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3-Chloro-4-Fluorophenylhydrazine

    • Product Name 3-Chloro-4-Fluorophenylhydrazine
    • Alias 3-chloro-4-fluorophenylhydrazine
    • Einecs 629-333-5
    • 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
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    Specifications

    HS Code

    938280

    Productname 3-Chloro-4-Fluorophenylhydrazine
    Casnumber 116219-67-7
    Molecularformula C6H6ClFN2
    Molecularweight 160.58
    Appearance Off-white to light brown solid
    Meltingpoint 67-71°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Storageconditions Store at 2-8°C, tightly closed
    Synonyms 3-chloro-4-fluorophenyl hydrazine
    Smiles NNc1ccc(Cl)c(F)c1
    Hazardclass Irritant

    As an accredited 3-Chloro-4-Fluorophenylhydrazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle, screw-capped, labeled with hazard warnings and “3-Chloro-4-Fluorophenylhydrazine, CAS 151355-19-2.”
    Shipping 3-Chloro-4-Fluorophenylhydrazine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported according to regulatory guidelines for hazardous chemicals, typically under ambient temperature with clear hazard labeling. Ensure compliance with all local and international shipping regulations for safe handling and transport.
    Storage Store 3-Chloro-4-Fluorophenylhydrazine in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from heat, moisture, and direct sunlight. Handle under inert atmosphere if sensitive to air. Use appropriate personal protective equipment to avoid contact with skin, eyes, and clothing.
    Application of 3-Chloro-4-Fluorophenylhydrazine

    Applications of 3-Chloro-4-Fluorophenylhydrazine in Industrial Manufacturing

    3-Chloro-4-Fluorophenylhydrazine serves as a key intermediate in several high-value chemical synthesis pathways. Our production meets the stringent quality and consistency requirements of strict industrial segments. Below we detail the dominant downstream application domains with specific use patterns and integration methods.

    1. Pharmaceutical Intermediate for Pyrazole Synthesis

    Major pharmaceutical manufacturers utilize this hydrazine derivative as a starting reagent in the construction of heterocyclic pyrazole drug scaffolds, including advanced anti-inflammatory compounds and central nervous system agents. Integration involves direct coupling with beta-diketones or alpha,beta-unsaturated ketones under mild conditions, typically employing solvents and acidic catalysts to drive the key condensation and cyclization steps. Each output batch undergoes comprehensive in-process QC to match pharmacopeial requirements for residual impurities and hydrazine derivatives.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • USP General Chapter <467> (Residual Solvents)
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals GMP)

    Typical usage ratio

    • Stoichiometry ranges from 0.95:1 to 1.2:1 (hydrazine to diketone) based on targeted medicinal compound and process route.
    • Process optimization adjusts ratio lower if side-product formation requires tighter control.

    Downstream process integration

    • Loaded at initial condensation stage with nitrogen inlets for safety
    • Isolated after primary cyclization using liquid-liquid extraction and recrystallization
    • In-line HPLC detects trace hydrazine carryover before API finalization

    Final product types

    • Non-steroidal anti-inflammatory drug actives (e.g., pyrazole analogues)
    • Selective kinase inhibitor lead compounds
    • Pyrazolone class CNS actives
    • Custom pyrazole-based intermediates for contract synthesis

    2. Agricultural Fungicide and Herbicide Precursor

    We supply bulk volumes to global agrochemical groups specializing in the manufacture of fungicides and herbicides that depend on arylhydrazine-based lead structures. The compound undergoes substitution reactions in controlled reactors to generate essential heterocyclic moieties for crop protection agents. Batch records systematically track raw material input, with periodic compliance audits to address environmental and worker safety standards.

    Industry compliance standards

    • FAO/WHO Guidelines for Pesticide Formulation
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) Annex II
    • China ICAMA Product Registration regulations
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • Formulation typically employs 0.8–1.3 mol equivalents versus coupling partners
    • Adjustments based on final active ingredient target and byproduct minimization needs

    Downstream process integration

    • Reacted in jacketed glass-lined reactors with phase-transfer catalysis for safety
    • Introduced during heterocyclic ring formation for systemic fungicide cores
    • Intermediates filtered and purified using continuous centrifugation

    Final product types

    • Triazole fungicidal actives (e.g., agricultural formulations)
    • Pyridazinone herbicide bases
    • Pre-emergent and post-emergent crop protection agents
    • Seed treatment compounds for major cereal crops

    3. Specialty Dye and Pigment Manufacturing

    Colorant producers incorporate 3-Chloro-4-Fluorophenylhydrazine to build high-purity azo dyes for plastics, synthetic fibers, and specialty inks. This precursor undergoes controlled diazotization followed by coupling with activated aromatic compounds to yield chromophoric systems with precise absorption profiles. Tight production parameters ensure pigment grade standards and robust batch-to-batch reproducibility, aligning with environmental and consumer safety mandates for colorant-containing products.

    Industry compliance standards

    • EN 71-3 (Toy Safety, Migration of Certain Elements)
    • ISO 9001 (Quality Management for Pigment Manufacturing)
    • EU REACH regulation for dyes and pigments
    • California Proposition 65 (Safe Drinking Water and Toxic Enforcement Act)

    Typical usage ratio

    • Azo coupling processes use 0.9–1.0:1 molar ratio with coupling agents
    • Ratio tuning depends on shade intensity and target chroma

    Downstream process integration

    • Direct addition to diazotization vessel under temperature-controlled conditions
    • In-process UV-Vis spectrometry for absorption curve monitoring
    • Purification through filtration and reprecipitation prior to pigment granulation

    Final product types

    • High-performance azo dyes for plastics and textiles
    • Inkjet and laser printer pigment dispersions
    • Industrial color concentrates
    • Colorfast coatings and paint pigments

    4. Fine Chemical Building Block for Material Science

    Leading specialty chemical companies employ 3-Chloro-4-Fluorophenylhydrazine as a tailored building block in the synthesis of advanced organic materials, such as custom ligands for catalysis, molecular switches, and smart sensor arrays. Strict material identity and impurity specifications underpin its integration in multi-step synthesis where selective reactivity is critical. The compound is charged under inert atmosphere conditions to minimize moisture and oxidation, with validated traceability throughout the synthesis chain.

    Industry compliance standards

    • ISO 17025 (Testing and Calibration Laboratory Accreditation)
    • ASTM E2879 (Impurity Profiling in Advanced Materials)
    • Internal SOPs for specialty organic synthesis (audited by customer QA teams)
    • Applicable national chemical inventory registrations (TSCA, NDSL, IECSC)

    Typical usage ratio

    • Multi-gram to kilogram-scale syntheses use 1.0:1.05 equivalents with cross-coupling reagents
    • Purity and reactivity drive ratio selection for functionalization steps

    Downstream process integration

    • Added in protected containment at early or mid-stage synthetic steps
    • Monitored by NMR and LCMS to verify incorporation and selective functionalization
    • Followed by sequential protection/deprotection or metal-complexation as required

    Final product types

    • Functionalized ligands for catalysis R&D
    • Organic semiconducting materials
    • Sensing layer molecules for advanced analytical devices
    • Photo-reactive intermediates for material modification
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    Certification & Compliance
    More Introduction

    3-Chloro-4-Fluorophenylhydrazine: A Reliable Intermediate for Modern Synthesis

    Understanding 3-Chloro-4-Fluorophenylhydrazine

    Every production batch in the fine chemical industry stands or falls on foundation chemicals. For aromatic hydrazines, the subtle choice in ring substitution changes how reactions unfold and the kinds of products customers can eventually make. 3-Chloro-4-Fluorophenylhydrazine brings together two powerful features: a chloro group and a fluoro group. This combination doesn’t often show up naturally, so it requires precise handling and reliable equipment. Over years of handling such aromatic intermediates, it's become clear that only through careful quality controls and hands-on adjustments to synthesis routes can a reproducible, clean product leave the reactor.

    Our production process for this compound focuses on minimizing unknown impurities and consistently reaching a crystalline product that meets tight melting point ranges. The product leaves our site with a typical appearance as a pale crystalline solid, an odor characteristic of substituted hydrazines—a reminder of both its safety considerations and its authenticity. Long-standing partnerships with analytical labs have fine-tuned our GC and HPLC testing; we track any trace byproducts and analyze for potential contaminants from earlier steps in the reaction, such as unwanted aniline derivatives or phenyl fluoride fragments. Our team learned long ago that robust purification steps—whether through layered recrystallization or repeated washings—often determine whether customers see the expected yield and purity, or end up with batch failures.

    Reliable Quality for Critical Synthesis Steps

    In our synthetic experience, even minor differences between batches cause headaches downstream for our customers. Whether customers pursue heterocyclic pharmaceuticals or novel agrochemicals, this intermediate ends up reacting with carbonyl compounds, other aromatic rings, or getting converted into more elaborate scaffolds. Each stage demands assured reactivity and minimal contamination. Controlling moisture is especially crucial. Water subtly catalyzes unwanted side reactions during downstream applications, often reducing yields or introducing difficult-to-separate impurities, a lesson we encountered back when we first scaled up. Now, our production lines employ closed filtration and vacuum-drying techniques. The final moisture content remains so low that it rarely disrupts sensitive further transformations.

    3-Chloro-4-Fluorophenylhydrazine operates as a “building block” in the sense that it slots neatly into multi-step syntheses. The electron-withdrawing chlorine and fluorine change how easily the hydrazine group reacts, often making these stages more selective. From years of working on these reactions in collaboration with scale-up partners, our chemists have seen fewer byproducts and simplified purification, especially compared to non-fluorinated or non-chlorinated phenylhydrazines. This direct experience confirmed for us that even slight changes to the substituents can determine the outcome of cyclizations or acylations.

    Comparison with Other Phenylhydrazines

    The market for phenylhydrazines includes many common and modified derivatives: unsubstituted phenylhydrazine, 4-chlorophenylhydrazine, 4-fluorophenylhydrazine, and more highly substituted products. Each has its niche, but our long-term customers, mainly those working on specialty pharmaceuticals and advanced agricultural actives, report that the simultaneous presence of both chloro and fluoro groups imparts unique reactivity. The combination shifts the electron density across the aromatic ring, making nucleophilic and electrophilic substitution reactions more predictable. When synthesizing new heterocycles, this predictable behavior can shave weeks off project timelines.

    Plain phenylhydrazine, while inexpensive and popular for academic work, often struggles with stability and safety. The lack of electron-withdrawing protection makes it hazardous to transport and store in large quantities. Chlorinated or fluorinated single-substitution analogues are more stable, but offer a narrower band of reactivity. Our experience producing and testing these analogs across various production runs showed that the separately chlorinated or fluorinated versions sometimes yield more side reactions or offer incomplete conversions during target molecule synthesis. By contrast, 3-Chloro-4-Fluorophenylhydrazine responds reliably to the destination substrate, and exhibits better control over side product formation.

    Cost pressures and environmental concerns remain front-and-center for every manufacturer. Many customers ask whether the extra cost of adding a chloro group or a fluorine pays off downstream. Our data, and that shared by process partners, show that the higher initial cost often results in cleaner end-products, easier separation of impurities, and safer operations. Jobs that start with carefully controlled intermediates end with higher-yield processes and fewer reprocessing cycles. In short, picking this more refined intermediate raises overall process efficiency.

    Applications: Innovation in Pharmaceuticals and Agrochemicals

    For pharmaceutical syntheses, 3-Chloro-4-Fluorophenylhydrazine stands out in forming complex heterocyclic structures—pyrazoles, triazoles, and other nitrogen-rich scaffolds. Many sunscreen actives, antimicrobial agents, and anti-inflammatory compounds take shape from these backbones. This intermediate reacts smoothly to give high-purity final products with fewer tars or persistent side-products, based on our customers’ feedback and our own field studies. The specific substitution pattern on the benzene ring, achieved through our controlled halogenation techniques, lowers the chance of oxidative byproducts, a weakness in less robust intermediates.

    In agrochemical innovation, this compound enables the development of new herbicides and pesticides with improved resistance to environmental breakdown. Our own in-house project teams have put this intermediate to work in multi-step syntheses targeting harder-to-control plant pathogens. By starting with a well-defined aromatic hydrazine, the synthesis team avoids the pitfalls of ambiguous reactivity, instead channeling every reaction toward cleaner, more selective transformations. End-users, especially those producing candidates for regulatory review, appreciate this kind of predictability.

    Material scientists often turn to 3-Chloro-4-Fluorophenylhydrazine for constructing specialty dyes and polymer intermediates—not just because of its versatility but because the halogen pattern imparts lasting electron-withdrawing capability. These characteristics matter when the end goal involves tuning conductivity, color fastness, or resistance to chemical attack. Our close work with partners in these sectors revealed just how much trace impurities or modest inconsistencies can undermine their project—catalyzing unwanted cross-links, changing melting profiles, or reducing photostability—so our internal programs now focus on minimizing batch-to-batch variability.

    Specifications: Defining Quality Through Experience

    Our best results come from settings in which quality control never relaxes. Target assay for 3-Chloro-4-Fluorophenylhydrazine typically exceeds 98 percent, with melting points consistently falling inside expected narrow bands. We record each batch’s analytical readings and supply several grams to internal and partner labs for third-party validation. Analytical chemists on our team run not just single-point checks, but trending analyses to identify drift over time—whether that means subtle changes in UV spectra or creeping impurity levels that might escape ordinary monitoring.

    Physical properties matter for handling as well as for reaction yield. The solid is slightly hygroscopic. Our packaging line, updated frequently, maintains anhydrous storage by using two-stage protection: first, a sealed, inert-gas-flushed bag, and second, a sturdy, light-resistant outer drum. On several occasions, we tracked batches through distribution and storage at several climates, then retested their physical and chemical properties after weeks on the road—the intermediate held up every time. This testing regime, while rigorous, paid off by removing doubts over shelf-life or reactive loss due to environmental moisture.

    Internal best-practices dictate that every production operator receives hands-on training with this material—safe handling, correct loading into reactors, and precautions during discharge and transfer. Operators report regularly at safety briefings about practical experience, identifying minor procedural gaps. Lessons learned with previous, less stable intermediates led to tighter monitoring of air and moisture intrusion at every transfer point.

    Why Small Differences in Synthesis Matter

    In the earliest days of synthesizing aromatic hydrazines, the entire industry struggled with unpredictable side reactions. Outdated halogenation steps, poorly controlled temperatures, or the use of sub-par raw materials all contributed to unpredictability, lower yields, and the potential for dangerous byproducts. Since revamping our synthetic sequence to rely exclusively on high-purity starting materials, and integrating semi-automated dosing, our line-level teams have seen improved conversion rates and fewer heat runaways.

    These adjustments came the hard way—after a few failed scale-up attempts and disappointing pilot batch yields. Each misstep sparked new lab-scale trials. We soon discovered, for instance, that using excessively aggressive halogen sources created more escaped halide ions, causing knock-on contamination in later steps and raising the risk of hazardous off-gassing. After revising the oxidation/reduction sequences and investing in better containment, quality went up and downtime dropped. Open dialogue across R&D, production, and analytical teams keeps mistakes from being repeated. Industry consortia, of which we are active members, now circulate best-practice guidelines, but the most valuable lessons come from direct experience with the nitty-gritty of running day-to-day reactions.

    Working With End-Users Beyond the Lab

    Most of our end-users are chemists and engineers, pressing forward with timelines and confronted with cost and quality constraints. Trusted feedback cycles help us keep our manufacturing responsive. Site visits to customer labs often reveal new information on how our intermediate behaves in their hands: an unexpected impurity surfacing after extended aging, a color change while blending into a new reaction, or a loss of crystallinity midway through a shelf-life test. Internal “lessons learned” meetings bring this outside knowledge back into our SOPs, and occasionally spark minor—even critical—changes in drying times, filtration media, or packaging types.

    One of our longest-running client projects involved adapting our process to supply 3-Chloro-4-Fluorophenylhydrazine for a multi-site pharmaceutical program. The customer’s analytical group flagged trace nitrosamine precursors after extended storage. This feedback pushed us to introduce further vacuum steps at the tail end of drying, followed by rapid sealing and lightproofing, changes that quickly translated into cleaner final API. Watching this cycle play out—customer flags problem, our lab confirms and identifies sources, production team retools, QC confirms solution—drilled into all of us that collaboration runs deeper than single purchase orders.

    Sustainability and Responsible Chemistry

    Manufacturers who handle halogenated aromatics face tight scrutiny: regulatory agencies and socially minded partners track not only what leaves the plant, but also the waste, the solvents released, and the potential for lingering pollution. Over the past decade, our team has adopted ongoing solvent recovery and secondary waste treatment. The intense scrutiny applied to chlorinated and fluorinated waste flows—the challenge of scrubbing, neutralizing, and responsibly disposing of them—often pushes our engineers to invest in new abatement systems. Routine audits focus both on the chemical yield and the environmental balance sheet.

    Customers often express concern over persistent pollutants—especially in the realm of perfluorinated compounds—but in our regional and international work, robust abatement and careful solvent selection keep our processes within strict limits on both air and water emissions. We maintain a continuous dialogue with regulators, keeping process transparency as a key value. Internal training and yearly external reviews reinforce this commitment. Larger industry shifts—such as movement toward greener genomes—shape goals for future process improvements, from more selective catalysts to better solvent management. The discipline imposed by working with challenging intermediates such as 3-Chloro-4-Fluorophenylhydrazine ultimately strengthens compliance across all production lines.

    Looking Ahead: Innovation Through Real-World Experience

    Every production batch reflects an accumulation of learned experience—successes and failures, real-world feedback, evolving quality standards. Product development never stalls at a fixed “model” number or set of paper specs. New applications for 3-Chloro-4-Fluorophenylhydrazine keep trickling in. Scientists and process engineers now push for even tighter controls on trace impurities and batch consistency, aiming for zero-defect performance in critical syntheses.

    Internal discussions increasingly circle around how to harmonize these expectations with hard realities—cost, throughput, energy use, and regulatory compliance. Our operations team tests each process tweak in pilot lines before transferring changes to full-size runs, recognizing the scale-up often exposes issues hidden at the bench. Co-investment in analytical equipment, process automation, and operator training keeps the whole chain, from raw input to finished drums, moving toward greater reliability and responsibility.

    3-Chloro-4-Fluorophenylhydrazine stands as a core intermediate not just for its chemical value, but because manufacturers across the world depend on stability, predictability, and ethical sourcing. The story of every kilogram produced traces back to daily choices—a fusion of chemistry, experience, ongoing collaboration, and a constant eye on sustainability. This approach, grounded in experience and close collaboration, ensures this compound continues to deliver reliable results for the industries shaping tomorrow’s medicines, crops, and materials.