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1-[2-(Trifluoromethyl)Phenyl]Hydrazine

    • Product Name 1-[2-(Trifluoromethyl)Phenyl]Hydrazine
    • Alias 1-(2-(Trifluoromethyl)phenyl)hydrazine
    • Einecs 276-687-3
    • 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
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    Specifications

    HS Code

    799534

    Product Name 1-[2-(Trifluoromethyl)Phenyl]Hydrazine
    Cas Number 774-56-3
    Molecular Formula C7H7F3N2
    Molecular Weight 176.14
    Appearance Light yellow to brown solid
    Melting Point 41-45°C
    Density 1.33 g/cm³ (estimated)
    Solubility Soluble in organic solvents such as ethanol and dichloromethane
    Purity Typically ≥98%
    Smiles FC(F)(F)c1ccccc1NN
    Inchi InChI=1S/C7H7F3N2/c8-7(9,10)5-3-1-2-4-6(5)12-11/h1-4,12H,11H2
    Synonyms 2-(Trifluoromethyl)phenylhydrazine
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Hazard Statements Harmful if swallowed, causes skin and eye irritation

    As an accredited 1-[2-(Trifluoromethyl)Phenyl]Hydrazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, labeled with chemical name, hazard symbols, CAS number, and manufacturer’s details for laboratory use.
    Shipping 1-[2-(Trifluoromethyl)Phenyl]hydrazine should be shipped in compliance with local and international regulations for hazardous chemicals. It must be packed in tightly sealed containers, clearly labeled, and cushioned to prevent breakage. Temperature control is recommended, and transport via approved carriers with appropriate documentation ensures safety and regulatory compliance.
    Storage Store 1-[2-(Trifluoromethyl)phenyl]hydrazine in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizers and acids. Keep it in a cool, dry, well-ventilated area, ideally in a flammables cabinet. Avoid heat and ignition sources. Properly label the storage container, and handle the substance with suitable personal protective equipment (PPE) to prevent exposure.
    Application of 1-[2-(Trifluoromethyl)Phenyl]Hydrazine

    Applications of 1-[2-(Trifluoromethyl)Phenyl]Hydrazine in Industrial Manufacturing

    As a specialized manufacturer, we supply 1-[2-(Trifluoromethyl)Phenyl]Hydrazine for critical roles in advanced synthesis processes. Below, we outline key industrial applications where this raw material supports innovation, quality, and process reliability in well-established downstream sectors. Each scenario highlights the integration profile, from compliance through to end-use, based on global best practices and customer production workflows.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    API manufacturers utilize this hydrazine derivative as a building block for various fluorinated pharmaceutical molecules, especially where trifluoromethyl aromatic structures impart targeted pharmacodynamic properties. Downstream partners rely on its reactivity in diazotization and condensation steps for assembling pyrazole, indazole, and related scaffolds critical in oncology and CNS therapies. Material purity, handling robustness, and residual hydrazine control form binding requirements throughout multi-stage synthesis under stringent quality regimes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monographs (for impurity and residual solvent control)
    • 21 CFR Part 211 (FDA cGMP for finished pharmaceuticals)
    • REACH Annex XVII (chemical restriction requirements, EU market)

    Typical usage ratio

    • 0.07–0.18 molar equivalents per target compound, adjusted through stoichiometric balancing of aryl hydrazine incorporation reactions; usage further tailored based on in-process yield and impurity formation monitoring.

    Downstream process integration

    • Introduced during early-stage diazotization to form diazonium salts for subsequent coupling or cyclization.
    • Engaged in batch or semi-continuous synthesis loops under controlled atmosphere and temperature to minimize decomposition and oxidative by-products.
    • Critical for step-growth reactions preceding isolation of heterocyclic pharmacophores.

    Final product types

    • Anti-cancer agents (e.g., fluorinated kinase inhibitors)
    • Neuropsychiatric and anti-inflammatory drugs with trifluoromethylaryl motifs
    • Bulk API intermediates for contract manufacturing organizations (CMOs)

    2. Agrochemical Synthesis: Triazole and Pyrazole Herbicide Intermediates

    Major crop protection formulators employ this compound as a key hydrazine moiety provider in the production of selectivity-enhanced triazole and pyrazole herbicides. Its role is critical for introducing the trifluoromethyl phenyl group through cycloaddition and stepwise condensation methods, which fine-tune field efficacy and environmental stability. Agrochemical production lines require rigorous process validation to meet regulatory residue and impurity controls, especially for global food safety alignment.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • OECD Guidelines for the Testing of Chemicals (analytical method validation, residue profiling)
    • ISO 9001:2015 Quality Management System in agrochemical manufacturing
    • National food safety and pesticide regulation bodies (e.g., US EPA 40 CFR 180, EU Regulation No 1107/2009)

    Typical usage ratio

    • 0.05–0.12 molar equivalents per active ingredient core, modulated in multi-step syntheses based on required substitution pattern and downstream crop residue limits.

    Downstream process integration

    • Used in the introductory cyclization stage for forming heterocyclic triazole/pyrazole skeletons from dicarbonyl precursors.
    • Part of closed reactor setups to tightly control by-product formation and optimize transformation yields.
    • Input material tracked using electronic batch records for full traceability in manufacturing batches destined for regulatory review and field release.

    Final product types

    • Broadleaf herbicides containing pyrazole or triazole backbones
    • Selective fungicidal active ingredients based on fluorinated scaffolds
    • Premix technicals and formulated crop protection products

    3. Fine Chemical Synthesis: Specialty Dyestuffs and Pigments

    Manufacturers in the fine chemicals sector deploy this hydrazine derivative as a selective nucleophilic agent for synthesizing high-performance aromatic azo and hydrazone pigments. Its trifluoromethyl group imparts superior weather and light fastness required in automotive and high-end architectural coatings. Batch production standards necessitate exacting control of reaction time, pH, and impurity management within permitted ranges for specialty colorant markets in regulated applications.

    Industry compliance standards

    • ISO 23157:2021 (Quality criteria for organic colorants, pigments, and dyestuffs)
    • EN 71-3 (Migration of certain elements for toys and child-contact coatings)
    • REACH Annex XVII and XVII (Substance restrictions and SVHC controls for pigments)
    • RoHS Directive 2011/65/EU (for use in electronic or painted items)

    Typical usage ratio

    • Typically 0.10–0.30 mole fractions relative to colorant skeleton; variation subject to target chroma and substrate compatibility.

    Downstream process integration

    • Charged directly into mono- or bis-azo coupling reactions following preactivation of the coupling component.
    • Process includes staged pH control and color precipitation under chilled, nitrogen-blanketed conditions to maximize purity and color strength.
    • Followed by filtration, washing, milling, and dispersion to achieve required rheological and particle size characteristics.

    Final product types

    • Specialty organic pigments for automotive and industrial coatings
    • High-durability azo dyes for polymer compounding and inks
    • Technical grade colorants for engineering plastics and elastomers

    4. Fluorinated Heterocyclic Material Synthesis for Electronic Applications

    Electronics material producers leverage this raw material in multi-stage syntheses of fluorinated heterocyclic compounds, particularly for use as charge transport layers and organic semiconductors. The strong electron-withdrawing properties of the trifluoromethyl group enhance thermal and chemical stability, critical for next-generation display and photovoltaic components. Clean-room compatible batches require uncompromising quality control, with trace metal, halide, and hydrazine residues kept within supplier-agreed technical specifications.

    Industry compliance standards

    • IEC 60747-1:2010 (Semiconductor device quality requirements)
    • JEITA ET-7302C (Organic electronics material standards, Japan)
    • RoHS Directive 2011/65/EU (EU hazardous substance control for electrical/electronic products)
    • ISO 14644-1 (Cleanroom standards for integrated material production)

    Typical usage ratio

    • 0.04–0.09 molar equivalents relative to the precursor aromatic core in cyclization and functionalization steps, adjusted to achieve precise doping levels and electronic properties.

    Downstream process integration

    • Reacted in closed, moisture-free environments for the synthesis of fused aromatic heterocycles.
    • Feedstock included at the initiating stage for N-heterocycle formation via transition-metal-catalyzed route.
    • Processes monitored by in-line analytics for byproduct and residual solvent control prior to device-grade purification.

    Final product types

    • P-type and n-type organic semiconductors
    • Charge injection and transport layers for OLED/OPV devices
    • Specialty intermediates for photoalignment and liquid crystal materials
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    Certification & Compliance
    More Introduction

    Introducing 1-[2-(Trifluoromethyl)Phenyl]Hydrazine: Shaping Performance through Precision Chemistry

    Product Focus: Experience Driving Real-World Value

    In hands-on production environments, certain intermediates set the tempo for everything that follows downstream. Few materials underscore that reality quite like 1-[2-(Trifluoromethyl)Phenyl]Hydrazine. As a manufacturer involved in consistent daily batches, our attention remains pinned to what clients actually expect from this molecule—uniform reactivity, reliable supply, manageable handling, and tight quality control. Down the line, minor batch-to-batch inconsistencies can ripple through workflows and inflame total project costs, so production strategies never drift far from tangible outcomes.

    Our facility crafts 1-[2-(Trifluoromethyl)Phenyl]Hydrazine, also known as 2-Trifluoromethylphenylhydrazine, for demand in both pharmaceuticals and specialty organic synthesis. The influence of the trifluoromethyl group is not theoretical in lab notes—it directly affects hydrazone formation, the selectivity of coupling reactions, and the yield from protected intermediate steps. Chemists routinely ask for ways to boost reaction efficiency or to shift selectivity, and real-world evidence shows this reagent can nudge process chemistry toward specific targets unavailable with conventional unsubstituted hydrazines. This advantage comes through both electronic effects and the steric modulation from the trifluoromethyl group, which can help steer product profiles when lower analogues simply can’t deliver.

    Consistency through In-House Process Control

    Our batch records capture every stage, from sourcing the base phenylhydrazine to refining the introduction of the trifluoromethyl group through patented fluorination techniques. Specifying a purity of at least 98.5% GC (by internal standards) and robust controls of water and inorganic fluoride content has proven essential. Trace amine and halogen impurities run well below customer thresholds. Delivering these guarantees over thousands of kilograms means daily hands-on oversight—nothing gets out the door until analytics align with defined targets. Decades of fine-tuning on our production line ensure minimal degradation during storage and transport, a challenge for many hydrazines that can darken or decompose if left unchecked or poorly stabilized.

    We rely on glass-lined and fluoropolymer-reactor vessels, not just for safety with aggressive intermediates but also to maintain a clean synthetic path. Routine online GC-FID checks accompany every transfer, with physical inspection of each finished lot. There’s no shortcut—every kilogram has a paper trail, and technicians flag the tiniest deviation. Where traders and distributors obscure origins, manufacturing in-house gives us both traceability and accountability.

    The Role of Trifluoromethyl Groups: Performance, Not Hype

    Throughout years of technical support calls, few topics have generated more on-the-ground interest than the effect of the trifluoromethyl group in aromatic hydrazines. Unlike speculative additives, the CF3 moiety locks in a strong electron-withdrawing profile, influencing N-N bond activation and coordinating the molecule’s nucleophilicity. In the synthesis of active pharmaceutical ingredients, this sometimes tips downstream reduction and cross-coupling reactions toward higher throughput. Customers have reported that the trifluoromethyl group’s steric and electronic profile not only enhances selectivity in heterocycle formation but also suppresses side reactions compared to toluidine-based hydrazines or compounds lacking fluorine altogether.

    Beyond typical bench-scale performance, actual production figures lead project managers to lean heavily on models like ours. Many have seen increased product stability during multi-step synthesis chains—feedback from teams scaling up pilot batches stresses the importance of predictable behavior, not just nominal purity. Even downstream formulation teams appreciate its role, as this molecule’s byproducts present less challenge during work-up than some chlorine- or nitro-substituted analogues.

    Responsible Handling and Transparency

    Our experience with hydrazine derivatives reminds us that safe processing beats regulatory friction every time. Both the trifluoromethyl group and hydrazine backbone call for direct oversight and engineered safeguards, not just paperwork. Manufacturers handle this chemistry at scale only by controlling exposure, capturing off-gases, and recirculating scrub systems on every batch. We publish every relevant SDS, and run consultation with customer safety teams before the first drum leaves the plant. For all the talk about technical merit, health and environmental controls make or break long-term viability.

    Customers carrying out one-off experiments tend to notice the smell, so we include odor control in transport packaging. At plant scale, positive-pressure airlocks and active filtration are “musts,” not afterthoughts. We cycle through one full review of containment every two years, and adjust process controls after any technical incident—better five minutes double-checking than an afternoon cleaning up an avoidable spill. Daily feedback from operators complements lab metrics, making adjustments a living, ongoing affair.

    Comparative Performance: Why Not Just Use Phenylhydrazine?

    Chemists want more than just another “aryl hydrazine.” Extended trials show the trifluoromethyl variant stands out precisely because the electron-withdrawing group changes how the molecule interacts with both metal catalysts and organic substrates. Classic phenylhydrazine tends to over-react in some settings, generating heavier waste loads and, in many cases, lowering selectivity during cyclization and azo-coupling stages. The trifluoromethyl-substituted product shifts the reactivity window, tailored for targeted applications that demand high yield and low byproduct formation.

    Testing over time has mapped out the performance difference—our industrial clients report fewer purification steps and smoother work-ups, especially when moving from benchtop routes to pilot or commercial production. Cost per kilo may run higher than basic phenylhydrazine, but improved atom economy and lowered waste-disposal costs counterbalance the input price on a full-cost basis. In pharmaceuticals, rigorous impurity control adds a premium, so knowing exactly what is (and isn’t) in your intermediate helps avoid costly surprises under GMP scrutiny.

    Some competing substituted hydrazines, such as those with halogen or alkyl substituents, introduce bulk or polarizability but lack the fine balance between steric and electronic effects delivered by the trifluoromethyl group. We notice this difference especially in partnered research syntheses, where even minor process improvements translate into months of saved work and decreased compliance burdens.

    Delivering a Material for Modern Laboratories and Factories

    We see 1-[2-(Trifluoromethyl)Phenyl]Hydrazine as more than just an upstream input—it’s a solution to a host of real-world headaches. Analytical chemists appreciate that the compound gives sharp chromatographic peaks and avoids streaking seen in some halogenated derivatives. Downstream, our packing team ships in sealed, nitrogen-flushed containers equipped with tamper-evident seals and reinforced liners, ensuring stability across long-distance or multi-modal transport. Lab managers who receive our product describe far less need for re-testing versus resellers’ goods, because the supply link stays direct and transparent.

    From kilo-scale distribution for synthetic R&D to tonnage for commercial manufacture, scale-up support never stops at shipment. We review customer NMR and GC-MS data for any suggestion of drift or breakdown. If the batch profile edges away from target profiles, our tech service team steps in, not just by phone but sometimes directly on site, to debug at the reactor rather than waiting for problems to appear downstream. Partnering with us gives access to years of trial-and-error experience—no third-hand interpretations or piecemeal fixes here.

    Meeting Global Regulatory and Technical Demands

    Working across borders, we interact with teams who require more than simple purchase orders and MSDS scans. We back every outbound order with detailed certificate-of-analysis data, and support full transparency for GMP and REACH pre-registration. Supply chain interruptions can grind development to a halt, especially when importing specialty intermediates. By holding multi-month safety stock, backed by supplier agreements at the point of key starting raw materials, we’ve insulated our customers from shortages caused by geopolitical shifts or sudden surges in demand.

    Direct experience with certification audits has forced us to reconsider every aspect of the process. Inspection doesn’t end at endpoint analysis—inspectors audit our waste treatment flows, emergency protocols, and even end-of-life management for discarded batches. By investing in solvent recovery and internal effluent processing, we’ve managed to stay ahead of tightening emission regulations, ensuring both approvals and ongoing client trust.

    Process Adaptation and Customer Outcomes

    Not every customer wants the same performance profile. Medicinal chemists target selective transformations to unlock novel heterocyclic scaffolds, often using this hydrazine variant for key pyrazole or triazole ring closures. Agrochemical researchers seek out antifungal and pesticidal agents where resistance breeched product lines built on more basic hydrazine chemistry. Our product finds both—a selective, strong nucleophile that withstands harsh process conditions while giving sharp selectivity. We’ve partnered with both segments, tuning batch specifications according to their validated process controls.

    Before a customer releases a new process chemistry, tech transfer meetings map out not only the desired endpoint, but each intermediate step. Much of the value in our product rests on expert support—problem-solving with clients, not just filling drums. We rely on shared trial data and feedback to tune everything from stabilizer levels to storage protocols. In place of boilerplate “solutions,” we iterate until customers see process yields and impurity profiles match their best-case scenario.

    Addressing Challenges in Sourcing and Storage

    Most hydrazine derivatives have both high sensitivity to oxygen and light, so warehousing and distribution cannot rely on generic logistics. By investing in cold-chain logistics, desiccants, and calibrated shipment, we’ve seen marked improvement in delivered shelf-life compared with common trading routes. Real losses from spoilage and requalification hit the bottom line, so we check drum integrity before and after shipment, logging all temperature excursions electronically. Every container is date-stamped and sealed with a QR code that links directly to production and testing records, ensuring transparency and real-time tracking.

    Even with firm control, bottlenecks can arise from external factors. Year-to-year, raw material volatility has threatened continuity, requiring forward commitment on key reagents and substitution testing on backup sources. We run periodic comparisons on every alternate feedstock, halting substitution unless full-spec match and downstream compatibility are demonstrated through plant-scale runs.

    Building for Tomorrow’s Chemistry

    Modern organic and medicinal chemistry increasingly targets fluorinated scaffolds for stability, metabolic resistance, and targeted activity. Fluorinated hydrazines such as this compound have become pivotal—often their synthesis enables new drug classes or specialty materials that would fail with legacy inputs. Our team collaborates with leading institutions and R&D sections across industries, constantly adding to both application knowledge and technical best practices.

    We update our production protocols yearly, integrating feedback from new reaction screening, thermal hazard analysis, and regulatory watchlists. The trend in green chemistry has brought renewed attention to process optimization, reducing both solvent load and byproduct formation at every turn. Many of our recent investments support closed-loop operations, upgraded scrubber systems, and cleaner reactor bases, reflecting both environmental and economic realities.

    Our technical staff routinely publishes anonymized process notes from customer projects (with permission), sharing hard-won knowledge of everything from unusual reaction enthalpy shifts to troubleshooting scale-up impurities. Manufacturing 1-[2-(Trifluoromethyl)Phenyl]Hydrazine is not a static challenge—a true process chemistry company measures progress by night-and-day improvements, not just certificates pinned to the wall.

    Supporting Partner Success from Lab to Plant

    Access to consistent, high-purity 1-[2-(Trifluoromethyl)Phenyl]Hydrazine shapes commercial and research-scale success alike. Academic collaborators regularly request technical backup to move from benchtop synthesis to pilot scale, or to shift from lab-time small-batch trials to kilo production. We support these initiatives, offering both direct technical input and logistics planning. Our personnel walk customer teams through material compatibility, safety protocols, and troubleshooting—nothing left to chance, with checklists and hands-on walkthroughs for every project.

    As more industries require reliable, fluorine-based chemical inputs, our ongoing investment in people, process, and infrastructure ensures long-term access to a product trusted by top-tier manufacturers, contract synthesis labs, and innovation-driven research groups. The track record behind 1-[2-(Trifluoromethyl)Phenyl]Hydrazine proves the value of full-cycle chemical manufacturing—not just as a pipeline to fill orders, but as a platform for building the next generation of performance-driven chemistry.