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HS Code |
851251 |
| Product Name | (R)-4-Amino-3-(Naphthalen-1-Yl)Butanoic Acid |
| Cas Number | 1187596-72-2 |
| Molecular Formula | C14H15NO2 |
| Molecular Weight | 229.28 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Solubility | Soluble in DMSO, methanol |
| Optical Activity | [α]D undefined (specified by R configuration) |
| Smiles | N[C@@H](CCc1cccc2ccccc12)C(=O)O |
| Inchi | InChI=1S/C14H15NO2/c15-11(14(16)17)8-7-12-9-5-6-10-3-1-2-4-13(10)12/h1-6,9,11H,7-8,15H2,(H,16,17)/t11-/m1/s1 |
| Storage Temperature | 2-8°C (refrigerated) |
As an accredited (R)-4-Amino-3-(Naphthalen-1-Yl)Butanoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, airtight, high-density polyethylene bottle containing 5 grams of (R)-4-Amino-3-(naphthalen-1-yl)butanoic acid, labeled with hazard warnings. |
| Shipping | (R)-4-Amino-3-(Naphthalen-1-Yl)Butanoic Acid is shipped in tightly sealed containers, protected from light and moisture. It is transported at ambient temperature unless otherwise specified, in accordance with all relevant safety regulations. Proper labeling and documentation are included to ensure safe and compliant handling during transit. |
| Storage | (R)-4-Amino-3-(Naphthalen-1-yl)butanoic acid should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep at room temperature or as specified by the manufacturer, in a well-ventilated, dry area. Avoid excessive heat and humidity, and clearly label the container. Follow local regulations for chemical storage and handling to ensure safety. |
Applications of (R)-4-Amino-3-(Naphthalen-1-Yl)Butanoic Acid in Industrial Manufacturing(R)-4-Amino-3-(Naphthalen-1-Yl)Butanoic Acid supports a range of advanced manufacturing sectors. Its unique chiral structure and aromatic properties enable downstream producers to achieve precise specifications in pharmaceutical synthesis, specialty intermediates, and high-end research chemicals. As the direct manufacturer, we ensure stringent process control for end-use applications requiring traceability, reproducibility, and full regulatory compliance. 1. Chiral Pharmaceutical Intermediate SynthesisPharmaceutical and biotech companies employ this compound as a key chiral building block in the synthesis of selective GABA analogues and neurological agents. Producers require enantiomerically pure amino acids to maintain target profile and clinical activity. GMP-grade supply and validated impurity profiles allow integration for API synthesis under strict audit. Industry compliance standards
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2. Peptide and Peptidomimetic R&DResearch laboratories and CDMO partners utilize this compound during sequence extension and side chain modification in the synthesis of peptidomimetic scaffolds. The regulated backbone allows for modulation of bioactivity in candidate drug screening, supporting high-throughput lead optimization under GLP. Industry compliance standards
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3. Advanced Chemical Synthesis of Aromatic IntermediatesProducers of specialty aromatics incorporate this material into multi-step syntheses for custom naphthyl-based intermediates. Its molecular rigidity and functional groups support ring construction and further substitution, often under strictly controlled reaction environments to meet electronics or polymer precursor specifications. Industry compliance standards
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4. Analytical and Chiral Reference StandardsCertified analytical laboratories and pharmaceutical QC teams source this material for use as a chiral reference standard and calibration substance in chromatographic assay development. The well-defined stereochemistry and robust supply traceability enable compliance in GLP/ISO environments, supporting both method validation and regulatory filings. Industry compliance standards
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At our production site, we’ve handled (R)-4-Amino-3-(Naphthalen-1-Yl)Butanoic Acid for over a decade, watching the requests and applications widen as science pushes forward. Each month, our synthesis line pulses with the familiar smell of naphthyl derivatives and the clink of specialty glassware. This compound shows up in both pharmaceutical inquiry labs and custom synthesis programs, standing out for its chiral structure and robust aromatic backbone.
From hands-on work, we’ve learned the importance of maintaining stricter temperature controls during both the resolution and final recrystallization steps. Crystallization drives the purity here; even small shifts in water content or solvent ratio can affect optical purity. We record the [α]D value batch by batch, finding that tight monitoring brings more consistent outcomes. We don’t cut corners—every batch reflects the hard lessons learned from the early days when a degree of racemization meant wasted time and resources.
Specs matter, but what matters more comes through in the lab: w/w purity of at least 99%, stable appearance, and sharp melting point. Our teams monitor every shipment, logging lot numbers and keeping retention samples to track stability over time. We know the end users often demand documentation down to enantiomeric excess, so every number we report has a team and a process behind it. It’s not just about meeting a spec, it’s about owning the whole process and making corrections ourselves, not leaving it to a third party.
It’s easy for lab catalogs to treat each compound as another entry in a long table. From the plant floor, though, the differences between these molecules jump out at you. The extended aromatic system of the naphthalene group brings solubility quirks not shared by more pedestrian aryl-aminobutyric acids. Researchers often chase additives or solvents to make naphthyl derivatives behave, but our team found that phase-transfer techniques and careful pH adjustment during the process make a major difference even before a chemist ever uncaps the bottle.
Our staff receives questions from formulators and chemists who work under tight timelines. They want assurance on polymorphism and storage stability, so we invested in solid-state characterization early on. It means we spot batches prone to clumping or minor hydrate formation before release. Most suppliers stop at purity numbers; we track shelf-life in real time, retesting lots a year down the line and sharing those real-world stats with regular clients.
We’ve partnered with academic teams, sending reference materials and discussing scale-up headaches. They bring up oxidation of the naphthalene ring during some transformations, so we reinforce inert atmosphere techniques during packaging. It’s these conversations that shape our process, not just feedback back-chained from a faceless sales channel.
In our experience, the (R)-enantiomer offers a steep challenge. Stereospecific synthesis doesn’t forgive slipshod methods or shortcuts in resolution. For butanoic acids with simple phenyl groups, resolving the two sides can run on simple crystallization. With the naphthyl analog, mechanical stirring, seed crystals, and solvent mix all play outsized roles. Our staff adjust conditions in real time, not just following a flowchart—making the result more reliable for labs and scale-up projects.
Compared to related γ-aminobutyric acids, this molecule’s extra size and aromatic heft alter both physical properties and downstream activity. The naphthyl group resists easy hydrogenation and adds both hydrophobic and stacking interactions. We’ve supported teams exploring CNS analogs, reporting that substitution on the naphthalene ring itself further shifts behavior in unpredictable ways. Making these derivatives with reproducible purity isn’t simple; once the batch comes out, the quality speaks for itself.
Over time, we’ve noticed more customers moving away from off-the-shelf, racemic mixes. Activity differences between enantiomers can drive big shifts in results—something that came into focus with the rise of chiral-specific research projects these last few years. Our batches consistently display optical rotation at the expected value, and our facility retains analytical documentation for customers who need compound-level traceability for regulatory filings or publication supplements.
Our product often lands in the hands of medicinal chemistry teams probing new receptor families for lead compounds. The extended aromatic core earns a spot in libraries where the simple benzene ring can’t probe sufficiently deep into receptor pockets. Early collaborations aimed at antineoplastic screening gave us a sense for just how small impurities could derail projects, so we instituted a two-step purification routine, followed by HPLC fingerprinting on each batch.
Other sectors come calling, too. Material science groups seek this compound for experimentation on organic electronics, owing to the rigidity and resonance of the naphthyl skeleton. We took their feedback about particle flow and static-dissipation needs and introduced new packaging methods to curb clumping, making the powder easier to dispense in finely-tuned syntheses.
Peptide research also saw (R)-4-Amino-3-(Naphthalen-1-Yl)Butanoic Acid step forward as a specialty building block. In the solid-phase world, reliable side-chain protection and compatibility matter. Early trials flagged deprotection issues, traced back to trace iron carryover from a prior supplier. Our in-house QA flagged it in ICP-MS rounds, so we swapped to non-metallic equipment in those steps. The result? Problems gone, and our partners reported higher coupling efficiencies and better yields.
Every manufacturer talks up their lab capabilities. For us, the proof lies in the stack of chromatograms and mass-spectra that map each batch’s true composition. We test on chiral columns and run NMR in-house, checking both for main peaks and possible side reactions. We keep tabs on limit tests for common trace impurities from solvents or starting materials, since these crop up in structure–activity work.
People ask why we bother holding reference vials so long after batches ship. In our history, a client flagged a bioassay drop-off linked to minor decomposition, spotted upon retest. That prompted us to retool both packaging choices and include more desiccant protection, which improved long-term stability. Every lot gets full traceability, not just for regulations, but because we want to be sure that what ships will work as it should—five months later, not just the week after release.
Rather than only offering a standard grade, we produce lots under distinct solvent systems for clients with specific downstream reactions. Some benefit from bulk shipments, some from lyophilized vials; having our own controlled lines means we can adjust readiness. Competing offerings tend to repackage or white-label from generic sources—leaving questions unanswered if process deviations creep in.
Aromatic building blocks bring their own set of wrinkles. Handling naphthyl-containing acids calls for careful environmental controls. Some molecules absorb moisture or degrade when exposed too long. We discovered shifts in melting point after shipments crossed humid regions in midsummer, so we adapted our internal packing process for better sealing and began recommending refrigerated shipping on some routes.
Early on, we learned solvent residues could stymie both analytical readings and downstream applications. We trained our team to tighten up rotary evaporation and added extra vacuum drying cycles. Now, customer feedback rings clearer, with fewer cases of unexplained NMR peaks or solvent “ghosts” in endotoxin testing from clients using our material in sensitive assays.
It pays to invest in staff training—chemists on our line get regular updates not only in GMP and analytical control, but also in chemical hazards, waste minimization, and cross-contamination prevention. By keeping production lines segregated for the most sensitive intermediates, we deliver on our promise for trace-element and by-product control.
Packaging choices evolved in response to real client lab conditions: antistatic jars for material scientists working in dry boxes, amber glass for UV-sensitive protocols, and customized weights to support automated dispensing systems. No single solution works for every research outfit, but drawing on conversations and hands-on feedback, we iterate to keep every batch fit for the purpose.
Far from being another catalog item, (R)-4-Amino-3-(Naphthalen-1-Yl)Butanoic Acid stands as a direct product of experience at the bench and in the warehouse. We recognize patterns in reactivity, stability, and crystallization habits that don’t always make it into the literature. Our teams work through the day-to-day realities: taking calls from researchers with rushed timelines, dialing in last-minute purity adjustments, and ensuring all batch data follows the compound from cleanroom to shipping crate.
The labs developing new CNS-active molecules or exploring custom peptide architectures put compound provenance under a microscope. Small differences in molecular structure translate to major consequences in biological systems. We base our reputation on meeting not only stated requirements, but also anticipating the next wave of questions from the scientists pushing the chemistry forward.
For the chemist juggling a dozen simultaneous screens, confidence in building-block reliability is non-negotiable. We live by those stakes, jumping in to troubleshoot downstream synthesis headaches, or rerunning tests to support a customer’s regulatory filings. Many talk about product stewardship. For us, that means being ready to answer for every shipment, every lot, and every gram.
In a sea of building blocks, naphthyl-ring analogs break the mold. The dense aromatic system brings both promise and necessary precautions. Some customers need the compound in crystalline form; others ask for fine powders. Getting this right called for practical adjustments: small-batch grinding, in-line particle sizing, and quick turnaround to preserve sharp melting behavior. We drop in with custom requests—without needing a committee review—because real research does not wait.
Clients have flagged clumping in poorly handled naphthalene compounds. We took that feedback and brought in improvements in blending and anti-caking, especially on rainy days when humidity spikes push powders toward unwanted agglomeration. Dry room packaging, tighter headspace control, and extra moisture checkpoints now come standard on sensitive shipments.
From a scalability perspective, larger runs demand extra vigilance in stirring, solvent ratios, and semi-batch feeding. The naphthyl core tends to resist full conversion, which calls for incremental feeds of reagents and in-process monitoring. No two runs are the same, but lessons from years in the plant shape every decision. Our scale-up team logs every deviation and outcome, learning from each project instead of stamping out cookie-cutter runs.
Transitioning new users to naphthyl-substituted butanoic acids often means troubleshooting solubility questions. Common organic solvents work, but the order of addition, pH, and even lot-to-lot quirks matter. We share not only specifications, but also detailed solubility profiles from in-house trials, saving clients time on method development. If questions arise mid-project, our technical support pulls lab records and advice from those who run the same reactions daily.
Every compound leaving our line carries a story of trial, error, and improvement. From the earliest batch syntheses, the value of open records and client dialog became clear. We invite process audits and welcome new analytical demands because every additional step deepens our understanding and improves the next shipment. We hold back representative vials from each run, following their progress in real time, and routinely refresh analytical runs to ensure accuracy.
Scientists preparing for publication or scale-up access our detailed batch histories. Whether it’s an NMR shift, a question about trace residuals, or the logistics of dry-ice packed deliveries, we stand by our product and those who depend on its reliability. Openness builds both better chemistry and lasting trust—two essentials in the world of specialty building blocks.
Our constant interaction with end-users shapes both daily practice and future plans. These interactions highlight that compound quality is never static; fresh queries, new project goals, and unplanned problems all push us to respond and refine. We engage directly with chemists, listen to unvarnished feedback, and never shy from revisiting process details as needs evolve.
For (R)-4-Amino-3-(Naphthalen-1-Yl)Butanoic Acid, custom work often involves tweaking isolation steps or developing entirely new analytical runs. Peptide shops sometimes request integration reports with more comprehensive impurity tracking. Pharma teams need Excel-ready data for regulatory submission. We designed our documentation system so requests funnel from the lab to the office, minimizing lag and preventing data bottlenecks.
Continued investment in plant infrastructure and staff knowledge broadens what’s possible for (R)-4-Amino-3-(Naphthalen-1-Yl)Butanoic Acid, allowing even small-batch runs to enjoy the same oversight and reporting as multi-kilo lots. The push for greener chemistry influences choice of solvents and waste-handling—never at the expense of product consistency. While the world chases breakthroughs, we keep our focus on supporting those efforts with honest, transparent, and technically robust building blocks.
Over years in manufacturing, providing this compound has shown that attention to detail in synthesis, packaging, and support makes the critical difference. With every gram produced, we draw from experience, adapt to changing conditions, and uphold the trust that enables serious research to move forward.