scale transformations.
Plant scientists, developing agrochemical actives, value not just purity and cost but also detailed impurity profiles. Active research programs request supply in different solvent carriers, and the facility has responded by expanding the offering to custom dilutions at no extra risk of cross-contamination, using dedicated reactor and transfer lines.
Shipping to remote sites or through multi-step third-party logistics is not always smooth. Customs officials sometimes raise questions on packaging or paperwork, so our logistics lead supports every shipment with photographs of sealed product, barcoded labels, and rapid certification response. Because customs issues result in unwanted storage or temperature fluctuations, team members often monitor at-risk shipments and intervene before product quality suffers.
Large buyers prefer reusable totes or bulk containers, while research groups seek 10–100 gram packs for rapid turnover. Our production team tracks these needs and turns out the right format for each user, whether it’s a small research sample or a multi-tonne drum for a pharma major. Few substitutions work for 3-iodobenzyl alcohol when downstream success depends on predictable coupling and ease of purification—switching to the cheaper halogens means risking a months-long process setback and extra purification cycles.
Specialty applications, such as imaging tracer precursor synthesis for radiodiagnostic drugs, further increase the calls for documentation clarity and batch reproducibility. Teams on both sides of the supply chain work closely to minimize contamination risk, especially for ultra-trace applications, and process validation runs include extra analytics on demand.
Real manufacturing stories usually circle back to feedback. Several industrial customers faced issues sourcing consistent-quality 3-iodobenzyl alcohol from the open market, reporting widely variable side-product content. We addressed these gaps by reworking our purification protocol and investing in better analytical controls. The impact: fewer project delays and a stronger working relationship with repeat customers.
The plant encourages customers to share use-case feedback, especially around new synthetic pathways, so staff can anticipate upcoming specifications. Internal process improvements—driven by operator input—resulted in faster batch turnaround, improved yields, and, ultimately, better pricing for frequent buyers. Engineers and chemists meeting with end users on-site gained a clearer view of where material differences arose in real process trials rather than waiting for reports after a campaign was already derailed.
Greater scrutiny in pharmaceutical and fine chemical markets drives continued upgrades in both reaction technology and QA systems. By staying close to industry trends—such as the shift toward automated and greener synthesis routes—the manufacturing team consistently tunes batch process parameters to favor both quality and efficiency. Research customers value not just bulk supply, but rapid technical response, full transparency in material characterization, and practical troubleshooting from an experienced production chemist’s viewpoint.
We see 3-iodobenzyl alcohol shifting from a specialty intermediate confined to niche projects, to an essential toolkit reagent for new-molecule innovation. As customer applications expand, so does the need for responsible, documented, and transparent manufacturing. Decades in chemical production taught our staff that consistent quality, open communication, and the willingness to adapt make a bigger difference than any single process tweak or cost-saving measure.
Customers working on deadline-driven projects learned the impact of real-time support from the actual plant rather than third-party sellers. Orders are tracked by the people who actually oversee synthesis and packaging. Batch problems don’t get bounced between middlemen—they get fixed at the source. Down-to-earth logistics, robust documentation, and plant-level oversight keep production moving and cut the risk of unexpected delays or paperwork stalling at the border.
With 3-iodobenzyl alcohol, chemists aren’t just buying a commodity. They’re securing a reagent crafted with care, subject to real-world constraints, and ready for immediate use. Every feedback call, every customizing request, and every batch release shapes how the team works, so each bottle speaks not just to a molecular formula but to an ongoing working relationship between manufacturer and user.