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Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid

    • Product Name Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid
    • Alias Boc-D-FPhe-OH
    • Einecs 848651-05-0
    • 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
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    Specifications

    HS Code

    719333

    Product Name Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid
    Cas Number 1173021-24-1
    Molecular Formula C14H18FNO4
    Molecular Weight 283.30
    Purity ≥98%
    Appearance White to off-white solid
    Melting Point 112-116°C
    Solubility Soluble in DMSO and methanol
    Optical Activity [α]D20 +7° (c=1, MeOH)
    Storage Temperature 2-8°C
    Protecting Group Boc (tert-butoxycarbonyl)
    Chirality (R)-enantiomer
    Smiles CC(C)(C)OC(=O)N[C@@](CC1=CC=C(C=C1)F)(C(=O)O)H

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

    Packing & Storage
    Packing White, tightly sealed HDPE bottle labeled "Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid, 25g," with hazard and lot information.
    Shipping Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid is shipped in a secure, airtight container to prevent moisture and contamination. It is typically handled as a non-hazardous substance but should be shipped with standard chemical safety protocols, avoiding extreme temperatures and direct sunlight. Shipping complies with all relevant regulatory guidelines.
    Storage **Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid** should be stored in a tightly sealed container under cool, dry conditions, ideally at 2–8°C (refrigerated). Protect from light, moisture, and sources of ignition. Store in a well-ventilated area and keep away from incompatible substances such as strong oxidizing agents. Use appropriate personal protective equipment when handling.
    Application of Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid

    Applications of Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid in Industrial Manufacturing

    Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid serves as a critical chiral intermediate in various industrial fields. Our manufacturing team supplies this raw material to pharmaceutical, peptide synthesis, agrochemical, new chemical entity (NCE) R&D, and specialty chemical producers. Below, we outline real application pathways, technical requirements, processing approaches, and examples of final downstream products.

    1. Chiral Pharmaceutical API Synthesis

    This intermediate supports asymmetric synthesis in the development of active pharmaceutical ingredients (APIs), particularly in producing chiral β-amino acid derivatives for antidiabetic, CNS, or oncology pipeline drugs. Pharmaceutical manufacturing relies on this material for introducing a fluorinated phenyl moiety with precise stereochemistry, supporting structure–activity optimization and patent protection in small-molecule APIs.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredients
    • USP, EP, JP monograph compliance for specific APIs
    • FDA 21 CFR 210/211 for finished drug manufacturing
    • Quality oversight under cGMP with traceability and impurity profiling

    Typical usage ratio

    • Custom synthesis: 1–1.5 molar equivalents per downstream chiral center
    • Final API step: 10–35% w/w in synthesis mixtures, adjusted for yield and target molecule design
    • Micro-scale development: variable, determined by route screening

    Downstream process integration

    • Introduced after critical resolution or protection group strategy in multi-step API synthesis
    • Boc deprotection prior to final condensation or reductive amination
    • Inline monitoring (HPLC or chiral LC) for stereopurity and residual protection groups
    • Incorporated into kilogram-scale process validation under GMP

    Final product types

    • Antidiabetic drug APIs with β-amino acid scaffolds
    • Central nervous system (CNS) drug candidates in IND or NDA stages
    • Oncology small-molecule libraries with fluorinated groups
    • Patent-protected single-enantiomer pharmaceuticals

    2. Peptide Synthesis for Research and Clinical Development

    Specialty peptide manufacturers integrate this amino acid derivative into automated solid-phase peptide synthesis (SPPS) and solution-phase assembly, targeting high-affinity analogs and modified peptides with enhanced metabolic stability. The Boc group provides temporary protection, facilitating coupling under mild conditions. The para-fluoro group aids in optimizing peptide–receptor interactions and metabolic profiles.

    Industry compliance standards

    • ISO 13485 for peptides intended for diagnostics and clinical development
    • ICH Q11 for control strategy in peptide API manufacturing
    • USP <1045> for peptide APIs and reference standards
    • Synthetic peptide guidance by EMA and FDA for preclinical development

    Typical usage ratio

    • Peptide chain assembly: 1 equivalent per incorporation site
    • N-terminal protection strategy: excess of 1.1–1.2 equivalents
    • Batch peptide synthesis (multi-gram scale): dosing based on resin loading and final sequence length
    • Scale-up processes: ratio adjusted to minimize racemization (pH and reagent excess monitored closely)

    Downstream process integration

    • Initial amino acid coupling step with Boc-protected strategy (Fmoc compatibility possible with deprotection protocol adaptation)
    • Placed at strategic positions for SAR library generation
    • Peptide chain elongation followed by Boc deprotection using TFA or alternative acids
    • Purification via preparative HPLC and lyophilization prior to downstream animal or cell assay use

    Final product types

    • Peptidomimetic drug candidates with specific fluorinated aromatic residues
    • Research-grade analogs for receptor binding studies
    • Clinical-grade peptides for vaccine development
    • Modified peptides for metabolic or stability profiling

    3. Building Block for New Chemical Entity (NCE) Discovery

    R&D divisions within pharmaceutical and specialty chemical firms incorporate this compound into combinatorial chemistry programs, building NCE libraries containing fluorinated chiral β-amino acids. Structural diversity and controlled stereochemistry accelerate hit-to-lead optimization in drug discovery campaigns targeting protein–protein interactions and enzyme modulation.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for chemical R&D
    • Internal IP documentation and compound tracking protocols
    • Lab safety handling and chemical hygiene best practices
    • Local regulatory controls for new chemical synthesis (e.g., REACH preregistration status where applicable)

    Typical usage ratio

    • Screening library synthesis: 0.1–0.5 mmol per reaction (multi-parallel format)
    • Lead expansion: up to 5–10% of total building block pool in mixture campaigns
    • Optimization projects: amount adjusted for diversity scaffold vs. focused analog work
    • Batch scale: based on availability and route design, typically several grams per series

    Downstream process integration

    • Included in parallel synthesis modules for automated or manual combinatorial work
    • Covalent incorporation or coupling modification before analytical QC and biological screening
    • Iterative analog design based on SAR data generation and computational chemistry feedback
    • Archival as reference standard in compound management platforms

    Final product types

    • Lead-like NCEs for early-stage pharma pipelines
    • Candidate molecules for protein–protein interaction inhibition
    • Enzyme inhibitor libraries containing chiral β-amino acid motifs
    • Diverse compound collections for CRO screening campaigns

    4. Intermediate for Fluorinated Agrochemical Synthesis

    Agrochemical manufacturers employ this raw material as a chiral precursor when developing active ingredients with fluorinated aromatic groups. It enters synthesis routes for crop protection actives such as herbicides or fungicides, leveraging the fluoro-phenyl moiety to achieve specific target selectivity and enhanced environmental stability.

    Industry compliance standards

    • FAO/WHO specifications for agrochemical intermediates
    • ISO 9001 production quality management systems
    • REACH registration where required for new agrochemical entities
    • Regulatory data submission standards for EPA, China ICAMA, or EU PPP authorizations

    Typical usage ratio

    • Synthesis scale-up: 5–30% w/w based on target molecule and synthetic yield
    • Laboratory development: milligram to multi-gram scale per reaction
    • Formulation optimization: adjusted per prototype and final actives property requirements
    • Custom synthesis: material usage matched to sequence and chiral purity needs of the process

    Downstream process integration

    • Used after precursor alkylation or addition of protection group steps
    • Typically introduced in mid-stage transformations en route to final active
    • Chiral purity evaluation critical before final condensation and formulation
    • Rotary evaporation or column chromatography for intermediate purification before agrochemical formulation

    Final product types

    • Chiral herbicide actives for row crop applications
    • Fluorinated fungicides with site-specific activity
    • Active intermediates for customized crop protection product lines
    • R&D agrochemical analogs for resistance management platforms
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    Certification & Compliance
    More Introduction

    Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid: A Direct View from the Manufacturer

    Real-World Experience Shapes Every Batch

    In our manufacturing facility, we handle compounds that researchers and drug makers use to solve tough challenges in healthcare and chemistry. Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid stands out from the crowd not because of buzzwords, but because of its genuine, repeatable performance, batch after batch. The world of unnatural amino acids continues to grow, and this compound demonstrates steady demand thanks to both its structural complexity and the role it plays as a vital synthon. Our journey with this molecule did not begin with a catalog listing. We started producing it long before it became popular in certain peptide design circles, learning through scale-ups, pilot runs, and feedback from researchers who needed a consistent starting point for crucial syntheses.

    Model and Key Features: What Sets Our Product Apart

    We adhere to specifications valued in synthetic chemistry, but it goes beyond technical jargon here. Our Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid, for reference as Model BA-43FPPA-R, consistently meets an enantiomeric excess above 99% as checked by chiral HPLC. Chemists focused on asymmetric synthesis and solid-phase peptide research have told us that trace amounts of the wrong enantiomer can derail months of work. We build our process around this feedback, monitoring every lot to ensure optical purity, checking for chiral integrity from raw materials all the way through to final packaging. Analytical chemists on our team confirm the identity, purity, and structure via NMR, LC-MS, IR, and elemental analysis; not just one test per batch, but a battery of approaches so that customers can run with our product right from the vial.

    Moisture content, residual solvents, and trace impurities get special attention because downstream reactions with carbamates and fluorinated aromatics show sensitivity to even minor contaminants. Chemists dislike working with unpredictable starting materials—one day the TLC reads clean, the next week a shadow ruins their sequence. By controlling each step of Boc protection, amino acid coupling, and final fluoride introduction, we reduce these frustrations. The crystalline powder we supply has a stable color and shelf stability that researchers in both process R&D labs and discovery teams appreciate.

    Usage and Value in Research and Manufacturing

    Our Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid sees its main use in the development of peptide drug conjugates and peptidomimetics. Medicinal chemists incorporate its fluoro-substituted phenyl ring to tweak bioactivity or alter metabolic stability. The (R)-configuration allows for chiral tuning not possible with racemic or (S)-form analogues. The compound acts as an intermediate in building protease inhibitors and neural receptor modulators. Some customers pursue it for its application in macrocyclic peptides or add it to screen for unexpected molecular interactions thanks to its steric and electronic properties.

    Direct use in solid-phase synthesis ranks high among applications. Automated peptide synthesizers depend on predictable protecting group stability; Boc offers that reliability. We optimize our product for resin coupling so that users don't have to troubleshoot side reactions or incomplete couplings. For experimentalists investigating enzyme-substrate binding, our material supports the introduction of a fluorine atom at the para position, which enables sensitive NMR and MS detection—a trick that seasoned analysts leverage to uncover fleeting interactions.

    Synthetic chemists working in discovery pipelines have pointed out that substituting a hydrogen with a fluorine atom can sometimes move a compound from “inactive” to “active” during screen testing. DDR1 inhibitors and CNS-targeted peptides have emerged from campaigns where our compound provided the right balance of size, hydrophobicity, and electronic character in the side chain. It also finds a niche among those developing new materials or catalysts, as the protected amino acid can serve as a starting block for custom polymers or fine-tuned ligands.

    Differences from Other Products in the Field

    It is tempting to think all protected amino acids look the same, but long-term experience says otherwise. We have handled plain Boc-protected phenylalanine derivatives, and many exhibit batch-to-batch color changes, stickiness from incomplete drying, or unexpected isomer content. The addition of the para-fluoro group on the phenyl ring in our product creates unique reactivity and poses challenges in purification. We’ve fine-tuned crystallization and solvent washes to separate side-products that show up as traces in the mother liquors—impurities that can kill an expensive peptide campaign.

    Many traders and brokers fill the market with products that look identical on paper but give inconsistent results at the bench. Our manufacturing protocol does not rely on random suppliers for intermediates; we work upstream, qualifying every input and scaling up under strict oversight. This focus has paid off for customers running FDA-audited or GLP-compliant labs, where hidden trace byproducts are unacceptable.

    Since this amino acid has both an α-carbon chiral center and a substituent on the β-position, it poses a tougher synthesis than more common α-amino acids. Competing products often contain measurable levels of the (S)-isomer or racemized material. Over the years, we’ve leaned on our chiral separation expertise, investing in both chemical resolution and modern enzymatic techniques. Our product does not just pass by a chiral column once and head out the door; lots are held and rechecked over time to catch rare late-appearing impurities.

    Transport stability and ease of handling set our grade apart from some generic offerings. Our compound ships as a non-hygroscopic powder, avoiding the sticky clumps that frustrate those using low-quality grades. We select packaging to minimize both static and cross-contamination. Many products in the market pick up odors from plasticizers or trace solvents during shipping—ours ships clean, so the only thing coming out of the vial is pure research-grade material.

    Pain Points We’ve Addressed from Years of Feedback

    A lot of feedback over the years has focused on problems with amino acid derivatives clogging lines or producing ghost peaks in analytical runs. Our QC team cross-tests every shipment for solubility in the common solvents used in peptide work—DMF, DCM, and acetonitrile—to make sure customers aren't left adjusting protocols or fighting insoluble clumps. Color stability under light and temperature changes comes from improved purification and minimal exposure to air during drying. These routine details add up for research teams on deadlines; nobody likes discarding peptide resins because a crucial step failed mysteriously from a hidden impurity.

    We’ve received frantic calls from researchers whose projects stalled due to ambiguous spectral data from off-the-shelf competitors. Our technical staff works closely with analytical chemists to verify not only structure, but also batch consistency over time. Customers have come to count on reproducible retention times and clean mass spectra that match reference data in every lot.

    Many academic labs operate under tight budgets and can only purchase a few grams at a time. Early on, we committed to offering exact weights and clear documentation even for small quantities. By avoiding large “overfill” bags or awkward aliquots, we keep waste to a minimum. Scale-up research teams have praised our ability to deliver custom bulk orders just as clean as our small batches, a difference that shows up in large-scale validation runs where impurity accumulation ruins yield.

    Making the Most of Each Step: Lessons Learned in Manufacturing

    A complex intermediate like Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid teaches a manufacturer more than just theoretical chemistry. Our chemists have tackled persistent side products—such as tarring during Boc protection, or overalkylation at elevated temperatures. We respond to these by adjusting temperature ramps, drying times, and even minor changes in purification solvents based on up-to-date analytical feedback.

    Process development became an iterative loop: adjust one parameter, observe three new effects. Initial scale-ups exposed vulnerabilities in glassware handling, especially at the low temperatures sometimes required for sensitive steps. We improved our facility’s solvent recovery system to avoid introducing trace water; trace moisture has ruined high-purity runs more than once in the past. These quality improvements feed back directly into the reliability our customers require in peptide synthesis.

    Beyond purity, we ensure the material’s integrity through long-term storage studies. We’ve had batches sampled and retested at intervals to see how stability holds up, data that only comes from holding inventory and putting it through its paces in a real-world warehouse, not just relying on lab-bench convenience. This approach has allowed us to support customers whose procurement cycles span months or even quarters, giving peace of mind that their material will perform just as reliably months after receipt.

    Real-World Applications and Stories from the Bench

    Lab teams using our material have discovered that this specific fluorinated propionic acid can create analogues with unexpected bioactivity. A couple of our industrial partners shared data highlighting enhanced blood-brain barrier penetration after a single para-fluorination. In early screening for antitumor peptides, medicinal chemists leveraged both the chiral center and the electron-withdrawing fluoride. This effect changes hydrogen bonding networks and boosts receptor binding affinity, practical benefits that go beyond theoretical speculation.

    Feedback from academic teams has pointed to the material’s clean handling in automated peptide synthesizers, especially where long, hydrophobic stretches cause trouble on the resin. Organic process teams in biopharma have detailed how our batch purity minimizes column fouling and reduces the need for extensive intermediate purification. These are issues that cost not just time, but hundreds or thousands of dollars in wasted reagents if the incoming amino acid fails QC.

    For teams involved in lead optimization, quick turnaround matters. Our local delivery model and bulk inventory allow us to ship material sometimes within hours of an urgent request. This cuts down the waiting times that disrupt tight medicinal chemistry campaigns. The reliability of each vial helps teams to design, synthesize, and test analogues in a single sprint, getting leads into animal models or on decision calls faster.

    Supporting Innovation, Not Just Supplying Material

    Manufacturing Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid is far more than producing another specialty chemical. Our experience stretches from synthesis and purification to application on the bench, translating to practical support for partners at every stage. For breakthroughs in peptidic drugs or new bioactive molecules, the ability to count on every reagent is a non-negotiable foundation.

    Because research projects run on innovation and sometimes on tight funding, technical advice comes included. We’ve helped customers troubleshoot pH drift during coupling reactions, optimized dissolution protocols for low-boiling solvents, and even walked through MS fragmentation analysis over video calls. These interactions keep us connected to the real-world needs of researchers, shaping every process update and informing future product improvements.

    Researchers have confided that inconsistent amino acid building blocks have derailed grant milestones, causing downstream failures in parallel synthesis or biomarker screening. Our depth of experience in quality control helps bridge this gap between catalog commodity and real-world requirement. We take the outcome seriously—each batch reflects hours of care from synthetic teams, quality assurance, and customer feedback loops.

    Closing the Loop on Transparency and Trust

    The journey from raw starting material to clean, ready-to-use Boc-(R)-3-Amino-3-(4-Fluoro-Phenyl)-Propionic Acid is full of checkpoints. Our philosophy remains straightforward: transparency, attention to detail, and an ongoing conversation with the community that relies on our product. Analytical test data remains available on demand; we do not hide behind minimal “meets specification” claims, and our technical support stays accessible post-purchase.

    Chemists who have tried multiple sources notice subtle differences: variations in melting point, consistency on the spatula, or even odor. These physical cues signal the underlying quality and care in manufacturing. We encourage partners to share feedback—good or bad—and routinely survey for suggestions to further improve usability or documentation. Each issue resolved shapes the next production cycle, making the product a little better each time.

    We believe that manufacturing is not a closed door operation, but a collaborative extension of the research effort itself. From the first inquiry to long-term supply partnerships, every batch we produce aims to be part of a reliable foundation for creative work and real-world discovery.