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HS Code |
745866 |
| Chemical Name | 4-Fluorophenylglycine |
| Cas Number | 771-61-9 |
| Molecular Formula | C8H8FNO2 |
| Molecular Weight | 169.16 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 255-259°C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Iupac Name | 2-amino-2-(4-fluorophenyl)acetic acid |
| Smiles | C1=CC(=CC=C1C(C(=O)O)N)F |
| Storage Temperature | 2-8°C |
| Synonyms | DL-4-Fluorophenylglycine |
As an accredited 4-Fluorophenylglycine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 4-Fluorophenylglycine (25g) is a sealed amber glass bottle, clearly labeled with compound details, hazard warnings, and batch information. |
| Shipping | 4-Fluorophenylglycine is shipped in tightly sealed, chemically resistant containers to prevent contamination and degradation. Packages comply with relevant regulations for handling and transport of chemical substances. Appropriate hazard labeling, documentation, and protective measures are included. Shipping may require temperature control depending on specific storage recommendations provided by the supplier or manufacturer. |
| Storage | 4-Fluorophenylglycine should be stored in a tightly sealed container, protected from light and moisture. Keep at room temperature in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Ensure the storage location is clearly labeled and observe standard laboratory safety procedures to prevent contamination or accidental exposure. |
Applications of 4-Fluorophenylglycine in Industrial Manufacturing4-Fluorophenylglycine demonstrates consistent value in several specialized sectors as a building block for pharmaceutical intermediates, fine chemical synthesis, peptide drug production, and agrochemical active ingredient development. As a primary manufacturer, we monitor real-world application standards and formulation requirements for each downstream industry. 1. Pharmaceutical API Intermediate SynthesisMajor pharmaceutical producers use 4-Fluorophenylglycine during multi-step synthesis of advanced intermediates for non-steroidal anti-inflammatory drugs (NSAIDs) and targeted oncology compounds. Its monofluorinated aromatic ring participates in amide-bond forming steps and undergoes further structural modification under controlled batch reaction conditions. Manufacturers select this raw amino acid for creating optically pure intermediates, ensuring chiral integrity throughout the route. Strict traceability and analysis of residual solvents occur at each step, following quality management protocols during upscaling. Industry compliance standards
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2. Peptide Drug Synthesis (Solid-Phase Peptide Synthesis, SPPS)Custom peptide producers rely on 4-Fluorophenylglycine as a non-standard amino acid component for constructing fluorinated peptide chains. The substituted aromatic structure can influence binding affinity and metabolic stability in clinical peptide candidates. During SPPS, our material is converted to Fmoc-, Boc-, or CBZ-protected derivatives before resin loading. Rigorous inspection for optical purity and resin loading consistency ensures downstream stepwise elongation proceeds with minimal sequence loss. Industry compliance standards
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3. Agrochemical Active Ingredient SynthesisResearch-based agrochemical companies utilize 4-Fluorophenylglycine to access phenylglycine-derived herbicidal and fungicidal compounds, often through combined aromatic fluorination and side-chain modification. This raw material enters at key synthetic stages where a fluorophenyl moiety is needed for bioactivity enhancement or metabolic resistance. Analytical verification of purity and absence of prohibited impurities is enforced to ensure acceptability for export formulation plants and regulatory dossier submission. Industry compliance standards
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4. Fine Chemicals – Fluorinated Aromatic Building BlocksSpecialty chemical manufacturers depend on 4-Fluorophenylglycine as a structural core in custom fluorinated aromatic compound synthesis. The raw material enables tailored electronic and steric properties for downstream intermediates, dyes, and advanced organic materials. Quality assurance involves monitoring racemization rates during transformations and confirming batch-to-batch homogeneity via HPLC and chiral GC methods. Analytical reporting supports customer R&D and process transfer documentation for specialized syntheses. Industry compliance standards
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Since the earliest batches rolled out of our controlled reactors, 4-Fluorophenylglycine has been one of those products that keeps pushing us to refine both our process and our understanding of fine chemistry. This compound, with its distinct para-fluoro substitution on the phenylglycine skeleton, stands out among the many specialized amino acids that pass through our facility. Our chemists have handled this molecule in volumes that make the quirks and nuances more than just theory—every day, we document adjustments, variations, and observations, ensuring each batch meets what the industry expects.
What makes 4-Fluorophenylglycine a frequent request from both established and up-and-coming pharma projects is its utility in advanced research chemistry. Chemists building modern peptidomimetics or crafting innovative APIs often reach for this derivative because it carries an additional dimension of electronic and steric tuning, thanks to the fluorine atom lodged in the para position. The creation process demands vigilance, especially during the electrophilic aromatic substitution and the delicate handling that follows. Years of scaling from grams to industrial multipurpose reactors has taught us more about the stability profile and how reaction impurities respond to purification steps.
Our main production focus circles around a model that sits within the highest purity grades demanded by pharma syntheses—typically, we control for a minimum of 98% GC purity in finished batches. Typical batches come out as white to off-white solids, with melting points matching established literature, and our QC teams run both HPLC and NMR to check not just for headline values but for subtler impurity fingerprints. Our batches move directly from reactor to isolation and through to carefully monitored drying rooms, all handled by staff trained to spot the early warning signs of moisture uptake or cross-contamination.
From a manufacturing perspective, 4-Fluorophenylglycine’s key difference from generic phenylglycine, or other substituted analogs like 3-fluorophenylglycine, lies in reactivity and downstream behavior. The para-fluoro moiety alters both electron distribution within the aromatic ring and the compound’s interaction with coupling reagents in peptide synthesis. In our plant, this translates to small but unmistakable differences in solubility and crystallization compared with non-fluorinated or differentially substituted variants.
Most material leaves our plant destined for peptide science, medicinal chemistry research, and pharmaceutical intermediate production. Our technical team works closely with several R&D groups focused on fluorinated amino acid analogs—these molecules are pivotal for tuning both metabolic stability and binding selectivity in drug candidates. Some customers use our 4-Fluorophenylglycine directly in solid-phase peptide synthesis, reporting stronger resistance to oxidative degradation and improved incorporation in automated synthesizers.
The demand for specifically para-fluorinated glycine, as opposed to meta- or ortho- varieties, comes down to balancing hydrophobicity with steric effects. The para-fluoro group occupies a spot that influences the adjacent amine and carboxyl in a way that suits certain targeted biological activities. From our reactor operators' point of view, controlling for this specific regiochemistry isn’t a trivial task—quality comes from deliberate process tuning: precise reagent atmosphere, staged additions, and vigilant monitoring. This is necessary because an off-spec batch that contains even small amounts of meta- or ortho-isomers disrupts downstream workflows for our pharmaceutical customers.
Working with the unsubstituted phenylglycine, or with analogs bearing other substituents like methyl, chloro, or bromo, brings a different slate of manufacturing headaches and opportunities. The fluorine atom, light as it is, creates a final product with markedly higher chemical resilience, influencing shelf life and storage requirements. In our facility, we’ve charted the hygroscopicity profile of every batch and compared it with similar structures—4-Fluorophenylglycine tends to resist moisture uptake, resulting in lower caking and fewer logistical hiccups during transportation.
In practical terms, our formulation teams noticed that 4-Fluorophenylglycine's distinct balance of lipo- and hydrophilicity carries over into ease of solvent exchange, direct crystallization, and recovery processes. Purification by standard re-crystallization or preparative HPLC gets a boost, reducing solvent consumption and shortening turnaround. As manufacturers, we appreciate these knock-on effects, since they make bulk production more rational and waste streams easier to manage. Periodic side-by-side evaluation with closely related molecules reminds us how slight shifts in molecular structure can ripple out into real savings—or real frustration—on the production line and beyond.
Scaling up 4-Fluorophenylglycine synthesis from glassware to jacketed vessels taught us plenty about solvent volume optimization, thermal stability, and work-up reliability. The para-fluoro group—while robust during the main synthetic route—sometimes introduces surprises in side-product distribution, especially in poorly controlled exotherms. Our team learned that precise temperature ramping and staged quenching avoids forming regioisomeric byproducts that otherwise draw out purification steps.
Handling 4-Fluorophenylglycine in its final solid form raised its own set of challenges for our plant crew. Granule flow properties remain stable under ambient conditions, making bagging and drum-filling more straightforward than other amino acids prone to clumping. That being said, the product’s finely divided powders can still generate airborne dust under forceful transfer, so we invested early in both dust abatement and staff training. Over years, we fine-tuned our handling protocols so that quality assurance keeps pace with increasing order volumes.
Our technical support desk often hears from users incorporating 4-Fluorophenylglycine into synthetic peptides and small molecule libraries. One common thread: users value the compound’s repeatable behavior under both manual and automated assembly conditions. Chemists working in high-throughput environments tell us the para-fluoro variant outperforms unsubstituted versions in terms of incorporation rates and finished product longevity, especially for preclinical candidates intended to probe peptidase resistance or altered pharmacodynamics.
Requests for custom purities and particle sizes continue to shape our batch scheduling. Some clients want fine powders for solution-phase use, while others request slightly coarser cuts for direct charging into reactor feed hoppers. Our willingness to adapt here comes straight from the floor, where process operators and QC staff coordinate tightly to deliver what researchers genuinely rely on.
Each round of quality analysis, from incoming raw material checks right through to final drum inspection, forms the backbone of our reliability. For 4-Fluorophenylglycine, we trace every reagent back to original supply, making real-time adjustments based on current analytical feedback. Since the para-fluoro route can show drift in impurity profile if the wrong oxidizing conditions crop up, we prioritize regular review sessions with both production and analytical teams. Working shoulder-to-shoulder with our own staff and trusted external labs, we examine FTIR, NMR, and GC-MS spectra to stay out ahead of potential batch deviation.
We also maintain reserves of retained material from each batch, allowing us to quickly investigate any end-user performance concern or shipment query. These housekeeping habits, built up over years of close work with demanding partners, help us both respond rapidly and minimize any risk of mismatch between what we ship and what our customers expect to unbox.
A significant share of our 4-Fluorophenylglycine output supports ongoing pharmaceutical research initiatives. Many partners now push for tighter impurity profiles or require trace impurity disclosure that wasn’t insisted upon a decade ago. Responding to these new pressures, we’ve upgraded both our analytical instrumentation and process transparency. Every gram of 4-Fluorophenylglycine that leaves our production lines comes with a comprehensive batch analysis, run by staff trained to detect trends before they grow into problems.
By working with researchers in real time—sharing insights about best practices for protection/deprotection steps, optimal solvent systems, and long-term storage tips—our technical team builds relationships grounded in practical knowledge. Often, we work together not only to solve immediate synthesis problems, but also to anticipate future needs should regulatory changes or novel pharma strategies demand more precise control over side-reactivity, metal trace content, or residual solvents.
Producing 4-Fluorophenylglycine at commercial scale forces us to look closely at the environmental and occupational health profiles of every step. Regular audits push us to cut down on solvent waste and engineer safer, more contained workflow designs. Since the introduction of our latest closed-loop solvent recovery system, total hazardous waste output per batch dropped measurably, and staff exposures fell in tandem. In practice, this translates to a cleaner, more predictable workplace which supports both material consistency and regulatory compliance.
By consulting with safety specialists, we adopted improved containment and ventilation, aligning our practices with the strictest of modern expectations. As our daily throughput and batch frequency rise, we maintain a readiness for greater scrutiny while sharing new insights about process safety with our industry peers.
Success with a molecule as nuanced as 4-Fluorophenylglycine does not rest solely on equipment or software upgrades. At our site, practical training and on-the-job knowledge transfer underpin every successful scale-up. Our most seasoned operators mentor new staff, passing on both the hard-won tricks for handling tricky intermediates and the less tangible ability to spot potential deviations early.
Each time we commit to investing in process improvements, the team deliberates over real-world returns: better yields, tighter purity brackets, faster order fulfillment. Through internal process audits and ongoing dialogues with end-users, we continuously adapt both our documentation and our manufacturing workflows.
Our direct relationships with research scientists, formulation chemists, and scale-up engineers fuel our own learning. Each feedback loop clarifies which parameters deserve the most attention—be it particle size and free-flowing properties for automated lines, or ultra-low residual solvent content in the final product. As global standards tighten and the pace of discovery accelerates in synthetic peptide chemistry, our process learnings compound, allowing the supply chain to deliver on both reliability and transparency.
Being at the manufacturing source, we witness firsthand how small changes ripple through both our own workflows and the wider industry. For every kilogram of 4-Fluorophenylglycine packed and shipped, our focus stays trained on supporting the most ambitious projects in contemporary drug design, enabling customers to move from bench to market with direct backing from a supplier that values both practical realities and scientific progress.
Through years of producing 4-Fluorophenylglycine on both modest and grand scales, we have gained perspectives that only direct manufacture and close cooperation with the scientific community provide. Our commitment is visible in every delivered batch: consistent quality, reliable documentation, and a willingness to solve each new challenge shoulder-to-shoulder with customers who trust us to help them go further. This compound may be a small piece of the puzzle, but it reflects a large portion of what responsible manufacturing can achieve.