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HS Code |
151298 |
| Cas Number | 90-97-1 |
| Molecular Formula | C13H8Cl2O |
| Molecular Weight | 251.11 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 105-108 °C |
| Boiling Point | 390 °C |
| Density | 1.32 g/cm3 |
| Solubility In Water | Insoluble |
| Refractive Index | 1.612 |
| Purity | Typically ≥98% |
| Synonyms | 3,4-Dichlorodiphenyl ketone |
| Storage Temperature | Store at room temperature |
| Smiles | Clc1ccc(cc1Cl)C(=O)c2ccccc2 |
| Ec Number | 202-022-0 |
As an accredited 3,4-Dichlorobenzophenone 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 3,4-Dichlorobenzophenone, sealed with a screw cap and labeled with hazard information. |
| Shipping | 3,4-Dichlorobenzophenone should be shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. Handle with care, labeling appropriately as a chemical substance. Follow all applicable transport regulations (such as DOT, IATA, IMDG), ensuring secure packaging to prevent leaks or spills during transit. Consult the SDS for detailed instructions. |
| Storage | 3,4-Dichlorobenzophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat and direct sunlight. Keep it separate from strong oxidizers and incompatible substances. Store in a chemical-resistant cabinet, and ensure proper labeling. Use secondary containment if necessary and avoid sources of ignition. Follow all applicable safety and regulatory guidelines. |
Applications of 3,4-Dichlorobenzophenone in Industrial ManufacturingAs the direct producer of 3,4-Dichlorobenzophenone, we supply this intermediate to multiple advanced chemical sectors. The following sections detail the principal industrial fields utilizing this compound, with specific focus on regulatory compliance, in-plant usage ratios, integration steps in customer processes, and downstream product forms exported globally. 1. Pharmaceutical Intermediate for Antifungal API SynthesisDownstream pharmaceutical manufacturers employ 3,4-Dichlorobenzophenone primarily in multi-step syntheses of antifungal active pharmaceutical ingredients, particularly in the preparation of certain azole derivatives. Bulk production requires rigorous tracking of input quality, and the intermediate is introduced after initial aromatic substitution steps. End-users implement tight controls on residual solvent and impurity profiles to fulfill global drug standards. Formulators select charge levels based on target yield and byproduct minimization, recalibrating during process optimization validations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate for Selective Herbicide SynthesisMajor agripharma companies utilize this compound in the synthesis of substituted benzoyl urea herbicides. It serves as a strategic carbonyl source for advanced intermediate formation during herbicide manufacture. Deployment of the intermediate occurs in automated batch reactors with strict material traceability. Process engineers determine charge percentage based on catalytic efficiency and extraction losses, maintaining compliance with strict production and environmental regulations acknowledged in key export regions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Dye Intermediate for Speciality PigmentsSynthesizers of high-performance pigments utilize 3,4-Dichlorobenzophenone as a core building block in the preparation of advanced azo dyes and specialty pigments. It enters production lines during diazotization or coupling stages, functioning as a controlled electrophilic component. These applications demand trace impurity management and conformance to heavy metal limits, especially for products bound for the textile and plastics industries. Ratios align with color intensity demands and final pigment loading, with close monitoring during each lot’s manufacture. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. UV-Absorber Intermediate for Polymer Additive ManufacturingKey polymer additive producers integrate this chemical as a precursor for benzophenone-based UV stabilizers, often for plastics and coatings requiring prolonged outdoor durability. Direct introduction occurs within high-temperature processing vessels after the main aromatic substitution stage. Teams apply precise dosing based on molecular weight calculations and end-use polymer matrix (such as polycarbonate, PET, or PVC). QA departments confirm each batch meets regulatory criteria for food contact and migration when appropriate. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Electronic Chemical Precursor for Specialty PhotoresistsManufacturers of high-end electronic materials leverage this product in the production of specialty photoresist systems, particularly for thin-film transistor and LCD panel fabrication. The compound is fed into coupling reactions forming key benzophenone photosensitive units, followed by proprietary downstream purification. QC teams tie input levels to crosslinking performance and spectral sensitivity, revising dose during pilot plant runs for substrate variations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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At our chemical facility, every batch of 3,4-Dichlorobenzophenone (CAS Number 90-98-2) brings with it an honest measure of pride and responsibility. Decades on the production floor have shown us that real consistency matters — not only to us but to every processor, formulator, and end user relying on reliable benzophenone derivatives. Our team has worked hard to take this compound from basic building block to trusted intermediate for specialized syntheses, always tuned in to where purity, stability, and process compatibility bring tangible real-world benefits.
Among chlorinated benzophenones, the 3,4-isomer stands out due to the dual chlorine substitution at positions three and four on the benzene ring. The arrangement changes its chemical reactivity, and we often see it enabling reactions where single-chloro or mixed-halogen benzophenones struggle. We produce our material with a focus on high purity (typically exceeding 99%), minimal byproducts, and reproducible particle size. Each of these factors arose not from paperwork or sales talk, but from listening to downstream users in pharma, dyes, and agrochemicals who needed clean, predictable input without surprises in their reactors.
It's easy to group all dichlorobenzophenones together, but practical results tell another story. The 3,4-isomer displays lower melting points than some of its cousins, which can simplify certain handling steps — especially when melting or blending into liquids at scale. The two-chlorine pattern also makes a real difference in subsequent chlorination, reduction, or coupling reactions. I remember running head-to-head comparisons for a dye manufacturer: 3,4-dichlorobenzophenone enabled cleaner coupling, fewer tar formation headaches at the kettle, and smoother crystallization steps. We see similar feedback from pesticide intermediate producers, who benefit from its reactivity and lower tendency to produce side products under normal catalytic conditions.
In our plant, we stick to an established manufacturing line for this product: crystalline powder, white to pale yellow under ambient light, and density ranging around 1.36 g/cm3. Most lots measure 99.0% minimum by HPLC assay, with no more than 0.3% single impurities and a moisture content below 0.2%. Those numbers carry the story of years tweaking thermal processing, upgraded filtration, and rigorous monitoring every step from raw material selection through to drum filling.
A few years back, a large customer ran into yield issues downstream. Investigation pointed to small changes in our particle size distribution. We responded by investing in finer grinding and sieving controls, and now particle size rarely drifts from 40-100 microns — enough flow for automated dispensers, but not so fine as to create dust and loss. No one in the chemical business wins by overlooking these 'details'—each change ripples into someone’s plant, affecting everything from pressure drops in feeders to washing times after a synthesis. That hands-on experience has kept us focused on physical properties as much as purity.
Where does 3,4-dichlorobenzophenone go, once it leaves our site? Customers put it to work mainly as a raw material or intermediate. Its most common uses center on the synthesis of pharmaceutical actives, specialty pigments, agricultural agents, and polymer modifiers. Chemists prize it for its reliable performance during Friedel-Crafts acylation and in the preparation of more complex biphenyl, indanone, or anthrone derivatives.
In one long-standing partnership, we support a pharmaceutical operation manufacturing antihistamine and anti-inflammatory compounds. Our 3,4-dichlorobenzophenone forms the critical acyl fragment in a multi-step synthesis. Failures in this step not only delay the rest of their schedule — they risk throwing off the entire batch. Tighter impurity profiles and stricter metal content limits (iron, copper, and nickel in the low ppm range) set by them shaped our entire purification process. We put real resources into extra hot-filtration and cooling steps to deliver on these requirements.
For pigment makers, shade and stability rely on each precursor. Even minor contaminants or color bodies in our dichlorobenzophenone can spoil hue and fade resistance in final products. In response, our QC team uses both instrumental and visual checks, comparing every sample against an internal library of standard lots. For these customers, color and clarity mean more than purity numbers — and our experience says you can never skip the simple visual checks, even in a modern lab.
Transitioning from lab preparation to full-scale tonnage requires more than copying a recipe. Over the years, the nuts and bolts of our process changed, not for the joy of tinkering but to address recurring issues. Early batches suffered from burnt odor and black specs. We overhauled solvent recovery and crystallization, switched to closed glass-lined reactors, and reinforced operator training around temperature ramp rates. These changes cost time, but established a repeatable, clean product—no more complaints about off-odors or filter-clogging particles from our partners.
Other facilities sometimes chase higher throughput with lower solvent ratios or by skipping purification passes. That path looks efficient on paper, but shortfalls appear in end-use complaints — stuck feeds in extruders, haze in polymers, or brittleness in finished pharmaceuticals. By holding to higher initial purity and tighter tolerance specs, we’ve actually reduced return rates and time spent troubleshooting with customers.
Packaging speaks just as loudly as the chemistry itself. Early on, we packed in bags; handling dust, slow pouring, and complaints about exposed surfaces became routine. After switching to high-integrity, lined fiber drums and regularly testing closure integrity, loss rates dropped, and downstream users reported easier, cleaner loading. On-site visits confirmed that good packaging protects more than just value; it maintains trust across complex supply chains.
People new to chlorinated benzophenones sometimes lump all the isomers together, thinking that 2,4-, 2,5-, or even 2,3-dichloro variants behave the same way. Our daily reality says otherwise.
Take reactivity in electrophilic aromatic substitution: 3,4-dichlorobenzophenone often reacts faster and more selectively than comparably treated 2,4- or 2,5-derivatives. The electronic effects of the chlorine atoms, positioned next to each other on the same ring, create both an activating and directive influence on certain reactions. Our in-house chemists have worked directly with formulators to replace alternative isomers in certain coatings and pharmaceutical intermediates, reducing unwanted chlorination side products and shortening cycle times. For polymer work, the melting point and handling temperature of 3,4-dichlorobenzophenone often offer a straightforward step up from its mono-chlorinated or non-chlorinated relatives. Lower melting means less thermal stress and easier incorporation in plastics blends or masterbatches, especially compared to old standards like pure benzophenone.
Another unseen but crucial factor is downstream safety and environmental outcomes. We have followed the regulatory and safety data for decades. The 3,4-isomer, due to its substitution pattern, avoids some of the generalized hazards seen with other isomers, such as higher volatility or greater persistence in certain environmental simulations. This has helped maintain acceptance with customers under increasingly stringent emission or residual solvent policies.
There’s an industry cliché that says quality is measured in certificates and paperwork. We know better. Our customers measure quality by how predictable the product behaves in their plant, how often we catch (and fix) problems before they do, and how open we are when unexpected snags arise.
For instance, we log every batch in real time, tracking small variables: ambient humidity, raw material supplier shifts, even changes in cleaning agents. It might seem obsessive to some, but it pays off. Years ago, we caught a pattern connecting faint orange tints in the output to one supplier’s change in toluene grade. Removing that supplier fixed a whole family of downstream complaints for pigment and pharma buyers.
No formal spec sheet fixes a batch run through contaminated tanks or sped up cooling zones. By putting qualified eyes and hands on every stage—sampling, sieving, filtration, packaging—we avoid the trap of treating production as a checkbox process. The record in our complaint logs, repeated audits, and customer feedback surveys tells us what’s working and what needs a closer look.
Our logistics staff works directly with end-users to find the right delivery schedule and packaging for each run. Some customers take full drums, others order smaller kegs for rapid sampling before main delivery. We temperature-map all shipments and run short-run stability checks to make sure that product integrity survives transport. After a cargo incident under high humidity, we replaced part of a lot preemptively and added water-absorption indicators to each shipment. Since then, none of our customers have reported degraded material upon arrival.
We do not wait for paperwork: our plant chemists answer technical questions directly by phone or email, often sharing process insight or troubleshooting tips based on real experience. No chatbot, just actual production chemists and site managers who know the quirks of our product. On several occasions, a conversation on spray drying conditions or filtration speeds helped a customer cut downtime by hours — lower loss, less frustration.
No chemical product lives in isolation from the rest of the regulatory world. Over the past decade, our team has tracked changing demands in REACH, TSCA, and similar global registration lists. More countries now require complete documentation of residual solvents, trace metals, and any persistent organic contaminants. Our plant built custom analysis suites — GC for solvents, ICP-OES for metals, and a rolling archive of COA data — to anticipate these changes.
As reporting moves from annual to live updating in some markets, we invest time not only in keeping documents current but in ensuring the underlying data comes from real samples, tracked from raw input to final loadout. Several years back, proactive clarification of impurity profiles allowed a Japanese partner to fast-track their cosmetic pigment registration without extra delays for new studies. Similar efforts for South American pharma clients saved months during regulatory audits. Keeping a living connection to both regulations and practical plant chemistry keeps us ahead of costly, disruptive changes.
Chemical production creates responsibility. Our management and plant supervisors see the impacts of process choices daily — from solvent recycling to byproduct capture. Early runs released small-scale volatile organics and excess wastewater; over time, we redesigned distillation columns, upgraded scrubbers, and switched to closed recapture systems. Those changes brought emissions and waste below regional requirements, but also improved the workplace environment. Cleaner air, lower odors, and quieter plant operation lifted morale and reduced nuisance complaints.
Some producers draw a hard line at regulatory minimums, but experience says going further builds trust with both clients and communities. Visiting customers’ plants, we talk openly about our waste minimization efforts, recycled solvent loops, and clean energy plans. Our staff has participated in studies looking at end-of-life handling for dichlorobenzophenone-containing byproducts, helping to close information gaps and improve downstream safety practices.
We work with partners on take-back and reverse logistics schemes — collecting used drums, refurbishing them, and reducing disposable packaging. The story of these practices traces through regulatory filings, but more importantly, it shows up in everyday conversations with our supply chain partners, who want assurance not only of quality but of a responsible, practical approach.
The market for intermediates like 3,4-dichlorobenzophenone does not sit still. Raw material fluctuations, evolving global trade, and periodic adoption of new synthesis routes keep our team on alert. The real challenge centers on delivering a consistent product when sources or specifications outside our control change.
We work closely with suppliers, sometimes pooling orders with other producers, to maintain quality raw materials even when prices or availability change. On two occasions in the past decade, alternate chlorobenzene sources forced us to re-qualify entire lots and run additional purification cycles. That experience reinforced the lesson that in-house analysis and process flexibility matter more than spot-price chasing.
Whenever new analytical techniques or greener process aids become available, we trial them first on pilot batches. Once, a new catalyst system promised higher yields and cleaner byproducts but required months of optimization and downstream compatibility testing. We involved key customers early in these trials, sharing both successes and the occasional failure. Openness created stronger partnerships, allowed for joint problem-solving, and prevented disruption during rollout.
Watching trends in specialty chemicals — especially active pharmaceutical ingredients, advanced dyes, and performance plastics — we predict continued strong demand for intermediates with well-defined physical and chemical properties. As more sectors adopt real-time process monitoring and push for zero-defect inputs, we see even greater emphasis on traceability, speed of technical support, and rapid troubleshooting. Our plant is investing in digital integration for live batch tracking, with direct customer access for transparency.
Increasing requests for low-residual, low-toxicity profiles suggest growth in life sciences, medical plastics, and specialty colorants that cannot tolerate out-of-spec starting materials. Investment in cleaner production lines, ultra-pure solvents, and enhanced spectral analysis helps us keep pace with these evolving expectations. Our involvement with industry groups and standards-setting bodies keeps us aware of upcoming shifts and gives us a voice in shaping new requirements.
Finally, as downstream users push for environmental accountability, our ongoing work in capture, recycling, and solvent minimization for 3,4-dichlorobenzophenone will only sharpen. By sharing these lessons, both successes and ongoing challenges, we hope to strengthen practical, transparent relationships with every partner in the journey from molecule to marketplace.