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HS Code |
310200 |
| Chemical Name | Meso-1,2-Diphenyl-1,2-Ethanediol |
| Molecular Formula | C14H14O2 |
| Molar Mass | 214.26 g/mol |
| Appearance | White crystalline solid |
| Melting Point | 137-139°C |
| Solubility In Water | Slightly soluble |
| Density | 1.22 g/cm³ |
| Cas Number | 606-05-3 |
| Smiles | C1=CC=C(C=C1)C(C(C2=CC=CC=C2)O)O |
| Chirality | meso compound (achiral) |
| Refractive Index | n20/D 1.605 |
As an accredited Meso-1,2-Diphenyl-1,2-Ethanediol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g, sealed with PTFE-lined cap, labeled with product name, CAS number, hazard symbols, and handling instructions. |
| Shipping | Meso-1,2-Diphenyl-1,2-ethanediol is typically shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be packaged according to standard chemical transport regulations, labeled appropriately, and kept away from incompatible substances. Transportation should ensure stable temperatures and protection from physical damage. Adhere to all relevant safety and regulatory guidelines. |
| Storage | Meso-1,2-Diphenyl-1,2-ethanediol should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Store at room temperature or as specified on the label, and handle using appropriate personal protective equipment to prevent skin or eye contact. |
Applications of Meso-1,2-Diphenyl-1,2-Ethanediol in Industrial ManufacturingMeso-1,2-Diphenyl-1,2-Ethanediol is widely utilized as an intermediate and chiral building block in several industrial fine chemical production routes. Its defined stereochemistry and physical properties enable precise functionalization in pharmaceutical synthesis, agrochemical manufacturing, specialty polymer production, and asymmetric catalysis. The below sections describe key downstream application scenarios, with details on usage, standards, downstream process conditions, and related end products. 1. Pharmaceutical Synthesis of Chiral IntermediatesPharmaceutical manufacturers incorporate this compound in the construction of chiral pharmaceuticals, such as active pharmaceutical ingredient (API) intermediates for antihypertensive and anticancer agents. The specific stereochemistry allows enantioselective transformations and resolution, required for regulatory approval of modern medications. Industry compliance standards
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2. Asymmetric Ligand Synthesis for Metal CatalystsCatalyst manufacturers apply Meso-1,2-Diphenyl-1,2-Ethanediol as a key diol in the preparation of chiral ligands for transition metal-catalyzed asymmetric reactions. Its rigid structure imparts defined spatial orientation in ligand backbones, leading to enhanced selectivity in hydrogenations and hydroformylations. Industry compliance standards
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3. Synthesis of Specialty Polycarbonate and Polyether MaterialsManufacturers of specialty plastics utilize meso-1,2-diphenyl-1,2-ethanediol as a comonomer in step-growth polymerizations to design engineered polycarbonates and polyether networks with tuned optical or mechanical properties. The diol units enable rigid linkages and enhance glass transition temperatures for niche industrial parts. Industry compliance standards
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4. Advanced Organic Synthesis for Agrochemical IntermediatesAgrochemical manufacturers integrate the diol in synthetic workflows for high-value intermediate compounds. Its phenyl and diol functionality enables tailored functionalizations, such as selective oxidation or halogenation, for the production of advanced pesticide and herbicide scaffolds. Industry compliance standards
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As a chemical manufacturer deeply involved in the daily realities of specialty synthesis, I see firsthand what makes a building block like meso-1,2-diphenyl-1,2-ethanediol stand out. We’re not just producing another entry in a catalog; we’re creating a material that supports innovation at the bench and on the plant floor. Over the years, this diol has found a steady place in synthetic chemistry due to its unique stereochemistry and physical properties, offering both academic and industrial labs a trustworthy tool for asymmetric synthesis, ligand development, and stereochemical studies.
Most products labeled as meso-1,2-diphenyl-1,2-ethanediol stem from the same fundamental reaction: the reduction of benzil using a mild reductant. Our process consistently yields a white crystalline solid, characterized by its high purity level—essential for reproducible research. We control each stage, from raw material selection to drying conditions, because even small impurities or inconsistent crystallization create headaches in chiral catalysis and pharmaceutical projects. Product stability holds up for long-term storage in sealed containers, provided they’re kept away from extremes of temperature or open air.
The two phenyl groups and the two adjacent hydroxyls in this compound define its performance. In our own checks, melting points range reliably near 136°C. We back repeated runs with both NMR and HPLC purity analysis, ensuring minimal contamination from starting materials or side products. Such attention matters since a trace of oxidation byproducts or a handful of off-stoichiometry crystals can ruin an experiment downstream, especially in sensitive ligation or resolution work.
Researchers value meso-1,2-diphenyl-1,2-ethanediol for different reasons, yet the core requirement boils down to trust in the material every single time it leaves our plant. In asymmetric catalysis, this diol pairs seamlessly with transition metals for the creation of C2-symmetric ligands, driving enantioselective transformations at both pilot and production scale. Graduate students tell us they rely on it as a standard in stereochemical assignments, exploiting the symmetry to confirm complex reaction pathways.
Outside the academic lab, demand comes from pharmaceutical manufacturing. Many stepwise chiral separations use this compound, and in some cases, it helps resolve racemic intermediates. Some facilities develop new ligands from this backbone, relying on the fact that each batch behaves the same, run after run. We keep hearing requests for bulk shipments timed to support one-off high-throughput screens, pilot process testing, or patent-driven synthesis—a testament to its flexibility.
For those curious about the specifics, our typical lot of meso-1,2-diphenyl-1,2-ethanediol rolls out as a free-flowing crystalline powder. Each drum or bottle matches the certificate of analysis on basic metrics: melting point within a two-degree window, water content below detectable limits, and HPLC assay above 99 percent. The model doesn’t carry a fancy proprietary mark—it needs only the correct CAS number and substance structure for the end user to recognize its reliability.
Logistics can prove trickier than expected with fine chemicals of this purity. We hear from customers facing issues with bridging, caking from ambient moisture, or contamination during storage. In response, we ship in nitrogen-flushed containers on request and update packaging as seasons change. Our site engineering team works quietly but persistently behind the scenes, installing improved vacuum filtration or more precise temperature controls, all to ensure the output fits what the protocol in your hands requires.
Unlike some diols that come with hard-to-purify regioisomers or mixtures of optical isomers, meso-1,2-diphenyl-1,2-ethanediol can be cleanly separated and isolated straight from the reaction mixture, under our process. Chiral centers in this molecule are mirror images but non-enantiomeric overall, which simplifies stereochemical assignment work and makes it an attractive starting point in ligand synthesis.
The real-world benefit? We have watched a formulation team shorten their optimization cycle by weeks thanks to a reliable, single-isomer diol. In pharmaceutical or agrochemical screening, where every run counts, eliminating the need for further chromatographic separation makes a real economic and scientific difference. Project managers, pressed for time, appreciate not having to chase after uncertain isomeric ratios or call back for repeat purity data.
Some chemists might look for alternatives among the family of 1,2-diols, ranging from 1,2-ethanediol (ethylene glycol) to substituted analogues. Ethylene glycol works as a solvent or antifreeze, but its reactivity profile offers none of the stereochemical control available from our product. Pinacol and its derivatives introduce complexity with tetrasubstituted centers, which makes their use in chiral ligand fields less straightforward.
The diol we produce stands out for its symmetrical structure and clean chirality. Racemic mixtures sold by traders or legacy suppliers often harbor inseparable impurities—sometimes in amounts that escape quick bench tests but show up as ghost peaks in critical LC-MS work or as side bands on NMR. By locking down production parameters in-house, we’ve been able to consistently outpace open-market sources, reducing time spent troubleshooting contamination or rerunning critical reactions. Synthetic routes that require regiospecific addition or tight control over secondary alcohol geometry depend on this kind of certainty.
The lab teams often want to know about the quirks of handling meso-1,2-diphenyl-1,2-ethanediol on scale. Over time, water uptake can become a nuisance, especially in humid climates or in facilities without full HVAC control. Our advice: reseal containers immediately after weighing, and avoid open-air transfer where possible. The product doesn’t absorb moisture as aggressively as some glycols, but its large surface area in powder form creates opportunities for slow degradation if left unprotected.
Workers have shared how small tweaks make lab life easier—simple changes like switching from wide-mouth bottles to sealed tubes for small-scale work reduced accidental contamination by a noticeable margin. For kilo batches, inline nitrogen blanketing at transfer helped keep the material in spec, heading off subtle shifts in water content or oxidation. At shipping, anti-static liners proved helpful in maintaining flow and reducing risk of particle clumping during bulk loadouts, especially in the rainy season.
We hear from both research and process teams using this diol in asymmetric syntheses, chiral resolution, and even as standards for instrument calibration. A recurring theme is relief when batches arrive on specification—no second guessing on melting point, no strange coloration, no hidden residual solvents. One formulation chemist reported improved resolution in a series of chiral separations just by switching raw material source over to ours. A catalyst development team shaved two weeks off their screening campaign, thanks to a consistent lot-to-lot performance. They didn’t have to wrestle with untracked contaminants throwing off their baseline reactions.
Such reports underline a fact we see in our own checks: real-world success depends more on reliability than on claims of “premium” status or extra processing steps. Costly purification doesn’t create true value if the initial synthetic step delivers a consistent and pure product. Material that behaves predictably lets chemists focus on creative problem-solving, not fire-fighting batch inconsistencies.
Scaling up for high-purity specialty products like meso-1,2-diphenyl-1,2-ethanediol reveals its share of challenges. Consistent quality at scale doesn’t come free. Every switch in raw material grade, every seasonal swing in humidity, or slight vessel contamination gets magnified in bulk runs. Early on, we battled inconsistent crystal morphology and batch-to-batch purity drift. By reworking reaction time, upgrading filtration units, and using tighter drying parameters, we reached a level where most internal samples from a run meet or exceed our targets.
Investing in analytical support, especially automated chromatography and updated spectroscopic methods, proved essential. We found that seemingly minor tweaks in drying or bottling made all the difference between customer complaints and smooth project launches. Our team makes it a point to regularly run retained samples against current production, checking for drift or off-notes that could hint at upstream issues. Transparency with clients also keeps us honest—labs often catch issues in downstream applications that we wouldn’t spot in standard in-process checks.
With increasing focus on green chemistry, end-users look beyond content and specification toward responsible sourcing and lower-impact synthesis. The starting materials for this diol draw from the benzil stream, mainly sourced from aromatic oxidation. Ever since clients began asking about carbon footprint and solvent management, we’ve responded by switching partial solvent streams to recyclable formats and lowering the use of resource-intensive inputs.
We’ve managed to cut solvent waste through closed-loop recovery for both reaction and recrystallization steps. The diol’s relatively benign profile—no heavy metals, low volatility, easy filtration—makes it a logical choice where downstream processing needs to avoid persistent pollutants. We share ongoing solvent use data and recovery rates with several larger customers, so that their own sustainability scorecards can transparently account for project resource use.
Chemists continue pushing the boundaries of asymmetric transformation, and our material, with its stable meso configuration, offers a platform for new ligands and transition metal catalysts. The diol’s predictable reactivity and convenient physical form let researchers iterate faster, test new concepts, and build on reliable precedents from published literature. As pressure grows on the entire industry to streamline step counts and reduce costs, intermediates that behave predictably look set to gain even more importance.
Across the projects we support, demand for this compound shows no sign of fading. Collaborators want rapid turnarounds, zero-hassle supply, and above all, confidence that each kilogram or gram matches specification. By keeping production rooted in hands-on, real-world feedback, we work to deliver results that matter at the synthesis bench—not just on paper.
Many of our own staff members began as chemists on the bench. We know that delays in raw materials, ambiguous documentation, or inconsistent performance end up costing both time and trust. That’s why our procedures stress traceability—down to the drum, filter, and operator involved in each run. Each bottle leaving our site carries with it daily effort and accumulated lessons from teams who have solved the same problems facing today’s research and production chemists.
The conversation doesn’t end at the point of shipment. We regularly reach out for feedback, analyze customer sample returns, and roll improvements back into production. Ultimately, real-world outcomes build our reputation—the papers written, the patents filed, and the drugs synthesized after our meso-1,2-diphenyl-1,2-ethanediol passes through a customer’s hands.
From our experience, manufacturers have a duty to do more than simply replicate data sheets. We integrate historical knowledge, evolving analytical methods, and direct feedback in every batch produced. Customers often highlight the time and cost saved by running with high-integrity materials. Troubleshooting a stubborn impurity or unclear melting point chews up valuable instrument time and people-hours. With growing constraints on R&D budgets and shorter project deadlines, product reliability becomes not just a technical feature, but a core business advantage.
Looking forward, we see advanced applications for meso-1,2-diphenyl-1,2-ethanediol springing up in every field, from next-generation pharmaceuticals to chiral polymer development and even specialty sensors, where its stable primary alcohol groups serve as anchor points in materials science. Each use case traces back to the reliability of the original material. By building a production system focused on consistent, feedback-driven results, we help create the conditions for real breakthroughs in chemical research and manufacturing.