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2-Chloro-6-Methylbenzamide

    • Product Name 2-Chloro-6-Methylbenzamide
    • Alias 2-Chloro-o-toluamide
    • Einecs 219-327-2
    • 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
    VTB
    Specifications

    HS Code

    462266

    Chemical Name 2-Chloro-6-Methylbenzamide
    Molecular Formula C8H8ClNO
    Molecular Weight 169.61 g/mol
    Cas Number 5332-50-7
    Appearance White to off-white solid
    Melting Point 143-146 °C
    Solubility Slightly soluble in water
    Purity Typically >98%
    Synonyms 2-Chloro-o-toluamide
    Storage Conditions Store at room temperature, in a dry and cool place
    Smiles CC1=C(C=CC=C1Cl)C(=O)N
    Inchi Key BDHZPFOEBROKRM-UHFFFAOYSA-N

    As an accredited 2-Chloro-6-Methylbenzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 grams, screw cap, chemical-resistant label showing “2-Chloro-6-Methylbenzamide,” hazard symbols, and handling instructions.
    Shipping 2-Chloro-6-Methylbenzamide is shipped in sealed, chemically resistant containers to prevent leakage and contamination. It is labeled according to regulatory requirements for hazardous materials. During transit, it is protected from extreme temperatures, heat, and moisture. Shipping follows all applicable safety regulations for chemical substances to ensure secure and compliant delivery.
    Storage **2-Chloro-6-Methylbenzamide** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling and limit access to authorized personnel. Always follow relevant safety guidelines and consult the SDS for additional storage information.
    Application of 2-Chloro-6-Methylbenzamide

    Applications of 2-Chloro-6-Methylbenzamide in Industrial Manufacturing

    2-Chloro-6-Methylbenzamide supports several specialized manufacturing sectors as a crucial intermediate. Our facility delivers this raw material with controlled purity and particle consistency, enabling precise downstream integration for international B2B clients. Below we present key application scenarios, each with specific compliance, formulation, and end-product details relevant to large-scale manufacturing environments.

    1. Agrochemical Synthesis: Herbicide Intermediate

    Producers in the agrochemical sector widely incorporate 2-Chloro-6-Methylbenzamide as an intermediate in constructing selective herbicides, particularly acetanilide and amide-type formulations. The compound enables reliable functional group introduction during amide coupling steps, maintaining target molecule performance and regulatory compliance in modern weed control products. Manufacturers optimize reaction sequences using this intermediate for improved batch yields and controlled impurity profiles to satisfy strict market entry demands.

    Industry compliance standards

    • REACH (EU Regulation No 1907/2006)
    • US EPA TSCA Inventory Listing
    • China MEE Order No. 12 (New Chemical Substance Registration)
    • ISO 9001:2015 for production management

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to primary amine in final coupling reaction
    • Adjustment based on target herbicide molecular structure and substitution pattern

    Downstream process integration

    • Charged into amide bond formation vessel after solvent activation
    • Optimized addition sequence with temperature control to limit side reaction
    • QC sampling after reaction to validate target intermediate assay and residuals

    Final product types

    • Pre-emergence and post-emergence herbicide active ingredients
    • Commercial weed control blends for row-crop agriculture
    • Bulk intermediates for branded crop protection formulations

    2. Pharmaceutical Intermediate: Antipsychotic Agent Precursor

    In regulated GMP environments, 2-Chloro-6-Methylbenzamide serves as a true building block for synthesizing substituted benzamide APIs, especially within atypical antipsychotic development. The compound provides targeted halogen and methyl functionalization at key ring positions, enabling precise downstream steps such as Suzuki coupling, acylation, or N-alkylation under manufacturing-level process controls. Pharmaceutical manufacturers rely on consistent purity and traceability from raw material supply through QC release, in alignment with global regulatory expectations for finished dosage production.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • EU EudraLex Volume 4, Part II (GMP guidelines for intermediates)
    • USP monograph verification for final API assay

    Typical usage ratio

    • 1.0–1.05 mole ratio to subsequent reactant in the amide coupling or substitution step
    • Process chemist adjusts based on scale, purity requirement, and impurity threshold

    Downstream process integration

    • Batch charged in closed reactors for derivatization with catalytic base
    • Purification via crystallization or preparative chromatography prior to API build-out
    • Extensive in-process and release testing for residual solvents and heavy metals

    Final product types

    • Antipsychotic active pharmaceutical ingredients (e.g., benzamide class agents)
    • Key advanced intermediates for CNS drug synthesis
    • Clinical trial pharmaceutical compounds under IND or NDA

    3. Specialty Dye Manufacturing

    Colorant manufacturers use 2-Chloro-6-Methylbenzamide as an intermediate in the synthesis of specialty azo and anthraquinone dyes. Its unique substitution pattern provides enhanced stability and colorfastness in the final dye structure, suiting both fiber and pigment dispersions. Strict formulation precision is required to achieve consistent hue intensity, and compliance validation focuses on environmental and end-use application standards within textile and plastic sectors.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile eco-safety)
    • EN 71-3:2019 (European Toy Safety for pigments)
    • EU REACH Annex XVII (restricted amines in dyes)
    • ISO 1833 (Textiles quantification of blend composition)

    Typical usage ratio

    • Depending on formulation, 0.5–1.5 mole equivalents per dye molecule synthesized
    • Adjustment by color shade and solubility target

    Downstream process integration

    • Amidation or coupling reaction under controlled pH and temperature
    • Batch purification using filtration and solvent extraction
    • QC colorimetric analysis and fastness testing after final dye crystallization

    Final product types

    • Textile-reactive dyes for cotton, wool, and synthetic fibers
    • Specialty color pigments for printing inks and plastics
    • Industrial coating colorants and engineered pigment dispersions

    4. Chemical Research and Fine Chemicals Production

    Institutes and contract manufacturers source 2-Chloro-6-Methylbenzamide for use as a synthetic intermediate or ligand building block in advanced research. Its defined functional groups facilitate rapid synthesis of candidate molecules, test probes, or fine specialty chemicals for industrial R&D. Usage often varies based on research protocols but consistently demands detailed COA documentation and batch-level impurity mapping to support publication or pilot trial requirements.

    Industry compliance standards

    • ISO 17025 for analytical method validation
    • GHS/CLP Regulation (EC) No 1272/2008 for laboratory safety labeling
    • Material Safety Data Sheet (MSDS) verification for shipping
    • RoHS assessment for any electronics-related R&D compounds

    Typical usage ratio

    • Lab scale: 0.1–5 g per target synthesis depending on reaction design
    • Pilot scale: 0.01–0.3 mole ratios based on exploratory production

    Downstream process integration

    • Direct addition to custom synthesis batches or combinatorial libraries
    • Flexible protocol entry point—often in initial functionalization or ring formation step
    • Post-reaction analysis includes NMR, GC-MS, HPLC for verification

    Final product types

    • Research-grade intermediates for academic or industrial use
    • Analytical reference compounds for method development
    • Novel fine chemicals for electronics, biotech, or catalyst development
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    Certification & Compliance
    More Introduction

    Product Spotlight: 2-Chloro-6-Methylbenzamide

    Precision Chemistry for Consistent Results

    As a chemical manufacturer closely involved in the synthesis and development of specialty aromatics, I’ve spent years observing the practical value of products such as 2-Chloro-6-Methylbenzamide across industries. The demand for reliable intermediates has grown alongside advancements in pharmaceuticals, agrochemicals, and specialty chemical production. This compound plays a practical role, delivering targeted performance and ease of integration into advanced molecular systems.

    A Closer Look at 2-Chloro-6-Methylbenzamide

    This molecule, distinguished by a single chlorine atom and a methyl group on a benzamide backbone, has secured a place in modern chemical catalogs due to its strategic substitution pattern. I’ve watched formulation labs return to this compound for its clean reactivity and reproducible performance. With a consistent white to off-white crystalline appearance, this material typically arrives in purity ranges exceeding 98%, supported by in-house HPLC and NMR analysis. Melt point ranges align reliably with recognized literature values, and stringent batch control keeps impurity levels tightly contained.

    Uses Driven by Trust in Reactivity

    For synthetic chemists, the subtle electronic effects brought about by the chloro and methyl groups direct downstream substitution or coupling reactions with predictability. Our partners often call for this molecule when constructing intermediates for pharmaceutical active ingredients, especially where ortho-substitutions streamline further transformations. In agrochemical R&D, derivatives of 2-Chloro-6-Methylbenzamide form core structures of herbicidal and fungicidal compounds, responding well to scale-up from pilot to commercial volumes. This extended compatibility with amide coupling, cyclization, halogen exchange, and cross-coupling reactions reduces surprises at the bench—a detail that matters to researchers on tight timelines.

    Why This Molecule Over Others?

    Through years of feedback and close work with users, I’ve seen that fine-tuning molecular substitution delivers advantages not always obvious at the catalog level. The 6-methyl group blocks unwanted ortho substitution during directed ortho-metalation routes, providing selectivity that’s harder to secure from more symmetrical alternatives. On the other hand, the 2-chloro group acts as a leaving group under certain conditions, inviting nuanced transformations not open to the parent benzamide or other regioisomers. Our chemists frequently mention that this dual-substitution pattern actually simplifies the work—by closing doors to certain reactive sites, it opens a cleaner route through multi-step syntheses. Compared to unsubstituted benzamide or alternatives like 2-chloro-benzamide, the methyl group subtly shifts reactivity, aiding in the design of more robust, less error-prone workflows.

    Manufacturing Consistency — A Non-Negotiable

    We have learned the hard way that downstream users will quickly flag even the smallest inconsistencies in starting material. As a manufacturer, I keep a close eye on the reproducibility of each lot, ensuring that particle size, purity, and moisture all land within a narrow band. We blend technical diligence with hands-on sampling at every critical stage, running each output against retained reference samples. Many of our long-standing partners rely on this batch-to-batch sameness for scaling up reactions, especially during tech transfer to full commercial production. The trust built doesn’t come from a certificate; it grows from years of reliably delivered quality.

    Environmental and Handling Notes

    With constantly evolving regulations and safety priorities, our facility has modified the production of 2-Chloro-6-Methylbenzamide to lower process waste and improve worker safety. Emissions control, solvent recovery, and green chemistry techniques have moved from theory into hardwired practice. While the molecule contains a halogen, we structure workflows to confine and recycle chlorinated byproducts. For sensitive users, our literature provides detailed guidance on optimal storage—dry, away from light and sources of heat—to keep hydrolysis at bay. Every effort is made to keep both our operators and customers free from risk, as careless handling of intermediates can quickly ruin more than just a batch.

    In the Lab and in the Field

    Customers in pharma and agrochemicals return to the properties of 2-Chloro-6-Methylbenzamide because trial-and-error in intermediate chemistry triggers delays and uncertainty. I have seen well-equipped labs discard days of effort due to poorly characterized starting materials, and the cost grows exponentially in commercial settings. Our tight process controls allow researchers to plan steps with fewer contingency budgets, knowing the amide backbone will react as expected. This isn’t just a raw material—it’s a building block for innovation, chosen by developers who want their chemistry to move forward without detours.

    Comparing Alternatives

    Within the family of benzamide derivatives, every substitution brings a shift in reactivity and compatibility. For applications demanding rapid aromatic substitution, other chlorinated isomers may perform better, but they sacrifice specificity in follow-up transformations. Adding a methyl group—or changing its position on the ring—directs reactivity and physical form. After years of customer feedback, it’s clear that the 2-chloro, 6-methyl combination outperforms in cases where selectivity and intermediate stability matter as much as absolute reactivity. For some projects, unsubstituted benzamide or 2-chloro-benzamide cannot deliver the required precision, frequently causing low yields or unwanted byproducts in late-stage synthesis.

    Feedback-Driven Refinement

    We have revisited and refined our process for making 2-Chloro-6-Methylbenzamide in response to user experience from both bench chemists and plant engineers. Early on, we fielded complaints about micron-scale insoluble residues and resolved them with an additional purification step. Questions on chloride contamination led us to tighter process analytics and filtration. A few years back, several long-term users needed scale-up batches for regulatory filings, and we demonstrated consistency from gram to multi-kilo scale, matching impurity profiles line for line. These practical lessons shape each lot we release, keeping output in line with expectations.

    Addressing Industry Challenges

    Change in any chemical process brings uncertainty, and for a manufacturer, shifting supply chains or input quality can ripple out through entire sectors. Sourcing high-purity raw materials for 2-Chloro-6-Methylbenzamide once proved tricky, given fluctuations in global chlorobenzene and toluene markets. By securing contracts with vetted upstream suppliers and building redundancy into key steps, we've kept material flowing even as peers experienced outages or recalls. Modernization of our equipment—through automation, online analytics, and improved waste treatment—helps shield downstream users from spikes in impurity or cost. In our experience, honesty in forecasting and signaling any supply issues early builds a reputation that withstands market turmoil.

    Fostering Collaborative Development

    Application chemists and scale-up teams often call for tweaks to meet a project's special needs—particle size shifts for improved dosing, alternate solvent systems for unique reactors, or split shipments timed to complex project schedules. We adapt our drying and milling processes and keep reserved capacity for sudden ramp-ups. Regular visits and feedback sessions have shown us that the biggest breakthroughs come from open discussion, not arm’s-length transactions. The evolution of 2-Chloro-6-Methylbenzamide production at our facility has been shaped by direct collaboration, allowing us to correct blind spots and chase improvements that deliver real-world value.

    Reliable Analytics Backing Every Batch

    Precision analysis supports every decision in our facility. Our lab team validates each batch of 2-Chloro-6-Methylbenzamide by comparing against standard spectra and running full profiles, not just endpoint checks. We use a mix of HPLC, GC-MS, and, where applicable, elemental analysis. Over the years we've added automated sampling to eliminate human error and catch any deviation before release. These checks matter when customers need supporting data for regulatory submissions, or when scale-up trials face scrutiny in validation runs. Trust isn’t earned by promises alone; it's secured batch by batch, through proof and rigorous record-keeping.

    Responding to Regulatory Demands

    Every year brings new regulations and shifting compliance targets for specialty chemicals. Documented traceability, secure handling of waste, and fully documented change control all now factor into the acceptance of a synthetic intermediate like 2-Chloro-6-Methylbenzamide. Our team tracks regional developments in chemical safety, from export controls to REACH updates and local discharge restrictions. Updates to our paperwork and reporting, along with batch documentation, make life easier for customers through audit trails and smooth importation. As the regulatory landscape evolves, we invest to stay ahead, ensuring our partners remain compliant and free from disruption.

    Serving Multiple Sectors

    Use cases for 2-Chloro-6-Methylbenzamide have expanded over the last decade, driven by new research and the shift toward more selective syntheses. In pharmaceuticals, it slots into strategies to build heterocycles and elaborate frameworks for investigational compounds. In agrochemicals, it appears as both an intermediate for bioactive molecules and a reference standard for analytical studies. Material science explorations use this compound for functionalizing aromatic polymers or advancing sensor development. This cross-industry demand has helped us sharpen supply logistics, plan inventory reserves, and maintain engagement with R&D teams who value rapid response and flexibility.

    Meeting Future Needs

    With sustainability at the core of industry evolution, our process for 2-Chloro-6-Methylbenzamide constantly evolves. Last year we piloted solvent minimization steps, and initial runs demonstrated a tangible reduction in emissions. Dialogue with equipment suppliers has sparked the introduction of closed system reactors, further reducing operator risk and release of volatiles. As customers ask sharper questions about lifecycle and footprint, we aim to be transparent—publishing process improvements, energy usage trends, and remaining nimble in accommodating greener chemistries as standards rise. It’s an ongoing challenge, pressing us to go beyond compliance and seek smarter paths from raw material to packaged product.

    Supporting Customers Beyond Supply

    As a specialist manufacturer, our role doesn’t stop at producing 2-Chloro-6-Methylbenzamide to spec. Researchers routinely need technical support for optimizing reaction conditions or troubleshooting unexpected reactivity. Our technical staff fields questions on solvent selection, batch stability, and byproduct suppression—solving issues that make the difference between a published result and an abandoned project. Years of feedback have made us responsive and ready with data, whether for new project launches or compliance audits requiring traceable lot histories.

    Listening to the End User

    Regular dialogue with process engineers and formulation scientists ensures that the final product truly integrates into real-world workflows. We track feedback on packaging, flow characteristics, and analytical performance, quickly adjusting procedures when minor tweaks will prevent major headaches downstream. If a batch displays atypical free-flow or minor caking, quality teams investigate and resolve with improved drying or repackaging. This close relationship with customers means that the 2-Chloro-6-Methylbenzamide received at the bench or reactor is designed not only to meet a formal specification, but also to work smoothly in daily practice. The value is measured by smooth, uneventful synthesis runs—and researchers able to focus on discovery, not troubleshooting inputs.

    True Value Adds Up Over Time

    The market offers an array of benzamide-based intermediates, but few come backed by years of process refinement, transparent quality assurance, and direct engagement with the end user. In my experience, advances in chemistry often hinge on the reliability of the inputs, with even small changes leading to compound failures or delays at commercial scale. We approach the manufacture of 2-Chloro-6-Methylbenzamide not as a commodity process, but as a collaborative effort with each customer. Every improvement is driven by mutual trust and constant feedback, and every challenge is met by a team tuned to the needs of synthetic chemistry in the real world.

    Anticipating Opportunities and Challenges

    Looking forward, the functions of 2-Chloro-6-Methylbenzamide continue to expand as downstream chemistry evolves. We’re tracking trends in novel drug development, green synthesis methods, and advanced materials—all of which demand more precise and well-characterized intermediates. Through active R&D partnerships, investment in cleaner production, and a practice of listening first, we remain ready to supply a product that serves today’s needs and tomorrow’s breakthroughs. We view every kilogram shipped as both a vote of confidence and an open invitation: challenge us, and join us in pushing the possibilities of chemistry forward together.