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HS Code |
650531 |
| Chemical Name | 3,5-Dichloro-2-Iodotoluene |
| Molecular Formula | C7H5Cl2I |
| Molecular Weight | 286.93 g/mol |
| Cas Number | 24390-14-5 |
| Appearance | White to off-white solid |
| Melting Point | 64-68°C |
| Density | 1.93 g/cm³ (estimated) |
| Purity | Typically ≥ 98% |
| Solubility | Insoluble in water; soluble in organic solvents |
| Synonyms | 2-Iodo-3,5-dichlorotoluene |
| Smiles | Cc1c(I)cc(Cl)cc1Cl |
| Storage Temperature | Store at 2-8°C |
As an accredited 3,5-Dichloro-2-Iodotoluene 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 3,5-Dichloro-2-Iodotoluene, tightly sealed with a screw cap, labeled with hazard information. |
| Shipping | 3,5-Dichloro-2-Iodotoluene is shipped in tightly sealed, chemical-resistant containers, compliant with applicable hazardous material transport regulations. The package includes appropriate labeling for hazardous organic compounds and is cushioned to prevent breakage. Direct sunlight, moisture, and extreme temperatures must be avoided during shipping to maintain product integrity and ensure safe handling. |
| Storage | 3,5-Dichloro-2-Iodotoluene 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. It should be kept away from sources of ignition, heat, and moisture. Proper chemical labeling and secondary containment are recommended to prevent leaks or accidental exposure. |
Applications of 3,5-Dichloro-2-Iodotoluene in Industrial ManufacturingAs a direct manufacturer of 3,5-Dichloro-2-Iodotoluene, we focus on its integration into key chemical synthesis processes across pharmaceuticals, agrochemicals, performance coatings, and advanced material intermediates. Below are several specialized applications derived from established industrial practices, each illustrating how our material is used in real-world downstream manufacturing lines. 1. Pharmaceutical Active Ingredient Synthesis3,5-Dichloro-2-Iodotoluene serves as a core building block in the multi-step synthesis of several pharmaceutical intermediates, notably in the preparation of substituted benzyl compounds for antihypertensive and CNS-acting agents. Pharmaceutical manufacturers utilize it during controlled halogenation and coupling reactions to introduce functional groups with precise regioselectivity. Strict compliance protocols guide handling, processing, and waste management at every stage, with in-process controls and full batch documentation. Industry compliance standards
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2. Agrochemical Intermediate FormulationMajor agrochemical producers incorporate 3,5-Dichloro-2-Iodotoluene as a halogenated aromatic nucleus for synthesizing advanced herbicides and fungicide precursors. The compound enables selective substitution in downstream transformations, often via Suzuki-Miyaura or Buchwald–Hartwig coupling pathways, yielding high-purity intermediates under controlled conditions. Production facilities observe rigorous documentation and residue control as mandated for plant protection ingredient synthesis. Industry compliance standards
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3. Electronic Material Intermediate SynthesisIn electronic chemical manufacturing, the compound functions as a precursor for high-performance aryl iodides and chlorinated toluidines, facilitating the creation of photoresist additives, liquid crystal molecules, and OLED intermediates. The ability to provide high-purity lots with low heavy metal and halide content directly supports stringent traceability in microelectronics chemical supply chains. Industry compliance standards
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4. Specialty Polymer Modifier SynthesisPolymer and resin formulators utilize the compound as a monomer modifier to introduce halogen functionality in specialty epoxy and vinyl ester resins. Its incorporation enables adjustments in flame resistance, dielectric properties, and chemical durability, with process QC focusing on uniform functional group dispersion. Manufacturers track halogen content and leachable limits to comply with end-user automotive and electronics requirements. Industry compliance standards
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Every day in the chemical industry, we weigh the complexities of synthetic pathways and the reliability of every intermediate that passes through our reactors. As direct producers of 3,5-Dichloro-2-Iodotoluene, our perspective on this compound is shaped by decades of hands-on experience, unpredictable market demand, and constant shifts in chemical research. This compound, known systematically as 1,3-dichloro-5-methyl-2-iodobenzene, holds a particular place in our lineup: it delivers reactivity yet provides control. These traits have led many of our clients—research chemists, pharmaceutical manufacturers, and agrochemical project leaders—to come back for batches that build on their past success stories.
Before diving into the specifics, let’s acknowledge what brings attention to this molecule. The iodine atom at the ortho position relative to the methyl group makes it an important building block. The two chlorine atoms at the meta and para positions modify electronegativity across the ring, giving chemists fine-tuned substrate behavior. This is not just theory: after producing dozens of halogenated aromatics, we notice consistent performance differences—both in crystallization and reactivity—when using this compound compared with alternatives like mono- or tri-halogenated toluenes.
As manufacturers, control starts from raw materials. Reliable supply chains for iodine and chlorinated precursors remain essential for consistent output. Fluctuations in halogen availability can quickly lead to material with unwanted color, odor, or off-spec melting points. In our daily process monitoring, we notice that proper order of halogen introduction matters. Adding the iodine after chlorination, rather than in reverse, contributes to cleaner conversions on a commercial scale, and this experience led us to design a protocol that keeps by-products to a minimum.
Our regular audits show that the purity threshold for this product needs to be tight: HPLC results frequently identify trace impurities, so we use additional recrystallization or vacuum distillation to avoid downstream headaches for customers. We keep a close eye on the methyl group’s position, since even minor isomerization interrupts reaction selectivity in our customers’ labs. This quality assurance isn’t just a claim; it’s built into every lot, each batch authenticated by NMR and mass spectrometry profiles matched to standard spectra from previous years’ reference vials.
In the market, generalized thinking about halogenated toluenes can cost time and money. Not all dichloro-iodotoluenes behave the same way. Our own records show that switching from 3,5-dichloro-2-iodotoluene to the 2,4- analogue can throw off coupling yields—even when catalysts, solvent, and base remain unchanged. The distinction isn’t academic; over the years, project reports from pharmaceutical labs using our product have shown that the reaction rate, product stability, and purification profile shift with ring substitution pattern. Such lessons are not widely circulated outside production sites, but they shape how we advise even our most seasoned formulators.
We do not manufacture this product for broad, undirected consumption. Most of our recurring orders come from teams that understand the implications of functional group tolerance and plan their routes around this compound’s specific halogen placements. They recognize that the presence of both electron-withdrawing chlorines and a large, polarizable iodine atom opens up coupling chemistry unavailable to substrates like 3,5-dichlorotoluene or 2-iodotoluene alone. Suzuki and Ullmann-type cross-couplings, for example, benefit from predictable reactivity and manageable side product formation, a point validated by returns of successful gram-to-kg upscaling feedback from medicinal chemistry clients.
In our plant, “specifications” goes beyond quoting purity or molecular weight. Every kilogram destined for shipment must pass clarity and color checks; even slight discoloration can indicate metal impurity or incomplete halogenation. We do not cut corners on particle sizing since reflux behaviors in large reactors demand uniform batch-to-batch solubility. Experienced synthetic teams tell us—often unprompted—that variations in morphology affect stirring and transfer rates more than datasheets let on.
Documentation does little to capture the subtleties here. For example, we strive for a moisture content below established thresholds, as NMR solvents or bases in customers’ reactions can amplify trace water’s effect, shifting yields. Flame-sealed glass ampoules for sample retention, installed as part of our routine, have often settled disputes by proving a product’s integrity months after delivery. We maintain open records on melting range, appearance, and residual solvent content, because any deviation can ripple downstream in the process chain.
Colleagues in pharmaceutical R&D and crop protection commonly build their syntheses on halogenated rings like this. Anecdotal evidence, matched by regular technical feedback, shows that 3,5-dichloro-2-iodotoluene plays a crucial role in generating key intermediates for both small-molecule drug and agrochemical candidates. Chemists involved in iterative synthesis, combinatorial libraries, and patent compound production often struggle to find a balance between cost, reactivity, and downstream functional group compatibility.
We do not see 3,5-dichloro-2-iodotoluene going unused on lab shelves. When it ships, it’s deployed in planned, measured steps—introduced as a handle for metal-catalyzed coupling or nucleophilic substitution at the iodine or chlorine, depending on the sequence. Many customers rely on it for selective halogen-lithium exchange, leveraging the iodine position while the chlorines remain robust to standard conditions. This strategy saves steps and cuts waste, and it has been engineered through years of close collaboration between production, research, and application chemists.
Some users pick this intermediate for radiolabeling projects using iodine isotopes. While we don’t handle radioactive materials ourselves, we’re aware from production consultation that isotopic substitution needs a consistent, reliable core structure. Structural guarantees mean more controlled downstream modification and fewer surprises, be it in a kilo run or a screening campaign.
Compared to 2-iodotoluene or its chloro-substituted counterparts with fewer or differently positioned halogens, our 3,5-dichloro-2-iodotoluene brings a unique blend of reactivity and stability. Much of this stems from how the two chlorine atoms, positioned next to the methyl group, decrease the overall electron density, taming the aromatic ring’s propensity for uncontrolled side reactions during coupling or alkylation. We’ve noticed in batch processing that this stabilization translates to higher yield and easier purification—benefits highlighted in satisfied customer reports, especially from scale-up teams.
In larger industrial synthesis setups, yields and throughput matter. We have worked with formulations using other dichloro- and trichloro-iodotoluenes, and we continue to find that 3,5-dichloro-2-iodotoluene offers an optimal compromise between energetic reactivity and ease of withdrawal from crude mixtures after workup. Users looking for mono-halogenated options often face more handling challenges—especially with more volatile iodine—while trihalogenated versions introduce unnecessary complexity and cost. For workflows requiring stepwise, selective functionalization, keeping the synthetic pathway flexible makes all the difference, as many organizations discovered after experimenting with alternate halogenation patterns.
Feedback shows that downstream emissions, especially volatile organoiodine species, are easier to monitor and capture with our product. We’ve developed handling packaging and in-plant transfer protocols after lessons learned from accidental volatilization events, reducing losses in storage and transfer. These subtle, seldom-advertised details shape process safety and long-term viability for plants dealing with increasingly strict environmental controls.
Over our years in chemical production, we watched the dialogue between research needs and market availability shift. Twenty years ago, requests for halotoluenes tilted toward broader, less-specific substitution. Today, research teams demand intermediates that suit precisely plotted synthetic sequences. Patented pharmaceutical and agrochemical targets require building blocks designed for compatibility with the next two or three reaction steps. Our participation in the industry’s learning process has reinforced the need for unwavering supply consistency and technical transparency.
Researchers and production chemists seek out 3,5-dichloro-2-iodotoluene because it spares them from unpredictable routes or unnecessary by-products. The cost of unvalidated intermediates, both in terms of lost time and incompatible results, can dwarf any up-front raw material savings. We’ve invested in dedicated production lines, process validation, and systematic customer feedback tracking to address these realities as efficiently as possible.
Transparency around trace contaminants, batch history, and production yields underpins the trust that buyers—and often regulatory auditors—place in us. Technical data requests, if they arrive post-shipment, do not uncover surprises. This approach, born out of real operational necessity, shows our commitment to reliability among the source manufacturers in the halogenated aromatic sector.
As managers and staff working on the plant floor, responsibility does not end at the gate. Chlorinated and iodinated compounds bring their own set of process, handling, and disposal challenges, and over the years, we have continually improved our internal protocols. Capture and treatment of off-gases, containment of solid and liquid wastes, and careful dosing remain standard. We know from environmental audits that even modest improvements in solvent selection, distillation conditions, and halogen handling reduce both emissions and hazardous by-product generation by double-digit percentages.
Plant operations have benefited from clearer, stepwise process hazard assessments, as certified through third-party reviews. Our internal incident logs show fewer close calls after implementing direct employee feedback on storage, transfer, and sparging systems specific to organoiodine work. Every weekly operations meeting includes a review of incidents, near-misses, and suggestions for incremental tweaks. This management culture delivers on both performance and compliance.
Process waste reduction is not just an environmental or ethical issue—it improves plant economics. Recovering mother liquor wastes and halogenated by-products, separating reusable solvents, and reclaiming iodine through reductive workup have become integral. Our efforts cut disposal costs, ease regulatory burdens, and often improve the recovery of saleable product in tandem.
Unlike companies mainly engaged in reselling or brokering, manufacturers deal with technical stopgaps first-hand. We’ve built our support network around the kind of real technical hurdles that research chemists and plant engineers face. This includes troubleshooting sluggish couplings, cleaning up stubborn by-products, or figuring out how to convert a winning lab-scale reaction to a steady kilo-a-week campaign. We do not see remote, hands-off advice get the job done. Instead, we trade stories, walk through real procedures, and iterate approaches based on facts, not just textbook prescriptions.
Failures, when they occur, often offer the most useful feedback. Bottlenecked reactions, incomplete washes, or unexplained shifts in product stability usually trace back to details in either the substrate or procedure. We advise our partners from an insider’s perspective, knowing where trace water, solvent residues, or shipment timing can break a process. Learning cycles like these have shaped how we present, ship, and track every drum, bottle, or sample lot from the plant.
Markets move fast. Regulatory lists expand, high-throughput chemistry surges, and process economics sharpen. By staying rooted in the front lines of chemical production, we anticipate changes in precursor demand, process bottlenecks, and emerging safety standards. Tools like real-time batch tracking, in-house quality verification, and detailed lot retention allow us to answer technical calls—sometimes months after a delivery—with confidence. Customers appreciate real traceability, not just empty assurances.
Part of our ethos revolves around partnering with research groups and scale-up teams, not just supplying materials as commodities. If a shift in synthesis runs into hiccups with a key intermediate, we know that it’s often a subtle interaction of structure, purity, and process. This understanding, not simply a chemical catalog number, maintains our position among modern chemical suppliers focused on specialty halogenated organics. We take pride in feedback—constructive or otherwise—from users who depend on our expertise to explore what boundaries their research or product development can push, using materials that function the same way every time they arrive.
Anyone relying on 3,5-dichloro-2-iodotoluene, whether for new molecule construction or process development, benefits from supplier experience built over production campaigns, quality scrapes, and customer collaborations. Our focus remains squarely on shared results—straightforward, effective, reliable. The lessons learned on the shop floor, supported by continuous improvement and technical transparency, shape the way we support teams striving for new synthetic milestones. We do not view ourselves as just another supplier, but as production partners invested in sustainable success for every downstream user.