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2-Amino-5-Chloro-N,3-Dimethylbenzamide

    • Product Name 2-Amino-5-Chloro-N,3-Dimethylbenzamide
    • Alias SCHEMBL1781012
    • Einecs 252-729-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    868258

    ProductName 2-Amino-5-Chloro-N,3-Dimethylbenzamide
    MolecularFormula C9H11ClN2O
    MolecularWeight 198.65 g/mol
    CASNumber 191282-48-9
    Appearance Off-white to light yellow solid
    MeltingPoint 120-125°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    StorageConditions Store at 2-8°C, keep container tightly closed
    Synonyms N,3-Dimethyl-2-amino-5-chlorobenzamide
    SMILES Cc1cc(N)ccc1ClC(=O)NC

    As an accredited 2-Amino-5-Chloro-N,3-Dimethylbenzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 100g amber glass bottle, tightly sealed, labeled with chemical name, hazard symbols, batch number, and handling instructions.
    Shipping The chemical **2-Amino-5-Chloro-N,3-Dimethylbenzamide** is shipped in tightly sealed containers under ambient conditions. Packaging complies with regulatory standards to ensure safety and prevent contamination. The product is labeled clearly with hazard, handling, and storage instructions. Appropriate documentation accompanies the shipment to meet transport and customs requirements.
    Storage 2-Amino-5-Chloro-N,3-Dimethylbenzamide should be stored in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Keep the container tightly sealed and protected from light and moisture. Store at room temperature and avoid exposure to excessive heat. Ensure appropriate labelling, and store in a designated chemical storage cabinet for hazardous substances.
    Application of 2-Amino-5-Chloro-N,3-Dimethylbenzamide
    Purity 98%: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity profile. Melting Point 142°C: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with melting point 142°C is used in fine chemical formulation, where it allows predictable process crystallization and optimal product recovery. Stability Temperature 60°C: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with stability temperature 60°C is used in bulk storage applications, where it maintains chemical integrity under controlled temperature conditions. Molecular Weight 198.66 g/mol: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with molecular weight 198.66 g/mol is used in active ingredient calibration, where it delivers accurate dosage formulation. Particle Size ≤20 μm: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with particle size ≤20 μm is used in solid dispersion manufacturing, where it improves dissolution rate and content uniformity. Water Content ≤0.5%: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with water content ≤0.5% is used in moisture-sensitive compound preparation, where it prevents hydrolytic degradation and enhances shelf life.
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    More Introduction

    2-Amino-5-Chloro-N,3-Dimethylbenzamide: Expanding the Toolbox for Modern Chemistry

    Anyone who spends time working with chemical intermediates knows the hunt for reliable, well-characterized ingredients shapes entire industries. One such compound, 2-Amino-5-Chloro-N,3-Dimethylbenzamide, keeps garnering attention for its performance in research and industrial chemistry. More than a mouthful of a name, this specialty aromatic amide stands out with a molecular structure that gives it an edge in synthesis applications and chemical modification. The seasoned chemist sees molecules not just as formulas on a page, but as opportunities to solve technical problems in creative and practical ways.

    The Structure That Makes a Difference

    Beneath the surface, the action often starts with chemistry’s smallest components. 2-Amino-5-Chloro-N,3-Dimethylbenzamide brings a unique combination: an amino group at the 2-position, a chlorine atom at the 5-position, and two methyl groups that change the chemical’s reactivity. The fused features on the benzamide ring are more than aesthetic—they determine everything from solubility to compatibility with reagents. During synthesis, these groups enable a range of substitutions and coupling reactions, making the compound a flexible building block for more complex molecular designs.

    The specificity of additions on the benzene ring isn’t trivial. Substitution can turn an inert skeleton into a highly active intermediate. That matters to those navigating the hurdles of organic synthesis, where control over reaction outcomes saves weeks of troubleshooting. Comparing 2-Amino-5-Chloro-N,3-Dimethylbenzamide with the broader set of benzamides, it’s not just one more cog in the machine; it’s a fine-tuned instrument with practical implications in planning multi-step syntheses. I’ve read work from R&D labs that highlights how smaller tweaks—like adding that chlorine—open up new reaction channels or suppress undesired side-products. When you look at reaction yields and impurity profiles, the advantages become tangible.

    Why Chemists Reach for this Compound

    In industry and the lab, reliability counts for more than any marketing claim. Reports indicate that this molecule holds its own where consistency and tractability are under the microscope. Compound purity sits at the center of the matter, where tight specifications (usually cited at greater than 98% by analytical HPLC) guarantee downstream results won’t get derailed by unknown contaminants. That matters whether the end use involves pharmaceutical discovery, pigment formulation, or specialty materials.

    Chemists often gravitate toward compounds like 2-Amino-5-Chloro-N,3-Dimethylbenzamide because synthesis challenges stack up as projects get more complex. For instance, the combined presence of the amino and chloro groups means the benzamide can serve as a divergent intermediate—one side opens to electrophilic substitution, the other to nucleophilic attachment. Practical synthesis routes that start from this benzamide streamline the path to more elaborate molecules, which reduces cost and development time.

    Compared to straight-chain or unsubstituted benzamides, this variant offers greater flexibility for late-stage modification. In drug development, such traits play a huge role when screening a wide swath of chemical space. The molecule takes well to common coupling partners including activated carboxylic acids and sulfonyl chlorides, and the dual reactive handles expand the possible combinations.

    Real-World Applications: Progress through Precision

    Research groups looking to tailor-make biologically active molecules find that 2-Amino-5-Chloro-N,3-Dimethylbenzamide gives them a valuable springboard. Some recent studies use it as a foundation to build kinase inhibitors and antimicrobial compounds. Others focus on leveraging its sterically distinct framework to control the three-dimensional arrangement of the next synthetic step, a make-or-break consideration in pharmaceutical work.

    On the industrial side, pigments, dyes, and specialty polymers benefit from using intermediates with predictable reactivity. The two methyl groups reduce the likelihood of unintended side-reactions, allowing for cleaner downstream processing. Those with experience in formulation chemistry point out how a robust intermediate minimizes the number of purification steps, which in turn keeps costs in check and throughput high.

    The presence of both electron-donating methyl groups and electron-withdrawing chlorine influences not just chemical stability but also influences how the benzamide integrates with other components. A trusted chemical supplier may highlight the compound’s track record: a strong batch-to-batch reproducibility, something that’s never a given in specialty chemical markets. My conversations with chemists confirm that such reliability takes years to establish and is highly valued when stakes run high.

    Safety and Environmental Considerations

    Experience in chemical handling tells anyone: working with aromatic amides demands vigilance. Safety protocols exist for good reason. While 2-Amino-5-Chloro-N,3-Dimethylbenzamide has no outlier hazardous properties compared to similar compounds, standard handling precautions apply—use of gloves, eyewear, and well-ventilated workspaces ranks non-negotiable.

    More companies and academic labs now factor sustainability and lifecycle impact into product selection. Many are reevaluating their intermediates to minimize environmental footprint without sacrificing performance. This compound generally allows for efficient reaction conditions that use less energy and generate fewer byproducts compared to older alternatives. That helps both bottom lines and the push for greener processes. Recyclability of process solvents and safe waste handling practices remain top priorities during scale-up; anyone involved in process chemistry knows that solvents often bring more environmental challenges than the reagents themselves.

    Why Product Differentiation Matters

    The specialty chemical world teems with similar-sounding names and close molecular cousins. What sets 2-Amino-5-Chloro-N,3-Dimethylbenzamide apart? Years of development in the field reveal that not all benzamides deliver the same performance. The placement and number of substituents matter greatly—not just on paper, but in the flask and in the final product.

    Turn to comparable products, such as 2-Amino-5-Methylbenzamide or 5-Chloro-N-Methylbenzamide, and you find differences in how they respond to standard reaction conditions. Those differences ripple down to downstream process reliability, final product quality, and compliance with tight regulatory standards. The combination found in the dimethyl analog produces improved selectivity for certain transformations, reducing the trial-and-error phase common in method development. Researchers I know often bring up that moving from a methyl-only to a chloro-methyl variant changes the project trajectory, letting new scaffolds come to life or opening up reaction conditions otherwise known for poor yields.

    Comparisons with established intermediates also bring regulatory compliance into focus. Where other benzamides or aromatic amines may raise red flags because of toxicological or environmental issues, this compound often slips through without causing new headaches. Industry prefers ingredients that promise predictable performance and minimal additional regulatory hurdles—this saves months during development cycles, particularly in regulated sectors such as pharmaceuticals and advanced materials. That preference comes not from marketing, but from learning hard lessons during scale-up and regulatory review.

    Consistent Supply: A Major Hurdle Overcome

    Reliability remains the unsung hero of any supply chain built on fine and specialty chemicals. Feedback from buyers and users points to consistency: the ability to source the same compound with assured quality year after year. Several decades ago, fluctuations in chemical purity or trace contaminants created major headaches for manufacturers. Now, with increased transparency and advances in process monitoring, compounds like 2-Amino-5-Chloro-N,3-Dimethylbenzamide hit the benchmarks without unwelcome surprises.

    The global nature of the specialty chemical market pushes suppliers to keep up with strict purity specifications and verified supply sources. Labs depending on dependable intermediates now enjoy greater supply security, thanks to a mature logistical network and transparent traceability. This has been especially important during disruptions brought on by global events; researchers and technical leads know that process continuity hinges on ingredients arriving exactly as ordered.

    Solutions for Common Synthesis Challenges

    Ask any experienced chemist about the biggest roadblocks in organic synthesis and you get a list: unpredictable reactivity, side products, inconsistent suppliers, and regulatory headaches. Choosing a versatile intermediate like 2-Amino-5-Chloro-N,3-Dimethylbenzamide addresses several challenges at once. Its balanced reactivity means chemists can introduce structural complexity without worrying about runaway reactions destroying product integrity. The molecule’s stability lets teams screen reaction conditions—from base-sensitive to acid-hardened routes—without risking decomposition or loss of yield.

    On the practical front, this intermediate helps sidestep lengthy purification sequences. With greater selectivity in each synthetic step, purification goes faster and final product purity stays high. That saves time in pharmaceutical research, where bottlenecks in purification slow everything down. Chemical manufacturers looking to streamline process safety and waste reduction have found that using well-behaved intermediates cuts operational costs. Instead of compensating for wayward byproducts or persistent impurities, teams direct resources to developing end products and scaling the chemistry.

    Addressing regulatory complexity stands as another benefit. When regulatory teams face a data package built from legacy chemicals with known tox profiles, new chemical intermediates often carry a burden of extra scrutiny. This compound’s documented use, low impurity profile, and routine analytical data make the approval process smoother. Pharmaceutical and advanced material engineers have enough on their plates without running gauntlets for ingredients that turn out to be problematic just before market launch.

    Continual Learning and Community Exchange

    The pace of change in chemistry means nobody works in a vacuum. Community exchange—whether through journal articles, open research platforms, or professional conferences—spurs knowledge transfer and enables smarter decisions over time. 2-Amino-5-Chloro-N,3-Dimethylbenzamide stands as a practical example of how collective experience sharpens product selection and method development.

    More researchers publish comparative studies that assess critical intermediates across different applications. Data from these papers provide real benchmarks—how does a compound perform in real synthesis campaigns, what byproducts surface, where do yields and throughput fall short or excel. Consistent feedback across the user community confirms what sales sheets alone cannot: reliability emerges from daily practice, not just theory.

    Looking Forward—Balancing Innovation and Practicality

    Chemistry continues to demand both creativity and discipline. No single compound solves every challenge, but smart intermediate choices make a huge difference over the course of a development project. The track record of 2-Amino-5-Chloro-N,3-Dimethylbenzamide demonstrates that small changes at the molecular level shape what’s possible in the lab and at industrial scale.

    New entrants into the field benefit from collective lessons. Using well-characterized, multi-functional intermediates simplifies the path from concept to outcome. That’s not just a matter of academic concern; it directly feeds into drug discovery timelines, material innovation, and even environmental responsibility. Carefully chosen intermediates mean fewer course corrections down the line.

    From my own time collaborating on early-stage discovery projects to speaking with process chemists in large-scale manufacturing, I’ve seen the appreciation for intermediates that truly perform. Performance is measured not in theory but in whether a product helps teams reach their goals without extra roadblocks. In my experience, advocating for robust, well-supplied building blocks reduces friction, keeps projects on track, and stacks the odds in favor of breakthroughs rather than setbacks.

    Conclusion: Incremental Gains with Lasting Impact

    While the broader market for fine chemicals moves fast, those who build success on incremental improvements often reap the most sustainable rewards. 2-Amino-5-Chloro-N,3-Dimethylbenzamide illustrates the quiet power of solid chemical workmanship: one well-conceived molecule, reliably produced, and thoughtfully used. As the chemical marketplace gets crowded with new options and evolving demands, focusing on compounds with a proven edge continues to deliver value. Thoughtful sourcing and deliberate selection ensure that investments in R&D, manufacturing, and compliance build lasting foundations instead of fleeting milestones.

    Every major advance in chemistry pivots on small, smart moves. For those making choices that shape products, drive research, and meet the challenges of tomorrow, building on strong intermediates represents a step toward resilience and progress. Whether you work at the bench, manage a supply chain, or define new products for an emerging market, the case for time-proven, versatile intermediates remains as compelling as ever.