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HS Code |
521623 |
| Iupac Name | fluorene-2-carbaldehyde |
| Cas Number | 1834-30-6 |
| Molecular Formula | C14H10O |
| Molar Mass | 194.23 g/mol |
| Appearance | white to light yellow crystalline solid |
| Melting Point | 108-112 °C |
| Boiling Point | unknown; decomposes |
| Density | 1.20 g/cm³ (approximate) |
| Solubility In Water | insoluble |
| Smiles | C1(C2=CC=CC=C2C3=CC=CC=C13)C=O |
| Pubchem Cid | 14238 |
As an accredited 2-Fluorenecarboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle, tightly sealed, labeled “2-Fluorenecarboxaldehyde,” with hazard symbols, batch number, and manufacturer details. |
| Shipping | 2-Fluorenecarboxaldehyde is shipped in tightly sealed containers to ensure stability and prevent exposure to air and moisture. It should be packaged according to local and international regulations for hazardous chemicals, typically within labeled, solvent-resistant bottles, and cushioned to minimize breakage during transit. Appropriate documentation and handling instructions accompany each shipment. |
| Storage | 2-Fluorenecarboxaldehyde should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Store in a designated chemical storage cabinet, preferable for aldehydes or flammable liquids, and ensure proper labeling to avoid accidental misuse or exposure. |
Applications of 2-Fluorenecarboxaldehyde in Industrial Manufacturing2-Fluorenecarboxaldehyde serves as a specialized intermediate in targeted chemical sectors requiring aromatic aldehydes. We supply manufacturers who integrate this compound into high-performance processes. Our production supports downstream clients with large-scale, consistent supply meeting strict technical criteria. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers use 2-Fluorenecarboxaldehyde as a key building block for several active pharmaceutical ingredients. Its unique structure enables selective condensation reactions essential in heterocycle formation, specifically for fluorenone-based antiviral and anticancer compounds. Customers must comply with validated process specifications for GMP manufacturing. This raw material enters multi-step syntheses where purity and trace isomer control critically impact final drug substance quality. Our technical support covers impurity profiling and scale-up batch consistency. Industry compliance standards
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2. Organic Photovoltaic (OPV) Material DevelopmentR&D and industrial producers of organic solar cells employ this compound in the synthesis of donor-acceptor polymers and small molecules. The aromatic aldehyde group enables controlled functionalization, enhancing charge mobility and film-forming parameters critical to device performance. This application requires high purity raw material for laboratory scale polymerizations and pilot-scale roll-to-roll manufacturing. Industry compliance standards
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3. Fluorescent Dye and Pigment ManufacturingSpecialty dye producers incorporate 2-Fluorenecarboxaldehyde into synthetic routes for advanced fluorescent and phosphorescent pigments. The molecule’s robust aromaticity and functional group reactivity support chemical transformations yielding high-brightness dyes for security inks and optical markers. Quality requirements target high fluorescence stability and consistent chromatic index. Multiple reaction routes utilize the aldehyde position for directed attachment of electron donor/acceptor groups. Industry compliance standards
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4. Agrochemical Active Ingredient SynthesisProducers of advanced agrochemicals use this building block in the synthesis of heterocyclic bases and modifications for selective pest and disease control agents. The aromatic route enables chiral and non-chiral transformations necessary for active ingredient scaffolds. Quality management addresses residual solvents and by-product formation, as crop protection manufacturing demands strict upstream impurity limits for regulatory submission. Industry compliance standards
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5. Specialty Polymer Modifier SynthesisManufacturers serving the specialty polymer sector introduce 2-Fluorenecarboxaldehyde as a functional monomer for controlled backbone modification. The aromatic aldehyde allows incorporation into copolymers, providing rigidity and specific thermal properties required for high-temperature engineering plastics. The raw material’s batch-to-batch purity manages final polymer ductility and processability. Advanced customers may further derivatize the core structure for customized block copolymer formulations. Industry compliance standards
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Everyday work inside our manufacturing facility brings a close relationship with materials like 2-Fluorenecarboxaldehyde. From its white crystalline presence to its characteristic aromatic scent, this compound brings a balance of stability and reactivity that chemists in organic synthesis count on. Our product, cataloged as Model FCA-98, regularly leaves the plant in powder form, boasting a purity that consistently exceeds 98%—a number we pay careful attention to. Once processed, every batch passes consistently strict quality checks before heading out to labs, research divisions, and production floors worldwide.
Handling 2-Fluorenecarboxaldehyde on the production line requires close attention, mostly because its application directly influences batch performance for downstream users. Most of our experience comes from supplying academic researchers, pharmaceutical research teams, and specialty intermediate formulators. These customers bring us questions each month, often rooted in differences they notice when switching between aldehydes, or even between different sources for the same material.
A simple glance at the process flow illustrates our resolve. Starting from fluorenone, a controlled approach under anhydrous conditions leads to the desired aldehyde. Avoiding impure or substandard intermediates saves hours and eliminates future headaches with purification. Our team’s hands-on experience has shown, again and again, that retaining trace impurities (even a fraction of a percent) causes major trouble in subsequent steps. The Fluorenecarboxaldehyde’s purity makes a difference in Grignard reactions, Suzuki couplings, reductive aminations, and in more niche syntheses of fluorescent dyes or liquid crystals. Over the years, we found that users notice improved yields and fewer side products when they rely on our tightly controlled output.
On the shop floor, the team packs this product primarily in 25 kg drums, but we’ve filled everything from 1-kg glass flasks for custom orders to 250-kg lots for bulk buyers. Each container matches the handling needs of research professionals as well as larger manufacturers. Those in air-sensitive labs appreciate packaging under an inert nitrogen atmosphere. Several regular research clients prefer this option because trace moisture disrupts sensitive reactions—the kind that can derail a week’s worth of work and thousands in labor and reagents.
Our standard FCA-98 meets or exceeds 98% purity as checked by HPLC, but we regularly produce higher grades for applications in optoelectronic research, where contaminants add noise or reduce device life. Trace metal content matters a great deal for these users, so we invested in ICP-MS capabilities to verify acceptable thresholds down to parts per million. These efforts grow from feedback directly from the receiving end—their complaints about inconsistent melting points or unexpected reactivity help us catch problems and tighten process parameters before they escalate.
Conversations with formulation chemists remind us how 2-Fluorenecarboxaldehyde’s specific structure—the fusion of the fluorene core and an aldehyde group—shows up again and again as a versatile building block. Researchers synthesizing fine organic pigments point out better thermal stability and colorfastness when starting with this material. Pharmaceutical R&D teams use it for custom intermediates, especially for projects seeking planar aromatic cores that enhance stacking interactions in drug candidates. In electronic materials development, teams prefer 2-Fluorenecarboxaldehyde because small tweaks in the aldehyde position shift the photophysical properties—key for OLED research.
A key difference from general aromatic aldehydes is the rigidity of the fluorene backbone. While benzaldehyde or naphthaldehyde bring their own reactivity, 2-Fluorenecarboxaldehyde offers increased planarity and a broader pi-conjugation system. These traits make it indispensable in certain cross-coupling reactions, such as the synthesis of conjugated polymers. Time and again, we see how these features improve the outcome and reproducibility for process chemists searching for robust building blocks.
Some customers have asked about substituting with more common aldehydes. After direct testing, R&D groups frequently report compatibility issues and insufficient performance, especially where electronic or photophysical demands run high. In downstream processes, cost savings from using a cheaper aromatic aldehyde rarely outweigh the losses in efficiency, purity, or target yield—experience confirms this within catalyst screening, polymer science, and pharmaceutical lead discovery environments.
In production, the lab and factory teams collaborate often. Small changes in raw material origin or reaction workup might go unnoticed in a casual analysis, but seasoned staff recognize telltale signs: a slight color change, a different melting point, or a change in solubility. These observations trigger deeper checks—even if last-minute. Clients pursuing gram-scale synthesis of specialty fluorophores depend on this attention to detail, because their own processes may not tolerate inconsistencies. Applications including organic electronics, imaging agents, and molecular sensors hinge on the optical and electronic qualities intrinsic to the fluorene core. Inconsistent starting material can throw entire research directions off course.
Every batch receives full spectral analysis—NMR, HPLC, FTIR, GC-MS—before approval. This rigorous approach does not result from regulatory mandates; rather, it grew naturally from experience. Customers forced to troubleshoot unpredictable fluorescence yields or chromatographic profiles often found the problem traced back to a minor flaw in a reagent. We learned the value of such extra checks after years of assisting with troubleshooting and root-cause analysis on the client’s end. It becomes less about a checkbox and more about respecting the time and efforts of everyone involved—from bench chemist to production engineer.
Within our own facility, we routinely handle several aldehydes: benzaldehyde, p-tolualdehyde, and naphthaldehyde, among others. Each brings a distinct set of properties, but few match the balance provided by 2-Fluorenecarboxaldehyde. One clear distinction is its photostability and the resulting improvements in the final product’s shelf life. Compounds built from this aldehyde exhibit greater resistance to UV degradation, a crucial property for dye manufacturers and organic semiconductor researchers. Clients constructing specialty OLED layers or polyaromatic frameworks choose this material specifically for its solid-state resilience.
Benzaldehyde-based products hold a price advantage, and their physical handling presents fewer challenges, especially in scale-up environments. Yet, for high-overlap polymer syntheses or applications needing extended conjugation, the planar structure and rigid backbone of 2-Fluorenecarboxaldehyde outperform. A technical comparison of melting points, solubility, or reaction selectivity all favor our product in demanding or precision chemistry. Teams working on asymmetric synthesis have reported fewer side products and less purification hassle when switching from flexible aldehyde substrates.
Another distinction stems from the chemical’s moderate reactivity. While some aromatic aldehydes display significant volatility or oxidation tendencies during long-term storage, our 2-Fluorenecarboxaldehyde’s stability impresses warehouse staff used to stricter controls for more volatile analogs. We pack and store this compound under mild conditions, yet shelf-life measured in years avoids wastage and additional costs. As feedback comes in from supply chain clients, we see recurring requests for certifications of extended stability and packaging that maintain this resilience.
As a manufacturer, fielding questions about batch consistency, impurity profiles, and downstream compatibility becomes a routine part of our work. In early years, trace levels of fluorenone or over-reduced byproducts occasionally slipped through and disrupted customer syntheses, leading to time-consuming troubleshooting. Over the years, we overhauled recrystallization procedures, set tighter drying protocols, and upgraded analytical equipment—all in response to hard-earned lessons from returned products or direct user feedback. These iterative improvements gradually produced an offering that is now trusted for demanding applications in advanced materials research and pharmaceutical discovery.
Specific feedback from dye chemists encouraged us to move beyond generic melting point checks. Instead, we began assessing impurity profiles by HPLC and GC-MS, which allowed us to spot and eliminate subparts-per-thousand fluorenone residues. Our present staff finds these steps second nature, yet they started with a single customer pointing out a reproducibility gap in their quantum yield measurements. Many process changes take shape after these kinds of collaborative troubleshooting moments, which ultimately benefit every stakeholder over time.
Applications in photonics and nanotechnology encouraged us to pursue higher-purity variants. Early efforts required significant investment in column chromatography and advanced filtration systems. Our results now match or exceed specifications set by leading research journals, keeping the material suitable for demanding electronic and photophysical experiments.
Most risk with 2-Fluorenecarboxaldehyde production revolves around contamination, moisture intrusion, or inconsistent handling. Open discussions with research and industrial partners have shaped our approach. Drums leaving our facility undergo moisture analysis using Karl Fischer titration, down to well below 0.1%. This strict attention reduced complaints of hydrolysis or side-product formation, especially among those operating at high temperatures or under basic conditions. In the past, skipping this step led some clients down frustrating paths, as hydrolyzed impurities dragged reaction yields down.
Our facility enforces consistent training for staff at every stage of material movement, from raw material reception through final package sealing. The value of on-the-ground experience means a seasoned operator often catches a slight discoloration or faint off-odor that would not show on a technical checklist but signals trouble. These subtle quality indicators lead to repeatable manufacturing outcomes and foster trust in supply relationships over the years.
A recurring request from users involves documentation of trace elemental contamination. We built a direct partnership with independent laboratories, offering third-party verification for trace metal levels and confirming every parameter that could impact downstream catalyst reactions. This shift reduces costly surprises for end-users, particularly for those running multi-tonne-scale syntheses or catalyst-driven processes with strict tolerance thresholds.
Within the plant, worker safety and environmental impact shape every step of production and packaging. Personnel handle 2-Fluorenecarboxaldehyde with gloves, eye protection, and localized ventilation, following procedures grounded in actual risk assessment, not simply regulatory minimums. Waste management includes solvent recovery and secure storage of residues. Operators trained in spill management respond instantly to minor incidents to prevent personal or environmental harm.
We also designed packaging to minimize potential exposure and promote safe transfer, particularly for smaller research clients. Batch-level documentation ensures all material shipped matches agreed specifications—each package leaving the facility logs storage life, quality analysis, and verification of seals. These measures grow directly from an ethos of shared responsibility. Our commitment goes beyond compliance; we know any shortcoming on our end ripples downstream, whether slowing promising research or compromising product safety.
Over time, optimizing processes to reduce waste sent to landfill became a central objective. Closed-loop solvent systems and targeted purification both reduce our footprint and align with expectations from partners focused on sustainable sourcing. Many buyers now ask for declared, traceable steps that confirm an ethical, environmentally sound origin. Our commitment to these principles rests on concrete changes in manufacturing workflow and regular third-party audits.
Relying on a stable product stream requires control over raw material procurement, storage, and logistics. Tight coordination with suppliers ensures feedstocks arrive clean and on schedule—a fact that goes unnoticed until a single late shipment throws weeks of downstream work into jeopardy. Over the past decade, sourcing disruptions have grown, whether from geopolitical events or market fluctuations. By maintaining multi-source supplier relationships and on-site analytical checks, we reduce the chance of impurities sneaking in through upstream channels.
For many of our partners, the cost of downtime outweighs fluctuations in input prices. Our regular conversations with purchasing coordinators, chemists, and logistics teams focus as much on contingency planning as on cost negotiations. Investment in additional storage, real-time monitoring, and quick-turn small-batch production gives us the flexibility to respond when conditions change suddenly. These layers of preparedness grew from past experience—missed deadlines or shortages rarely get a second chance in high-stakes, innovation-driven industries.
The manufacturing landscape for fine chemicals continues to evolve. Keeping pace demands an enduring commitment to problem-solving, transparency with clients, and respect for the delicate balance between innovation and reliability. With 2-Fluorenecarboxaldehyde, practical experience within the plant and across supply networks stands as the surest measure of consistent quality.
We field questions about emerging applications, newer regulatory pressures, and bespoke purity requirements with an outlook shaped by direct involvement. Every step, from reformulating a process step to optimizing shipment for a novel application, connects us more closely to the community that depends on these materials.
At the end of a production run, the compound sitting in the final container reflects thousands of tests, dozens of process adjustments, and countless quality conversations up and down supply chains. These efforts form the backbone of a reliable partnership—one batch and one challenge at a time.