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HS Code |
929990 |
| Chemical Name | 3-Nitrobenzyl Chloride |
| Cas Number | 536-90-3 |
| Molecular Formula | C7H6ClNO2 |
| Molecular Weight | 171.58 g/mol |
| Appearance | Pale yellow to yellow crystalline powder |
| Melting Point | 42-44°C |
| Boiling Point | 156-157°C at 14 mmHg |
| Density | 1.356 g/cm3 |
| Solubility | Insoluble in water; soluble in organic solvents such as ethanol and ether |
| Purity | Typically ≥98% |
| Refractive Index | 1.608 (Predicted) |
| Flash Point | 110°C (closed cup) |
| Smiles | ClCC1=CC(=CC=C1)[N+](=O)[O-] |
| Storage Conditions | Store in a cool, dry place, tightly closed container, away from light and moisture |
As an accredited 3-Nitrobenzyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Nitrobenzyl Chloride, 25g: Supplied in an amber glass bottle with a secure screw cap, labeled, and chemical hazard warnings. |
| Shipping | 3-Nitrobenzyl Chloride must be shipped in accordance with hazardous materials regulations. It should be packed in tightly sealed containers, protected from moisture and physical damage, and labeled with appropriate hazard symbols. Ensure transport in compliance with local, national, and international guidelines, including the use of protective packaging and documentation. |
| Storage | 3-Nitrobenzyl chloride should be stored in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong bases and oxidizers. Keep the container tightly closed and properly labeled. Store in a chemical-resistant container, preferably glass or polyethylene, and ensure access is restricted to trained personnel. Use secondary containment to prevent accidental spills or leaks. |
Applications of 3-Nitrobenzyl Chloride in Industrial Manufacturing3-Nitrobenzyl chloride serves as a critical intermediate in fine chemical synthesis across specialty chemicals, advanced materials, and pharmaceutical manufacturing. As an experienced manufacturer, we supply this raw material to downstream industries with strict attention to quality, compliance, and process needs. Below we detail key industrial application areas with their respective compliance, ratios, process stages, and end products.
Many pharmaceutical companies use this compound to produce intermediates for nitrobenzyl-based antimicrobial APIs. It undergoes nucleophilic substitution for further derivatization and subsequent reduction or coupling steps. Control over residuals and purity is essential to meet global regulatory standards for finished drugs. Our technical support includes guidance on qualification requirements, impurity profiling, and documentation for regulated markets. Industry compliance standards
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The compound plays a key role in agrochemical synthesis as a benzylating agent for producing selective herbicide intermediates. Its reactivity supports construction of nitroaromatic building blocks that form the active cores of high-value crop protection formulations. Downstream processors monitor reactant ratios to optimize yield while maintaining active ingredient stability throughout formulation and packaging. Industry compliance standards
Typical usage ratio
Downstream process integration
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Specialty polymer manufacturers use the compound as a precursor for crosslinking agents and custom photoinitiators. Its nitro group and benzyl moiety enable design of high-performance polymers with targeted UV or thermal activation properties. Processors balance the input ratio to optimize crosslink density and determine end-use attributes such as flexibility, curing time, and material longevity. Industry compliance standards
Typical usage ratio
Downstream process integration
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Dye and pigment producers rely on this material for controlled benzylation, introducing nitrobenzyl groups into dye molecules for enhanced lightfastness and color intensity. The process demands close monitoring of purity, water content, and stoichiometry to minimize by-product formation and meet stringent color quality specifications required by end-users in textiles and plastics. Industry compliance standards
Typical usage ratio
Downstream process integration
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Competitive 3-Nitrobenzyl Chloride prices that fit your budget—flexible terms and customized quotes for every order.
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Producing 3-nitrobenzyl chloride means working with a compound that has shaped the field of fine chemical synthesis for decades. Factories like ours, operating for years under strict safety and operational standards, don't just sling barrels down the line. Our entire process starts with carefully sourced raw materials and ends with quality checks at each stage, because chemists and plants downstream rely on consistent purity. The substance we make isn’t a commodity meant for mass consumption. Its main demand comes from specialist manufacturers, research institutions, and sector-specific developers whose work requires more than surface-level quality control.
3-nitrobenzyl chloride, with CAS number 6892-52-2 and formula C7H6ClNO2, belongs to the family of nitroaromatic benzyl chlorides. Its molecular structure—chlorine next to a methyl group attached to a nitrobenzene backbone—makes it reactive in targeted reactions, which labs and industrial users prize. In our line, the most frequently produced model meets 98% minimum purity, measured by HPLC and verified by GC. Visual checks and melting point readings mark each batch, but we lean on consistency in chemical specs above all else.
Purity isn’t a slogan. Days in a chemical plant are spent minimizing side reactions, purifying with precision, and measuring every stage. Even minor byproducts can spell disaster for an end-user working through a multi-step synthesis, so we rely on controlled nitration and benzylation, paired with an optimized distillation routine. Over time, we found the right temperature and pH controls limit impurities such as 4-nitrobenzyl chloride or unreacted benzyl chloride. These aren’t just traces—they impact downstream product quality and cost.
Before shipping, each lot faces HPLC analysis and moisture checks, since 3-nitrobenzyl chloride has a tendency to hydrolyze with prolonged exposure. That reactivity, so useful in the right hands, can turn into ring-opening—or even render the batch unsuitable for precision biochemistry. With this experience, our quality department pushes for glass or PTFE-lined transport containers, keeping exposure to air and light at a minimum. For large orders, we pack under nitrogen and monitor for any pressure build-up.
Chemists know that a reactivity step with 3-nitrobenzyl chloride gives access to intermediates not easily made from other reagents. Alkylation of nucleophiles and formation of nitrobenzyl ethers or esters stands out in our feedback from pharma labs and dye manufacturers. In early stage drug synthesis, it’s used for blocking groups or attaching aromatic fragments. Diagnostics use it to label or derivatize sensitive substrates, exploiting its predictable reactivity and, once attached, the unmistakable fingerprint the nitro group gives in analytic instruments.
We’ve supplied batches destined for specialty pigment manufacture. There, end-users utilize the selective reactivity to install the nitrobenzyl moiety, knowing downstream reduction yields amines that integrate colorant systems. As a manufacturer, we see inquiries tied to non-pharmaceutical research, especially in polymer chemistry, where the product modifies chain ends or introduces photo-switchable links.
Many outside the business lump “benzyl chloride derivatives” together, but our experience tells a different story. The presence of a nitro group distinctly changes both physical and chemical properties. Compared with unsubstituted benzyl chloride, 3-nitrobenzyl chloride has a significantly higher boiling point and greater polarity. That doesn’t just affect storage behavior; it alters reaction kinetics and selectivity in ways a synthetic chemist tracks closely. Our users in flavor, fragrance, and pharmaceutical sectors don’t just swap in related molecules—they calibrate entire reaction schemes around the behavior of this specific reagent.
In practice, 2- or 4-nitrobenzyl chloride show markedly different reactivity and separation characteristics. The ortho or para positions lead to unwanted byproducts in some routes and less stability in others. We’ve fielded calls from research labs trying to troubleshoot failed reactions, only to discover they ordered a positional isomer or used a technical grade product with broad impurity bands. Decades of batches and customer feedback have made it clear—consistent, pure 3-nitrobenzyl chloride works when the rest don’t cut it.
Beyond structural isomers, we often hear requests for mixed product lines, like 3-nitrobenzyl alcohol or bromide. Chloride, as a leaving group, occupies a unique niche: it’s reactive enough under mild conditions to work in most nucleophilic substitutions, but stable enough for scale-up and safe handling at industry scale. The bromide and iodide analogues bring higher reactivity but come with cost, supply constraints, and less favorable handling for long-distance shipments. The chloride option thus finds a balance that manufacturers, R&D shops, and formulators gravitate to.
From a producer’s standpoint, one of the chronic headaches among downstream users is batch-to-batch inconsistency among low-tier traders or resellers. We have seen first-hand the supply chain problems caused by inconsistencies in particle size, purity fluctuations, or containers improperly sealed and transported. Using a batch that’s been repacked, handled by multiple brokers, or stored in sub-par conditions almost guarantees incomplete reactions or costly purification later on. We eliminated these risks over years by labeling every container from the source plant, tracking shipments for temperature excursions, and fielding technical support for any lot discrepancies.
Industries that need gram to multi-ton orders tell us that inconsistent color, off-odors, or visible particulates in 3-nitrobenzyl chloride can set entire production runs back. There’s no faking a clean product: quality failures show up in analytic traces and failed syntheses, not at the order desk. By operating our own reactors, distillation, and purification lines, we prioritize source-to-end consistency, reducing reliance on spot buying and middlemen who may not understand exactly what’s required from the start.
Handling nitroaromatic chemicals requires a thorough risk management approach. Our process includes extensive air handling, waste reduction, and monitoring, as safety doesn’t stop at the laboratory door. 3-nitrobenzyl chloride brings particular risks: skin and eye irritation, and respiratory sensitivity if exposed as vapor or fine mist. Factory teams rely on closed systems, not just gloves and goggles, limiting personal exposure through proper engineering controls. Waste streams, including residual organics and wash waters, receive on-site pre-treatment, using carbon beds and scrubbing towers.
Decades of manufacturing experience have shown us that minor changes in process flow—adjusting solvent types, using phase-separation techniques, or implementing staged purification—meaningfully reduce emissions and waste. Each operational update, well beyond regulatory minimums, wouldn’t exist without feedback from operators on the ground and chemists driving process R&D. Rather than relying on generic safety advice, we invest directly in staff training and technical troubleshooting, making safety and environmental compliance an everyday culture.
Market demand shifts with new pharmaceutical projects, dye chemistry trends, and sensitizer usage in specialty materials. From our vantage point, regulatory moves on aromatic chlorides and increasing scrutiny on legacy solvents have prompted formulations toward greener profiles. Our plant invested in solvent recovery and process intensification for this reason. Sometimes clients request alternate packaging due to weight or disposal requirements, and we have adapted by offering volumes from kilogram increments up to full-scale drums, always in chemically compatible linings.
We monitor global market trends and policy updates directly, not through layers of brokerage chatter. Direct input from R&D partners abroad helps us structure our own product releases, plan for shifts in order volumes, and preemptively qualify new supply routes if geopolitical or supply threats arise. Experience in this industry often means learning to predict, not just react, to changes—one season’s new product launch can double nitric acid consumption or require weeks of raw material testing before the first new batch is shipped.
Manufacturers like ours play a quiet but crucial role in enabling early-stage research. Institutes developing novel probes or exploring new drug mechanics count on us to deliver more than standard batches. Some require custom packaging, more rigorous impurity profiling, or batch history documentation for their own traceability. We keep technical staff on hand to answer in-depth questions about expected impurity profiles or differences in reactivity. Rather than shifting those questions down the line, we believe in open communication between production, quality, and the final user.
chemistry often advances through small, incremental improvements to reagent purity or handling safety. Our role has evolved from simply supplying a raw material to collaborating with researchers—sharing experiences with structure-reactivity relationships or troubleshooting purification steps after complex reactions. Over the years, we have maintained relationships with university spin-offs, pharmaceutical startups, and process engineering groups not by selling, but by sharing technical knowledge gleaned from real production setbacks and optimization success stories.
Some buyers arrive at our door after being undersold by generic product listings promising “pure” or “technical” material. We see, again and again, the costs that creep in from chasing low price over process reliability. Handling nitrobenzyl chlorides from questionable sources can mean months spent treating failed reactions or debugging analytics. Real cost savings come from robust, repeatable batches with predictable reactivity—not just the number on an invoice.
Investing in direct purchase from the manufacturer means access to real production logs, impurity profiles, and batch traceability. Brokers and repackagers rarely provide that detail, and even less often understand why it matters in process scale or sensitive synthesis. We’ve worked with firms cleaning up after cross-contamination in their lines, scratching heads over a change in crystal morphology, or chasing a stubborn color body—all of which trace back to overlooked, seemingly “minor” differences in the original supply.
We don’t pretend chemical manufacturing is risk-free, easy, or static. Our own learning curve has been steep—every transition to a new reactor setup, adjustment in order volume, or incoming regulatory hurdle prompts a review of existing processes. Where material trends shift, such as increased demand for custom derivatives or more environmentally benign production, we adapt by updating purification columns, re-examining solvent usage, and trialing new process controls.
Research partners increasingly look to us for support with scale-up challenges, not just a sample on a spec sheet. By keeping feedback loops open, tracking patterns in reported failures or unexpected reactivity, and investing in plant upgrades, we ensure 3-nitrobenzyl chloride remains reliable as chemistries develop. Our teams discuss new safety guidance, international shipping relevance, updated documentation requirements, and application-specific troubleshooting in regular technical meetings—experience developed over decades, not just summarized in bullet points.
Producing chemicals like 3-nitrobenzyl chloride never feels routine. There’s pride in meeting the challenge of each order—a sense among everyone, from plant operators to logistics coordinators, that the consequences of a sloppy batch ripple down the line. Lessons from the floor that led to more uniform heating, cleaner condensers, or smarter handling find their way into the procedures we share with end-users. If there’s a way to anticipate and prevent a problem, experience tells us it’s better than cleaning up after one.
We’ve visited customer plants, watched processes falter due to overly reactive or sluggish product, and fielded midnight calls about a mysterious solid left at the bottom of a drum. This feedback doesn’t vanish—it refines how we approach storage conditions, labeling, and support. While other manufacturers may skimp on stabilization or package in reactive materials to trim costs, we insist on inert atmospheres and unreactive drum linings.
Industry standards continually evolve, and regulatory frameworks only grow more complex. Meeting expectations for traceability, environmental controls, and batch documentation means building these practices into our daily work, not just ticking compliance boxes during audits. Each improvement in our facility—whether a monitoring system update, operator training session, or a new sealant for packaging—emerges from direct operational realities, balancing production costs with customer outcomes.
3-nitrobenzyl chloride holds a distinct spot in specialty manufacturing. Years spent navigating production challenges, optimizing purification, and building safety into our infrastructure show there’s no replacement for first-hand experience. The industry’s best practitioners have learned the hazards of cut corners the hard way. Our clients recognize the difference between industrial supply and true manufacturing expertise. With each batch, we aim to deliver not just a chemical, but a partnership grounded in reliability, transparency, and the collective lessons learned from years of hands-on work. Choosing a manufacturer who shares that experience means better outcomes, more predictable research, and fewer unwelcome surprises in the process.