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HS Code |
490803 |
| Chemical Name | 2,2-Diphenylacetic acid |
| Cas Number | 117-34-0 |
| Molecular Formula | C14H12O2 |
| Molecular Weight | 212.25 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 146-150°C |
| Solubility In Water | Slightly soluble |
| Density | 1.222 g/cm³ |
| Flash Point | 200°C |
| Smiles | C(C(=O)O)(c1ccccc1)c2ccccc2 |
| Inchi | InChI=1S/C14H12O2/c15-14(16,12-8-4-2-5-9-12)13-10-6-3-7-11-13/h2-11H,1H2,(H,15,16) |
As an accredited 2,2-Diphenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 2,2-Diphenylacetic Acid is supplied in a sealed amber glass bottle, labeled with hazard information and batch number. |
| Shipping | 2,2-Diphenylacetic Acid is shipped in tightly sealed containers to prevent contamination and moisture exposure. Handle with care using appropriate personal protective equipment. Transport according to local and international chemical regulations. Avoid sources of ignition and store away from incompatible substances. Shipping documentation should clearly identify the substance and its hazards. |
| Storage | 2,2-Diphenylacetic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area. It should be kept away from moisture, heat sources, and incompatible substances such as strong oxidizing agents. Ensure the storage area is clearly labeled and complies with relevant chemical safety regulations. Personal protective equipment should be used when handling the compound. |
Applications of 2,2-Diphenylacetic Acid in Industrial Manufacturing2,2-Diphenylacetic acid serves specialized roles in various industrial sectors, primarily as a key intermediate in pharmaceutical synthesis, advanced material manufacture, and dyes and pigments production. Our manufacturing expertise ensures reliable compliance, consistent quality, and process adaptability for diverse application environments. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical manufacturers use 2,2-Diphenylacetic acid as a critical intermediate in the synthesis of central nervous system agents and antiepileptic drugs. The compound participates in Grignard and condensation reactions to form complex molecules, meeting stringent purity standards. Production batches undergo rigorous control to minimize impurities and ensure regulatory compliance for subsequent API stages. Industry compliance standards
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2. High-Performance Polymer Building BlockIn advanced materials manufacturing, the compound functions as a co-monomer or chain extender for specialty polyesters and polyamides, providing enhanced rigidity and thermal stability. Industrial formulators precisely control addition levels to achieve specified glass transition and melt point characteristics. Accurate analytical monitoring ensures batch-to-batch reproducibility for materials headed into automotive and electronics assemblies. Industry compliance standards
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3. Pharmaceutical Analytical Reference Standard PreparationControl laboratories employ 2,2-Diphenylacetic acid as a non-endogenous reference compound for analytical method development and calibration of chromatographic systems. Its high purity supports validation protocols for active pharmaceutical ingredient identification and quantitative purity assays. Preparative steps include accurate weighing, solubilization in certified solvents, and validation per regulatory guidance. Industry compliance standards
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4. Dye and Pigment Synthesis IntermediateSynthetic dye manufacturers incorporate 2,2-Diphenylacetic acid in the construction of complex aromatic structures for specialized colorants. It reacts in Friedel–Crafts acylation and condensation steps, supporting chromophore development for textile, leather, and plastic applications. Strict in-process controls verify reaction completion and colorimetric consistency prior to blending and formulation. Industry compliance standards
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Years of managing reaction vessels, adjusting formulas, and serving demanding chemists have solidified how we approach each batch of 2,2-diphenylacetic acid. This white, crystalline compound—sometimes recognized by its CAS number (117-34-0)—has played a quiet but robust role in research and manufacturing for decades. It’s not just a string of atoms or another inventory line on the books. Every sack, every drum that leaves our site has its origin story: where each reactant came from, how the temperatures rose, how the precipitate looked under the glass.
2,2-Diphenylacetic acid doesn’t bounce between endless brand names or variants. We produce it in its pure acid form, with a molecular formula of C14H12O2, ensuring a clear-cut identity for everyone who opens the container. It typically arrives as off-white to fine crystalline powder. The melting point typically ranges between 148 and 150°C, a detail we check relentlessly. Water solubility sits on the low side; solvents such as ethanol and ether take it readily—the sort of thing you learn after clarifying more than a few extractions after a late shift.
Purity in this realm isn’t just a checkbox—it determines reactivity, color, odor, and often, shelf-life. Most of what leaves our production floor focuses on 99% or higher purity (by HPLC or GC, depending on client demand), because every stray impurity can make itself known mid-reaction or in the end-use performance of a drug intermediate or specialty compound.
Our long familiarity means we can spot the difference between a good batch and a great one just from physical characteristics, even before the lab finishes up the latest chromatogram. Moisture content, residual solvents, and trace metals can each cause headaches downstream. So we pull tests, we grind and sift, and we double-check consistency. That philosophy doesn’t come from a manual, but from the phone calls you remember: the drug developer who wanted a “ruined” batch traced back, the materials scientist who needed a cleaner signal in their NMR spectra.
Our core buyers induce transformations with this compound across several verticals. Many see it as a valued intermediate in advanced organic synthesis—no surprise, given how the phenyl rings and acetic acid core lend themselves to customizations. Chemists prize the stability and ease of substitution on the benzylic position. Laboratories working on analgesics, anti-inflammatories, and other pharmaceutical candidates run recurring orders, and for good reason: a pure starting point avoids cascades of side-products later in synthesis.
Companies making dyes, perfumes, fine chemicals, and specialty polymers have also found transformative flexibility in the structure. We’ve watched small teams turn our acid into custom esters, fit it into experimental liquid crystals, and even use it as a ligand in coordination chemistry. The simplicity on paper belies the amount of possibility seen in real-world projects.
Some are drawn to 2,2-diphenylacetic acid because it yields to straightforward Grignard, halogenation, or reduction reactions. Its carboxylic acid group responds predictably in multi-step synthesis. As far as protection and deprotection strategies go, working with a clean sample speeds things up—no gels, no odd hues in the TLC plates, no excess washing.
We’ve dealt with both pharma titans and green startups. The feedback often points to one hard lesson: chasing lower costs by buying outside QC-driven environments often causes pain down the line. It’s tempting to try a cheaper source, sometimes sourced outside regulated supply chains. Those who return seldom ask for a "faster" batch—they ask for reliability, batch documentation, and up-to-the-mark characterization. Once you’ve had to stop a kilo-scale run due to an odd impurity profile, small savings no longer sound wise.
Several shops can yield diphenylacetic acid these days, but the differences become obvious in any practical application. Everyone has heard "purity ≥98%," but as a maker, we know this doesn’t reveal the whole truth. Consistency isn’t just a nice-to-have—it’s an operational requirement. Moisture absorbs readily, especially in humid climates—a poorly sealed bulk bag can affect dissolution rates or react unpredictably in moisture-sensitive steps.
Granularity brings another factor into play. Overly fine powder can clump or show static buildup during handling; coarser product can delay dissolution or complicate automated dosing. Over years of tweaking, our production lines have shifted sieve sizes and adjusted drying protocols to consistently land right where researchers and line chemists want—easy transfer, little dust, no big crumbs.
Another repeated request: documented absence of heavy metals and residual solvents. We’ve revised SOPs to ensure tighter controls than the standard method. Especially in regulated industries, trace elements like iron, lead, or cadmium trigger scrutiny. Our process monitoring uses validated equipment, not just periodic spot-checks. That attention became part of our workflow after a recall scare—something never forgotten by anyone who lived through the aftermath.
Solvent residues speak volumes about a manufacturer’s discipline. Over-aggressive drying can char product, destroying value. Insufficient drying leaves background peaks on customer’s reports. We implemented a vacuum-drying sequence after seeing solvent carryover spike in product shipped amid rush orders. That switch dropped GC-detectable residues well below regulatory requirements, earning us repeat contracts on high-value pharmaceutical projects.
We’ve experimented with temperature and pH throughout the synthesis route, suiting reaction scale-up or customized batches for research customers. The yield and impurity profile both hinge on minor tweaks. We’ve learned to avoid overusing oxidizing agents, as these tend to spike colored by-products, which can plague downstream synthesis. Batch aging, humidity controls, and careful selection of glassware and solvents often tip the balance between flawless and underperforming product.
Customers sometimes request tailored particle size or "brighter" product. While it’s tempting to rush solutions or over-hype minor advantages, long-term buyers care more about reproducibility. For chromatographic applications, a consistent melting point means far more than marketing glitter. The professional chemist running a pilot doesn’t call us to praise branding—they call because the batch “worked” and the project moved forward without avoidable surprises.
Feedback never arrives in a set script; it comes in urgent phone calls, panicked emails, or methodical test results comparing batches over years. After supplying tons of this compound globally, we’ve adapted processes to factor in atmospheric pressure changes, local humidity swings, and even electrical grid inconsistencies. Each alteration is measured, trialed, and checked—trust with research partners isn’t gained through claims, but through delivered results.
Flow chemistry and continuous processing have emerged as promising trends. We watch the field closely, adjusting lot sizes and delivery forms as customers demand faster, smaller-batch outputs for experimental synthesis. Some request pre-packed columns, others pre-diluted solutions. Scaling up for industrial supply introduces a whole layer of complexity, particularly as environmental and safety requirements tighten. Our reaction design always considers waste minimization and active capture of by-products.
Two close relatives, phenylacetic acid and benzylacetic acid, tempt some buyers when pricing or regulatory lists dictate. In application, the difference shows up in both molecular stability and downstream reactivity. The two phenyl rings on 2,2-diphenylacetic acid grant more steric bulk and, sometimes, altered hydrophobicity—benefits in some contexts, drawbacks in others. It resists unwanted side reactions better than mono-phenyl options. This stability improves reliability for multi-step synthesis or in situations requiring extended shelf-life.
Phenylacetic acid draws appeal due to its lower price point and broad use in fragrances or as a precursor in some generic pharmaceuticals. Its reactivity can lead to higher rates of by-products during complex synthesis, creating more challenges at the purification stage. Benzylacetic acid sits in another niche, with a structural layout that encourages different reactive paths.
In terms of handling, 2,2-diphenylacetic acid shows lower volatility and a robust melting range. The added rings bring not just mass, but a tactile difference noticeable on the shop floor: it cakes less, flows easily out of liners, and does not cling in hoppers as stubbornly as lighter cousins. This saves time in automated dispensing operations. Some users switching away from more volatile analogs cite safety as a significant benefit.
Environmental aspects come into sharper focus for those comparing options. 2,2-diphenylacetic acid, like its near cousins, requires thorough management of solid waste, filtrates, and spent solvents. Though not classified as highly hazardous, treating every by-product stream with respect remains non-negotiable. Our facility relies on in-house waste capture and aggressive effluent treatment, knowing that every unmonitored discharge can set back hard-won environmental accreditation.
The value of 2,2-diphenylacetic acid only proves itself during actual chemistry. Researchers may favor it for substitution, alkylation, or condensation steps. In this respect, consistent purity and reliable logistics matter more than the theoretical advantages on a spec sheet. We have bulk clients formulating active pharmaceutical ingredients, but we also serve advanced research labs chasing custom molecules for small-scale study.
The biggest lesson: tiny differences in specification can matter. We once supplied material for a drug candidate where water content measured 0.3% rather than the requested 0.1%. The downstream reaction stalled, prompting a flurry of retesting and investigation. The learning: even trusted process steps can drift, and double-checking remains part of the daily routine. It’s not enough to hit an average—a real production environment calls for tightening the spread, batch to batch, season to season.
We take pride in our technical support. Teams across Europe and Asia have called late at night chasing batch documentation ahead of regulatory submissions, or troubleshooting mid-run challenges. Years of dialogue make it clear: buyers don’t just want powder in a jar—they want answers, assurance, and a problem-solving partner. One major benefit we offer lies in established documentation—COA, batch traceability, and impurity profiles delivered with every order.
Manufacturers of specialty acids walk a tightrope: maximizing throughput while maintaining strict purity and safety. Industry regulations require full transparency. Batches are traceable from raw benzoin or benzil through final packaging. Inspections by external auditors, routine proficiency testing for our analytical crew, and data logging on every critical process variable are part of daily protocol.
Trust takes years to build, and a single misstep—a contamination event, a mislabeled shipment—can erode it overnight. We still remember a case where a single drum, swapped at a distributor’s warehouse, upended a delivery chain and left our customer facing fines for missed deadlines. The correction process drove home the importance of maintaining full custody, direct delivery, and uncompromised packaging standards.
Worker safety forms another pillar of responsible operations. We design workflow with careful handling of acids and minimizing airborne dust exposure. Closed transfer systems, regular PPE training, and air monitoring protect both staff and end-user product purity. As the expectations from regulatory bodies rise worldwide, compliance is no longer a regional affair—customers in one country now benchmark standards globally.
Supply chain logistics bring their own hurdles. Delays in precursor shipments, natural disasters, or geopolitical developments can ripple through raw material sourcing. Being vertically integrated offers one layer of resilience. Having alternate suppliers for high-purity benzil, for instance, ensures we rarely face stockouts or sudden quality drop-offs. Our customers deserve predictably high quality, even when broader markets wobble.
Counterfeit and adulterated chemical products remain an industry-wide concern. Over the years, we have seen substandard “2,2-diphenylacetic acid” samples laced with cheap fillers, unreacted precursors, or hazardous by-products. Our in-house LC-MS detection capability typically spots these imposters immediately. We run a verification program for customers facing questionable supply or unusual analytical results, reviewing suspect samples and lending advice—even for batches we didn’t supply.
Some sites continue to struggle with off-spec batches due to uncontrolled moisture, poor packaging, or unreliable third-party sampling. Over time, we invested in moisture-barrier drums, dehumidified storage, and batch-level barcoding. This allows us to trace any field complaint back to original process variables—reactor, date, weather conditions, and operator involved. That way, the solution is targeted. Customers benefit from having documentation ready for audit at a moment’s notice, minimizing regulatory headaches.
A recurring challenge is the tension between cost and compliance. Unregulated or unauthorized suppliers can offer remarkable prices on paper but often fail to provide full quality assurance or react quickly to quality issues. Some clients must learn the hard way before returning to long-term, reliable makers. We recommend reviewing COA data for more than just the main assay—dig into residual solvents, heavy metals, and trace impurities before deciding. A transparent producer welcomes questions and provides lot-specific results.
Environmental controls also demand real action. We have implemented solvent recovery systems, energy-efficient drying, and on-site treatment of waste streams. These investments don’t just tick regulatory boxes—they future-proof the business and shield end users from environmental liabilities. Many downstream users seek sustainability certifications, so supply chains linking back to our plant gain a reputational edge.
In process troubleshooting, we’ve opened virtual lines for regular customers to consult with technical experts. From NMR troubleshooting to purification tips, our years in the field often translate into practical, time-saving advice. Even when problems originate outside our supply—an unplanned humidity spike, a filter rupture, a stray peak on analysis—we share insight to get production moving again. Problem-solving doesn’t end at shipment.
Transparent dialogue builds resilience. Incoming feedback, even in the form of complaints, helps shape our protocols. The cycle is constant: listen, adapt, document, verify. That is the cornerstone of continuous improvement in a modern chemical facility.
2,2-Diphenylacetic acid is more than a line on a spec or a commodity on a warehouse shelf. For those of us involved in synthesis, packaging, and quality assurance, every step adds up. Years of vigilance, careful adjustment, and honest feedback have shaped both what we produce and how we support each project using our product.
The challenges of keeping up with evolving customer needs, regulatory change, and environmental standards never pause. Only direct experience on the production line—fixing hot plates at midnight, investigating yield dips, listening to scientists desperate for a purer lot—can teach the lessons needed to do better. And every batch carries these lessons forward, from our facility to your bench or reactor.
We don’t claim perfection, but we stand by the track record of consistency and proactive support forged over years of production. For those seeking a reliable partner in 2,2-diphenylacetic acid, there is no substitute for a producer invested in both product and partnership.