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4-Nitrobenzyl Chloride

    • Product Name 4-Nitrobenzyl Chloride
    • Alias p-Nitrobenzyl chloride
    • Einecs 208-868-7
    • 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

    269983

    Chemical Name 4-Nitrobenzyl Chloride
    Cas Number 100-14-1
    Molecular Formula C7H6ClNO2
    Molecular Weight 171.58 g/mol
    Appearance Pale yellow crystalline solid
    Melting Point 44-46 °C
    Boiling Point 285 °C
    Density 1.34 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Refractive Index 1.603
    Flash Point 138 °C
    Storage Conditions Store in a cool, dry place, tightly sealed

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

    Packing & Storage
    Packing 4-Nitrobenzyl Chloride, 25g, is supplied in a tightly sealed amber glass bottle with hazard labels and tamper-evident cap.
    Shipping 4-Nitrobenzyl chloride is shipped in tightly sealed containers made of compatible materials, kept away from moisture, heat, and direct sunlight. Proper hazard labeling and documentation are required, as it is a hazardous chemical. Transportation must comply with local and international regulations for toxic and irritant substances, ensuring safe handling and storage.
    Storage 4-Nitrobenzyl chloride should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong bases and oxidizers. Keep the container tightly closed and out of direct sunlight. Use a corrosion-resistant storage container. Proper labeling and secondary containment are recommended to prevent spills or accidental exposure.
    Application of 4-Nitrobenzyl Chloride

    Applications of 4-Nitrobenzyl Chloride in Industrial Manufacturing

    4-Nitrobenzyl Chloride supports key transformations in chemical synthesis, especially supplying high-value sectors that require specific nitration and benzylation functionality. As an original manufacturer, we supply 4-Nitrobenzyl Chloride to carefully defined markets that rigorously control ingredient quality, process traceability, and verification to meet industry and regional standards. Below we detail proven downstream industrial segments, with reference to unique process and compliance needs in each.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers use 4-Nitrobenzyl Chloride as a key intermediate in constructing complex organic molecules for certain APIs. Its role centers on selective protection of alcohol or amine groups, followed by deprotection or reduction steps depending on the target molecule. Controlled addition and strict residue control are essential to meet regulatory limits for residual starting materials in finished APIs.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • ChP (Chinese Pharmacopoeia) for registered intermediates

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to substrate; adjusted by target molecule synthesis pathway and protection/deprotection efficiency

    Downstream process integration

    • Used during early to mid-stage of multi-step batch synthesis, typically for benzyl ether or benzyl amine protection
    • Reacted with alcohols or amines in presence of base catalysts under strictly inert conditions
    • By-products removed during subsequent purification (crystallization or chromatography)

    Final product types

    • Piperazine-based antihistamines production intermediates
    • CNS-active compounds (e.g., psychoactive pharmaceutical intermediates)
    • Pain management molecule precursors
    • Specialty bulk drug intermediates exported for API finishing

    2. Photochemical Protecting Group for Peptide and Oligonucleotide Synthesis

    Specialist laboratories and peptide manufacturers employ 4-Nitrobenzyl Chloride in the design of photolabile protecting groups used during solid-phase peptide synthesis (SPPS) and oligonucleotide manufacturing. The compound enables precise UV-triggered group removal under mild conditions, supporting high-purity yield in custom biomolecule production for research or clinical use.

    Industry compliance standards

    • ISO 13485 for medical device and diagnostic reagent components
    • Good Laboratory Practice (GLP) for reagent validation
    • National Institutes of Health (NIH) guidelines for research reagents

    Typical usage ratio

    • 1.0–1.2 equivalents per functional group to be protected; quantity optimized to minimize excess and ensure complete coverage

    Downstream process integration

    • Introduced in the coupling stage for synthesis resins or solution-phase steps
    • Reaction controlled for short duration to avoid overprotection or cross-reactivity
    • Protection removed with defined UV irradiation prior to final deprotection and purification

    Final product types

    • Peptide libraries with cleavable side-chain modifications
    • Photo-removable nucleic acid fragments for molecular biology
    • Labeled research probes for protein function studies
    • Specialty oligonucleotide reagents for genomic assays

    3. Agrochemical Intermediate Manufacturing

    Agrochemical producers integrate 4-Nitrobenzyl Chloride as a building block for synthesis of specific selective herbicides and insecticides. The compound introduces a nitrobenzyl group which modulates the biological activity and environmental properties of the final molecules, requiring strict adherence to regional agrochemical registration regulations.

    Industry compliance standards

    • FAO/WHO specifications for pesticide intermediates
    • Regulation (EC) No 1107/2009 (EU approval of plant protection products)
    • China ICAMA (Institute for the Control of Agrochemicals, Ministry of Agriculture) requirements

    Typical usage ratio

    • 0.5–1.0 molar ratio with primary reactant; range determined by downstream syntheses, with close balance to minimize unreacted residue

    Downstream process integration

    • Participates in nitrobenzylation of base skeletons, either batch or continuous
    • Subsequent steps involve reduction, further functionalization, and formulation into technical concentrates

    Final product types

    • Nitrobenzyl-substituted triazine herbicide intermediates
    • Precursors for sulfonylurea insecticides
    • Intermediates for research and development of new agrochemical formulations

    4. UV-Activated Crosslinker Raw Material for Polymer Chemistry

    Producers of specialty polymers and coatings use 4-Nitrobenzyl Chloride for introducing crosslinkable groups that activate under ultraviolet (UV) light. This application supports development of negative photoresists and advanced lithographic materials in electronics and high-resolution printing, where controlled release or patterning is essential.

    Industry compliance standards

    • RoHS Directive (Restriction of Hazardous Substances) for electronic grade materials
    • ISO 9001 for manufacturing quality systems
    • IEC 61249-2-21 for materials in electronic substrate manufacturing

    Typical usage ratio

    • 0.5–3.0% by weight in photoresist resin formulations; dosage tailored by sensitivity and film thickness requirements

    Downstream process integration

    • Reacted into acrylic or methacrylate polymers in solution or melt processing
    • Precursor solution cast or coated onto substrates, then UV-cured in patterned exposure steps

    Final product types

    • Negative photoresists for PCB fabrication
    • Micro-patterned polymer films for microelectronics
    • Photocrosslinkable adhesives for medical or display assembly

    5. Fine Chemical Building Block for Fragrance Intermediates

    In the aroma chemicals sector, 4-Nitrobenzyl Chloride functions as a reagent for producing specific musk and aromatic intermediates. The compound is incorporated by chemoselective benzylation processes, supporting small to mid-batch production with close analytical following of purity due to the sensitivity of perfume applications.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • COSMETICS EU Regulation (EC) No 1223/2009
    • ISO 22716 (Cosmetic GMPs for production and control)

    Typical usage ratio

    • 0.8–1.2 molar equivalents based on reacting aromatic/phenolic substrates; adjusted for targeted substitution without excess residue

    Downstream process integration

    • Used in first or second step of multi-stage musk synthesis
    • Reaction progress monitored by GC-MS or HPLC for trace impurities

    Final product types

    • Aromatic aldehyde intermediates for musk production
    • Fine aroma molecules for perfumery blending
    • Ingredient bases for luxury fragrances and specialty formulations
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    Certification & Compliance
    More Introduction

    4-Nitrobenzyl Chloride: From Our Plant to Your Lab

    Getting to Know 4-Nitrobenzyl Chloride

    Anyone specializing in fine chemical synthesis or pharmaceutical R&D comes across 4-Nitrobenzyl Chloride sooner or later. In our production facility, we handle this compound every day—its chemical structure, C7H6ClNO2, forms the basis for one of the more reliable benzylating agents found in modern industrial and academic chemistry. Our own manufacturing history with it traces back more than a decade. Our engineers and lab technicians have worked out the most consistent preparation process to maintain high purity, color stability, and ease of downstream processing.

    We produce 4-Nitrobenzyl Chloride with strict batch monitoring to reduce byproduct levels, aiming for purity levels above 99%. This doesn’t just come down to analytics; it’s also the choice of raw nitrobenzene feedstock, attention to reaction temperatures, and a careful chlorination process. After the main reaction, we don’t cut corners in the way we separate, dry, and package every lot. The pale yellow crystalline powder pouring out of our reactor isn’t just a commercial product—it reflects our direct technical problem-solving to get rid of typical off-odors or colored tars that can ruin downstream reactions.

    Why Choose 4-Nitrobenzyl Chloride Over Other Benzyl Halides?

    Chemists have their pick of benzyl chlorides and bromides for alkylation, but 4-Nitrobenzyl Chloride stands out when selectivity and reactivity are both in play. The nitro group at the 4-position deactivates aromatic substitution on the benzene ring while making the benzylic position more susceptible toward nucleophilic attack. From experience, this higher reactivity in SN2-type alkylations makes it the go-to for protective group installation, labeling, or building more elaborated molecules.

    Our customers often ask why they shouldn’t just use regular benzyl chloride or the cheaper 2-nitro version. In our own trials, and in customer processes, the 4-nitro variant cuts down side reactions, doesn’t suffer as much from overalkylation, and typically leads to cleaner product isolation. With some aromatic substitution reactions, the ortho-nitrobenzyl clogs up with undesired regioisomers; the para-nitro compound avoids all that fuss and gives a more straightforward work-up.

    Some may bring up price—4-Nitrobenzyl Chloride is costlier than standard benzyl chloride, and the demand level is smaller. But for pharmaceutical or specialty chemical operations, the real cost arises from purification headaches and lost batches. We see fewer such issues with this compound. The higher upfront chemical cost translates into savings on labor, solvent, and wasted time on chromatography or recrystallizations that bulk route alternatives can create.

    Production Process Insights You Won’t Find on a Data Sheet

    Manufacturing 4-Nitrobenzyl Chloride is a pretty unforgiving process at scale. We’ve experimented for years with various routes, but direct chlorination with controlled temperature and humidity works best. Small upgrades in reactor lining, agitation settings, and condenser flow have all contributed to safer handling and more consistent output.

    Nobody talks much about how moisture melts this compound into sticky lumps or darkens it in storage. Early batches used to clump and decompose before they even made it to the packing stage. After investing in proper drying columns and handling silos, we now get granular, free-flowing crystals that don’t cake up. And because some of our clients run automated powder feeders, we’ve tailored the filtration and drying stages to limit fines that can clog up their machines. No one likes tracing losses to powder stuck inside vacuum lines or filter bags.

    Our operators still check every drum for caking, color, and even odor—years of production have taught us it’s not just about the chromatogram or the purity certificate. We sometimes stop entire batches if the color drifts toward brown or yellow-orange, not because it always affects reactivity, but because clients expect reliability time after time. It saves headaches later, especially for those using this intermediate in API or photochemistry production. We invest in training for our teams to recognize these visual and olfactory cues; human quality control still beats software for some non-quantifiable characteristics.

    Applications Across Industry and Research

    Walk into any lab running photo-caging chemistry, and you’ll see 4-Nitrobenzyl Chloride somewhere on the shelves. Extended to pharmaceutical manufacturing, this compound occupies a foundational role in constructing protected building blocks, with the para-nitro group serving as a leaving group or as a trigger in photochemical release. During enzyme studies, researchers use it to introduce photolabile protections that cleave under UV irradiation, offering exquisite control during bioassays. Our product in particular has moved from molecular biology sites in China to top academic centers in Germany and the US.

    Industrial clients rely on this intermediate when producing dyes and optical brighteners, where certain colorfast properties require precise substitution patterns. The precision and high-purity grade we deliver translates to straighter paths during coupling reactions, reductive deprotection, or further processing to benzyl alcohols and ethers. In fine fragrance and specialty flavor production, the nitrobenzyl motif carves out a unique scent spectrum, and our consistency ensures repeatable olfactory results.

    Some companies ask us about using this as a precursor for more complex nitroaromatic scaffolds. We’ve worked on both large multi-ton batches and 10-kg research-scale runs tailored for very specific end-user requirements. Larger clients may run campaigns of this compound over several weeks, demanding consistency from batch to batch as they feed downstream reactors. We accommodate special requests for size or packaging to make everything work on their automated lines.

    Product Specifications Directly From the Shop Floor

    Every lot we ship meets long-standing process controls honed over years. Product typically shows up as a pale yellow to light beige crystalline solid—darker color hints at degradation. We check for a melting point that falls within a tight range, close to 70–72°C, with the right purity confirmed by GC and NMR. Our team uses hands-on SLAs, not just paperwork, to decide when a batch meets our standards. Impurities like 4-nitrobenzyl alcohol, 4-nitrobenzaldehyde, or unreacted para-nitrotoluene are tracked and suppressed below 0.5%, well under most customer needs.

    The final product’s solubility in common lab solvents like dichloromethane, acetone, and acetonitrile opens up a range of reaction conditions. We’ve also made tweaks over the years to manage dustiness—a key concern for workers and for automated weighing systems. We listened when a pharmaceutical client needed larger, less dusty granules, which spurred hardware investment on our end.

    We’re upfront about product hazards, too. Direct contact or inhalation can irritate skin and respiratory passages—full PPE and ventilated handling are non-negotiable in our facility. Packaging is done in thick-walled polyethylene-lined containers, double-sealed to minimize any escape of dust during shipment. We’ve also tested for chloride ion ingress and product leaching to confirm long shelf life, provided it’s kept cool and dry.

    What Sets Our Material Apart

    Over the years, we’ve seen more and more clients switching over from distributor-sourced 4-Nitrobenzyl Chloride to our directly produced batches. Many mention the simple fact that we answer technical questions from people who actually run the plant. We’ve been able to locate and fix subtle differences in product quality that others overlook—matters like trace yellowing or the presence of odorous markers, which can make or break certain applications.

    Early on, a customer batch showed micro-scale tar formation. Rather than blame the client process, we ran a process review, identified minute feedstock impurities, and rerouted supply—even though we had already passed purity by standard analytics. The new raw material vendor cost more, but our batches improved. This kind of hands-on troubleshooting is only possible when you’re making it yourself, and not simply picking up drums from a bulk trader.

    We also pay attention to sustainability and environmental impact. While 4-Nitrobenzyl Chloride synthesis can generate waste containing organic chlorides, we’ve upgraded to closed-loop solvent recovery and scrubbing systems. Solvent vapor from chlorination isn’t vented untreated; we trap, condense, and reprocess much of it, both saving on material cost and reducing discharge. Because we run both semi-batch and continuous systems, we’re able to adapt to changes in demand while minimizing idling and deadtime losses.

    Tackling Common Problems With Real Solutions

    Feedback has driven nearly every improvement to our process. Some years back, persistent clumping in summer shipments led to complaints from a customer in humid regions. It wasn’t enough to throw in a desiccant packet; we reworked our packing line and redesigned tamper-proof seals that also block out moisture. Another time, a regular user noted a lingering solvent-like smell not detected in our standard panel. This spurred us to recalibrate our drying and vacuum transfer steps, cutting that impurity down below sensory thresholds.

    We regularly field application questions directly, often advising on solubility, dilution, or optimal compounding for a target downstream product. For first-time users, we share real-life data from our lab showing handling quirks and storage points learned the hard way. If a drum doesn’t meet our published color or granule spec, we investigate and, if needed, recall before end use to avoid downtime for our clients.

    Many labs demand documentation for GMP and environmental compliance. We maintain full batch traceability; our production runs are registered with standardized batch reports and HPLC/NMR spectra archived for seven years. This is not just about ticking boxes—traceability matters any time an irregularity pops up in downstream synthesis or packaging.

    Large projects sometimes challenge our capacity, but we keep a standing inventory and run partner logistics for clients needing just-in-time deliveries. Our technical staff don’t shy away from troubleshooting, whether it’s supporting pilot-scale transitions, advising on dust control, or analyzing downstream reaction hiccups. Everything is coordinated directly from our production plant, not through third-party call centers.

    Environmental and Regulatory Responsibility

    The industrial production of aromatic chlorides means running processes that, unless carefully managed, can be rough on both worker safety and the community. Years of operational oversight and investment in our plant’s environmental controls show up in our lower than average waste output and the lack of workplace incidents. We audit our incoming material suppliers for responsible sourcing, not just to satisfy downstream customers, but to protect our own workers and neighbors.

    In meeting evolving Green Chemistry guidelines, we limit chlorinated waste, make use of solvent distillation columns, and operate close-cycle cooling throughout our production line. Our approach has drawn direct praise from environmental auditors and third-party process safety consultants. We don’t just talk about compliance—we submit to quarterly reviews and third-party monitoring to catch anything we could miss. Every operator knows the environmental risks, and our facility hosts regular safety drills.

    Not every chemical manufacturer takes this hands-on role. Because we don’t hand off our products to trading houses or distributors with no technical oversight, we track what leaves our plant and who uses it. This direct line provides a quick response path if any environmental, technical, or regulatory issue arises. Our workers, their families, and our local community all benefit from an operation that’s both economically and ethically solid.

    Looking Forward With 4-Nitrobenzyl Chloride

    We believe a chemical manufacturer’s true worth doesn’t show up only in its certificates or test results but in the depth of its technical service, operational reliability, and ability to solve problems. We’ve partnered with academic labs, biotech startups, and global pharmaceutical companies to tailor our 4-Nitrobenzyl Chloride product range for their unique needs. Over the years, we’ve remodeled pieces of our plant and invested in technician education and safety just as much as in hardware upgrades.

    Upcoming expansions will address both increasing demand for photolabile protecting groups and the tightening regulatory landscape for aromatic chlorides. Our R&D staff keep close ties with end-users so we never lose track of what the next generation of users expects in purity, particle characteristics, and packaging.

    For those exploring new synthetic applications, building complex molecules, or scaling up pharmaceutical ingredients, our 4-Nitrobenzyl Chloride stands up to real-world production challenges, not just analyst’s requirements. Continuous improvement, client-led innovation, and technical experience—all grounded in years of making, not just trading, chemistry—set our approach apart.