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HS Code |
991333 |
| Chemical Name | (S)-3-Amino-3-Phenylpropanoic Acid |
| Synonyms | L-β-Phenylalanine |
| Molecular Formula | C9H11NO2 |
| Molecular Weight | 165.19 g/mol |
| Cas Number | 1138-83-8 |
| Appearance | White to off-white solid |
| Melting Point | 250-255°C (dec.) |
| Optical Rotation | [α]D20 +35° (c=1, H2O) |
| Solubility | Soluble in water, slightly soluble in ethanol |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C in a tightly sealed container |
| Inchi | InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m0/s1 |
| Smiles | C1=CC=C(C=C1)C(CC(=O)O)N |
| Chirality | S-enantiomer |
As an accredited (S)-3-Amino-3-Phenylpropanoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | (S)-3-Amino-3-Phenylpropanoic Acid, 5g, is supplied in a sealed amber glass bottle with a tamper-evident cap and labeling. |
| Shipping | (S)-3-Amino-3-Phenylpropanoic Acid is shipped in tightly sealed containers to prevent contamination and degradation. The product is packaged according to regulatory standards, and typically transported at ambient temperature. Proper labeling, including hazard information and safety precautions, is provided to ensure safe handling during transit. Shipping generally complies with relevant chemical transport regulations. |
| Storage | (S)-3-Amino-3-Phenylpropanoic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature (15–25°C) in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Avoid prolonged exposure to air to prevent degradation, and always handle under appropriate laboratory safety conditions. |
Applications of (S)-3-Amino-3-Phenylpropanoic Acid in Industrial Manufacturing(S)-3-Amino-3-Phenylpropanoic Acid serves as a high-purity chiral intermediate tailored for specialized industries where enantiomeric purity and precise formulation parameters are crucial. Our team ensures strict process control from synthesis to quality assurance, supporting various manufacturing segments requiring advanced organic building blocks. 1. Active Pharmaceutical Ingredient (API) SynthesisThe pharmaceutical industry uses this amino acid as a critical chiral precursor in the synthesis of several enantiomerically pure APIs, including CNS-active drugs, enzyme inhibitors, and peptide-based therapeutics. Its inclusion in synthetic routes improves target molecule specificity and reduces side product formation, complying with stringent GMP standards in multi-step organic and peptide synthesis. Our material undergoes stringent chiral purity and residual solvent testing before delivery to formulation plants. Industry compliance standards
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2. Peptide Synthesis for Diagnostic ReagentsBiotechnology and IVD companies incorporate this material as a non-proteinogenic amino acid for customizing peptide sequences required in diagnostic tests and targeted detection kits. The chiral center allows specific antigen-mimetic properties in biosensors and immunoassays, supporting reliable signal generation and repeatable performance in critical in vitro diagnostics. Industry compliance standards
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3. Chiral Auxiliary in Fine Chemical SynthesisFine chemical producers use this compound as a source of chiral induction to direct stereoselective transformation steps in enantioselective synthesis of specialty compounds. Its defined stereochemistry plays a critical role in achieving high enantiomeric excess for next-stage intermediates, essential in fragrance, agrochemical, and specialty material development. Industry compliance standards
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4. Reference Standard Production for Analytical LaboratoriesReference material manufacturers use this amino acid to formulate calibration standards for chromatographic and spectrometric analysis of enantiomeric and structural purity. Laboratories deploy these standards in pharmaceutical batch release, forensic drug screening, and regulatory compliance testing, ensuring reproducible chiral separation and detection of trace contaminants. Industry compliance standards
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5. Research-Grade Building Block in Medicinal ChemistryContract research organizations (CROs) and academic R&D units employ this compound for the rapid development of novel analogues and structure-activity relationship libraries. Its stereochemistry is exploited to differentiate chiral pathways in lead optimization for therapeutic and probe discovery, enhancing data integrity in preclinical compound screening. Industry compliance standards
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We produce (S)-3-Amino-3-Phenylpropanoic Acid in our facility by focusing on accuracy and consistency from raw materials through to packaged product. Every batch comes off our line as a result of careful control, hands-on oversight, and deep respect for the chemistry behind this valuable compound. The chemical formula, C9H11NO2, and chiral specificity carry real consequences in the phytochemical or pharmaceutical space. In our hands, purity isn’t a vague claim—it's tracked daily, measured, and confirmed using established chromatographic and spectroscopic methods.
Our expertise covers all stages, from feedstock selection to crystallization. We remember earlier years when small inconsistencies in temperature could throw out the final enantiomeric excess. Years of steady, iterative improvement have built a robust production route: low-temperature asymmetric synthesis stands as the key step, not a shortcut. Laboratories and downstream partners test our output randomly because they’ve seen real-world reproducibility. With each cycle, we tighten tolerances, log every deviation, and use the same NMR and HPLC instruments as the verification labs down the road.
(S)-3-Amino-3-Phenylpropanoic Acid, sometimes called L-β-phenylalanine, serves as a core building block for precise, enantiomer-specific formulations. It isn’t just any β-amino acid. The S-configuration gives it a unique biological profile, making it critical in peptide synthesis and medicinal chemistry research. Whether a team is optimizing CNS-targeted ligands or exploring artificial enzyme scaffolds, one detail stands out: enantiopure raw material is not optional. Impurities in the S-enantiomer muddy data and can derail entire projects. We’ve worked shoulder-to-shoulder with synthetic chemists who rely on us because lower optical purity means wasted time, wasted reagents, and lost confidence in end results.
This material reaches 99%+ chemical purity by HPLC, with chiral purity repeatedly exceeding 98%. Laboratories probing for trace contaminants don’t need to ask about leftover catalyst levels; we know their screening routines because our QA team uses the same panels. Reproducibility in melting point, particle size, and color arise from solid process fundamentals. The crystalline white powder isn’t just for show; it reflects real removal of colored byproducts and thorough drying.
Across every lot, the specifications reflect years of tweaks honed by direct user feedback. Early complaints about hydration or tangled solid-state forms led us to change drying protocols and invest in new jacketed vessels. Results today feature a tight moisture control, minimal need for post-purchase drying, and rapid dissolution in standard solvent systems used for coupling reactions.
Beta-amino acids span a large landscape, each with their own quirks—hydrophobicity, reactivity, and stability. (S)-3-Amino-3-Phenylpropanoic Acid sets itself apart by virtue of its chiral center and rigid aromatic side chain, which influence both physical and pharmacological behavior. Through our own scale-ups for peptide research partners, we’ve learned to respect these differences: beta-alanine, lacking the phenyl ring, cannot mimic the spatial or electronic properties of the S-phenylpropanoic core. Researchers develop beta-peptides with defined secondary structures, often leveraging the rigid, hydrophobic nature of the phenyl group here, which alters folding, aggregation, and biological function.
Selection isn’t just about price or supply. It’s about locking in results—our feedback from peptide chemists and neuroscientists is clear. Beta-alanine or racemic phenylalanine open doors to ambiguity and inconsistent yield in cyclization or elongation. Only pure (S) configuration achieves the correct chirality for high-fidelity studies, guaranteeing reliable SAR (structure-activity relationship) explorations.
Structural differences pay off in real applications. In small molecule design, for instance, the (S)-enantiomer fits certain transporters and receptors with impressive selectivity. Without careful attention to stereochemistry during production, unintended side products or racemates undermine both efficiency and safety in scale-up.
Most of our clients work in pharmaceutical discovery, custom peptide synthesis, or advanced molecular research. They choose (S)-3-Amino-3-Phenylpropanoic Acid to construct beta-peptides, peptidomimetics, CNS drug candidates, and complex combinatorial libraries. Academic and industrial teams use our product for synthesis of highly specific modulators, enzyme inhibitors, and biologically active oligomers. Locking down chirality at the monomer stage makes downstream separation cleaner, cost of purification lower, and reliability across preclinical screens far higher.
In some fields, such as neuropharmacology, this compound plays a role in reference standard assays or in building block toolkits for their analog screening. We’ve shipped hundreds of grams at a time into custom combinatorial synthesis, supporting lead development within timelines that chemical patent offices won’t wait for. That chance to save a week means new candidates reach early assessment ahead of competitors or regulatory deadlines.
Peptide chemistry groups know from frustrating bench failures that even trace levels of racemization can compromise yield or introduce unpredictable structure into cyclic or stapled peptides. Our QC data isn’t just for shelf appeal—it stops surprises mid-campaign, saving precious time and expensive, hard-to-source protected amino acids. We support buyers directly, whether for small batches in a startup pipeline or larger volumes tuned for API intermediate production.
This work draws on decades of incremental innovation. We recall clogging filters, losing product in poor crystallization, and chasing lost yield during the notoriously finicky resolution stages. Many beta-amino acid syntheses rely on chiral resolution, asymmetry enforced by organocatalysts, or direct enantioselective hydrogenation. Over time we chose a route blending direct Strecker-like synthesis and careful, temperature-driven optical resolution using modern chiral auxiliaries. Learning by direct feedback—both in yield metrics and hands-on inspection—kept us grounded.
Peer review of our intermediates with customers allowed us to spot trouble early, modify steps in response to on-the-ground test results, and adapt to supply fluctuations of critical raw reagents. We've replaced older purification sequences with more sustainable solvent systems and reduced energy consumption during crystallization.
Not every batch runs smoothly, yet our system logs each irregularity for root-cause review before the next synthesis cycle. Technicians pull comparison samples, supervisors run double-checks, and production teams keep every timeline transparent. This transparency has allowed our partners to conduct independent forensic checks without surprises. We weren’t always so methodical—experience forced us to trust measurement, not hope. This is why our reputation rests not on advertising, but on documented repeat orders from research teams who demand performance, not rhetoric.
Our role doesn’t stop with a COA or batch record. We step into labs where temperature, humidity, and scale can vary widely. We’ve visited peptide manufacturing lines and seen exactly how a high-purity, non-hygroscopic powder cuts prep time, avoids cross-contamination, and fits straight into their finely-tuned workflows.
We answer questions about handling, storage, and shelf-life routinely. Since (S)-3-Amino-3-Phenylpropanoic Acid can degrade with mishandling, we package with robust sealing and desiccation. This practice stems from hard-earned history—in early years, slight exposure meant caking and a rising moisture content, which directly affected solubility and weighed-inaccuracy. Now all product leaves our hands with moisture checked not just by loss-on-drying, but by Karl Fischer titration, and the desiccant inside is both reliable and non-reactive.
Our lines run year-round, but we reserve buffer stocks for researchers handling urgent, accelerated projects. Quick turnaround can spell success for labs competing to secure the next patent or journal publication. We make sure packaging is universal, easy to open without spillage, and always labeled to recognize through heavy gloves. These aren’t afterthoughts—they reflect hard feedback from working chemists who’ve lost time to sticky caps or unreadable labels.
Direct comments from the floor have shaped our specification sheets. We’ve shifted away from glass ampules because enough synthetic teams flagged storage issues and risk of breakage. Packing in wide-mouth HDPE jars eliminated frustrating bottlenecks during handling. Analytical teams test trace element content and want documented batch homogeneity, so we’ve invested in in-house ICP analysis to keep up with tightening analytical standards.
Quality reports aren’t thrown together—they’re based on live runs, not textbook theory. Early adopters pointed out frustrations with batch consistency and late shipments. We overhauled order tracking and batch scheduling to ensure better predictability. Careful process design now supports both kilogram-scale lots for process development and small gram units for initial screening.
Chirality makes or breaks biological performance. The S-form of 3-amino-3-phenylpropanoic acid interacts differently with biological receptors and enzymes compared to its R-enantiomer or the racemic mixture. We’ve supported teams working in drug discovery, peptide engineering, and enzyme modulation—they noticed dramatic changes in binding affinity or selectivity rooted directly in choosing the correct enantiomer.
We’ve seldom encountered a lab where “close enough” passes muster. Even one percent racemization can throw off biological activity profiles or peptide folding. Our responsibility includes routine chiral HPLC and NMR verification—not just at release, but pulled from storage after three, six, or twelve months so we can stand behind our labeled shelf-life.
Manufacturing at scale means juggling demand upticks, regulatory questions, and unforeseen shipping delays. By keeping real-time inventory and redundant equipment, we’ve supported consistent supply even amidst raw material shortages or transport snags. Years in the business taught us that lost production time from a single broken pump or kettle doesn’t just cost us money; it cripples the research timetables of every client counting on a shipment.
During peak demand cycles, our team stocks up ahead of forecast to buffer against market spikes. We remember the sting of missing a deadline because a single lot needed rework. Our monthly reviews go beyond the numbers—we focus on real process bottlenecks, update predictive maintenance, and prioritize critical shipments to customers who simply can’t wait.
Regulatory requirements for pharmaceutical raw materials keep climbing. We update internal records to document traceability at every stage, from supplier to final drum. This helps both our team and our clients to move swiftly in case of internal or external audits.
Beyond production, sharing technical know-how with other labs benefits our work. We take part in symposia on chiral synthesis and regularly publish minor process tweaks in industry journals. Collaborating with academic groups keeps our team grounded, encouraging adoption of the latest catalytic systems or analytical tricks. This cycle of feedback and adaptation helps drive future innovation and keeps our product offering current.
We also support method development or troubleshooting at the application stage—guides for solvent choices, coupling conditions, and safe handling see regular updates based on both our in-house findings and our partners’ needs. Custom solutions, often simple process changes, help peers solve persistent problems nobody else would flag as significant. This culture of dialogue helps push boundaries and lifts quality across the sector.
Looking at the rapid changes in molecular sciences, the need for reliable, stereochemically pure building blocks is only growing. AI-driven design, new high-throughput screening, and exciting progress in peptidomimetic drug development all depend on repeatable, standardized starting points. Through years of working alongside small and large partners, we see our role as both a supplier and technical support. Our focus remains firmly on product that empowers discovery—refined, consistent, and manufactured with care, not just at scale.
Locally and globally, we keep reinvesting in better facilities, more precise chemical processes, and sustainable raw material sourcing. These aren’t luxuries. They’re answers to real questions posed by the researchers tackling tomorrow’s challenges.