|
HS Code |
183093 |
| Chemical Name | 3-Iodo-4-Methylaniline |
| Cas Number | 6968-73-2 |
| Molecular Formula | C7H8IN |
| Molecular Weight | 233.05 g/mol |
| Appearance | Light brown to beige solid |
| Melting Point | 61-64 °C |
| Density | 1.78 g/cm³ (estimated) |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | CC1=CC(=C(C=C1)N)I |
| Inchi | InChI=1S/C7H8IN/c1-5-2-3-6(9)7(8)4-5/h2-4H,9H2,1H3 |
| Ec Number | 230-219-2 |
| Storage Conditions | Store at room temperature, keep container tightly closed |
As an accredited 3-Iodo-4-Methylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g 3-Iodo-4-Methylaniline is packaged in a sealed amber glass bottle with a tamper-evident screw cap and hazard labeling. |
| Shipping | 3-Iodo-4-Methylaniline is shipped in secure, chemically resistant containers compliant with safety regulations. The packaging is clearly labeled and includes hazard information. During transit, temperature and handling precautions are maintained to ensure product integrity. All shipments adhere to relevant local, national, and international transport regulations for hazardous chemicals. |
| Storage | 3-Iodo-4-Methylaniline should be stored in a tightly sealed container, placed in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Store at room temperature, avoiding excessive heat or moisture. Ensure proper labeling, and keep the chemical out of reach of unauthorized personnel. Use designated chemical storage cabinets if available. |
Applications of 3-Iodo-4-Methylaniline in Industrial Manufacturing3-Iodo-4-methylaniline supports several high-value industrial sectors as a crucial intermediate. Its stable halogenated aromatic backbone delivers unique reactivity required for precise downstream chemical synthesis. We supply directly to manufacturers applying this material in active pharmaceutical ingredient (API) synthesis, specialty dyes, agrochemical active production, and advanced electronic material sectors. 1. Pharmaceutical Intermediate Synthesis for Anticancer CompoundsMajor global and regional pharmaceutical manufacturers use 3-iodo-4-methylaniline as a key starting material in the targeted synthesis of kinase inhibitor actives for oncology therapeutics. During API route development, its selective iodination and methylation support transformations such as Buchwald-Hartwig aminations or Suzuki couplings under GMP conditions. Material purity and trace metal content must meet strict industry release specifications before use in regulated drug substance routes. Our internal quality systems support multi-kilogram batch supply aligned with site-specific process validation requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Specialty Dye and Pigment SynthesisDye and pigment manufacturers in the fine chemicals sector employ 3-iodo-4-methylaniline for the preparation of high-performance azo and anthraquinone colorants used in inkjet, textile, and plastics coloration. Its position-selective substitution profile enables building blocks for unique hues and solubility profiles. The QC team tests each batch for reactivity performance, ensuring compliance with established sector-specific purity and contaminant limits, including halide content, as demand grows for pigment dispersions and specialty ink systems. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Active Ingredient ManufacturingManufacturers of herbicide and fungicide actives select 3-iodo-4-methylaniline for its role in constructing halogenated aromatic rings, critical to biological selectivity and field durability. Used within registered process chains for advanced crop protection compounds, the raw material supports scalable conversion under controlled batch conditions with dedicated process monitoring, tracking and documentation for independent regulatory submission. We offer technical support to achieve industry-mandated traceability and full substance disclosure as required by local authorities and global crop protection chemical standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Advanced Electronic Materials SynthesisProducers of specialty electronic materials and molecular semiconductors require highly pure, halogen-functionalized aromatic intermediates during development of organic light-emitting diodes (OLEDs), organic thin-film transistors, and advanced resist materials. 3-iodo-4-methylaniline allows precise control over spatial and electronic properties in custom monomer synthesis, impacting charge mobility and stability in the final material stack. Each supplied batch undergoes extra sub-ppm control for trace metal and ionic contamination, as leading-edge customers set strict quality requirements pursuant to their end-use device qualification protocols. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Iodo-4-Methylaniline 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!
In the chemicals industry, progress often depends on access to robust and reliable building blocks. 3-Iodo-4-Methylaniline stands as a prime example of an intermediate favored by research teams and production lines that value clean reactions and well-characterized properties. We produce this specialty aniline derivative in-house using a batch process that keeps close watch on purity standards at every stage. Every time research and development teams approach us with a challenge grounded in the need for high specificity, 3-Iodo-4-Methylaniline regularly surfaces as a tool that handles difficult substitutions on aromatic rings effectively, particularly for those seeking a halogenated and methylated aromatic amine.
Our production model for 3-Iodo-4-Methylaniline (also known under CAS 6967-82-4) focuses on reproducibility, consistency, and minimizing byproducts that can impact downstream reactions. The finished product presents as a crystalline solid. From in-house records and internal QA, HPLC purity regularly exceeds 98%, and water content falls below 0.5% as monitored by Karl Fischer titration. Limit tests for metals and other halides meet the threshold needed for fine chemical synthesis and advanced pharmaceutical intermediates. During our internal process controls, GC-MS and NMR confirm the structure and help us keep isomeric impurities below detectable levels. Every lot undergoes rigorous analytical checks to ensure the iodo and methyl groups are precisely in the 3- and 4-positions, which matters a great deal for those engineering structure-activity relationships in heterocyclic development.
In our experience, users depend on this compound to streamline syntheses that require selective introduction of nitrogen and iodine groups to aromatic systems. The electronics sector calls for molecules bearing halogen substitutions, which impart increased reactivity at precise sites on the benzene ring. Many research protocols for agrochemical candidates demand aromatic amines as key precursors, especially where a methyl group at the 4-position fine-tunes solubility and biological profile. Our customers in medicinal chemistry leverage this product as a stepstone in the creation of kinase inhibitors, CNS modulators, and other bioactive scaffolds where careful positioning of iodo and methyl marks on the ring can determine binding activity and selectivity profiles.
Multi-step synthesis frequently requires that intermediates survive harsh reaction conditions and avoid undesired rearrangement. The stability profile of 3-Iodo-4-Methylaniline, according to feedback from lab and pilot-scale operations, reduces the need for constant repurification. Users performing Suzuki, Buchwald-Hartwig, or amination couplings benefit from the electron-donating methyl group, which can accelerate reactions, while the ortho iodo atom provides a targeted handle for palladium- or copper-catalyzed transformations. The outcome: higher yields, faster reactions, and less scrambling of the aromatic backbone.
Manufacturing specialty anilines involves more than simply following a literature procedure. Process optimization at larger scale requires patient troubleshooting, particularly to keep the introduction of the iodo group selective and controllable. From our own line runs, we recognized long ago that side reactions, such as diiodination or partial demethylation, posed a risk to lot-to-lot consistency. By tuning solvent ratios and precisely controlling the stoichiometry and addition rate of iodine reagents, we minimize the formation of unwanted isomers and over-iodinated byproducts.
Operators who have worked with halogenated aromatics can attest to the challenge posed by strong odors or skin sensitivity. We run dedicated air handling and ensure full containment to protect the workforce, relying on automated sampling and in-line analytics. The final product, once dried and packaged, passes through a dust-control filter that limits losses due to hygroscopicity and helps improve shelf life during storage. That kind of hands-on control pays off later, reducing the odds of surprises on downstream process lines or supply chain rejections.
The aniline family covers a wide spectrum, both in terms of structure and physical properties. Our years manufacturing alkyl- and halogen-amines have shown that the placement of each functional group influences both how the compound reacts and how cleanly it can be purified. For instance, 4-methylaniline alone holds promise for pharmaceutical use, but lacks the directed reactivity provided by a halogen atom. 3-iodoaniline features the iodine, but without a methyl group on the ring, it leaves process chemists without an additional handle to modify lipid solubility or electronic properties.
Working with 3-Iodo-4-Methylaniline brings a unique combination. The electron-donating methyl group stabilizes diazonium salts during functionalization, avoiding the tendency of unsubstituted anilines to decompose or tar up under acidic conditions. That difference manifests in better yields when users want to construct azo dyes, specialty pigments, or benzotriazoles for advanced materials. The iodine not only serves as a coupling point, but also lends the molecule weight, which is valued for radio-labeling, imaging agent development, or as a stepping stone to further fluorination.
In direct side-by-side comparisons of purification runs, the 3-iodo-4-methyl variant produces sharper melting and boiling points, which helps users avoid product carryover during vacuum distillation – a task notoriously difficult with lower boiling mono-alkyl derivatives. Sample feedback from API manufacturers points out fewer tar impurities and more reproducible spectra compared to other halogenated aromatics we've supplied. In the hands of experienced chemists, those traits shorten development timelines and de-risk scale-up.
The pressure to meet regulatory and environmental standards continues to mount – particularly with halogenated intermediates. We’ve adopted greener iodine sources and solvent recovery on our 3-Iodo-4-Methylaniline lines before these changes became official requirements. The business case for investing in these upgrades became clear once stricter wastewater treatment rules took effect. In process intensification trials, switching to microreactor technology during iodination steps helped cut overall iodine and acid use by over 30%. That, in turn, lowered both energy bills and the need for costly secondary waste treatment.
Some buyers in the biopharma and diagnostics spaces request proof of freedom from nitrosamines and low residual solvent profiles. We share full analytical documentation and encourage plant tours so partners can see process controls in action. In everyday operations, this means holding to better than ICH Q3C solvent residue limits and confirming that critical metal catalysis residues fall well below agreed specs. Our role as manufacturer doesn’t stop at producing grams or kilos: we help users trace each batch from raw iodine to final product, supporting internal compliance and market access.
As with any specialty intermediate, keeping down-time low during changeover matters. The dust and static risk with finely divided iodoaniline powder prompted us to redesign the discharge chute for easier flow, and to adopt nitrogen blanketing during larger operations. Slow pours and low-pressure transfer keep static below threshold and cut back on operator exposure.
Limited solubility in some organic solvents can present bottlenecks for users, especially at high concentrations. Our technical team mapped solubility profiles in a broad range of reaction media to help formulators avoid unexpected precipitates. That led customers to switch from toluene to NMP or DMF in coupling steps, with a measurable impact on both crystallization time and yield. The bottom line, as we see in their feedback and our own plant audits, is that process knowledge and willingness to tackle unforeseen headaches separates routine suppliers from genuine solutions partners.
Few intermediates sit at a perfect intersection of reactivity, selectivity, and compatibility. Over years producing iodoanilines, we’ve seen how compromised purity, even at tenths of a percent, can wreak havoc. Impurities such as diiodinated or ortho-methylated analogs tend to poison catalysts, disrupt isolation, and sometimes lead to phase separation issues during extractions. By setting our detection limits below those of most third-party labs, we hand users a tool that needs less troubleshooting downstream.
Market shifts, regulatory changes, and unforeseen logistics hurdles all test a manufacturer’s commitment. Data from the last several years have shown cost spikes for iodine sources and some aromatics due to geopolitical volatility. Our position as a primary producer allows us to absorb some cost volatility and buffer partners from short-notice price swings that hit traders and resellers harder. Direct plant-to-user shipping with real-time tracking lets us keep foreign object and contamination claims to virtually zero. When issues do arise – material returns, transit exposure, or regulatory audits – we provide forward and backward traceability for every 3-Iodo-4-Methylaniline drum or bag, using in-house labeling and bulk handling records.
Feedback channels show just how pivotal product reliability has become in specialty chemical supply. One multi-national client in crop protection outlined their bottlenecks with out-of-spec halogenated intermediates, including lost time at downstream granulation and formulation steps. R&D inputs for molecule optimization, particularly for those chasing patentable fungicide backbones, demand confidence that every batch of iodoaniline delivers identical performance. In another case, a diagnostics company developing radiolabels for imaging asked for pre-packed aliquots to minimize degradation during transport – both to cut on-site QC time and meet GMP standards.
Each use scenario sheds new light on the characteristics that matter most: precise substitution pattern, minimal trace impurities, reliable logistical support, and data-rich transparency from manufacturing through delivery. Communication with these partners challenges us to keep raising the bar and shows that process improvements rarely follow a single template.
As functionalized aromatics play larger roles in the design of next-generation electronic materials, energy storage, and genomics, manufacturers of 3-Iodo-4-Methylaniline face growing calls for ever-purer product. The days of batch-to-batch variability forcing research teams to hedge bets with increased analytical overhead are drawing to a close. For us, that means deeper integration of inline analytics, tighter process documentation, and ongoing engagement with end-users to anticipate new requirements.
In-house experience repeatedly shows that production of 3-Iodo-4-Methylaniline involves much more than access to raw materials or off-the-shelf procedures. Each reactor run, analytical report, and customer conversation builds an accumulative record that shapes not only this product line, but also the way specialty chemicals are delivered and supported as the industry changes.
A deep familiarity with the nuances of 3-Iodo-4-Methylaniline production, from raw iodine supply management to mitigation of dust during packaging, defines what manufacturers bring to the table. We shape each batch informed by both long-term hands-on process data and ongoing user feedback. This approach, grounded in technical integrity and willingness to adapt, makes a real difference for organizations seeking more than commodity intermediates. With a product as versatile and chemically influential as 3-Iodo-4-Methylaniline, an experienced manufacturing partner enables confidence in both chemistry and supply, letting innovators concentrate on the breakthroughs that matter.