|
HS Code |
839011 |
| Name | 3,5-Dichlorophenol |
| Cas Number | 591-35-5 |
| Molecular Formula | C6H4Cl2O |
| Molecular Weight | 163.00 |
| Appearance | White to light tan solid |
| Melting Point | 69-71°C |
| Boiling Point | 227°C |
| Density | 1.5 g/cm³ |
| Solubility In Water | Slightly soluble |
| Iupac Name | 3,5-dichlorophenol |
As an accredited 3,5-Dichlorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3,5-Dichlorophenol is packaged in a 500g amber glass bottle, featuring hazard labels and a tightly sealed screw cap for safety. |
| Shipping | 3,5-Dichlorophenol should be shipped in tightly sealed, labeled containers designed for hazardous chemicals. It must be protected from moisture and heat, and stored away from incompatible substances. Transportation should comply with relevant regulations (such as DOT, IATA, or IMDG) for toxic and environmentally hazardous materials, ensuring secure handling and spill prevention. |
| Storage | 3,5-Dichlorophenol should be stored in a cool, dry, and well-ventilated area, away from incompatible substances like oxidizers and strong bases. Keep it in a tightly closed, clearly labeled container. Protect from direct sunlight, heat sources, and moisture. Ensure storage areas have appropriate spill containment and are equipped with suitable ventilation to avoid accumulation of hazardous vapors. |
Applications of 3,5-Dichlorophenol in Industrial Manufacturing3,5-Dichlorophenol is a specialized halogenated phenolic compound with established functions in multiple chemical industry segments. Through years of production experience and technical exchanges with downstream partners, we have mapped its industrial deployment to key sectors where the compound directly enters process streams, contributes to end-product characteristics, and must meet stringent regulatory expectations. Below are the principal application scenarios verified by actual plant use. 1. Agrochemical Intermediate for Herbicide SynthesisAs a core intermediate in the synthesis of selective herbicides, 3,5-Dichlorophenol is charged into multi-step organic condensations for active ingredient production, primarily for post-emergence weed control products. Its precise chlorination pattern contributes to the bioactivity and environmental profile of the final herbicidal substance. Synthesis facilities demand traceable supplier documentation according to both export and in-market safety mandates, ensuring downstream product registration and audit compliance. Industry compliance standards
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2. Intermediate in Pharmaceutical API ManufacturingCertain downstream pharmaceutical API producers rely on 3,5-Dichlorophenol for chlorophenol ring introduction in the biosynthesis of antibacterial and antifungal drugs. Quality and impurity profiles must fulfill pharmacopoeia monographs and cGMP documentation. Integration demands careful quantitation to ensure consistent yield in multi-stage chemical transformations, especially the formation of etherified and acylated API scaffolds. Industry compliance standards
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3. Biocide and Preservative Precursor in Industrial FormulationsThis compound is introduced as an upstream reactant for the production of halogenated phenolic biocides found in paints, metalworking fluids, and wood preservatives. Ensured batch uniformity aligns with strict environmental and consumer protection norms, as the downstream biocidal active formulations must exhibit validated purity and controlled residue levels. Industry compliance standards
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4. Synthesis of Specialty Dyes and Pigment Intermediates3,5-Dichlorophenol functions as a critical intermediate during the manufacture of chlorinated azo dye precursors and pigment compounds used primarily for plastics and fiber coloration. Compliance tracking ensures vendor batch-to-batch consistency since off-ratio inputs may cause downstream quality deviations in pigment intensity, migration, or thermal stability. Industry compliance standards
Typical usage ratio
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Years in the chemical industry teach you to spot certain workhorse compounds long before their names show up in procurement docs. 3,5-Dichlorophenol—known across the lab benches and reactors by its CAS number 591-35-5—ranks high on that list. In the practical business of synthesis, intermediates don’t always get the spotlight, but this molecule stands out by reputation and by its fundamental role as a building block for downstream goods.
We produce 3,5-Dichlorophenol in our facility from chlorinated benzene derivatives through well-controlled processes that hinge on batch purity and contamination avoidance. Market needs have driven us to offer this compound at a high-purity level (often >99.0% on GC) with careful controls around residual solvents and background chlorinated impurities. We keep a sharp eye on every run for off-odor and discoloration, since even minor flaws can pass down the line, impacting synthesis yields or regulatory acceptance for customers making agrochemical or pharma intermediates.
There’s often some confusion among buyers about what sets this compound apart from other dichlorophenol isomers. The beauty of the 3,5-configuration sits in those chlorine atoms arranged meta to each other, influencing reactivity and solubility. Compared with 2,4-dichlorophenol or 4,6-dichlororesorcinol, the 3,5-variant offers distinct behaviors when introduced as a synthetic handle. For example, nucleophilic substitutions on the ring respond differently, making our compound ideal for certain biocidal formulations and dye intermediates where steric access or further substitution matters.
Daily production of 3,5-Dichlorophenol brings its own challenges. The specificity of chlorination requires careful stoichiometric control—overshoot the reagent charge and polychlorinated byproducts take over. Our operators pay special attention at stage separation and distillation. Temperature rigors demand the right glass-lined reactor, as iron catalysis from a corroded batch kettle can cause off-color that downstream users pick up quickly. Our quality department pulls composite samples from every lot, comparing retention times and mass spectra against validated standards.
We’ve watched the market lean in on documentation. End-users especially from regulated markets (like EU or NA agrochem manufacturers) ask for full impurity profiles, not just COA basics. Audits now look for process transparency—raw material sourcing, chlorination agents, and waste streams. We invested early in in-house analytical equipment—GC-MS, NMR for batch validation—because lab results are only as good as the tale they tell. If a shipment deviates, feedback comes fast and clear; some customers run our product in high-throughput combinatorial setups where even minor variance drags operations.
Physical properties often matter more than the typical numbers on a page suggest. Freshly made 3,5-Dichlorophenol forms light crystals with a mild phenolic scent. Clumping or discoloration signals moisture ingress or temperature cycling. Our standard packaging—high-grade polyethylene drums with desiccant liners—arose from years of hearing about lost batches from storage conditions. Transportation also gets a tailored touch: for routes exposed to prolonged high summer heat, we mobilize climate control staging or expedited shipping.
We first gained notice with customers in the herbicide and fungicide sectors. There, 3,5-Dichlorophenol finds its way as an intermediate for a lineup of active ingredients (AIs). Its two chlorine atoms turn out to be reactive anchor points for groups attached during later stages, leading to molecules that inhibit fungal growth or block unwanted plant tissue development. It’s not just the biology—the regulatory framework for actives looms large, so every impurity level we report takes on added weight. Certain residue levels, if missed, can mean rejection by end-product quality control.
Other manufacturers employ our product as a starting point for antiseptic and disinfectant agents. The phenolic scaffold, toughened by the electron-withdrawing chlorines, widens the antimicrobial spectrum and boosts stability under sunlight. Some specialty resin and dye makers also prefer 3,5-Dichlorophenol for its unique electronic structure, which leads to colorfast pigments or more robust crosslinkers upon functionalization. In the art and science of chemical synthesis, isomer selection becomes a matter of both yield and downstream processing cost. Using the wrong dichlorophenol can spike waste rates or force roundabout purification steps.
Questions sometimes come in from R&D: Why not pivot to alternative phenols or other ring-substituted aromatics? Frankly, availability and price matter, but so does the predictability of transformations. 3,5-Dichlorophenol boasts ring activation poised for functionalization, with fewer ortho chlorines to hinder further group installation. Trying to mimic downstream AIs with a different dichlorophenol often results in higher halide waste burden or lower conversion in the critical coupling stages.
Some buyers ask directly what sets our 3,5 isomer apart from more commonly available variants like 2,4-dichlorophenol. The answer traces back to reactivity and downstream process fit. 2,4-dichlorophenol, while similar, often leads to non-selective substitution patterns on the aromatic ring. The difference seems subtle, but once secondary reactions start, especially in making fine chemicals, the devil’s in the detail. We have tracked user feedback over years and see that process chemists choose our product where selective activation, fewer stages, and manageable byproduct profiles help hit tighter production timelines.
We regularly run demo syntheses alongside R&D partners. One recent batch comparison found higher yield and less unwanted cross-chlorination with 3,5-Dichlorophenol than with 2,4- or 3,4- variants under otherwise identical Suzuki coupling conditions. Our team shared this insight at a recent technical session, and customers responded by piloting our grade for agricultural intermediate production. These are real-world metrics that weigh heavier for procurement teams than generic catalog comparisons.
Some industries consider cost per kilo as the deciding factor, but applications in pharmaceuticals or high-value materials manufacturing tip the balance toward purity and reliability. Contaminants like polychlorinated phenols or ring cleavage products not only lower batch yields—they can introduce toxicity concerns, or breach tight international specifications. By focusing on clean profiles and robust documentation, we support customer audits and regulatory submissions. Plant managers once facing delays from residue analysis come back when their in-house checks show cleaner conversion and less downtime from column fouling.
As chemical manufacturers, we view EHS standards as more than regulatory line items. Everyday operations aim to reduce worker exposure and limit emissions, especially with phenolic compounds like 3,5-Dichlorophenol. Its moderate vapor pressure asks for local extraction in reactor halls and transfer points. Engineering controls—a legacy of past solvent incidents—provide our staff with enclosed handling and automatic dosing stations so direct skin or vapor contact rarely occurs. Regular staff training reinforces not just compliance, but a basic understanding of the chemistry hazards.
Our waste management system channels spent mother liquors through both internal treatment units and authorized external handlers. Historically, the focus on dichlorinated organics pushed our process to adopt multi-stage neutralization and carbon filtration to meet water discharge limits. Where outdated protocols might have seen byproducts vented or incinerated, customer demand for greener profiles pushed us into closed-loop reclamation for some solvents and even considered routes for spent phenol reuse.
Clients—especially outside our national borders—grow more curious about life cycle impact. We field questions on source raw material traceability. Some buyers, particularly those aligning with ISO certifications or meeting REACH registration, look for detailed dossiers on intermediates. Our documentation spells out not just product purity, but also upstream footprint: raw source, energy demand, and disposal routing.
Feedback cycles matter in this business. Early on, we saw our role as ending at the warehouse door. Over the past decade, customer needs transformed that view. Now we routinely field application troubleshooting: clogged filter press? Unexpected color in downstream? We help trace analytical fingerprints, running split samples, or sourcing alternative packaging. Occasionally, R&D teams approach us for modifications—adjusting particle size, moisture, or providing pre-ground material. We have responded by customizing certain lots, improving flow or handling properties to suit niche process needs.
We also react quickly to documentation needs. Many users send agents for site audits—tracking both product and process. We maintain batch records, validated cleaning procedures, and storage logs accessible for major client partners. Whenever regulatory frameworks shift, our teams adapt documentation and adjust production, maintaining up-to-date REACH, EPA, and GHS conformity. Traceable chain of custody tracks back to our storage tanks, an assurance critical in regulated, high-liability markets.
Supplying 3,5-Dichlorophenol brings its own headwinds. Raw material price volatility keeps everyone wary. A sudden spike in chlorinated benzene can ripple down quickly, squeezing margins and prompting supply chain recalibration. Over time, we built reserves and diversified sourcing, forging direct relationships with upstream producers. Sourcing strategies paid off during recent global logistics chokepoints. The experience told us that maintaining product flow sometimes requires investing ahead of actual demand—a tough balance for smaller operators.
On the technical side, process intensification remains a goal. We constantly scout new catalytic systems, greener oxidants, and low-residue purification steps. The promise of continuous flow chemistry in dichlorophenol production gets discussed often. Transitioning from batch to continuous opens lots of potential, not just for throughput or cost, but also for reproducibility and waste minimization. We have observed pilot success in parallel fields and keep a close watch for crossover opportunities.
The evolving regulatory landscape also affects even entrenched intermediates like ours. Tightening control over aromatic chlorinated compounds in several regions forces us to continually invest in emission management and impurity reporting. Rather than treating this as a box-ticking exercise, we treat every new guideline as a prompt to revisit cleaning protocols, product labeling, and emergency response planning. The changing rules also reflect market pressures; customers in pharma or agriculture must provide more transparency in filings than ever before, so we remain ready with the data they need.
Sustainability—a term sometimes thrown around loosely—anchors more of our daily discussions. Longview, greener production pathways for chlorinated aromatics mean less reliance on legacy reagents and more attention to closed-loop systems. Colleagues in the research group continue working on alternative chlorination strategies and solvent recycling upgrades. These aren’t just gestures: waste reduction, energy savings, and risk mitigation at the source all bring measurable operating benefits. Customers see cleaner, more predictable intermediates and share that value with their own stakeholders and regulators.
Looking ahead, we expect downstream users will keep pushing for even tighter specification windows—lower ppm targets, more detailed impurity accounting, wider sustainability data sets. Learning from every feedback—whether a successful scale-up or a process hiccup—fuels the upgrades we pursue. Our teams treat each order as both a technical challenge and a relationship in practice; when a customer’s downstream process tightens limits or pivots chemistry, we drive process improvement to keep pace.
Through years of producing 3,5-Dichlorophenol, none of its applications or specifications stand still. Working directly with users—taking calls about an odd color during a production campaign or collaborating on a customized drying cycle—cements our place not just as a supplier, but as long-term partners in manufacturing. Each unit shipped, inspected, and tracked marks a joint effort in safely and reliably moving all kinds of chemistry forward.