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HS Code |
579858 |
| Chemical Name | 2-Amino-5-Chloro-N,3-Dimethylbenzamide |
| Molecular Formula | C9H11ClN2O |
| Molecular Weight | 198.65 g/mol |
| Cas Number | 130283-24-0 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 146-150°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Temperature | Store at 2-8°C |
| Smiles | CC1=CC(=C(C=C1Cl)N)C(=O)NC |
| Inchi | InChI=1S/C9H11ClN2O/c1-6-4-8(11)7(10)3-5(6)9(13)12-2/h3-4H,11H2,1-2H3,(H,12,13) |
| Synonyms | N,3-Dimethyl-2-amino-5-chlorobenzamide |
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 | The packaging is a sealed, amber glass bottle labeled “2-Amino-5-Chloro-N,3-Dimethylbenzamide, 25 grams” with safety and handling instructions. |
| Shipping | 2-Amino-5-Chloro-N,3-Dimethylbenzamide is securely packaged in sealed containers to prevent contamination and degradation. It is shipped according to relevant chemical safety regulations, often as a non-hazardous material, but with precautions against moisture, extreme temperatures, and physical damage during transit. Handling instructions and safety data sheets accompany each shipment. |
| Storage | **2-Amino-5-Chloro-N,3-Dimethylbenzamide** should be stored in a tightly sealed container at room temperature, in a cool, dry, well-ventilated area. Keep away from incompatible substances, such as strong oxidizers and acids. Protect from light, moisture, and direct heat sources. Always ensure that storage areas are clearly labeled and follow all relevant safety protocols and regulations. |
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Purity 99%: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with a purity of 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures minimal side reactions and greater yield of target compounds. Melting Point 148°C: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with a melting point of 148°C is utilized in solid-state formulation processes, where its defined phase transition temperature supports precise process control. Molecular Weight 198.68 g/mol: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with a molecular weight of 198.68 g/mol is incorporated in organic chemistry research, where accurate stoichiometric calculations enhance experimental reproducibility. Particle Size <50 µm: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with particle size below 50 micrometers is used in fine chemical blending, where small particle size enables uniform mixing and consistent product quality. Stability Temperature 60°C: 2-Amino-5-Chloro-N,3-Dimethylbenzamide stable up to 60°C is applied in temperature-sensitive formulations, where thermal stability maintains compound integrity during processing. Assay 98% min: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with a minimum assay of 98% is used in analytical reference standards, where high assay guarantees the accuracy of analytical measurements. Solubility in DMSO: 2-Amino-5-Chloro-N,3-Dimethylbenzamide soluble in DMSO is utilized in biological screening assays, where excellent solubility ensures homogeneous test solutions for reliable bioactivity results. Residual Solvents <0.1%: 2-Amino-5-Chloro-N,3-Dimethylbenzamide with residual solvents below 0.1% is selected for active pharmaceutical ingredient development, where minimal residual content supports regulatory compliance. |
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In chemistry, some molecules serve as quiet workhorses. 2-Amino-5-Chloro-N,3-Dimethylbenzamide belongs in this group, punching above its weight in research and development labs that focus on pharmaceuticals, specialty materials, and organic synthesis. I’ve worked in chemical sourcing and small-batch synthesis for years, so I know how tricky and rewarding it can be to find the right building block for a complicated synthesis. Objective knowledge, careful handling, and collaborative expertise shape the value we draw from each molecule. In my experience, 2-Amino-5-Chloro-N,3-Dimethylbenzamide brings an intriguing balance—its reactivity offers both possibilities and challenges.
Let’s unpack what this compound brings to the lab bench. With a straightforward benzamide core, two methyl groups add both bulk and fine-tuned electronic effects, and a chlorine atom creates a handle for rather interesting transformations. Chemists value this “toolkit” effect: three key substituents on a single aromatic ring give options for further reactions and combinations. The amino group at position 2 is reactive enough for functionalizations and modifications, but not so unruly that it gets in the way during workup or purification. In practice, this setup helps with planning syntheses and saving time on route scouting. This matters when you’re chasing complex targets—an intermediate that doesn’t play games on the bench is worth its weight in gold.
Modern syntheses demand clarity, so let’s talk about what specialists monitor closely with 2-Amino-5-Chloro-N,3-Dimethylbenzamide. Purity measurements usually hit the 97-99% range or better; nobody wants to waste time cleaning up side products or guessing about contamination. Physical appearance needs to match expectations—powder, off-white or cream, as deviations sometimes hint at problems upstream. Melting point and elemental analysis anchor the quality assessment. I’ve worked with providers who run advanced NMR, HPLC, and MS checks, even on small batches, since small impurities can trip up pharmaceutical research and slow regulatory approval.
Packaging speaks volumes about a company's standards: tightly sealed glass or HDPE with tamper-evident closures prevents moisture uptake or cross-contamination, especially for sensitive molecules. For storage, the compound likes a dry, cool environment, safe from light. Deviation from these routines tends to degrade sample reliability faster than anyone wants to accept. Every experienced lab tech has stories of compounds ruined by careless storage or slipping shelf-life. Simplicity in handling means lower training thresholds—good for both efficiency and safety.
People working on drug discovery or agrochemical R&D see this compound pop up under different names but with one shared purpose: a versatile intermediate ripe for transformation. That versatility plays out in heterocycle construction, urea-linked frameworks, and custom ligand systems for catalysis. I’ve watched researchers streamline synthesis pathways by using this one compound, shaving days off reaction sequences by skipping unnecessary protection or deprotection steps.
In process chemistry, speed and accuracy matter. A robust starting material keeps downstream operations running smoothly. 2-Amino-5-Chloro-N,3-Dimethylbenzamide brings this dependability to a range of targets, especially in tightly regulated environments, where each synthetic route faces multiple regulatory reviews. Documentation must be ironclad, and the global push for greener chemistry means every atom counts. Reagents like this one make new, less wasteful methods possible—something that most of my colleagues take pride in chasing.
With so many chemicals out there, why pick this one? It’s about the harmony between functional group positioning and chemical stability. Direct comparison with other substituted benzamides shows that the specific arrangement of amino, chloro, and methyl groups opens up room for efficient cross-coupling, halogen-exchange, and directed ortho-metalation. These methods cut steps and lower reagent costs. In synthetic organic chemistry, every avoided procedure brings cost and time savings.
Contrast this with compounds bearing alternative substituents—a para-methyl or an extra halogen, for instance. They often introduce steric bulk or electron density shifts that complicate reactivity. I’ve seen teams scrap entire branches of research after a supposedly “minor” substitution gummed up a key reaction, shattering meticulously laid plans. The specific substitution pattern of 2-Amino-5-Chloro-N,3-Dimethylbenzamide delivers a sweet spot where reactivity, selectivity, and processability meet, which acts as an advantage when developing patentable new molecules.
The barrier to entry for new pharmaceuticals keeps climbing. Reliable intermediates like this one serve as quiet engines that drive pipelines forward. A failed lot or non-reproducible intermediate can set back whole projects by weeks, sometimes months. Sharing stories among fellow scientists often circles back to the everyday nuts and bolts: purity, shelf-stability, predictable behavior in solution. I remember an early project where we compared three related benzamides; the version with this precise functional set finished reactions more cleanly, handled scale-up to the pilot phase without trouble, and simplified purification at every step. The mundane details carried weight far beyond their immediate context.
For those who work in high-stress, high-throughput screening environments, consistency in chemical supply builds trust in the R&D chain. A lab’s faith in its sources grows with every shipment that meets spec, every successful scale-up, every smooth downstream purification. The chemical acts as the backbone—sometimes unremarked on, always valued, never wholly visible to end-users. This background labor sets the stage for safer medicines, better crops, and new materials. My colleagues and I bond over those “quiet successes” where a dependable reagent saves the day, even when outside observers only see the ultimate product.
Sourcing and manufacturing bring ethical responsibilities. I’ve seen firsthand how supply chain disruptions, questionable provenance, or subpar quality can taint a promising project. The recent push for Enhanced Quality Standards, including good manufacturing practice (GMP) and rigorous traceability, finds enthusiastic uptake among serious producers. With 2-Amino-5-Chloro-N,3-Dimethylbenzamide, clear documentation trails, supplier certifications, and routine analytical verifications shape its reputation among chemists. For those positioning new pharmaceutical candidates for clinical testing, an unreliable intermediate has no place. The risk of cross-contamination, off-specification lots, or unreported impurities lingers like a cloud over otherwise groundbreaking work.
Meeting environmental standards also holds weight. Synthesis routines that avoid toxic byproducts or minimize hazardous waste gain traction. Cheaper routes may save short-term cash, but in my experience, the long-term reputational risks and disposal headaches cost more. Collaborating with environmentally conscious suppliers of intermediates like this one paves the way for clean, transparent progress. Researchers and quality managers increasingly ask for provenance—what route made this, how much waste occurs, have alternatives been considered?
Laboratory realities rarely appear in public-facing dock sheets. 2-Amino-5-Chloro-N,3-Dimethylbenzamide’s solid-state stability is a plus, but solubility in some solvents varies. Scale-up for pilot batches can introduce flow challenges; at larger volumes, particle size, mixing behavior, and process filters all shape the final outcome. The occasional attempt to push reactivity can yield unanticipated byproducts, especially when researchers modify protocols meant for similar-looking compounds but with different site reactivity. I’ve seen process chemists adapt by tweaking solvent polarity, reaction temperature, or even mechanical stirring regimes to unlock full performance.
Human error also plays a role. Mislabeled containers, poorly calibrated scales, or a momentary oversight in drying can lead to setbacks. At one facility, an unplanned spike in humidity spoiled an entire lot, triggering awkward phone calls and rush resupply. Smart policies, double checks, and a culture that values reliable routines cut down on such mishaps. Training and purpose-built laboratory infrastructure matter—a reminder that what seems easy on paper still demands real experience in practice.
Chemistry culture prizes the sharing of “tricks of the trade”—small, specific practices that maximize success with each compound. For intermediates like 2-Amino-5-Chloro-N,3-Dimethylbenzamide, standard protocols go a long way: monitor batch records, keep a regular inventory check, and communicate clarity regarding shipments and analytical data. Advanced users push for high-resolution NMR and consistent mass spectrometry validation, not just an off-the-shelf certificate.
In sourcing, forming partnerships with vendors who invest in systematic quality control, rapid shipping, and full regulatory documentation pays dividends. Collaborative relationships with suppliers open the doors to technical troubleshooting and responsive problem-solving—more like joint stewards than mere transactional ties. In my own work, this means asking direct questions about shelf life, container specification, and pre-shipment analysis rather than making assumptions. Distributors who cut corners often do so at the pivotal expense of quality; ongoing dialogue invites accountability and improvement.
On the lab side, verification remains essential: run spot-checks on new lots, store records in secure digital archives, and document user feedback for continuous improvement. In larger facilities, integrating lot tracking and digital batch management reduces risk and aligns outcomes with evolving regulatory demands. Teams that take these steps report lower incident rates and smoother audit experiences.
Chemical innovation moves at the speed of its weakest link. In fast-evolving areas like medicinal chemistry or functional materials, the right building block can unlock a new design strategy or spark better outcomes. I’ve contributed to early-stage projects where access to specialty intermediates like 2-Amino-5-Chloro-N,3-Dimethylbenzamide pushed the group’s ideas from theory to practice, shaving months off project timelines.
For early-career scientists, these intermediates represent an accessible entry point for advanced experimentation. They offer enough functional diversity to support a wide range of synthetic ideas, yet avoid the operational headaches that come with extremely unstable or highly hazardous compounds. Mentors often select such molecules deliberately, aiming to combine educational growth with practical, publishable results.
Pharmaceutical scale-up or custom synthesis does not run on autopilot. Downstream decision-making grows simpler when each intermediate behaves predictably. Users benefit from batch-to-batch consistency in melting point, reactivity, and impurity profile. Having spent time troubleshooting pilot plant runs, I appreciate the moments where the feedstock “just works as it should”—no fuss, no last-minute process edits, no nervous post-game autopsies. For 2-Amino-5-Chloro-N,3-Dimethylbenzamide, predictability shapes smooth transitions between kilo-scale and full production, a big win for developers under tight deadlines.
Industry leaders look for flexibility but also reliability. Some other similar secondary benzamides require higher temperatures to react or fight back with difficult purification steps. The specific arrangement here lends itself to mild reaction conditions, compatibility with a broad set of reagents, and lower energy consumption. That marks it as a favorite for method development, where safety, cost, and time matter together.
In the sciences, lessons seldom come cheaply. Anyone who’s handled dozens of intermediates knows the headaches that can come from unreliable shipments. I remember a project where a less well-characterized intermediate with similar structure to 2-Amino-5-Chloro-N,3-Dimethylbenzamide arrived three days late, slowed downstream reactions, and jeopardized our progress toward a publication deadline. That’s the difference solid sourcing and clear communication make—a lesson every research team absorbs, sometimes the hard way.
People respect the simple formula: invest in quality at the upstream link, and things break less often downstream. 2-Amino-5-Chloro-N,3-Dimethylbenzamide demonstrates this dynamic, bridging the practical needs of working chemists with the ambitions of those chasing new discoveries. The stakes—publication, patent protection, progress—depend on such intermediate successes.
Modern chemical development walks a fine line between speed and stewardship. Choices about intermediates like 2-Amino-5-Chloro-N,3-Dimethylbenzamide do more than affect cost or workflow; they reverberate into broader questions of safety, transparency, and ethical progress. Labs that prioritize traceable, high-purity materials equip themselves to explain decisions to regulators, collaborators, and the wider public. That transparency builds community trust.
Thoughtful chemical sourcing offers more than a technical fix; it supports environmental goals and aligns with the expectations of a world increasingly focused on sustainability and accountability. Any lab looking to build a culture of integrity starts with the basics—what’s on the shelf, how well it’s understood, and how carefully it’s managed.
For buyers, bench chemists, and managers alike, every purchase shapes outcomes. Investing in solid, well-characterized intermediates pays off in faster results and safer operations. A culture of knowledge-sharing, meticulous documentation, and ethical supply choices pushes back against short-term savings that come with hidden costs. My advice, forged on the back of good runs and bad: start with a compound you can trust. Evaluate sources critically, demand documentation, and open lines of communication with your suppliers and colleagues. 2-Amino-5-Chloro-N,3-Dimethylbenzamide stands out as a reliable player that forms the foundation for new solutions in complex industries. That reputation is built molecule by molecule, delivered package by package, and maintained by everyone in the chain.