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HS Code |
600493 |
| Product Name | Boc-3,3-Diphenyl-L-Alanine |
| Cas Number | 162870-09-3 |
| Molecular Formula | C20H21NO4 |
| Molecular Weight | 339.39 |
| Appearance | White to off-white powder |
| Purity | Typically ≥98% |
| Melting Point | 118-120°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Storage Temperature | 2-8°C |
| Iupac Name | (2S)-2-[(tert-butoxycarbonyl)amino]-3,3-diphenylpropanoic acid |
| Smiles | CC(C)(C)OC(=O)N[C@@H](C(=O)O)C(C1=CC=CC=C1)C2=CC=CC=C2 |
| Optical Rotation | [α]20/D +23° (c=1, MeOH) |
| Synonyms | N-Boc-3,3-diphenyl-L-alanine |
As an accredited Boc-3,3-Diphenyl-L-Alanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Boc-3,3-Diphenyl-L-Alanine is supplied in a sealed amber glass bottle, 5 grams, labeled with product name, quantity, and safety data. |
| Shipping | Boc-3,3-Diphenyl-L-Alanine is shipped in secure, airtight containers to protect from moisture and contamination. It is transported at ambient temperature, unless otherwise specified, and labeled according to chemical safety regulations. Appropriate hazard documentation and handling instructions are included to ensure safe transit and compliance with relevant shipping regulations. |
| Storage | Boc-3,3-Diphenyl-L-Alanine should be stored in a cool, dry, and well-ventilated area, protected from light and moisture. Keep the container tightly closed and stored at 2–8 °C (refrigerator conditions). Avoid sources of ignition and incompatible substances such as strong oxidizing agents. Ensure proper labeling and handling to prevent contamination or degradation of the chemical. |
Applications of Boc-3,3-Diphenyl-L-Alanine in Industrial ManufacturingBoc-3,3-Diphenyl-L-Alanine finds widespread adoption in industrial organic synthesis, particularly in peptide chemistry and pharmaceutical process routes, due to its unique chiral and sterically demanding backbone. As direct manufacturer, we supply this protected amino acid to leading downstream sectors where strict compliance, accurate dosing, and controlled integration are required for advanced intermediates and finished formulations. 1. Peptide API SynthesisPharmaceutical companies employ Boc-3,3-Diphenyl-L-Alanine in the multi-step synthesis of peptide drug candidates. Its bulky side chain and Boc protection support selective coupling and minimize racemization in solid-phase and solution-phase peptide assembly. Process chemists integrate it as a specialty building block, especially in the elongation stages for complex API structures involving non-natural amino acids. After deprotection and downstream purification, the finished peptide meets injectable or oral therapeutic standards. Industry compliance standards
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2. Development of Protease-Resistant Peptide TherapeuticsBiotech R&D and specialty pharma integrate Boc-3,3-Diphenyl-L-Alanine in designing peptide drugs where enhanced resistance to metabolic degradation is essential. Its pronounced steric shielding at the α-carbon delivers improved peptide half-life in vivo. Formulators introduce the protected amino acid at lab-scale during resin loading and later during clinical lot upscaling, ensuring batch-to-batch reproducibility and process traceability for regulatory documentation. Industry compliance standards
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3. Chiral Intermediate Sourcing for Asymmetric SynthesisManufacturers of advanced pharmaceutical intermediates employ Boc-3,3-Diphenyl-L-Alanine as a chiral pool substrate for further functionalization in asymmetric synthesis routes. Its conformational rigidity benefits stereoselective transformations, including amide bond formation and diazotization reactions, producing optically pure chiral amines and acids essential for high-value small molecule APIs. Production lines integrate this amino acid at the key transformation node, with careful solvent control and chiral analytics as per batch records. Industry compliance standards
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4. Modified Peptidomimetic Production for Drug DiscoveryContract research organizations and medicinal chemistry labs rely on Boc-3,3-Diphenyl-L-Alanine in the iterative synthesis of modified peptidomimetics, targeting enhanced receptor binding and proteolytic resistance. Integrated into secondary structure motifs such as β-turn inducers or helix stabilizers, it enables structure–activity relationship studies during library generation. Chemists monitor regulatory and intellectual property boundaries, using full traceable batch records from protected intermediate through to purified lead compounds. Industry compliance standards
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5. Custom Amino Acid Derivatives for Specialty Chemical SectorsProducers in the specialty chemicals industry utilize Boc-3,3-Diphenyl-L-Alanine as a precursor for developing non-proteinogenic amino acid derivatives incorporated into catalytic ligands, polymer additives, or as functional groups in advanced material applications. Reactive groups on the aromatic rings and steric bulk support bespoke compound synthesis for high-precision industrial uses, with rigorous batch documentation and full impurity profiling to meet downstream performance and safety criteria. Industry compliance standards
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Competitive Boc-3,3-Diphenyl-L-Alanine prices that fit your budget—flexible terms and customized quotes for every order.
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In our world of chemical synthesis, progress walks hand-in-hand with accuracy and purity. Every step counts, every atom matters. Some intermediates help us solve problems that stall research, while others quietly play critical roles in designing new compounds. Boc-3,3-Diphenyl-L-Alanine, also known as Boc-Dip-L-Ala, holds its ground in the toolkit of chemists tackling peptide chains with challenging motifs. For years, our facility has grown alongside the swelling needs for high-fidelity building blocks that drive pharmaceutical innovation, and this material remains among those staples genuinely tested by time and practical lab experience.
At its core, Boc-3,3-Diphenyl-L-Alanine is an amino acid derivative with a Boc (tert-butoxycarbonyl) protecting group. This structure opens doors for peptide chemists who want to install unique side-chain features into their sequences. The 3,3-diphenyl moiety sets it apart from standard alanine derivatives, giving rise to bulky, hydrophobic characteristics that influence folding, bioactivity, and binding affinity. We manufacture this compound in solid, crystalline form, with batch consistency reflecting real demands of process-scale chemistry.
Peptide synthesis relies on reliable reactants. Even small shifts in purity, moisture, or byproduct levels can disrupt cyclization or cause downstream impurities. Our own methods cut those risks: multiple crystallization steps follow the primary reaction to secure high-purity product, while we monitor residual solvents and ensure chiral integrity using trusted chromatographic techniques. Whether scaled for kilogram lots or supplied for research, our commitment to thoroughness comes from watching researchers in protein engineering, enzyme mimicry, and drug discovery put their trust in our reagents.
Handling Boc-3,3-Diphenyl-L-Alanine is straightforward: the powder dissolves cleanly in DMF, DCM, or acetonitrile, and peptide coupling protocols using EDC/HOBt or PyBOP move efficiently. Hard-won experience shows that impurities tracked back to inferior starting materials often crop up as troublesome shadows in analytical traces, so we chase these out at every step. As a result, even researchers pushing for clinical-grade peptides have circled back to our lots when lesser materials left them with analytical dead-ends or purification headaches.
Use of this amino acid in peptide design is not just about novelty. The bulky diphenyl group deeply influences conformational behavior, imparting stiffness and spatial restriction. This changes how peptides fold and interact with targets, sometimes sharpening receptor selectivity or improving resistance to enzymatic degradation. As a chemical manufacturer rooted in continual contact with medicinal chemists, we see these demands emerge not from academic curiosity alone, but practical aims—targeting proteases, mimicking protein-protein interfaces, or reinforcing bioactive helices in small, functional peptides. Many clients turn to us because they face similar synthetic bottlenecks: shelf-stable, high-purity intermediates that unlock new structural space.
Amping up production from grams to kilograms taught us where corner-cutting hurts downstream users. We standardize purity to exceed 98% by HPLC, maintain optical rotation above 99% of theoretical value for the L-enantiomer, and analyze each batch for residual heavy metals and volatile organics. Color, particle shape, and bulk density change little across multiple campaigns. It takes hands-on expertise to know how slight inconsistencies may come back to bite during process validation at a customer’s site, so we stay vigilant. We store finished lots in low-humidity chambers, pack in moisture-barrier bags, and provide spectral data with every shipment. Our investment in these procedures comes from pragmatic necessity, not regulatory checkboxing.
Clients sometimes ask how our Boc-3,3-Diphenyl-L-Alanine differs from what they have purchased elsewhere. Cost variations hold little value if the material misbehaves in their reactors or produces unexpected byproducts that soak up hours in purification columns. The key distinctions emerge from hands-on handling: ease of solubility, lack of crystalline fines, predictability in coupling yield, low batch-to-batch drift, and direct access to our technical team. As a manufacturer, our conversations don’t end with the invoice—we discuss loading ratios, resin compatibility, and real-world troubleshooting for solid-phase or solution-phase peptide assembly.
Working chemistry tells the difference. In contrast to unprotected 3,3-diphenylalanine—which can suffer from side reactions or instability—our Boc-protected variant handles exposure to common peptide coupling conditions without fuss. Fmoc-3,3-diphenyl-L-alanine, the other common protecting option, finds fans among those using Fmoc solid-phase platforms; yet, Boc offers greater flexibility for those who rely on acid-sensitive protocols or perform multi-step modifications where base lability would be a liability. Each protecting group carves out space for a particular strategy, and firsthand lab results guide these decisions more than generic literature. We see researchers switch back and forth based on project-specific needs rather than brand allegiance, because downstream results matter most.
Standard Boc-protected amino acids, such as Boc-L-alanine, miss the rigid, hydrophobic influence of the diphenyl group. This difference can determine whether new analogs exhibit potent biological activity or fall short of design goals. Peptide chemists value Boc-3,3-diphenyl-L-alanine’s steric impact in DNA-mimetic oligomers, foldamers, or when stabilizing β-turns. We field requests from teams aiming to replicate published results, and they frequently emphasize how lot purity and verified stereochemistry directly affect reproducibility. A string of unsolved chromatographic impurities can derail timelines or blunt painstaking structure-activity relationship studies. Our role as a direct producer is to cut down these headaches with careful stewardship over every step from raw materials to final packaging.
Research environments evolve. We’ve watched the shift toward automation in peptide synthesis, and even small process differences get amplified at scale. For industrial projects, a sluggish coupling step or troublesome filtration can introduce major inefficiencies. Our feedback loop from bench to production line lets us adapt: we gather real-world complaints and use them to refine drying methods, alter milling procedures for optimal particle size, and tweak purification regimens to maintain brightness and solubility. We invest in quality because we see the outcome not only in product, but in steady relationships with repeat customers.
Stable pricing goes hand-in-hand with predictable supply. While global events jostle logistics, this doesn’t excuse interruptions for those who rely on us for their process development milestones. Our raw material sources are vetted, and we keep safety stocks not just for contract obligations, but for a sense of reliability that our customers value. Over time, clients have pointed out saved days or weeks simply because their chemists didn’t have to rework mediocre lots or suffer preventable delays. These details, often overlooked in flashy brochures or reseller pages, drive our own pride of craft.
Making Boc-3,3-Diphenyl-L-Alanine at bench scale is relatively simple for one-off syntheses: secure the starting L-alanine, install the phenyl groups, then cap with Boc. Going larger exposes tricky issues. Side reactions threaten chiral purity, solvents need strict control, and even glassware becomes a critical variable. Our team’s greatest lessons stem from these scale-up hurdles—examining every step by TLC, NMR, and HPLC, monitoring for off-flavors in the odor of intermediates, training operators to look for subtle color shifts in crystals. Every customer who has been frustrated by something as subtle as a 0.5% drift in optical rotation knows the cost of unseen batch variation.
The other area where we provide real value lies in transparency. Customers often have to guess what went into their starting material. We openly share spectral prints, let visitors inspect processes, and accommodate special requests for custom lot parameters when necessary. This level of access simply does not exist in distribution-driven commerce. The result: fewer surprises, better alignment of expectations, and steady progress toward research goals. We don’t chase novelty for its own sake, but anchor each improvement to concrete customer insight.
Academic groups, pharmaceutical companies, and biotech startups look for reagents that solve both short-term needs and future scalability. Our interactions with project leaders reveal an appreciation for building blocks that confidently step from the 100 mg scale used for screening up to multi-gram and kilogram lots used in pre-clinical batches. For those engineering new peptide therapeutics or peptidomimetic architectures, 3,3-diphenylalanine’s geometry yields backbone conformations that can resist breakdown, change binding modes, or unlock new bioactive topologies. Projects in targeted drug delivery or next-generation antibiotics often require these features—sometimes dramatically boosting half-life, sometimes merely nudging a lead compound from ‘maybe’ to ‘yes’.
Our team has supplied Boc-3,3-diphenyl-L-alanine to groups working on peptide dendrimers, macrocycles, and synthetic antibodies. This sort of cross-pollination of methods sharpens our own expertise, driving iterations that improve both the product and the service around it. Where off-the-shelf reagents may fall short—such as batch contamination, unpredictable crystallization, or frequent handling issues—we adjust, absorb feedback, and design process tweaks to keep ahead of expectations.
Every experienced chemist knows that product quality goes beyond a purity number on a piece of paper. It’s the way a powder pours, the absence of lingering odor, the sharp melting point, the consistency in chromatography peaks, and the ease of redissolution as reactions scale. We select raw materials through rigorous assessments, separate impurity fractions with analytic finesse, and safeguard stereochemistry with double redundancy in our checks. Our technical backup gives customers peace of mind—questions get direct, informed answers rather than sales pitches. For years, this has meant more than a fleeting competitive edge; it has laid a foundation of trust.
We’ve heard accounts of how even small residual levels of unwanted side-products can wreak havoc with peptide purity. Sensitized to these risks, our protocols favor overkill in purification: running an extra chromatographic pass, extending a crystallization soak, or re-testing samples after simulated storage scenarios. Customers often return with their own HPLC data, confirming or challenging our claims. We see these dialogues not as criticism, but as partnership—a two-way improvement channel that strengthens both sides.
Sustainable chemistry is not a buzzword here, but a framework for real improvement. Waste minimization, solvent recycling, and strict energy use controls pepper all our production campaigns. Staff receive routine hazard and waste handling refresher training—even for seemingly benign solids like Boc-3,3-diphenyl-L-alanine—because good habits prevent incidents. In consultation with environmental chemists, we’ve swapped out some harsher reagents, reduced isolated yields from post-use materials, and continually retrofit our waste lines with improved sensing equipment.
Safety data accompanies every shipment, not because regulations require it, but because customers appreciate transparency and actionable information. Our own facility has lived through batch spill events, process upsets, and recovery plans that taught hard-won lessons in chemical stewardship. This approach carries into everything we do, from delivery vehicles to documentation practices, shaping a culture that supports both our staff and the customers relying on us.
A real partnership in synthetic chemistry emerges from upfront honesty, rapid response to technical questions, and a nimble approach to evolving demands. We’ve watched clients grow from academic labs to commercial pilot facilities. Some come to us at the 11th hour, stumbling over unreliable shipments or tricky quality setbacks elsewhere. The most common question is: “Can you help make this work in our process?” The answer takes more than shipping a drum of material—it involves dissecting exactly what reaction conditions, solvents, and coupling agents are in use, and sometimes performing side-by-side runs at our own benches to troubleshoot together.
Product documentation flows from experience. We don’t just list numbers; we share observations from actual coupling trials, prepare tips for dissolving, and caution on routes that have proven problematic during scale-up. For Boc-3,3-diphenyl-L-alanine, subtle details like order of reagent addition, solution pH, and agitation rates matter more than brochure copy. The only way to support users is to remain in conversation: take their feedback, examine failed runs, review missed yield, and steadily improve. Our biggest wins come when we help a project move past a sticking point and the customer circles back for the next challenge, not just the next purchase.
Producing Boc-3,3-diphenyl-L-alanine means more to us than moving product from one bin to another. Each batch is the culmination of hard work, lessons learned from mishaps, and direct connections with those pushing boundaries in modern peptide science. Our approach—steady technical improvement, honest dialogue about performance, and transparent sharing of methods—shapes better results, both for our operation and those we serve. New collaborations, emerging methodologies, and continual learning all carry forward in the quality of what leaves our doors. The story of Boc-3,3-diphenyl-L-alanine doesn’t end in a drum or bottle; it travels forward in every discovery it makes possible.