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HS Code |
804822 |
| Cas Number | 611-72-3 |
| Molecular Formula | C10H12O3 |
| Molecular Weight | 180.20 g/mol |
| Iupac Name | Ethyl 2-hydroxy-2-phenylacetate |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 284 °C |
| Melting Point | 16-18 °C |
| Density | 1.13 g/mL at 25 °C |
| Refractive Index | n20/D 1.505 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Flash Point | 132 °C |
| Odor | Mild, aromatic |
| Smiles | CCOC(=O)C(O)C1=CC=CC=C1 |
As an accredited Ethyl Mandelate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ethyl Mandelate is packaged in a 100g amber glass bottle with a secure screw cap and tamper-evident seal for protection. |
| Shipping | Ethyl Mandelate is shipped in tightly sealed containers made of compatible materials, protected from moisture, heat, and light. The chemical is labeled per regulatory requirements, with documentation on handling and hazards. It is transported according to relevant safety guidelines to prevent contamination, spillage, or exposure during transit. |
| Storage | Ethyl Mandelate should be stored in a cool, dry, well-ventilated area, protected from direct sunlight and sources of ignition. Keep the container tightly closed and away from incompatible materials such as strong oxidizing agents. Store it in a designated chemical storage area, preferably in glass or compatible plastic containers, and clearly label all storage vessels to prevent accidental misuse or contamination. |
Applications of Ethyl Mandelate in Industrial ManufacturingEthyl Mandelate serves specialized roles across several advanced manufacturing sectors. Our direct supply to these downstream applications emphasizes process consistency, regulatory compliance, and efficient formulation. The following sections detail authentic industrial usage scenarios for this raw material. 1. Pharmaceutical Intermediate for Chiral Drug SynthesisDownstream pharmaceutical producers incorporate this compound as a key enantiomeric intermediate in the multistep synthesis of chiral active pharmaceutical ingredients, including antihypertensives and CNS medications. Its use stems from its stereospecific properties and high purity, essential for medicinal chemistry. Integration requires adherence to validated batch records, rigorous analytical controls, and traceability per regulatory filings. Quality requirements relate directly to targeted final APIs, with specifications for residual solvent and impurity profiling. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Cosmetic Ingredient for Skin-Lightening FormulationsEthyl Mandelate functions as a controlled-use ingredient in cosmetic and personal care formulations targeting skin tone improvement. Its ester profile offers both mild exfoliation and tyrosinase inhibition, supporting claims of radiance and clarity in finished goods. Compliance necessitates raw material traceability, allergen labeling, and performance validation in line with region-specific cosmetic regulations. Downstream processors require documentation on heavy metal content and toxicological safety for leave-on applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Fragrance and Flavors IntermediateThis material is used in the synthesis of aroma compounds due to its structural similarity to naturally occurring mandelic derivatives. It acts as a versatile starting block for the preparation of esters, lactones, or aldehydes, contributing floral and fruity notes in both fine fragrances and flavor blends. Adherence to strict food/contact material standards is required when employed in edible flavor compositions, including allergen declaration, residue testing, and trace origin records. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Synthesis of Specialty Polymer AdditivesEthyl Mandelate is processed as a functional comonomer or reactive intermediate during the formulation of specialty polymers and resins, especially for optical materials and high-performance coatings. It imparts improved film clarity, gloss, and chemical resistance to thermoplastic and thermoset systems. Compliance covers registration under polymer-specific guidelines, documentation of reaction byproducts, and product-specific migration testing for regulated market entry. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Every batch of ethyl mandelate leaving our reactors carries with it years of knowledge and careful handling. As chemical manufacturers, we understand what research labs and industrial clients expect—reliability in supply, consistent purity, transparent quality control. Ethyl mandelate sits at the intersection of fine chemistry and practical application. Creating this molecule isn’t just about achieving textbook yields; true value comes from controlling side products, packing stability, and ensuring customers never pause their lines because of unpredictable supply.
We produce ethyl mandelate through a precise esterification using high-purity mandelic acid and ethanol under controlled conditions. What sets our approach apart is our investment in purification. Extra steps after synthesis—multiple filtration stages, monitored crystallization—remove trace byproducts like residues of unreacted acids or solvents. This makes a difference in downstream applications where even a slight impurity skews analytical results or throws off subsequent reactions. These lessons didn’t come overnight; they came after collaborating with specialists in pharmaceuticals and flavors, hearing their feedback, and fine-tuning our protocols to narrow down the product’s variability.
The ethyl mandelate we ship to our clients averages purity levels above 99%. Moisture content stays tightly controlled—low enough for HPLC work and precise enough for those scaling up flavor or aroma syntheses. Each batch goes through rigorous in-house analysis: GC and NMR confirm identity and purity, and spot checks catch anything off-spec long before packing. Years ago, we optimized our drying and packing lines so ambient humidity never becomes a variable customers need to factor in.
We know trace metals bother some end users, especially those developing chiral drugs or sensitive analytical reagents. Close control of our raw materials and careful maintenance of our glassware and steel reactors means metal contamination never creeps into the final product. For those with even tougher standards, we’ll run extra rounds of testing and tailor our QC to match their requirements, but the baseline product already covers most.
While methyl mandelate and benzyl mandelate sometimes join request lists, experience tells us ethyl mandelate stands out for a reason. It combines better solubility profiles with moderate volatility—both helpful attributes for flavor work and fine chemical reactions. Those working on organic syntheses often mention that ethyl mandelate’s reactivity strikes a good balance: active enough for downstream functionalization without the headaches of over-reactivity or instability.
Clients in the pharmaceutical and analytical industries have pointed out another edge: the lack of heavy aromatic residues after use. Ethyl mandelate leaves behind clean, manageable byproducts, which helps avoid cross-contamination and speeds up clean-up steps—something you only appreciate after years on the production floor. We observe fewer off-odors and lower risk of lingering contamination in batch setups using ethyl mandelate instead of some higher-boiling relatives.
Pharma researchers reach out to us for ethyl mandelate as a starting material in the synthesis of several biologically active compounds. It appears in research journals as a chiral intermediate and a building block for new drug candidates. Because our process allows for optical resolution, we can provide enantiomerically pure material for those working on stereoselective syntheses. Years of custom batch work for academic groups and R&D arms of pharmaceutical houses taught us that getting enantiomeric purity right on the first try prevents costly scale-up setbacks.
In the flavor and fragrance space, product formulators appreciate ethyl mandelate’s mild, fruity profile and ease of incorporation into complex blends. It serves as a bridge component—adding subtle character without dominating the mix. This feedback came straight from artisan perfumers and industrial flavor chemists after experimenting with dozens of esters. Beverage innovation labs have sent us reports showing how ethyl mandelate performs well in both alcohol-based and aqueous systems, which not every mandelate derivative can boast.
One thing clients mention after switching from methyl or benzyl mandelate lies in handling and storage. Ethyl mandelate remains liquid at room temperature, making bulk transfer and metering straightforward. Technicians no longer wrestle with semi-solid or crystalline materials—a small operational benefit that becomes visible at production scale.
From our vantage point inside the plant, another difference shows up: ethyl mandelate tends to resist hydrolysis better than more volatile esters. Tanks stay clean, and less product loss occurs during storage, which saves real money for users buying by the drum.
We also keep in touch with academic labs and universities who use ethyl mandelate for teaching organic chemistry. They mention that the compound’s straightforward structure allows students to practice a variety of transformations, and the relatively low toxicity profile enhances safety in the teaching lab.
Feedback loops from our customers often drive our incremental process improvements. Some years ago, a client came to us with issues using ethyl mandelate in a solvent-free formulation—minor yield losses and difficulty scaling up. We re-examined our production metrics and used modified distillation to trim lingering volatiles that had gone unnoticed. The next batch passed their internal protocols, and that relationship bolstered our reputation as a responsive partner.
We keep tabs on machine learning-based prediction models in chemical R&D. They often suggest new applications for molecules like ethyl mandelate, pushing demand for tighter quality control and higher purity standards. Because we handle all production steps in-house, we are always ready to adapt. Our engineers discuss proposed changes with synthetic chemists rather than just following spec sheets, allowing us to make tweaks that save time and cost at our clients’ facilities.
Supplying chemicals for regulated industries means anticipating audit requirements and documentation needs. Every lot of ethyl mandelate leaving our site comes with a complete analytical package—chromatograms, full spectroscopic records, and details on raw material sourcing. This complete trail backs up our production claims and gives our clients confidence when scrutinized by regulators.
Supply interruptions can cripple projects. We address this by maintaining an inventory buffer and redundant production equipment capable of stepping in if a line goes down. Years of dealing with volatile market conditions for starting materials have shaped a procurement team skilled at securing reliable sources for mandelic acid and ethanol. Open communication with suppliers and regular on-site audits mean surprises stay rare, and knock-on effects remain contained.
Modern chemical manufacturing cannot ignore the environmental angle. Over the past decade, we’ve retrofitted our process to recycle solvents and minimize water use. We operate a solvent recovery system that consistently cuts waste output, and energy-efficient reactors keep power consumption in check. This isn’t just a public relations angle—it carves out cost savings we reinvest into QA improvements.
Responsible waste treatment forms another key area of focus. By-products from ethyl mandelate production get neutralized and sent for responsible disposal. Local regulators tour our facilities without warning, and our records have always passed their scrutiny. Our environmental footprint is a concern we treat with the same seriousness as any technical variable in our process.
We see manufacturers and labs cycle through different fashionable molecules year after year. Ethyl mandelate remains a steady performer. Whenever a new use case crops up or a regulatory requirement shifts, we talk directly with end users to sort out whether we need to tighten specs, change packaging, or offer smaller or larger pack sizes. This flexibility only comes when the whole operation—from purchasing to QA—answers to manufacturing, not marketing.
Every time a customer shares their results or points out an equipment quirk, we listen. Advice from a flavorist or a process chemist who has burnt through kilograms of test samples steers us in directions generalist suppliers overlook. Through these exchanges, ethyl mandelate keeps evolving, shaped not just by what’s possible in the lab, but by the lessons learned under real industrial constraints.
No manufacturing operation runs better than its people. Trainings run year-round for QC staff, plant operators, and logistics teams. We cross-train our crew on analytical equipment and batch documentation, so disruptions stay uncommon and teams grow more skilled every year. Recent investments in automated packing lines help maintain accuracy as batch sizes grow, letting us keep pace with larger clients without sacrificing the same attention to detail we started with.
Clients regularly approach us with issues the spec sheet can’t capture. Maybe a process fouls during scale-up, or an allergy warning crops up in consumer testing. By having our process chemists in-house and open lines to formulation teams, we dig into feedback, offer sample batches with slight tweaks, and help partners work through problems. This hands-on approach makes ethyl mandelate from our lines more than just a commodity; it’s a tool shaped by user insight and adapted through dialog.
We see biotech and pharmaceutical innovation leaning on specialty esters like ethyl mandelate more each year. Molecular libraries grow, and the demand for reliable chiral building blocks rises right alongside algorithm-driven drug discovery. Because we sit close to these changes, we prepare for more diverse requests—higher optical purity, deeper documentation, green chemistry credentials.
Newer applications continue to surprise. Last year, a team working on biodegradable plastics tested ethyl mandelate as a modifier. Another group sourced material for experimental anti-microbial coatings. These collaborations often start small but lead us to reexamine our synthesis, scale up in new reactor sizes, or rethink packaging. Our decision-making—whether upgrading purification steps or trialing different packaging films—owes more to customer partnerships than spreadsheets.
From our experience, real innovation comes out of collaboration and transparency between manufacturer and user. Ethyl mandelate has carved its place in research labs and production lines not because it’s a generic option, but because decades of incremental improvements, customer feedback, and rigorous attention to manufacturing detail make the difference. Every drum or bottle that leaves our floor benefits from this approach—tested, traceable, and manufactured by people who take pride in doing the job right, batch after batch.