|
HS Code |
921784 |
| Chemical Name | 2-Bromo-4-Chloro-6-Methylaniline |
| Molecular Formula | C7H7BrClN |
| Molecular Weight | 236.50 g/mol |
| Cas Number | 89389-87-9 |
| Appearance | Light brown to beige solid |
| Melting Point | 68-72°C |
| Purity | Typically ≥97% |
| Solubility | Slightly soluble in organic solvents |
| Smiles | Cc1cc(Cl)cc(N)c1Br |
| Inchi | InChI=1S/C7H7BrClN/c1-4-2-6(9)3-5(8)7(4)10/h2-3H,10H2,1H3 |
| Storage Conditions | Store in a cool, dry, and well-ventilated place |
| Synonyms | 2-Bromo-4-chloro-6-methylbenzenamine |
As an accredited 2-Bromo-4-Chloro-6-Methylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | |
| Shipping | |
| Storage |
Competitive 2-Bromo-4-Chloro-6-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!
Among the many options for aromatic amines, one product that has gained notable traction is 2-Bromo-4-Chloro-6-Methylaniline. This chemical stands out not simply for its molecular structure, but for the practical advantages it brings to both research and scalable synthesis in pharmaceuticals, agrochemicals, and dye intermediates. As someone who has spent years in both academic laboratories and production-level settings, it’s clear how slight tweaks in substitution patterns on the benzene ring can lead to big changes in downstream chemistry. In comparison with plain aniline or simple chloroaniline variants, the addition of both bromine and chlorine along with a methyl group creates a compound with unique reactivity and selectivity, driving innovation in synthetic routes.
2-Bromo-4-Chloro-6-Methylaniline is typically supplied as a crystalline solid, with a molecular formula of C7H7BrClN. Each of these atoms serves a role—not just in the shelf life or appearance of the product, but in its behavior during coupling reactions, substitutions, and protection steps. A methyl group at the 6-position gives increased electron density, sometimes shifting the reactivity in ways that simpler amines can’t match. In solution, this translates to a predictable interaction with standard solvents and reagents, delivering cleaner results instead of muddy byproducts.
Quality matters. From my own experience, impurities in aromatic amines tend to creep forward in a synthesis pathway, leading to hard-to-remove contaminants at the final step. Well-prepared 2-Bromo-4-Chloro-6-Methylaniline, with a high purity level confirmed by HPLC and NMR, shaves hours off purification work. Instead of endless column runs, users see sharp TLC spots and good yields with less waste. This makes a difference in both small-scale laboratory work and multi-kilogram batches.
This compound doesn’t only fill a gap left by more basic starting materials. In multi-step synthesis schemes, specialists often look for ways to introduce diverse functional groups on a single aromatic core. The bromo and chloro atoms allow for stepwise cross-coupling—such as Suzuki-Miyaura or Buchwald-Hartwig reactions—to introduce various substituents while retaining a high degree of control. Compared with similar anilines containing just one halogen, this dual-halogen version offers greater flexibility.
Agrochemical and pharmaceutical innovators often seek to build libraries of molecules by combining different electron-donating and electron-withdrawing groups. 2-Bromo-4-Chloro-6-Methylaniline can access those targets more efficiently thanks to the position and nature of its substitutions. I recall one project developing herbicidal compounds, where this aniline scaffold allowed chemists to implement late-stage diversification. Instead of retracing steps or restarting, the team used this product to snap in new fragments via palladium-catalyzed reactions, avoiding both wasted time and costly raw materials.
The chemical industry presents an almost overwhelming lineup of aniline derivatives. Still, not all serve the same purposes. Simpler options, like aniline itself or 4-chloroaniline, can feel appealing for their price and widespread availability. Their lack of structural complexity reduces cost, but often forces researchers to build more steps into a synthetic route or risk producing less-selective reactions. Adding bromine and a methyl group, as seen in 2-Bromo-4-Chloro-6-Methylaniline, addresses certain bottlenecks.
Some chemists stick with cheaper, unsubstituted intermediates hoping to cut costs, but this strategy sometimes backfires. When reactions require selective functionalization or reliable downstream coupling, using a more sophisticated scaffold can reduce overall project timelines and lower total expenses by streamlining purification and minimizing failed batches. In real-world terms, this means moving from gram-scale to kilogram-scale with far fewer headaches—a point anyone who has managed a process scale-up will appreciate.
Few people outside advanced chemistry realize how much time is spent troubleshooting unclear reaction pathways when using less functionalized starting materials. Over the years, I’ve seen both students and senior researchers wrangle with inconsistent results, varying between reactions. Once 2-Bromo-4-Chloro-6-Methylaniline entered the lab’s regular inventory, many of those uncertainties dropped. Its defined structure adds predictability, which matters both for yields and for the reproducibility demanded in regulated industries.
In drug discovery, rapidly creating analogs often decides which company or team crosses the finish line first. Time lost in the synthesis phase directly eats into any competitive edge. Leveraging arylamines with optimal groups pre-installed enables high-throughput screening without lengthy detours into protecting group chemistry or multiple-step halogenations. Libraries broaden, options open up, and the likelihood of breakthrough candidates rises. Choosing a starting material like 2-Bromo-4-Chloro-6-Methylaniline changes the pace at which new molecules are born.
Scaling up any chemical process brings a unique set of hurdles. Product consistency drifts, yields can wobble, and minor impurities at the beginning magnify as the path continues. Going through scale-up exercises with various aniline derivatives, sharp contrasts always emerge in how easily a synthetic protocol transfers from milligram to multi-kilogram levels. With 2-Bromo-4-Chloro-6-Methylaniline, those transitions feel smoother.
Process chemists benefit from high-purity, well-characterized materials. The solid crystalline nature of this compound aids in efficient charging and measuring during manufacturing runs. Instead of dealing with sticky oils or volatile materials, operators can rely on manageable, doseable batches. Workflow interruptions drop, with less need for costly rework, and engineered control over reaction chemistry increases. The bottom line: fewer delays and more reliable outputs.
The chemical sector faces strong scrutiny around waste streams and worker exposure, which keeps everyone on their toes. Compared to other aromatic amines requiring aggressive treatment or producing difficult-to-treat byproducts, working with a well-understood and reasonably stable compound like 2-Bromo-4-Chloro-6-Methylaniline can reduce hazards, provided proper protocols are followed.
Disposal of halogenated intermediates always deserves attention. Facilities with existing acetone, methanol, and organic waste streams find that the compound integrates smoothly with existing protocols. Experience in both university and industry has shown that adopting reagents requiring less aggressive post-process cleanup wins favor from both environmental auditors and practicality-focused engineers. Instead of days spent neutralizing or treating unexpected side-products, reliable input materials set the stage for safer workflows.
With increasing focus on reducing the environmental footprint of chemical processes, chemists now consider both the overall step count and the atom economy of each transformation. Whereas some fallback aromatic amines generate mountains of waste by requiring unnecessary protection and deprotection stages, the intelligent substitution pattern in 2-Bromo-4-Chloro-6-Methylaniline helps chemists skip entire classes of auxiliary reactions. Streamlined synthesis means not just shorter project timelines, but reduced solvent use and lower emissions.
Green chemistry isn’t just a catchphrase—it’s an operational reality for many modern producers. By selecting intermediates that minimize the generation of hazardous side-products, manufacturers build safer plants. Personal experience has shown that processes running with this aniline require fewer emergency workarounds, resulting in more stable regulatory compliance, improved worker safety, and lower insurance premiums. Stakeholders see a real difference on both the spreadsheet and the operating floor.
There’s a gulf between making a few milligrams for research and producing tons for industry. Early in my career, I watched as promising research molecules stumbled during transfer to commercial plants due to impractical or dangerous intermediates. Sometimes, the issue wasn’t poor science but a poorly chosen starting material: something too reactive, challenging to isolate, or prone to decomposition. 2-Bromo-4-Chloro-6-Methylaniline bridges this gap by providing a versatile and manageable platform for both rapid screening and robust scale-up.
Pilot facilities appreciate feedstocks that stand up to storage, temperature changes, and varied humidity. As someone who has spent long nights in both university labs and plant control rooms, I know reliability means fewer surprises, lower storage costs, and more predictable process controls. This aniline has a track record of stability not matched by more volatile or less crystalline options. As a result, scheduling isn’t constantly threatened by delays from material recalls or re-qualification tests.
The modern chemical marketplace often brings together suppliers from Asia, Europe, and North America. Ensuring a steady pipeline of raw materials causes real headaches for both procurement managers and scientists. A starting material like 2-Bromo-4-Chloro-6-Methylaniline becomes attractive partly for the predictable synthesis methods and partly for global accessibility.
During pandemic years and periods of volatility in international shipping, I’ve seen firsthand how easy-to-produce intermediates like this one kept projects alive, while less common or patent-locked compounds led to weeks-long wait times. A robust supply network supporting this chemical, whether refined for GMP compliance or not, ensures that research programs, pilot projects, and commercial launches maintain their timelines.
Competition among pharma and agrochemical developers isn’t limited to the lab bench. Patent claims often hinge on the specific substitutions brought to an aromatic core, influencing both freedom to operate and the strategic direction of new research programs. The unique combination of bromine, chlorine, and methyl groups on this aniline offers an entry point for designing novel molecules less likely to infringe on crowded technology spaces.
Selecting differentiated starting materials helps teams innovate without constant fear of litigation or last-minute reformulation. By embedding hard-to-replicate structural elements early in the synthesis, companies gain strategic advantages and reduce both risk and uncertainty. This has been a consistent lesson throughout both consultancy projects and in-house roles: distinguish your chemistry at the input stage, and downstream hurdles shrink in number and height.
Few chemical components find a spot at the intersection of fine chemical research and industrial production as frequently as substituted aromatic amines. In medicinal chemistry, projects pivot quickly. Days matter. Medicinal chemists prize building blocks that accommodate a wide variety of final targets, from kinase inhibitors to novel herbicides.
In my experience, 2-Bromo-4-Chloro-6-Methylaniline lands among those rare intermediates with tangible upstream and downstream advantages. Researchers can introduce polar or nonpolar groups on the benzene core with pinpoint control, yielding novel structures efficiently. Whether the goal is to create a new class of antifungal agents or tweak a known structure to skirt resistance, this product simplifies problem-solving at the bench and at scale.
Over years working alongside experienced synthetic chemists and operators, certain truths emerge. Reliability in feedstocks translates directly to reliability in projects. 2-Bromo-4-Chloro-6-Methylaniline shows up not just as a number on a material list, but as a trusted member of a formulation arsenal. It handles laboratory mishaps well: easy to recover from, with a low tendency toward mysterious decomposition that can tank weeks of effort.
As chemists shift projects from R&D to pilot plant, new priorities emerge: dust control, metering accuracy, regulatory documentation, and batch traceability. This compound supports those needs through its manageable physical state and well-understood analytical profile. I’ve watched projects speed through validation, hitting regulatory metrics and customer requirements without cavernous re-testing expenses.
Many of the industry’s biggest pain points stem from inconsistent input material, unpredictable supply chains, and brittle regulatory compliance. Streamlining synthetic routes with robust intermediates like 2-Bromo-4-Chloro-6-Methylaniline helps address all three. For supply chain resilience, wide international availability and the use of common synthesis methods shield projects against shortages. For regulatory compliance, well-documented spectral data and batch certificates remove many last-minute doubts. For synthetic challenges, built-in functional handles empower creative chemistry with less need for late-stage troubleshooting.
Looking forward, adoption of such intermediates—driven by quality-first thinking and anchored in practicality—pushes the entire sector closer to dependable, scalable, and safer innovation.
Stepping back, the lessons aren’t just about molecules, costs, or timelines. Whether developing new medicines, crop protectants, or pigments, success comes from making smart choices early. In the toolkit of modern synthetic chemistry, 2-Bromo-4-Chloro-6-Methylaniline stands as more than just another name on a list. It’s a tool that brings together efficiency, versatility, and safety, carrying advantages into research, production, and market strategies. Those seeking to advance in the fast-evolving landscape of customized chemicals would do well to consider what this unique building block offers—not in abstraction, but in lived, day-to-day results where outcomes matter.