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HS Code |
621093 |
| Productname | Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid |
| Casnumber | 1346568-64-2 |
| Molecularformula | C16H20F3NO4 |
| Molecularweight | 347.33 |
| Appearance | White to off-white solid |
| Purity | ≥98% |
| Meltingpoint | 110-115°C |
| Solubility | Soluble in DMSO, methanol |
| Storagetemperature | 2-8°C |
| Opticalactivity | [α]D +15 to +25° (c=1, MeOH) |
| Smiles | CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C(F)(F)F)C=C1)C(=O)O |
| Inchikey | LFDMSISWNFUSHF-LBPRGKRZSA-N |
As an accredited Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle, sealed with a white screw cap, labeled with compound details. Contains 5 grams of Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid. |
| Shipping | **Shipping Description:** Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid is shipped in tightly sealed containers to prevent contamination and moisture absorption. It is transported under ambient conditions unless otherwise specified, compliant with standard chemical shipping regulations. Ensure proper labeling and documentation for safe and efficient handling during transit. Not classified as hazardous for transport. |
| Storage | **Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid** should be stored in a tightly sealed container, protected from moisture and light. Keep at 2-8 °C (refrigerated) in a dry, well-ventilated area. Avoid exposure to heat, oxidizing agents, and acids. Ensure container is properly labeled, and access is restricted to trained personnel. Follow all relevant safety and storage guidelines. |
Applications of Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid in Industrial ManufacturingBoc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid serves as a key intermediate in the precision synthesis of pharmaceuticals and related advanced compounds. Our years of production experience and technical collaboration with active pharmaceutical ingredient (API) manufacturers ensure that this material meets stringent downstream requirements across several advanced synthesis routes. Below, we present dedicated application scenarios based on established industry uses. 1. Chiral Intermediate in Protease Inhibitor SynthesisSeveral global pharmaceutical companies integrate this compound as a chiral building block for the synthesis of protease inhibitors, including next-generation antiviral APIs. The reliable stereochemical configuration and the stability of the Boc-protected amino group support efficient peptide coupling steps in their multi-step production campaigns, especially under large-scale cGMP conditions. Industry compliance standards
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2. Stereoselective Intermediate for CNS Active Pharmaceutical IngredientsLeading specialty pharmaceutical manufacturers employ this compound in the multi-stage synthesis of central nervous system (CNS) agents where the introduction of a trifluoromethyl-phenyl group is required for receptor binding specificity. The Boc group maintains integrity throughout harsh reaction conditions needed for key coupling reactions, minimizing racemization and optimizing throughput. Industry compliance standards
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3. Core Building Block for Peptidomimetic Research ReagentsResearch reagent manufacturers utilize this product as a core protected amino acid for the solid-phase synthesis of non-natural peptidomimetics. The molecule’s trifluoromethyl-substituted aromatic ring is crucial for introducing hydrophobicity and metabolic resistance in experimental peptide analogs produced for in vitro drug discovery and lead optimization. Industry compliance standards
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4. Intermediate for Custom Synthesis of Fluorinated Amino Acid MonomersAdvanced chemical companies synthesize functionalized, fluorine-containing monomers for high-performance polymer and specialty material R&D using this compound as a key intermediate. The Boc group allows selective transformation and late-stage modification while protecting the reactive amino group throughout multiple synthetic operations involving strong bases or electrophiles. Industry compliance standards
Typical usage ratio
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Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid stands as a reliable component for advanced synthesis in the pharmaceutical and fine chemical industry. Our hands-on experience, day in and day out, connects us directly with the transformations, challenges, and nuanced behaviors of this building block. This product, with the model identifier CAS 69895-10-9, is crafted to serve researchers, chemists, and process engineers who expect consistency and clarity from each batch they handle.
Producing Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid is never a task for surface-level chemistry. Our process takes steric specificity and purity seriously, focusing on keeping the (S)-enantiomer intact at every checkpoint. The Boc protection guards the amino group, making this compound suitable for multi-step peptide or pharmaceutical syntheses without risking side reactions or tedious purification stages.
Our production pairs decades of technical know-how with monitoring at each step, from selection of raw stock to the final isolation and packaging. This compound consistently displays a white to off-white solid appearance, with HPLC showing purity above 98%. Moisture and residual solvents present risks; strict drying and inert atmosphere packing habits minimize those uncertainties.
Many labs and process engineers notice subtle but critical changes between batches of specialty amino acids. From our vantage point behind every batch, physical contaminants, stereochemical drift, and minor side-products can threaten both research and scale-up production. We’ve committed to tight control over stereochemistry, so the (S)-form remains dominant batch after batch, with optical rotation and chiral HPLC validation on every lot.
Boc-protected analogs can often display batch-dependent lability, manifesting as foam, tackiness, or unwanted discoloration. Our procedure addresses these pitfalls, employing mild workups and low-temperature stages to foster sharp crystallinity and reduce hydrolysis risks. Seasoned chemists know the cost of dusting off unstable intermediates; for this compound, reliable shelf life and physical stability translate directly to project timelines and confidence at the bench.
Our team has spent years refining the trifluoromethylation step, a process notorious for creating exothermic, difficult-to-reproduce outcomes. We use staged addition and gentle solvent selection, which helps suppress unwanted side-products and ensures a reproducible trifluoromethyl signature on the aromatic ring—too often the weakest link in generic commercial routes.
Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid usually finds a home in the world of peptide drug development and medicinal chemistry. Pharmaceutical researchers pick this product for constructing analogs that improve metabolic stability, alter substrate selectivity, or drive binding affinity studies. Its unique combination of a Boc-protected amine and trifluoromethyl-moiety opens doors to custom peptidomimetic building, targeting disease pathways with improved pharmacokinetics.
From our workshop, the daily conversations with customers revolve around reliability: Does the product dissolve consistently in common organic solvents? Will it stand up to coupling conditions with peptide activation agents? Our QC group regularly tests for solubility in DMF, DCM, and even acetonitrile, making sure that tight timeframes and complex synthetic designs can proceed without hesitation. That approach has minimized the “trial-and-error” cycles researchers often face with off-brand alternatives.
Down in pilot plants and kilo-lab settings, technicians bring up a series of practical concerns: smooth filtration, easy extraction, minimal waste, and predictable yields. We have spent years responding to these points. In our experience, keeping trace metals and residual mineral acids out of the product matters as much as enantiomeric excess, especially with scale-up production. Impurity carryover, once overlooked, has become a central attribute in our internal checks, reducing headaches for downstream process validation and regulatory filings.
Manufacturing specialty building blocks looks straightforward on paper; in practice, every batch throws up new surprises. In one memorable scale-up run, a slight drift in reagent supplier resulted in a faintly yellow product and lower-than-usual melting point. Through a series of analytical checks—NMR, LC-MS, and IR—our team pinpointed a minute overreaction during trifluoroacetylation, affecting just one lot but nearly derailing a customer’s regulatory filing. After this experience, we integrated additional QC checkpoints and doubled back on raw material traceability. These lessons have sharpened the way we handle change control, preventing similar issues for every kilogram since.
Real improvements often come from the floor, where operators notice subtle shifts in filtration rates or spot persistent traces in waste streams. Consulting with end-users, we realized a certain solid form led to losses during phase transfer steps. Tweaks in recrystallization yield a slightly larger crystal habit, reducing dusting and making for easier handling at the next stage. Sharing these lessons with our partners builds trust, and detailed feedback loops translate to worthwhile gains for research timelines outside our walls.
Working at the intersection of scale-up chemistry and environmental responsibility, our team takes solvent selection, waste minimization, and operator safety seriously. Each batch of Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid leaves the plant with a full record of solvent recovery rates and critical process parameters. That transparency builds trust with regulatory partners and environmental audits.
Handling trifluoromethylated moieties demands careful air-handling and proper personal protective equipment—volatiles and fine powders can become issues quickly. We keep dust exposure low and train all shift teams on best practices, minimizing both acute and chronic risks. Our solvent recovery routines pull double duty: cutting costs and reducing our site’s emissions.
Feedback from the user side often highlights the need for manageable waste handling, especially during downstream processing or Boc-deprotection. Our R&D chemists continue to refine procedures to minimize salt build-up and aqueous waste, knowing that lab and plant teams both benefit from easier compliance work.
Every order for Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid draws on a deep technical back-and-forth between our team and the chemists at the bench. We don’t just pack the drums and send them off; our support team helps consult on process bottlenecks, solubility tweaks, purification choices, and even alternate coupling methodology. We never treat these as off-the-shelf widgets—each order is a request for technical experience as much as for material.
Synthesis rarely follows a straight path. Several customers have tackled unique peptide designs, only to realize that alternate coupling agents or protective group regimes shake up solubility or compatibility profiles. Our technical staff shares data and practical notes from real-world experiences, giving synthetic chemists the details they need to keep projects on track. By keeping open communication, we bridge the gap from raw material production all the way to active pharmaceutical ingredient synthesis.
Analytical support backs up our technical work. Each batch leaves the site with full spectroscopic and chromatographic documentation, and our specialists remain available to interpret tricky spectra or support custom method development.
A quick search reveals a marketplace filled with dozens of specialty amino acid manufacturers and resellers. The differences rarely come down to price alone. In our experience, the source and the technical backbone supporting a given product line make up most of the value. For Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid, physical characteristics, impurity profiles, and post-shipment follow-through deliver far more than simple specification sheets ever can.
Resellers and traders too often work from third-hand stock, lacking connections to process tweaks and material origin. We keep each production batch linked directly to experienced chemists, not just machines. That chain of accountability matters when a deviation appears or a project faces an unexpectedly tight timeline. First-hand manufacturing means data sharing, open technical dialogue, and a voice at the table if a reformulation or additional testing phase comes up.
Production sites and workflow matter more than ever in the wake of tightening compliance standards worldwide. We’ve adapted batch records, operator training, and analytical standards to match the expectations of both established multinationals and local regulatory authorities. That groundwork hasn’t come easily. Analytical validation, documentation of every critical processing step, and full traceability keep us on the right path and support users preparing regulatory submissions of their own.
Our analytical teams keep pace with developments in impurity profiling, focusing on the kind of detail demanded in current good manufacturing practices and modern documentation. The fine points—chiral excess, heavy metal residues, and residual solvent content—receive ongoing monitoring and reporting, so project teams can make informed decisions before launching downstream campaigns.
Reliable sourcing only grows more valuable in a world beset by logistics turbulence and global supply shocks. We maintain close partnerships with raw material producers and shipping partners, staying ahead of shortages and delays. That hands-on involvement with both upstream and downstream partners means tighter scheduling, a lower risk of lost shipments, and better real-time response to any hiccups that appear.
The manufacturing cycle for advanced building blocks like Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid plays out over weeks, not just days. We keep safety stock on hand, buffer capacity, and raw materials in reserve, smoothing out the surprise outages that can upend R&D or project launches. These practical measures arise from direct experience, not just planning.
Peptide synthesis often acts as a proving ground for advanced amino acid analogues. The (S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid core brings together backbone versatility and medicinal chemistry flexibility. We’ve seen medicinal chemists and process development teams use our product to introduce new ligand scaffolds, boost bioavailability, or build resistance into metabolic breakdown pathways.
Our technical team has supported researchers adapting Boc-deprotection steps for both classic acidolysis and milder condition regimes, balancing speed with functional group compatibility. The Boc group survives a wide range of coupling agents, and the trifluoromethyl-phenyl substituent brings added electron-withdrawing capability and hydrophobic bulk, shifting bioactivity where simple phenylalanine analogues cannot.
Drawing from project feedback, the ease of incorporating this product into both solid-phase and solution-phase peptide synthesis matters as much as purity. We keep the lot-to-lot variation narrow, making repeat runs or scale-up smoother. Success for us is measured by fewer failed syntheses and more straightforward downstream purifications, as shared by our customers after months of project work.
Challenges in specialty amino acid manufacturing rarely disappear. The cost and environmental impact of fluoro-organic chemistry calls for ongoing innovation in waste minimization, solvent recycling, and greener processing. We sponsor in-house R&D that cuts reaction steps, reduces high-boiling solvent loads, and adopts safer alternatives wherever possible.
Early trials with new trifluoromethylation chemistries—looking past traditional metalation for milder catalytic regimes—show promise, though scale and reproducibility remain hurdles. We invite feedback from users willing to try novel procedures, closing the gap between bench-scale innovation and larger-volume production. By keeping the dialogue open, we see future tweaks to product profile, sustainability, and even regulatory standing.
Producing Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid in-house puts us closest to every advantage and every challenge—direct responsibility for every kilogram. Being on-site means responding quickly to quality issues, learning from every setback, and continuously tweaking the process in response to customer feedback and regulatory shifts. Over years of direct involvement, we’ve built a product that serves not just as a chemical entity, but as a combination of reliable performance, useful technical exchange, and an open line for continuous improvement.
Working from base chemicals to finished product, our staff sees every aspect: reaction hazards, purity rollercoasters, and the all-important handoff to the end user. That experience sharpens our commitment to more than just checkboxes—it means staying available when project launches approach and post-launch questions pop up at unexpected hours. We believe first-hand manufacturing isn’t just about higher quality; it’s about a partnership that endures and supports innovation across the entire research and production chain.
Every kilogram of Boc-(S)-3-Amino-4-(4-Trifluoromethyl-Phenyl)-Butyric Acid that leaves our site reflects years of technical expertise, constant refinement, and daily attention from chemists viewing the process up-close. The result is more than just a white powder. We deliver certainty in stereochemistry, performance in synthesis, and a dedication to technical partnership. The difference comes not from slogans, but from the daily conversations with scientists, engineers, and project leaders, and the lessons taken directly from the production floor. For anyone needing advanced building blocks capable of supporting research, scale-up, and real-world innovation, our team stands ready with product and experience in equal measure.