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HS Code |
870062 |
| Chemical Name | 2-(Chloromethyl)Naphthalene |
| Cas Number | 86-52-2 |
| Molecular Formula | C11H9Cl |
| Molecular Weight | 176.64 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 160-162°C at 12 mmHg |
| Melting Point | 28-30°C |
| Density | 1.17 g/cm³ at 25°C |
| Refractive Index | 1.631 |
| Flash Point | >110°C (closed cup) |
| Solubility | Insoluble in water; soluble in organic solvents |
| Pubchem Cid | 72946 |
As an accredited 2-(Chloromethyl)Naphthalene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 250 grams of 2-(Chloromethyl)Naphthalene, labeled with hazard warnings and handling instructions. |
| Shipping | 2-(Chloromethyl)Naphthalene is shipped in tightly sealed containers, protected from moisture and light, and labeled according to hazardous material regulations due to its flammability and potential toxicity. Transport typically follows UN class 6.1 (toxic substances) guidelines, ensuring secure packaging and clear hazard labeling for safe handling and delivery. |
| Storage | 2-(Chloromethyl)naphthalene should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Store in a cool, dry, well-ventilated area separated from incompatible materials such as strong oxidizing agents. Proper chemical labeling and secondary containment are recommended to prevent leaks or spills. Personal protective equipment should be used when handling the substance. |
Applications of 2-(Chloromethyl)Naphthalene in Industrial Manufacturing2-(Chloromethyl)Naphthalene serves as an advanced chemical intermediate in diversified downstream synthesis, playing a pivotal role in high-value aromatic transformations. As a direct manufacturer, we support formulation engineers, process chemists, and technical buyers by consistently supplying this specialty raw material to suit specific end-use disciplines. Main industrial applications include agrochemical intermediates, specialty dye production, pharmaceutical synthesis, advanced liquid crystal monomer development, and polymer modifier manufacturing. 1. Agrochemical Intermediate SynthesisThis compound is widely adopted for constructing naphthyl-based herbicide and fungicide intermediates, particularly via C-alkylation or condensation pathways, which allow for precise molecular tuning of bioactivity. Modern agrochemical sites rely on chloromethyl-naphthalene derivatives to enable next-generation crop protection agents through aromatic substitution and cyclization reactions. Industry compliance standards
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2. Specialty Dye and Pigment ManufacturingIndustrial colorant producers employ chloromethyl-naphthalene as a key aromatic building block for synthesizing advanced naphthalene-based azo and anthraquinone dyes. Its activated chloromethyl group permits targeted substituent introduction, which directly influences hue, shade fastness, and solubility for performance-critical organic pigments. Industry compliance standards
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3. Pharmaceutical Active Ingredient IntermediatesSeveral pharmaceutical manufacturers utilize this aromatic chloromethyl compound as a strategic precursor during the assembly of advanced naphthalene-ring drugs and specialty APIs (Active Pharmaceutical Ingredients). Medicinal chemists leverage its reactivity for selective functionalization, which ultimately benefits the development of new therapeutic molecules in oncology and anti-inflammatory research. Industry compliance standards
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4. Liquid Crystal Monomer and Advanced Material SynthesisDevelopers of high-performance electronic and optical materials incorporate chloromethyl naphthalene moieties into specialty monomers for advanced liquid crystal systems and high refractive index polymers. Its unique chemical structure facilitates the introduction of rigid aromatic segments, essential for controlling anisotropic properties in display technology and photonic applications. Industry compliance standards
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5. Polymer Modifier and Crosslinking Agent ProductionChloromethyl-naphthalene derivatives function as high-activity crosslinkers and performance modifiers for thermoset resins and advanced engineering plastics. By introducing rigid aromatic linkages, compounders enhance matrix durability, heat resistance, and dimensional stability in final polymer systems targeting high-demand industrial applications. Industry compliance standards
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Working the line in chemical synthesis, we see time and again which compounds keep up with demand—2-(Chloromethyl)Naphthalene has shown its worth both in pilot projects and commercial runs. We’ve been producing this material for years, refining our approach based on the feedback from research labs, specialty formulators, and process engineers. While every molecule comes with a spec sheet, our experience teaches us that what matters more is how it performs in the real world: reaction predictability, batch-to-batch consistency, and practical storage and handling considerations.
Our 2-(Chloromethyl)Naphthalene rolls off the reactors as a crystalline solid, usually colorless to light yellow. The molecular formula is C11H9Cl. We have standardized its purity levels, confirming by HPLC analysis and NMR, hitting benchmarks above 98%. During the aging or storage processes, we have noticed slight shifts in color under improper conditions, so we package in light-resistant containers under controlled environments. We run residue solvent checks and moisture content analyses before signing off final lots, which ensures stable behavior during downstream reactions.
We set up particle size controls on equipment to prevent dusting and to help users handle material efficiently at any production scale. Each batch undergoes GC-MS screening for trace contaminants—chloronaphthalenes have a reputation, deserved or not, for stubborn byproducts, so we keep the fraction of isomeric impurities minimal. Whether the lot size calls for kilos or drums, we offer the same stringent checks right through to the last pallet.
From our floor, no product leaves without confirming melting point—routinely falling between 63 and 66°C, checked every run. Water solubility is extremely low, and we remind end-users to expect oily residue if not kept in dry conditions. For anyone managing inventory across seasons, we have found that storing under nitrogen prolongs freshness and purity, so that's our standard packing method.
2-(Chloromethyl)Naphthalene often gets a starring role in complex organic synthesis. Labs and plants use it as a starting block for building naphthalene derivatives—structurally dense intermediates found in crop protection products, specialty polymers, and advanced electronic chemicals. Our partners in the dye and pigment industry request this compound for its predictable reactivity during the attachment of sulfonic or nitro groups. From sulfonation to Grignard reactions, we see requests from formulators developing high-performance colorants for modern plastics. Research teams pushing boundaries in pharmaceuticals rely on our pure material for making naphthalene-based ligands and drug lead compounds.
Several catalyst developers in the hydrogenation area prefer our material's consistent structure, allowing for specific testing of reaction kinetics. Not everybody realizes this, but slight impurities or shifts in molecular formula can throw off adding catalytic metals by even a fraction of a percent, especially in sophisticated homogeneous catalysis. We regularly discuss directly with process engineers to confirm compatibility, whether their setups use batch reactors or continuous flow systems, taking note of the subtle ways physical and chemical purity becomes critical at scale.
We have seen subtle issues arise over the years—an off-specification methyl chloride residue once created confusion for a pharmaceutical client. Since adopting a tighter distillation process and improving our inert gas purge, those spikes disappeared. Sometimes the smallest impurity can compromise reactivity, especially in sequential steps where a contaminant can trigger side reactions. By working directly with chemists and production teams at user sites, we've been able to hone not only our analytical procedures but also our physical packaging materials. While paper specs build confidence, ongoing field feedback and collaborative troubleshooting keep our processes honest.
Customers usually compare 2-(Chloromethyl)Naphthalene against its isomer, 1-(Chloromethyl)Naphthalene. In reality, the attachment point on the naphthalene ring changes reaction profiles rather significantly. For those seeking ortho-substitution, our version—substituted at the 2-position—delivers specific advantages in terms of electron density and steric factors, which shows up clearly in subsequent synthesis performance. Niche polymerization processes, for instance, have shown increased yield consistency and fewer byproducts when using our 2-substituted material vs. other available isomers.
Having filled, sealed, and shipped more containers than we care to count, we keep our eyes open to practical safety issues. Bulk chemical handling brings the predictable set of questions. While this compound doesn’t fume or leak like some chlorinated aromatics, it does carry toxicity concerns, demanding gloves and proper ventilation. One hard-won lesson from a production incident: avoid statically charged surfaces, as the crystalline powder can accumulate and then release unexpectedly—good grounding in all receiving areas prevents this. We monitor ventilation in our filling rooms and regularly swap out filters using chemical-resistant equipment. Training staff goes far beyond compliance checklists—hands-on familiarity with the feel, texture, and odor patterns (a faint, sweet-chloride edge) reduces error before anything escalates.
Disposal procedures matter as well, since the compound resists breakdown in regular water systems. Building solid partnerships with certified waste processors, we track every lot right back to its disposal pathway once it leaves production. Sampling incoming raw materials for halide content has prevented upstream contamination, cutting off future headaches halfway through processing. Attention to this detail alone has paid dividends in both customer trust and operational uptime.
Regular feedback from compounders and formulators gives us a grounded view of the unique value of 2-(Chloromethyl)Naphthalene compared to other chlorinated aromatics and methylated naphthalenes. The position of substitution creates a different reactivity platform for follow-up reactions. Colleagues working in the synthesis of functionalized naphthalenes report cleaner reactions and better selectivity, particularly when introducing further groups at other positions on the ring. Where other chloromethylnaphthalenes tend to leave more persistent chlorinated impurities in downstream processes, our 2-position material, produced under fine-tuned reactor conditions and using consistently high-grade feedstocks, stands out for fewer contaminants.
Other manufacturers sometimes cut corners by running high-volume reactions at the expense of rigorous purification. That shortcut echoes in real-world tests—off-colors, low yields, fouled membranes in pharma separation processes. Direct conversations with plants using both types reveal stark contrasts under microscope and in production line stability, even when apparent analytical readings seem close. We maintain a hands-on approach, testing side-by-side with end users, ready to tweak reaction sequences, adding step-down washes, or even adjusting crystal growth rates just to hit the sweet spot our partners demand.
While multi-chlorinated naphthalenes make sense for some specialty uses, their handling risk and byproduct spectrum look quite different. Our experience emphasizes that a single chloromethyl at the 2-position serves broader applications, fewer headaches during compliance review, and allows full control for specialized downstream modification—especially in custom synthesis assignments.
Quality in a product like this depends on the vigilance applied at each production stage. We source our naphthalene from narrow-cut, hydrogenated streams—having chased down supplier traceability and built relationships with miners and refineries, we don't gamble with the base stock that determines ninety percent of the final outcome. During chlorination, we monitor both temperature and agitation, logging every variable shift and correlating with downstream analytical checks. The entire team—operators, QC analysts, supervisors—draws from a process manual that’s updated based on the year’s lessons, not just regulatory mandates. Someone using the compound in an advanced polymer composite wants what they've been promised, and it’s our job to hit and maintain that mark, day after day.
We’ve faced supply bottlenecks and have been forced to adapt—sometimes that meant processing longer batches through our purification columns, at other points investing in filtration systems overhauls. Adjusting parameters like solvent ratios, wash durations, and filtration media feels tedious, but small gains in impurity removal stack up in large-scale performance. We respect customer deadlines. If that means running a pre-shipment check afterhours or doubling up on HPLC controls for an urgent drum, so be it. The result turns up as lower reject rates and fewer service calls after delivery.
End-users often need more than a product drop-off. We appreciate genuine conversations where a user describes a sticky point in a particular transformation—maybe a decarboxylation step runs slower than protocol, or a scale-up leads to dust inhalation risk for operators. Our technical team works shoulder-to-shoulder with process chemists, running side lab tests or modifying shipment packaging to make handling safer or cleaner. Feedback loops from these real-world trials have driven changes in our drying cycles, our protective wrapping materials, and our short-haul logistics. Being upstream in the supply chain means anticipating what can go wrong and adapting rapidly—the mark of a manufacturer, not just a shipper.
With experience comes a sense of which uses stretch the product’s capabilities. Gentle persuasion from our side has often led R&D teams to try our 2-(Chloromethyl)Naphthalene instead of generic isomers when reaction conditions are especially demanding, or when subtle byproducts cause headaches downstream. Over time, the relationships built on these problem-solving efforts return as loyalty—turning a one-off test batch into a steady supply agreement.
Traceability forms the spine of our manufacturing effort. Each lot has a documented path from raw material intake to reactor batch logs, QC checkpoints, and outbound packaging. Our teams archive not only the expected analytical reports but also line logs, deviation records, and environmental monitoring data attached to every lot. Downstream, we track customer returns and feedback, using statistical process control to tie back issues and prevent future occurrence. Regulatory compliance sits beside real operational transparency; users see every test result and handling note that leaves our plant. Over years, this embedding of traceability leads to fewer disputes, and a deeper trust from partners who need their chemicals to perform reliably under pressure.
Modern manufacturing cannot ignore the need for responsible practice. Every batch starts and finishes with a focus on resource efficiency and waste reduction. We closed solvent recovery loops years ago, meaning recovered chlorinated solvents now cycle back into the system rather than heading out as hazardous waste. We audit disposal vendors and document outgoing waste streams, tracking the fate of every kilogram leaving our plant. Regular audits by third parties (not just internal checks) force us to keep practices honest, and keep environmental impact front-of-mind.
Supply partners are evaluated not just for price or delivery performance, but for their own environmental and occupational health performance. With upcoming global regulations cracking down on chlorinated emissions and potential bioaccumulation, developing alternatives or innovations in process containment remains a serious focus in our plant meetings. We also work with research partners on catalytic improvements and alternative feedstocks—sometimes these don’t pan out in the commercial sector, but our willingness to explore does translate into safer, more future-proofed chemistry for all involved.
Seeing the full cycle—from weighing the crude naphthalene to tightening the last drum seal—reminds us that chemical manufacturing depends on more than a single transaction. It’s about reliability tested under the tough lights of production scale, openness with technical details, and being ready to troubleshoot the unique challenges each user faces. In the field, where every step from raw material to final use matters, we believe in direct, honest partnerships. Beyond marketing claims, the true test runs in the reactors, the analytical labs, and on the floor with your teams.
We stand behind our 2-(Chloromethyl)Naphthalene not with empty guarantees, but with years of hard-won technical know-how, a network of continuous improvement, and the understanding that the right molecular fit opens the door for lasting progress. Working directly with users on both the science and the logistics, we’ve shared in both the setbacks and the breakthroughs. That’s what sets a true manufacturer apart from a trader or middleman—the stakes are real, and so is the commitment.