|
HS Code |
929570 |
| Cas Number | 214821-24-4 |
| Molecular Formula | C13H8F2O |
| Molecular Weight | 218.20 |
| Iupac Name | 2,3'-Difluorobenzophenone |
| Appearance | White to off-white solid |
| Melting Point | 51-54°C |
| Boiling Point | Unknown |
| Density | Unknown |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, methanol) |
| Smiles | C1=CC(=CC=C1C(=O)C2=C(C=CC=C2)F)F |
| Inchi | InChI=1S/C13H8F2O/c14-11-6-2-5-9(7-11)13(16)10-4-1-3-8-12(10)15/h1-8H |
As an accredited 2,3'-Difluorobenzophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,3'-Difluorobenzophenone, 25g, is packaged in a sealed amber glass bottle with a tight screw cap for protection. |
| Shipping | 2,3'-Difluorobenzophenone is shipped in a tightly sealed container, protected from light and moisture, and typically packaged according to local and international regulations for hazardous chemicals. Transportation should comply with DOT, IATA, and IMDG guidelines to ensure safety and prevent spillage, with clear labeling indicating its chemical nature and any hazard warnings. |
| Storage | 2,3'-Difluorobenzophenone should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the container tightly closed when not in use. Store at room temperature, and avoid exposure to moisture. Use appropriate chemical storage cabinets, especially if storing large quantities, to minimize potential hazards. |
Applications of 2,3'-Difluorobenzophenone in Industrial Manufacturing2,3'-Difluorobenzophenone is a key intermediate for producing advanced materials and specialty chemicals. Its consistent quality and high purity are required across multiple industrial sectors with strict regulatory and technical demands. Below are the main application routes based on real-world industry scenarios. 1. High-Performance Polyaryletherketone (PAEK) SynthesisMajor polymer manufacturers use 2,3'-Difluorobenzophenone as a difluorinated monomer for producing PEEK, PEK, and related high-temperature aromatic polymers. The compound provides enhanced chemical resistance, heat stability, and mechanical property control. Experts adjust loading levels to influence crystallinity, molecular weight, and melt viscosity to match end-use requirements in aerospace, electronics, and automotive sectors. The material enters production at the monomer condensation phase, with precise stoichiometric calculation and rigorous polymerization control under nitrogen atmosphere to minimize side reactions and ensure target polymer chain structure. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Photoinitiator Intermediate for UV-Curable MaterialsSpecialty chemical companies use this material as a benzophenone-based intermediate to synthesize photoinitiators for UV-curable coatings, inks, and adhesives. The two fluorine atoms allow for specific absorption characteristics adjustment and increased stability of derived photoinitiator molecules. The process involves acylation or nucleophilic substitution, giving rise to tailor-made photoinitiators for industrial applications such as electronic encapsulants and 3D printing resins. Strict impurity limits and traceability apply throughout synthesis, ensuring batch-to-batch consistency and regulatory compliance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Synthesis IntermediateFine chemical plants employ 2,3'-Difluorobenzophenone as an intermediate in synthesizing agrochemical actives, specifically for certain fluorinated benzoyl-substituted herbicides and fungicides. Its unique substitution pattern increases activity spectra and metabolic stability in target formulations. Downstream producers control process pH, temperature, and solvent to ensure selectivity in subsequent amide or hydrazone formation. Manufacturers adhere to international crop protection raw material purity guidelines, and the raw material’s batch release links directly to regulatory dossier documentation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Pharmaceutical Intermediate for Fluorinated APIsActive pharmaceutical ingredient (API) manufacturers select 2,3'-Difluorobenzophenone as a building block for certain fluorinated pharmaceutical compounds. Its dual-fluorine substitution pattern enables medicinal chemists to access target molecules with tailored pharmacokinetics and bioactivity for intensive R&D applications. In regulated GMP environments, the compound is introduced in the late-stage synthesis of core scaffolds, and producers utilize validated crystallization and impurity control protocols. Audited traceability and full batch documentation apply for every step entering clinical or commercial API supply chains. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2,3'-Difluorobenzophenone prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Those of us working in chemical synthesis know every small molecular tweak can carry far-reaching consequences for downstream work. 2,3'-Difluorobenzophenone (CAS 456-57-3) stands out as one of those specialty building blocks that continues to be a mainstay in both established and emerging segments. Years of watching this molecule flow through vessels, seeing it change hands across quality labs and pilot facilities, have shaped our perspective on both where it's used and what sets it apart.
Our plant doesn’t see model numbers as mere technical markings—they reflect batches completed, purity reports checked, extractions verified, and clocks ticked during crystallization. The 2,3'-Difluorobenzophenone we put out reaches a minimum purity of 99%, with an appearance that falls between white to off-white—always checked under neutral light. Typical melting point for our product measures at 68–71°C, with GC and HPLC analysis completed on every batch. We maintain water content below 0.3% by Karl Fischer analysis. These specs come from direct experience with our reactor network and robust quality controls; the figures hold because the teams repeat the tasks, keep attention on cooling steps, clean reactors properly, and calibrate instruments regularly.
You won’t find fillers, unknown stabilizers, or post-synthesis blending agents in our output. Handling residues and maintaining cleanliness between runs keeps contamination below detection levels, and parallel syntheses for custom orders are always isolated. Most plant operators want to keep these standards even higher, because once a batch falls below our cut-offs, nobody can relax—not engineers nor sales, and certainly not our lab staff.
2,3'-Difluorobenzophenone sits at an intersection between traditional and modern molecules. The pharmaceutical sector uses our compound in key intermediate syntheses, especially for developing API side chains and selective aromatic capping. In agrochemicals, it enables targeted fluorinated substitutions that boost product resilience without straying from permitted regulatory frameworks. Advanced materials research, in university and commercial groups, treats this benzophenone variant as a foundation for photoinitiator precursors and cross-linking studies. Our long-time customers in OLED and specialty coatings labs request this compound for the clear-cut reactivity of both fluorine atoms, which remain less hindered than in many symmetric benzophenones. From our end, we’ve seen more cumulative value from selling a solid molecule, at consistent purity, year after year, than from any half-promised upgrades or unknown blends.
For the specialty chemicals world, where experimentation happens at both 5g and 500kg scales, usage almost always depends on scalability. We run synthesis both at pilot and at full production scale, and by constantly comparing notes with R&D teams, we see how minor impurities or batch inconsistencies can disrupt an entire project’s downstream chemistry. Consistency here doesn’t mean chasing an arbitrary standard: it means that whatever is delivered in January keeps the same spectral signature as September’s shipment, because a change disrupts method validation—not just in academic studies, but also in compliance documentation and production timelines.
Our chemists appreciate that even with a simple structure, yield improvements require patience and a careful approach. Fluorine’s presence on the 2- and 3'-positions adds both electron-withdrawing and steric effects, which shows up fast in condensation reactions—especially during sequence attachment or cross-coupling. Many clients mention lower byproduct formation compared to mono-fluorinated or para-fluorinated benzophenones. Fewer purification steps after reaction means less solvent is used, and waste disposal numbers drop. During aromatic halogenation or further functionalization, our batches repeatedly show tight spot profiles on TLC—one of the first signs that the aromatic ring is ready for custom work.
We often share analytical data directly with partner labs so they can check for trace metals, halogens, or residual solvents. This open data flow wasn’t always standard in the chemical world, but it has proven essential in both pharma and electronics projects, where a small impurity can mean the difference between an accepted batch and a return shipment. If a customer gets results they don’t expect, our team checks instrument calibration and runs side-by-side analysis; this feedback circle helps us improve—not just react to complaints.
Some ask what actually separates our 2,3'-Difluorobenzophenone from other benzophenone derivatives. Working with dozens of benzophenone-based intermediates, it becomes clear that even a switch between two fluorine atoms, or swapping location from 2,4- to 2,3'- substitutions, changes the whole game. Electron distribution alters reactivity, which either speeds up or slows down key reactions—McMurry couplings, Friedel–Crafts acylations, reductive amination, and photochemical cleavages all show different kinetics and selectivities as a result of such changes.
Our product combines high electronegativity with predictable aromatic substitution patterns. For clients aiming for highly specific fluorinated backbones or planning downstream coupling, this means less unpredictability, fewer side-reactions, and better reproducibility when scaling from milligram to kilogram synthesis. Some benzophenone analogues can clog up columns, crystallize unpredictably, or even degrade during storage—experiences we all want to avoid. By sticking to rigorous process control, double-checking solvent purity at every stage, and avoiding cut corners, our batches keep their performance both on the bench and on the balance sheet.
Another practical difference comes up in safety and handling—our teams have learned over years that this compound maintains physical integrity during normal laboratory transfers and offers higher shelf stability compared with perfluorinated or ortho-heavy analogues. Fume hood time stays reasonable, and handling protocols are already familiar to most safety officers. Many engineering leads report easier management of this compound in their own storage facilities, with packaging compatible with standard procedures and no special hazard communication needed above routine chemical care.
No synthesis route ever runs itself. Every time weather conditions change, utilities go offline, or a shipment arrives late, the risk to yield and purity jumps. During cold months, certain steps require longer mixing times to prevent crystallization inside transfer lines. Dirty or uncalibrated glassware has resulted in off-target product before; that memory drives us to audit every washing step, no shortcuts.
Our site’s process chemists keep logs of reaction irregularities, documenting even the small drifts. For example, we noticed our NMR reporting once missed a minor impurity peak—leading to a thorough review and a shift in our internal method SOPs. Open mistakes and shared lessons mean every operator knows to look for subtle process problems before the product hits the final QC check. These lessons have built a production culture where every step gets cross-checked, resulting in higher yields and fewer recalls.
One scaling challenge comes in the energy cost: fluorinated benzophenones require more precise temperature control, since decomposition can occur above a certain threshold. This fact led us to invest in more efficient, digital temperature regulators for all our main reactors. Another hurdle appears in solvent recovery—the solvents used for this compound can carry trace acidic impurities from raw material streams, so we implemented extra purification cycles on spent solvents. Although this adds time, it cuts costs in waste disposal and brings our final product cleaner than what most third-party suppliers offer.
We often get asked about application details and process optimization for using 2,3'-Difluorobenzophenone in new projects. Our engineers and chemists do not hesitate to share process notes, storage tips, or even reaction troubleshooting—because building strong customer collaboration matters far more than chasing new sales leads. Working directly with pharmaceutical process teams has taught us that speed and openness are essential—waiting days for answers on batch or contaminant questions derails carefully planned trials.
One recurring request comes in custom batch sizing: some R&D teams need just a few grams, others want shipments ramped up as pilot work progresses. Our flexibility here is grounded in day-to-day operational experience—teams keep small-scale and full-scale facilities ready to ensure that nobody waits weeks for either a laboratory sample or a large-scale order. We keep customer communication active, with our production managers available to discuss order timing, any potential delays, or changes in demand forecasting.
On the material handling side, our warehouse and shipping division works closely with regulatory staff to maintain full compliance with local and international transport standards. This means that, no matter where a client operates, our shipments arrive with the right paperwork, tamper-evident seals, and lot-specific documentation. We treat these steps as safeguards, not just paperwork—because a missed document can mean delayed trials, wasted time, and lost credibility on all sides.
Direct manufacturing experience leaves little doubt about the environmental impact of specialty chemicals production. With 2,3'-Difluorobenzophenone, waste reduction starts at the reactor itself. Our facility invests in compressed solvent recovery, in-line purification, and closed-loop handling to limit direct emissions or uncontrolled disposal. Rather than view compliance as a burden, our experience shows that treating these steps as central to daily work actually creates value—reducing audit risk, improving safety for workers, and strengthening partnerships with both domestic and international clients who demand clean supply chains.
We routinely review evolving chemical safety guidelines and compliance standards for both local and foreign regulatory agencies, adjusting our methods to stay ahead of changing requirements. Our documentation team works hand-in-hand with certified environmental auditors, providing full traceability on every outgoing batch. Over time, regular internal audits have lowered our incident rates, reduced waste processing costs, and attracted more long-term contracts from clients who prioritize green chemistry principles.
For plant workers and product formulators, the direct benefit is seen in fewer hazardous spills, lower VOC readings, and safer air quality inside workspaces. By sharing these outcomes with our buyer teams and research partners, we help raise industry-wide expectations on supply chain transparency and sustainability.
Shifts in global supply chain logistics have taught everyone in the industry that reliable access to key building blocks like 2,3'-Difluorobenzophenone isn’t a given. Sudden export controls, raw material shortages, and transportation bottlenecks can all threaten supply, forcing project timelines to slip and budgets to overrun. By focusing on robust local sourcing for critical inputs, and by keeping more than one synthesis pathway open, we hedge against unpredictable market swings. Adjusting order cycles and stocking strategies may not sound glamorous, but these slow, daily choices mean that research teams never wait for inventory and project managers avoid shutdowns due to missed deliveries.
We monitor demand drivers directly by keeping contact with downstream users, not just through third-party sales data or rumor. Noticing an uptick in demand for fluorinated benzophenones in battery research, we ramped production and honed our purification protocols. Early warning systems—both technical and economic—allow us to keep prices stable, even through short-term raw material swings.
With counterfeit materials and diluted intermediates appearing more often on unregulated supplier lists, our clients turn to us for verified authenticity and full-chain traceability. Serial tracking, tamper-resistant packaging, and batch analytics all trace back to years of manufacturing experience and the knowledge that only a consistent, transparent supplier can keep end-users protected from supply chain threats.
Our teams don’t sit in isolation. Operators, QC analysts, and client-facing chemists collect feedback from every stage—be it slow crystallization in a customer’s pilot process or unexpected side reactions in late-stage pharma synthesis. Sometimes, a returned drum or a flagged impurity alert leads to an internal investigation and process change. Everyone in our plant—from the night shift reactor crews to the analytical chemists—has learned not to hide process issues behind blank reports or generic statements.
By sharing direct experiences and addressing concerns as they come up, we grow both as a team and as a link in the larger chemical industry. Our product development meetings openly review process hiccups and client suggestions. As new applications for 2,3'-Difluorobenzophenone emerge—be it in advanced electronics, fluoropolymer chemistry, or medical device synthesis—we keep learning and adapting. Applying small tweaks, testing minor process variations, and listening closely to customer trials have proven more valuable than any single process innovation. Every conversation and every adjusted protocol leads to a better product, and the people behind it take pride in these incremental gains.
We see a future filled with evolving synthesis techniques, more stringent quality standards, and a growing need for specialty building blocks that do exactly what chemists expect. 2,3'-Difluorobenzophenone continues to carve out new roles in both classic and cutting-edge chemistry, from late-stage pharmaceutical synthesis to advanced functional polymers and optoelectronic research. The real edge comes not from chasing every trend, but by maintaining a production process guided by direct feedback, solid data, cross-functional expertise, and a willingness to learn with every new batch. Rather than dilute our core strengths or overload production with unsustainable shortcuts, we keep our focus steady: produce quality, deliver on what is promised, and listen to the people using the product every day.
From years inside the plant, the lesson holds: consistency—batch to batch, drum to drum, year after year—is what customers value most. That’s the foundation on which our 2,3'-Difluorobenzophenone stands, and it’s what we will continue to build on as science, industry, and technology move forward.