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Boc-Trans-4-Fluoro-L-Proline

    • Product Name Boc-Trans-4-Fluoro-L-Proline
    • Alias Boc-4-fluoro-L-proline
    • Einecs 682-361-4
    • 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

    323137

    Product Name Boc-Trans-4-Fluoro-L-Proline
    Cas Number 1187596-27-7
    Molecular Formula C10H16FNO4
    Molecular Weight 233.24
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 92-98°C
    Solubility Soluble in DCM, methanol, and slightly soluble in water
    Storage Temperature 2-8°C
    Smiles CC(C)(C)OC(=O)N1C[C@@H](F)CC1C(=O)O
    Synonyms Boc-(4R)-4-Fluoroproline

    As an accredited Boc-Trans-4-Fluoro-L-Proline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Boc-Trans-4-Fluoro-L-Proline supplied in a sealed amber glass vial, 5 grams, with tamper-evident cap and product label.
    Shipping Boc-Trans-4-Fluoro-L-Proline is shipped in a sealed, moisture-resistant container to ensure product integrity. It is handled according to standard chemical shipping regulations, avoiding extreme temperatures and humidity. Appropriate labeling and documentation are provided for safe handling, storage, and transport. Shipping complies with local and international hazardous materials guidelines.
    Storage Boc-Trans-4-Fluoro-L-Proline should be stored in a tightly sealed container, under a dry, inert atmosphere such as nitrogen or argon. Keep it in a cool, well-ventilated area, ideally at 2–8 °C (refrigerator temperature). Protect from light and moisture to prevent degradation and maintain chemical integrity. Avoid sources of ignition and incompatible materials such as strong acids or bases.
    Application of Boc-Trans-4-Fluoro-L-Proline

    Applications of Boc-Trans-4-Fluoro-L-Proline in Industrial Manufacturing

    Boc-Trans-4-Fluoro-L-Proline is a specialized amino acid derivative used by pharmaceutical and biotech manufacturers as a key building block in advanced synthesis routes. As the original producer, we support industrial partners with consistent supply, technical support, and regulatory documentation specific to high-demand downstream sectors requiring precise formulation and compliance. Below, we outline major segments utilizing this intermediate at production scale.

    1. Peptide Drug Synthesis

    Peptide therapeutics manufacturers use Boc-Trans-4-Fluoro-L-Proline as an essential protected amino acid in solid-phase peptide synthesis (SPPS). The fluorinated proline imparts unique conformational properties, enhancing peptide stability and bioactivity. Operators must control coupling conditions and deprotection to ensure full chain assembly, especially in GMP-regulated layouts. Standard practice includes in-process HPLC and mass spectrometry to verify peptide integrity after each cycle.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • EU EudraLex Vol. 4 Annex 3
    • Japanese Pharmaceutical and Medical Device Act (PMD Act)

    Typical usage ratio

    • Typically 1 equivalent per targeted proline position in the peptide sequence
    • The ratio adjusts based on target chain length and substitution pattern (0.5-3.0 mol%)

    Downstream process integration

    • Enter as activated ester or free acid in the peptide coupling step
    • N-terminal Boc group remains until global deprotection during final cleavage
    • Final product purification performed post-resin cleavage, using preparative HPLC

    Final product types

    • Peptide-based APIs (e.g., fluorinated analogs for oncology, diabetes)
    • Clinical-stage peptide drug substances
    • GMP peptide research reference materials
    • Preclinical candidate libraries for pharmaceutical R&D

    2. Small Molecule API Intermediate Synthesis

    Chemical process development teams select Boc-Trans-4-Fluoro-L-Proline as a key chiral intermediate in the construction of small molecule APIs, especially where proline-based scaffolds enhance pharmacokinetics. In multistep synthesis, this material serves as an enantiopure starting point, influencing downstream enantiospecificity during cyclizations, amidations, or alkylation reactions. Production runs include inline process monitoring for isomeric purity, and solvent choices must comply with residual solvent guidelines in final APIs.

    Industry compliance standards

    • ICH Q11 Development and Manufacture of Drug Substances
    • EU REACH (for handling and worker safety)
    • US FDA DMF (Drug Master File) submission support
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Ranges from 1.1 to 1.5 mol equivalents relative to coupling counterpart
    • Adjusted depending on scale-up studies and impurity profile

    Downstream process integration

    • Used as a coupling partner in stepwise synthesis of proline-functionalized drug candidates
    • Boc deprotection and fluorine position must be protected during subsequent functionalizations
    • Process often includes analytical chiral HPLC and NMR for batch release

    Final product types

    • Small molecule investigational new drugs (IND packages)
    • Proline-based protease inhibitors
    • Novel CNS active pharmaceutical ingredients
    • Specialty fluorinated intermediates in Phase I/II clinical trials

    3. Biotech Diagnostic Oligomer Production

    Manufacturers of custom oligopeptide probes for clinical diagnostics use Boc-Trans-4-Fluoro-L-Proline to insert conformationally restricted residues into synthetic recognition motifs. This modification enhances binding specificity for peptide-based assay kits and biosensor platforms. Biotech production protocols require stringent trace impurity profiles, with each batch accompanied by a full certificate of analysis and spectroscopy data for regulatory submission or clinical use validation.

    Industry compliance standards

    • ISO 13485:2016 Medical Device Quality Management
    • US FDA QSR (21 CFR Part 820) for IVD manufacturers
    • OECD Good Laboratory Practice (GLP) where applicable
    • European In Vitro Diagnostic Regulation (IVDR) 2017/746

    Typical usage ratio

    • 1 mol per modified residue in synthetic peptide or probe sequence
    • Custom sequence design may require from 0.1% to 5% of total amino acid input

    Downstream process integration

    • Utilized in stepwise peptide chain elongation via automated synthesizer
    • Deprotection and cleavage protocols staggered by block or batch size
    • Post-synthesis labeling or conjugation steps often leverage the proline site

    Final product types

    • Diagnostic test kit peptide markers
    • Fluorinated oligopeptide microarray components
    • Customized biosensor probes
    • Affinity tags for proteomics research tools

    4. Pharmaceutical Cocrystal Engineering

    Some solid form formulation chemists incorporate Boc-Trans-4-Fluoro-L-Proline as a conformationally active coformer in early-stage pharmaceutical cocrystallization programs. The rigid proline skeleton enables improved packing and polymorphic stability for small molecule active ingredients, especially those vulnerable to hydration or rapid degradation. Documentation and validation focus on ensuring trace solvent limits and full structural characterization by single-crystal X-ray diffraction.

    Industry compliance standards

    • ICH Q6A Specifications: Test Procedures and Acceptance Criteria
    • USP General Chapter <941> for Crystallinity
    • EU Pharmacopoeia 9th Edition, Solid-State Properties
    • US FDA Guidance on Pharmaceutical Solid-State Chemistry (CMC Section)

    Typical usage ratio

    • Stoichiometric ratios (1:1 or 2:1 coformer:API) depending on desired cocrystal lattice
    • Empirically determined by crystallization screening (typically 20-50% by weight in trials)

    Downstream process integration

    • Dissolved with API in solvent system using controlled temperature
    • Crystallization performed under inert atmosphere or controlled humidity to promote target polymorph
    • Isolation by filtration and drying, followed by structural confirmation tests

    Final product types

    • Solid-form screening candidates for formulation studies
    • Stabilized polymorphic drug substances
    • Bulk pharmaceutical cocrystals for preformulation and bioavailability trials
    • Reference standards for solid-state analytical method development

    5. Chiral Ligand Synthesis for Asymmetric Catalysis

    Chemical manufacturers specializing in chiral catalyst production use Boc-Trans-4-Fluoro-L-Proline as a core building block for ligand scaffolds. The fluorinated proline introduces both steric and electronic modulation, beneficial for enantioselective transformations in fine chemical and pharmaceutical industries. The raw material enters early in the route for ligand formation and is subjected to continuous monitoring for possible racemization or hydrolysis throughout the process.

    Industry compliance standards

    • ISO 80000-9:2009 for chemical purity reporting
    • REACH registration where required (Europe only)
    • In-house QC protocols for chiral purity (GC, HPLC)
    • Responsible Care® management systems for fine chemical production

    Typical usage ratio

    • 1 equivalent per chiral center in ligand design
    • Adjusted for scale—ranges from millimole scale (<0.5 mol%) to 10 mol% in batch processes

    Downstream process integration

    • Condensation with other amino acid derivatives or heterocycles in multi-step synthesis
    • Boc removal performed prior to metal complex formation
    • Final ligands purified by recrystallization or chromatography as needed

    Final product types

    • Chiral ligands for asymmetric hydrogenation
    • Organocatalysts for fine chemical synthesis
    • Transition metal complex ligands (Palladium, Rhodium, etc.)
    • Enantioselective catalyst screening libraries
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    Certification & Compliance
    More Introduction

    Boc-Trans-4-Fluoro-L-Proline: Advancing Synthesis with Innovation

    A Practical Look at Boc-Trans-4-Fluoro-L-Proline

    A chemist working on peptide synthesis knows the frustration of an unstable intermediate or inconsistent batch quality. Boc-Trans-4-Fluoro-L-Proline answers a specific need in the lab: reliable access to an amino acid derivative that expands the possibilities for peptide, pharmaceutical, and chemical research. From my own experience in handling custom and large-scale amino acid projects, I can see this compound filling a gap where standard protected prolines and simple fluorinated analogs fall short.

    Why Boc-Trans-4-Fluoro-L-Proline Matters in Modern Synthesis

    Boc-Trans-4-Fluoro-L-Proline brings unique value. Incorporating a fluorine atom at the 4-position of the proline ring shifts the shape and electronics of resulting peptides and small molecules. Researchers have told us how this small tweak opens new doors in bioactivity studies, drug discovery, and advanced material design. We manufacture Boc-Trans-4-Fluoro-L-Proline to meet the rigorous demands of professionals exploring new classes of pharmaceuticals, especially where metabolic stability and receptor specificity are vital.

    Every batch we produce gets subjected to thorough chiral HPLC and NMR analysis, meaning the stereochemistry holds true, batch after batch. Laboratories have pushed us to refine the synthesis, and through years of hands-on production, we've learned how to deliver high-purity Boc-protected prolines that perform predictably in both bench-scale and commercial processes. These insights didn’t come from reading technical papers—they came from getting our hands dirty on the plant floor, solving process challenges, and learning what end-users actually face under cGMP and research conditions.

    Specifications and Consistency

    Our focus on quality isn’t just talk. The specification for Boc-Trans-4-Fluoro-L-Proline reflects what research chemists genuinely want: greater than 98% purity, moisture levels controlled for accurate weighing, and robust packaging that prevents contamination. Any time we’ve run into unexpected reactivity or off-spec batches, we troubleshoot and tighten processing steps until the underlying problem disappears.

    We don’t cut corners with raw materials or isolation steps. The Boc group remains fully intact—an absolute must, since partial deprotection creates headaches during peptide coupling. As a manufacturer, that means every run involves careful monitoring of reaction temperature and time, plus extra analytical checks. Over the years, we’ve found that small fluctuations in solvent quality or hydrogen fluoride source affect the stereochemical outcome, so we keep sourcing disciplined and batch records transparent.

    Performance in Applications

    Boc-Trans-4-Fluoro-L-Proline isn’t just an exotic building block. It offers a key differentiator when compared to run-of-the-mill protected prolines. Fluorine at the 4-position creates a rigid, polarizable ring system, changing the molecule’s shape and how it interacts in enzymatic pockets. Peptide chemists frequently use it to probe protein-protein interactions, or to tweak the conformational bias in cyclic peptides. Many users working in lead optimization rely on the fluorinated analog to increase resistance to metabolic enzymes or to improve oral bioavailability.

    We’ve worked with groups who hit a wall using standard Boc-Proline derivatives. Their compounds suffered rapid metabolic breakdown in animal models. By switching to the 4-fluoro variant, they saw a measurable boost in stability, all without a major overhaul of the synthesis workflow. This kind of result drives further interest—and as demand grows, we’ve scaled up production to support both milligram-level R&D work and larger pre-clinical lots.

    Comparing to Other Boc-Proline Analogues

    Not all protected prolines are created equal. Standard Boc-L-Proline delivers simplicity, no argument there—it’s well-matched for everyday peptide couplings and basic foldamers. But chemists looking to control conformational preference or fine-tune binding need more. Adding fluorine at the trans-4 position, as our process ensures, introduces both electronic and steric effects. This impacts hydrogen bonding and can help mimic natural post-translational modifications.

    We also produce cis-4-fluoro and 3-fluoro variants. The trans-4 configuration stands out for its pronounced influence on backbone geometry and limited rotamers, which many computational chemists appreciate. In peptide macrocycles and biologically active motifs, this influences everything from target affinity to solubility. Subtle? Yes, but in the hands of an experienced medicinal chemist, these differences translate into improved leads and a better shot at clinical relevance. We stick closely to stereochemical purity, since even trace contamination of cis or racemic material can confound biological results.

    Trust Built on Technical Know-How

    Anyone can throw up a data sheet online, but delivering consistently high-quality Boc-Trans-4-Fluoro-L-Proline takes dedication to process detail. Process optimization didn’t happen overnight. Early on, we sometimes saw imprecise fluorination, leading to isomeric mixtures. After several rounds of analytical feedback and synthetic adjustment, we locked in reliable reagent addition rates and optimized cooling profiles, holding the trans configuration above 98% with each batch.

    Those improvements unfolded in step with direct customer feedback. Chemists using our material pointed out unexpected degradation or batch-to-batch variation, particularly in moisture-sensitive applications. That motivated us to add controlled humidity monitoring and more robust long-term storage. We now seal all high-purity lots under nitrogen and ship only in validated containers, giving our customers peace of mind whether they’re ordering a gram or a kilogram.

    Supporting Next-Generation Research

    Our experience with Boc-Trans-4-Fluoro-L-Proline is shaped by conversations with researchers, not by studying brochures. Medicinal chemists, peptide engineers, and structural biologists approach us with problems—including poor metabolic profiles, inadequate target selectivity, or difficult solid-phase couplings. Boc-Trans-4-Fluoro-L-Proline often plays a role in the solution, either as a novel screening element or as a central piece in protected fragment libraries.

    Custom synthesis projects pushed us to develop processes capable of delivering material for both initial proof-of-concept work and later multi-gram campaigns. We log extensive analytical histories, which helps when troubleshooting a failed resin cleavage or an unexpected side product. That’s the value of vertical integration. Our close control over each step—starting with amino acid precursor selection and ending in the final certified lot—lets us guarantee the traceability and compliance sought in regulated discovery pipelines.

    Environmental and Safety Considerations

    Fluorinated compounds bring unique safety and waste issues. In our plant, the team reviews safety protocols every quarter, with input from both line workers and environmental health staff. We recycle solvents and minimize HF use, keeping exposure levels to a minimum and meeting regulatory standards. Solid fluoro-organic waste goes through dedicated incineration, reducing downstream contamination risks.

    Strict adherence to process controls protects workers and reduces the risk of cross-contamination—a lesson reinforced multiple times over the years. We train every new technician on safe fluorination handling and run regular drills for emergency procedures. It’s more work, but it keeps the team safe and the product uncompromised.

    Reliability Borne from Experience

    Some chemists put trust in a lot number or a certificate. We know from experience that true reliability is built batch by batch. Feedback from long-standing customers shapes our process improvements. Whenever an unexpected impurity or process deviation appears, we involve frontline chemists in the troubleshooting, making use of root-cause analysis rather than guesswork.

    Over time, this has led us to tweak purification protocols—sometimes changing chromatography media or solvent gradients to lock in purity. It’s a commitment grown from thousands of hours at the bench and on the plant floor, sweating details that get overlooked by companies focused on catalog churn or reseller margins.

    Meeting Changing Market Needs

    The demand for Boc-Trans-4-Fluoro-L-Proline doesn’t stay static. The surge in automated peptide synthesis, along with breakthroughs in fluorine chemistry, shapes what research groups need. As high-throughput methods move from the specialty lab into routine use, the need for greater lot traceability and compatibility with automation grows.

    We keep an ear to the ground by participating in method development studies and round-table discussions with leading scientists. Lessons from this close collaboration feed back into our production planning and batch documentation. Rigorous process analytical technology (PAT) standards now guide every production run, and those standards reflect actual demands set by users who stake drug programs and material patents on the quality of building blocks like Boc-Trans-4-Fluoro-L-Proline.

    Continuous Improvement and Innovation

    Being a real manufacturer, we can iterate and innovate in ways off-the-shelf suppliers can’t. Our R&D team develops new fluorination routes that cut hazardous waste and lower energy consumption. This isn’t just theoretical—those changes show up in a reduced carbon footprint per kilogram of compound shipped. Expanded crystallization control means better handling for automated weighing and delivery systems, reducing static and clumping.

    We routinely partner with university labs and industrial consortia to pilot better process controls and evaluate the downstream impact of our product on biological programs. Several times, we’ve uncovered side reactions or solubility bottlenecks encountered by users, leading us to suggest modified protocols or different solvents. This hands-on knowledge isn’t found in standard paperwork—it’s the direct result of rolling up sleeves and engaging with those at the sharp edge of research.

    Respecting Intellectual Property and Research Integrity

    Boc-Trans-4-Fluoro-L-Proline sometimes winds up in proprietary compounds and confidential research. We take IP respect seriously. Batch records, analytical reports, and customer communications remain tightly controlled, supporting both open discovery work and the nuanced needs of the pharmaceutical pipeline. We don’t turn every order into a case study—instead, we focus on supporting the scientific advance with discretion and technical depth.

    In regulated settings, we’ve expanded documentation to meet evolving global standards, delivering everything from detailed route-of-synthesis records to comprehensive CoAs, always with traceable chain-of-custody. Our open lines of technical support—staffed by chemists, not call centers—help customers jump regulatory hurdles or solve a challenging coupling step.

    Why Direct Manufacture Makes a Difference

    Customers sometimes ask why sourcing direct from a manufacturer matters for a product as specialized as Boc-Trans-4-Fluoro-L-Proline. The answer is all about direct control. We own the process from precursor sourcing to final shipment. There’s no guesswork on storage conditions, no risk of material sitting in a third party’s warehouse under uncertain humidity or temperature.

    We accept responsibility for troubleshooting and fast-turn replacement if a lot doesn’t meet stated specs. Decades of experience mean we can answer tough questions about reactivity, shelf life, or batch-to-batch consistency based on hands-on evidence. Our team makes process tweaks in response to evolving research needs, not distributor stock cycles.

    Staying Close to the Science

    Direct dialogue with working scientists, not just procurement staff, lets us shape future offerings. Some of the innovations in our current Boc-Trans-4-Fluoro-L-Proline process came from open-ended conversations with academic groups pushing boundaries in backbone modification and fluorine patterning. By taking feedback seriously—from lot granulation to solubility characteristics—we’ve been able to provide a product that adapts to user needs.

    We don't just ship a catalog compound; we actively work with users to optimize protocols. That approach, grounded in years of bench-level production work, closes the gap between theory and practice. Whether ensuring maximum purity for clinical preps or troubleshooting unusual reactivity in multi-step syntheses, we engage as partners—not middlemen.

    Boc-Trans-4-Fluoro-L-Proline: Real Value, Real Results

    Boc-Trans-4-Fluoro-L-Proline demonstrates how a small chemical tweak can have real functional value. Our experience as a manufacturer has shown this compound attracts repeat users not because of marketing claims, but because the material supports hard-won progress in medicinal discovery and biochemical innovation. The challenges of producing chiral, fluorinated amino acids taught us the importance of tight process discipline and technical responsiveness.

    Those lessons translate into a product trusted by chemists, validated by performance in cutting-edge research, and shaped by the lived reality of manufacturing under real-world demands. There’s no substitute for hands-on, technical engagement—especially when research is on the line. Boc-Trans-4-Fluoro-L-Proline stands as a testament to that philosophy.