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HS Code |
463870 |
| Cas Number | 13340-83-3 |
| Molecular Formula | C9H7F3O |
| Molecular Weight | 188.15 |
| Iupac Name | 1-(3-(Trifluoromethyl)phenyl)ethan-1-one |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 77-80°C at 13 mmHg |
| Density | 1.232 g/cm3 at 25°C |
| Purity | Typically ≥98% |
| Synonyms | 3'-Trifluoromethylacetophenone, m-(Trifluoromethyl)acetophenone |
As an accredited M-Trifluoromethylacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | M-Trifluoromethylacetophenone, 25g: Clear glass bottle with screw cap, white label detailing chemical name, hazard symbols, and supplier information. |
| Shipping | M-Trifluoromethylacetophenone is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material and transported according to applicable chemical safety regulations. The packaging complies with international standards for chemical transport to ensure safe handling and prevent leaks or contamination during transit. |
| Storage | **M-Trifluoromethylacetophenone** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect the chemical from direct sunlight and sources of ignition. Store at room temperature and ensure proper labeling. Always follow institutional safety protocols and consult the material safety data sheet (MSDS) for additional guidance. |
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Purity 99%: M-Trifluoromethylacetophenone with purity 99% is used in pharmaceutical intermediate synthesis, where it enables high-yield and low-impurity end products. Melting Point 40°C: M-Trifluoromethylacetophenone with a melting point of 40°C is used in fine chemical formulations, where it ensures process consistency at ambient temperatures. Molecular Weight 186.15 g/mol: M-Trifluoromethylacetophenone with a molecular weight of 186.15 g/mol is used in agrochemical research, where it offers precise stoichiometric calculations for reaction planning. Boiling Point 226°C: M-Trifluoromethylacetophenone with a boiling point of 226°C is used in high-temperature organic synthesis, where it maintains chemical integrity under reaction conditions. Stability Temperature Up to 180°C: M-Trifluoromethylacetophenone with stability temperature up to 180°C is used in industrial chemical production, where it prevents decomposition during heating processes. Particle Size <10 μm: M-Trifluoromethylacetophenone with particle size less than 10 μm is used in catalyst carrier preparation, where it enhances surface area and reaction efficiency. Water Content <0.5%: M-Trifluoromethylacetophenone with water content below 0.5% is used in moisture-sensitive polymer syntheses, where it reduces risk of unwanted hydrolysis. Chromatographic Purity ≥98%: M-Trifluoromethylacetophenone with chromatographic purity ≥98% is used in analytical method development, where it allows for reproducible calibration standards. Refractive Index 1.525: M-Trifluoromethylacetophenone with refractive index 1.525 is used in optical material testing, where it provides reliable light transmission characteristics. Storage Condition 2-8°C: M-Trifluoromethylacetophenone under storage conditions of 2-8°C is used in specialty material warehouses, where it preserves physicochemical stability during long-term storage. |
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In the world of organic chemistry, picking the right building block for synthesis makes a real difference in efficiency and outcomes. M-Trifluoromethylacetophenone stands out, not just for its mouthful of a name, but for its robust role in crafting complex molecules. Its model, distinguished by the meta arrangement of the trifluoromethyl group on the acetophenone structure, delivers a distinct reactivity that more basic acetophenones struggle to offer. I’ve seen how chemists and product developers rely on compounds like this for their reliability when the stakes are high – especially in pharmaceutical and agrochemical research, where precision matters as much as yield.
Describing a chemical like M-Trifluoromethylacetophenone isn't just about naming a carbon skeleton and three electronegative fluorines. Here, the meta position of the CF3 group shifts both electronic and steric properties. This configuration leads to different reactivity compared to para or ortho variants, impacting selectivity during downstream reactions. The presence of the trifluoromethyl group offers an electron-withdrawing effect, toughening aromatic rings against unwanted side reactions, which I’ve witnessed in bench-scale lab environments.
Purity often sits above 98%, a threshold that helps synthetic chemists trust their precursors. In real work, I've found that knockoff grades with questionable purity introduce a risk of stalled reactions or contamination. This level of certainty lets process engineers scale up without babysitting every flask. Good solubility in organic solvents adds another layer of flexibility, so whether you work in benchtop stirred tanks or need consistent behavior under pilot plant conditions, the compound fits right in.
Every step in a synthesis plan carries its own risks, and the choice of starting material can make or break both timeframes and budgets. M-Trifluoromethylacetophenone pulls its weight as a precursor in medicinal chemistry, where fluorinated motifs have seen a surge. Adding a trifluoromethyl group isn’t purely for looks – these groups influence metabolic stability and bioavailability in drug candidates. That comes from the high electronegativity of fluorine, which reduces the tendency for drugs to break down in the human liver or soil microbes, giving them a longer active profile.
I've read reports showing its usefulness in synthesizing anti-inflammatory and oncology-focused compounds. CF3-substituted aromatics also show up in agrochemical products, helping control how pesticides behave in different crop environments. Researchers benefit from its role as a synthon, allowing direct derivatization into more complex targets. I’ve observed how this flexibility reduces the need for deep multi-step reaction sequences.
Beyond pharma and agriculture, this compound crops up in producing specialty polymers, electronic materials, and fragrance chemistry. I once encountered a specialty flavor application where trace fluorinated ketones shifted the aroma profile without introducing toxicity. These less-obvious uses keep the compound relevant beyond laboratories, expanding its marketplace presence.
It's easy to lump all acetophenones together – until you work with them side by side. Traditional acetophenone lacks the trifluoromethyl punch, making it less suitable for high-performance chemical synthesis. The meta trifluoromethyl variant offers a different electronic interplay than ortho or para analogs. In this context, the meta position balances influence between the ring and the carbonyl, so downstream reactions take a different path. Anyone who’s tried a Friedel–Crafts acylation with the wrong isomer knows the frustration of getting unexpected byproducts.
Fluorinated versions cost more to produce compared to standard aromatics. The value they add often outweighs this premium, especially in late-stage pharmaceutical development or high-stakes material synthesis. The thermal and chemical resilience imparted by the CF3 group means processes handle sharper conditions, reducing the odds of thermal degradation or side-product formation. I’ve talked with process chemists who appreciate having a compound that resists breakdown during lengthy heat treatments, something unmodified acetophenone rarely achieves.
Some users consider para-trifluoromethylacetophenone for electronic effects, but the meta version brings a middle ground – not as electron-poor as para, not as crowded as ortho. This niche placement gives medicinal chemists flexibility in tuning pharmacokinetics without swinging too far toward instability or inactivity.
Getting your hands on high-purity M-Trifluoromethylacetophenone isn’t always a sure thing. Several factors influence access: regulatory approvals, supply chain consistency, and manufacturing scale. I've seen shortages ripple through R&D teams due to delays in fluorinated intermediates, pushing delivery deadlines. Reliable sources protect projects from these disruptions, and based on my experience, buyers now spend more time double-checking supply chain transparency.
Sustainability poses another layer of complexity. Fluorination on an industrial scale calls for safe handling protocols and careful waste management; these processes generate byproducts that demand attention. Factories with a focus on green chemistry tend to recycle solvents, minimize halogenated waste, and look for cleaner fluorine sources. Not all vendors offer this level of stewardship. As someone who tries to make responsible lab choices, I see buyers asking for documentation on environmental safeguards, making supply contracts contingent on cleaner manufacturing methods.
Local regulations shape the market. Some regions complicate import and handling due to fluorinated content or ketone structure. Labs working under tight guidelines may favor suppliers that carry compliance documentation or meet specific national requirements. Walking this fine line between accessibility and compliance, responsible manufacturers offer transparent batch information and clear certifications, making life easier for both buyers and regulators.
No one wants avoidable incidents in a workplace. M-Trifluoromethylacetophenone follows many safety rules common to aromatic ketones, but the addition of fluorine ups the ante for personal protection. This effort isn’t about fear, just careful practice. The compound’s volatility means chemists rely on well-ventilated spaces and standard protective gear. I recall a senior researcher pointing out how the trifluoromethyl group, while stable in a synthesis, doesn't eliminate risks of skin or respiratory exposure. Dense, sweet-smelling vapors can lead to complacency, so most organizations wrap storage and handling procedures with redundant safety checks.
Fire resistance stands higher than many standard organics, but its ketone backbone still counts as flammable. Storage away from oxidizers and ignition sources forms the backbone of any chemical inventory protocol I’ve run across. Spill management relies on containment and targeted disposal, not washing down drains. These day-to-day efforts, supported by ongoing training and regular review, limit incidents and keep both people and communities safe.
I’ve sat through enough lab safety briefings to see best practices become habits. Workplace safety isn’t about eliminating risk, but understanding it well enough to manage it — a lesson that extends to every chemical but becomes crucial for those with unusual electronic or physical properties.
Demand for trifluoromethylated intermediates continues to climb with the steady growth in pharmaceutical R&D and specialty material sectors. Global attention on energy-efficient electronics and high-performance polymers brings even more focus on robust, reliable building blocks like M-Trifluoromethylacetophenone. Innovators look to this molecule for its ability to drive reactions forward with minimal fuss and maximum consistency.
At the same time, the pressure to lower environmental impact grows. Industry and academia confront the realities of fluorinated waste and process emissions, forcing a rethink in production and downstream processing. I’ve participated in brainstorming sessions where ideas ranged from using lower energy synthetic routes to employing recyclable fluorinating agents. Some teams now explore biocatalysis or electrochemistry for installing trifluoromethyl groups, hoping to bypass hazardous reagents entirely. Every step forward here shrinks the environmental burden but requires close cooperation between producers and researchers.
There's also movement toward digitalization in chemical supply chains. Digital tracking for each batch provides a level of quality assurance and traceability that manual paperwork never achieved. This tech-backed accountability reassures customers, and based on my experience, it speeds up troubleshooting when batches fall short of expectations.
One problem stands out in the production of M-Trifluoromethylacetophenone: tight process windows. Selective fluorination at the meta position calls for fine-tuned reaction conditions, not just textbook knowledge. Sometimes, small adjustments in temperature or pressure yield different ratios of side products — something I’ve watched lab teams struggle with in pilot runs. To get around this, some companies now employ flow chemistry instead of batch methods, which smooths out temperature swings and allows operators to collect purified product continuously.
Waste stream management remains another hurdle. Traditional fluorination routes, especially those dependent on older reagents, kick out difficult-to-dispose organofluorine byproducts. Green chemistry practices push for replacement of tough reagents with milder alternatives and offer pathways to capture or neutralize fluorinated waste. On one project, introducing solid-phase scavenger columns shaved down organic fluorine content in wastewater, making regulatory compliance much simpler. While not every solution is perfect, each tweak brings reduction in downstream environmental load.
Supply-side disruptions, especially during global upheavals, forced buyers to seek backup sources. Foresighted firms keep surplus inventory or set up dual supply agreements. A few have explored partnerships with custom synthesis providers to guarantee production capacity. Having seen what a single-supplier failure can do to a project timeline, I value redundancy in sourcing.
Personnel training also plays a role. Rotating staff through advanced handling and storage workshops, alongside regular safety drills, sharpens team readiness for emergencies. In my experience, this not only cuts accidents but makes compliance with evolving regulation smoother.
Many issues tied to specialty chemicals track back to limited knowledge among end users. Distributors and producers who invest in education, whether through documentation, live seminars, or open consultations, lower misuse rates and improve satisfaction. I’ve seen purchasing decisions influenced by nothing more than a clear, straightforward explanation of the compound’s options and differences. Detailed but readable resources — including application guides and troubleshooting tips — replace dense technical jargon with actionable instructions.
Tight-knit collaboration between academia and industry also bears fruit. University-led research on sustainable synthetic routes feeds back into production, reducing costs and environmental impact. Sometimes, direct outreach by academic groups leads to modifications in production scale strategies, while cross-training programs ensure both sides speak the same technical language.
Organizations that build a reputation for openness, accuracy, and transparent sourcing find their products welcomed in crowded spaces. In a crowded field, reputation influences buying decisions as much as performance figures. Consistently delivering trusted information and honest results fosters loyalty well beyond the first sale.
The chemical industry faces unprecedented scrutiny over environmental footprint and workplace safety. Products that once sold on technical merit now carry expectations for lifecycle stewardship. Clients increasingly ask where raw materials originate and press suppliers on details of energy use or waste generation. M-Trifluoromethylacetophenone, like many specialty intermediates, stands at this crossroads. Innovative suppliers see opportunity — if they lean into transparency, green manufacturing, and vouched quality, they can secure a spot in future-focused supply chains.
I’ve heard from customers who prize suppliers willing to open their labs for audits or share third-party certifications. Others stick with established names but demand regular updates on process changes, especially those impacting environmental or social responsibility. Staying relevant in modern chemical distribution calls for investment in both relationships and process improvements.
Walking through the evolving needs of research labs, manufacturing floors, and regulatory offices, M-Trifluoromethylacetophenone has carved out a unique position. Its distinct structure drives specific reactivity, helping chemists achieve results that would stump conventional acetophenones. The extra cost and need for vigilant sourcing reflect the value it brings, but these factors also underline the importance of thoughtful selection, responsible use, and dedication to continual improvement.
Each stakeholder — from supplier to end user — shapes the compound’s journey from synthesis vessel to finished product. By focusing on smart chemistry and responsible stewardship, the community ensures that products like M-Trifluoromethylacetophenone not only perform well in the lab but contribute positively to bigger picture goals: safer workplaces, lower emissions, and more transparent supply chains. Having worked across different facets of the industry, I know real advances happen not in perfect labs, but among dedicated professionals willing to share knowledge and solve practical problems as they appear. This compound, unassuming as it may seem on paper, continues to help specialists tackle challenges at the intersection of innovation and responsibility.