|
HS Code |
945863 |
| Cas Number | 3097-21-4 |
| Molecular Formula | C13H9ClO3 |
| Molecular Weight | 248.66 |
| Iupac Name | 4-chloro-3,4-dihydroxybenzophenone |
| Appearance | Off-white to light beige solid |
| Melting Point | 177-180°C |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC=C(C=C1)C(=O)C2=CC(=C(C=C2Cl)O)O |
As an accredited 4'-Chloro-3,4-Dihydroxybenzophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g quantity of 4'-Chloro-3,4-Dihydroxybenzophenone is securely sealed in an amber glass bottle with a tamper-evident cap. |
| Shipping | 4'-Chloro-3,4-Dihydroxybenzophenone is shipped in compliance with chemical safety standards. It is securely sealed in a suitable container, properly labeled, and cushioned to prevent breakage during transit. Transport follows regulations for hazardous materials, including documentation and handling instructions, ensuring safe and efficient delivery to the designated recipient. |
| Storage | 4'-Chloro-3,4-Dihydroxybenzophenone should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Ensure the storage area is equipped for handling chemicals and clearly labeled. Avoid direct sunlight and sources of ignition. Always follow relevant safety protocols. |
Competitive 4'-Chloro-3,4-Dihydroxybenzophenone prices that fit your budget—flexible terms and customized quotes for every order.
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Every chemist in our plant understands the meticulous work it takes to produce specialty benzophenone derivatives, and 4'-Chloro-3,4-Dihydroxybenzophenone remains a perfect example. Our technical team continually refines the route for chlorination and controlled hydroxylation to ensure that each batch brings consistent, stable results. Years on the line have taught us that small variances in reaction conditions—temperature, solvent choice, purity of raw materials—have a measurable impact on product quality. This chemical sits on our roster precisely because of its dual functionality: the chloro group provides sites for further reaction or coupling, and the two hydroxy groups offer anchoring or chelating potential. Solid quality means manufacturers downstream, whether in pharmaceuticals or advanced polymers, rely on predictable reactivity and product purity.
We pour considerable attention into crystallization and drying steps. This product finishes as a pale, fine powder, reflecting a purity that comes from multi-step purification—confirmed by our in-house HPLC and NMR checks. Our process delivers a content regularly above 99 percent, beating the standard technical grades offered elsewhere. Water content, measured by Karl Fischer titration, never exceeds 0.3 percent in our QC checks, because excess moisture in downstream syntheses can create side-products or incomplete conversions.
The melting range, typically cited at 188–191 degrees Celsius, allows formulators to easily handle and blend into subsequent reactions without concern for decomposition at standard process temperatures. A notable feature: the molecule’s robust aromatic backbone provides chemical stability, resisting oxidation in ambient storage over six months with only minimal discoloration if properly shielded. On user requests, we tailor the sieving and particle size, an option valued especially by those running precision batch reactors.
Years of feedback from our partners have highlighted how this compound functions as a building block for high-value products. Research teams in life science sectors often select this intermediate for assembling small molecule drugs. The para-chloro substituent serves as a handle for cross-coupling variants in aromatic chemistry, while the two hydroxy groups readily undergo either etherification or esterification. This dual reactivity expands options for synthetic routes, especially those aiming to introduce functional complexity onto benzophenone scaffolds. The flexibility increases the appeal for both medicinal and agrochemical projects where intermediate diversification speeds project lead time.
Our customers in specialty coatings and UV absorber manufacturing rely on this exact molecule as a precursor for more functionalized benzophenones. The electron-rich hydroxy groups impart high UV absorption, protecting polymers used in paints, adhesives, and plastics. By adjusting the substitution pattern on the benzophenone core, we help compounders design photoprotective materials with greater longevity, a layer of innovation that starts with our intermediate’s reproducibility.
Our lab’s focus on target purity distinguishes our product from offerings featuring similar scaffolds. The addition of the chloro group at the para-position, compared to 2,4-dihydroxybenzophenone or standard 2-hydroxy-4-methoxybenzophenone, increases the molecular weight and enforces a more controlled reactivity profile under nucleophilic substitution. We find that, in catalyzed reactions, the presence of the halogen group often directs reagents in ways that simpler benzophenones do not, contributing to improved yield and selectivity in follow-up steps.
The two adjacent hydroxy functionalities on the aromatic ring set this material apart from mono-hydroxy analogues. Chemically, this opens up route planning for complex chelate formation and for functional groups that need specific proximity—something unattainable with asymmetrical alternatives. In our daily batch work, monitoring by TLC and HPLC has shown the stability of our product, with minimal side product formation compared to less pure materials, which contributes directly to more predictable downstream procedures.
Our in-house produced 4'-Chloro-3,4-Dihydroxybenzophenone contains controlled amounts of trace impurities. We keep halo-substituted biphenyls well below detection limits of 0.05 percent, a threshold not always maintained in generic market offerings. These details matter greatly for users in pharmaceutical discovery and photochemical applications, where safety and repeatability govern process scale-up decisions.
An R&D team working on a novel fungicidal agent approached our engineers after issues arose with a previous supplier's less pure batch. Their synthesis suffered from inconsistent conversion rates, traced back to high levels of organic chloride residues and peroxo impurities. Upon switching to our high-purity intermediate, batch failures dropped to nearly zero and their synthesis windows widened, providing flexibility and less need for post-reaction cleanup. This feedback loop—hearing issues, seeing our product in use, and improving our process—drives how we continue to invest in better purification cycles and more granular quality controls.
Another example comes from partners in the UV-stabilizer sector. Uniformity in aromatic substitution and low moisture levels allowed their continuous polymerization processes to run without interruption or fouling. By actively monitoring free acid levels in every lot, we preempted hydrolysis during their lengthy thermal runs. Their gains in extrusion throughput translate directly into cost savings, showing how careful chemical stewardship at the intermediate stage creates value down the line.
No chemical plant escapes the realities of sourcing variability and environmental compliance. In the case of 4'-Chloro-3,4-Dihydroxybenzophenone, chloroarene raw materials often fluctuate in market purity. Our procurement team has learned, through repeated batch-to-batch QC, to audit every new delivery using side-by-side NMR fingerprinting. Years of integrating supplier controls with our plant batch records has built up layers of traceability, which gets reflected in every certificate we issue.
Chromatographic purification, while resource-intensive, has proven indispensable to removing trace phenolic and halogenated byproducts. Choosing greener solvents for extraction and crystallization remains a work in progress. Investments in solvent recovery and closed-loop wastewater treatment, made over the last decade, show our direct commitment to eco-friendly operations. It isn’t just about meeting regulatory checklists—cutting waste streams and water demand helps us stabilize costs, meet community expectations, and, simply put, do better chemistry.
Staff training plays a vital part. Operators rotating from our other specialty lines receive targeted instruction on safe handling and reaction quenching. The presence of activated chloro and phenolic sites means even trace acidic or basic contamination in plant piping could cause product degradation or safety incidents. By encouraging open reporting of near-misses or line fouling events, we cultivate a hands-on safety culture, shored up by twice-annual review boards and ongoing maintenance investment.
Steady supply is inseparable from process reliability. Over years, working as a manufacturer means we accept delays from energy shortages, logistics snarls, and seasonal export blockages. Though bulk chemical markets fluctuate, our bulk storage systems, forward contracts with trusted suppliers, and in-house buffer inventories enable us to keep our downstream partners stocked. We see firsthand that a delay of even a week can stall research timelines or cost a customer far more than any product discount could offset.
Tracing quality from the bottom-up—the lot numbers of shipments, the timeline of synthesis in the plant, real-time process sensor logs—brings peace of mind to both seasoned buyers and new start-up formulators who lack large procurement teams. We build relationships not from canned email responses, but via direct technical calls that sort out the “why” and “how soon” in the context of each user’s end-goal.
Years ago, we received requests from high-throughput screening labs for smaller packaging to reduce bench waste. Listening closely, our packaging team developed resealable, inert-lined containers in multiple batch weights. Some customers importing under air-sensitive conditions opt for vacuum-sealed, double-bagged shipment. Our logistics crew, skilled in cold chain and compliant labeling, scrupulously tracks temperature excursions and notifies clients of any deviations before the shipment lands.
We also learned from large-volume users in the resin sector that even slight off-gassing from packaging can affect sensitive blends. Our current container materials, chosen for low permeability and absence of phthalate plasticizers, came about only through failures and revisits to packaging suppliers. This iterative growth traces back to dozens of application engineers who agreed to pilot test new formats, seeking lower risk of physical or chemical contamination.
We see increasing demand from fields like photochromic devices, advanced coatings, and medicinal scaffolds. The aromatic core, bolstered by multiple points of reactivity, attracts custom synthesis clients. As industries push for sustainable, high-performance materials, the need for specialty intermediates with tailored substitution will only rise.
Upcoming research in our own labs explores catalysts and alternative oxidants, aiming for reduced byproduct formation and energy savings. Colleagues elsewhere in the industry increasingly call for closed-cycle solvent handling and reduced carbon footprint. We have begun sharing batch-level process emission reports, enhancing transparency and giving partners deeper insight into the upstream impacts of their purchases.
Direct dialogue with regulatory bodies and international compliance teams keeps our workflow aligned with evolving standards in chemical manufacturing. Each shipment runs through routine screens for restricted impurities and compliance with industry norms, whether destined for Europe, the Americas, or Asia-Pacific. Quality assurance teams maintain detailed batch histories going back more than five years, which ensures full traceability—critical for regulatory inspections or customer audits.
Adaptation comes not as an afterthought but as a continuous process, integrating new safety data, international registration requirements, or advanced user needs into what we make. By mining our own production and quality data, we pre-empt trends and can react with agility to changes in the regulatory landscape—sparring unnecessary downtime or sudden shortages for our partners.
Today, producing 4'-Chloro-3,4-Dihydroxybenzophenone isn’t just a technical pursuit; it’s an ongoing conversation between our engineers, operators, and downstream innovators. End users expect not just purity, but reliability, consistency, and support. They want the facts, want clarity, and want the assurance a “real” chemical producer stands behind what’s delivered.
We back up every claim with batch-specific analysis reports—real yield, water content, spectroscopic features. As scale-up projects or market priorities shift, our technical liaisons remain available, drawing from years handling this molecule from conceptual chemistry to full-scale dispatch. Every kilogram of intermediate reflects the lived experience and day-to-day vigilance of factory staff, quality chemists, and logistical planners who understand that a specialized compound represents both risk and opportunity.
4'-Chloro-3,4-Dihydroxybenzophenone only became a mainstay because we listened to critical partners, learned from in-the-trench mistakes, and invested in the best purification and process control we could afford. Its value gets proven every week, in every lab project moving from test tube to drum scale. We remain committed to constant process refinement, eco-conscious production, and full, open engagement with those who use our products to build tomorrow’s technology, formulations, drugs, and materials.
In sharing our viewpoint—not just what this chemical is, but what it does and how it's made—we invite direct dialog, technical exchange, and shared problem-solving. The real story of 4'-Chloro-3,4-Dihydroxybenzophenone belongs as much to those who craft with it as to those who bring it into being.