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2-Chlorobenzylamine

    • Product Name 2-Chlorobenzylamine
    • Alias o-Chlorobenzylamine
    • Einecs 217-987-0
    • 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

    288075

    Chemical Name 2-Chlorobenzylamine
    Molecular Formula C7H8ClN
    Molecular Weight 141.60 g/mol
    Cas Number 89-98-5
    Appearance Colorless to pale yellow liquid
    Boiling Point 220-222 °C
    Melting Point -4 °C
    Density 1.153 g/cm³
    Flash Point 111 °C
    Refractive Index 1.576
    Synonyms o-Chlorobenzylamine
    Solubility In Water Slightly soluble

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

    Packing & Storage
    Packing A 100-gram amber glass bottle labeled "2-Chlorobenzylamine," features hazard symbols, batch number, and manufacturer details, tightly sealed.
    Shipping 2-Chlorobenzylamine should be shipped in tightly sealed, appropriately labeled containers, protected from physical damage, moisture, and direct sunlight. It must be handled as a hazardous material, following all relevant regulations for transport (such as DOT, IATA, or IMDG), and accompanied by safety documentation and proper hazard labeling indicating its irritant and toxic properties.
    Storage 2-Chlorobenzylamine should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Use appropriate secondary containment to prevent spills, and ensure the storage area is equipped with proper ventilation and spill response measures.
    Application of 2-Chlorobenzylamine

    Applications of 2-Chlorobenzylamine in Industrial Manufacturing

    2-Chlorobenzylamine is a specialized intermediate used in several high-value chemical manufacturing sectors. As a direct manufacturer, we supply this material to customers requiring reliable consistency, traceability, and technical support through a range of critical downstream applications.

    1. Pharmaceutical Intermediate for Antihypertensive API Synthesis

    Pharmaceutical manufacturers use 2-Chlorobenzylamine in the synthesis of key active pharmaceutical ingredients (APIs), especially in the production of antihypertensive agents within the imidazoline and substituted benzylamine classes. Chemical process engineers introduce 2-Chlorobenzylamine as an alkylamine building block during the main condensation or nucleophilic substitution phase. Quality control protocols demand strict batch-to-batch consistency and low impurity profiles to ensure regulatory acceptability of the final API.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for APIs
    • USP-NF and European Pharmacopoeia reference monographs
    • Good Manufacturing Practice (GMP) for Pharmaceutical Intermediates
    • FDA Drug Master File (DMF) registration for regulated markets

    Typical usage ratio

    • Employed in 1–1.4 molar equivalents per API batch, adjusted based on the downstream substitution yields and purging of side-products

    Downstream process integration

    • Introduced into multi-step synthetic routes after halogen substitution and prior to cyclization or protective group chemistry; monitored via in-process HPLC and purity control

    Final product types

    • Antihypertensive tablets and capsules (API: Imidazoline derivatives)
    • Bulk pharmaceutical intermediates for contract manufacturers
    • Precursor for antiarrhythmic and CNS-active APIs

    2. Agrochemical Synthesis for Selective Herbicide Intermediates

    Agricultural chemical formulators utilize 2-Chlorobenzylamine for the production of selective post-emergence herbicide intermediates. The compound undergoes condensation with acid chlorides or carboxylic acids to yield amide structures found in modern phenoxyalkanoic, triazine, and pyridine-based herbicides. Granular process control is vital to minimize residual amine content in the technical concentrate before final blending and formulation.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Active Ingredients
    • ISO 9001:2015 for agrochemical raw material supply
    • REACH Regulation (EC) No 1907/2006 compliance for European production
    • China National Standard GB 20811-2020 (for pesticide manufacturing)

    Typical usage ratio

    • 0.85–1.1 mol per target molecule, adjusted for downstream acylation efficiency and process waste

    Downstream process integration

    • Input after initial halogen-substitution step and before amide bond formation; usually dissolved in polar aprotic solvents for high reactivity in batch or semi-continuous systems

    Final product types

    • Technical-grade herbicide active substances
    • Water-dispersible granules (WDG) formulations
    • Stabilized crop protection concentrates

    3. Synthesis of Specialty Dyes and Pigments

    Dye and pigment manufacturers incorporate 2-Chlorobenzylamine as a nucleophile in diazotization reactions, especially for producing chlorinated benzyl-substituted azo dyes. Production lines require this intermediate to introduce controlled chlorine and amino functionality, helping fine-tune solubility, hue, and stability profiles of synthetic colorants. QA systems verify trace impurity levels and batch color consistency to meet textile and plastics standards.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textiles
    • EN 71-3:2019 Chemical Safety for pigments in toys
    • ISO 9001:2015 for pigment and dye production
    • Registration compliance under US TSCA

    Typical usage ratio

    • 0.95–1.2 equivalents, routinely adjusted based on target dye chromophore structure and color yield

    Downstream process integration

    • Added in the primary diazotization or coupling reactor; process steps include controlled temperature and pH, followed by washing and drying for pigment isolation

    Final product types

    • High-performance azo dyes for polyester and nylon fibers
    • Plastisol and inkjet color pigments
    • Direct application pigments for automotive plastics

    4. Intermediate in Custom Polymer Modifier Production

    Polymer compounders use 2-Chlorobenzylamine to create specialty polymer modifiers, including functionalized polyamides and custom polyurethanes. It participates as a chain extender or end-group modifier in solution or melt-phase processes, enabling the introduction of chlorinated amino groups that adjust polymer flexibility, adhesion, or flame retardancy. Product lines require strict control of monomer dosing to achieve consistent polymer architecture and downstream material certification.

    Industry compliance standards

    • UL 94 Flammability Standard for plastics
    • EPA 40 CFR Part 63 (NESHAP) for polymer facilities
    • ISO 14001 for environmental management
    • RoHS (2011/65/EU) for electronics-related modifiers

    Typical usage ratio

    • 3–15% by weight in prepolymer or resin blends, adjusted for target mechanical and thermal properties of custom formulations

    Downstream process integration

    • Charged during prepolymer formation or in post-polymerization chain extension steps; monitored using GPC and DSC to confirm polymer structure and thermal response

    Final product types

    • Fire-retardant electrical encapsulants
    • High-adhesion polyurethane foams
    • Specialty thermoplastic elastomers used in automotive gaskets and electronics
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    Certification & Compliance
    More Introduction

    Introducing 2-Chlorobenzylamine: Direct from the Production Floor

    Our Experience with 2-Chlorobenzylamine

    Every batch of 2-Chlorobenzylamine rolling out from our facility carries more than just a synthetic intermediate—it carries the story of decades spent mastering chemical processes. Across shifts and seasons, our operators and engineers have seen demand for fine, reliable benzyl amines rise steadily. 2-Chlorobenzylamine (also known by its chemical name, 2-chlorophenylmethylamine) has built that reputation in industrial labs and manufacturing plants worldwide, and each order we ship builds on those years of collaboration and real-world feedback.

    We work with raw materials sourced for purity and trace elements well below industry tolerance. As we scale up, our approach has barely changed: evaluate material at every step and adjust parameters based on actual data, not just theory. This practice shows in the finished product—free from unnecessary impurities, kept dry, and handled only by veteran hands from start to finish.

    Understanding 2-Chlorobenzylamine Through Application

    In the process chemistry sphere, few aromatic amines have proven as flexible as 2-Chlorobenzylamine. This molecule, distinguished by a chlorine atom ortho to the benzylic position, offers unique reactivity. Pharmaceutical intermediates often rely on the aryl chloride for selective substitution or further transformation. Its straight amine function encourages coupling reactions that unlock dozens of routes for downstream synthesis.

    We field calls from R&D chemists seeking scale-up support for pilot processes, and from multinational crop science groups requiring multi-ton lots with exact impurity profiles. 2-Chlorobenzylamine appears routinely in investigations of antihistamine pipelines, fungicide development, and as a linker or building block for active pharmaceutical ingredients. In these roles, researchers look for sharp melt points, consistent bulk density, and well-documented impurity maps, all points we monitor batch after batch.

    The difference between lab quantities and commercial shipments can be night and day. All too often, bench-grade stocks appear clean but fail to deliver consistent conversions when reactors fill 400-liter vessels. Sticky residues, colored byproducts, and unknown ions can all bleed into later process steps unless the starting amine comes genuinely clean. Over the last ten years, we have invested in low-ppm water removal, inline GC analysis, and storage protocols that maintain both shelf stability and shipping safety. We keep the pathway simple—each drum loaded onto a truck is traceable to its raw input and in-process records.

    Real-World Impact: Why Purity Tells the Story

    Purity figures more than just as a number on paperwork. The stakes climb fast as end uses drift from research toward regulated production. The chlorine substituent in 2-Chlorobenzylamine creates a reactivity profile that amplifies trace contaminants—so even half a percent of unknowns can derail whole syntheses or surface in final active ingredients. We have worked shoulder-to-shoulder with process development scientists, troubleshooting unexpected side reactions or color changes during scaling.

    These experiences pushed us to improve phase separations and invest in analytical equipment. NMR, HPLC, Karl Fischer titration—all standard tools, though we see them as ongoing investments, not just checkmarks. The exacting standards of an FDA-audited process or an agricultural registration do not tolerate paperwork purity if the batch itself falls short.

    On occasion, we partner with innovators on non-standard grades. Some projects benefit from ultra-low sulfate specifications; others call for custom packaging to minimize risk in automated lines. We document every modification, supply lot-specific COAs, and welcome lab visits. Each step is verified, not just assumed.

    Comparing 2-Chlorobenzylamine with Other Benzylamines

    Our perspective grows from years of handling a range of benzylamine derivatives. Aniline, para-chloro, and even methylated analogs all have places in custom syntheses. 2-Chlorobenzylamine stands out because of both its structural features and its consistent industrial demand.

    The presence of the ortho-chlorine makes it less nucleophilic than unsubstituted benzylamine. This can slow undesired side reactions in some coupling or alkylation steps, offering cleaner product streams. Some analogs, such as 4-chlorobenzylamine, display different selectivity or volatility, but few can match the performance profile of the ortho isomer in certain medicinal chemistry projects and pigment manufacture.

    Not all benzylamines are created equal regarding odor, handling, and long-term storage. 2-Chlorobenzylamine brings a manageable, less aggressive aroma, and when dried and stored correctly, resists yellowing or polymerization. Some grades of unsubstituted benzylamine discolor quickly and emit strong, irritating fumes. Plant operators and QC techs respect the difference—there’s less downtime spent fixing leaks or scrubbing air.

    We know many customers weigh price and availability above other specs. Our production model relies on semi-continuous reactors and robust recycling of by-products, letting us maintain consistency and keep pricing competitive even as global feedstock markets fluctuate. We commit to transparency in cost structure and do not cut purity to chase short-term gains.

    Specifications We Put Our Name On

    Our 2-Chlorobenzylamine typically leaves the plant as a clear to pale yellow liquid with an assay of at least 99% by GC or HPLC. Water stays below 0.2%, and heavy metal content remains well under global thresholds. Packing options include coated steel drums and HDPE kegs, purged under dry nitrogen if required. Each container leaves with a unique batch number and analytic documentation.

    We carefully avoid contaminant crossflow by dedicating lines for aromatic amines and scheduling turns to accommodate different customer needs. Our environmental controls exceed standard regulatory frameworks—effluent and reactor off-gas undergo third-party monitoring, and internal audits occur year-round. Everything about manufacturing 2-Chlorobenzylamine, from solvent selection to final packaging, happens in one location, under one roof, and with full traceability.

    Choosing the Right Supplier—Why Origin Matters

    Over the last decade, the chemical supply chain for fine organics has grown tangled. Middlemen, blenders, and brokers often obscure product origin and handling practices. We hear from direct buying groups that tracking actual manufacturer identity can feel impossible in the current market. As a company producing 2-Chlorobenzylamine ourselves, we back every unit with records reaching back to raw feedstock delivery.

    Plants buying for API intermediates appreciate knowing there has been no repack or transfer along the way. There’s real value in visiting the site, reviewing SOPs, and seeing reactor trains in action. That visibility means less risk when regulatory reviews happen, or if root cause analysis becomes necessary. Each of our customers retains access to in-depth analytical documents, and we make a point of reviewing any change control or process modifications before shipment. Our relationships with clients are built on this openness, not just as transactions but as partnerships that extend across project lifespans.

    Examples from the Field—Collaborative Problem Solving

    One agricultural formulary approached us after struggles with off-color crop-protection actives. Together, we traced the problem to low-level bromide residues from their then-current supplier’s upstream chlorine sources. By redesigning the purification steps for our 2-Chlorobenzylamine process, we produced a low-halide variant, resulting in finished agrochemicals that finally passed visual inspection globally. No generic supplier could offer that bespoke solution so quickly, nor back it up with process logs.

    In another project, a start-up pharma manufacturer approached us with concerns about unwanted N-alkylation during drug intermediate synthesis. Working onsite with their chemists, we adjusted our lot’s pH and moisture parameters. Our modified amine provided a reliable conversion and reproducibility, slashing their troubleshooting cycle. These collaborations sharpen our understanding and keep our staff tuned to the actual needs of industrial chemists.

    The People and Equipment Behind the Product

    Every ton of 2-Chlorobenzylamine starts with process control staff who have fine-tuned these reactors for years. QC teams run round-the-clock sampling and verify standards against both external and internal benchmarks. Skilled technicians supervise solvent recovery—each drum reused is logged and its contents tested to ensure purity, reliability, and cost savings are not sacrificed for expediency.

    Investment in training and technology drives our manufacturing ethos. Chromatography, spectrometry, and automated water content checks run alongside older but proven methods for impurity tracking. We reach beyond paperwork quality by keeping open lines of communication between production, QC, and shipping.

    Adapting to Changing Markets and Regulations

    Stringent industrial regulations keep shifting, especially where pharmaceuticals and advanced agrochemicals are concerned. Maintaining compliance requires us to track updated guidelines, tweak process variables, and document everything. Auditors and regulators want to see these changes in real-time, not rewritten weeks later.

    Shipping documentation, packaging, and safety protocols must meet standards in all receiving jurisdictions. We coordinate closely with logistics partners to ensure 2-Chlorobenzylamine stays within specified temperature and physical protection during transit, even as that means extra cost and effort. We see ourselves not just as a supplier but as a compliance partner.

    Future Prospects: R&D and Market Trends

    Upstream producers of raw materials are shifting away from some older chlorination methods due to stricter safety controls. We prepare by regularly reviewing our supply agreements and maintaining backup sources to avoid shortages. Product purity that once defined high-quality aromatic amines has become baseline expectation. Rapid innovation in pharmaceutical and agricultural chemistry is encouraging us to experiment with new production routes, and we are piloting greener synthesis solutions, pursuing less hazardous solvents and reduced process emissions.

    Cutting-edge downstream applications often demand not only high purity and narrow impurity profiles but also environmental transparency regarding process waste and solvent recovery. Collaborating with research teams outside our own plant, we continue to adapt grades that better suit next-generation applications, such as green solvents or sophisticated catalytic pathways for selective syntheses. Our goal remains to not only keep up with market demands but to push the boundaries where possible—always drawing from our hands-on familiarity with the product and its real-life uses.

    Building a Future for Quality-Driven Supply

    Experience has taught us that paperwork can only take a product so far. Real performance shows up in reactors and makes itself known through higher product yields, shorter turnover times, and less plant downtime. Feedback from end users—both critical and complimentary—has shaped our plant configuration, product lineup, and even the culture within our production teams.

    We see 2-Chlorobenzylamine not just as a commodity, but as a staple in ongoing research and manufacturing. We back its quality with years of direct manufacturing experience, investments in best-in-class infrastructure, and the adaptability required to solve unexpected process hurdles. By staying close to our customers and our processes, we ensure every shipment stands up to the scrutiny demanded by high-stakes industries worldwide.

    From our manufacturing line to your plant, you receive far more than a drum of chemical—you get the results of persistent effort, attention to detail, and a commitment to doing things the right way, every day.