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HS Code |
880050 |
| Name | Ethyl (R)-2-Hydroxy-4-Phenylbutyrate |
| Cas Number | 77910-68-0 |
| Molecular Formula | C12H16O3 |
| Molecular Weight | 208.26 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 335.4°C at 760 mmHg |
| Density | 1.103 g/cm³ |
| Optical Rotation | +19° to +23° (c=2, MeOH) |
| Purity | Typically ≥98% |
| Smiles | CCOC(=O)C(CO)CC1=CC=CC=C1 |
As an accredited Ethyl (R)-2-Hydroxy-4-Phenylbutyrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ethyl (R)-2-Hydroxy-4-Phenylbutyrate is packaged in a 25g amber glass bottle, sealed, and labeled for laboratory use. |
| Shipping | Ethyl (R)-2-Hydroxy-4-Phenylbutyrate is shipped in tightly sealed containers to prevent contamination and moisture exposure. The chemical is handled according to standard regulations, with proper labeling and documentation. It is typically transported at ambient temperature and protected from direct sunlight and extreme conditions to ensure product integrity during shipping. |
| Storage | Ethyl (R)-2-Hydroxy-4-Phenylbutyrate should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2-8°C (refrigerator temperature). Avoid exposure to heat sources, oxidizing agents, and incompatible materials. Proper labeling and secure storage prevent contamination and ensure safety during handling and use. |
Applications of Ethyl (R)-2-Hydroxy-4-Phenylbutyrate in Industrial ManufacturingEthyl (R)-2-Hydroxy-4-Phenylbutyrate is a chiral intermediate used by multiple downstream sectors. With its stable configuration and high enantiopurity, this material supports high-value synthesis, especially in pharmaceutical, fine chemical, and specialty fragrance manufacturing. Our facility supplies industrial grades tailored for precise process requirements across these application tracks. 1. Chiral Pharmaceutical Intermediate for Oncology APIsAPI manufacturers use Ethyl (R)-2-Hydroxy-4-Phenylbutyrate as a building block in the enantioselective synthesis of anti-cancer drug molecules. It enters amidation and subsequent cyclization stages to construct core scaffolds for high-purity actives, such as certain kinase inhibitors. Control over residual solvents and optical purity is crucial to pass regulatory registration and process validation. Industry compliance standards
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2. Stereospecific Synthesis for Cardiovascular Drug PrecursorsCardiovascular pharmaceutical synthesis chains use this ester as a starting compound for high-purity chiral precursors. Manufacturers prioritize strict enantiomeric control to meet regulatory submissions for beta-blockers and anti-hypertensive agents. Downstream reactions involve reduction, protection, and asymmetric hydrogenation under validated protocols. Industry compliance standards
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3. Fine Chemical Intermediate for Flavors and FragrancesFragrance and flavor manufacturers utilize this compound as a chirality source for certain musk and floral note molecules. Downstream blending lines adopt it for functional group transformations, such as reduction and esterification, under strict food safety standards. Major applications include synthesis of aromatic and masking agents with safe metabolic profiles. Industry compliance standards
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4. Precursor for Specialty Polymer AdditivesIn specialty polymer additive production, Ethyl (R)-2-Hydroxy-4-Phenylbutyrate gets applied as a source of chiral functionality in high-performance plasticizers and UV-stabilizer intermediates. End-users in the engineering plastics sector integrate it where optical activity and thermal stability matter. Process conditions demand strict control of moisture and temperature to prevent side reactions. Industry compliance standards
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At our plant, Ethyl (R)-2-Hydroxy-4-Phenylbutyrate isn’t just a chemical on a shelf. We draw on years of experience with enantioselective synthesis to bring a product prized for its clarity, stability, and reliable chiral purity. The compound stands out in the catalog of chiral building blocks, not just for its R-configuration, which aligns with many research and industrial targets, but for the consistent quality that tight internal procedures deliver with every batch.
We produce Ethyl (R)-2-Hydroxy-4-Phenylbutyrate in its purest form, weighing experience against every run. Specification matters to our clients: optical purity, color, melting point, and spectral clarity are tested not to fit a generic box, but to suit rigorous standards in chiral synthesis and pharmaceutical research. Packing in clear containers under inert gas, every measure is taken to prevent oxidation and moisture uptake.
Our chemists have fine-tuned asymmetric synthesis methods over the years. Catalysts, solvents, and conditions are measured for every lot, and equipment is checked from glassware integrity to calibration on modern chromatography. By running repeated small-batch tests and applying direct feedback from downstream applications, we keep making process refinements. Solvent choice affects stereochemical outcome. Reaction temperature and time make a difference in optical rotation. Knowing this affects yield, cost, and purity—a lesson only gained by years on the floor.
Chiral control in the synthesis process remains a centerpiece. Minute variations impact downstream pharmaceutical or research applications. There aren’t shortcuts with this compound—a point shared among those who’ve struggled to get a clean R-enantioselective product at laboratory scale. So control of raw material sourcing, oversight on every lot, and in-process checks ensure the end user isn’t left compensating for our mistakes further down the line.
Purity and chiral excess routinely exceed 98%, but we monitor for other quality indicators. Thin layer chromatography, NMR, IR spectra, and HPLC trace impurities—anything that could cause batch-to-batch surprises. Pharmaceutical researchers count on this level of transparency to reduce time spent troubleshooting or discarding out-of-specification product. These details matter when a week lost on poor material disrupts a discovery program.
Our product is neither a generic intermediate nor a semi-pure sample batch. Ethyl (R)-2-Hydroxy-4-Phenylbutyrate hasn’t just passed a routine test—it’s tracked and documented against an internal reference with historical trends. Melting point, appearance, and moisture content are checked each time because any change signals a drift that could hurt your process. This comes from hands-on experience: chemists who have spent late nights tracking down mysterious peaks or underperforming reactions know how much trouble one overlooked parameter can bring.
Ethyl (R)-2-Hydroxy-4-Phenylbutyrate opens doors in pharmaceutical research, especially where stereochemistry decides biological activity. Several selective beta-blocker syntheses, certain anti-epileptic compounds, and advanced synthetic pathways put this compound right in the middle of crucial bond-forming steps. Where an enantiopure alpha-hydroxyester sits in the synthetic plan, labs can’t afford to gamble on racemic mixtures or dubious origins. Our repeat clients have returned for this specific purpose—they are seeking trustworthy input materials for higher value chiral drugs and advanced research.
Over time, we’ve watched trends in how the product supports different methodologies. Grignard additions, esterifications, and direct aminations built on reliable chiral centers foster fewer surprises at scale-up. Contract research organizations and small-batch pharmaceutical startups rely on this stability. We’ve seen projects rescued simply by bringing in high-purity, well-characterized (R)-2-Hydroxy-4-Phenylbutyrate instead of the variable-quality material they previously tolerated.
Beyond drug synthesis, it finds limited use in some flavors and fragrances, where a chiral center shifts perception or reactivity depending on the configuration. In those cases, trace contaminants not only impact purity but subtly alter the final product’s profile, something experienced manufacturers learn to guard against.
For many of our clients, hitting the favored chiral configuration removes the tedious cleanup steps and prevents costly repeat reactions. More than a cost-saving, it determines regulatory acceptance in pharmaceutical and life science streams. In our plant, attention to chiral excess is built into the verification loop. HPLC on chiral columns with strict sample handling gives real numbers, not ballpark figures.
Different from the many racemic compounds on the market—or poor attempts at resolution—our batch-to-batch approach minimizes the risk of variable outcomes. Where others settle for above 90% chiral purity, we push past this, and any hint of stereochemical drift sets off a process review. We have chased false peaks, isolated micro-impurities, and retraced sourcing history, not because it’s required, but because these details haunt downstream research if left unchecked.
Researchers mention the ease with which synthesis proceeds with reliable building blocks. They finish routes sooner, make fewer chromatography passes, and trust their assay results. We’ve heard everything from stories of almost-failed multi-week synthetic runs saved by proper starting material, to long-term collaborations built because one reliable batch led to extended partnerships.
A focus on (R)-enantiomer production is rooted in hands-on lessons. Customers in academic, startup, and major industrial labs talk to us about needing products that don’t deviate in quality between shipments. For them, data sheets alone don’t deliver confidence; stability and purity have to translate outside the test tube. Incoming goods testing catches slip-ups with humidity, byproducts, or oxidation. Shipment storage advice (keep cool, avoid light, watch for moisture) amounts to real knowledge, passed to users after long-term stress tests in our own facility.
Handling protocols were put in place after batches showed susceptibility to hydrolysis in damp conditions. New sealing processes and rapid packaging have cut down exposure time. Over the years, we’ve shifted from simple glass ampoules to specialized moisture-barrier vials without waiting for customer complaints. Attention to these details has ensured we avoid problems seen in early years when inconsistent supply caused headaches for both users and those of us standing behind the product.
Anyone who’s sourced poorly documented material from a reseller or broker has felt the pain of unreliable composition or inconsistent performance. Unidentified side-products or racemization cost valuable time and can throw synthetic routes off course. One of our earliest supply partners struggled to tell the difference between batches by spectral data alone, only learning the hard way through repeated downstream failures.
Direct manufacturing allows us to maintain strict control of the supply chain. Every raw material batch is traced and documented. Employees run double checks on solvent lines for contamination. Recently, a supposed clean lot showed up with trace sulfur, something that only appeared after monitoring new reagent sources. Immediate flagging and intervention prevented an entire production run from being compromised. Documentation process and electronic batch records reflect this vigilance. These efforts support our stance that direct chemical manufacturing offers reliability where distributors often can’t see below the surface.
Our product stands beside—and apart from—other chiral hydroxyesters through both its level of purity and continuous process review. While several other hydroxybutyrate derivatives see use in the market, their production sometimes relies on less selective routes, leading to racemates, high impurity levels, or unstable mixtures requiring complex remediation. Users working with generic 2-hydroxy-4-phenylbutyrate often face extra separation steps or spend extra time characterizing incoming material before it can be used.
The difference is pronounced when moving from a commercial racemate to our pure R-enantiomer. Downstream efficiency improves, waste steps disappear, and performance issues shrink. We have worked with research programs confronted with bottlenecks attributable to supplier inconsistencies; having direct control over each production detail, we help clients cut down repeated verification steps and focus on the chemistry that matters.
Use of well-characterized chiral catalysts and controlled environment conditions anchors every step of synthesis. Every batch runs against both historical internal standards and modern analytic techniques to track not just what’s expected, but what might be lurking at low levels: trace side-products, minor diastereomers, residual reactants. We have caught rare incidents of double-alkylation and run side-by-side comparisons to older product lines to guarantee improvements in chromatographic cleanness.
Material handling, re-crystallization, and drying are never rushed. Every misstep during isolation—rushing the dryness or cutting down on solvent—has shown up later as a problem, so practices have changed to favor time and care. Shipping procedures ensure material leaves the plant as it left the lab: dry, protected from light, and inerted where necessary. Each of these points is learned from dealing with products that spent long weeks in subpar warehouses and arrived at the customer in far-from-optimal state.
Clients often ask about solubility behavior in various solvents, impact of alternate storage conditions, or compatibility with specific reagents. Not every compound gets this sort of hands-on attention after it leaves the manufacturing line. Staff here collect these questions and track user outcomes over months and years. Tips for storage or reminders on minimizing moisture contact have come from direct feedback—users caught product breakdown and let us know, leading to improved advice and packaging upgrades.
We track customer project goals and take pride in seeing our material make its way from bench chemistries to pilot plant production. Sometimes that means adjusting preparation conditions, shifting packaging format, or providing detailed production history to satisfy regulatory scrutiny. Each of these pieces comes from partnership—a two-way exchange rooted in respect for those who apply our materials in cutting-edge, high-stakes research.
In one recent example, a scale-up customer faced yield drops during an amide coupling step. Working side by side, we reviewed full batch records, cross-checked chiral analysis, and provided parallel material from a retention sample. This direct involvement solved the matter; the problem traced to a plant-side issue with coupling reagent rather than the hydroxyester, validated by matching analytic results between fresh and retained product. Connections like these—born of transparency and technical dialogue—illustrate why clients favor a direct manufacturing relationship.
At scale, achieving the same chiral purity as the laboratory requires adaptation. Reaction vessels grow larger, temperature control becomes more complex, and mechanical mixing has to preserve both yield and configuration. Careful engineering of reactors and adoption of modern monitoring minimize the risk of temperature spikes or unexpected phase changes. Real-time analytic feedback shines here; in-process HPLC checks keep each run on track and give early warnings for problems.
Waste handling becomes a real concern—spent reagents, solvent recovery, and batch washing are handled in dedicated facilities. We’ve upgraded to sustainable solvent recovery on the back of both regulatory demand and personal respect for people and the environment outside our doors. The benefit becomes clear: less contamination risks, lower operating costs, and safer working conditions for everyone involved.
Supply chain interruptions, whether from raw material delays or changing regulations, pose real risks. Keeping close contact with our material suppliers and maintaining onsite reserves of core reagents helped us weather disruptions that saw other suppliers falter. Staff stay ahead by reading both the regulatory landscape and listening to customer forecasts—preparing for spikes in demand during certain project cycles.
Our approach to Ethyl (R)-2-Hydroxy-4-Phenylbutyrate stems from firsthand mistakes and successes. We’ve adjusted protocols based on user feedback and continued to test, not rest, after each improvement. Each advancement in purity, analytical methods, or packaging reflects direct lessons from chemists—both inside and outside our facility—who demand more than theoretical compliance.
We know the difference reliability makes from talking to scientists who bet their research timelines on good input material. Careful attention at each step means fewer headaches for end users. Long-term customers value honest data and practical support over flashy claims. They rely on us to let them know if a batch performed slightly outside our historical mean, not just if it met the standard. In turn, we see those customers return project after project, counting on dependable performance based on a partnership built in the lab, not the boardroom.
Expectations for chiral intermediates keep rising. Researchers want sharply defined purity, clear supply lines, regulatory-ready records, and authenticity from manufacturers. Our team welcomes these standards. Each challenge introduced by customer demand or evolving research goals pushes us to revisit old assumptions and refine production methods. The tight feedback loop—from in-house analytics to field application—keeps the product moving ahead.
By keeping every part of the process close, from first catalyst selection to container closure, our team delivers value beyond just molecules. That value shows up in clear, useful analytic data, reliable supply, and practical expertise shared across the table. These efforts reinforce the role of direct manufacturers in scientific advancement. We stand ready to keep raising the standard for Ethyl (R)-2-Hydroxy-4-Phenylbutyrate and beyond, supporting those who take these building blocks and turn them into tomorrow’s breakthroughs.