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HS Code |
590634 |
| Productname | 2-Amino-3-Chloro-5-Nitrobenzonitrile |
| Casnumber | 38734-54-4 |
| Molecularformula | C7H4ClN3O2 |
| Molecularweight | 197.58 |
| Appearance | Yellow crystalline powder |
| Meltingpoint | 163-167°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | Approx. 1.57 g/cm3 |
| Synonyms | 2-Amino-3-chloro-5-nitrobenzenecarbonitrile |
| Structuralformula | NC1=CC(Cl)=C(C=N1)N(2)NO2 |
| Storageconditions | Store in a cool, dry place, away from direct sunlight |
| Hazardclass | Irritant |
As an accredited 2-Amino-3-Chloro-5-Nitrobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Amino-3-Chloro-5-Nitrobenzonitrile is packaged in a sealed 25g amber glass bottle with a tamper-evident cap. |
| Shipping | 2-Amino-3-Chloro-5-Nitrobenzonitrile is shipped in tightly sealed containers, protected from light and moisture. Handle with care, using appropriate personal protective equipment. The chemical is classified as hazardous; transport must comply with local, national, and international regulations. Store at room temperature in a ventilated area, away from incompatible materials and sources of ignition. |
| Storage | **Storage Description for 2-Amino-3-Chloro-5-Nitrobenzonitrile:** Store 2-Amino-3-Chloro-5-Nitrobenzonitrile in a tightly sealed container in a cool, dry, and well-ventilated area. Keep away from direct sunlight, heat, and sources of ignition. Segregate from incompatible substances such as strong oxidizers and acids. Use proper labeling, and ensure access is restricted to trained personnel. Handle with appropriate protective equipment. |
Applications of 2-Amino-3-Chloro-5-Nitrobenzonitrile in Industrial Manufacturing2-Amino-3-Chloro-5-Nitrobenzonitrile serves as a critical intermediate in specialized chemical synthesis for sectors requiring high-purity building blocks. Our vertically integrated production facilities support downstream manufacturers seeking consistent quality, traceable supply chains, and documented compliance for advanced chemical preparations. Below are the focused industrial applications where our material meets the demanding requirements of global industrial operators. 1. Agrochemical Intermediate ProductionMajor agrochemical formulators rely on this compound as a key starting material for synthesizing several classes of selective herbicides. Its unique substitution pattern provides high compatibility in nucleophilic aromatic substitution reactions, facilitating downstream chlorination or further functionalization steps. Companies in this field utilize it in multi-step manufacturing of active ingredients for pre-emergence weed control, supporting robust acreage-scale deployment. Industry compliance standards
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2. Pharmaceuticals: Advanced API IntermediatesPharmaceutical companies use this compound selectively in the synthesis of complex heterocyclic intermediates, especially for small-molecule active pharmaceutical ingredients (APIs) where electron-withdrawing groups influence regioselectivity. It enables precise functionalization in nitroaromatic-to-amino conversions and is integral to manufacturing steps for certain antihypertensive, antitumor, and antiviral candidates. Industry compliance standards
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3. Dyes and Pigments: Specialty Colorants ManufacturingDye houses and pigment producers employ this compound as an essential feedstock for synthesizing high-performance disperse dyes and specialty colorants. Its integrated electron-withdrawing groups enable formation of vivid, stable colorant structures, particularly in the manufacture of azo and anthraquinone-based dyes used for demanding textile and plastic industry applications. Industry compliance standards
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4. Specialty Chemical Synthesis: Electronic Chemicals and Fine ChemicalsThis intermediate finds strategic use in the preparation of fine chemicals for liquid crystal display (LCD) intermediates, photoresist compounds, and custom synthesis projects where halogenated, nitrated aromatics are vital. Electronics-grade manufacturers rely on its consistent purity to ensure downstream yields and minimize side reactions in highly controlled, cleanroom-based synthetic operations. Industry compliance standards
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Producing 2-Amino-3-Chloro-5-Nitrobenzonitrile seems straightforward from the outside, but those who work with it know this molecule demands real diligence at every step. We have years of experience in handling aromatic nitrile synthesis, and this compound sits right at the intersection of complexity and utility. By carefully adjusting temperature, pH, and choice of reagents, a consistent product emerges, one with balanced purity, color, and granularity. Over multiple production cycles, feedback from end-users shaped our processes: persistence with purification methods, patience in crystallization, and tight control over reagent quality.
Chemically, 2-Amino-3-Chloro-5-Nitrobenzonitrile carries an aromatic ring decorated with four functional groups. The amino, chloro, and nitro substituents, combined with a cyano group, create distinct electron-rich and electron-deficient sites on the molecule. Each function changes the compound’s reactivity in downstream syntheses. Over time, we’ve fine-tuned the reaction stages to avoid unwanted side products, especially considering how nitro-group orientation can trigger unexpected rearrangements during coupling. The refined methods lead to material that holds up under scrutiny and performs in specialized transformations.
Looking at the market, 2-Amino-3-Chloro-5-Nitrobenzonitrile carves out its identity as more than just an intermediate. Pharmaceutical research draws on this molecule for a starting scaffold during heterocyclic ring assembly. Both the electron-donating amino and electron-withdrawing nitro group make it a versatile building block for constructing substituted anilines, diazonium salts, or even certain pyridine derivatives. Agrochemical developers ask for this product by name as they design crop-protection agents, and pigment chemists rely on it for synthesizing high-stability colorants.
Our colleagues in the lab often point out that not all benzonitriles offer the same resilience during demanding multi-step syntheses. We see regular requests for this specific chloro-nitro arrangement since it holds up better when exposed to reductive or nucleophilic conditions. Customers working on target-oriented syntheses reported stronger yields when switching to our material, remarking that the purity and consistent crystal habits minimize unpredictable side reactions down the line.
Down to the specifics, we manufacture 2-Amino-3-Chloro-5-Nitrobenzonitrile targeting a purity of no less than 99%. Melting point range and HPLC chromatograms are posted with every lot for full transparency. Our team goes beyond mere compliance with compendial standards; batch records and process change logs are accessible for audit upon request. This traceability reflects deep engagement with the production process that third-party handlers simply don’t offer.
By controlling the entire synthetic route, starting from precisely chosen precursors, we ensure minimal carryover of chloro or nitro byproducts. End users benefit from consistently white to light yellow crystalline solids, with no streaking or dark discoloration, which often signals incomplete purification. We run additional vacuum-drying sessions to reduce residual moisture to below 0.5%, based entirely on hands-on experience that even a slight increase can jeopardize downstream reactions.
Over the years, we’ve compared our product’s performance against other offerings on the market. Some samples sourced from brokers reveal off-odors, sticky caking, or spectral impurities—all problems traced back to shortcut-laden processes or insufficient environmental controls. Field feedback revealed that certain trace organics negatively impact high-yielding couplings or render pilot-scale batches unworkable. By maintaining granular oversight from raw material input to packaged output, we sidestep common bottlenecks and ensure batch reproducibility.
Practical application drives every improvement in our workflow. Pharmaceutical chemists testing library expansions depend on intermediates that won’t stall or introduce side products in late-stage modifications. Sample requests prompted our team to pilot smaller, more frequent batches to guarantee freshness and prompt, stable delivery schedules. Agrochemical formulators use feedback about compatibility with different catalytic systems to suggest minor process adjustments, which we’ve incorporated without sacrificing scale.
A leading polymer additive developer visited our plant last year. Their technical lead expressed relief that our benzonitrile derivative resisted cross-reactivity during high-temperature curing—outperforming a competing batch sourced from a general-purpose trader. The experience led to a joint quality review and, ultimately, expanded cooperation between our technical departments. End-user observation remains the truest metric: improved shelf stability, visual uniformity, and reduced requalification work for every new lot.
Synthesis of this molecule requires careful manipulation at each ring substitution step. Early mistakes in reaction sequence, especially with nitro-group directionality or overchlorination, translate directly into lower yields or challenging separations. Years ago, we struggled with inconsistent batch color and aromatic overchlorination until a more finely metered addition was implemented. Adjusting pH during amino group introduction created a marked improvement, seen firsthand by our purification technicians as clearer filtrate and less fouling on filter media.
Those practical improvements make a difference where operators and chemists work side by side, scrutinizing every lot before release. Regular in-process controls, visual checks, and hands-on sampling drive day-to-day decisions—a contrast to more hands-off or batch-blind approaches seen in bulk-trade environments. Every adjustment, whether in cooling rates or endpoint detection, comes from direct observations and data, rather than theoretical paper yields. These lessons find their way into our site-specific manufacturing protocol, reducing rework and building trust with buyers who demand more than just “compliant” product.
It’s tempting to assume all substituted benzonitriles behave similarly, but years of feedback show otherwise. Swap the positions of the amino, nitro, or chloro group and photostability, reactivity, and solubility can change unexpectedly. The 3-chloro, 5-nitro, and 2-amino arrangement produces unique cross-coupling and cyclization behaviors not found in para- or ortho-substituted analogs. Customers exploring neighboring compounds soon discover drift in color development, inconsistent filtration rates, or unexpected byproduct formation.
Working hands-on with different substituted benzonitriles, our chemists noticed better compatibility with both basic and acidic reagents in this configuration. Attempts to use similar nitrile intermediates either slowed process development or increased the cost of downstream purification by requiring more solvent or longer recrystallization schedules. Chemical differences, while subtle on paper, translate into meaningful productivity gains for synthetic teams charged with both innovation and throughput.
Raw material sourcing plays a major role in consistency. Long ago, inconsistent lot performance exposed weaknesses in our nitrochlorination step; batches produced from unvetted suppliers led to visible clumping and non-uniform color. Engineers worked with our procurement team, establishing strict vendor audits and backup sources to keep supplies uninterrupted. Where others opt for the cheapest available inputs, we select based on supplier transparency and their documented quality measures.
Process safety also matters. Nitro-containing aromatics require precise temperature and pressure control, not just for quality, but for plant safety. We invested in automated monitoring, and our skilled crew watches for foaming or runaway reaction signatures at each critical stage. Incidents dropped dramatically after integrating dynamic feedback controls, and lost-time accidents from fugitive exposures became rare. Other manufacturers, focused mainly on batch volume, sometimes shortchange investment in robust controls or operator training. By contrast, we see both product quality and workplace safety as linked goals, learned from direct experience rather than after-the-fact fixes.
Dealing with waste streams from aromatic nitrile production requires a commitment to responsible stewardship. Early refinements focused on recycling wash solvents and optimizing reaction sequences to minimize bleed-through of unwanted organics into plant effluent. We track every kilogram of reagent and product, always looking for new routes to reduce overall footprint and comply with the latest environmental benchmarks.
Across thousands of kilograms shipped to research, manufacturing, and pilot plants, attention to detail defines our planning. Each batch undergoes checks for water content, melting point, residual catalyst, and spectroscopic properties. In some cases, a single degree cooler during crystallization dialed down insoluble particle count on QC. We learned to record each experiment, update process windows, and adapt based on customer and internal feedback. Flexibility in operating procedures avoids the “one-size-fits-all” approach that leads to production hiccups as scale increases.
Packaging is kept clear and consistent to prevent exposure to light and moisture, with double-bagging as our standard practice. Operators cycle storage-room samples into real production environments to anticipate temperature swings or humidity spikes. Material destined for global shipment receives an additional round of environmental stress testing, based on firsthand experience with product sensitivity at extended transit times.
Our long-term clients in the fine chemical and pharmaceutical industry care about more than just paperwork. Routine calls between our product managers and a customer’s synthetic team become chances to share new observations, both strengths and weaknesses. On several projects, observing catalyst fouling or color change before full scale-up proved invaluable, allowing us to adjust particle size distribution or adjust lot sequencing. The result is not simply a “sale” but an ongoing technical partnership, informed by accurate record-keeping, field visits, and honest feedback.
Once, a researcher flagged subtle lot-to-lot differences in performance, which we traced back to a minor alteration in bath temperature control. In-house trials duplicated their findings, and we made the corresponding changes before shipping the next order. Such troubleshooting demonstrates respect for the technical skills of both producer and user, strengthening a feedback loop that keeps standards high long after certificates expire.
Handling, storage, and use often throw up more challenges than any bench experiment predicts. Over time, field technicians reported dusting and slight clumping for shipments exposed to prolonged humidity. We responded with modified storage protocols, improved barrier linings, and a direct channel for customer troubleshooting. Several synthetic chemists faced problems with batch carryover into aqueous extractions. We helped optimize their protocols, even supplying mock contaminated samples to simulate “worst-case” scenarios. Other companies offering the same product can’t always close that loop with hands-on advice.
Many production hiccups arise from trying to force a single protocol on all facilities. Our style emphasizes adaptability—finding a solution that works for large industrial reactors or smaller academic pilot lines without compromising product integrity. The experience that comes from repeated observation, collaborative troubleshooting, and mutual learning with users establishes a level of insight that bulk resellers rarely match.
Beyond refining our own process, we listen carefully to R&D teams pushing boundaries in both established and emerging applications. The trend in “green synthesis” pushed us to test alternative, less hazardous solvents; a shift from batch to continuous production in several facilities prompted further automation upgrades. These changes allowed for sharper reaction control, safer operator conditions, and better overall yields. Our company recognizes that successful adaptation comes from open communication at all levels of the supply chain—from engineers on the plant floor to principal investigators designing novel synthetic routes.
Growth in fine and specialty chemical production calls for more than technical knowledge. Keeping pace means investing in state-of-the-art equipment, regular skills training, and robust data collection. Annual audits of production logs by seasoned staff catch small variations before they turn into big issues. We pass those lessons back to customers through transparent documentation and updates to our manufacturing standards.
As more industries look to advanced intermediates like 2-Amino-3-Chloro-5-Nitrobenzonitrile, we stand ready with both the experience and infrastructure required for ongoing collaboration. Direct sourcing from a dedicated manufacturer builds trust: the technical questions get immediate answers, unexpected challenges receive practical support, and everyone benefits from open, honest communication.
Operators on the production line and chemists at the bench know the difference between off-the-shelf and purpose-prepared chemical intermediates. Each lot of 2-Amino-3-Chloro-5-Nitrobenzonitrile carries the collective knowledge of continuous improvement, field learning, and straightforward commitment to chemical craftsmanship. Reliable supply, technical transparency, and long-term partnership distinguish the manufacturer’s approach—qualities that matter for every experiment and every process scale.