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HS Code |
538757 |
| Productname | 5-Amino-2-Chlorobenzoic Acid |
| Casnumber | 6352-18-1 |
| Molecularformula | C7H6ClNO2 |
| Molecularweight | 171.58 |
| Appearance | Light yellow to beige powder |
| Meltingpoint | 243-247°C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Density | 1.53 g/cm³ |
| Synonyms | 2-Chloro-5-aminobenzoic acid |
| Storageconditions | Store at room temperature, keep container tightly closed |
| Smiles | C1=CC(=C(C=C1N)Cl)C(=O)O |
| Inchikey | QGDDONIRJIBAIX-UHFFFAOYSA-N |
As an accredited 5-Amino-2-Chlorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 5-Amino-2-Chlorobenzoic Acid is supplied in a sealed amber glass bottle with a printed chemical safety label. |
| Shipping | 5-Amino-2-Chlorobenzoic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It should be handled and transported in compliance with chemical safety standards, including accurate labeling and documentation. Protect from physical damage, direct sunlight, and extreme temperatures. Ensure compatibility with surrounding shipments and follow relevant regulatory guidelines for chemical transport. |
| Storage | 5-Amino-2-chlorobenzoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Store at room temperature and avoid excessive heat. Ensure proper chemical labeling and follow standard laboratory safety protocols while handling and storing this compound. |
Applications of 5-Amino-2-Chlorobenzoic Acid in Industrial Manufacturing5-Amino-2-Chlorobenzoic Acid serves as a critical intermediate across several specialized manufacturing sectors. Our facilities provide high-purity material directly suited for industrial synthesis, ensuring reliable downstream conversion at commercial scale. 1. Pharmaceutical Intermediate in Non-Steroidal Anti-Inflammatory Drug (NSAID) Synthesis5-Amino-2-Chlorobenzoic Acid acts as a core building block in complex stepwise synthesis routes for selected NSAID actives. Our material undergoes direct amide coupling or halogen exchange steps during active pharmaceutical ingredient production. Quality consistency supports multi-ton batch operations for international formulators supplying regulated markets, optimizing purity for downstream active isolation. Industry compliance standards
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2. Dye and Pigment Precursor for Specialty ColorantsIn industrial dye synthesis, 5-Amino-2-Chlorobenzoic Acid provides a key aromatic amine function enabling diazotization and subsequent coupling reactions. Formulators use our high-purity grade as a foundational block for custom color branches in azo and anthraquinone pigment manufacture, where substitution patterns directly impact spectral performance and fastness. Industry compliance standards
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3. Agrochemical Synthesis for Herbicide and Plant Protection ProductsProduction lines in agrochemical complexes incorporate 5-Amino-2-Chlorobenzoic Acid as a valued intermediate within targeted herbicide synthesis, especially for benzamide or benzoic acid derivative actives. Its chemical structure supports customization of electron-withdrawing patterns, which improve target selectivity and environmental fate in regulated crop management solutions. Industry compliance standards
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4. Polymer Additives and UV Stabilizer SynthesisProducers of performance polymers and specialty plastics utilize 5-Amino-2-Chlorobenzoic Acid as an anchor for synthesizing tailored UV absorbers and stabilizing agents. Its reactivity with carboxylic or sulfonic functionalities facilitates the construction of high-efficiency stabilizer molecules, crucial for applications demanding long-term exterior durability under UV exposure. Industry compliance standards
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5-Amino-2-Chlorobenzoic Acid, with CAS number 635-21-8, draws the attention of chemists and manufacturers who need reliable building blocks for performance-driven materials. Looking at its white to pale yellow crystalline appearance, we recognize both the purity and versatility valued in specialty synthesis. From the earliest days fabricating this compound in our reactors, we realized the impact of meticulous raw material controls and vigilant batch monitoring. The character of each production run reflects not just our technical skills, but also the chemistry knowledge built into our systems over time. Every batch introduction to our reactors brings another round of careful observation; a subtle color shift can signal a deviation in precursor clarity or an unexpected impurity, and the expertise of our team shapes the outcome.
In our manufacturing experience, batches typically achieve purity above 99%, supported by HPLC and melting point analysis. Slight variations in melting point (usually within 2-4 degrees Celsius of the literature value) reveal much about subtle structural differences and minor impurities — this is where manufacturing skill meets analytical insight. After years on the line, we know the details that matter.
Our daily work with 5-Amino-2-Chlorobenzoic Acid stems from clear market needs, not abstract ideas of what might be possible. In pharmaceutical synthesis, research teams often demand this intermediate for creating non-steroidal anti-inflammatory drugs, particularly where the amine and chloro positions influence biological activity. Process chemists look for an acid that stays stable across multiple reaction steps and meets ICH Q3A guidelines for residual solvents and elemental impurities. In dyes, the compound serves as a core structure for developing metal complex dyes where functional group substitution yields desired color properties and fastness. Pigment producers and electronics component developers appreciate consistent granularity and filterability in wet reaction processes – factors heavily shaped by upstream manufacturing diligence. Delivering this product, we’ve learned to anticipate the challenges technical customers face: solubility constraints in mixed-organic systems, filter cake properties, and pH stability through crude extractions to recrystallization.
Academic researchers have also leaned on our batches for developing new benzoic acid derivatives, often running side-by-side controls across other positional isomers. Each time a research partner shares feedback on how our material performs in combinatorial syntheses or coupling reactions, it sharpens the way we control our reaction conditions and post-synthesis filtration setups.
No two benzoic acid derivatives behave exactly the same. 5-Amino-2-Chlorobenzoic Acid stands apart from the 2,4- and 3,5- isomers both in reactivity and downstream usability. In our process, we've compared yields and filtration rates side by side: the 5-amino position often improves nucleophilic aromatic substitution results and crystallizes more readily, making purification steps less laborious than with the 3-amino analogs. The ortho chloro substituent in our compound sometimes acts as a directing group in further electrophilic substitution, opening up synthetic pathways that remain less accessible in other isomers. We’ve optimized our reactor parameters and workup conditions through trial and error, sometimes running parallel fermentations just to understand which purification protocols realistically scale beyond lab scale.
The market regularly asks about 5-Chloro-2-Aminobenzoic Acid or 2-Amino-5-Chlorobenzoic Acid thinking they bring similar downstream attributes, but our practical experience supports a different picture. Small shifts in the substitution pattern develop into significant differences during coupling reactions or amidation steps, leading to batch failures or poor conversion rates with incorrect isomers. Years working directly with downstream formulators and syntheses highlight that even small differences — as little as the placement of a chloro or amino group around the aromatic ring — alter reaction rates, catalyst compatibility, and product yields.
Every kilogram of 5-Amino-2-Chlorobenzoic Acid results from raw material diligence, reaction environment control, and effective waste handling. We source high-purity starting materials, verifying every lot against established specs with FT-IR and UV-visible checks. Batch monitoring through the reaction phase makes use of in-line spectrometry, which picks up on unexpected by-products faster than end-point testing alone. Temperature ramps, nitrogen blanketing, and continuous agitation shape the formation of the amino and chloro pattern, avoiding common pitfalls like over-chlorination or incomplete amination.
One unchecked spike in temperature can cause hydrolysis or unwanted by-product formation. We learned this early, as scaling up from glassware to full-plant reactors frequently highlighted heat transfer inefficiencies. Correcting those lessons through improved reactor jacket design and better process controls has paid off with each subsequent campaign. Regular input from maintenance and cleaning teams has refined the workability of our reactor setups, reducing downtime caused by cross-contamination or residue build-up.
Downstream, careful crystallization and centrifugal separation determines both product appearance and handling properties. Ferric impurities, often left behind from steel process vessels or raw materials, provoke regulatory scrutiny and real-world reactivity issues. DDS, or drum drying systems, deliver more consistent granularity and moisture content than open-air tray drying, especially in humid weather and variable seasonal conditions.
Packing into double-lined fiber drums or high-density polyethylene drums comes only after a final check on residual solvents and uniform bulk density. Our QC managers reject any batch showing out-of-spec particle morphology, as end-user downstream processes can clog filters or create dust hazards in closed and open transfer systems.
Our team draws on extensive analytical capability to make sure that every lot conforms — not just to specs, but to what real world chemists expect under process conditions. HPLC with photodiode array detection quickly flags residual impurities. Each production campaign starts with a review of solvent residue profiles and checks for compliance with regional environmental and pharmaceutical guidance to avoid issues downstream. Where customers request customized documentation for DMF filings or additional impurity profiling, we provide detailed results — this goes far beyond the standard certificate of analysis. Risk assessments gain added detail from process simulation data gathered across multiple years; whenever a trend appears (such as changing energy, filtration efficiency, or operator error rates), we adapt our SOPs and distribute learnings throughout the site.
Shipping logistics, too, reflect risk awareness. Climate-sensitive compounds need refrigerated transport, but our 5-Amino-2-Chlorobenzoic Acid formulation and packaging design simplifies handling for most moderate climates. For end users with specific transportation requirements, we integrate stability data and coordinate directly — this approach stems from years overcoming real logistical setbacks, not just reading data sheets.
Field feedback from pharmaceutical processors, dye manufacturers, and R&D partners has reshaped how we approach both consistency and documentation. Stories of filter press clogging or unexpected gel formation in solution pushed us to refine both our crystallization and washing protocols. At one point, several partners in pigment formulation flagged inconsistent melting ranges that we tracked down to hidden trace residues in solvents sourced after a regional supply disruption — a good reminder that quality assurance isn’t a checkbox, it is a daily reality.
Some customers run extended stability testing and feed back findings we didn’t get in our own accelerated shelf-life protocols. When they show how minor batch-to-batch differences in moisture uptake changed flow in automated dosing systems, that insight feeds directly into our batch drying schedules and controls.
Supplying pharmaceutical and electronic intermediates means regulatory frameworks influence nearly every workflow. Agencies and third-party auditors expect full transparency about raw material provenance, batch trackability, and impurity profiling. Our production records incorporate complete batch genealogy, electronic recordkeeping, and digital signatures for traceability. Third party audits, both announced and surprise, have shaped the rigor of our production logs and deviation investigations. Where a trend line shows a potential compliance drift, our QA and regulatory affairs staff join forces to resolve root causes before challenges make it to customer lines or regulator inquiries.
We support due diligence investigations for both generic and R&D-focused partners, providing access to original data sets, not just summary tables. This level of openness reflects the mutual trust needed for longer partnerships, particularly with formulators who rely on our material for multi-stage syntheses. In our experience, straightforward discussion about process capabilities and limitations makes for smoother problem resolution when issues surface.
What sets our 5-Amino-2-Chlorobenzoic Acid apart isn't just what the molecule can do; it's how our collective expertise and willingness to innovate shape each batch. Continuous improvement isn't about abstract value statements; it comes from daily work in process optimization, waste minimization, and energy efficiency. We retooled our hydrochlorination line to cut solvent losses by 14% over two years, investing in in-line vapor recovery instead of waiting for regulatory deadline pressure. Energy audits across the plant sparked changes in heating protocols, lowering utility consumption during cooling and washing cycles. These incremental victories deliver cost and quality gains not because a standard required them, but because our bottom line and customer trust depend on them.
Often, we see opportunities for collaborative trials with downstream innovators. Chemists seeking new coupling agents or process tweaks use our material in exploratory runs, reporting both successes and hurdles. We learn more from failed experiments and reworking material than from smooth, textbook runs. No lab manual or reference guide can substitute for the field realities and feedback loops developed with customers invested in the outcome.
Those who rely on benzoic acid derivatives for process consistency, reactivity, and compliance know that a commodity product approach won’t cut it. The distinctions between 5-Amino-2-Chlorobenzoic Acid and its isomers reveal themselves most clearly to those who have faced real-life troubleshooting in the plant. From filtration behavior to reaction rate, subtle differences in batch controls, process design, and packing finish show up in the end product. Our story with this chemical, shaped by years of scale-up, process tweaking, and open dialogue with customers, has given us a sharp understanding of what really matters. We don’t just make 5-Amino-2-Chlorobenzoic Acid – we build it alongside end users, driven by the kind of detail-focused care you only develop through hands-on manufacture.
Future directions for this product point toward growing demand from specialty pharmaceutical synthesis, colorants, and performance electronics. Each new requirement, whether for higher purity, reduced trace metals, or more sustainable production, has pushed us to refine every detail of our manufacturing workflow. The path forward isn’t about resting on standard benchmarks; it’s about staying close to the chemical’s nuances and real-world performance. Experience earned at the reactor – not just extracted from a datasheet – makes the difference for our team and our partners around the world.