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2,5-Dichlorobenzylamine

    • Product Name 2,5-Dichlorobenzylamine
    • Alias Benzenemethanamine, 2,5-dichloro-
    • Einecs 216-927-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    649986

    Cas Number 89-98-5
    Molecular Formula C7H7Cl2N
    Molecular Weight 176.05 g/mol
    Appearance White to off-white solid
    Melting Point 72-74°C
    Boiling Point 282°C
    Density 1.3 g/cm³
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Synonyms 2,5-DCBA; Benzylamine, 2,5-dichloro-
    Iupac Name 2,5-dichlorobenzylamine
    Smiles C1=C(C=CC(=C1Cl)Cl)CN

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

    Packing & Storage
    Packing 250g of 2,5-Dichlorobenzylamine is supplied in a sealed, amber glass bottle with a screw cap and hazard labeling.
    Shipping 2,5-Dichlorobenzylamine is typically shipped in tightly sealed containers made of compatible materials, safeguarded from moisture and sunlight. It should be labelled according to hazardous material regulations and handled by trained personnel. Transport must comply with local, national, and international regulations for hazardous chemicals to ensure safety and prevent environmental contamination.
    Storage 2,5-Dichlorobenzylamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible materials such as strong oxidizing agents and acids. Avoid exposure to heat, moisture, and direct sunlight. Properly label the container, and ensure storage is in accordance with local regulations and safety protocols to prevent leaks or environmental contamination.
    Application of 2,5-Dichlorobenzylamine

    Applications of 2,5-Dichlorobenzylamine in Industrial Manufacturing

    As a direct manufacturer of 2,5-dichlorobenzylamine, we support established global industries with consistent supply for advanced synthesis. Below, we detail its principal application segments, highlighting compliance requirements, formulation experience, process integration points, and specific downstream product categories.

    1. Pharmaceutical Intermediate for Psychiatric Medication Synthesis

    Pharmaceutical manufacturers rely on this amine as an essential intermediate in the multi-step synthesis of select active pharmaceutical ingredients (APIs), especially within the tricyclic antidepressant and atypical antipsychotic classes. The compound’s unique dichloro substitution enables specific site-directed substitutions and amide coupling steps, optimizing downstream pharmacokinetics and minimizing byproduct formation. We supply to partners with established continuous synthesis lines and batch reactors designed for high-purity API development under regulatory controls.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) compliance by US FDA (21 CFR Parts 210/211, ICH Q7A)
    • European Pharmacopoeia for qualifying intermediates (Ph. Eur.)
    • China National Medical Products Administration (NMPA) registration for intermediates
    • ICH Q11: Development and Manufacture of Drug Substances

    Typical usage ratio

    • Forms 0.05–0.2 molar equivalents in multi-step syntheses, based on target API yield and stoichiometric conversion rates. Actual charge adjusted to control impurity profile under process validation protocols.

    Downstream process integration

    • Introduced after halogen–amine exchange in the early or mid-stage synthesis, prior to final cyclization or coupling. Close coordination with solvent addition, temperature ramping, and post-reaction workup are standard.

    Final product types

    • Benzylamine-derived tricyclic antidepressant APIs
    • Substituted phenothiazine antipsychotic APIs
    • Novel CNS therapeutic candidate APIs
    • Research-use only (RUO) pharmaceutical intermediates

    2. Agrochemical Building Block for Fungicide Synthesis

    Production teams in major crop protection chemical plants use this compound as an amine source for the construction of benzylamine-based fungicide molecules. Its electron-withdrawing dichloro groups increase metabolic stability and environmental persistence, making it a favored core for manufacturing modern broad-spectrum agricultural fungicides that meet regional residue and safety requirements.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (GLP compliant synthesis)
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) standards
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • China GB/T 1600 and 1834 quality standards for pesticide intermediates

    Typical usage ratio

    • 1.0–1.5 molar equivalents relative to primary aryl halide precursors; charge ratio tailored to specific fungicide backbone and to maximize product yield during batch or continuous flow synthesis.

    Downstream process integration

    • Amine addition performed during nucleophilic aromatic substitution or amide bond formation steps, preceding sulfonation or protective group removal, under rigorous in-process monitoring for trace impurity removal.

    Final product types

    • Chlorinated benzylamine-based fungicides (such as formulations for rice, wheat, and fruit crops)
    • Intermediate compounds for combination fungicide platforms
    • Active ingredients for crop seed treatments
    • Bulk active technical concentrates for downstream formulators

    3. Specialty Polymer Monomer for Anti-Microbial Materials

    Polymer manufacturers exploit the reactive amine functionality and dichloro groups to create specialty monomers for antimicrobial additive polymers. Incorporation into condensation polymer chains enhances final polymer resistance to fungal and bacterial colonization, which is critical in healthcare facility surfaces, medical devices, and specialty coatings demanding certified bio-barrier properties.

    Industry compliance standards

    • ISO 22196: Measurement of Antibacterial Activity on Plastics
    • US EPA Antimicrobial Testing Program requirements for polymeric materials
    • EU REACH registration for monomer and polymer safety
    • USP Class VI biocompatibility assessment (when targeted for medical-grade polymers)

    Typical usage ratio

    • Monomer content typically 1–5 mol% of gross reactive monomer pool, adjusted for required antimicrobial performance and physical resin properties.

    Downstream process integration

    • Amine monomer charged at the start of solution or bulk polycondensation, monitored for complete reaction and uniform incorporation via in-line spectroscopy or wet-chemical titration.

    Final product types

    • Antimicrobial polyamide and polyurethane resins
    • Hospital-grade polymeric coatings
    • Extruded films for food-contact use (EU/FDA regulated)
    • Medical equipment housings and facings

    4. Intermediate in Dye and Pigment Synthesis for Industrial Inks

    Industrial dye manufacturers use the dichlorinated benzylamine as a key intermediate for synthesizing specific classes of azo and anthraquinone pigments that demonstrate high chemical resistance and lightfastness. The compound’s substitution pattern improves pigment stability in solvent-based and waterborne ink formulations targeted at automotive, packaging, and specialty printing sectors.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Responsible Care Program
    • EN 71-3 Safety of Toys (for pigments in toy and packaging inks)
    • ISO 2846-1 for colorant conformity in printing inks
    • China GB 9685: Hygienic standards for use of additives in food containers and packaging materials

    Typical usage ratio

    • 0.1–0.5 molar equivalents per main chromophore precursor; quantity tuned to hue intensity and to meet customer-specific UV or chemical resistance targets.

    Downstream process integration

    • Entered in the amination or coupling stage of pigment synthesis, preceding purification by crystallization or column chromatography. In-line HPLC and spectrophotometric monitoring ensure correct endpoint and purity profile.

    Final product types

    • High-durability pigments for automotive paints
    • Solvent-based and aqueous industrial printing inks
    • Food packaging inkjet and flexographic inks
    • Stain- and fade-resistant architectural coatings
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    Certification & Compliance
    More Introduction

    2,5-Dichlorobenzylamine: Crafting Consistency and Reliability in Each Batch

    Precision Comes From Experience With 2,5-Dichlorobenzylamine

    Every kilogram of 2,5-Dichlorobenzylamine coming off our reactors reflects a deep understanding of the chemistry and the practical demands of those who rely on this raw material. In our line of work, 2,5-Dichlorobenzylamine isn’t a forgettable intermediate; it’s an anchor for diverse reactions, structural building in pharmaceutical and agrochemical fields, and in bringing about selectivity when exact substitution is vital.

    We approach its manufacture with an awareness of the molecule’s sensitives. The dichlorination at the 2 and 5 positions changes more than just the N atom’s basicity or solubility in polar solvents. It creates steric and electronic effects that make it an essential intermediate when chemists need substitutions only monochlorinated amines can’t provide. Our technicians have tuned reaction times, temperatures, and purification steps over years to safeguard against the subtle side products that can trip up downstream reactions. It’s not unusual for our lab to run a series of micro-scale checks, rifling through impurities at the ppm level using both HPLC and GC, before releasing full lots to the next stage.

    The Distinction Behind Our Specification and Testing

    We routinely offer 2,5-Dichlorobenzylamine with a purity of 99% and above. This isn’t simply a number on a certificate of analysis, but the outcome of tailored solvent systems in crystallization, and an unwillingness to settle for “good enough” in drying. We monitor residual solvents because we know how they might influence next-step reactivity or toxicity profiles in pharmaceutical applications. Particle size—important for certain continuous feed systems—is tracked in every batch, not simply as a checkbox in documentation, but to keep performance consistent for customers running automated addition or in-process blending.

    The product’s melting range, color, and moisture content are all scrutinized using both traditional and instrumental analysis, such as NMR and FTIR, ensuring the actual physical sample matches reference standards. For clients using 2,5-Dichlorobenzylamine as an intermediate in active ingredient synthesis or as a blocking group precursor, we’re available to discuss analytical protocols in depth—not just sending a spectrograph but sharing our full sample prep method. Taking ownership for each variable, from trace halide levels to packing integrity, creates reliability batch after batch.

    Where 2,5-Dichlorobenzylamine Matters Most

    For synthetic chemists charting out new routes or scaling up already published reactions, the difference between theory and shop floor practice usually emerges. 2,5-Dichlorobenzylamine isn’t simply swapped for other chlorinated amines. Its double chloro-substituent forms a unique platform for introducing further functional groups under controlled, predictable conditions, which is tough with other benzylamines. That’s why it’s picked in heterocycle synthesis in pharma intermediates, or in constructing bioactive molecules where regioselectivity affects patentability and safety.

    Our product supports scale-up processes where traditional hazards, like exothermic handling during amination or unexpected gas evolution, translate to real-world plant risks. By tightly controlling mother liquor composition, temperature ramp rates, and filtration methods, we minimize such complications—not theoretically, but in day-to-day factory runs. This prevents plant stoppages and lost yield, which means our own schedules remain reliable. Behind each bottle lies decades spent learning exactly where an emulsion might form and how quickly a seed crystal will set off precipitation.

    Advantages Over Closely Related Substances

    The major comparison usually comes up with 2,4- and 3,5-dichlorobenzylamines or their mono-substituted siblings. Our own plant has produced many of these on contract, and we’ve seen how small shifts in the chlorine placement dramatically alter boiling points, solubilities, and downstream intermediate formation. For instance, 2,5-Dichlorobenzylamine resists unexpected side-reactions better in oxidative steps, thanks to the stabilization conferred by its particular substitution pattern. During hydrogenation or alkylation downstream, operators have reported fewer byproduct peaks in their final LC-MS analyses—something that translates to lower purification costs and steadier throughput for the end-user.

    Switching from a mono-chlorinated derivative to our 2,5 is usually driven by need, not by price. A few customers, having run into bottlenecks on scale, reported that using 2,5-Dichlorobenzylamine eliminated formation of certain chloro-coupled tars and intractable colored side products. Some medicinal chemists rely on our material to get reproducible yields on key lactam-cyclizations, or to avoid regulatory headaches associated with unidentified impurities. Here in the plant, we’ve participated in troubleshooting these exact issues, working with clients’ teams to confirm root causes and then shipping targeted test lots to confirm the fix in practice.

    Usage in Synthesis, at Lab and Industrial Scale

    At the bench, it’s often handled by synthetic teams preparing nitrogen-containing frameworks—pushing towards heterocycles that show antiviral, antibacterial, or herbicidal activity. Its two electron-withdrawing chloro groups set the scene for controlled nucleophilic aromatic substitution or for anchoring groups during ring construction. You rarely find it left out in the open: it enters flasks with care, weighed out for selective incorporation where over-reactivity or poor specificity from less substituted amines wouldn’t pass muster.

    For commercial-scale users, we’ve shipped multi-metric-ton orders to fine chemical, specialty pharma, and agro intermediates producers. Our QA team’s focus on reproducible quality has made us a go-to source when unexpected variability hits other supply chains. Whether it’s reacting with isocyanates, forming urea linkages, or coupling with acid chlorides, our 2,5-Dichlorobenzylamine’s purity and stability trim hours off downstream clean-up. Operational feedback from blenders, packagers, and maintenance techs comes directly to our production team. This feedback loop is why we planned upgrades to our dryer and solvent recovery systems last year—practical, operator-driven improvement rather than simply following a trend.

    Our product’s chemical profile makes it less prone to auto-oxidation during longer storage periods. This is no small thing when pallets head across continental or maritime shipping lanes. To minimize hydrolysis or exposure to ambient moisture, we pack each lot only after verifying dew point conditions in the warehouse, and each drum comes flush with minimal head-space air, preserving the sample for up to a year. Customers with just-in-time supply practices value a stable reagent that doesn’t suddenly drift out of spec a few months on the shelf.

    Technical and Hands-On Support: Built On Dialogue, Not Templates

    Having spent decades producing chlorinated aromatic amines, we know project challenges don’t always show up on the batch record. We field calls and lab visits from technical buyers, R&D chemists, and even plant operators troubleshooting mixing or handling on-site. Our staff doesn’t just direct people to read a spec sheet—they compare runs, help with analytical work-ups, and suggest batch pharmacy tweaks based on raw data from our own trial runs.

    It’s not rare for buyers to ask for custom particle size ranges. We set up small-scale test mills, measure particles before and after, and run comparative dissolution trials. If a customer’s process requires 2,5-Dichlorobenzylamine at a nonstandard purity spec, the team adjusts filtration, crystallization, and solvent stripping to match. These projects run in real partnership; every special spec becomes part of our in-plant knowledge base, refining our own manufacturing for future orders.

    Many users find themselves encountering lingering bitterness in their final products—a legacy from residual solvent or halide traces in intermediates. We built additional monitoring steps using ion chromatography, not as a checkbox, but in direct response to discovering that conventional wash cycles weren’t enough for certain downstream applications. By fixing these practical points, we help users avoid expensive rework and guarantee smoother compliance audits.

    Environmental and Regulatory Awareness

    We’ve seen the impact of tightening chemical regulations, especially where chlorinated aromatics are concerned. For us, compliance isn’t an add-on but embedded in plant upgrades and daily practice. Our extraction and waste handling process recycles solvents wherever feasible, reducing halogenated waste output year by year. All emissions—vapor, liquid, or solid—are tracked with the same meticulousness as our final product quality.

    Clients sometimes ask about the regulatory backdrop for 2,5-Dichlorobenzylamine vis-à-vis other related amines. It’s true the dichloro pattern brings a different risk profile compared to mono-chloros or the unchlorinated base structure. We keep current with Reach, TSCA, and regional Asian and EU guidelines, updating technical files as regulations shift. Being directly in touch with downstream users, we keep our documentation ready for quick access in regulatory submissions or safety dossiers, not simply archiving data on a server.

    Almost every audit from a pharmaceutical major or global agro brand brings up persistent organic pollutants or trace contamination risks. We share not just making docs, but full traceability data from raw inbound receipt through outbound batch. This is how we maintain trust with repeat clients, showing a willingness to submit not just data but also samples for third-party verification—because our business survives or dies by real trust on both sides.

    Practical Solutions for User Challenges

    2,5-Dichlorobenzylamine seldom raises alarms for seasoned chemists, but we have seen the surprises: Clogging of filters due to unexpected crystallinity, foaming during exothermic neutralizations, even odor complaints linked to trace volatiles. To address these head-on, we run batch-specific pre-dispatch tests depending on season, shipping route, or even anticipated warehouse humidity at client sites. The production team regularly joins remote troubleshooting sessions, compares physical property data, and—where necessary—assembles custom test kits that customers can use to assess batch-specific factors before full-scale integration.

    Large site operators, juggling multiple synthetic routes, sometimes find solubility and compatibility quirks that aren’t flagged in conventional literature. We offer pilot-batch samples at scale for direct compatibility trials, sharing our own learning on solvent exchange, dissolution, and filtration times. Downturns in process throughput or unexpected discoloration in finished goods prompt a cycle of investigation and adjustment—never simply shifting the responsibility. Our plant recognizes the economic stress production halts cause for our partners, so we bring our own QA and R&D together to guide solution-driven trials on both sides.

    Occasionally, we field requests for high-purity, ultra-trace certified lots for human pharma or crop protection actives. These aren’t routine orders—they require extra validation for things like specific enantiomeric ratios or undetectable secondary amines. Our lab dedicates time to custom runs, adjusting steps, and willingly reruns quality assays, even when it slows throughput, because we understand an unreliable intermediate is worse than a delayed one.

    Looking Ahead: Evolution Through Reliable Craftmanship

    Continuous improvement remains our push. Having manufactured 2,5-Dichlorobenzylamine since before online catalogs made raw materials look like commodities, we know that genuine reliability earns loyalty. Every upgrade—in drying, packaging, analytical testing—comes as response to feedback or process learning. We plan for more solvent recycling, further reductions in water and energy use, and enhancement of our impurity profiling, knowing these directly benefit users.

    We watch for shifting patterns in demand, requests for greener synthesis, and new end applications in regulated industries. Our team keeps close ties with university researchers and contract manufacturers, sharing knowledge and co-developing improvements. This isn’t simply selling a molecule, but a full partnership to solve real-world problems where purity, reliability, and safety matter at scale.

    Our Commitment: More Than A Product

    2,5-Dichlorobenzylamine, manufactured directly in our facilities, is the output of sustained learning, attention to detail, and ongoing partnership with those who use it every day. Each ton carries the weight of regulatory compliance, technical support, and process know-how accumulated over decades. Consistent, timely, and predictable: this is what our clients expect, and what we deliver—not in abstraction but in each drum, every batch, and every collaborative discussion for as long as demand requires.