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HS Code |
194067 |
| Cas Number | 3018-12-0 |
| Iupac Name | 2,2-Dichloroacetonitrile |
| Molecular Formula | C2HCl2N |
| Molar Mass | 109.94 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.387 g/cm³ (at 20°C) |
| Boiling Point | 112-114°C |
| Melting Point | -28°C |
| Solubility In Water | Slightly soluble |
| Flash Point | 38°C (closed cup) |
| Vapor Pressure | 17 mmHg (at 25°C) |
| Refractive Index | 1.426-1.428 (at 20°C) |
As an accredited Dichloroacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed, labeled with hazard warnings and handling instructions, containing 500 mL of Dichloroacetonitrile. |
| Shipping | Dichloroacetonitrile should be shipped in tightly sealed containers, protected from moisture and incompatible materials. It must be transported as a hazardous chemical, typically under UN2810, in accordance with local, national, and international regulations. Ensure proper labeling and documentation, and handle with care to prevent leaks or spills during shipment. |
| Storage | Dichloroacetonitrile should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and bases. Store in a tightly sealed, clearly labeled container made of compatible material. Protect from moisture and direct sunlight. Ensure storage area has appropriate spill containment and access to safety equipment like eyewash stations and showers. |
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Purity 98%: Dichloroacetonitrile with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Stability temperature 60°C: Dichloroacetonitrile with a stability temperature of 60°C is used in agrochemical formulation, where it maintains structural integrity during process heating. Low moisture content: Dichloroacetonitrile with low moisture content is used in specialty chemical production, where it prevents unwanted side reactions and increases reaction selectivity. High volatility: Dichloroacetonitrile with high volatility is used in laboratory-scale organic synthesis, where it allows for rapid solvent removal and efficient process workflow. Density 1.32 g/cm³: Dichloroacetonitrile at a density of 1.32 g/cm³ is used in liquid-phase extraction processes, where it provides optimal phase separation and recovery rates. Molecular weight 109.93 g/mol: Dichloroacetonitrile with a molecular weight of 109.93 g/mol is used in analytical reagent preparation, where it enables precise stoichiometric calculations and reliable analytical results. Boiling point 83°C: Dichloroacetonitrile with a boiling point of 83°C is used in controlled temperature reactions, where it minimizes thermal decomposition and ensures operational safety. |
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Walking into any modern laboratory, you spot rows of chemicals lined up, each bottle carrying value far beyond its label. Among these, dichloroacetonitrile sits as a staple for anyone working in synthesis and specialty chemical production. I’ve handled plenty of intermediates over the years, but few offer the same blend of reactivity and selectivity as dichloroacetonitrile. This compound’s role extends from pharmaceuticals to specialty polymers, serving as both a building block and a reactive agent in multiple pathways. Unlike many bulk chemicals that end up in detergents or fuels, dichloroacetonitrile feels almost surgical in its use—delivering targeted reactions whether you’re tweaking an active pharmaceutical ingredient or advancing a crop protection molecule.
At first glance, its structure looks straightforward: a two-carbon backbone, two chlorine atoms, and a nitrile group. Under the hood, that simplicity masks a serious punch—strong electrophilicity and the capacity to trigger demanding halogenation and cyanation steps. Working with this compound, I grew to respect its dual nature: highly effective yet challenging for those who don’t understand its quirks. Its ability to react under mild conditions allows chemists to bypass harsher reagents and more taxing environments. The nitrile moiety pulls electron density while the chlorines increase reactivity—a one-two combo that rarely misses.
I’ve watched skilled chemists use dichloroacetonitrile to introduce cyano groups into aromatic rings, build specialty isocyanides, and even to generate herbicidal agents. One memorable project involved synthesizing a narrow-spectrum antibiotic precursor—the clean, high-yield conversion we achieved owed much to the selectivity of dichloroacetonitrile. Technically, fewer by-products and easier purification make downstream processing smoother. That distinctive sharp aroma—the telltale sign in the fume hood—reminds you to respect its potency, but also points to its volatility and need for proper handling.
Dichloroacetonitrile typically comes in a few main grades, ranging from technical to high-purity forms designed for research or active ingredient production. Over time, I’ve tested both sides. Technical grade finds its place in manufacturing where trace contaminants do not upset the process, like in bulk agricultural synthesis or intermediates for dyes. In contrast, when the stakes grow higher—imagine prepping an intermediate for an injectable drug—only the highest-purity material cuts it. Microscopic contaminants in those settings spark unwanted side reactions, waste costly reagents, and sometimes stall entire projects. Even trace moisture content can hydrolyze dichloroacetonitrile, reducing yields. For meticulous work, I always insist on material with guaranteed GC assay results, low water content, and minimal halide impurity.
Those years in process optimization taught me that purity isn’t only lab fetishism; it’s plain economics. Lower waste translates to less clean-up, fewer surprises during scale-up, and tighter control in regulated industries like pharma. Batch consistency remains crucial. Sometimes suppliers will tout pricing, but I’ve seen cost savings dissolve in the face of unpredictable side products and yield losses. If your synthesis hinges on dichloroacetonitrile as a key step, skimping on grade rarely pays off in the long run.
Some chemists ask: Why work with dichloroacetonitrile when so many halogenated nitriles are out there? This isn’t a knee-jerk choice. Alternatives like trichloroacetonitrile, dichloroethanenitrile, or simple acetonitrile each bring different properties. Trichloroacetonitrile, for instance, goes harder as an electrophile but can overshoot and introduce too much reactivity—great when you need it, disastrous if you want control. Acetonitrile’s milder character makes it a staple solvent, but its lack of reactivity means it cannot step in where dichloroacetonitrile shines.
I remember one scale-up where a synthetic route originally relied on trichloroacetonitrile. The process worked perfectly in the flask, but as volumes increased, material control issues cropped up, consistency flagged, and purification grew costly. We pivoted to dichloroacetonitrile and saw an immediate improvement in selectivity and yield. Comparing the two under real plant conditions made the distinction clear—sometimes you don’t need the “strongest” agent, you need the right balance.
In the pharmaceutical world, dichloroacetonitrile appears across a spectrum of preparations—especially for introducing cyano functional groups for further conversion. These reactions serve as key junctions in antiviral, anti-inflammatory, and cardiovascular drug development. The crop science sector leans on it for producing advanced herbicides, often relying on dichloroacetonitrile’s halogenation power to unlock new, potent actives. Its selectivity supports the creation of intermediates that withstand tough field and environmental conditions.
Research always pushes boundaries, and dichloroacetonitrile holds up under challenging conditions. Take specialty polymer synthesis: here, custom monomers often start life as complex halogenated nitriles. This compound’s unique balance of reactivity and stability lets researchers prepare monomers without catastrophic side reactions. The semiconductor industry sometimes draws on it as well, leveraging the clean transformations possible with this intermediate during the fabrication of organic semiconductors and advanced coatings.
I’ve even seen it put to use outside textbooks: small companies developing UV-cured adhesives or specialty resins seek out dichloroacetonitrile for its ability to yield highly crosslinked, durable polymers. Many of these novel materials stem from clever applications of reactive intermediates, showing just how impactful a compound like this can be in the hands of a skilled chemist.
Experience with dichloroacetonitrile quickly teaches a healthy respect for its hazards. Safety data sheets warn about acute toxicity, corrosiveness, and environmental persistence. Some see it as a barrier, but commercial labs deal with compounds like this every day, provided protocols are robust. Working in a well-ventilated fume hood and wearing proper PPE—lab coat, gloves, goggles—stand as the minimum standard. Long hours at the bench made these habits second nature for me. Proactive spill control, fixing eyewash stations, and using sealed transfers become part of the routine. Storage away from acids, alkalis, and moisture prevents runaway reactions and equipment corrosion.
One slip almost cost us time and money—a minor leak due to a neglected gasket in storage led to contamination and additional disposal costs. That incident drove home how discipline in handling correlates with smooth operations and safety. Site managers and bench chemists need buy-in from leadership; strong safety culture lowers risk for everyone involved.
Dichloroacetonitrile’s power comes with responsibility. Chlorinated organics draw scrutiny because of their persistence in soil and groundwater. Factories and laboratories have a duty to capture fugitive emissions and properly destroy spent materials. Shortcuts invite regulatory trouble and hurt credibility. Incineration remains the gold standard, but even here, incomplete combustion can allow toxic byproducts to slip through—only high-efficiency thermal oxidizers guarantee thorough breakdown.
Throughout my career, I’ve seen both responsible operations and regrettable shortcuts. Facilities that invest in robust waste treatment keep audits clean, maintain good relationships with local authorities, and avoid production pauses or fines. Integrating strict environmental management with production pays dividends over time. Green chemistry principles also guide route selection: if you can swap in less persistent reagents or recover and reuse more feedstock, the entire process improves. It’s not just about compliance; resources saved often translate to real bottom-line benefits.
The chemical landscape never stands still. Recently, I’ve watched ventures pursue cleaner and safer synthetic pathways, reducing process steps by leveraging dichloroacetonitrile’s unique reactivity. Automated reactors and smart process controls allow safer, more precise dosing, minimizing exposure and running reactions with greater efficiency. Some innovators experiment with flow chemistry, showing that dichloroacetonitrile lends itself to continuous, closed-system operation, reducing both waste and operator risk.
Academic collaborations push the material even further. I’ve seen teams work on catalytic cycles that temporarily “mask” toxic reactivity until a critical synthetic step. Pharmaceutical chemists use advanced analytical tools to track even trace byproducts, getting ahead of regulatory demands for “greener” profiles. Data-driven process control helps keep emissions low, providing transparency and accountability across the supply chain.
The drive for sustainable solutions continues as both product developers and regulatory bodies raise the bar for what’s acceptable. Demand for cleaner, safer, and more efficient intermediates means suppliers constantly revisit purification, packaging, and delivery options. Many producers shift to safer bulk handling formats—stabilized drums, pre-weighed ampoules—cutting manual exposure and improve traceability from production to user.
No chemical comes without risk. Dichloroacetonitrile’s strengths—reactivity, volatility, strong functional groups—translate into challenges around transportation, worker safety, and downstream waste. Modernizing old plant equipment or building out new capacity always includes secondary containment, enhanced ventilation, and automated monitoring. Software-based recordkeeping tracks every drop, closing gaps where human error can creep in. These investments stretch capital budgets, but in my time, the companies that skimped on safety rarely lasted; one major spill or recall erases a thousand small savings.
Worker training forms the backbone of risk management. Sitting in quarterly refreshers might feel tedious to some, but it’s these sessions that build muscle memory in crisis situations. The best facilities encourage open reporting—near misses and incidents get logged, analyzed, and shared, shifting the culture from blame to learning. This feedback loop catches weak points before they cause harm.
On the research side, green chemistry’s rise means chemists continuously seek alternatives or remediation strategies. Process intensification—making more with less by skipping intermediary steps—often leverages dichloroacetonitrile’s reactivity while optimizing for less waste. Even incremental improvements, like switching to closed-transfer systems or in-line scrubbing, can greatly reduce emissions. It isn’t always glamorous work, but incremental changes drive safer and more sustainable outputs over the long haul.
Supply disruptions, regional differences in regulation, and the ever-present fluctuation in feedstock costs shape dichloroacetonitrile’s availability and pricing. Unlike some commodities, where massive swings are rare, specialty intermediates can see sharp shifts if a key plant goes offline, or if environmental rules squeeze production in one area and shift demand elsewhere. Procurement teams need deep relationships with suppliers, along with backup sources. I witnessed a year where floods shut down a major European plant—users who diversified their sourcing or held inventory fared better than those who played too lean.
At the same time, demand keeps growing, especially from fast-expanding pharmaceutical and agrochemical sectors. Global trends point to a rising need for efficient and selective building blocks. Markets that a few years back viewed dichloroacetonitrile as niche now see it as essential. Innovators in Africa, the Middle East, and Southeast Asia are scaling up, eager for reliable supply and technical support.
Forward-thinking suppliers invest in both capacity and technical support. Some offer tailored customer service, supporting not only delivery but also method development, troubleshooting, and regulatory support. My experience suggests the old transactional approach—buy, use, dispose—grows less sustainable. Collaboration across the supply chain yields stronger resilience when disruptions inevitably arise.
Choosing the right supplier means checking more than the catalog. Quality assurance teams should vet every lot using not just purity assays, but also trace impurity screens and spectroscopic analysis. Batches need to align with internal specifications—and where they deviate, open dialogue with the supplier matters. One of the most costly project delays I ever saw came from subpar material that passed the supplier’s tests but failed downstream in our formulation. Bringing these issues forward quickly, supported by thorough in-house data, shortened resolution time and kept the project on track.
Verification doesn’t end with product in hand. Ongoing monitoring—routine spot checks, third-party verification, and recordkeeping—remains important for regulated sectors. Maintaining traceability protects businesses in the event of recalls or regulatory queries. Big investment upfront saves headaches later. As regulatory environments tighten, processes for batch release and post-market vigilance grow more sophisticated.
Chemical manufacturing pushes onward, driven by both tradition and transformation. I talk with young chemists who see compounds like dichloroacetonitrile not just as reagents, but as jumping-off points for greener, smarter synthesis. They build on the lessons of past generations—prioritizing both safety and efficiency, seeking out process improvements that leave less waste, and collaborating across specialties. Tracking where the field moves next, I see digital twins, machine learning, and automation changing routine work—every stage from ordering to reactor control to waste disposal benefits from fresh thinking.
Policy also shapes the future. Governments and watchdogs update guidelines, asking manufacturers to justify not only performance, but lifecycle impacts—how a chemical touches both workers and the environment throughout its journey. Compliance moves from paperwork to real-time monitoring, supported by digital logs and remote audits. It’s no longer enough to say a process is safe; demonstrating that with data becomes table stakes.
As demand shifts and new uses emerge, the spotlight on quality, safety, and sustainability shines brighter. From my years in the lab and time spent overseeing production, the formula for success sounds simple: respect the reagent, invest in people and systems, and never let complacency settle in. People working hands-on with dichloroacetonitrile trust in its capabilities, provided the steps are right and the culture supports diligence.
Whether synthesizing a life-saving drug, upgrading materials for new tech, or pushing environmental stewardship, dichloroacetonitrile remains a workhorse for the modern laboratory. Its versatility, coupled with real-world challenges, means that success relies as much on chemistry as on culture, quality, and care. Each year brings new methods, sharper insight, and tighter controls—never losing sight of the human element behind every bottle and every bench. In a field where progress marches on, the lessons of experience still matter most.