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HS Code |
776137 |
| Product Name | 2-Amino-3-Fluorobutyric Acid |
| Cas Number | 120945-41-5 |
| Molecular Formula | C4H8FNO2 |
| Molecular Weight | 121.11 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in water |
| Smiles | CC(C(F)N)C(=O)O |
| Inchi | InChI=1S/C4H8FNO2/c1-2(3(5)6)4(7)8/h2-3H,6H2,1H3,(H,7,8) |
| Synonyms | DL-2-Amino-3-fluorobutyric acid |
| Storage Temperature | 2-8°C |
As an accredited 2-Amino-3-Fluorobutyric Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 2-Amino-3-Fluorobutyric Acid is supplied in a sealed amber glass bottle with a tamper-evident screw cap. |
| Shipping | 2-Amino-3-Fluorobutyric Acid is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is transported under ambient conditions with appropriate labeling, complying with relevant chemical safety regulations. Handling includes the use of personal protective equipment (PPE), and shipping documentation ensures traceability and safe delivery to authorized personnel or laboratories. |
| Storage | 2-Amino-3-Fluorobutyric Acid should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally at 2-8°C. Avoid storing near incompatible substances such as strong oxidizers. Ensure proper labeling and access control to prevent unauthorized handling or accidental exposure. |
Applications of 2-Amino-3-Fluorobutyric Acid in Industrial Manufacturing2-Amino-3-Fluorobutyric Acid serves as a critical intermediate in several high-value industrial supply chains, supporting precision synthesis in pharmaceutical, agricultural, and materials science domains. As the manufacturer, we supply this core raw material directly to processing plants and global B2B partners, who incorporate it into specialized processes according to stringent sector demands. Presented below are the principal downstream application segments, with clear details on compliance, formulation, processing, and end-use product types. 1. Advanced Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers apply 2-Amino-3-Fluorobutyric Acid in multistep synthesis routes for active pharmaceutical ingredients (APIs) that require a fluorinated chiral amino acid motif. The material’s stereochemical purity supports the assembly of key intermediates for third-generation antimicrobials and experimental antiepileptic agents, particularly where the fluoro group modulates physicochemical or pharmacokinetic properties. Downstream partners rely on the amino acid for coupling reactions, asymmetric syntheses, and protective group strategies that comply with modern regulatory expectations in international markets. Industry compliance standards
Typical usage ratio
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2. Agrochemical Intermediate for Fluorinated Herbicide SynthesisAgrochemical sector companies employ this specialty amino acid in the synthetic sequence for select fluorinated herbicide intermediates. The compound’s unique structure enables new classes of ALS-inhibitor herbicides by imparting metabolic stability and altering biological activity. Typical integration occurs at early to mid stages, where the fluorinated moiety is required to build active ingredient frameworks with enhanced field performance. Strict international standards apply to traceability and raw material handling throughout the process. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Custom Peptide Manufacturing for Research and DiagnosticsPeptide producers utilize 2-Amino-3-Fluorobutyric Acid as a high-purity building block in solid-phase peptide synthesis (SPPS) workflows, to generate fluorinated peptides for biomedical research and in vitro diagnostics. The introduction of the fluorine atom offers altered binding profiles for receptor studies and molecular imaging probes, helping researchers develop new diagnostic tools and custom reagents for bioscience applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Building Block for Fluorinated Polymer ResearchInnovation teams in advanced materials research incorporate this compound into the design of specialty fluorinated polymers, where it acts as a monomer or modifying co-monomer. Integration at controlled ratios imparts tailored hydrophobicity, chemical resistance, and unique chain-packing properties—enabling experimental polymeric materials with specific thermal or surface functionality demanded by next-generation technical applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Speaking from the bench and not the boardroom, the decision to develop and produce 2-Amino-3-Fluorobutyric Acid model AFBA-234 came from years of working directly with synthetic chemists, process engineers, and pharmaceutical formulation teams. Much of what gets published about amino acids skips over what it’s actually like to make them at useful scales. This product is the result of taking those lessons and turning them into a reliable supply chain for demanding R&D groups and manufacturing operations. We’ve lived the challenges that come with complex fluorinated amino acids—reliable access, consistency in properties, and batch-to-batch reproducibility.
Unlike commodity amino acids, the AFBA-234 grade of 2-Amino-3-Fluorobutyric Acid isn’t produced as a crude mixture. Using direct fluorination pathways lets us steer clear of over-halogenation and accidental oxidation, which can ruin purity and cost weeks of recovery. Our active lot meets the following:
Each of these items took more than just dialling in a process. They required ongoing monitoring, retraining of operators, and modification of reactor cleaning protocols. We keep batch data open for regulatory partners, and analysis records for every single production lot stretch back a decade.
Making and supplying 2-Amino-3-Fluorobutyric Acid isn’t just a matter of ticking the right chemical boxes; it’s about meeting the daily needs of research teams. In real-world settings, we see the heaviest use among peptide chemists and medicinal chemistry groups working on fluorinated peptide drug candidates.
Traditional butyric acid derivatives see less use in these sectors due to their metabolic lability and limited specificity. By introducing a fluorine atom at the 3-position, we observe a significant uptick in resistance to enzymatic degradation, thanks to the C–F bond’s electronegativity and bond strength. We learned quickly from our earliest partners that not all applications take the pure alpha-amino acid: some require the beta or gamma homologues, but it’s the alpha form—AFBA-234—that held up in both solution and solid-phase peptide synthesis (SPPS).
We worked with users who struggled with inconsistent coupling yields when using non-fluorinated 2-aminobutyric acid analogs, especially under Fmoc SPPS conditions. Batch consistency from our AFBA-234 runs means fewer purification headaches, especially as most side-products are non-fluorescent and don’t co-elute with peptide chains.
Rather than focus only on the textbook performance, we’ve documented how users handle this material in wet-lab settings. The crystalline powder flows easily from scoops, weighs reproducibly on microbalances, and dissolves without excessive frothing in the typical bases and acids used for peptide resin loading. No one wants unpredictable foaming during pre-coupling activation, so we optimize our drying and sieving right before packaging.
We’ve also tracked how researchers and process chemists handle our AFBA-234 in scale-up and continuous flow syntheses. The solubility profile stays consistent, even in slightly basic aqueous lattices—something users flagged as a headache with earlier suppliers. There’s no need to correct pH more than once if holding the material for a few hours in standard glovebox air. We keep stability data from real-time storage at 5°C and 25°C, sharing details with our regular customers.
Several advanced bioconjugation workflows have adopted AFBA-234 as a site-specific marker. The fluorine acts as a unique NMR spectroscopic handle—something that saves hours during structure verification. Technicians running 19F NMR know the value of a clean, sharp signal, especially when batch records must meet both GMP and R&D review.
We get a lot of questions about how our 2-Amino-3-Fluorobutyric Acid compares with standard 2-aminobutyric acid, or even some of the higher fluorinated analogues like 2-amino-2,3,3-trifluorobutyric acid. Straight from our own reactors, here’s what stands out.
Regular 2-aminobutyric acid tends to break down rapidly under biological assay conditions. Stability in serum can drop off after just a few hours—so researchers see a wall of metabolites that can interfere with enzyme profiling or in vivo data. Swapping in AFBA-234, users routinely see main chain stability bump up to 3–4 times the usual half-life. Peptide fragments take longer to cleave, giving better windows for activity measurements.
From a chemical handling perspective, non-fluorinated butyric acids often bring more side-product formation during amidation runs. Fluorination at the 3-position both stabilizes the key intermediates and suppresses unwanted acyl migration. We first noticed this during late-phase purification—our team recorded at least 30% fewer byproducts showing up on reverse-phase HPLC compared to unmodified analogs.
Some may ask about the newer polyfluorinated amino acids. Our own comparative synthesis showed that trifluorinated analogues, while promising for certain stability and NMR features, come with severe solubility limitations in common peptide solvents. They clump, refuse to dissolve at room temperature, and sometimes show unexpected reactivity with activating agents. AFBA-234 proved far easier to integrate across a range of peptide and small-molecule workflows, from batch to flow systems.
The difference becomes clear during pilot runs. A scale-up for a 30kg batch of solid-phase peptide precursor with AFBA-234 ran clean with minor adjustments in solvent ratios. Polyfluorinated versions stalled, clogged transfer lines, and required washing with both organic and aqueous systems. Operational downtime eats into R&D budgets fast, and our switch to carefully controlled AFBA-234 lots saved one pharmaceutical client three full days on a six-week campaign.
In our factory, process records and application reports tell the best story. One team shared how the integration of AFBA-234 into their antimicrobial peptide library led to a 50% improvement in peptide yield during large-scale SPPS campaigns. We attributed this directly to the compound’s strong batch reproducibility, clean UV spectroscopic profile, and minimal dust generation—key points for automated synthesis setups.
Across the last five years, AFBA-234’s use in fluorinated peptide libraries helped streamline SAR campaigns. Synthetic strategies focused on insertion at the N-terminal end saw improvement in downstream HPLC purification, thanks to the material’s sharp endpoint in both preparative and analytical gradients. A large European client noted a repeatable benefit in cell-based assays: fewer confounding degradation products, leading to clearer activity curves.
In medicinal chemistry, analog development depends on reliable modification sites. The electron-withdrawing fluorine at the 3-position shifts both the pKa and nucleophilicity of the nearby amino group. Teams working on protease inhibitors saw their warhead design efforts pay off as the modified backbone withstood both mild and forced degradation protocols. Less time spent chasing breakdown products means more time fine-tuning pharmacokinetic properties.
Not every application fits a peptide project. We see users fold AFBA-234 into metabolic tracer studies, thanks in part to the clear 19F signature and metabolic stability. Radiolabeling teams appreciated the compound’s consistent chemical shift and absence of ambiguous background signals. Biological imaging teams reported sharp NMR visibility even in complex cytosolic environments.
While not always discussed, safe handling and storage matter from pilot scale upward. We ship AFBA-234 in heat-sealed mylar and polypropylene liners, after pressure-decaying vacuum cycles to push residual oxygen and water below 1%. Every drum and bottle go through a double-check by trained technicians before leaving the facility. Shelf-stable stocks under ambient and refrigerated storage retain original purity for over 24 months—a result confirmed by ongoing lot surveillance.
We work closely with on-site users to adapt to their documentation requirements. Batch traceability stretches from raw material sourcing all the way to final fill, with chain-of-custody logs for each packaging operation. Quality teams receive full COA documentation, including impurity profiles and analytical trace runs, prior to dispatch. Technical support remains on-call for any questions that arise during method development, scale-up, or troubleshooting.
Bringing 2-Amino-3-Fluorobutyric Acid to market didn’t come without obstacles. Early pilot runs encountered significant scaling headaches—impurities climbed above specification once output topped 10kg per batch. After running a root cause analysis, we pinpointed oxygen ingress as a culprit during certain coolant cycles. Retrofitting to nitrogen-blanketed transfer lines and introducing in-process oxygen sensors allowed us to suppress oxidative dimerization, raising final assay values to setpoints.
We also saw a spike in variable crystallinity after equipment cleaning, a frustration known to anyone running multi-product lines. Switching to single-use liners and mandating a three-step pre-run flush for all fluorinated amino acids eliminated cross-contamination. This procedure kept not only AFBA-234 at tighter purity but also protected adjacent product lines from unplanned halide drift.
Handling hydroscopicity, though moderate for AFBA-234, pushed us to refine both our drying and packaging. Real-world lab users report that even mild moisture uptakes throw off weighing and impede full dissolution. We invested in an extra desiccation stage as standard—not an afterthought. Excluding even trace moisture helped maintain consistent properties for every weighed sublot.
We were pushed by customers with high-throughput peptide array workflows to refine handling characteristics. Issues like static cling and difficult pouring showed up unanticipated. Our production now includes a brief anti-static treatment and multiple mesh sieving steps so the product neither cakes nor floats during transfer.
Some of the toughest problems arose during remote shipments in hot, humid months. During a summer shipment, surface caking showed up on arrival at a client’s site, sparking a full review. Faster regional partners helped us re-route supply on the fly while we improved packaging—now incorporating humidity and temperature monitoring tags so even intercontinental transit doesn’t catch us off guard.
No batch process remains perfect over time. We run constant reviews with both maintenance and R&D teams to anticipate reactor fouling and off-ratio feeds. Every adjustment in a fluorinated amino acid process must balance between maximizing throughput and avoiding trace-level impurities that can derail downstream synthetic campaigns.
Clients rely on us not just to deliver product, but also continuity. Global demand for high-purity fluorinated amino acids shows no signs of slowing, and we recognize that price squeezes and raw material tightness cause cascading headaches for project leaders. In these cases, open communication, honest forecasting, and agile manufacturing serve as our strongest solutions.
We maintain close relationships with raw material vendors, qualifying alternate sources well in advance and conducting parallel validation runs. Substituting inputs is never taken lightly; every switch triggers new stability and performance testing in both solution and solid forms. End users get informed early, long before any material change reaches their facility.
Our analytical and technical staff stay in regular contact with R&D leads at customer sites, providing guidance for method transfer or troubleshooting. We collect application data, process feedback, and documentation requests to better tailor subsequent production parameters.
Consistent manufacturing only proves itself when backed by extensive analytics. Each lot of AFBA-234 goes through both in-house and third-party labs for cross-validated purity, identity, and stability testing. HPLC, NMR, and mass spectrometric data go into a digital batch record, accessible to authorized clients.
We encourage users to request full analytical packs before undertaking new regulatory filings. Many of the groups we support operate under GLP or GMP requirements, and our quality infrastructure matches these demands with rigorous record keeping.
Even with top-end analytical gear, the human factor matters most. Our on-shift analysts have trained on the full spectrum of amino acids and catch subtle deviations before they become customer-facing problems. Every complaint, no matter how rare, prompts a full-scale investigation and open reporting back to the affected customer.
Making 2-Amino-3-Fluorobutyric Acid the right way means more than just finishing a batch or shipping on time. It relies on knowing the unforgiving standards our customers face every day—whether it’s hitting a synthetic milestone, passing a regulatory audit, or scaling a new drug candidate to clinic. The value comes from standing behind every drum, every gram, and offering the direct support only a manufacturer can provide.
Daily conversations with our user community drive our ongoing improvements. We listen to early warnings about processing quirks, adjust specs to fit emerging workflows, and share our accumulated experience. Our focus stays on delivering material that not only meets analysis but also stands up to the unpredictable demands of laboratory and manufacturing life.
AFBA-234’s ongoing refinement is the direct result of listening, experimenting, and putting in the unglamorous work year after year. While the molecule itself doesn’t change, the real difference comes from those of us on the production and support teams, working to earn our customers' trust in each new project. This approach means you get a product shaped by practical realities—not just another listing on a catalog page.