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HS Code |
964491 |
| Iupac Name | (S)-4-Amino-3-p-tolylbutanoic acid |
| Molecular Formula | C11H15NO2 |
| Molecular Weight | 193.24 g/mol |
| Cas Number | 131463-80-6 |
| Appearance | White to off-white solid |
| Melting Point | 174-178 °C |
| Solubility In Water | Slightly soluble |
| Optical Rotation | [α]D25 = +19° (c=1, MeOH) |
| Smiles | CC1=CC=C(C=C1)C[C@H](CN)C(=O)O |
| Purity | Typically ≥98% |
| Storage Condition | Store at 2-8°C |
As an accredited (S)-4-Amino-3-P-Tolylbutanoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 1-gram quantity of (S)-4-Amino-3-P-Tolylbutanoic Acid is supplied in a sealed amber glass vial with a tamper-evident cap. |
| Shipping | (S)-4-Amino-3-P-Tolylbutanoic Acid is shipped in secure, airtight containers to preserve purity and prevent contamination. Packaging complies with chemical safety regulations and includes proper labeling. The product is transported under ambient conditions, unless otherwise specified, and accompanied by documentation including a Safety Data Sheet (SDS) for safe handling and regulatory compliance. |
| Storage | (S)-4-Amino-3-P-tolylbutanoic acid should be stored in a tightly sealed container, protected from light and moisture, at a cool temperature (2–8°C). Ensure the storage area is well-ventilated and away from incompatible substances such as strong oxidizers. Proper labeling and secondary containment are recommended to prevent accidental exposure or contamination. Avoid prolonged exposure to air and humidity. |
Applications of (S)-4-Amino-3-P-Tolylbutanoic Acid in Industrial Manufacturing(S)-4-Amino-3-P-Tolylbutanoic Acid supports diverse advanced manufacturing segments, serving as a key intermediate where controlled stereochemistry and aromatic substitution are vital for downstream synthesis and final product performance. 1. Chiral Pharmaceutical API SynthesisPharmaceutical companies employ this compound as a chiral building block in the synthesis of several active pharmaceutical ingredients, particularly anticonvulsants and central nervous system agents. Its defined stereochemistry guarantees precise molecular architecture in the end formulation, supporting strict regulatory and therapeutic requirements. The acid is typically introduced at the initial or intermediate coupling stage, where both purity and enantiomeric excess must be strictly controlled during peptide synthesis or carbon backbone extension. Industry compliance standards
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2. Custom Peptide Synthesis and ModificationSpecialty peptide manufacturers utilize this amino acid as a non-proteinogenic module to introduce specific structural and functional attributes in custom peptides and peptidomimetics. Its side-chain configuration impacts secondary structure, optimizing binding properties in therapeutic and diagnostic peptides. The compound is adopted after solid-phase synthesis deprotection cycles or as an Fmoc/Boc-protected building block, ensuring compatibility with established peptide assembly protocols. Industry compliance standards
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3. Agrochemical Intermediate ManufacturingAgrochemical producers rely on this chiral acid as a precursor in the synthesis of specific herbicide and fungicide molecules, especially those requiring controlled aromatic substitution for biological selectivity. The compound integrates into multi-step synthesis streams, where the amine and aryl functionalities enable further derivatization or cyclization crucial for activity spectrum tuning. Strict impurity profiles and stereochemical consistency are necessary to comply with international agro-regulations. Industry compliance standards
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4. Advanced Material and Specialty Polymer DevelopmentPolymer and advanced material manufacturers incorporate this compound as a functional monomer or chain modifier in high-performance applications where aromatic amine and carboxylic acid functionalities drive unique electrical and mechanical properties. Its inclusion enables synthesis of conductive polymer backbones or tailored side-chain interactions, often under controlled radical or condensation polymerization protocols. Plant QC teams verify purity and reactivity profile prior to scaling to batch-level blending. Industry compliance standards
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5. Analytical Reagent and Chemical Probe ManufacturingProducers of research chemicals and analytical reagents apply this molecule in synthesis of chiral probes and derivatization agents for chromatographic and spectroscopic analysis. Its resolved stereochemistry and aromatic functional groups provide critical reference standards in method development for enantioselective separation or biological activity assays. Precise documentation, purity analysis, and stability data are mandatory prior to global supply to academic and industrial labs. Industry compliance standards
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Producing (S)-4-Amino-3-P-Tolylbutanoic Acid starts well before the reactor warms up. This compound, with its specific S-configuration and p-tolyl group, comes from years of listening to what researchers and developers need in their daily workflow. Every batch brings lessons. From raw material sourcing to purification, many small decisions make a difference in final purity, color, and stability. The significance of a single chiral center seems technical on paper, but it’s practical in labs where optical activity influences performance. In practice, this molecule often finds a home in pharmaceutical investigation, and occasionally in the development of specialized intermediates. Structural requirements for downstream chemistry press us to pay strict attention to everything from substrate melting points to potential trace solvents.
We’ve met many customers who ask why our (S)-4-Amino-3-P-Tolylbutanoic Acid comes out with such a reliable HPLC trace and consistent lot-to-lot analysis. The answer ties directly to how each run gets monitored for enantiomeric excess and residual moisture. Experienced chemists know that chiral consistency can affect the entire synthetic route, not just this step. If a chiral intermediate skews off the mark, columns won’t resolve, unwanted byproducts can appear, and downstream cost climbs. Producing this compound requires far more than chiral reagents: every solvent, every piece of glassware, even air quality goes under scrutiny. These steps are not extras — they’re responses to honest feedback and decades of returns, scale-ups, and hard lessons.
Researchers and manufacturers often come to us with real deadlines and unique projects. They need assurance that 99+% e.e. means every molecule is pulling its weight in the same direction, not just in a certificate on paper. So, each lot gets verified by chiral HPLC, but those reports are only the surface. We test optical rotation out of habit, and scrutiny over trace metal content started after a single customer’s catalyst fouled several years ago. Over time, specifications grew out of genuine setbacks and trial-by-fire improvements. These days, our (S)-4-Amino-3-P-Tolylbutanoic Acid typically shows bright, consistent crystalline character and low water content. Impurities tell a story; we keep records so that any anomaly prompts an immediate root-cause check.
Using only USP water and high-purity solvents pays off when the downstream chemistry runs without surprises. No shortcut at this stage goes unpunished. Failures in strict purification might only show up after weeks of legwork on the user’s side; our experience has made that pain personal. Before packaging, vacuum drying and humidity tests are a given. Some might call it overkill. We call it not repeating the same mistakes twice.
Scale brings its own headaches. Early syntheses were often gram-scale and focused on making just enough for structure-activity work in medicinal chemistry groups. We learned the hard way how batch size changes can play tricks on conversion rates and impurity profiles. Now, during kilogram runs, careful cycle times and continuous filtration have to match standards set at the bench. On the application side, (S)-4-Amino-3-P-Tolylbutanoic Acid commonly enters reaction schemes as a building block for both active pharmaceutical ingredients and custom organic materials. Every customer’s process has quirks—solubility in specific solvents, sensitivity to heat, or interactions during coupling reactions.
There was a time a client needed a faster-dissolving variant for automated high-throughput synthesis. That meant not only tweaking the crystallization solvent but also rethinking drying procedures to avoid forming persistent clumps. It sounds mundane, yet those improvements became the new norm. Even the packaging—double-bagged, foil-wrapped units for moisture-sensitive processes—originated from feedback after a shipment arrived during a humid monsoon week. Using our product should make the next step in the synthesis easier, not introduce another source of worry.
We’ve watched trends in demand for chiral amino acids and related substituted butanoic acids. Some projects compare this compound to unsubstituted analogues or racemic mixes. Chemical differences show clearly in stereo-selective reactions: the p-tolyl group on our product grants more rigidity to downstream targets, supporting cyclization or specific coupling reactions that looser analogues can’t manage as effectively. The S-stereochemistry locks in potential bioactivity, turning a true single key in complex targets, where racemates introduce unnecessary variables and, sometimes, undesired pharmacological effects.
In our own trial reactions, we discovered that switching from (S)-4-Amino-3-P-Tolylbutanoic Acid to a related non-chiral intermediate cut a route short when stereochemical purity mattered. These lessons didn’t come from journals—they came from lost material, repeated attempts, and customer calls asking for troubleshooting help. Real-world comparison often comes down to how quickly researchers can move from intermediate to target molecule. Reducing purification steps, improving yields, and ensuring chiral accuracy have direct cost benefits. Some labs even tell us they come back because repeated synthesis with less pure chiral material added unnecessary complexity that our tighter controls manage to avoid.
Feedback loops shape the way we handle (S)-4-Amino-3-P-Tolylbutanoic Acid from start to finish. Sometimes feedback comes as an emailed NMR spectra with an “unusual bump” annotated, or as a supplier audit requesting extra documentation. We rely on these touchpoints. The compound’s use skews toward pharmaceutical research, but some groups explore materials science applications such as chiral ligands for asymmetrical catalysis. Each purpose brings a new checklist of requirements.
For pharmaceutical development, we learned that the specification for residual solvents can’t just match general standards—they need to meet precise, sometimes unpublished, expectations set by regulatory filings. A lot of the real improvement on our end came from solving repeated moisture concerns. One customer flagged a single lot drifting just above 0.3% moisture. That feedback led us to overhaul our drying cycle and revisit the design of our desiccators. Tweaks like longer vacuum steps slowed production for a short stint, but the payoff resided in fewer rejections and better overall acceptance rates.
Supplying (S)-4-Amino-3-P-Tolylbutanoic Acid means staying close to the front lines of laboratory science. Technical support often goes beyond answering questions about solubility or shipping. We trace every raw material batch and maintain backup aliquots for quick comparison if a complaint surfaces. Once, we solved an impurity issue not by scouring purity certificates but by comparing batches side-by-side with mass spectrometry in-house. Issues flagged by end users often highlight aspects we might not notice from a manufacturing view—such as trace acid sensitivity that only shows up under very specific coupling conditions.
Some newer projects now demand materials fully mapped for trace contaminants down to single-digit ppm. So, analytical investments have grown with customer sophistication; NMR, LC-MS, and Karl Fischer titrations are standard checks now. Our in-house standards shift yearly depending on customer expectation. Fielding these requests might mean retooling a grinding method or regrowing crystals to meet a sharper spec. These cycles turn feedback into genuine process upgrades. We’ve found technical curiosity among our staff frequently matches the persistence of our clients. No test or protocol update sounds like wasted time after a single tough audit.
Over years, manufacturing (S)-4-Amino-3-P-Tolylbutanoic Acid has pushed us away from static ways of working. Early on, we followed the published route with minor tweaks. What customers endured on batch-to-batch variability inspired more robust process control. Adjusting temperature ramp rates prevented side-product formation seen in larger reactors. Every deviation logged on our electronic batch record system gets reviewed with a question “will this matter downstream?”.
A few labs asked about “scalable green chemistry” for this compound. That led us to replace traditional halogenated solvents with lower-impact options, sometimes taking months to match the yield and enantiopurity of our original method. The end result produced less waste and made our colleagues handling the final product happier about lab air quality. These moves don’t happen in isolation—they’re responses to shared goals across organizations focused tightly on safety and sustainability. Major process overhauls happened only after tightening the loop with real end-user collaboration and sharpening our in-house expertise in both classical and modern analysis.
One takeaway from years spent making (S)-4-Amino-3-P-Tolylbutanoic Acid: shortcuts don’t last. Behind each improvement stands some team member who found a problem worth fixing. We keep a watchful eye on batch reactivity, check every delivery against customer commentary, and never skip verification steps for speed. While specs matter, relationships and open lines of honest feedback move things forward.
Questions still come in about suitable solvents, optimal storage, or compatibility with tricky transformations. We’ve gotten used to sending a photograph of our crystals next to a reference batch so customers can see what typical material really looks like. This trust is hard-won after seasons of support calls and side-by-side troubleshooting. Long-term reliability requires more than certificates: it rests on living up to real-world expectations and backing up claims with batch data, open access to problem-solving, and open-mindedness to ever-changing needs.
Plenty of building blocks claim high purity and chiral integrity. What puts (S)-4-Amino-3-P-Tolylbutanoic Acid in a different bracket comes from a combination of technical and practical edges: true S-configuration, clean isolation, and steady responsiveness to ongoing needs. Across countless discussions and orders, it’s become clear that delivering more than a catalog entry builds real partnerships and better chemistry. We don’t just tick checkboxes; every fresh request sends us scouring our logs for lessons and improvements.
Instead of just dropping material on a loading dock, we see ourselves as a partner for researchers who want fewer variables, clearer answers, and accountable manufacturing. This perspective grew from handling everything in-house—from raw material qualification to process refinement and shipment packaging. Our team goes beyond specs and strives to offer product that stands up to real scrutiny, blending technical rigor with openness to feedback.
The importance of (S)-4-Amino-3-P-Tolylbutanoic Acid comes from its proven track record in progressing challenging syntheses and supporting rapid drug discovery. This reputation builds batch by batch, through patience, exploration, and willingness to adapt established protocols for better practical outcomes both in our labs and in those of our customers.
Manufacturing specialty chemicals involves more than hitting numbers on a specification sheet. Every analyst and production team member becomes a stakeholder in the downstream science our customers pursue. This connection drives us to keep improving every aspect of our process, whether through new analytical checks, packaging upgrades, or broader communication channels with our partners in research and development.
We continue to learn from each batch, every unique order, and every conversation about a stubborn impurity or a subtle change in color. If future projects shift demands even further—toward greater environmental awareness, faster delivery, or tighter specs—we’re ready with both open ears and proven know-how. The role of a manufacturer today involves standing behind what we produce, learning from every setback, and sharing honest results that make real progress possible in each round of discovery or production.
At its best, the process of making (S)-4-Amino-3-P-Tolylbutanoic Acid links practical manufacturing insight with a deep respect for the science carried out with every shipment. We see firsthand the difference attention to detail and direct experience make for everyone further down the chain. Our goal remains: Deliver material that supports exacting research without hesitation, shaped by hands-on feedback and a history of serious engagement in both process and results.