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HS Code |
239619 |
| Product Name | 4-Fluorophenoxyacetic Acid Hydrazide |
| Cas Number | 83506-92-7 |
| Molecular Formula | C8H9FN2O2 |
| Molecular Weight | 184.17 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 142-146°C |
| Solubility | Soluble in DMSO, methanol |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Synonyms | 2-(4-Fluorophenoxy)acetohydrazide |
| Smiles | NNCC(=O)Oc1ccc(F)cc1 |
As an accredited 4-Fluorophenoxyacetic Acid Hydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging contains 25 grams of 4-Fluorophenoxyacetic Acid Hydrazide in a sealed amber glass bottle, labeled with chemical details. |
| Shipping | 4-Fluorophenoxyacetic Acid Hydrazide is shipped in sealed containers, protected from moisture and light. It is handled as a potentially hazardous chemical and packed according to international regulations for chemical transport. Proper labeling and documentation ensure safe handling, with expedited delivery in temperature-controlled conditions when required to maintain product integrity. |
| Storage | Store 4-Fluorophenoxyacetic Acid Hydrazide in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and clearly labeled. Avoid moisture, heat, and ignition sources. Use appropriate chemical storage cabinets and ensure proper handling with suitable personal protective equipment to prevent contamination and exposure. |
Applications of 4-Fluorophenoxyacetic Acid Hydrazide in Industrial ManufacturingAs a manufacturer of 4-Fluorophenoxyacetic Acid Hydrazide, we supply this specialty intermediate to leading chemical sectors with direct applications in pharmaceutical synthesis, agricultural chemical formulation, fine chemical production, and advanced material R&D. The following industrial uses reflect real-world implementations in high-value downstream processes, supported by established compliance protocols and formulation expertise. 1. Active Pharmaceutical Ingredient (API) Synthesis: Anti-Tubercular AgentsAPI developers utilize 4-Fluorophenoxyacetic Acid Hydrazide as a hydrazide intermediate in the preparation of heterocyclic active molecules for anti-tubercular and related antimicrobial drugs. Medicinal chemists employ this building block for functional group transformations, introducing fluorinated structures to enhance the metabolic stability and bioavailability of final actives. The typical workflow includes hydrazinolysis, condensation with carbonyl compounds, or further derivatization. Material QC, process control, and documentation must align to ICH, cGMP, and pharmacopoeial expectations. Industry compliance standards
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2. Agrochemical Discovery: Herbicide Intermediate ManufactureResearchers in agrochemical discovery use 4-Fluorophenoxyacetic Acid Hydrazide to introduce selective hydrazide motifs necessary for the rational design of novel herbicidal and fungicidal agents. Its incorporation enables structure-activity relationship studies and enhances molecular binding affinity toward plant enzyme targets. Application requires strict attention to active substance registration and OECD guidelines during scale-up and pilot production. Industry compliance standards
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3. Fine Chemical & Specialty Synthesis: Building Block for Aromatic Hydrazones4-Fluorophenoxyacetic Acid Hydrazide serves fine chemical manufacturers as a key building block for hydrazone ligands and precursors deployed in coordination chemistry, sensor materials, and dye formulation. The hydrazide's electronic properties facilitate targeted condensation reactions with carbonyl compounds to create stable, conjugated hydrazones used in analytical assays and specialized pigment preparations. Industry compliance standards
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4. Advanced Materials Development: Fluorinated Monomer IntermediateMaterials R&D teams use 4-Fluorophenoxyacetic Acid Hydrazide in the design of specialty polymers and high performance coatings, leveraging the hydrazide’s bifunctional reactivity and aromatic fluorination. It supports the synthesis of monomers for fluorinated polyhydrazides and, after further chemical modification, introduces thermal and chemical resistance into electronic, membrane, and filter materials. Regulatory and QC procedures follow ISO, ASTM, and technical customer specifications. Industry compliance standards
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5. Chemical Sensor Development: Precursors for Fluorinated ProbesAnalytical instrument manufacturers and sensor developers employ 4-Fluorophenoxyacetic Acid Hydrazide as a precursor in synthesizing fluorinated chemosensors and indicator molecules for metal ions and reactive species. Its fluorine content enhances probe sensitivity for modern spectroscopic and electrochemical detection platforms. Compliance with chemical substance regulations and rigorous method validation are essential at this development stage. Industry compliance standards
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In chemical manufacturing, clear distinctions define how products behave, how they’re handled on the plant floor, and how clients approach their application goals. The product 4-Fluorophenoxyacetic Acid Hydrazide didn’t appear overnight as a simple catalog addition. Our plant teams saw its growing inquiries from research laboratories, pharmaceutical developers, and agrochemical innovators. We’ve observed its rise out of direct, hands-on demands: a compound with genuine differentiation from both simple hydrazides and related functionalized benzoic acid derivatives.
We produce 4-Fluorophenoxyacetic Acid Hydrazide under the model identifier FPAH-104. Process engineers have traced the development path since the pilot reactors. The core structure couples phenoxyacetic acid's flexibility with the reactivity of a para-positioned fluoro. In practical terms, this core lets formulators target site-specific transformations. Out on the floor, tech staff know they’re handling something that will do more than just serve as a stock intermediate. It’s a matter of direct synthetic value. Every time we scale a batch, the fluoro group delivers subtle electronic effect–not too pronounced, just enough to tune the hydrazide’s activity for downstream synthesis or bioactivity modulation.
Working with 4-Fluorophenoxyacetic Acid Hydrazide, we focus on purity and consistency for labs performing organic synthesis or preclinical development. Our product comes as a fine, white powder, reflecting the tight control we maintain on reactor temperature and solvent selection. Moisture content, homogeneity, and trace impurity tracking have practical significance. These aren’t abstract checkboxes but daily checkpoints for our QA analysts—to avoid processing hiccups in partner labs where a foreign ion or secondary byproduct can derail an entire synthetic campaign.
We keep the melting point in the range that assures shelf-stability and ease of handling, usually confirmed between 134 and 137°C. Our customers don’t need granules that cake or powders that degrade after a month. We audit against that risk at discharge and packing. Handling safety also ranks high. Real-world loading, unloading, and weighing shape our process design decisions just as much as published chemical hazards. In this case, the hydrazide’s dustiness sometimes worries lab workers, which is why we sample particle size and ensure the final product flows without creating clouds during opening or dosing.
In boardroom presentations, it’s easy to read out a list of technical points. On the manufacturing floor, experience with product batches teaches the actual differences. We have made standard phenoxyacetic acid hydrazide, and the absence of the fluoro handle changes both the electronic and physical aspects. The para-fluoro group plays a real role—it tempers the hydrazide’s chemical reactivity, shifting pathways that influence downstream reactions, especially where selectivity and yield matter in pharmaceuticals or advanced agrochem intermediates. This distinction surfaces when we compare applications. A client focused on hydrazide exchange will report different kinetics with the 4-fluoro product, noting smoother transformations or improved control in their reductive aminations.
We’ve seen research chemists working on semi-synthetic APIs gravitate toward this molecule for the fine-tuning the substituent brings. Its modulated electron density often translates to better compatibility with certain protecting agents, more reliable coupling, and reduced side reactions that complicate scale-up. These outcomes are visible not in theory but in the yield logs and chromatograms that come back to us for batch-to-batch evaluation.
Researchers and process chemists rely on our 4-Fluorophenoxyacetic Acid Hydrazide to develop active pharmaceutical ingredients, crop protection agents, and sometimes, specialty polymers. In practice, our partners find this product suits reactions where the hydrazide function needs to be both activated enough to participate efficiently and stable enough to avoid runaway decomposition. Its behavior is not interchangeable with similar compounds. Conventional hydrazides sometimes degrade or react with unwanted haste. The para-fluoro substitution brings that middle-ground reactivity, letting pathways proceed cleanly—not too aggressive, not too inert.
We’ve received feedback from contract research organizations who value that our batches consistently match their incoming inspection numbers. That repeatability lets them work out robust procedures, since the compound’s reactivity and physical handling don’t vary unpredictably between shipments. This reliability comes from years of refining our reactor conditions, drying strategies, and post-synthesis purification.
Some developers focus on hydrazide-based linkage or chain-extension in their molecular scaffolds. With 4-Fluorophenoxyacetic Acid Hydrazide, side reactions linked to aromatic overactivation or nucleophilic attack appear less often, reducing byproduct handling and post-reaction cleanup. Analytical chemists in our client labs have praised this, seeing sharper peaks in their HPLC and easier product isolation. These comments emerge from use, not from literature abstracts.
It’s easy to get lost in a sea of catalog acids and hydrazide derivatives, but we’ve observed practical and economic distinctions. Regular phenoxyacetic acid hydrazide offers a baseline for building, but lacks the nuanced activity the fluoro group brings. Other halogenated analogs—such as chloro or bromo—show reactivity profiles that complicate certain downstream steps. Our 4-fluoro choice provides just the right electron-withdrawing effect, which smooths functional group transformations without introducing the bulk or reactivity extremes seen in heavier halides.
This real-world balance has caught the attention of both medicinal chemists pushing for novel enzyme inhibitors, and agrochemical chemists looking for improved metabolic stability. Since the fluoro substituent shapes the product’s behavior in living systems, our partners have reported less problematic bioactivation and cleaner metabolic breakdown, as reflected in their in vivo screens.
We’ve supplied both small development kits and larger process quantities, noting that synthetic pathways relying on 4-Fluorophenoxyacetic Acid Hydrazide tend to scale with fewer troubles. Yields hold steady, side products run minimal, and the chromatic and thermal profiles align from milligram to kilogram quantities.
Long-term clients contact us not as anonymous suppliers but as process partners. Their feedback loops drive our plant upgrades. When an academic group finds a hydration byproduct in our hydrazide, their NMR spectra get shared directly, and we push for root cause analysis—tracing lots back to solvent lots, storage shelf, even drum material. This back-and-forth never appears in a glossy brochure, yet it’s where real reliability builds. Reproducibility isn’t a marketing term in the chemical plant; it’s the hard result of daily diligence, with attention to both synthetic and mechanical integrity.
We don’t just manage raw material purity; we observe line operators as they handle each batch, watching how powder flows, where static forms, and whether bagging lines run into snags. For 4-Fluorophenoxyacetic Acid Hydrazide, these realities shape our process improvements. We invest in upgraded HVAC filtration just as much for product quality as for operator safety, minimizing both particulate release and cross-batch contamination. Our QA crew has revised their sample collection methods, favoring split batch sampling to catch rare anomalies before they become field issues.
Users sometimes seek advice on improving solubility or working around precipitation during formulation. The solubility profile of 4-Fluorophenoxyacetic Acid Hydrazide reflects its balanced polarity—soluble enough in polar aprotic solvents like DMF or DMSO, with limited miscibility in water. We routinely run bench-scale solvent trials in our demos, sharing guidance rooted in first-hand observations, rather than just data sheets. Our R&D chemists have even co-developed solvent blends, or suggested slight warming and mechanical agitation to dissolve denser samples. We’ve seen this help both bench chemists during preps and pilot operators during transfer and scale-up.
Packaging remains another real-world constraint. We have upgraded from standard PE-lined fiber drums to antistatic, lined steel containers for bulk deliveries, responding to client experiences of package ruptures or siphoning during seasonal humidity swings. Each year, we work through feedback from client warehouses to tweak liner thickness and drum closures. Lab-scale clients prefer amber glass for storage longevity, so we cold pack some kits to hold up during summer shipping. Packaging is more than an afterthought; it shapes the entire experience, from receiving dock to dispenser.
Our team also advises partners on parallel control reactions using both substituted and non-substituted hydrazides to distinguish reactivity origins—saving time troubleshooting batch failures that can trace to subtle differences in substrate behavior or on-site humidity. These are practical lessons, learned from years of direct collaboration, not from out-of-touch technical warnings.
Manufacturing and distributing 4-Fluorophenoxyacetic Acid Hydrazide involves not only technical skill but a commitment to safekeeping people and the environment. Our production process uses closed reactor systems, high-performance ventilators, dust suppression, and solvent recycling units. We’ve reduced both airborne particulates and liquid waste to negligible levels, investing in operator training to identify spills or leaks and act with urgency, rather than waiting for external audits.
For staff working with labile hydrazides, real-world training materials go beyond standard manuals—we hold hands-on drills, reviewing donning and doffing personal protective equipment, powder transfer, and spill response. Every shift rotation includes a rapid review, reinforcing the idea that each technician’s actions shape not just individual safety, but end-customer product reliability too. Our experience isn’t taught in classrooms; it’s ingrained through daily routines and earned trust.
From a sustainability standpoint, our team looks for new solvent systems that cut energy consumption or support more benign waste streams. These don’t arise as quick fixes, but through multi-season trials and feedback from plant engineers who have mapped every drain and flask in the workshop. We see real results: reduced scrubbing chemical consumption, better solvent recovery, and smaller waste holding areas. Over time, these choices drive down overhead and environmental risk, all while serving the needs of advanced synthesis and formulation.
We see each batch of 4-Fluorophenoxyacetic Acid Hydrazide as a result of shared knowledge, extending from the earliest trial reactions to fully commercial runs. We frequently welcome visiting chemists who wish to witness pilot plant operations, or offer trial batches for new project starts. This transparent approach pays off: for our pharmaceutical and agrochemical clients, confidence in starting material quality often determines the breakthrough or stumble of a new candidate. Our field representatives double as technical consultants, closing the loop between manufacturing reality and research ambition.
Each year, we re-invest in pilot-scale improvements, production analytics, and traceability. We know newcomers to 4-Fluorophenoxyacetic Acid Hydrazide search for reliable supply and technical support. Through long-term supply contracts, standing batch reserves, or expedited small-quantity deliveries, our aim is simple: assure researchers and formulators of batch-to-batch continuity, quick response times, and deep-rooted technical support.
Having worked through hundreds of synthesis runs, fielded endless questions from troubleshooting chemists, and watched dozens of pilot campaigns rise and fall, we recognize where the nuances lie. 4-Fluorophenoxyacetic Acid Hydrazide emerges not just as another entry on a price sheet, but as a tool with demonstrable value for those striving for both efficiency and specificity in their chemical designs.
We don’t view the product as a static offering. New process tweaks, analytical advances, and user insights shape future lots. By maintaining open communication with our users and staying grounded in the real pressures of chemical manufacturing, we commit to delivering more than just material—we build ongoing relationships. Our measure of success ties not to shipment volumes alone, but to the stories of success each client achieves with the help of tailored chemical components like 4-Fluorophenoxyacetic Acid Hydrazide.
Through this approach, we bridge the daily demands of manufacturing reliability with the pursuit of chemical innovation, ensuring that every batch upholds the trust placed in us by scientists and engineers pushing the boundaries in their fields.