|
HS Code |
943524 |
| Cas Number | 608-14-6 |
| Iupac Name | 1,2-dichloro-3-methylbenzene |
| Molecular Formula | C7H6Cl2 |
| Molecular Weight | 161.03 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 208-210 °C |
| Melting Point | -19 °C |
| Density | 1.25 g/cm³ at 20 °C |
| Refractive Index | 1.542 at 20 °C |
| Flash Point | 89 °C (closed cup) |
| Solubility In Water | Insoluble |
| Vapor Pressure | 0.32 mmHg at 25 °C |
As an accredited 2,3-Dichlorotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,3-Dichlorotoluene is packaged in a 500 mL amber glass bottle, tightly sealed with a safety cap, and labeled for laboratory use. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 80 drums x 250 kg, total 20,000 kg (net), liquid, securely packed for chemical transport. |
| Shipping | 2,3-Dichlorotoluene should be shipped in tightly sealed, appropriately labeled containers, away from oxidizing agents and sources of ignition. It is classified as a hazardous material and must be transported according to local, national, and international regulations for flammable and environmentally hazardous liquids. Proper safety documentation and labeling are required during shipping. |
| Storage | 2,3-Dichlorotoluene 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 oxidizers. Protect from direct sunlight and moisture. Store away from heat to prevent decomposition, and ensure proper labeling. Use secondary containment to avoid environmental contamination in case of spills or leaks. |
| Shelf Life | 2,3-Dichlorotoluene typically has a shelf life of 2-3 years when stored properly in tightly sealed containers, away from light. |
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Purity 99%: 2,3-Dichlorotoluene with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and consistent product quality. Boiling Point 197°C: 2,3-Dichlorotoluene with boiling point 197°C is used in agrochemical manufacturing, where it facilitates controlled distillation and reduces process losses. Low Water Content: 2,3-Dichlorotoluene with low water content is used in electronic chemical production, where it prevents hydrolysis and maintains product stability. Density 1.25 g/cm³: 2,3-Dichlorotoluene with density 1.25 g/cm³ is used in specialty resin formulation, where it enhances solvent compatibility and improves dispersion. Stability Temperature up to 60°C: 2,3-Dichlorotoluene stable up to 60°C is used in dye intermediate processes, where it ensures safe handling and prevents decomposition. |
Competitive 2,3-Dichlorotoluene prices that fit your budget—flexible terms and customized quotes for every order.
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As chemists and long-time producers of aromatic halides, we understand how key intermediates often go overlooked despite powering dozens of critical processes. 2,3-Dichlorotoluene, or 2,3-DCT as it’s called in our laboratory records, stands as one of those quiet workhorses in specialty chemical synthesis. Attention to purity, reliability batch-to-batch, and understanding end-user application shapes the way we approach each drum and tanker load we ship. Rather than treating this molecule as just a catalog entry, we see the many challenges and opportunities it brings to the table.
The molecular structure of 2,3-Dichlorotoluene is deceptively simple but opens a toolkit for synthetic chemists. With two chlorine atoms occupying the second and third positions of the toluene ring, the electron density shifts just enough to change its reactivity compared to the more common 2,4- or 3,4-dichlorotoluene isomers. This isn’t just a matter of intellectual interest; the placement of these substituents determines how this compound can serve as a precursor for pharmaceuticals, agrochemicals, and advanced materials. Based on our experience processing both mono- and dichlorinated toluenes, we notice the reactivity difference during halogenation and coupling reactions is substantial. These differences dictate what downstream partners our 2,3-DCT can be paired with and which patented processes it supports.
Take, for example, the development needs of modern herbicides and fungicides: 2,3-Dichlorotoluene can offer an optimal balance between reactivity and selectivity for chlorination sequences leading to active molecules. Over the years, we’ve also dealt with contract synthesis projects that call for maximum chemical yield in as few steps as possible; here, the isomeric configuration of 2,3-Dichlorotoluene often delivers more streamlined synthesis routes compared to its 2,5- or 3,4- siblings. Chemically, this impacts not just lab feasibility but production costs for our customers down the line.
From a production point of view, the expected purity for 2,3-Dichlorotoluene varies based on where the product is headed. For downstream pharmaceutical intermediates, we receive requests for material at or above 99.5% purity accompanied by low ppm levels of isomeric impurities and residual acids. Our process control must stick to these standards—when large-scale chiral catalysis is involved, even trace contaminants can derail reactions or poison expensive catalysts. We achieve that level of purity not through shortcuts but through a tightly controlled chlorination and distillation sequence, further refined as per the end-use requirements.
Some industrial users of 2,3-Dichlorotoluene for non-critical applications may seek a technical grade in the range of 97–98.5%. We can accommodate that without much issue, though we always communicate to R&D and procurement teams that even small increases in contaminants can impact scaling experiments or formulation tests. Ultimately, our blending, distillation, and analytical verification processes adjust to meet whatever target specification the buyer has validated in their own formulations.
Storage and shipment details may sound routine, but with chlorinated aromatics, neglect can lead to surprises. Ensuring an airtight seal throughout transit prevents moisture ingress, which helps safeguard both the product and any activated packing material. Some years ago, we introduced upgraded steel drums with specific lining technologies—this reduced risk of hydrogen chloride off-gassing in tanks under extreme temperatures, based on lessons learned during shipments to subtropical regions. Physical properties such as boiling point around 205–207 °C and relative density roughly 1.27 g/cm³ may seem minor, but they matter when building out equipment and safety protocols for large batch operations.
First-time users often ask about volatility, toxicity, and how 2,3-Dichlorotoluene stacks up against similar halotoluenes in terms of workplace safety. Over decades, we have tested, improved, and documented proper ventilation, PPE, and spill control for a wide range of aromatic halides. 2,3-Dichlorotoluene brings with it the faint but unmistakable characteristic chlorinated aroma. Its moderate vapor pressure doesn’t usually present polymerization risk in ambient environments, but prolonged exposure to its vapors will cause irritation and, in poorly ventilated spaces, can be a safety concern.
We share safety data transparently and make sure our delivery trucks supply major users—including those running continuous synthesis or multi-week campaigns—with proper training resources. Our teams regularly conduct their own risk audits, recognizing that actual site conditions often diverge from textbook scenarios. Periodic third-party validation of our handling procedures confirms that our approach remains forward-looking. Many young engineers from our process group now help customer sites draft their first batch operating instructions, bridging gaps that technical data sheets never cover in such detail.
Over the past twenty years, the growth in custom synthesis and flow chemistry has shifted the way 2,3-Dichlorotoluene features in new projects. No longer do most users rely on this intermediate only for classic coupling or Grignard reactions. Its role has matured in tandem with the advance of cross-coupling chemistries—the increased selectivity offered by the ortho and meta chlorine atoms provides an edge in certain C-H activation pathways. For specialty pigments, the orientation of the substituents enables subtle color tuning, leading to brighter, more stable shades when compared to meta-only or para-only substituted chlorotoluenes.
As a manufacturer, we notice clear cycles in demand tied to the pipeline of new active ingredient launches in agriculture and pharmaceuticals. When a new patent emerges referencing this intermediate, we often partner directly with the R&D teams for technical feedback on solubility, stability, and compatibility with their pilot reactors. Compared to other dichlorotoluene isomers, 2,3-DCT often fills a gap where steric effects matter or where yield optimization depends on site-specific chlorination. Its physical state as a colorless to slightly yellowish liquid also eases handling in bulk compared to solidified derivatives, which require costly melting and more involved transfer lines.
Scaling production batches smoothly means we deal with the compound’s quirks in real time—such as minor variations in boiling point impacting the separation of side products or the occasional anomaly in freeze-point when cold storage is necessary. These production insights, collected during hundreds of runs, allow us to tweak process variables and further inform downstream users of what to expect beyond the chemical formula.
Ensuring reliability in every shipment, regardless of batch size, builds the backbone of our business. Customers tell us time and again the value they find in consistent, traceable performance—one failed batch can translate into lost opportunity and unnecessary regulatory reviews. We assign every lot of 2,3-Dichlorotoluene a unique identifier, embedded in both our in-house and customer-facing documentation, so in case of process deviations every part of the chain gets checked.
Our commitment to transparency extends to open conversations with process engineers and production managers at our client sites. If a subtle change in impurity profile shows up in post-run analysis, we work hand-in-hand to correct course, whether the issue stems from upstream solvent changes or a need to retune our distillation parameters. Thorough process mapping and willingness to share analytical data means clients can dig deeper than face-value certificates. We’ve invested steadily in process analytical technologies such as GC-MS and NMR to screen for even minor contaminants, helping our partners achieve regulatory and performance milestones without surprises.
Expectations for environmental performance in chemical manufacturing have never stood still. As stewards of both our own production facility and the wider communities we share, we adopt pollution prevention and minimization strategies at every stage of 2,3-Dichlorotoluene production. Our chlorination section is equipped with closed-loop capture for HCl gas, treating all vent streams to prevent fugitive emissions. Waste streams undergo on-site neutralization before either recycling or safe disposal.
For downstream users, regulatory due diligence often focuses on residual aromatic chlorides in formulations. Each delivery can be accompanied by detailed trace impurity breakdowns, and our compliance team monitors international shifts in acceptable thresholds for chlorinated byproducts in finished drugs and agro-agent exports. This careful documentation meets or exceeds the expectation set by key markets, helping clients avoid customs complications or audit delays during registration of new finished products.
Having participated in a number of peer-reviewed site audits, we view third-party validation as a net gain for all parties involved. Our policies evolved based on feedback not just from regulators, but also from frontline chemists at customer sites—practical improvements such as faster batch release protocols or additional tank monitoring arose directly from user input. This approach to continual improvement, grounded in technical exchanges more than box-ticking exercises, keeps quality and compliance at the center of what we do.
The world isn’t standing still, and global sourcing strategies for intermediates like 2,3-Dichlorotoluene keep changing to keep up with supply security and cost pressures. In the past decade, fluctuations in raw material availability or tightening shipping controls have presented challenges for every manufacturer. We responded by diversifying sources for toluene and chlorine, building redundancy into our supply chain rather than relying on a single vendor or geography. We encourage potential users to look for this resilience in their suppliers; the ability to recover quickly from upstream disruptions matters more than ever.
Production costs for halogenated aromatics often depend on energy prices and regulatory compliance fees. Our energy recovery systems make better use of exothermic heat released in chlorination, mitigating the worst impact of regional energy spikes. This focus on efficiency not only stabilizes costs but also supports sustainability commitments that many of our industrial partners now require as standard. Keeping our emissions well below set targets gives reassurance to customers eager to meet investor and public expectations on ‘green’ chemistry sourcing.
Across the industry, we notice a steady trend toward increased transparency and collaboration. Gone are the days of opaque pricing or guesswork about lead times; our commercial teams offer clear estimates and regular production updates without burying details in jargon. That openness has drawn in new global customers who, in turn, share their roadmaps with us, allowing earlier alignment on production starts or custom grades.
Success in producing 2,3-Dichlorotoluene isn’t just a function of technical excellence. The strongest relationships grow from understanding the needs that drive a purchase. In our experience, pharmaceutical companies often seek this intermediate for the synthesis of certain substituted benzimidazoles, benzothiazoles, or for core scaffolds in anti-infective drugs. One long-term collaboration involved a new CNS-active molecule where 2,3-Dichlorotoluene served as the anchoring aryl starting material. Throughout each phase, we coordinated analytical schedules, stability samples, and even tailored grade specifications to ensure developmental timelines remained on track.
Agrochemical producers use this intermediate for making selective pre-emergent herbicides that require exacting standards for both performance and environmental impact. In feedback sessions, chemists noted that 2,3-Dichlorotoluene’s substitution pattern reduced the formation of certain unwanted by-products, which smoothed the registration process in some jurisdictions with strict environmental safety requirements. For producers of specialty dyes and pigments, the controlled introduction of chlorine atoms results in vibrant, stable hues—benefiting industries from plastics to high-performance inks.
We work closely not only with global corporations but also small startups driving innovation in specialty chemicals. Several years ago, a university startup approached us for support in developing new cross-coupling chemistries based on dichlorinated toluenes. Their curiosity drove process changes at our site, and their technical demands pushed us to develop a higher-purity grade we had never before produced at scale. This kind of customer-led innovation demonstrates that robust supplier partnerships can move both science and commerce forward.
Manufacturing both 2,3-Dichlorotoluene and related isomers gives us a unique perspective on their differences beyond what a database or handbook provides. Isomeric variation governs reactivity, safety, and—of no small importance—cost. The 2,4- and 3,4-dichlorotoluene isomers see more use in certain legacy processes where positional effects are less critical. 2,3-Dichlorotoluene, with its ortho-meta arrangement, often fits newer synthetic methods targeting specific molecular frameworks or improved yields.
In practical terms, the purification challenge stands out most. Isomeric by-products arising from incomplete chlorination steps call for meticulous distillation techniques. Our distillation team keeps detailed logs of temperature and pressure variances, learning from years of both successful and suboptimal runs, to ensure efficient isolation without product degradation. This commitment pays off for customers seeking robust, repeatable outcomes. We have found that our 2,3-Dichlorotoluene consistently produces higher confidence with specialists running site-selective coupling or stepwise halogenations, compared to isomers that might introduce more side reactions or less-desirable secondary products.
Pricing differences among isomers usually mirror both synthetic value and production complexity. 2,3-Dichlorotoluene’s place in modern organic synthesis, especially in regulated industries or where fewer process steps are possible, means it carries both technical advantages and cost effectiveness in the right context. Customers benefit from an honest assessment of these trade-offs rather than a simplistic comparison; we welcome technical discussions to ensure that selection optimizes both process efficiency and product performance.
Looking ahead, we anticipate that demand for novel heterocycles, new materials, and greener synthesis pathways will continue to drive interest in precision intermediates like 2,3-Dichlorotoluene. We’ve set aside development resources for pilot projects with clients aiming for new uses, such as next-generation UV absorbers or functionalized polymers. As end-use regulations evolve and consumer expectations shape purchasing trends, we work alongside partners to assess life-cycle impact and track improvements in waste minimization, emissions, and supply reliability.
Our facility invests in continuous process improvement based on robust operator feedback and frequent customer input. We encourage prospective partners to reach out for technical exchanges, share challenges, and celebrate shared wins that stem from real-world experience rather than theoretical promises. We remain committed to manufacturing excellence, transparency, and collaboration—a philosophy that continues to define our approach to 2,3-Dichlorotoluene and every specialty intermediate we produce.