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HS Code |
172730 |
| Chemical Name | 5-Chloro-1,3-Dimethoxybenzene |
| Molecular Formula | C8H9ClO2 |
| Molecular Weight | 172.61 g/mol |
| Cas Number | 3430-16-8 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 235-237 °C |
| Density | 1.18 g/cm3 |
| Refractive Index | 1.546 |
| Smiles | COC1=CC(=CC(=C1)Cl)OC |
| Pubchem Cid | 256649 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
As an accredited 5-Chloro-1,3-Dimethoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 5-Chloro-1,3-Dimethoxybenzene, tightly sealed with a screw cap and labeled clearly. |
| Shipping | **Shipping Description:** 5-Chloro-1,3-dimethoxybenzene should be shipped in tightly sealed, chemical-resistant containers. Store and transport in a cool, dry, well-ventilated area, away from incompatible substances. Label packages according to regulatory requirements. Handle with appropriate safety measures and ensure compliance with local and international chemical shipping regulations. |
| Storage | Store 5-Chloro-1,3-dimethoxybenzene in a tightly sealed container within a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect it from moisture and direct sunlight. Clearly label the storage area and container, and ensure it is accessible only to trained personnel. Follow all relevant safety and regulatory guidelines. |
Applications of 5-Chloro-1,3-Dimethoxybenzene in Industrial ManufacturingAs the original factory producer of 5-Chloro-1,3-Dimethoxybenzene, we supply this aromatic intermediate to established industrial chains with concentrated, compliant downstream operations. Below are the key application domains where 5-Chloro-1,3-Dimethoxybenzene functions as a critical building block, enabling value-added synthesis and specialty formulation for high-precision manufacturing. 1. Pharmaceutical Intermediate for API SynthesisIn pharmaceutical chemical synthesis, 5-Chloro-1,3-Dimethoxybenzene acts as a core intermediate for preparing various active pharmaceutical ingredients, including certain antifungal and anti-infective agents. Multi-step routes use it as a substituted benzene segment, where strict traceability and material consistency influence downstream yield and impurity control throughout API batch production. Industry compliance standards
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2. Agrochemical Synthesis: Key Intermediate in Pesticide ManufacturingAgricultural chemical formulators utilize 5-Chloro-1,3-Dimethoxybenzene as a key aromatic building block when producing specific broad-spectrum herbicides, fungicides, and plant protection compounds. Its unique substitution pattern allows targeted ring construction critical for downstream bioactive agents that pass national residue and environmental safety evaluations. Industry compliance standards
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3. Fragrance and Aroma Chemical IntermediateFragrance manufacturers employ 5-Chloro-1,3-Dimethoxybenzene for the synthesis of specialty aromatic compounds essential for high-end perfumery and flavoring agents. The compound contributes to the formation of complex ether and acetal structures, imparting unique olfactory notes and enhancing product differentiation for fragrance blending. Industry compliance standards
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4. Dye and Pigment IntermediateSynthetic dye and pigment producers source 5-Chloro-1,3-Dimethoxybenzene to prepare select functionalized aromatic dyes and pigment precursors. The molecular structure enables synthesis of mono- or di-chloro aromatic colorants, with significant performance in color stability and molecular compatibility for ink and fabric applications. Industry compliance standards
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We have been working with aromatic compounds for decades, and 5-Chloro-1,3-Dimethoxybenzene stands out for its remarkable stability and reliability in chemical synthesis. This compound, often recognized by its CAS number 7051-53-0, belongs to the family of chlorinated methoxybenzenes. Our team produces it with a focus on purity and consistency, essential traits for downstream processes in pharmaceuticals, agrochemicals, and fine chemicals manufacturing.
Synthesizing 5-Chloro-1,3-Dimethoxybenzene requires careful control of reaction conditions. Over years of optimization, we arrived at a process that minimizes over-chlorination and reduces unwanted by-products. The challenge isn’t limited to reaction stage alone; purification demands expertise as trace impurities—even those below 0.5%—can impact performance for downstream users.
Our chemists selected a pathway that starts with 1,3-dimethoxybenzene as the base molecule and introduces chlorine via electrophilic aromatic substitution. This avoids isomeric mixtures and preserves high yields. We invest as much effort in waste stream management as we do in yields; using activated carbon filtration, distillation under inert gas, and solvent recovery systems, we reduce environmental impact substantially. These steps help keep heavy metal content and halogenated by-products below thresholds acceptable in regulated sectors.
Some believe the margin for error in chlorination is generous, but our experience disproves that. At scale, even small fluctuations in temperature or reactant ratio give rise to 2,3- or 2,4-dimethoxy by-products that disrupt downstream synthesis. Reworking batches has a cost in both time and raw materials, pushing us to set narrow process windows and invest in rigorous online monitoring. HPLC and GC-MS analysis on every lot delivers confidence not just for us but for our clients, some of whom have zero-tolerance policies for cross-contamination.
Our typical product runs with purity of at least 99.5%. Moisture and inorganic chloride content sit at fractions of a percent, and we actively monitor for residual solvents left from synthesis or purification. Over the years, some clients expressed concern about trace metals or UV-active impurities. Strict adherence to validated cleaning protocols and the use of inert materials for storage address these issues before they arise.
A sample lot tested by our QC team may show the following figures: melting point between 40 and 42°C, free from sulfur-containing by-products, and free-flowing crystalline solid form. Color can drift slightly—pure samples appear almost white but can show faint yellowing if left exposed to air, due to slow oxidation. Protecting product from both light and moisture extends shelf life beyond two years with no noticeable degradation.
Some ask how 5-chloro-1,3-dimethoxybenzene compares to related benzene derivatives such as 4-chloro-1,3-dimethoxybenzene, 1,3-dichloro-5-methoxybenzene, or 2-chloro analogs. From a synthetic chemist’s view, the placement of the chlorine atom influences both reactivity and selectivity in downstream reactions. For instance, the electrophilic substitution reactions onsite heavily favor the 5-chloro pattern for ortho/para directors, which matters for certain synthesis pathways in active pharmaceutical ingredients.
In our line of work, the specific orientation of substituents determines which intermediates are practical versus those that result in low yields or inert by-products. For example, 1,3-dimethoxy-5-chlorobenzene directs substitutions to the 2- and 6-positions, which is critical if the next step requires selective activation. When comparing with the 4-chloro variant, we notice the 5-chloro isomer typically allows for greater regioselectivity in palladium-catalyzed cross-couplings.
Another distinction resides in solubility profiles. While the chloro group slightly reduces solubility in polar solvents compared to the non-chlorinated 1,3-dimethoxybenzene, its presence actually enhances compatibility in halogenated solvent systems—a feature important during multi-step syntheses involving protective groups and metal complexes.
As a manufacturer, we see our material heading downstream into a range of industries. The leading use remains in pharmaceutical intermediate synthesis. Many research groups rely on this compound as a scaffold to build more complex benzene derivatives, especially in the search for new antipsychotic and anti-inflammatory agents. The methoxy groups increase electron density and alter the reactivity of the ring, making selective functionalization much more predictable.
Agrochemical producers value its combination of chemical stability and low inherent toxicity when building herbicide and pesticide active ingredients. Our batches consistently pass stringent raw material inspection from their R&D groups. Unlike some benzene derivatives that require heavy metal catalysis or carry residual by-products that challenge analytical detection, our 5-chloro-1,3-dimethoxybenzene offers a predictable synthetic handle.
Fragrance and flavor makers rarely approach us for this molecule, but its structural relatives do find niche uses in synthetic musk and spice aromas. We focus on meeting the far tighter specifications required by pharmaceutical regulation than by the flavor industry, so quality remains exceptionally high even for less regulated applications.
Years spent trouble-shooting customer synthesis issues taught us the true value of consistency. With every batch, teams down the line know exactly how our product will behave under various temperature, pressure, and pH conditions. This predictability supports reliable yields, reduces troubleshooting, and allows end-users to focus research and production resources on their products instead of re-validating raw materials. For applications subject to regulatory filing—such as GMP-grade pharmaceuticals—documentation, traceability, and process transparency all stem from a stable raw material base.
Some grow frustrated by off-spec imports or “equivalent” products sourced outside controlled supply chains. We have run side-by-side comparisons and observed dramatic differences in side-product profiles, trace impurities, and even physical form. These factors add costs that rarely show up on a price sheet but emerge quickly during process validation or scale-up.
In daily operations, our team treats 5-chloro-1,3-dimethoxybenzene as a low- to moderate-hazard substance. It produces minimal dust, does not generate persistent or bioaccumulative breakdown products, and poses a modest inhalation risk when handled as a fine powder. Direct skin or eye contact during blending or weighing can cause local irritation. We recommend use of nitrile gloves, goggles, and basic dust extraction. Users with continuous exposure, such as those unloading drums or charging reactors, benefit from local ventilation or enclosed handling systems.
Transport doesn’t involve the same level of rigor as for some more hazardous aromatics. Our containers, usually HDPE or steel drums lined for chemical compatibility, protect the product until its point of use. Provided users store containers away from oxidants and moisture, breakdown risks remain low. A few clients requested custom labeling and color-coded drums to support lean manufacturing and mistake-proofing; these solutions cut risk of material mix-up and complement on-site quality assurance.
Lately, regulatory agencies emphasize lifecycle analysis and traceability—not only for end-products but for each raw material used upstream. We see increasing demand for audits, environmental impact documentation, and disclosure of residual solvents or by-products. Over the last five years, we replaced halogenated processing solvents with greener options, introduced energy-saving reactor systems, and launched a solvent recycling initiative. These moves reduced our carbon output per ton of product, which we now track annually.
Some competitors source basic chemicals through less regulated supply chains. In contrast, we verify both legal compliance and environmental reporting down to our starting materials. This reduces the risk of production interruption or unexpected compliance checks for us and our customers. For 5-chloro-1,3-dimethoxybenzene buyers seeking regulatory submission in North America, Europe, or Japan, we supply full trace documentation and change notification protocols.
A few batches in years past fell short, mostly due to trace sodium chloride contamination. Catching these outliers before packing took investments in rapid-response analytics and real-time reporting electronics at key process steps. Training makes a measurable difference; a well-trained operator noticed an odd “crust” at the crystallization stage, confirmed by lab tests to be poor filtration, and the affected batch did not leave the plant. Building a culture where anyone can raise a flag has saved hours of headaches for both us and our customers.
Audits by demanding pharmaceutical partners push us to constantly review protocols, calibrate instruments, and maintain a transparent record of corrective actions. We document each control point, report deviations promptly, and maintain digital signatures on batch records. End users audit not just test results but also underlying process logic—from source traceability to waste management and data integrity. Internal reviews catch small issues before they balloon to large-scale problems.
Our role doesn’t stop at manufacture. Early-stage discussions with R&D chemists often reveal process bottlenecks or yield issues not visible in spec sheets. We encourage direct field feedback and periodic technical exchanges to tailor crystal size distribution or optimize for specific solubility demands. Many of our longest-running partnerships began with a production trial, followed by mutual trouble-shooting to achieve a better fit for their process. This approach beats a one-size-fits-all standard.
Custom packaging, barcoding, or drum sizes improve handling at the customer’s site. Often, the simple act of repackaging at smaller increments minimizes risk of exposure to air or moisture. Over time, these practical adjustments cut loss and waste.
Markets aren’t static. We see increasing pressure for shorter supply chains, local procurement, and lower-carbon products. These drivers encourage continuous investment in process automation, recycling, and digital solutions. Demand for stricter documentation, down to trace-level impurity profiles and full residue solvent disclosure, grows each year, particularly among multinational buyers. Staying responsive means continually training staff in both process safety and data integrity.
We anticipate growth in specialty chemical uses for 5-chloro-1,3-dimethoxybenzene, particularly in high-value research backgrounds and targeted synthesis of complex pharmaceutical scaffolds. Adaptability stands as our greatest asset—a lesson learned through years of direct, hands-on experience. Constant technical dialogue with end users, real-time optimization, and a willingness to innovate along with changing market needs keep us competitive while delivering a reliable, quality intermediate.
Producing 5-chloro-1,3-dimethoxybenzene isn’t just about ticking off a specification sheet. It’s a daily cycle of hands-on problem-solving, refinement, and collaboration with partners who depend on our knowledge and consistency. Every improvement, each feedback session, and every quality check builds a track record that helps industries move forward. We take pride in the role we play, both as a manufacturer and as a partner ready to meet technical and regulatory challenges head-on.