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Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid

    • Product Name Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid
    • Alias (R)-Boc-3-Amino-4-(3-methylphenyl)butyric acid
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    210492

    Product Name Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid
    Cas Number 173352-49-9
    Molecular Formula C16H23NO4
    Molecular Weight 293.36 g/mol
    Appearance White to off-white solid
    Purity Typically >98%
    Smiles CC1=CC(=CC=C1)C[C@H](N)CC(=O)O
    Protecting Group Boc (tert-butoxycarbonyl)
    Optical Activity (R)-configuration (chiral center present)
    Solubility Soluble in DMSO, DMF, methanol

    As an accredited Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque screw-cap bottle labeled “Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid, 25g,” with lot number and hazard warnings.
    Shipping Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid is shipped in sealed, chemical-resistant containers under ambient or refrigerated conditions as required. Packages are clearly labeled and handled in compliance with local regulations for non-hazardous organic compounds, ensuring product stability and safety during transit. Shipping documentation accompanies all orders for traceability.
    Storage Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid should be stored in a cool, dry, and well-ventilated area, away from sources of moisture and direct sunlight. Keep the container tightly closed and store at 2–8°C (refrigerated) to ensure stability. Avoid exposure to incompatible substances such as strong oxidizers, acids, or bases. Store under an inert atmosphere if long-term stability is required.
    Application of Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid

    Applications of Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid in Industrial Manufacturing

    Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid serves as a specialized chiral building block for pharmaceutical, peptide synthesis, API manufacturing, and chemical research sectors. As a manufacturer, we support customers in meeting regulatory, formulation, and performance requirements across their industrial value chains.

    1. Chiral Intermediate in Small Molecule API Synthesis

    Pharmaceutical manufacturers use the raw material as a protected chiral amine intermediate for enantioselective synthesis in non-beta lactam small molecule APIs. The Boc-protected structure enables precise amide bond formation, crucial for active pharmaceutical ingredients requiring stereochemical integrity. Production lines implement multi-step API routes where this intermediate influences purity and batch consistency.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA GMP)
    • European Pharmacopoeia monographs
    • USP General Chapter <1078> GMPs for Bulk Pharmaceutical Excipients (as applicable to intermediates)

    Typical usage ratio

    • 0.5–1.2 molar equivalents per target API molecule, adjusted for route design and chiral purity requirements

    Downstream process integration

    • Introduced during protected amine-coupling stage in API synthesis; deprotection and further derivatization follow custom route steps

    Final product types

    • Chiral antihypertensive agents
    • Antiviral intermediates
    • Non-beta lactam therapeutic APIs
    • Pipeline drug candidates for CNS disorders

    2. Protected Amino Acid for Peptide Synthesis

    Custom peptide manufacturers leverage this material for introducing rigid chiral side chains during stepwise solid-phase peptide synthesis (SPPS) and solution-phase coupling. Its sterically protected amine assists in minimizing racemization and enhancing sequence fidelity, supporting the creation of high-purity research peptides and peptide-based drug candidates.

    Industry compliance standards

    • ICH Q11 Development and Manufacture of Drug Substances
    • EP 2.6.1 Identification Tests for Amino Acids
    • ICH Q3A Impurities in New Drug Substances
    • ISO 9001:2015 for peptide manufacturing processes

    Typical usage ratio

    • 1.0 equivalent per side-chain-modified residue, relevant to sequence design and target coupling efficiency

    Downstream process integration

    • Loaded onto resin or added in coupling solution during peptide chain elongation; Boc deprotection precedes linkage to next residue

    Final product types

    • Synthetic peptide APIs
    • Bioconjugate precursors
    • Peptide reference standards
    • Therapeutic peptide candidates

    3. Intermediate for Custom Chemical Research and Lead Optimization

    CROs and pharmaceutical research labs employ this protected amino acid during hit-to-lead and lead optimization projects that require enantiomerically pure amine precursors with defined aromatic substitution. Rapid scale-up batches demand high chemical purity and consistent stereochemistry for downstream reaction scouting and novel scaffold construction.

    Industry compliance standards

    • OECD GLP (Good Laboratory Practice) for research intermediates
    • REACH registered substances (as applicable in EU chemical research services)
    • ISO/IEC 17025 for laboratory reagents
    • GMP only for non-clinical or preclinical process R&D, if scaled for clinical candidate production

    Typical usage ratio

    • Variable, typically 0.1–2.0 equivalents per reaction, guided by experimental protocol and synthetic target

    Downstream process integration

    • Added at chiral amine installation steps or used for rapid analog library synthesis during medicinal chemistry productivity cycles

    Final product types

    • Chiral libraries for SAR (Structure–Activity Relationship) studies
    • Screening fragments for drug discovery
    • Custom chemical intermediates for academic or industrial R&D
    • Non-cGMP project samples

    4. Building Block for Specialty Fine Chemicals

    Producers of advanced intermediates and specialty chemicals integrate Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid as a core element for constructing N-protected, aryl functionalized molecules required in catalog chemical production. Applications center on customizing scaffolds with unique steric and stereoelectronic profiles demanded by high-value fine chemical markets.

    Industry compliance standards

    • ISO 9001:2015 certification for fine chemicals manufacturing
    • Chemical industry Responsible Care® programs
    • REACH pre-registration for commercialized, notifiable substances in the EU
    • Annual company-specific quality audits for catalog suppliers

    Typical usage ratio

    • 0.2–1.0 part per part of target molecule, adjusted based on reaction yield optimization in batch or flow processes

    Downstream process integration

    • Feeds into multi-step aryl amination, asymmetric reductions, or custom condensation reactions within fine chemical batch reactors

    Final product types

    • N-protected specialty building blocks
    • Functional aryl intermediates for proprietary catalogs
    • Platform molecules for further synthetic elaboration
    • Tool compounds for advanced chemical biology
    Free Quote

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    Certification & Compliance
    More Introduction

    Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid: Reliable Chiral Building Block for Peptide Synthesis

    Rooted in Real Manufacturing

    Manufacturing Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid takes specialized expertise beyond standard amino acid chemistry. As a direct producer, we approach each batch through an established flow, starting with high-purity starting materials and quality-controlled steps at every stage. Having produced this Boc-protected amino acid for many years, we understand both the technical demands and the opportunities it brings to biopharma R&D and custom synthesis.

    With years in custom amino acid synthesis, we've built our reputation on consistency at every scale. Customers who work closely with us often say they notice the lack of batch-to-batch deviations in chiral purity or moisture content – something we've prioritized since switching to more selective crystallization and drying processes. Researchers need steady and predictable raw materials, especially for medicinal chemistry work, and our hands-on approach removes the uncertainty that comes from spot buying or relying on less rigorous sources.

    Specifications and Physical Qualities That Matter in the Lab

    Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid, or (R)-Boc-AMBA, contains a tert-butyloxycarbonyl (Boc) group to protect the amine during coupling reactions, while the (R) configuration at the alpha carbon preserves the stereochemistry critical in active pharmaceutical ingredients. We produce this compound as a white to off-white crystalline powder. Most lots fall within a narrow melting point range, reflecting uniformity in molecular structure and minimization of isomeric impurities.

    Product quality goes beyond purity on paper. Each batch receives full chiral HPLC analysis, because even minor enantiomeric contamination causes headaches downstream. Our established process delivers >99% chiral purity consistently. Water content remains low, typically under 0.5% as confirmed by Karl Fischer titration. In our experience, residual solvent risks drop sharply using our modern vacuum drying set-up. Any trace metals or inorganic residues are checked through elemental analysis when required for protocols downstream.

    Gram to kilogram batches respond faithfully to similar reaction conditions during peptide bond formation. We've spoken with scientists in drug discovery, diagnostic peptide synthesis, and enzyme mechanism studies. What stands out most in lab feedback is predictable coupling efficiency. Controlling impurities such as unprotected amino acid or over-alkylated analogs gives real improvements in yield. Our fully documented production history reinforces that consistency.

    Understanding Usage in Peptide and Small-Molecule Synthesis

    Chemists reach for Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid because it brings together chirality, aromatic character, and a protected amino group. As part of a solid-phase peptide synthesis route, it provides the chiral backbone and extra rigidity to help peptides mimic natural biological targets or block degradation by peptidases. This compound fits well in medicinal chemistry, where subtle changes to side chains tune activity and pharmacokinetics.

    Our direct interactions with peptide scientists and medicinal chemists inform our perspective on why (R)-Boc-AMBA is valued. The presence of the 3-methylphenyl group elevates binding affinity in certain ligands without pushing solubility below usable thresholds. Additionally, the acid’s carboxy group is receptive to coupling with activating reagents across different solid supports—Wang resin, Rink amide resin, and others. The Boc group releases under mild acid conditions, making deprotection straightforward.

    Lab teams synthesizing SAR analogs, macrocycles, or peptidomimetics count on prompt access to both small and mid-size lots. We provide tailored packaging and rapid shipment, so rare supply interruptions don’t stall research. Often, customers draw comparisons to less refined sources; feedback points to easier coupling, fewer chromatographic separations, and less need for intensive purification with our product in the synthetic pipeline.

    Differences that Set This Compound Apart

    Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid fills a set of requirements not all Boc-amino acids match. From hands-on process control, we've learned that minor changes to the aryl ring—such as moving the methyl group to a different position—affect reactivity and steric hindrance in coupling reactions. Unlike common amino acid derivatives that might lack aromaticity or specific substitutions, the 3-methylphenyl unit grants both rigidity and hydrophobicity, often sought in the design of non-natural peptides or inhibitors.

    As a manufacturer, we’ve compared our (R)-Boc-AMBA head-to-head with (S)-enantiomers and analogs missing the Boc protection. Results from direct user feedback reveal more efficient downstream deprotection, less racemization during peptide synthesis, and smoother transitions between solvents—a meaningful boost in process reliability. Medicinal chemists highlight improved selectivity in enzyme inhibition assays and a higher hit rate in fragment-based screening compared to bland, aliphatic derivatives.

    The Importance of Stereochemistry and Protection

    In an era where chiral purity and reliable side chain protection can decide the success or failure of a synthetic route, we approach Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid formulations with a focus on process reproducibility. We found that diastereomeric impurities easily propagate through synthetic cascades, especially in automated or combinatorial work. Our close attention to stereochemical control—maintained from raw materials through isolation—limits costly reruns and troubleshooting for scientists under tight timelines.

    Peptide assembly lines and custom fragmentation strategies rest on the fact that the Boc group strips away under standard TFA conditions, allowing introduction of further modifications or linkers without side reactions. We see less incidence of over-alkylation or deprotection artifacts compared to Fmoc-protected analogues, especially in longer or sterically demanding peptides. This insight comes from hundreds of successful syntheses and troubleshooting calls with customers running automated solid-phase equipment.

    Process Improvements for Reliable Supply

    Consistency in Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid doesn’t spring from luck; it relies on tight production discipline. Over the years, we replaced some classical purification methods with high-efficiency crystallization, letting us tune both yield and product homogeneity. On-site analytical assessment—rather than offloading to third-party labs—lets us catch deviations immediately. Such hands-on adjustments mean that specification drift, which can slip through in contract-manufactured lots, becomes nearly impossible here.

    Investments in modern reactor controls, solvent recovery, and material handling guarantee that scale-up doesn’t introduce unexpected variance. Multiple chiral center checks, along with routine process validation, keep quality stable whether researchers order grams or multi-kg quantities. Years of scale-up data show our approach avoids common pitfalls—random racemization, unexpected isomer formation, and particulate contamination—that can plague less-controlled supply chains.

    Supporting Advanced Research and Discovery

    With the steady demand from biopharma innovators, we notice that Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid finds roles anywhere structure and function matter. Ligand design for GPCR screening, optimization of peptidomimetic scaffolds, or fine-tuning ADME properties in drug candidates—each scenario benefits from the extra level of predictability and chiral stability. Teams working in next-generation therapeutics, including targeted payload delivery, IVF adjuvants, and even agrochemical research, regularly find new uses for this distinctly substituted amino acid.

    We’ve worked shoulder-to-shoulder with scientists developing high-throughput screening libraries, where reagent and intermediate consistency cuts weeks from timelines. In one project, the transition from an inconsistent external source to our material resulted in fewer purification cycles and higher final yields for a neuroactive macrocycle series—the cumulative effect became clear in both cost savings and research progress.

    Direct Feedback from Real-World Synthesis

    Our technical team receives steady updates from the field. Troubleshooting requests often come when a project stalls due to subtle quality dips in critical starting materials. Trouble spots include shifts in HPLC retention, new unknown peaks, or erratic reaction yields. By analyzing returned samples and comparing them against our robust production history, we help end users track down root causes—often highlighting the importance of steady, fully traceable manufacturing.

    Feedback cycles create a two-way street. We actively update production protocols when lab data or applications suggest room for improvement. In one case, after speaking with a university group focused on NHS ester conjugations, we tailored an anhydrous packaging format that ensured optimal reactivity for difficult couplings. Direct support allows customers to move faster, tackle new synthetic targets, and avoid the frustration common with impersonal suppliers.

    Why Knowledge Direct from Manufacturer Matters

    Many sources claim to offer Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid, but only a hands-on manufacturer develops the experience needed to resolve emerging issues—solvent compatibility, storage longevity, and new synthetic demands. In conversations with procurement and R&D, common complaints about non-manufacturer sources center on missing documents, lack of real traceability, or unpredictable lead times. Every batch we supply comes from a lot we oversaw directly—end-to-end records, real-time analytical data, and custom support enable research teams to keep momentum, regardless of project changes or regulatory requirements.

    By investing in our production process and building strong feedback loops with the synthetic community, we deliver more than just chemical material. We deliver peace of mind, knowing each unit meets a shared standard for reliability, quality, and integrity.

    Solutions to Challenges in Custom Synthesis

    Chemists request Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid with specific requirements for solvent content, particle size, or chiral excess, tied to their unique workflows or regulatory filings. We help by offering tailored lots—whenever feasible—to avoid delays in scale-up, regulatory submission, or pilot-stage validation. Building these protocols demands real-world production experience, including the ability to control and document subtle analytical parameters for specialized users.

    Through years of supporting early-stage drug projects, we’ve seen the cost of inconsistent raw materials. Missed timelines, extra purification campaigns, and stalled patents emphasize the role of traceable, consistent supply. To address these pain points, we run stability studies, stress testing, and proactive release checks for every major customer segment. By tracking storage, moisture ingress, and long-term packaging trends, we cut down on last-minute surprises, supporting programs from synthesis through process development and QC approval.

    Traceability and Regulatory Readiness

    Today’s regulatory environment for pharmaceutical intermediates and peptide starting materials expects more than simple certificates of analysis. We provide complete documentation on origin, analytical data, and full material traceability. Our ability to share real manufacturing records proves especially important for IND-enabling research or cGMP-related project launches. Long-term customers tell us this level of transparency streamlines tech transfer, supports regulatory audits, and saves management time.

    Beyond documentation, we respect the evolving landscape in pharmaceutical and biotech R&D. As more researchers innovate around new indications or dosing regimens, being able to guarantee chiral stability and trace impurity profiles becomes a key asset. Direct manufacturer involvement shortens lines of communication—no waiting for intermediary responses, no conflicting analytical reports, just answers and support direct from the source.

    Continuous Improvement Through Scientific Collaboration

    Innovation does not stand still. As new synthetic strategies develop in academia and industry, so do requests for modified or improved forms of Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid. We pursue collaborations with both established partners and newer biotech startups, supporting process tweaks, access to reference standards, or impurities for analytical work. These interactions help us anticipate future trends and maintain high standards, driven by real user needs.

    Practical improvements—such as more inert packaging, further reduction in residual solvents, or extra chiral purity checks—stem from close ties to customers who push the limits of chemical synthesis. Like the time we responded to a surge in demand for water-free lots amid a wave of solid-phase resin compatibility studies, scaling up with no loss in product integrity or reactivity.

    Why We Continue to Invest in Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid

    The market for tailored chiral building blocks never stands still. As treatments become more targeted and research more sophisticated, solid, reproducible supply of advanced Boc-protected amino acids forms a cornerstone of drug and diagnostic innovation. By offering full production oversight, analytical support, and direct partnership, we make Boc-(R)-3-Amino-4-(3-Methyl-Phenyl)-Butyric Acid not just a product, but a solution trusted by medicinal chemists and synthesis experts worldwide.

    Drawing on operational knowledge, direct analytical insight, and ongoing dialogue with the scientific community, we commit to supporting new methods, troubleshooting real problems, and delivering uncompromised material batch after batch. At the end of the day, the success of any research lab, pilot plant, or scale-up depends on materials that perform exactly as needed—with no surprises, no unnecessary delays, and unwavering quality. In our experience, this is the difference that defines true manufacturing leadership.