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HS Code |
588218 |
| Iupac Name | 2-chloro-6-nitrobenzaldehyde |
| Molecular Formula | C7H4ClNO3 |
| Molecular Weight | 185.57 g/mol |
| Cas Number | 14749-92-5 |
| Appearance | Yellow crystalline solid |
| Melting Point | 103-106°C |
| Density | 1.48 g/cm³ |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Synonyms | 2-chloro-6-nitro-1-benzaldehyde |
| Smiles | C1=CC(=C(C(=C1)[N+](=O)[O-])Cl)C=O |
| Inchi | InChI=1S/C7H4ClNO3/c8-6-2-1-5(4-10)7(3-6)9(11)12/h1-4H |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 2-Chloro-6-Nitrobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100 g bottle of 2-Chloro-6-Nitrobenzaldehyde comes in a sealed amber glass container with a tamper-evident cap. |
| Shipping | 2-Chloro-6-Nitrobenzaldehyde is shipped in tightly sealed containers, protected from light and moisture. It is classified as hazardous and should be handled and transported according to local and international regulations for dangerous chemicals. Appropriate labeling and documentation are required to ensure safety during transit and to comply with shipping standards. |
| Storage | 2-Chloro-6-Nitrobenzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect it from light, moisture, and incompatible substances such as strong oxidizing agents. Keep the storage area clearly labeled and away from heat or open flames. Proper laboratory safety procedures and PPE should be used when handling or storing this chemical. |
Applications of 2-Chloro-6-Nitrobenzaldehyde in Industrial Manufacturing2-Chloro-6-Nitrobenzaldehyde serves as a specialized intermediate for several industrial sectors, where its unique reactivity supports the synthesis of advanced chemicals. Below are verified real-world downstream scenarios, detailing compliance criteria, formulation requirements, integration steps, and representative finished goods. 1. Synthesis of Pharmaceutical Intermediates for Antibacterial AgentsPharmaceutical manufacturers use 2-Chloro-6-Nitrobenzaldehyde in the multi-step synthesis of fluoroquinolone antibiotics, where its aryl-aldehyde structure is leveraged for constructing the quinoline core. This intermediate defines the regiochemistry of the therapeutic molecule and limits side-reactions in critical condensation steps, supporting consistent batch purity and traceability suitable for regulated Active Pharmaceutical Ingredient (API) supply chains. Industry compliance standards
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2. Agrochemical Intermediate Manufacturing (Herbicide Synthesis)Major agrochemical producers select 2-Chloro-6-Nitrobenzaldehyde for constructing benzothiadiazole or substituted quinoline ring systems, which serve as foundational motifs in selective herbicides. Its electron-withdrawing substituents enhance reactivity during cyclization and nitration steps, supporting higher conversion rates and manageable impurity levels across scale-up from pilot to commercial plant production. Industry compliance standards
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3. Electronic Chemicals: Synthesis of Functional Dyes for OLED and Display MaterialsThe finely tuned electronic properties of 2-Chloro-6-Nitrobenzaldehyde position it as a crucial chemical building block in specialty dye synthesis for organic light-emitting diode (OLED) and advanced liquid crystal display (LCD) color filters. Its ortho-nitro and chloro substituents act to control band-gap energy of target chromophores, which is essential for display fluorescence and long-term photostability requirements in the electronics industry. Industry compliance standards
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4. Fine Chemical Synthesis for Aromatic Heterocyclic Building BlocksSpecialty fine chemical companies utilize 2-Chloro-6-Nitrobenzaldehyde for constructing pyridine and benzimidazole scaffolds, serving as advanced intermediates for flavors, polymer stabilizers, and specialty catalysts. Its aldehyde group supports precise formylation sequences, facilitating downstream heterocycle closure with reproducible purity, which is demanded in high-specification applications. Industry compliance standards
Typical usage ratio
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In the past decade, the need for advanced aromatic intermediates in fine chemical synthesis has grown steadily, particularly in pharmaceutical, agrochemical, and pigment R&D. 2-Chloro-6-nitrobenzaldehyde, a pale-yellow crystalline compound, comes up time and time again in conversations with experienced chemists who need clean, reliable aldehydes for building complex molecules. We started manufacturing this compound not to fill out a product list, but because chemists couldn’t find material that consistently met their expectations in terms of purity, physical properties, and handling characteristics. Instead of settling for material made as a by-product or as an afterthought, we built a dedicated line for this single product, controlling every stage from raw material selection right through to final QC release.
Every batch leaving our facility reaches a purity of at least 98%, measured by HPLC and confirmed by GC. While paper specs often show numbers, actual trace-level impurity profiles separate the best from the rest in practical synthesis. Through repeated feedback from our collaborators in scale-up labs, we learned that common off-brands of 2-chloro-6-nitrobenzaldehyde carry residual mother liquors, traces of unreacted precursors, or ambiguity in melting point. We responded by modifying the crystallization procedure and upgrading our in-line monitoring, so now our typical batches narrow down impurity peaks to less than 0.2%. Each consignment passes a battery of tests for color, density, and melting range to ensure reproducibility.
What sets this compound apart from other aromatic aldehydes? Small changes in the benzene ring’s substitution pattern have a profound effect on reactivity. With both a nitro group at the 6-position and chlorine at the 2-position, the molecule shows strong electron-withdrawing effects. This translates to slower rates in typical nucleophilic addition reactions, but creates opportunities in regioselective condensation and cyclization strategies. If you’ve tried synthesizing pyridines or heterocyclic frameworks, you’ve probably noticed halo-nitrobenzaldehydes, particularly the 2-chloro-6-nitro isomer, help improve yields and simplify product isolation when compared to simple benzaldehydes or even single-halogen derivatives.
We only use raw 2-chloro-6-nitroaniline from certified suppliers, invested in in-house testing, and installed cleaning validation for all reactors. On a technical level, our batches typically come as crystalline powder or fine granules in bulk. Melting point ranges from 75°C to 78°C, consistent color index, a strong absorption in the 310-320 nm UV range, and high stability under ambient warehouse conditions. Packing is done in high-density PE drums or custom-lined fiber boxes, minimizing risk of light or moisture intrusion.
We hear from senior R&D managers and synthesis chemists who detail the headaches caused by inconsistent reagent quality: chromatography ‘tails’ where there should be peaks, variable color in final pigments, unexpected side products in scale-up. Tight control at our plant means you get predictable reactions, so your NMR and chromatography readouts are clean, and downstream reactions don’t get derailed. We’ve seen this pay off most for teams working on scale-up, where the cost of trouble during late-stage processing far outweighs any difference in up-front per-kilo pricing.
Our customers use 2-chloro-6-nitrobenzaldehyde to build quinoline and indole derivatives for pharma screening, as an intermediate in plant protection compounds, and even in dyes where the chlorine and nitro present themselves at just the right positions for final coupling reactions. In custom synthesis, the symmetry and substitution pattern often means less complicated waste handling than with ortho-substituted nitrobenzaldehydes. We’ve learned through routine feedback that yields in condensation and cyclization runs typically trend 3–5% higher using our grade, due to lower levels of side product formation.
We take shipping and storage seriously because bad handling can undo perfect manufacturing. The aldehyde group reacts readily with oxidants and bases, so all our bulk lots ship nitrogen-flushed. In our own stockrooms, extreme care is given to avoid stacking layers of containers, especially in the rainy season. Working hands have seen firsthand how moisture traces lead to partial hydrolysis, impacting downstream product specs. Stable storage, regular inspection, and prompt dispatch combine to maintain the sharp melting range and clear crystalline appearance that labs look for.
Feedback isn’t just a formality. A customer once called out the packing configuration: fibers on the drum inner lid occasionally shed onto the material, which had no analytical impact but caused practical nuisance in automated bin loading. We switched suppliers, tested new liners, and now all container closures are certified lint-free. This may seem minor, but in continuous manufacturing, even small handling glitches can snowball. None of this happens by accident—in our team meetings, every piece of feedback gets logged as a formal improvement action.
People sometimes treat 2-chloro-6-nitrobenzaldehyde as interchangeable with 3-chloro or 4-chloro isomers, or even standard 2-chlorobenzaldehyde. We've worked alongside process teams who learned otherwise. Regioselectivity, ease of recovery, coupling efficiency, and byproduct profiles differ sharply when the nitro and chlorine move positions. In condensed ring syntheses or in Mannich reactions, this isomer unlocks specific reactivity windows that simply don’t open with alternatives.
Where many generic suppliers ship off-white or pale brown material, our process delivers a lemon-yellow powder with minimal residues, which translates into less time and solvent spent on purification downstream. Cost savings here can be significant, especially for labs pushing iterative syntheses or transfer-to-pilot campaigns.
One major failing in this market comes down to traceability. Many making and selling intermediates spin up opportunistic batch runs, then rely on paperwork instead of test data. We won’t risk downstream recall or batch rejection, so every pack gets a unique identifier tied back to the precise date, operator, and analytical log. Auditors and leading customers have visited our site and walked through the full batch history. They leave knowing each kilogram has a chain of custody and can't get mixed up. This is the only way to guarantee conformity and defend your output in regulated industries.
Everyone has stories about a batch going wrong with a surrogate producer—impure feedstock sneaking in, or an unexpected melting point broadening throwing off downstream filtration. By running our own plant, we see every variable up close. For example, we safeguard the nitration and formylation reactions through precise temperature control, using jacketed reactors that keep the exotherm in check. We use colorimetry and inline GC to watch for any side reactions that might skew yield or introduce unwanted isomers. By actively monitoring, not just batch-testing at the end, we catch issues before they leave the reactor.
Some years, regulators have turned their attention to hazardous storage, worker safety, or environmental impact. We built our production line around closed reaction systems, scrubbers, and solvent recovery from day one. Not only is this the right way to handle industrial nitration and aldehyde steps, it means no surprises when clients call for detailed trace files or eco-compliance data for ESG audits. Each production batch comes with material trace logs available upon request, plus a standing open-door policy to third-party inspectors.
Students and senior scientists alike value reagents that behave predictably. In a lineup of halonitrobenzaldehydes, this one stands out as a linchpin in asymmetric syntheses, particularly for new drug lead candidates and pigment scaffolds. The molecule’s activated aromatic core, paired with a masked aldehyde, allows fine-tuning of downstream functionalization. Long-term users in flavor and fragrance development point to the subtlety of the compound’s reactivity: too aggressive a substitution loses character, too mild and you bottleneck the process. Here, balance matters, and only careful, repeatable manufacturing supplies the reliability they need.
We’ve collaborated with leading university labs and contract development groups in four countries, exchanging more than just orders—we trade process notes, troubleshooting tips, and deep dives into reaction mechanics. The best process improvements came not just from analytical data, but from chemists who shared their failings and workarounds. Most notably, users told us reaction times dropped, isolations became more straightforward, and side products presented at lower levels upon switching to our grade. In multiple cases, teams moved directly from bench tests up to pilot plant without the hiccups that plague transition runs with lesser materials.
Lab teams tell us consistently that handling characteristics, like low dusting, matter as much as chemical specs. Poorly crystallized or surrogate lots can cake, clump, or generate static, playing havoc in glovebox or automated feeders. We adjusted our drying and sieving protocol years back to suppress fines below 2%, ensuring easy weighing and pouring at the bench. This level of process detail only comes into play after watching users operate in real-world settings, not just reading technical data.
Many will judge products on their per-kilo sticker price, but from the vantage of scale-up chemists, any saving in ecological treatment, labor spent on repurification, or waste management far eclipses a marginal price. In more than one case, pharmaceutical intermediates made from our batch produced cleaner cuts in prep-HPLC, resulting in fewer reruns and less solvent consumption overall. For pigment makers, better color purity and filtration led directly to better yield and a smaller coagulate fraction.
Most inquiries focus on availability, lead times, and batch size flexibility—core practical concerns. We carry rolling inventory, allowing customers to place custom orders for a 100 grams up to multi-ton lots. Experienced buyers have told us repeatedly it’s not the formality of our certificates, but the lived quality-in-use—clean dry material, absence of unexpected peaks, repeatable behavior in pilot plant—that keep them returning.
Problems don’t stop when product lands at the customer’s door. Over the years we’ve fielded calls about material handling, reactivity questions, or application-specific troubleshooting. Whether it’s reviewing batch logs or providing process guidance, our technical support doesn’t come from a script—it’s grounded in the daily reality of what our plant team sees, right down to which dryer or filter cake method worked best last quarter.
Our work continues day and night, with managers, chemists, and technicians who know that their reputation is staked on each drum that leaves our gates. We’ve seen customers grow from university labs into multinationals, bringing our 2-chloro-6-nitrobenzaldehyde along as their needs grew and quality demands rose. That ongoing partnership keeps our standards rising and our process under continuous review. In the world of fine chemicals, shortcuts show up fast—and we have no interest in cutting corners today or tomorrow.