| HS Code | 830421 |
| Chemical Name | 2,6-Dichlorophenol |
| Molecular Formula | C6H4Cl2O |
| Molecular Weight | 163.00 g/mol |
| Cas Number | 87-65-0 |
| Appearance | White to pale yellow crystals |
| Melting Point | 67-69 °C |
| Boiling Point | 208 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.49 g/cm³ |
| Odor | Phenolic |
| Flash Point | 88 °C |
| Pka | 7.08 |
| Vapor Pressure | 0.2 mmHg at 25 °C |
As an accredited 2,6-Dichlorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,6-Dichlorophenol is packaged in a 500g amber glass bottle, featuring a secure screw cap and hazard warning labels. |
| Shipping | 2,6-Dichlorophenol is shipped as a hazardous material due to its toxicity and potential environmental impact. It is typically packed in tightly sealed containers, protected from moisture and direct sunlight, and labeled according to international regulations. Appropriate safety documentation accompanies each shipment to ensure safe transport and handling. |
| Storage | 2,6-Dichlorophenol should be stored in a tightly closed, clearly labeled container, away from heat, sparks, and open flames. Store in a cool, dry, well-ventilated area, separate from incompatible substances like strong oxidizers and bases. Protect from moisture and direct sunlight. Use corrosion-resistant shelving and keep away from food and drink. Handle with appropriate personal protective equipment. |
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Producing 2,6-Dichlorophenol over countless batches and shipments, I have gained firsthand appreciation for what makes this compound a staple in specialty chemical applications. The compound’s formula C6H4Cl2O and its signature chlorinated, phenolic structure set it apart from relatives in the wider phenol family. As a manufacturer, I see requests for various models—crystalline powder, flakes, sometimes custom ground particle sizes. These reflect how different customers approach problem-solving with the same substance.
Demand for this compound reaches seasonally high marks in agrochemical development, dyestuff production, and medicinal precursor synthesis. The reason traces back to its unique combination of two chlorine atoms attached to the aromatic ring, positioned at the 2 and 6 slots. With both chlorine atoms anchored on the ortho positions, we find increased resistance to biochemical degradation compared to lighter or para-substituted isomers. For buyers in the pesticide or herbicide precursor market, this higher resistance translates directly into the extended activity of their end-products, which is rarely achievable with single-chlorine derivatives.
Producing pure 2,6-Dichlorophenol at scale exposes strengths and challenges that never show up in a standard brochure. Even high-quality feedstock can carry trace contaminants; single-digit ppm levels of cresols, polychloro derivatives, or water residues can trip up downstream syntheses. Maintaining consistent melting points in the 68°C to 71°C range and color indices matters—the slightest inconsistency risks batch failure later in the chain. As someone responsible for quality control and remediation, I can say: small deviations in color purity and moisture are often the best predictors of complaints or downtime from clients further along.
Compared to mono-chlorinated analogs (like 2-chlorophenol or 4-chlorophenol), 2,6-Dichlorophenol requires a more controlled halogenation process. Out of experience, failing to control temperature gradients can generate unwanted isomeric impurities or polychlorinated phenols. This precision in handling also lets us meet GMP and high-purity standards for pharmaceutical intermediates—important for customers with sensitive downstream requirements. Large volume buyers from fine chemical sectors emphasize transparent documentation and real batch records because, as they tell us, “one outlier contaminates an entire process.”
Over time, I have seen that published specs only tell part of the story. We target >99% minimum assay for the main fraction, using HPLC and GC methods tailored to our own production quirks. Water impurities below 0.1% and color below APHA 20 don't just look good on a certificate—they cut rework and scrap costs for blending and formulation lines. In dye manufacture, the faintest excess of pink or yellow hue from by-product tars can throw off hundreds of kilograms of finished colorant.
An on-site perspective also reveals that particle size distribution matters more than most think. A coarse granular product may work well in reactors with strong agitation, but when feeding small-volume syntheses or working with older transfer screws, blockages are real and production halts cost the client money. Listening to what users in their labs and plants report, we fine-tune drying protocols and invest in automated sieving as an ongoing effort, not just to make a sale, but because it saves trouble for all parties down the road.
Users often group various dichlorophenol isomers together because of similar-sounding names, but distinct outcomes emerge based on position. As a long-time producer, I have witnessed repeated confusion between 2,6- and 2,4-dichlorophenol from research teams new to the downstream chemistry. The difference in reactivity stems from the blocking effect of both ortho chlorines; 2,6-dichlorophenol is much less susceptible to ring-activation, which changes how it behaves in further chlorination or coupling reactions. Those pursuing phenoxy herbicide chain extension or anti-microbial resin manufacture prefer 2,6- for its stability, even if it comes at a slightly higher cost comparatively.
Older chemical safety reports used to generalize hazards across all dichlorophenols. Realistically, our in-plant experience, combined with new regulatory studies, reveals that 2,6-Dichlorophenol hydrolyzes slower and volatilizes less during production than its meta and para isomers. This pattern means less fugitive release and easier compliance with local emission norms. For buyers facing increasingly strict air and water discharge permits, this distinction can make all the difference when choosing between similar products.
Some clients request help picking between 2,4-; 2,5-; and 2,6- dichlorinated phenols, plus occasional interest in trichlorophenol neighbors. Over hundreds of consultations, I have learned to guide decisions based on actual end-functionality instead of textbook differences. For resin modification—especially where thermal stability is critical—2,6-Dichlorophenol’s steric hindrance reduces crosslinking drift and color instability. In wood preservative formulation, its enhanced persistence balances increased cost. In contrast, 2,4-isomer suits rapid, metabolically degradable applications, making it better for temporary microbiocidal use.
Understanding demand signals also lets us predict market scarcity periods or pricing pressures. Regulatory shifts in Europe and the US have repeatedly altered demand for 2,4- variants due to changing views on environmental persistence. This leaves 2,6-Dichlorophenol as a backstop for long-acting agricultural formulations, for clients who need fewer application cycles and can justify higher up-front purchasing costs. Recent years have brought greater scrutiny to halogenated organic intermediates, but our investment in process stewardship keeps us qualified to supply customers with tighter eco-label requirements.
Our factory’s location, sourcing arrangements, and storage methods play a role in the product’s reliability. 2,6-Dichlorophenol stores best in low-humidity, fully sealed containers—oxidation and hydrolysis begin degrading product quality within weeks under the wrong conditions. We line steel drums with phenolic coatings; this step, while not strictly required by regulatory code, emerged from repeated incidents in which uncoated drums caused trace iron contamination and batch spoilage. Clients using the material in polymerization or electronics intermediates now mandate full trace metal records, a trend I saw begin nearly a decade ago and only intensify each year.
Truthfully, volatility in bulk chlorinated benzene and caustic soda feedstock supplies from upstream impact both output schedules and raw material quality. Our team monitors shipment integrity in transit as closely as the reaction vessels inside the plant. In recent years, several major logistical bottlenecks—weather events, port closures, export regulation delays—reminded us that hands-on supply chain management often marks the difference between predictive reliability and frantic interruptions across a customer’s production cycle.
Years of handling, storing, and packaging 2,6-Dichlorophenol have shaped our facility’s best practices. Though not as acutely hazardous as some chlorinated solvents, its skin and respiratory sensitization risk grows during powder transfers. As a producer, we improve containment systems beyond regulatory minimums not for compliance’s sake, but because an experienced operator recognizes that visible dust escape anywhere usually signals invisible carries elsewhere. We upgrade dust recovery and vessel vent filters after finding elevated exposure readings in real, working conditions.
With international buyers keenly tracking REACH and TSCA registries, documentation transitions from procedural to essential. Customers developing green chemistry credentials press for full disclosure of trace dioxin or furan impurities. Our historic records of each lot, dating back years, have salvaged more than one audit for overseas partners. After all, manufacturers who cut corners rarely stay undetected once downstream product failures or external audits begin.
Customization has become almost routine in our daily work. A pharmaceutical client demanded residue-free, sub-ppm inorganic contamination after an issue with a generic supplier. We reconstructed the entire process line, replaced an aging neutralization vessel, and requalified new filters with independent labs. Costly at the outset, these changes slashed out-of-spec notifications and improved our uptime. Other clients in the plastics sector requested narrow-range bulk deliveries in reusable containers for batch production, citing environmental impact targets. Changes like these build loyalty by aligning operational reliability with shared sustainability goals.
Small-volume research buyers frequently approach us for advice on solvent compatibility and intermediate handling—not all of it found in technical guides. I have lost count of the inquiries about the behavior of 2,6-Dichlorophenol in nonpolar solvent systems. Based on our trials, it dissolves efficiently in ether and chlorinated solvents, but requires temperature control to avoid recrystallization. Insights like these only come from practical experience, taught by occasional failures and the motivation to improve.
Green chemistry initiatives and corporate social responsibility commitments influence our ongoing process improvements. New catalysts for selective dichlorination reduce waste chlorinated by-products, addressing environmental audit points and saving on tipping fees. Traceability for every raw material batch and digital record-keeping meets demand from both regulatory authorities and future-minded buyers. On balance, the investment in analytics, safer process agents, and error-proof packaging means lower overall operational risk that customers notice and value.
Regulatory pressure on global halogenated organics markets is increasing. We adapt by anticipating changes—qualifying bio-based feedstocks, upgrading monitoring tools, and engaging proactively with NGOs driving the dialogue. We communicate openly with buyers about these trends, clarifying why a price shift occurs or why a certain impurity threshold has moved. Transparent relationships like this—grounded in process knowledge rather than faceless transactions—enable our clients to plan their own operations confidently and meet new market expectations efficiently.
Our position as a longstanding producer of 2,6-Dichlorophenol creates an unusual accountability. We are invested not only in the product’s technical attributes, but in our customers’ successful outcomes. That means continual learning—staying abreast of academic literature, conducting pilot-scale reaction monitoring, and sending teams into client plants for feedback. We listen to what each customer says about batch behavior, safety improvements, and performance in final use.
Adjustments in process, packaging, or delivery scheduling emerge from these real interactions, not hypothetical scenarios. By bridging technical know-how with operational experience, we offer more than a shipment of chemicals—we deliver reliability measured in clean batches, reduced rework, and material stewardship that stands up to scrutiny. With every lot, we commit to making 2,6-Dichlorophenol a decisive advantage in our partners’ product lines and a model for responsible chemical manufacturing.