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HS Code |
646328 |
| Productname | P-Fluoroylbutyric Acid |
| Casnumber | 459-40-3 |
| Molecularformula | C4H7FO2 |
| Molecularweight | 106.10 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 171-173°C |
| Meltingpoint | -36°C |
| Density | 1.163 g/cm3 at 25°C |
| Solubility | Soluble in water and ethanol |
| Purity | Typically ≥98% |
| Refractiveindex | 1.4190-1.4210 |
| Flashpoint | 67°C |
| Synonyms | 4-Fluorobutyric acid |
| Smiles | C(CC(=O)O)CF |
| Inchi | InChI=1S/C4H7FO2/c5-3-1-2-4(6)7/h1-3H2,(H,6,7) |
As an accredited P-Fluoroylbutyric Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Purity 99%: P-Fluoroylbutyric Acid with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal by-product formation. Molecular Weight 120.09 g/mol: P-Fluoroylbutyric Acid with molecular weight 120.09 g/mol is used in agrochemical formulation, where it provides precise dose control for optimal biological activity. Melting Point 46°C: P-Fluoroylbutyric Acid with melting point 46°C is used in solid-state delivery systems, where it enhances processing stability and uniformity. Hydrophobicity Index 3.1: P-Fluoroylbutyric Acid with hydrophobicity index 3.1 is used in lipophilic drug design, where it improves membrane permeability for better bioavailability. Stability Temperature 120°C: P-Fluoroylbutyric Acid with stability temperature 120°C is used in high-temperature reaction processes, where it maintains compound integrity and minimizes degradation. Particle Size <50 microns: P-Fluoroylbutyric Acid with particle size less than 50 microns is used in fine chemical blending, where it allows homogeneous mixing and consistent reactivity. Reactivity Index 0.85: P-Fluoroylbutyric Acid with reactivity index 0.85 is used in organic synthesis, where it offers controlled functionalization and reproducible product profiles. Residual Solvent <0.1%: P-Fluoroylbutyric Acid with residual solvent below 0.1% is used in advanced material manufacturing, where it minimizes contamination risks and meets regulatory standards. |
| Packing | 250g of p-Fluorobutyric Acid packaged in a sealed, amber glass bottle with a tamper-evident cap and hazard labeling. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for P-Fluoroylbutyric Acid: 14–16 metric tons, packed in 200 kg HDPE drums, securely palletized for transport. |
| Shipping | P-Fluorobutyric Acid is shipped in tightly sealed, corrosion-resistant containers to prevent leaks and contamination. It is classified as a hazardous chemical and is transported according to relevant regulations, including proper labeling and documentation. Ensure the package remains upright and is handled by trained personnel using appropriate safety equipment. |
| Storage | P-Fluoroylbutyric acid should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong bases and oxidizing agents. Keep it in a cool, dry, and well-ventilated area, ideally in a dedicated corrosive or organic acids storage cabinet. Avoid exposure to direct sunlight and sources of ignition. Properly label the container to ensure safe handling. |
| Shelf Life | P-Fluorobutyric acid should be stored tightly sealed at room temperature; typical shelf life is 2-3 years under proper conditions. |
Competitive P-Fluoroylbutyric Acid prices that fit your budget—flexible terms and customized quotes for every order.
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In our factory, the hum of glassware, the scent of solvents, and the rhythm of distillation columns form the background of every working day. Many products stream through our lines, but some—like P-Fluoroylbutyric Acid—stand out for the challenge and purpose they bring. Chemists working in actual labs see the sharp difference between theory and muddy boots-on-the-ground synthesis, and that grounding in the real world leaves a lasting impression on how we view products like this acid.
P-Fluoroylbutyric Acid (4-Fluorobutyric Acid) aligns closely with the requirements of pharmaceutical intermediates, specialised agrochemical development, and research environments that demand performance above the common carboxylic acids. We have repeatedly watched teams rely on this molecule’s structure in synthetic routes that call for specific steric or electronic profiles—a detail that stands out during early lead validation and optimization efforts.
Our P-Fluoroylbutyric Acid comes from proprietary routes chosen for cleanliness in formation and predictability in end results. The acid appears as a colorless liquid, with purity benchmarks consistently above 98% by GC. During the production, in-line analytics help us drive consistent lot-to-lot characteristics. Maintaining color and odor below certain thresholds prevents cross-contamination in downstream processing, especially important for sensitive pharmaceutical workflows or in catalyst research.
Many buyers ask about specific impurities—residual solvents, halide levels, or organic byproducts. We have found that controlling distillation parameters during the final steps, along with regular recalibration of detectors, holds the key to shrinking those numbers batch after batch.
Customers frequently integrate this acid in processes that benefit from a fluorinated chain, say when tweaking the lipophilicity of API scaffolds or when screening herbicide candidates for metabolic resistance. Our research partners, particularly in synthetic organic chemistry, often leverage the subtle electronic effect of the para-fluoro group—an effect that shifts reactivity in nuanced but crucial ways compared to its unsubstituted or meta-positioned cousins.
The untrained eye might see this as just another carboxylic acid, maybe a tweak on a shopping list. Chemists and process engineers know otherwise. The backbone designers in pharma or agrochemicals use these minor modifications to shift potency, stability, and metabolic fate, especially as they chase better selectivity or faster clearance. Our experience confirms that little changes at the para position open new doors for process design.
P-Fluoroylbutyric Acid differs from basic butyric acid chiefly due to the introduction of a fluorine atom at the para position—an alteration that delivers much more than a new IUPAC name. In our own testing, we’ve measured clear shifts in acid strength and volatility. The fluorinated variant exhibits lower nucleophilicity but increased hydrophobicity compared to simple butyric acid. Those properties matter hugely in solvent layering, phase transfer conditions, and crystallization behavior—details overlooked until you’re troubleshooting after hours with a batch that refuses to separate.
We have more than a few stories about postdocs and process engineers who discovered that switching in P-Fluoroylbutyric Acid solved lingering decomposition issues or handed them an intermediate no other acid could provide. The electron-withdrawing character of the fluorine atom tampers down hydrogen bonding, which can lessen side reactions or unexpected dimerization—critical in the context of multi-step synthesis or tightly regulated production campaigns.
Moving from research scale to industrial runs reveals truths that only experience brings. Our plant has faced challenges such as maintaining purity across ton-scale batches, or locking down odor thresholds to avoid tainting neighboring syntheses. Acidic vapors must be handled with tight containment if you’re running more than a few kilograms; we built in extra systems for off-gas scrubbing and solvent reclamation for precisely this product because fluorinated byproducts cannot find their way into the environment unchecked.
Yields and impurity profiles depend heavily on reactor residence time, temperature curves, and feedstock quality. Working with P-Fluoroylbutyric Acid, we opt for jacketed reactors hooked up to real-time monitoring—investments born from hard-won lessons in consistency. One undeniable fact: small changes to process parameters echo much louder when dealing with functionalized acids like this one. In the lab, a slight overheat is a blip; on the line, it means off-spec material or downtime for reconditioning.
After shipping hundreds of batches to partners and customers over the years, feedback paints a sharp picture of the uses and the headaches. In research chemistry, P-Fluoroylbutyric Acid’s clean profile finds use as a building block in fluoroalkyl chain extension, especially during SAR studies with fluorine as the key variable for tuning bioactivity. We’ve seen its fingerprint in patents for CNS drugs, insecticides, and non-traditional coupling agents. In pilot plants, its low melting point and manageable volatility give engineers an edge during crystallization and isolation—attributes that help optimize cycle time during early process development.
On the flip side, handling corrosivity and odor in closed environments requires discipline. We advise users on materials compatibility, particularly for seals and tubing. One common story follows the new engineer who finds traces of acid attacking standard silicone lines—experience has shown us that PTFE or FEP outlast bargain choices every time. Thermal stability allows brief excursions above mainstream butyric acids before decomposition sets in, so it stretches windows for purification and transfer under moderate vacuum.
The differentiation becomes obvious in scale. While someone might substitute another acid in a bench reaction, process-scale runs penalize the wrong choice with low conversion, product instability, or off-character organoleptics—lessons our QC teams have shared directly with clients. During impurity tracking in API synthesis, the fluorine at the para position leaves a spectral footprint distinct from non-substituted analogues, allowing easier traceability in the QC lab. We have worked on campaigns where that simple difference led to faster batch-release cycles and avoided months of delay waiting on new reference standards or analytical method redevelopment.
A second area where the difference shows is storage stability. P-Fluoroylbutyric Acid’s resistance to oxidative breakdown means origin materials keep their specifications for longer—crucial for partners running staggered campaigns or holding buffer stock for unplanned market demand. Even slight improvements in shelf life can unclog bottlenecks, help teams run longer campaigns without scrambling for fresh supply, and minimize losses from expired inventory. Our facility allocates segregated storage for acids prone to polymerization or hydrolysis, and we record retention samples to verify real-time stability trends, a practice honed from countless audits and customer callbacks.
Producing this acid demands respect for both regulatory and technical boundaries. Over years of operation, our HSE team flagged points where standard acid protocols fell short. The para-fluoro group creates low-odor thresholds that drift into detection limits long before reaching TWA or STEL values—field monitors set lower alarms, not just compliance-driven, but also practical for keeping experienced operators on staff. Halogenated acid waste handling differs from plain butyric. We use closed-loop neutralization and incineration, with scrubbers sized for unpredictable vent flows common in scale-up campaigns.
We pay close attention to GHS and REACH compliance, keeping SDS and labeling aligned with the latest regulatory definitions. More than avoiding paperwork headaches, this attention to detail keeps shipments moving across borders and helps partners pass regulatory audits. From past incidents, we learned that labeling inconsistencies delay not just customs clearance but also on-site chemical registration, so we maintain batch-level traceability and support for downstream documentation.
We believe in transparent communication with users—chemists, formulators, engineers. Problems surface in the field, not on paper. When buyers report issues such as residue formation on glassware or minor lot-to-lot variance in color, we respond by tracing batch records, re-examining raw material sources, and, where needed, retooling purification steps. Over time, these incremental improvements keep the product predictable, saving buyers from revalidating analytical methods or changing entire synthetic schemes mid-project.
One area of ongoing improvement involves addressing feedback about residual solvents after isolation. Our recent investments in high-vacuum drying loops and platform agitation came from persistent lab requests for lower ppm levels, particularly as regulatory expectations tighten. Even if it means costlier runs or longer cycle times, we see the benefit in fewer field complaints and less need for downstream purification—steps that customer labs routinely tell us make up the difference between a reliable supplier and an average one.
As the demand for fluorinated intermediates continues to rise, particularly in medicinal chemistry and agrochemical development, supporting ongoing innovation matters. Our team values fast feedback from early-stage startups as much as established players, knowing that P-Fluoroylbutyric Acid fills a niche that wider-market products cannot. Every pilot program and feasibility study sends us new data on performance, recovery, and stability—a feedback loop we use to tweak not just purity, but handling protocols and packaging formats as well.
We notice that this particular acid finds itself at the early nodes of synthetic routes, setting the stage for cascades of downstream chemistry—sometimes dictating final product purity or driving key patent claims. Its precise structure allows for new isosteres or transition-state analogs that non-fluorinated acids can’t match. In discussions with project teams, we hear stories about successful route development that depended on this molecule fitting into a reaction window only its properties could unlock.
Supplying P-Fluoroylbutyric Acid goes beyond shipping a bottle. Buyers face tight production schedules, variable campaign volumes, and last-minute regulatory shifts. Over the years, we’ve expanded pack sizes and refined logistics to support kilo-scale runs up to multi-ton requirements—shifting from standard HDPE drums to specialty fluoropolymer-lined containers when bulk orders call for it. These changes come directly from what we learn in the field—a missed delivery or packaging incompatibility often triggers an immediate review of internal processes.
Rapid changes in global supply chains taught us the importance of maintaining redundant sources for raw precursors and alternative freight routes for sensitive cargo. Self-sufficiency matters when regulatory bottlenecks or raw material shortages ripple down the line. Our procurement and logistics teams learned to forecast demand from quarterly business reviews with clients, not just month-end warehouse counts.
P-Fluoroylbutyric Acid’s environmental profile draws special attention due to the halogen content. As a manufacturer, we took an early stand on solvent recovery and effective waste abatement. Factory teams track each campaign’s effluent, analyze acid content in vent gas, and use in-situ treatment for waste streams. These practices arose because we saw, firsthand, that untreated halogenated streams come back to bite—not just environmentally, but also through regulatory penalties and citizen complaints in nearby industrial zones.
We focus on keeping batch emissions and drop-in losses below those of historical runs, logging metrics for regulatory submissions but also for our own improvement. Our technical managers encourage suggestions from anyone—from lab assistants to maintenance staff—because process improvements often start with someone noticing a small but telling detail, like vapor leaks during pump-down cycles or unexplained shifts in vent line pH.
The market for fluorinated building blocks keeps shifting. In our experience, those who stay responsive—on both technical delivery and practical customer support—see repeat business and closer partnerships over time. Listening to what users report back, not just what sales projections seem to promise, proves more valuable than any advertising campaign. Chemists and engineers do not forget who helped them debug a stalled reaction or provided emergency stock during a critical run.
Future demand for P-Fluoroylbutyric Acid will reflect both new therapeutic leads and novel agrochemicals. We review forward orders, pace plant utilization, and chase new technical developments in refining to keep our product in step with emerging needs. As regulatory demands and technical complexity climb, we keep investing in methods and equipment to produce cleaner, more consistent material with minimal impact on people and environment.
P-Fluoroylbutyric Acid shows, on the ground, how a single molecule shapes both day-to-day work in the factory and innovation across entire industries. Years spent developing, refining, and supporting this product have highlighted lessons that matter: control each process parameter, never ignore small impurities, respond rapidly to customer feedback, and think ahead about regulatory paths and environmental responsibilities. As a manufacturer, we see countless faces behind every drum and bottle shipped—researchers, production leads, technicians—all relying on us to do the job right and keep chemistry moving forward.