|
HS Code |
548161 |
| Chemical Name | N-(Chloromethyl)phthalimide |
| Cas Number | 1071-13-8 |
| Molecular Formula | C9H6ClNO2 |
| Molecular Weight | 195.60 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 87-90°C |
| Boiling Point | No data available |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.39 g/cm3 |
| Purity | Typically >98% |
| Synonyms | N-(Chloromethyl)phthalimide; Chlormethylphthalimide |
| Inchi | InChI=1S/C9H6ClNO2/c10-6-11-9(12)7-4-2-1-3-5-7/h1-5H,6H2 |
| Smiles | ClCN1C(=O)c2ccccc2C1=O |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Hazard Statements | Irritant to skin, eyes, and respiratory system |
As an accredited N-(Chloromethyl)Phthalimide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 g of N-(Chloromethyl)Phthalimide is supplied in a sealed amber glass bottle with tamper-evident cap and hazard labeling. |
| Shipping | N-(Chloromethyl)phthalimide should be shipped in tightly sealed chemical-resistant containers, protected from moisture and direct sunlight. It must be labeled as a hazardous material, complying with applicable local and international transport regulations. Adequate packaging, cushioning, and labeling for toxic and irritant chemicals are required. Only trained personnel should handle shipping procedures. |
| Storage | N-(Chloromethyl)phthalimide should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it isolated from incompatible materials such as strong bases and oxidizing agents. Properly label the container and handle under a fume hood with appropriate personal protective equipment to prevent exposure. |
Applications of N-(Chloromethyl)Phthalimide in Industrial ManufacturingN-(Chloromethyl)Phthalimide serves as a critical intermediate for specialized chemical syntheses in pharmaceutical, agrochemical, pigment, and advanced material production. We manufacture this compound to consistent high purity, ensuring compatibility with regulated industrial workflows demanding precise formulation, controlled reactivity, and traceable compliance. Below, we outline key established downstream scenarios where this raw material directly participates in the manufacture of performance-critical end products. 1. Pharmaceutical Intermediate SynthesisN-(Chloromethyl)Phthalimide is extensively adopted as an alkylating agent and protected amine precursor in multi-step syntheses of antihypertensive agents, anticonvulsants, and beta-lactamase inhibitors. Major pharmaceutical plants utilize it in batch and continuous flows under GMP protocols, often in the formation of protected amino compounds via Gabriel synthesis routes before further elaboration into licensed APIs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Ingredient ManufacturingN-(Chloromethyl)Phthalimide functions as a key starting material in the synthesis of nitrogen-containing heterocyclic building blocks, particularly in the creation of functionalized pyridines, triazoles, and imides. Agrochemical formulators use the compound within highly regulated synthesis lines to form crop protection actives via N-alkylation or ring-closing reactions, often followed by post-synthetic modifications meeting national pesticide authority requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Pigment and Dye IntermediatesChemical plants utilize this compound in the preparation of advanced azo and phthalimide-based pigment intermediates, enabling the stable introduction of nitrogen groups onto aromatic rings for high-performance coloring agents. This stage requires precise reaction monitoring and controlled addition regimes to comply with environmental regulations and batch reproducibility expectations essential for textile, ink, and paint pigment producers. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Advanced Polymer and Specialty Resin Additive SynthesisIn functional polymer and engineered resin manufacturing, N-(Chloromethyl)Phthalimide serves as a crosslinking or chain-modifying agent, introduced to facilitate the attachment of protected amine groups or to graft nitrogen functionalities within specialty thermoplastics and heat-resistant resins. Producers operating closed-system extrusion or custom batch reactors value its reactivity profile for forming tailored application polymers in electronics, automotive, and specialty adhesive sectors. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive N-(Chloromethyl)Phthalimide prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In our industry, small details shape real progress. N-(Chloromethyl)phthalimide, also known by its CAS number 524-36-7, often doesn’t grab attention the way flashier advanced materials do. Yet within countless synthetic steps, this compound plays an essential part that chemists appreciate at the bench. Having spent years watching each drum leave our facility, I’ve seen how quality and consistency here lay a foundation for reactions downstream.
We’ve tailored our process to get N-(Chloromethyl)phthalimide right, batch after batch. The product comes to you as a pale to white crystalline solid. Our typical manufacturing targets a purity of not less than 99%, measured by gas chromatography, with a loss on drying not exceeding 0.5%. Moisture content and residual solvent levels stay well-controlled, so that every reaction step you plan can proceed with high confidence. This is not a commodity item for us—it’s a specialty intermediate, and we have invested years refining each parameter.
Plenty of phthalimide derivatives appear on spec sheets, but N-(Chloromethyl)phthalimide offers a unique combination of reactivity and selectivity. The distinguishing feature stems from its chloromethyl sidechain. In synthetic organic chemistry, this group enables highly efficient N-alkylation reactions. The electron-withdrawing power of the imide position increases the leaving group ability of the attached chlorine, opening up direct substitution steps other phthalimide derivatives don’t allow.
If you compare it to plain phthalimide or N-methylphthalimide, their lack of a reactive site means extra steps or harsher conditions. N-(Chloromethyl)phthalimide slots directly into routes that demand a mild but effective alkylating agent, especially for introducing phthalimide protection to amines in a controlled manner. Some competitors make the material as a co-product in limited quantity; we dedicate entire production lots to it, which means every kilogram you receive has been produced for this specific function.
Ask a synthetic chemist or process engineer what matters: clean reactions, predictability, and throughput. N-(Chloromethyl)phthalimide turns up often as a core intermediate for preparing phthalimide-derived amines. This route remains one of the most reliable for converting primary amines to phthalimide-protected products, especially for preparing Gabriel reagents. What we ship out regularly finds its place in pharmaceutical synthesis, agrochemical research, and specialty fine chemicals where protecting group strategies underpin multi-step synthesis.
Our partnering customers, including those in drug discovery, fine chemicals, and materials science, have integrated this intermediate into both trial syntheses and scale-up processes. The suitability of N-(Chloromethyl)phthalimide for alkylation reactions means that it often forms the backbone for compounds with more complex functionalization to follow. It tolerates a range of conditions, and its crystalline nature helps with logical inventory management and accurate dosing during batch processing.
Through years of feedback, we’ve come to understand what our partners expect. Predictable batch consistency ranks at the top, because even minor changes in impurity profile can complicate purification or downstream yields. In our facility, we carry out in-process controls at multiple stages, not just final product testing. Real insight from the shop floor involves talking directly to the chemists who use the material—not just skimming specification sheets—and adapting as project requirements grow or shift.
We also see practical concerns about safety and handling. The chloromethyl group requires appropriate controls due to its reactivity. Our packaging team takes great care to minimize exposure and ensure the product handles predictably in both manual and automated feed systems. As a company that has dealt firsthand with scale-up from grams to tons, we prioritize both worker safety and process reliability. The solid, stable nature of N-(Chloromethyl)phthalimide eliminates some headaches found with more volatile alkylating agents. Controlled moisture content ensures flowability, limiting caking or compaction over time.
If you compare N-(Chloromethyl)phthalimide to traditional alkyl halides like benzyl chloride, the contrast is immediate. Benzyl chloride offers similar alkylating potential but frequently introduces unwanted side reactions or by-products. In contrast, the imidic structure of N-(Chloromethyl)phthalimide provides both selectivity and ease of purification, with crystalline by-products that can be filtered or removed easily. Our customers have documented higher product purities and reduced waste disposal costs by shifting to this intermediate.
Against common phthalimide derivatives lacking the chloromethyl group, the product offers broader application and operational advantage. Many downstream users need tight control over the timing and specificity of N-alkylation: N-(Chloromethyl)phthalimide addresses this need more directly. Some downstream processes require direct coupling or deprotection steps under mild conditions. In those cases, the unique balance of stability and reactivity in this molecule saves both time and raw material input.
Producing N-(Chloromethyl)phthalimide at scale means handling strict process validation, batch records, and reproducibility. Every batch receives a unique lot designation and we maintain records pulled from continuous in-line sensors and periodic laboratory check points. This isn’t just about ticking boxes for certification. Our own reputation hangs on whether your next reaction performs as expected. Tracing sources of raw phthalimide, solvents, and chlorine donors back to established suppliers cuts down the risk of contamination or unexplained off-spec batches.
We keep logs of customer suggestions for process tweaks. Several years ago, we received reports of inconsistent melting points between production runs in summer and winter. Turns out, subtle changes in crystal morphology related to temperature swings in the plant led us to install dedicated environmental controls across our drying suites. Today, complaints on that front have vanished—another lesson learned and implemented based on real-world, boots-on-the-ground experience.
Most of the interesting work with N-(Chloromethyl)phthalimide happens after it leaves our doors. We keep in touch with our network of chemists, R&D directors, and scale-up managers who use it in ways rarely covered in textbooks. Some have shared successes optimizing Gabriel synthesis routes with fewer purification steps, others cut down on hazardous waste by swapping out more aggressive alkylating agents. Our product finds applications from custom pharmaceutical intermediates, where tight impurity control spells the difference between a pass and a failed batch, to advanced polymer synthesis.
When a new compound route demands a material with proven reliability, the focus lands on upstream quality. Several partners have shared back that swapping from a generic supplier to a batch-tracked lot from our site led to smoother process qualification and regulatory review. Our in-house chemists run trial reactions using our latest lots, not just relying on certificates but on actual synthetic performance—yield, work-up ease, and crystallinity all matter.
Manufacturing intermediates like N-(Chloromethyl)phthalimide involves more than putting product in a drum. We put strong controls in place to limit worker exposure to chlorinated reagents and to capture all emissions from process vents. Our facilities employ closed-system handling, and we’ve invested in real-time monitoring to intercept any deviations rapidly. Our focus on best practices in handling and process safety reflects lessons learned the hard way.
We routinely review the regulatory landscape affecting N-(Chloromethyl)phthalimide, applying updates where necessary. Many of our customers operate under strict documentation requirements for pharmaceuticals and specialty chemicals. Transparent supply chain records and open communication help everyone stay ahead of challenges, from changing REACH compliance to routine audits.
Advances in medicinal and agrochemical synthesis depend on reliable performance from every building block. N-(Chloromethyl)phthalimide’s utility comes not just from its structure but from how it’s produced, tested, and delivered. Having spent decades scaling with our customers—from research bench projects to multi-ton commercial launches—we see our role as more than a supplier. Close partnerships drive practical solutions, whether that means scaling up a new impurity removal step, switching to eco-friendlier solvents, or just providing timely technical support for process troubleshooting.
We’ve noticed more attention paid to green chemistry in recent years. N-(Chloromethyl)phthalimide already scores well relative to many alternatives for reaction waste minimization due to its selectivity and cleaner cleavage routes after use. We continue to evaluate solvent recovery systems, process intensification, and greener purification strategies to further improve our offering. Investing in these developments means that as customer priorities shift, our product keeps pace—not just on paper, but in real-world application.
No two chemists run the exact same process. Needs evolve—sometimes faster than product catalogs can follow. This product, which we’ve made part of our core line-up for decades, holds up not because of hype, but because it continues to deliver reproducible results across industries. We believe in listening to the people who use our N-(Chloromethyl)phthalimide, adapting processes and documentation based on lived experience, and sharing what we learn along the way.
Your successes, challenges, and feedback drive us to make each batch a little better than the last. Chemical manufacturing isn’t about just meeting a number on a cert—it’s about understanding, partnering, and building a track record of trust with every new synthesis.