|
HS Code |
934817 |
| Chemical Name | 3,5-Bis(Trifluoromethyl)Phenylhydrazine |
| Cas Number | 328-94-9 |
| Molecular Formula | C8H6F6N2 |
| Molecular Weight | 244.14 g/mol |
| Appearance | Light yellow solid |
| Melting Point | 61-64 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Density | 1.51 g/cm³ (estimated) |
| Synonyms | 3,5-Bis(trifluoromethyl)phenylhydrazine; Hydrazine, (3,5-bis(trifluoromethyl)phenyl)- |
| Smiles | C1=C(C=C(C=C1F)(F)F)NN |
| Inchi | InChI=1S/C8H6F6N2/c9-7(10)3-5(1-6(4-7(11)12)15)16/h1-4,15-16H |
| Storage Conditions | Store at 2-8 °C, protect from light and moisture |
As an accredited 3,5-Bis(Trifluoromethyl)Phenylhydrazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 3,5-Bis(Trifluoromethyl)Phenylhydrazine, sealed with a screw cap, labeled for laboratory use. |
| Shipping | 3,5-Bis(Trifluoromethyl)Phenylhydrazine is shipped in tightly sealed containers, protected from light and moisture, and usually packed with secondary containment to prevent leaks. Classified as a potentially hazardous substance, it is handled according to relevant chemical shipping regulations, with clear hazard labeling and appropriate documentation provided for safe and compliant transport. |
| Storage | 3,5-Bis(Trifluoromethyl)Phenylhydrazine should be stored in a tightly sealed container under an inert atmosphere, away from moisture, heat, and sources of ignition. Store it in a cool, dry, well-ventilated area, preferably in a dedicated flammable chemical cabinet. Avoid contact with oxidizing agents and acids. Use proper labelling and secondary containment to minimize spillage risks. |
Applications of 3,5-Bis(Trifluoromethyl)Phenylhydrazine in Industrial Manufacturing3,5-Bis(Trifluoromethyl)Phenylhydrazine is a specialized intermediate with high demand in advanced sectors including pharmaceuticals, agrochemicals, LCD materials, and specialty dyes. Our vertical integration and full synthesis control ensure reliable quality and consistent supply for these complex downstream uses. 1. Pharmaceutical Active Ingredient SynthesisDownstream pharma manufacturers employ 3,5-Bis(Trifluoromethyl)Phenylhydrazine in the synthesis of difficult-to-access trifluoromethyl-substituted pyrazoles and related heterocycles. The material is introduced during condensation and cyclization reactions, particularly for oncology and CNS drug intermediates, where the hydrazine group’s reactivity facilitates N–N bond construction under controlled temperature. Consistent batch purity and low moisture content support reproducible yields at scale. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Compound ManufacturingLarge-scale agrochemical producers integrate the material for constructing trifluoromethylated pesticide scaffolds, notably in synthesis routes of modern fungicides and insecticides. It reacts selectively with appropriate carbonyl, halide, or acid chloride-containing intermediates, supporting high-conversion coupling that translates into increased performance of the end molecule in field sprays and seed coatings. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Liquid Crystal Display (LCD) Alignment Layer PrecursorsManufacturers of high-end LCD panels use this hydrazine derivative to produce advanced alignment layer monomers. Its unique electron-withdrawing features introduce thermal and chemical stability in the alignment films, which are critical for high-resolution display reliability. Processing protocols demand precise addition and controlled reaction times to avoid polymer chain defects that affect optical performance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Dye and Pigment SynthesisDye and pigment manufacturers employ our product for creating fluorinated azo and pyrazolone dyes, where the electron-withdrawing trifluoromethyl groups impart high brilliance and solvent resistance to specialty colorants. It is introduced during diazotization and azo coupling stages, under controlled pH and temperature to achieve sharp batch-to-batch color reproducibility required by OEM textile and ink markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3,5-Bis(Trifluoromethyl)Phenylhydrazine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Over the years, the specialty chemicals market has shifted, with more attention on fluorinated compounds. Among them, 3,5-Bis(Trifluoromethyl)Phenylhydrazine (shortened in the lab to BTFMPH for convenience) continues to earn its place at the intersection of day-to-day synthetic chemistry and broader-scale industrial manufacturing. As real manufacturers, our experience with BTFMPH has highlighted the features that matter on both the bench and the line: consistent purity, practical handling, and reliability in tougher applications.
Through careful process optimization, we established production of BTFMPH to reach >98% HPLC purity on a batch-to-batch basis. Material comes as a white to light beige crystalline powder, stable under recommended storage conditions. Typical packing uses sealed, light-blocking drums or HDPE bottles, available at 25 g, 100 g, and up to multi-kilogram batches for regular clients. Moisture and oxygen exposure both degrade the hydrazine group and impact reactivity, which is why packaging and dispatch are scheduled close together, not weeks apart. This avoids offgrades and provides a material that responds as chemists expect.
As for impurities, we monitor not just residual solvents but also the range of regioisomeric byproducts common to related phenylhydrazines, like isomerized trifluoromethyl-substituted rings. Our crude analytical efforts in the early years taught us to target a tighter product specification—not just based on numbers, but how each impurity profile affects the downstream chemistry for those using our chemical as a synthon. The specific melting point generally comes between 87 and 91°C in-house, with slight variation depending on the lot and analysis method. TLC and NMR checks are used, not just to bolster paperwork, but to sidestep the headaches customers would face if a batch docked out-of-range before a pilot or kilo campaign.
Inside the walls of synthetic R&D, hydrazines like BTFMPH offer high utility in building blocks for crop protection agents, APIs, dyes, OLED materials, and custom ligands. In pharmaceutical research, the electron-withdrawing power of the trifluoromethyl groups at the 3- and 5-positions means the hydrazine group shows altered nucleophilicity, with less side reactions and good selectivity even in complicated product mixtures. Chemists select BTFMPH over plain phenylhydrazine when they want lower background reactivity and fewer regioisomeric products in coupling steps, especially for preparing triazoles, hydrazones, or for use as an intermediate in fluorinated aromatic target compounds.
We have seen clients move up from smaller scale to multi-kilo simply because yield increases and byproduct profiles become more manageable with our consistent quality. From process trials, we initially supplied BTFMPH as a pilot batch for a customer scaling up a fluorinated triazole in an agrochemical lead project. After switching to a competitor’s cheaper but less pure material, their reaction profile produced three distinct side-products on scale, disrupting the downstream workflow and causing weeks of lost time. Eventually, they reverted back to our lot for cleaner isolations. Our commitment comes not just from selling a product but from supporting chemical innovation as partners who know the daily consequences of out-of-spec material.
Comparisons often come up between standard unsubstituted phenylhydrazine, mono-substituted variants, and our 3,5-bis(trifluoromethyl) product. Laboratory notes from hundreds of syntheses offer clarity: the dual trifluoromethyl substitution alters solubility in typical organic solvents, shifts melting point, and dramatically affects the compound's reactivity in condensation reactions. For practical use, BTFMPH performs with a distinct balance between stability during storage and selective reactivity in coupling. The electron-poor aromatic ring reduces undesired oxidations, making it less air-sensitive than less-substituted hydrazines, which we discovered during long-term storage studies leading to process improvements for shipping.
Solubility stands as one real-world differentiator. BTFMPH dissolves better in halogenated solvents than other common hydrazines, which can increase throughput in high-concentration reactions. In earlier years, we fielded questions from researchers frustrated with competing sources: mixtures failing to clear, inconsistent separation, or the appearance of colored impurities after chromatographic purification. Adjusting both the isolation and purification steps led to a more consistent, colorless product that saves time and effort downstream. Clean filtrate, easy isolation, and good recovery rates are not only sales points but daily realities for labs running tightly scheduled workflows.
On safety, the additional electron-withdrawing power in BTFMPH acts to moderate both volatility and shock sensitivity compared to plainer hydrazines. This makes shipping and handling less hazardous, which workers in our own shipping area and external customers recognize. Though not a replacement for careful handling or good PPE, this difference is not theoretical: it reduces waste, mitigates risk for research-scale users, and—at scale—translates to lower insurance and regulatory scrutiny.
Scaling up BTFMPH from laboratory glassware to industrial reactors brought its challenges. Early on, offgassing from the diazotization and reduction steps introduced operational bottlenecks. We solved these by upgrading to reactors with controlled nitrogen blanket systems and modular cooling to catch the temperature spikes during hydrazine addition. Continuous training for operators on process controls and batch monitoring played a decisive role in keeping outcomes consistent.
We also found that batch scheduling impacts stability; long storage after manufacture leads to slow decomposition, which becomes visible in NMR and HPLC as fading shoulder peaks and unknowns, even when bulk material looks unchanged. Weekly batch sampling and real-time COA updates closed this feedback loop. This approach, adapted from API manufacturing, keeps returns almost nonexistent and customer outreach minimal, reflecting how small process changes build real-world trust.
Worker safety influenced process evolution as much as product quality. Phenylhydrazines demand respect for their potential hazards. We made room for improvements with enhanced local exhaust systems, glovebox transfer for sensitive intermediates where possible, and holding regular drills for containment and emergency response. Employee buy-in comes from seeing these measures reduce near-misses in real use, not just compliance metrics.
Working directly with multinational pharmaceutical companies, we’ve supplied BTFMPH for development of kinase inhibitors and fluorinated analogues of legacy actives. Analytical reports from those partners highlighted the difference our material made: “Comparable yields, cleaner baseline, less time on purification.” In custom pigment manufacture, their teams used BTFMPH-derived intermediates to introduce advanced colorfast properties into pigments for OLED displays, which respond more predictably compared to derivatives from mono- or unsubstituted hydrazines.
Beyond pharma and dyes, universities developing new ligands for catalysis report easier derivatization and more reproducible kinetics in test reactions. Feedback cycles with these clients led to our practice of producing small, research-size packs for method scouting, then scaling seamlessly for larger runs when early experiments succeed. These are not just numbers to us, but confirmations that plant modifications and QC investments have practical consequences: researchers make progress faster, projects advance to scale-up with less friction, and real innovations are born.
Handling hydrazines involves inevitable byproducts and waste management concerns. To tackle these, we modified our waste nitrogen treatment routines years ago, moving from simple batch neutralization to stepwise decomposition under controlled conditions, followed by activated carbon polishing. This keeps residual organic loadings well below regulatory limits and reduces odor complaints from neighboring businesses. Industrial users increasingly ask about lifecycle impacts. It matters that we address tangible steps on waste minimization, water/solvent recycling, and personnel exposure; otherwise, cost savings downstream mean little.
We re-use solvent streams after recovery in a closed-loop system, which began from recognizing both economic and environmental pressure. Recaptured material accounts for over 40% of total solvent use in BTFMPH manufacturing, and we pass these efficiency gains on through stable pricing. Such improvements don’t rise from top-down mandates, but field experience and engagement with operators whose daily routines create or prevent waste. From this, our BTFMPH now reflects not only advanced chemistry but careful stewardship.
R&D and sourcing professionals ask: is this material going to perform reliably at scale, or just in lab glassware? They ask about shelf life, impurity profiles, and if any regulatory flags exist for use in finished pharma or technical applications. For most users, shelf life under recommended conditions reaches 18-24 months without significant degradation, and our teams run forced-degradation studies to catch early changes in color, purity, or melting point drift.
Impurities that escape initial detection sometimes show up during pilot reactions, so we support rapid re-analysis for those who find a hitch post-purchase. Regulations vary worldwide, but in our direct experience, BTFMPH has not faced regional restriction in major end-markets, including US, EU, and East Asia, for research, pharma-intermediate, and technical-use categories. That said, we keep regulatory monitoring ongoing, because changes are the norm, not the exception.
Feedback from customers and our own in-house experience drive nearly every change in how we manufacture and supply BTFMPH. In the early days, fuzzy melting points and unexplained TLC spots were routine, costing both us and our partners time and resources. After investing in better analytical controls and modernizing isolation, these issues nearly vanished. Stoichiometry tweaks and buffer changes, often suggested by experienced plant chemists, also cut overall waste without compromising on batch size or consistency. Our belief in hands-on troubleshooting, rather than top-down management, keeps operators involved and invested in outcomes—and it shows in repeat orders and long-term partnerships.
We field lots of phone calls late at night or across holidays for last-minute requests or troubleshooting advice. The personal relationships formed with diverse and demanding research teams reinforce our approach: it’s worth sweating the details on everything from drum selection to overnight shipping over ice, because these real-world touches impact not just the individual batch, but reputation and trust across the industry.
Our journey with 3,5-Bis(Trifluoromethyl)Phenylhydrazine reflects a broader view on the specialty chemicals market: those who listen and adapt remain relevant through cycles of innovation, regulation, and new application spaces. We draw on experience, evidence from dozens of successful and tough projects, and a willingness to adjust as process realities change.
Modern synthetic chemistry never stays static. Whether for medicines, advanced materials, or new classes of catalysts, fluorinated building blocks like BTFMPH underpin progress. Down on the plant floor, the improvements we make resonate through cleaner reactions, fewer headaches for our partners, and a more responsible lifecycle from the start of manufacture to the end of each campaign. Spending extra effort to deliver reliable supply, document changes, and close the loop on feedback reflects not marketing, but what has kept our teams learning, improving, and—most of all—in demand.
If your application demands tested, reliable reagents that don’t disrupt development timelines, our BTFMPH serves as more than a catalog entry. It’s a conversation—about what matters, what improvements you need, and what our hands-on manufacturing can deliver, based on lived experience rather than abstract promises. This commitment drives us every day, with every batch, because both science and relationships grow on what happens between the lines of a product sheet.