|
HS Code |
759123 |
| Product Name | 3,5-Dimethyl-4-Iodophenol |
| Cas Number | 134901-85-6 |
| Molecular Formula | C8H9IO |
| Molecular Weight | 264.06 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 80-84 °C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC1=CC(=C(C=C1I)C)O |
| Inchi | InChI=1S/C8H9IO/c1-5-3-7(2)8(10)4-6(5)9/h3-4,10H,1-2H3 |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 4-Iodo-3,5-xylenol |
As an accredited 3,5-Dimethyl-4-Iodophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 3,5-Dimethyl-4-Iodophenol (5 grams) is a tightly sealed amber glass bottle with a clear label. |
| Shipping | 3,5-Dimethyl-4-Iodophenol is shipped in tightly sealed containers, protected from light and moisture. The chemical is handled as a hazardous material, complying with applicable transportation regulations (DOT, IATA). Packaging ensures minimal risk of spills or contamination, and each shipment includes proper labeling and documentation for safe handling and identification during transit. |
| Storage | **3,5-Dimethyl-4-iodophenol** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from light and moisture. Store at room temperature, and ensure that the storage area is clearly labeled and compliant with all applicable chemical safety regulations. |
Competitive 3,5-Dimethyl-4-Iodophenol prices that fit your budget—flexible terms and customized quotes for every order.
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In our decades of working directly with phenolic intermediates, we’ve seen the industry’s standards grow and change. 3,5-Dimethyl-4-Iodophenol stands out in any catalog of halogenated phenols. Our plant relies on high-precision synthesis lines, where we monitor every reaction step, keeping the final product consistent from drum to drum. Over the years, chemists and production managers visiting our facility have brought up a familiar set of questions: how pure can we make it, how dependable is the supply, and what makes our process different from a simple trading house? Years of answering these questions and adapting our techniques guide the following explanation.
The molecule carries two methyl groups at the 3 and 5 positions on the phenol ring, and an iodine atom at the 4 position. This pattern is not just for show. It creates a reliable intermediate for more complex synthesis. Our team synthesizes this compound without shortcuts—each batch undergoes control checks for positional isomers and residual solvents. Chemists working on drug candidates, dyes, and specialty agrochemicals prefer this intermediate for its reactivity, the selectivity it offers in metalation or cross-coupling reactions, and the lack of unwanted byproducts.
We manufacture 3,5-Dimethyl-4-Iodophenol under controlled temperature profiles and verify it with NMR, GC, and HPLC. Our standard grade exceeds 98% assay, with water below 0.2%. That moisture number isn’t an arbitrary cut-off; it comes from seeing how phenolic iodides hydrolyze or decompose when exposed to water during storage or during coupling reactions. Impurities result in lower yields and extra work during downstream purification. Sourcing directly from us means a clear chain of custody for each batch, supported by records linking raw material lots to finished drums.
The physical appearance is an off-white powder, sometimes faintly yellow, with a melting point that hovers around 97-101°C. We pack this material in HDPE-lined drums after nitrogen-purging to reduce oxidative discoloration, so users don’t lose potency before they open the container. If a customer needs a certificate of analysis on a particular lot, we run the specifics as requested: detailed NMR spectra, residual iodide analysis, and attention to trace metals critical in some pharmaceutical pathways.
3,5-Dimethyl-4-Iodophenol behaves very differently from monoiodo phenols without methyl groups. We’ve seen practitioners in the field favor this compound for Suzuki and Buchwald-Hartwig couplings due to its higher selectivity and lower susceptibility to overreaction compared to less hindered phenol iodides. The two methyl groups change the reactivity landscape of the aromatic ring, making certain substitutions possible that won’t work with unsubstituted phenol derivatives.
One customer, a mid-size pharma firm, once illustrated the contrast. Their pilot-scale group compared 3,5-dimethyl analogs to simple 4-iodophenol, reporting more robust C–C couplings, fewer side products, and easier purification. These details, coming from people running real reactors—not just bench-scale flasks—keep surfacing in our feedback loop. Months later, their procurement manager told our technical team that their waste streams became easier to work up, and their reduced purification steps significantly lowered their solvent consumption.
Early on, most requests for 3,5-Dimethyl-4-Iodophenol came from pharmaceutical research. Medicinal chemists like using this molecule to build up advanced scaffolds, especially for structures that benefit from halogen “handles” for further transformation. Experience has shown that the methyl substitution pattern steers the reactivity of the iodine atom—this leads to more predictable outcomes in sensitive bond-forming reactions. Aromatic iodides like this are also a base for synthesizing radioiodinated tracers, where purity and isotopic cleanliness become even more critical.
Specialty pigments companies purchase this intermediate to access complex diaryl ethers and functionalized biphenyls. If the substitution pattern shifts—if the methyls are on other positions, or the iodine sits elsewhere—the resulting colorants or dyes shift markedly in shade and solubility. That sort of observation doesn’t come from reading literature abstracts; it’s what several customers have told our team during site visits.
Crop protection research facilities have adopted this compound too. The halogenated phenol core appears in fungicide syntheses, where reliable, high-purity intermediates prevent bioactivity loss in new lead compounds. The low water and heavy-metal content guarantee reproducible pilot results—a necessity when registration trials burn through kilograms at a time.
Making high-purity iodophenols requires attention beyond basic quality benchmarks. In our plant, staff regularly review crystallization temperatures, drying cycles, and solvent changes. Even a slight drift in chromatographic purity from one lot to the next ends up flagged in our batch records. We log and trend performance metrics—impurity profiles, melting point ranges, and color development over time. Experienced plant operators know pure product doesn’t just mean a high assay on paper; it means keeping trace levels of oxidative byproducts and residual halides below limits that interfere with catalytic reactions.
Feedback from process scale-ups led us to adjust our purification protocols over the years. Early runs often delivered material that met basic purity, but customers mixing it in transition-metal-catalyzed couplings began seeing minor side products. We worked repeatedly with these users, modifying solvent and crystallization steps until downstream issues disappeared. That’s not something distributors bother with, but as a manufacturer, our team gets hands-on with customer troubleshooting.
Years ago, a customer scaling a new API synthesis reported inconsistent yields. Our technical liaison worked directly with their process chemist, reviewing both the analytical data and their handling protocols. Moisture absorption during storage proved to be the culprit. This led us to tighten up our packaging, implement batch-specific moisture reports, and follow up with regular cold-chain shipping in more sensitive projects.
Another specialty polymer producer needed extremely tight control over trace iodine content in post-reaction waste. We designed a purification and rinsing step purely for them, confirmed by multiple external laboratories, which protected their product qualification and long-term reputation. This approach comes from understanding the stakes of each batch—it’s not just about pass–fail; it’s about keeping every link in the manufacturing chain stable.
Working on both ends—production floor and customer lab—teaches a lot about what matters in a real synthesis. Analytical methods evolve in response to new regulatory scrutiny. We provide full spectral characterization and comply with REACH and other regulatory demands without making compliance an afterthought. With feedback cycles from our own R&D and clients’ technical challenges, we continually upgrade our filtration, analytical, and drying systems.
Clients working under GMP conditions rely on our detailed batch tracking. No shipment leaves our facility without a corresponding analytical workup and clear traceability to the starting raw materials. This transparency comes from years of seeing how quality lapses elsewhere force costly recalls or process shutdowns. Direct manufacturing control gives us levers that trading companies cannot pull—reactor cleaning protocols, in-process sample analytics, and transparent documentation.
Halogenated aromatics, particularly iodophenols, raise concerns over environmental and process safety. Our site’s EHS program features integrated waste tracking, effluent treatment, and solvent recovery at every step. Operators are trained to minimize manual handling, and all iodinated waste streams run through an in-house deiodination unit before final disposal. We’ve worked alongside local and national regulators during audits, sharing data publicly and inviting regular site inspections. These practices keep our product and our community secure, and protect customers’ reputations when regulatory scrutiny tightens.
For transportation, robust containment lays the groundwork. We use tested, leak-resistant drums with detailed labeling. Each drum’s journey—from our lines to your loading dock—receives attention from dedicated logistics staff. Import and export paperwork is validated through our compliance office, not just for smooth customs clearance, but to support traceability under national chemical regulations. This reduces downstream risks for our customers, while protecting our own safety record.
Being directly involved in both synthesis and customer support, we've built a feedback-driven cycle. Decisions on batch sizes, purification routes, and process adjustments come from years on the line, listening to research chemists and process engineers. Supply chain reliability starts with our access to precursor chemicals—longstanding supplier relationships, regular quality audits, and inventory strategies that weather market swings.
Process engineers often bring up scalability. We run both small-lot and bulk campaigns, matching run size to customer forecasts. When shortages of key precursors hit, years of direct sourcing ensure limited downtime. Instead of gambling on spot markets, we lock in raw materials earlier, ensuring consistent output. Manufacturing skill shows up between the lines—adapting reactor cleaning procedures, optimizing solvent changes, translating lab protocol overruns into stable commercial output.
Today's market doesn’t tolerate slow adaptation. Demand for 3,5-Dimethyl-4-Iodophenol tracks closely with shifts in pharmaceutical, pigment, and agrochemical innovation cycles. Our technical team attends industry roundtables to keep up with the next wave of synthetic challenges—new transformations, emerging impurity limits, or alternative coupling strategies. When new detection limits shrink or international rules become stricter, we implement in-line analytics so process drift doesn’t put customer compliance at risk.
Each year brings new regulatory requirements. REACH, US TSCA, and Asian chemistries all set new thresholds for purity and environmental impact. We don’t just update paperwork—we invest in analytical and process upgrades so compliance doesn’t slip through the cracks. Many large-volume customers ask for third-party analytical certification, and we respond by double-checking our in-house results against certified external labs.
Proper packaging and secure logistics play a role in consistent quality. Our team selects packaging to withstand humidity, temperature swings, and stacking in global transport. Nitrogen-flushed, internally lined drums keep the material stable until use, while barcoded labels link every drum to analytical reports and manufacturing history. This transparent logistics chain gives end users confidence in what they receive.
We learned over time that delays in customs or mishandling at ports can harm both timeline and product integrity. Our logistics group stays in touch with shippers to clear containers efficiently, monitoring for any signs of mishandling. Unbroken communication from our dock to your storeroom keeps outages to a minimum and ensures that you never wonder where your batch stands.
Customers sometimes underestimate the storage sensitivity of iodinated aromatics. Even tightly closed containers left in variable temperatures risk slow oxidative degradation, which appears as a faint yellowing in bulk materials. Over years, we’ve developed storage protocols and drum liners that hold up under transit stress and long-term warehouse conditions. On rare occasions, users outside controlled environments saw minor discoloration after months on the shelf—an issue quickly traced to faulty third-party warehousing. Sharing these lessons with new users prevents costly surprises.
Another recurring challenge arises from side reactions in catalytic couplings with low-purity starting material. Even small amounts of non-target isomers or halide impurities act as catalyst poisons, crippling activity and hiking waste. In response, our QA teams doubled analytical frequency during both synthesis and final blend-up, keeping these contaminants consistently below customer-reported critical thresholds.
Every drum leaving our facility includes not just a certificate of analysis, but decades of experience running and troubleshooting this chemistry. We hold regular in-house reviews when customer feedback comes in—whether praise, a rare complaint, or a special purchase request. Our chemists and technicians work directly with end users to interpret analytical data, investigate lot anomalies, or suggest real-world solutions that avoid market claims or costly resynthesis.
Technical exchanges inform continuous improvement. One major pigment company reworked a synthetic route based on input from our process lab, improving overall yield and lowering solvent use. With open channels across the supply chain, both routine and novel issues see quick response, and better products reach the market without protracted problem-solving cycles.
Industry changes faster than ever. Sourcing 3,5-Dimethyl-4-Iodophenol from a manufacturer invested in reliability, deep technical support, and end-to-end quality assurance cuts risk in every downstream step. Lessons learned from working shoulder-to-shoulder with research labs, process teams, and regulatory groups guide us every day. Our team’s focus remains simple: deliver dependable material that meets or beats expectations, document every step for full transparency, and keep improving with every lot produced.
In short, 3,5-Dimethyl-4-Iodophenol plays a subtle but crucial role in countless synthetic projects. Experience, transparency, and long-term industry commitment ensure that each kilogram not only meets the specification but supports the bigger picture—safer production, better outcomes, and less risk for every user down the line.