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HS Code |
773616 |
| Cas Number | 100-14-1 |
| Molecular Formula | C7H6ClNO2 |
| Molecular Weight | 171.58 g/mol |
| Iupac Name | 1-chloro-4-nitro-2-methylbenzene |
| Appearance | Light yellow crystalline powder |
| Melting Point | 70-73 °C |
| Boiling Point | 282 °C |
| Density | 1.377 g/cm³ |
| Solubility In Water | Insoluble |
| Refractive Index | 1.583 |
| Flash Point | 116 °C |
| Un Number | 2811 |
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 | 4-Nitrobenzyl Chloride is supplied in a 100g amber glass bottle with a secure cap, labeled with hazard and handling information. |
| Shipping | 4-Nitrobenzyl chloride is shipped in tightly sealed containers, protected from light, heat, and moisture. It is classified as a hazardous material and requires handling according to regulatory guidelines (such as DOT or IATA). Safety measures include appropriate labeling and documentation, with transit under controlled temperature and secure conditions to avoid leaks or spills. |
| Storage | 4-Nitrobenzyl chloride should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong bases, oxidizing agents, and moisture. Keep it in a tightly closed container, preferably made of amber glass to protect from light. Properly label the container and avoid exposure to heat, direct sunlight, and open flames. |
Applications of 4-Nitrobenzyl Chloride in Industrial Manufacturing4-Nitrobenzyl chloride is a high-purity, specialty intermediate with well-established roles across several key fine chemical manufacturing sectors. Our production processes and quality management systems align with stringent industry requirements, ensuring reliable batch-to-batch consistency for advanced downstream integration. Below, we outline specific industrial applications, each with particular compliance demands, process points, and end-use products. 1. Photolabile Protecting Groups for Peptide and DNA SynthesisIn peptide and oligonucleotide manufacturing, 4-nitrobenzyl chloride serves as a critical precursor for photolabile protecting groups (PPGs). Its nitrobenzyl structure allows precise, light-triggered deprotection during the stepwise assembly of sensitive biomolecules. Downstream synthesis protocols use controlled UV exposure for timed removal, streamlining the production of high-purity, sequence-defined polymers for pharmaceutical development and molecular diagnostics. Industry compliance standards
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2. Synthesis of Nitrobenzyl Derivatives in Pharmaceutical IntermediatesPharmaceutical intermediate producers rely on 4-nitrobenzyl chloride as a key alkylating agent in multi-step synthesis of active molecules. Its selective reactivity with nucleophilic sites enables introduction of the nitrobenzyl moiety into heterocycles and aromatic scaffolds. Precise control of temperature, solvent type, and pH ensures minimal byproduct formation and meets purity criteria for subsequent conversion to high-value intermediates used in CNS, oncology, and antimicrobial APIs. Industry compliance standards
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3. Light-Sensitive Polymer Additives for Photoresist FormulationProducers of advanced photoresist materials for photolithography utilize 4-nitrobenzyl chloride as an organic additive to generate controlled photosensitivity in polymer matrices. Its incorporation facilitates precise pattern transfer at micro and nano scales. Material formulators tailor additive concentration to achieve specific solubility and etching response curves, critical for electronics fabrication such as printed circuit boards (PCBs) and semiconductor wafers. Industry compliance standards
Typical usage ratio
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4. Intermediate for Agrochemical SynthesisManufacturers of specialized crop protection products exploit the reactivity of 4-nitrobenzyl chloride for introducing nitroaromatic motifs in fungicides and herbicides. Its use as an alkylating intermediate supports the synthesis of new-generation actives with targeted bioactivity and improved environmental persistence profiles. Downstream teams emphasize throughput, reaction yield, and minimal environmental release in integrated production setups. Industry compliance standards
Typical usage ratio
Downstream process integration
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At the heart of many synthetic transformations in the fine chemicals sector, 4-Nitrobenzyl chloride (CAS 100-14-1) has carved out an indispensable niche. From our manufacturing floor to shipping bays, this compound travels a well-honed path guided by hands-on stewardship and a deep-rooted commitment to reliability. Over the years, we’ve worked closely with research scientists, process chemists, and technical directors who have relied on this material not only for its purity but for its consistent reactivity. Each batch owes its characteristics to choice raw materials, careful monitoring, and years of cumulative operational improvements.
Our 4-Nitrobenzyl chloride leaves the reactor as a pale yellow crystal, often with a mild odor reminiscent of chlorinated aromatics. It’s a chemical that demands attention at every stage. Whether we’re scaling a batch for pharmaceutical R&D or fine-tuning a run for photochemical research, its melting point, odor, and crystalline form offer early signs of purity and correct process control. High purity—often greater than 99% by GC—isn’t just a sales figure to us; it’s the measure of repeated solvent recrystallizations and calibrated distillation runs.
We define our product by more than just assay: hydrochloric acid content, moisture by Karl Fischer, and GC area percent all tell part of the story. Over time, we’ve learned how even small fluctuations in these values can shift the performance in a key step of a synthesis. Our operators and QC analysts track subtle color variations and the index of refraction—tiny cues that make the difference between a smooth downstream alkylation and hours lost to troubleshooting.
Talk to process chemists about their wishlist for benzylating agents, and reliability usually tops the list. 4-Nitrobenzyl chloride brings robust alkylation potential without the unpredictability sometimes seen with other benzyl halides. The nitro group at the para position doesn’t just affect electronics; it offers a lowering of the nucleophilicity, which actually assists in controlling side reactions. As a manufacturer, we field questions weekly on batch certifications and reactivity comparisons—not just from industrial buyers, but from university researchers studying reaction mechanisms.
Our customers often share feedback rooted in real workbench stories: a higher yield in amine protection steps, cleaner byproduct profiles after deprotection, and more straightforward purification post-reaction. These anecdotes matter, because they feed into our lot adjustments and give us insight into how changes in our process parameters affect labs down the supply chain.
The real power of 4-Nitrobenzyl chloride lies in its structure. Unlike its ortho- or meta-nitro counterparts, the para-nitro configuration influences how it participates in nucleophilic substitution. You see less steric hindrance and a pronounced activating effect for certain deprotection strategies, especially in solid-phase peptide synthesis (SPPS) and oligonucleotide work. Photoreactive work benefits too—the para-nitro group enables photolytic cleavage applications, a fact that gets overlooked in favor of the more generic “benzyl chloride” designation.
Down in the trenches, it’s not just about “does this meet purity spec?” but about tuning the chlorination protocol to minimize ortho or meta isomers. Our team keeps operations tight, routinely running small-scale HPLC checks to look for less than 0.5% total impurity, because even low-level contamination from the wrong nitro isomer can show up as difficult-to-remove colored impurities in a downstream pharmaceutical process.
We often get calls from formulators and process engineers who are troubleshooting unexpected byproducts in their syntheses. It helps to remember that not all benzyl chlorides offer the same electronic environment. Simple benzyl chloride acts quickly in many reactions, but has a habit of promoting side alkylations. The nitro group on 4-Nitrobenzyl chloride changes that landscape. It pulls electron density from the benzene ring, creating a more easily controlled reaction for specific nucleophiles. This selectivity is exactly why drug developers and peptide chemists keep coming back after trialing other options.
Subtle differences show up in photolabile protection chemistry as well. 4-Nitrobenzyl chloride provides a sharper trigger for photodeprotection, often at wavelengths more compatible with less photodamage to sensitive biomolecules. We’ve learned, through detailed feedback and shared experimental logs, that this often means easier purification—and for specialty applications, even a half-day saved on the prep bench can be a deciding advantage.
Our product gets built into photoremovable protecting groups, or “cages,” used in the activation and deactivation of biological targets with light. Many modern neuroscience protocols depend on stable, reliable batch-to-batch performance of the protecting group moiety. A single off-grade shipment can disrupt months of experimental timelines. We take that risk seriously, monitoring each run for trace organics and ensuring packing lines are free from cross-contamination.
Polymer chemists report advantages with 4-Nitrobenzyl chloride when synthesizing advanced materials—specifically, polymers that require clean initiators. By providing a reproducible cleavage profile and strong reliability in Friedel–Crafts reactions, our material sidesteps longstanding issues associated with variable reactivity. These niche but crucial applications challenge us to keep a tight grip on process variables and to share openly about any plant modifications or raw material supply changes that could introduce variability.
We work upstream of many regulated industries—pharma, diagnostics, electronics. Each sector brings a slightly different interpretation of what counts as “quality.” For some, a narrow melting point range and spectral match to reference standards matter most. For others, residual solvents or heavy metal content can be a sticking point. We have implemented a block-wise sampling plan, pulling representative aliquots at each critical stage of production, not just the final drum.
Much of this work stems from direct dialogues with auditors and purchasing managers who’ve seen enough paperwork to know when something doesn’t add up. They look for chain-of-custody details, raw material traceability, and evidence of process robustness. We encourage their visits, because, frankly, our plant team learns with each conversation. Auditors’ questions often drive upgrades—sample handling equipment, data logging, even storage protocols for intermediate samples waiting for final approval.
As regulatory standards evolve, especially around impurities and potential genotoxins, we adapt not only our HPLC protocols, but also our cleaning and validation cycles. This isn’t an academic exercise. We’ve seen the fallout from cross-lot contamination and the real-world impact that a single off-spec shipment can have downstream. Clear communication, transparent documentation, and strict adherence to Good Manufacturing Practice don’t just protect business—they help scientists reach important breakthroughs without “what-if” worries about their starting materials.
The pharmaceutical sector demands both flexibility and rigor. We serve customers at every scale, from bench-top to bulk. Over the years, we’ve modified batch reactor size, implemented secondary containment, and optimized solvent recovery, all to ensure the needs of each client group are met. We’re used to running in 50-liter glasslined reactors for developmental scale projects, then ramping up to multi-ton batches for routine manufacturing. With each ramp-up, cycle time and mother liquor composition can shift slightly, so we track every detail—not just to meet our own standards, but to meet the increasingly challenging requirements of custom synthesis partners.
Some customers look for tighter controls on trace metals; others want customized packaging or solvent residue specifications for highly sensitive electronic or analytical processes. We offer both standard and tailor-made specifications. Tighter specifications are a real advantage in photochemistry, where even trace contamination can throw off optical clarity and reaction kinetics. It’s not just about following a checklist—it’s about tuning each production run to the intended application, often in direct collaboration with the customer’s technical team.
Run-of-the-mill data does not always address the practical realities of a busy lab. 4-Nitrobenzyl chloride, being sensitive to both moisture and light, needs attention to storage conditions at every step. As a manufacturer, we ship in sealed, light-blocking containers to guard against early degradation and hydrolysis. Our warehouse staff maintain strictly controlled environmental conditions, and every outgoing drum lives in nitrogen-flushed packaging until it’s on the truck.
Chemists tell us that even minor lapses in closing bottles or delays in use can lead to the formation of hydrolyzed or polymerized byproducts. We pass along practical advice, drawn directly from our own storage protocols: limit exposure to open air, refrigerate after opening, and use within six months for critical reactions. By sharing stories of both successful and problematic storage practices, we help research teams avoid unplanned reruns and waste.
Working with 4-Nitrobenzyl chloride day in, day out, our production team has developed a good feel for what can go wrong, and more importantly, how to keep things right. For instance, we’ve had batches where a minor excursion in chlorination temperature led to hard-to-remove color impurities. Catching those early, through hands-on monitoring and frequent in-process checks, saves months in troubleshooting. Feedback loops with R&D teams let us follow how small upstream choices manifest in isolation steps, byproduct formation, or yields on the user’s bench.
Past process deviations have taught us to avoid excessive heating, which can drive decomposition or form unwanted tars. Operator vigilance matters just as much as sophisticated instrumentation. We’ve written SOPs that focus not just on the big picture, but on routine checks—simple observations, employee training, and empowering frontline staff to flag anything that looks off. Years of partnership with analytical chemists have underscored the value of robust record-keeping and ready access to retained samples for every batch.
On paper, 4-Nitrobenzyl chloride looks like a straightforward commodity. In practice, the quality swings wider than many new buyers expect. By offering open doors to our plant, sharing batch records, and supporting troubleshooting, we commit ourselves to accountability. Long-term relationships with technical directors and procurement specialists have evolved into collaborations that outlast ordinary purchase cycles.
Sometimes, issues come up outside our immediate expertise—an impurity spike after scale-up, unexpected results in a new multi-step protocol. We don’t claim to know every answer, but our on-site chemists work across time zones to replicate user conditions and resolve challenges. Reaching out to other manufacturers, academia, and regulatory specialists has widened our toolkit of solutions.
The landscape for 4-Nitrobenzyl chloride is never static. Greener chemistry, stricter auditory standards, and more complex applications push us forward. We’ve made headway by optimizing chlorination reactions to cut down on waste and lower energy use. Catalysis improvements and more efficient solvent recovery allow us to offer a cleaner, more sustainable product. We’re reducing hazardous byproducts—not just because of regulation, but because it frees users from lengthy purification work downstream.
On the end-user side, advances are equally rapid. New methods in photolabile protection, gene editing, and responsive polymer development rely on predictable, batch-to-batch supply. We keep up by investing in pilot programs, funding collaborative synthesis research, and actively exchanging know-how with the customers who ultimately shape demand patterns. It’s a feedback-oriented approach that sometimes means tearing up the playbook and working from scratch, but that’s where major improvements begin.
As expectations climb, so do the technical hurdles. Today’s 4-Nitrobenzyl chloride applications often involve high-throughput automation, compact reactions, and real-time analytics. Ready adjustment and openness to process innovation give us an edge, making it possible to keep up with customers racing ahead in their own fields.
Quality no longer just means “meets spec”—it means sharing risk, sharing data, and responding with agility to changing needs across international markets. By maintaining visibility into every production step and listening carefully to customer feedback, we work to ensure each bottle and drum carries the same level of care our team invests in its production. The compound may be small, but its impact rides on a larger culture of accountability and long-term partnership.