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4-Chlorobenzylamine

    • Product Name 4-Chlorobenzylamine
    • Alias p-Chlorobenzylamine
    • Einecs 219-459-2
    • 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

    747399

    Cas Number 104-83-6
    Molecular Formula C7H8ClN
    Molar Mass 141.6 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 232-234 °C
    Density 1.17 g/cm³
    Refractive Index 1.574
    Solubility In Water Slightly soluble
    Flash Point 110 °C
    Purity Typically ≥98%
    Smiles Clc1ccc(cc1)CN
    Synonyms p-Chlorobenzylamine; 4-Chlorophenylmethanamine
    Storage Temperature Store at 2-8 °C

    As an accredited 4-Chlorobenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 4-Chlorobenzylamine, 100g, is packaged in a sealed amber glass bottle with a tamper-evident cap and detailed hazard labeling.
    Shipping 4-Chlorobenzylamine is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. Classified as a hazardous chemical, it is transported according to relevant regulations (e.g., UN/IMDG/IATA), using appropriate labeling and documentation to ensure safety during transit. Personal protective equipment is recommended when handling during shipping and receipt.
    Storage 4-Chlorobenzylamine 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 and acids. Protect from moisture and direct sunlight. Clearly label the container and keep it in a designated chemical storage area with appropriate safety signage. Use secondary containment to prevent spills.
    Application of 4-Chlorobenzylamine

    Applications of 4-Chlorobenzylamine in Industrial Manufacturing

    We supply 4-Chlorobenzylamine for integration into multiple advanced industrial processes across pharmaceuticals, agrochemicals, dyes, and specialty chemical synthesis. Our material supports precise synthesis due to its controlled purity and consistent quality, ensuring reliable performance and compliance at large-scale production environments.

    1. Pharmaceutical Intermediate Manufacturing

    Pharmaceutical manufacturers select 4-Chlorobenzylamine for use as a key building block in active pharmaceutical ingredient (API) synthesis, particularly for antihypertensive, antipsychotic, and anti-infective drugs. This raw material enters alkylation and condensation reactions during multi-step synthesis, enabling production of complex benzyl-substituted compounds with controlled regioselectivity. Our 4-Chlorobenzylamine meets stringent quality parameters to minimize impurities, crucial for API downstream purification. Operators adjust the amine addition during batch or continuous reactor charging, maintaining close monitoring for process control and regulatory inspection traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) residue and impurity limits for starting materials
    • EU GMP for APIs, Part II
    • REACH Regulation (EC) No 1907/2006 (substance registration and use)

    Typical usage ratio

    • 0.5–1.2 molar equivalents per target API intermediate, adjusted based on stoichiometry and side-reaction profile; precise ratio guided by drug master file and process validation data

    Downstream process integration

    • Added in Stage 2 or 3 of API multi-step synthesis, usually after core ring construction, via closed transfer systems into jacketed reactors equipped for inert atmosphere and controlled agitation

    Final product types

    • Antihistamine (e.g., Loratadine intermediates)
    • Antipyschotic drugs (e.g., Chlorprothixene intermediates)
    • Antibacterial agents (benzylamine-based APIs)
    • Specialty pharma intermediates with chlorinated benzyl cores

    2. Agrochemical Synthesis

    In agrochemical production, 4-Chlorobenzylamine serves as a precursor for selective herbicides, fungicides, and plant growth regulators. The raw material enters amidation, urea formation, and carbamate reactions, producing active ingredients for pre- and post-emergence crop protection. Formulators require consistent amine content and minimal by-products to meet strict product labeling and residue control by agricultural authorities. Quality control programs routinely verify batch-to-batch reproducibility and compatibility with in-plant continuous flow reaction systems.

    Industry compliance standards

    • FAO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System for agrochemical manufacturing
    • EU Regulation (EC) No 1107/2009 (authorisation of plant protection products)
    • US EPA pesticide chemical residue tolerance requirements (40 CFR Part 180)

    Typical usage ratio

    • 23–41% by weight in technical-grade active ingredient syntheses, varied based on product registration dossier and calculated reaction yield

    Downstream process integration

    • Charged into synthesis reactors alongside isocyanates or carbamoyl chlorides for final stage condensation prior to crystallization or solvent extraction

    Final product types

    • Herbicide intermediates (e.g., substituted phenylureas)
    • Systemic fungicides using benzylamino scaffolds
    • Registered plant growth regulators with chlorinated phenylamines
    • Agrochemical formulation components for combination products

    3. Dye and Pigment Manufacture

    Producers of specialty dyes and colorants use 4-Chlorobenzylamine for modifying chromophore structures, imparting specific hue adjustments, and enhancing dye-fiber affinity. The amine introduces electron-donating properties, tailoring dye aggregation and stability for textile, leather, and ink applications. Production relies on precise addition during diazotization, coupling, or reductive alkylation steps. Stringent monitoring ensures controlled substitution while preventing excess formation of secondary amines or tars, critical for downstream application approval and end-user color fastness requirements.

    Industry compliance standards

    • OEKO-TEX Standard 100 (harmful substances in textiles)
    • EN 71-3:2019 (Safety of toys – migration of certain elements)
    • ZDHC Manufacturing Restricted Substances List (MRSL) for textile and leather processing
    • REACH Annex XVII (restriction of aromatic amines in consumer products)

    Typical usage ratio

    • 4–15% by weight as modifying amine depending on the dye class and target performance; ratio set by color strength and solubility demands

    Downstream process integration

    • Blended during controlled heating and stirring in diazo or azo dye synthesis stages, typically under acidic or neutral pH with precise reaction timing

    Final product types

    • Reactive dyes for cotton and cellulose fibers
    • Azo pigments for printing inks
    • Benzylamine-based mordant dyes for leather finishing
    • Color-fast textile auxiliaries containing halogenated amines

    4. Synthesis of Fine and Specialty Chemicals

    Chemical manufacturers employ 4-Chlorobenzylamine as a core intermediate for the preparation of fine chemicals, including custom synthons and complex molecular building blocks. The controlled nucleophilic reactivity allows for site-selective modifications and coupling in heterocycle construction, polymer additives, and advanced material monomers. In this context, material traceability and contaminant profile must comply with electronic industry and specialty market specifications. Ongoing process validation ensures reproducible performance in high-purity batches needed for fine chemical synthesis workflows.

    Industry compliance standards

    • ISO 9001:2015 for fine and specialty chemical manufacturing
    • GHS classification and labelling as per local regulation
    • RoHS Directive (2011/65/EU) for chemicals in electrical/electronic products where applicable
    • REACH substance registration for import and use verification

    Typical usage ratio

    • Varies from 1–30% by molar ratio depending on downstream molecule structure and complexity, strictly calculated per custom synthesis route

    Downstream process integration

    • Directly coupled or condensed with activated aromatic or aliphatic substrates in batch or continuous stirred tank reactors following in-line quality sampling

    Final product types

    • Specialty polymer crosslinkers containing halogenated benzyl groups
    • Photoresist intermediates for electronics
    • Liquid crystal material intermediates
    • Charge-control agents for toner and imaging applications
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    Certification & Compliance
    More Introduction

    Understanding the Role and Value of 4-Chlorobenzylamine in Modern Synthesis

    Hands-On Perspective: The Process Behind 4-Chlorobenzylamine Production

    As a manufacturer, the backbone of our work comes from direct engagement with raw materials, process controls, and countless test batches that form the final product: 4-Chlorobenzylamine. This organic intermediate finds steady demand in the pharmaceutical and fine chemical sectors, built on reliable chemistry and predictable results. In our facility, 4-Chlorobenzylamine primarily originates from 4-chlorotoluene using a stepwise synthesis involving either chlorination or reductive amination methods, which tones the final content of residual solvents and impurities. The technical model we provide regularly achieves purity above 99%, since failure to maintain strict process control could result in mixtures that delay downstream reactions or, worse, initiate unwanted side chemistry.

    Unlike products supplied through trading houses or general distributors, in-house production brings active selection of catalysts and solvents. The facility runs continuous purification cycles on the amine, all monitored with calibrated HPLC, GC, and NMR instrumentation freshly validated by our QA lab. This hands-on process sharpens the chemical profile batch by batch. Everyday vigilance, not just recipe, sets apart our 4-Chlorobenzylamine. For instance, regular supplier checks for starting materials cut the risk of mineral contamination and aromatic impurities, since a misstep here passes directly into final purity and color. Consistency starts with what comes through the warehouse door.

    Where 4-Chlorobenzylamine Stands in Organic Synthesis

    4-Chlorobenzylamine shows up as a critical link in a chain of chemical transformations. In our experience, customers leaning into pharmaceutical R&D want a primary amine that won’t muddle their synthesis with side reactions. The presence of a 4-chloro group gives this benzylic amine unique reactivity, allowing precise nucleophilic substitution or reductive amination routes. Some of our partners use it to build antihypertensive active ingredients, agrochemical scaffolds, and even special dyes for advanced photochemistry.

    Working directly with bench chemists, we learned that tolerance for trace halides, amine overalkylation, or oxidized impurities hovers near zero during critical coupling steps. If just one batch drifts from the norm, a new series of analytical headaches can emerge, including off-color, hygroscopic "stickiness," or unexplained TLC streaks during intermediate workups. Our practical response is hands-on: repeated drying, repurification, and even small-batch pilot checks before scaling to the next 500-kilo drum. Trust in this raw material doesn’t form through a certificate; it grows only through years of feedback and iteration.

    Specifications That Matter to the User—Not Just Numbers

    Most industry requests for 4-Chlorobenzylamine zero in on purity, water content, and byproduct levels. In practice, purity alone tells only part of the story. The crystalline form, solid state, and even the lot’s odor offer early signals of performance. From frequent feedback, we switched from flexible packaging to airtight HDPE liners, since tiny leaks or ambient moisture can alter both shelf life and purity. Moisture content, strictly controlled in-house to below 0.2%, determines actual reactivity—an amine with excess water blocks smooth condensation, clogs tubes, and ruins precious reagents. We monitor light transmittance and melting range, which help spot contamination invisible in standard HPLC or GCMS scans.

    Our scale-up team chased one recurring problem during warm months: batches exposed to prolonged heat occasionally yellowed or clumped. In that season, a cold-room dispatch gets triggered every time product heads for storage. This sort of detail doesn’t show up on generic data sheets, but it matters when building genuine reliability into the supply chain. Each specification comes from hard lessons and customer requests over the years, not from templated paperwork.

    What Sets 4-Chlorobenzylamine Apart from Similar Amines?

    4-Chlorobenzylamine sits alongside a family of benzylic amines—each fit for a different job. Value comes from knowing how it behaves compared to related molecules like benzylamine or other chlorinated amines. The para-chloro group isn’t just cosmetic; it shifts electron density, which modulates reactivity in acylation or reductive alkylation. Some labs report higher selectivity in C-N bond formation, and we saw that our 4-chlorinated amine resists oxidation under tested oxidative conditions better than the plain benzyl version.

    Comparing with ortho- or meta-substituted isomers, the 4-position chlorination provides less steric interference and cleaner reaction kinetics during N-protection or when forming active pharmaceutical intermediates. Other benzylic amines require more purification steps post-reaction to clear unexpected color or tar. We understand these details through hundreds of scale-up batches and dialogue with R&D chemists, not just by reading published literature. Our own process confirms that fewer byproducts and manageable volatility keep the workup more consistent. In our workflow, the 4-chloro compound purifies faster on silica columns and evaporates with less residue, giving direct practical handling benefit.

    Beyond composition, physical form differences matter in the shop. Our product remains free-flowing at a wider range of temperatures compared with several ortho- or di-chlorinated relatives. Packing, handling, and transfer systems show lower static build-up, so there’s less powder loss and easier weighing on production floors. These are details easy to overlook until a batch needs to be reworked or an operator flags buildup in the feed chute. The right physical characteristics come from repeated feedback, not a one-size-fits-all approach.

    Requirements for Downstream Synthesis: What Chemists Value

    Our most frequent users work at the intersection of scale and precision. Whether developing a new beta-blocker, a selective herbicide, or an advanced photoinitiator, repeatability matters more than theoretical purity claims. The para-chloro-substituted amine behaves predictably in multi-step syntheses, and feedback from pharmaceutical clients points to time saved on downstream chromatographic separations.

    We often hear that, while other amines drag through post-reaction workups or require repeated crystallization, 4-Chlorobenzylamine gives a cleaner break between organic and aqueous phases. This means less time spent drying extracts or chasing lost yield. In custom projects, one medicinal chemistry group cited our tighter impurity profile as a reason for faster initial lead screening. No roundabout claims—just grounded observations from colleagues tackling new synthetic targets every week.

    Handling ease matters just as much as reactivity. Bench chemists appreciate the relatively mild odor and limited toxicity, so regular use in open labs comes with fewer concerns and less need for additional PPE. Shipping and storage demand less oversight compared with more volatile or moisture-sensitive amines. Our technical staff respond directly to user questions—every lot comes with a full trace file, chromatograms, and a straightforward water content check, since small surprises in one batch can set back whole project schedules.

    Why Manufacturing Source Matters—Confidence in Every Drum

    With increased regulatory scrutiny, traceability and audit-readiness now count as much as traditional clean-room handling. Supplying directly from the manufacturing line, our quality systems track each batch from raw material through the reactor and all the way into the final container. Real-time process monitoring—GC scans, NMR checks, and water analysis—catches trends earlier than later. A misplaced or uncontrolled temperature fluctuation in the reduction step can ripple through the batch and derail planned timelines. The responsibility for fixing root-cause incidents sits with the producer, not the trader, and ownership of the challenges results in faster, more reliable corrective action.

    Audit teams visiting our facility comment on our paper trail and strict segregation of process streams, especially in the chlorination area. On-site analysts check that every drum matches the lab’s outgoing sample, not just a randomly selected QC tube. Any outlier result triggers a stop and full review; we learned from hard experience that guessing through a borderline QC report exposes customers to much greater risk than pulling and remaking a batch. Our goal remains straightforward: sending out 4-Chlorobenzylamine we would want to receive at our own bench.

    Tracing Safety and Environmental Responsibility in Synthesis

    The chemistry behind 4-Chlorobenzylamine creates unavoidable challenges for worker safety and waste management. The chloro group introduces risks in handling, so our teams undergo routine retraining on safe charging, venting, and emergency response. All ammonia-related synthesis happens under tight negative airflow with multiple scrubber backups, since small leaks risk onsite exposure or offsite odor complaints.

    Process wastewater undergoes onsite neutralization and chloramine separation before release. Our solid waste containers stay locked and tracked until confirmed inert, and annual site reviews by environmental auditors drive further upgrades. Recent investments in catalyst recycling and closed-loop batch filtration reduced non-degradable byproduct levels. As chemical manufacturers, shifting from generic compliance toward proactive risk reduction marks the difference in winning the trust of both local communities and globally compliance-oriented customers.

    Supply Security and Market Adaptation

    Market cycles and supply chain interruptions affect specialty chemicals as much as bulk commodities. The 4-Chlorobenzylamine stream depends on both upstream chlorotoluene supply and global logistics for solvents and catalysts. We insulate downstream teams from these shocks by keeping a rolling inventory buffer and qualifying backup sources for key raw materials. Routing finished material through secured, climate-controlled warehouses prevents seasonal spoilage and off-spec drift—lessons learned directly from some hard-won logistics battles in the past few years.

    Customers look for manufacturers who can stabilize deliveries even through raw material crunches or energy outages. We keep an active file of real-time inventory, forward contracts, and alternate synthesis plans, sharing disruption alerts and realistic lead times. One example came during a regional port slowdown last year. Our team ramped up local synthesis, pulled from spot solvent reserves, and kept supply flowing with minimal delivery slot changes. That event shaped our new protocols for minimum on-site storage levels and backup supplier specifications. Staying nimble through direct production beats over-promised, undersupplied offers that fall through at the last minute.

    Innovating for the Needs of Next-Generation Chemistry

    Each year, new applications and tougher technical demands push us to review the fundamentals. In recent collaborations, R&D groups testing photoinitiated processes or rare transition metal couplings leaned on the electron-withdrawing effect of the chloro group in our 4-Chlorobenzylamine. Even incremental shifts in isotopic purity or trace halide content can dictate success or failure in such advanced applications.

    Feedback prompted us to invest in new drying and handling suites. Trial batches under inert gas, sealed transfer lines, and tighter online moisture sensors produced more reactive amine for critical use. We record and feed this data back into our internal quality system, updating process parameters as soon as real differences (not just theoretical ones) arise in direct user feedback. This responsive approach fosters deeper partnerships—chemists on both sides speak the same technical language and quickly spot new bottlenecks.

    Next Steps for Users Seeking Responsible Supply

    Partners sourcing from a grounded manufacturing origin gain more than product—they get a history of analytical process data, technical troubleshooting access, and practical advice from operators who’ve cleaned stuck reactors, diagnosed color instability, and talked real-time with bench users. Our production line supports both kilo-lab R&D users and tonne-scale process plants. The goal remains steady: deliver 4-Chlorobenzylamine with real performance, not just a list of specifications.

    Questions sometimes cross a surprising technical range—from scale-up kinetics for a new active pharmaceutical ingredient to waste stream disposal for multi-tonne campaigns. We welcome direct discussion about packaging, delivery format, or integration into automated systems, recognizing that trade partners rarely offer tailored details. This open approach shortens problem-solving timelines and adapts readily to shifts in regulatory expectations or new synthesis requirements.

    Our commitment stands grounded in direct experience: straightforward handling, robust process transparency, and ongoing dialogue with the chemists shaping tomorrow’s molecules. We remain ready to discuss, advise, and deliver practical solutions for shifting demands—building quality batch by batch, feedbacks addressed as they arise, and every kilogram coming direct from our reactor floor. That’s the difference hands-on chemical manufacturing brings to 4-Chlorobenzylamine supply, year in and year out.