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HS Code |
666301 |
| Chemicalname | 4-(Diethylamino)salicylaldehyde |
| Synonyms | 4-(Diethylamino)-2-hydroxybenzaldehyde |
| Casnumber | 2769-80-6 |
| Molecularformula | C11H15NO2 |
| Molecularweight | 193.24 |
| Appearance | Yellow powder |
| Meltingpoint | 140-143°C |
| Solubility | Soluble in organic solvents such as ethanol and DMSO |
| Purity | Typically ≥98% |
| Smiles | CCN(CC)C1=CC=C(C=C1O)C=O |
| Inchi | InChI=1S/C11H15NO2/c1-3-12(4-2)10-6-5-9(8-13)7-11(10)14/h5-8,14H,3-4H2,1-2H3 |
| Storageconditions | Store at 2-8°C, tightly closed |
As an accredited 4-(Diethylamino)Salicylaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 4-(Diethylamino)salicylaldehyde is packaged in a sealed amber glass bottle, labeled with hazard, safety, and handling information. |
| Shipping | 4-(Diethylamino)Salicylaldehyde is shipped in tightly sealed containers designed to prevent moisture and light exposure. It is classified as a chemical reagent and may be subject to specific transportation regulations. Standard shipping involves labeling for safe handling, typically via ground or air transport, with all relevant safety data and documentation included. |
| Storage | 4-(Diethylamino)salicylaldehyde should be stored in a tightly sealed container, away from direct sunlight, heat, and moisture. It must be kept in a cool, dry, and well-ventilated area, separated from incompatible substances such as strong oxidizers and acids. Proper labeling and secondary containment are recommended to prevent accidental exposure or spills. Always follow relevant safety and regulatory guidelines. |
Applications of 4-(Diethylamino)Salicylaldehyde in Industrial ManufacturingAs a direct manufacturer of 4-(Diethylamino)Salicylaldehyde, we supply this specialty chemical to a range of advanced downstream sectors. Below, we detail distinct industrial applications, aligning with demanding compliance systems, specific usage ratios, and real formulation needs in key subfields where the material is applied. 1. Fluorescent Dye Synthesis for Analytical ReagentsMajor analytical chemistry laboratories and dye intermediates manufacturers use this material as a core aldehyde intermediate in the production of coumarin-based fluorescent dyes. The compound acts as a selective condensation partner in forming benzopyrone structures, enabling precise emission wavelength engineering. Facilities optimize reactions using controlled alkaline or neutral pH and, depending on the downstream target, may introduce protective group strategies for sensitive substituents. Final dyes must undergo batch QC for photostability, quantum yield, and impurity profiling before formulation into analytical kits used in spectroscopy and imaging assays. Industry compliance standards
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2. Pharmaceutical Intermediate in API DevelopmentAdvanced pharmaceutical manufacturers utilize this compound as a fine chemical intermediate in the synthesis of heterocyclic scaffolds for investigational drug molecules, especially those targeting central nervous system and cardiovascular disorders. The electron-rich aldehyde functionality is vital in controlled Mannich-type or Knoevenagel condensation reactions, where strict moisture and trace metal controls are enforced. All procedures follow multi-step GMP synthesis pathways, incorporating solvent recovery and closed-system handling to ensure batch traceability and impurity minimization as required by finished API regulatory dossiers submitted under the ICH Q7 guideline. Industry compliance standards
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3. Organic Photovoltaic and Light-Emitting Device MaterialIn electronic materials manufacturing, the compound is integrated into small-molecule dye structures designed for organic semiconductors, organic photovoltaics (OPVs), and solution-processed OLED devices. R&D teams select the compound for its extended π-conjugation and electron-donating properties, delivering fine-tuned absorption and emission characteristics in active layer blends. The material is introduced during precision-controlled Suzuki or Heck cross-coupling steps. Resulting organic films undergo cleanroom fabrication, solvent annealing, and device encapsulation to meet rigorous electronics reliability requirements. Industry compliance standards
Typical usage ratio
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4. Chromogenic Substrate Manufacturing for Biochemical AssaysKey producers of diagnostic and monitoring reagents adopt this aldehyde as a precursor in the synthesis of enzyme- or protein-targeted chromogenic substrates. The material supports formation of highly responsive benzaldehyde-derivatives that, upon enzymatic cleavage, yield distinct color changes. Manufacturers run batch reactions under controlled pH and temperature to yield the correct para-substituted products, followed by rigorous QC for purity, identity, and stability to avoid interference in downstream assay protocols. Finished materials ship to end users in pre-measured reagent kits for hospital and research laboratory environments. Industry compliance standards
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5. Custom Synthesis for Research Chemical LibrariesContract research organizations and chemical library suppliers integrate our raw material during the construction of high-diversity benzaldehyde and aromatic amine compound libraries for pharmaceutical and agrochemical screening. Synthesis teams use standardized solution-phase or solid-phase combinatorial chemistry processes, balancing batch and parallel microscale synthesis needs. The compound is introduced at targeted condensation steps, with building block selection guided by design-of-experiment (DoE) protocols to maximize compound novelty and screening coverage. Strict compound tracking and LIMS documentation govern every process stage. Industry compliance standards
Typical usage ratio
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In our chemical plant, the sheer diversity of aromatic aldehydes used for advanced organic synthesis always amazes our team. Among these, 4-(Diethylamino)salicylaldehyde stands out for good reasons. Anyone who has worked with fine chemicals in research, diagnostics, or dye production probably knows this molecule for its versatility. Its formal molecular formula reads C11H15NO2, and it comes from the salicylaldehyde class, tweaked at the four position with a diethylamino group—small changes on paper, big changes in application.
Batch after batch, we carefully monitor the crystallization of this compound. Proper storage and handling start right here at the manufacturing stage. The solid usually presents a yellow to greenish tint when pure. This hue comes from the electronic influence of the diethylamino group. Our spectroscopic analysis—mainly HPLC and NMR—ensures that impurities do not slip through. With a molecular weight of 193.24 g/mol, this compound always draws the attention of our QC team, especially since high-purity standards are crucial in downstream synthesis.
On the production line, we synthesize 4-(Diethylamino)salicylaldehyde with careful calibration of temperature and pH. Oxidation and work-up steps can introduce subtle impurities if not vigilantly controlled. Unlike some vendors who source from multiple plants, we maintain a single-stream process from raw materials to finished product. This control makes a real difference for repeatability and analytical consistency, whether our customer is developing a new fluorimetric sensor or pushing the boundaries of non-aqueous staining.
Every researcher who has colorimetrically detected trace metals or amino acids in a test tube will recognize the unique value of substituted salicylaldehydes. The electron-donating effect from the diethylamino group modifies the aldehyde’s reactivity profile. You see strong selectivity and heightened chromogenic response compared with unsubstituted analogues. Among its uses, 4-(Diethylamino)salicylaldehyde is a top choice for forming Schiff bases with primary amines—crucial for color development in certain clinical or food safety tests.
Our standard manufacturing model for this compound centers on a purity threshold of at least 98%. Such high levels do not happen by accident. We don’t simply rely on crystallization; column purification and careful distillation count for much of the workload. In academic work, students sometimes assume that trace byproducts are harmless. From experience, even one percent of byproduct can throw off analytical readings or dye color in a formulation. For those scaling up to kilogram quantities or more, a 98% pure product eliminates many headaches.
On the surface, 4-(Diethylamino)salicylaldehyde resembles other aromatic aldehydes—phthalaldehyde or vanillin come to mind. Process chemists think in terms of reaction rate and selectivity, which sets this compound apart. The diethylamino substituent acts as an electron donor, increasing the molecule’s nucleophilic response and changing its electronic transitions. This effect delivers marked advantages in applications like fluorescent probe development or when preparing metal complexes. A simple swap to 4-methoxy or methyl analogs does not recreate the same signal intensity or selectivity, particularly in aqueous detection methods.
Our team supplies many diagnostic labs that rely on 4-(Diethylamino)salicylaldehyde in specialized staining kits. The compound reacts readily under mild conditions, forming deeply colored complexes when exposed to certain biological analytes. These properties make it a go-to molecule in colorimetric ammonia assays, which detect trace levels in clinical samples. The color intensity and wavelength shift—attributes measured in our QC lab before shipping—provide superior contrast against other detection reagents.
In dye chemistry, molecular tweaks impact brightness and stability. Our customers who manufacture fluorescent probes often use 4-(Diethylamino)salicylaldehyde as a precursor for Schiff base formation. Once incorporated, the diethylamino group enables longer-wavelength fluorescence and higher quantum yields compared with non-substituted salicylaldehydes. More than controlling the synthetic procedure, we watch for trace triamino and methylated byproducts, because even minor impurities can impact dye performance, shelf stability, or signal-to-noise ratio.
Moving up from research-batch to full production presents plenty of challenges. Our experience guiding customers through this process often leads to useful feedback. For instance, those transitioning a 10-gram method to several kilos quickly realize the impact of reaction heat and mixing consistency. We learned early to optimize heat transfer during condensation and avoid local concentration spikes, which can form colored side products and lower batch yield. These insights inform every scale-up batch we run, just as much as the analytical purity targets.
Repeatedly, missteps in purity have derailed even the most sophisticated R&D projects. A researcher asked why his fluorometric assay produced inconsistent results—turns out, his supplier couldn’t guarantee batch purity on a regular basis. Even with relatively simple detection chemistry, impurities in this compound introduce noise, reduce sensitivity, and slow down troubleshooting. This experience spurred us to improve column purification and enhance our analytical reporting, so each lot record shows GC, HPLC, and NMR confirmation. We know who is accountable for each deviation—often it’s the batch handling step during drying and packing, not the reaction itself.
In storage, 4-(Diethylamino)salicylaldehyde resists air oxidation better than some less-functionalized aldehydes. The diethylamino group stabilizes the aromatic system, pushing shelf life beyond a year if stored dry at room temperature. Handling in the plant demonstrates the difference: batches remain powdery and free-flowing with proper desiccation, and packing in amber bottles avoids photodecomposition. Colleagues using simple aromatic aldehydes like p-anisaldehyde have often reported brown tars forming after a few months; our own experiences with this product leave such worries behind.
Even the best facility sees occasional problems. We’ve seen clumping from excess humidity, which can be reversed with gentle warming under nitrogen. If spectral discrepancies hint at residual solvents, a slow vacuum dry solves the issue without risk of decomposition. One of our chemists caught a high-water-content batch early, before packaging, by noticing the product stuck to the glove. This kind of hands-on vigilance makes more difference than any number of SOPs. Maintaining batch records with regular moisture analysis—Karl Fischer titration remains the most reliable—helps us keep on top of these practical issues before they reach the customer.
4-(Diethylamino)salicylaldehyde often exits our doors destined for high-stakes environments. One notable area lies in environmental monitoring, where rapid reagents for ammonia or hydrazine rely on this molecule’s unique reactivity. Researchers have shared results showing detection limits below five parts per billion, a standard impossible with basic salicylaldehydes. In other labs, protein biochemists use specially designed Schiff bases to visualize tiny quantities of amino acids on gels or plates, taking advantage of this compound’s deep coloration and sensitivity.
It’s easy to overlook the edge that comes from a repeatable process, but real-world chemistry punishes shortcuts. We source aniline derivatives from partners we’ve worked with for years, test them before each run, and optimize our condensation reactor parameters just as closely. Upgrading from batch to semi-continuous processing kept impurity levels low, and allowed us to meet bulk orders without sacrificing quality. Our technicians record each deviation—not out of bureaucracy, but because the next unexpected result often traces back to that one overlooked variable.
Long-term exposure data on 4-(Diethylamino)salicylaldehyde remains limited, but routine handling protocols reduce operator risk and protect the workforce. Scrupulous use of fume hoods, powder handling enclosures, and PPE keep the work environment safe, and we find a little experience goes a long way in preventing skin contact or dust inhalation. Each veteran on our team can recount stories of learned caution—quick closing of a vial, prompt neutralization of a spill, a sharp eye on the benchtop balance—all small actions that keep the day running smoothly. Over time, we see the lowest incident rates in teams who treat every drum with respect, not only regulated hazards.
Waste management in fine chemical manufacturing matters, both for environmental compliance and for community trust. In earlier days, aromatic aldehydes often meant mixed solvent streams and difficult recycling. We invested in closed-loop recovery for most of our organic solvents, greatly reducing effluent and improving process efficiency. Process water and spent catalysts receive full attention before disposal. Our neighbors and downstream water treatment teams rely on this commitment. Positive feedback from regulators or neighboring industries comes not from promises, but from quietly returning clean water and managing air emissions as strictly as any other tier-one producer.
Over the past years, global supply chains for specialty amines and aldehydes faced real strains. At the height of shortages, competitors who depended on third-party procurement floundered. We have a small, steady team for in-house substrate synthesis, with secondary sources lined up for emergencies. The result: our customers faced fewer interruptions in pharmaceutical, dye, and diagnostic production schedules. The lesson holds that reliability grows out of contingency planning, not simple inventory buffers.
A chemical is only as good as the result it helps achieve. Customers often approach us well after a project begins, looking to resolve technical or logistical issues. By fielding real-time analytical data, repacking bulk lots on demand, or troubleshooting synthetic workup steps, we play a small but important part in countless research and production successes. Our partners’ feedback—more than sales statistics—drives every process refinement and batch improvement. Some of our best improvements have come from a single customer request: finer milling for more even powder dispersion, tighter control on residual solvents, or custom packaging for sensitive applications.
With each order leaving the plant, we see new fields adopting 4-(Diethylamino)salicylaldehyde. Increasingly, chemists use it for supramolecular complexation, where subtle electronic effects dictate molecular recognition in sensors or materials. Environmental labs value the robust signal this molecule delivers in screening kits, helping maintain safe food and water. Organic electronics researchers, intrigued by the strong charge transfer properties, now explore new dyes and functional materials based on this backbone. The smallest tweak on a molecule may open surprising new chapters—years of refinement at the production level mean that the building blocks will keep pace with whatever challenge comes next.
At our facility, the story of 4-(Diethylamino)salicylaldehyde mirrors the wider evolution of chemical manufacturing: never static, always open to improvement and partnership. Close attention to process detail, commitment to purity, and focus on customer collaboration have shaped both our product and company. Our team knows that each lot represents more than simple inventory. It’s the sum of careful chemistry, thousands of tests, supplier relationships, and countless small decisions made on the production floor. With every new application or research breakthrough, we celebrate the direct—and often unheralded—role that a precisely manufactured aromatic aldehyde can play in scientific and industrial progress.