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4-Chlorobenzyl Chloride

    • Product Name 4-Chlorobenzyl Chloride
    • Alias p-Chlorobenzyl chloride
    • Einecs 202-707-5
    • 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

    514218

    Cas Number 104-83-6
    Molecular Formula C7H6Cl2
    Molecular Weight 161.03
    Appearance Colorless to pale yellow liquid
    Boiling Point 213-215°C
    Melting Point -14°C
    Density 1.244 g/cm3
    Refractive Index 1.565
    Flash Point 92°C
    Solubility In Water Insoluble
    Synonyms p-Chlorobenzyl chloride, 1-(Chloromethyl)-4-chlorobenzene
    Purity Typically ≥98%
    Odor Pungent
    Storage Temperature Store at 2-8°C
    Ec Number 203-241-6

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

    Packing & Storage
    Packing 500g of 4-Chlorobenzyl Chloride is supplied in a sealed amber glass bottle with safety labeling and a tamper-evident cap.
    Shipping 4-Chlorobenzyl Chloride is shipped as a hazardous chemical under UN 3276. It should be transported in tightly sealed, corrosion-resistant containers, away from moisture and incompatible substances. Proper hazard labeling, documentation, and protective packaging are required to comply with local and international regulations. Handle with care to prevent leaks or exposure.
    Storage 4-Chlorobenzyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and direct sunlight. Keep it separated from oxidizing agents, strong bases, and strong acids. Use suitable corrosion-resistant containers and avoid all contact with moisture, as the compound reacts with water. Proper labeling and access restriction are recommended.
    Application of 4-Chlorobenzyl Chloride

    Applications of 4-Chlorobenzyl Chloride in Industrial Manufacturing

    4-Chlorobenzyl chloride serves as a key intermediate in several established manufacturing sectors, providing precise reactivity and stable integration within advanced syntheses. As a direct manufacturer, we ensure consistent supply, stringent quality control, and documented traceability in every shipment, supporting accurate formulations and regulatory compliance in global downstream operations. The following application scenarios illustrate real-world industrial adoption of 4-chlorobenzyl chloride, each with well-defined compliance expectations, process parameters, and finished goods.

    1. Pharmaceutical Intermediates: Synthesis of Antihypertensive APIs

    Downstream pharmaceutical manufacturers incorporate 4-chlorobenzyl chloride primarily for N-alkylation or acylation steps in the multi-stage synthesis of certain antihypertensive active pharmaceutical ingredients, such as AT1 receptor blockers. The controlled electrophilic substitution reactivity enables targeted side-chain modifications under GMP plant conditions. Typically, developers optimize batch input loads according to specific reaction yields, process safety limits, and required product purity for downstream isolation and purification under validated protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • EU GMP Annex 8: Sampling of Starting and Packaging Materials
    • 21 CFR Part 211 (U.S. cGMP for finished pharmaceuticals)
    • Ph. Eur., USP, or JP pharmacopoeial monograph (depending on the API)

    Typical usage ratio

    • 0.8 to 1.2 molar equivalents per reaction batch, fine-tuned to the stoichiometry of the target synthetic step; adjusted for reaction conversion efficiency and impurity control

    Downstream process integration

    • Added during the intermediate functionalization step, usually by controlled addition under anhydrous conditions to avoid hydrolysis
    • Isolated intermediates then proceed through subsequent cyclization, reduction, or protection group deprotection as part of the API route
    • Column chromatography or crystallization applied post-reaction for intermediate purification

    Final product types

    • Active pharmaceutical ingredient bulk powders (e.g., certain sartans)
    • Synthesized drug intermediates for further downstream transformations
    • Final medicinal tablets and capsules formulated from purified API

    2. Agrochemical Synthesis: Herbicide Active Ingredient Manufacturing

    Agrochemical formulators employ 4-chlorobenzyl chloride as a crucial alkylating intermediate for creating specific benzyl-substituted heterocycles widely used in herbicidal compounds. The high selectivity and reliable chlorination profile result in structurally uniform active ingredients required for large-volume field application formulations. Tight mass balance control ensures maximal use of charged intermediates while maintaining effluent compliance within regulated agrochemical plants.

    Industry compliance standards

    • FAO/WHO Main Specifications for Agrochemical Technical Materials
    • ISO 9001:2015 for process quality management in agrochemical plants
    • REACH (EC) No 1907/2006 obligations for chemical registration in the EU
    • OECD Principles of Good Laboratory Practice (GLP) for R&D labs

    Typical usage ratio

    • 1.05 to 1.2 equivalents per target chemical entity, with precise adjustment based on target herbicide yield, side reaction minimization, and environmental discharge permits

    Downstream process integration

    • Reacted during early-stage alkylation of heterocyclic scaffolds under base-catalyzed conditions
    • Product mixture typically neutralized and washed before isolated via phase separation or distillation
    • Further synthetic modifications occur on alkylated core to achieve final herbicidal properties

    Final product types

    • Technical-grade herbicide actives (e.g., benzyl-substituted pyridines or triazoles)
    • Mother liquors for scale-up to formulated suspension and emulsifiable concentrate products
    • Field-ready commercial pre-mix solutions

    3. Dye and Pigment Precursor Formulation

    Industrial dye and pigment manufacturers integrate 4-chlorobenzyl chloride as a foundational benzylating reagent for creating specialty chlorinated benzenes used in pigment dispersions and persistent textile dyes. The compound's stability in concentrated acid and controlled chlorination behavior enable production of intermediates with needed colorfastness, UV endurance, and solubility tailored to textile or polymer applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for restricted dye component safety)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • EN 71-3 Child Toy Safety (for pigment applications in toys)
    • GHS/CLP labeling rules for workplace chemical safety

    Typical usage ratio

    • 8–15% by total batch mass for pigment syntheses; adjusted for product line concentration requirements and reactive loss to side products

    Downstream process integration

    • Added during nucleophilic substitution in mono- or di-chlorinated benzene syntheses
    • Blended with additional modifiers to create water-dispersible pigment pastes or powder dyes
    • Undergoes filtration and stability testing before downstream blending into concentrates

    Final product types

    • Azo and phthalocyanine pigment powders
    • Dispersed textile dye concentrates
    • Masterbatch colorant granules for plastics and fibers

    4. Perfume and Aroma Chemical Manufacture

    Within the aroma and perfumery sector, manufacturers process 4-chlorobenzyl chloride as an alkyl donor for constructing key aromatic building blocks with controlled halogen profile. These intermediates impart unique olfactory notes for high-value blends and must meet allergen labelling and residue specifications validated through rigorous QC testing. Selection of charge ratio and quenching steps drive both fragrance intensity and toxicological acceptance in luxury-grade formulations.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • EU Cosmetics Regulation EC No 1223/2009 (residual impurity constraints)
    • ISO 9235:2013 (Aromatic Natural Raw Materials)
    • ISO 16128 (Guidelines on fragrance ingredient origin for natural and organic claims)

    Typical usage ratio

    • 2–4% of reactant blend for typical aroma intermediates; reduced for lighter top-note building blocks or increased for base-note fixatives as determined by perfumer formulation

    Downstream process integration

    • Introduced during Friedel–Crafts alkylation steps to modify ring structure of precursor alcohols or phenols
    • Intermediate then submitted to distillation and rectification to meet residual solvent thresholds
    • Blended post-reaction in aroma matrices for stability and sensory testing

    Final product types

    • Synthetic aromatic bases for fine fragrance manufacturing
    • Functional perfumes for detergents and personal care
    • Flavoring intermediates for food-contact approved fragrances (subject to further conversion)
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    Certification & Compliance
    More Introduction

    4-Chlorobenzyl Chloride: Product Introduction and Manufacturer’s Perspective

    Practical Insights from Production to Application

    Our team has dedicated years to refining the manufacturing process of 4-chlorobenzyl chloride, recognizing its solid demand in chemical synthesis, pharmaceuticals, and specialty materials. This compound, identified with the CAS number 104-83-6, consistently attracts interest from professionals who value purity, precise physical parameters, and efficiency in their operations.

    Chemists seek out 4-chlorobenzyl chloride for its reliable performance as an alkylating agent. We maintain strict controls during each production step to manage both the chlorination and benzylic chloride functionalities. The manufacturing flow focuses on minimizing impurities—every batch emerges with a typical purity of 99% or above, evidenced by straightforward analytical checks on site. Such attention to process detail means reaction yields, when using our product, tend to be higher and downstream purification simpler.

    Production Challenges and How We Solve Them

    Industrial synthesis of 4-chlorobenzyl chloride requires not just the right starting materials but also careful engineering. Our lines are fitted with corrosion-resistant reactors because the hydrochloric acid generated during reaction aggressively attacks ordinary steel. Between temperature control and continuous phase separation, the process leaves little room for error or short-cuts.

    Many new entrants to the field underestimate the importance of tight control. Even a modest fluctuation in temperature or chlorine delivery can jump-start unwanted side reactions. By running pilot-scale batches, we fine-tune conditions before scaling up. Each plant operator undergoes specialized training to recognize shifts in the chemistry in real time—human oversight is a factor automation never fully replaces.

    Waste management sits at the center of any chlorination chemistry. Stringent in-house procedures guarantee that off-gas scrubbers and solvent recovery systems function at peak efficiency, which aligns not just with local regulatory standards but with our experience of what supports reliable long-term manufacturing. We treat spent wash lines with active carbon and neutralize acidic residues before discharge. Our plant reports incident rates for these units that markedly beat the regional average, giving us confidence that environmental risks remain contained.

    Physical Properties and In-Process Control

    The compound crystallizes at room temperature in areas of the plant with good climate control. As a colorless to pale yellow liquid below its freezing point, 4-chlorobenzyl chloride presents a manageable viscosity, essential for pumping and metering. We measure density at 1.2 g/cm3 and boiling range between 210 and 213°C at atmospheric pressure—all verified with each production run.

    Chlorinated aromatic substances, if produced to insufficient quality, reveal themselves fast. Even a slight brownish tinge signals potential contamination with polychlorinated byproducts, usually the result of over-chlorination. That’s why our operators check each sample directly from the reactor before permitting transfer to holding tanks.

    Purity and Assay: More Than a Number

    End-users commonly demand specifications that state an assay value—often 99% or above by GC. What those specs do not always show is the unseen detail: residual solvents, trace unreacted benzyl chloride, or side products that can poison catalysts or block synthetic routes downstream. Our team screens every batch for those byproducts with a focus that stems from routine customer feedback. A single customer returning a shipment, even if rare, creates costs for all parties and delays schedules that every partner in the chain depends on.

    Storing the material under nitrogen blankets and in colorless glass ensures shelf life extends beyond published expectations. We prefer drums with lined interiors to prevent contamination from leaching metals—a lesson learned from crude storage over a decade ago, when a single out-of-spec shipment pushed us to redesign our container protocols from scratch.

    Comparisons to Other Chlorinated Benzyl Derivatives

    4-chlorobenzyl chloride stands apart from other isomers and derivatives, such as 2-chlorobenzyl chloride or benzyl chloride itself. The location of the chlorine atom on the aromatic ring impacts reactivity, with our product favored for nucleophilic substitution reactions by formulators of pharmaceuticals and advanced agrochemicals. We have seen research groups try to substitute with ortho- or meta-analogs, only to report altered reaction rates or troublesome impurity profiles in scale-up.

    Not all benzylic chlorides are interchangeable. Benzyl chloride, lacking a ring chloro-substituent, reacts more readily but also invites unwanted side reactions in applications where selectivity governs product quality. In contrast, 4-chlorobenzyl chloride delivers a balance between stability and functional reactivity. We receive regular inquiries from new customers puzzled by failed reactions using the base compound, seeking advice on selectivity and practical substitution.

    Safe Handling and Best Practices Learned Over Years

    Years of experience in the plant have shown us that personal safety extends beyond compliance paperwork. 4-chlorobenzyl chloride releases acid fumes when exposed to moisture and attacks unprotected skin. All operators suit up in acid-resistant gear, and we run constant air monitoring. It is tempting to cut corners with short-term use of lesser gloves, but even brief exposure leads to chapping and irritation. We invest in operator training that covers not only how to handle emergencies but also how to recognize early warning signs on the packaging and plant lines.

    The main packaging format chosen for this product is 200-liter drums fitted with tight gaskets and tamper-evident closures. Each drum is batch-marked so traceability runs from raw material to finished lot. Customers often choose repackaging into smaller units for laboratory use, and we recommend transferring only under fume extraction, using low-pressure nitrogen to minimize vapor release.

    Applications and Evidence from Our Partners

    Pharmaceutical manufacturers rely on 4-chlorobenzyl chloride as a building block in antihistamines and certain local anesthetics. Agricultural labs develop herbicides and fungicides from the same intermediate. In both sectors, our site partners have documented that reaction sequences using purified material enjoy higher conversion rates and fewer troublesome color bodies in the final products.

    We sometimes receive feedback from R&D teams who run exploratory work with less-pure technical grades, noticing surprise gelation or darkening of solutions during their syntheses. Our history in the market has shown that controlling the fine details in process chemistry translates to more robust process validation and ultimately cuts batch release times for our customers.

    Anecdotally, one customer in custom flavors and fragrances reported that the ortho-analog of chlorobenzyl chloride produced off-odors not present in our para-substituted material. These are the types of differences that rarely show up in textbooks but become obvious in application testing and final product assessment.

    Trends and Regulatory Developments

    In recent years, regulatory scrutiny around chlorinated aromatics has tightened noticeably. Our manufacturing approach anticipates periodic surprise audits, not only from domestic authorities but from export destinations. By documenting every modification to our procedures and product specifications, we make the audit process smoother for everyone involved.

    Regulatory limits on allowable residuals, especially concerning impurities like benzyl chloride and related monochlorotoluenes, motivate us to run continual process optimization. We track both industry publications and customer-reported incidents. One notable regulatory push has been towards lowering workplace exposure limits, prompting newer ventilation systems in our handling areas and the installation of continuous ambient air quality monitors.

    Environmental Responsibility: From Process to Shipping

    Runoff from chlorination processes contributes significant polluting potential if not treated correctly. Our plant features a closed-loop solvent recovery system—over 90% of the solvents introduced in the reaction return to the front end after purification, drastically reducing demand for fresh chemical stocks.

    Drums destined for domestic and international shipment meet both UN and local hazardous goods standards. Rather than relying solely on static labels, each shipment includes a product passport summarizing recent QC data and any relevant regulatory or logistics updates. This approach developed after long-running customer discussions about documentation needs during customs inspections and product registration.

    Customer Feedback and Continuous Improvement

    Direct engagement with end users sets our roadmap for continuous improvement. During technical support calls, we consistently hear that transparent communication about trace contaminants and storage recommendations makes a difference. A customer in specialty polymers once described significant improvements in process yield after adjusting their purification strategy based on a minor impurity we highlighted in the accompanying certificate of analysis.

    We run annual analysis of returned products and claims, mapping any trends directly to plant upgrades when justified. It is not rare for small tweaks in batch sequencing to cut reject rates and support higher customer satisfaction. A collaborative approach, grounded in experience at the plant and in close consultation with the people who actually use the product, remains our guiding principle.

    From the plant floor, every drum of 4-chlorobenzyl chloride delivered out the door represents a two-way conversation. As end-users bring new chemistries and processes to market using our material, we take pride in seeing those innovations succeed with a product that has been shaped by real-world requirements and feedback from many hands.

    Innovation and Future Prospects

    Looking forward, we invest regularly in pilot trials for greener synthesis approaches. One recent project targeted byproduct reduction by running the chlorination in continuous-flow microreactors—a technology that, while requiring upfront investment, delivers more predictable output quality and safer operating conditions.

    Feedback from research partners in sustainability has encouraged us to explore less-volatile alternatives for downstream processing and to support the growing trend towards greener chemistry. Basing decisions on real data, whether from product returns or inline process sensors, helps us target upgrades where they make practical sense, not just in response to regulatory pressure.

    Conclusions Drawn from Years in Manufacturing

    Experience teaches that successful production of 4-chlorobenzyl chloride means more than scaling a batch recipe. It calls for invested teams, robust process infrastructure, and a willingness to adapt as chemistries and regulatory landscapes evolve. The material’s value is confirmed at every stage: in the hands of production operators, the workflows of our application labs, and the project outcomes of customers who rely on it as a trusted intermediate.

    Through continuous adjustment based on operator input and customer feedback alike, we aim to provide a consistent, high-quality product that keeps pace with the growing needs of the sector. Our real reward comes from seeing how each slight improvement—whether in purity, handling, or transparency—pushes not just our capabilities but those of our customers, suppliers, and partners forward.