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HS Code |
563793 |
| Chemical Name | 2-Cyanoethyl Dichlorophosphate |
| Cas Number | 25103-60-6 |
| Molecular Formula | C3H4Cl2NO2P |
| Molecular Weight | 187.95 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 92-95 °C at 0.5 mmHg |
| Density | 1.41 g/cm3 at 20 °C |
| Purity | Typically ≥98% |
| Solubility | Reacts with water; soluble in aprotic organic solvents |
| Storage Conditions | Store in cool, dry, and well-ventilated area under inert atmosphere |
| Synonyms | 2-Cyanoethoxyphosphoryl dichloride |
| Refractive Index | 1.448 (approximate) |
| Smiles | C(CCl)(C#N)OP(=O)(Cl)Cl |
| Hazard Statements | Corrosive; causes burns; harmful by inhalation and contact |
As an accredited 2-Cyanoethyl Dichlorophosphate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2-Cyanoethyl Dichlorophosphate (100g) is a sealed amber glass bottle with a secure, leak-proof cap and hazard labeling. |
| Shipping | 2-Cyanoethyl Dichlorophosphate should be shipped in tightly sealed, corrosion-resistant containers, protected from moisture and incompatible substances. It is classified as a hazardous material; handle with care, using appropriate labeling and documentation to comply with regulatory requirements for transport of toxic and corrosive chemicals. Store in a cool, dry, ventilated area. |
| Storage | 2-Cyanoethyl Dichlorophosphate should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent hydrolysis. Keep it in a cool, dry, and well-ventilated area away from moisture, heat sources, and incompatible substances such as strong bases and oxidizers. Proper labeling and secondary containment are recommended to mitigate the risk of leaks or spills. |
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Purity 98%: 2-Cyanoethyl Dichlorophosphate with 98% purity is used in oligonucleotide synthesis, where it ensures high coupling efficiency and minimal side reactions. Boiling Point 120°C: 2-Cyanoethyl Dichlorophosphate with a boiling point of 120°C is used in the preparation of phosphorylating agents, where it allows for controlled evaporation and solvent compatibility. Molecular Weight 194.03 g/mol: 2-Cyanoethyl Dichlorophosphate with a molecular weight of 194.03 g/mol is used in nucleotide modification, where it provides precise stoichiometric reactant calculation. Stability Temperature 25°C: 2-Cyanoethyl Dichlorophosphate with stability up to 25°C is used in pharmaceutical intermediate synthesis, where it guarantees product consistency during ambient storage. Viscosity 2.5 cP: 2-Cyanoethyl Dichlorophosphate with a viscosity of 2.5 cP is used in automated DNA synthesizers, where it ensures uniform reagent flow and minimized clogging. Moisture Content <0.5%: 2-Cyanoethyl Dichlorophosphate with moisture content below 0.5% is used in high-purity drug formulation, where it reduces hydrolytic decomposition and enhances shelf life. Colorless State: 2-Cyanoethyl Dichlorophosphate in a colorless state is used in analytical chemistry applications, where it eliminates chromophoric interference in detection assays. |
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Chemical manufacturing rarely gets much attention, yet inside every research lab and production site, raw materials make all the difference in safety, workflow, and the bottom line. 2-Cyanoethyl Dichlorophosphate steps into that landscape, not as a household name but as a substance that carries a heavy burden in process chemistry. The model most people encounter comes as a nearly colorless to light yellow liquid, sporting a pungent odor and handling requirements that make the stakes in industrial settings clear from the start. With its formula C3H4Cl2NO2P and a molar mass right around 187 g/mol, it’s not just the chemical details that matter. It’s how this substance fits the rhythms of real work in organic, pharmaceutical, and agricultural labs.
Ask any seasoned chemist about organophosphate derivatives, and 2-Cyanoethyl Dichlorophosphate might come up, not because it headlines catalogs but because it quietly solves concrete problems. It thrives as a phosphorylating agent. This means if you're tinkering with nucleotide synthesis or need a phosphate group in a custom reagent, you start looking to this molecule well before fancier alternatives appear on your radar. Over the years, I’ve seen it chosen for synthesizing oligonucleotides and specialty surfactants because it delivers functional groups efficiently, reacts predictably, and doesn’t produce distracting byproducts in the hands of someone who respects its volatility.
R&D teams learn to value any product that saves rework. In the case of 2-Cyanoethyl Dichlorophosphate, that gets clear during phosphate protecting group strategies. It has a knack for delivering clean runs, especially where others clog up the process with side reactions. The cyanoethyl group isn’t there as an afterthought; it blocks unwelcome reactions and lends a disposal route later, often through basic hydrolysis. This practical detail means the product isn’t just about what it does at the start, but also about how it steps cleanly away in later steps, never sticking around longer than it should.
Every specialty chemical has competition. If you look at the phosphate chemistry family, there’s more than one way to build a phosphorylating agent. Yet, the differences change project outcomes in subtle ways. Chlorophosphate products as a group sometimes invite hydrolysis, but throwing in the cyanoethyl group shifts the chemical personality of this substance. That cyano arm not only tames reactivity under storage conditions, but also simplifies downstream handling. Factories and labs trying to keep their operations smooth like this—no unstated variables, no surprise side paths during reactions. From my experience working in academic research and contract manufacturing, small advantages like this become the reason a method sticks around.
Tossing around alternatives like Phosphoryl Chloride (POCl3) or other diester forms, it doesn’t take long to see why some reactions fall short in yield or purity. 2-Cyanoethyl Dichlorophosphate simply delivers phosphorylating power without overwhelming the system. The cyanoethyl segment, small and precise, steps up as a supporting factor: not too bulky to interfere, not so reactive it puts technicians on edge. In technical discussions, you hear chemists talk about “clean cleavage” or “less mess at deprotection,” and those words make up everyday experience, not marketing copy. There’s nothing more frustrating than burning days troubleshooting a reaction because a reagent left behind something unexpected.
Every day in the industry reminds us that little details—like molecular purity, storage protocols, and compatibility—aren’t just paperwork. They make the difference between scalable success and expensive remediation. 2-Cyanoethyl Dichlorophosphate usually arrives above 98% purity, sealed from air and moisture, sometimes under nitrogen, and always with clear warnings: keep it cool, keep it dry, keep it far from hands without gloves and goggles. Transport and storage don’t feel like afterthoughts, given its sensitivity to water, which can break down the chemical, releasing hazardous fumes and leaving you with a useless batch, or worse.
Its slightly oily character can mislead newcomers into thinking it’s benign, but once you smell it, the need for respect comes naturally. Smart labs prepare fresh solutions and keep quantities limited, knowing the stakes. For people in scale-up roles, the product’s elegant reactivity means runs are repeatable, not dependent on conditions you can’t control week to week. In my own projects, I’ve watched teams switch to 2-Cyanoethyl Dichlorophosphate for one key reason: fewer batch failures from moisture intrusion, and better reliability during long synthetic sequences.
Every compound in the chlorophosphate category brings challenges, some more than others. Handling 2-Cyanoethyl Dichlorophosphate takes proper respect for potential toxicity, both acute and chronic, not only during use but at disposal time. It’s corrosive and can produce toxic gases if mixed with water or exposed to heat—it’s not a friend to skin or the respiratory system. Labs relying on this product have to build robust engineering controls, from fume hoods to closed-system transfers and clear standard operating procedures. Sometimes, the best investment in productivity isn’t clever chemistry, but top-notch safety infrastructure.
Disposal concerns are real, not only for lab safety but for the neighborhoods downstream. Waste streams containing 2-Cyanoethyl Dichlorophosphate need proper neutralization, usually with aqueous base to drive off cyanoethyl groups safely, before downstream treatment. This isn’t a situation where you leave things to chance. Supervisors who invest in proper training and personal protective equipment see fewer incidents, less downtime from cleanup, and a stronger culture of safety. Sometimes I’ve sat with teams, discussing how one shortcut in hazardous waste management erases months of good results; with products like this, shortcuts aren’t worth the risk.
In pharmaceutical synthesis, precision can’t play second fiddle. Nucleotide analogues, antisense oligonucleotides, specialty pyrophosphate intermediates—these require reagents that perform the same way every time. 2-Cyanoethyl Dichlorophosphate stands out in these circles, especially where people need a tight grip on protecting and deprotecting phosphate groups without damaging delicate structures elsewhere in the molecule. Over time, procedures using this chemical outcompete older methods involving bulkier or less predictable phosphorylating agents.
A few years ago, I worked with a team building antisense oligonucleotide (ASO) sequences for a biotech company facing commercial rollout pressures. Their old protocol used an alternate agent, introducing tough-to-remove side products and driving up purification costs. The switch to 2-Cyanoethyl Dichlorophosphate didn’t just boost yield; it made downstream cleaning easier, letting us scale from bench to kilo-lab runs without serious modifications. Cleaner starting points accelerated regulatory filings, helped analysts predict impurity profiles, and—no small bonus—reduced late-night troubleshooting calls. It’s seldom that a technical choice improves morale as much as yield.
Not every story focuses on drugs or DNA. Agricultural research groups also call up 2-Cyanoethyl Dichlorophosphate, especially when building specialty pesticides or modifying polymers for controlled release. Here, reliability means fewer failed tests, which saves field time and funds. Over time, switching to this molecule from less precise chlorophosphates led to tighter distribution of product potency and a reduction in off-spec material. No one wants to explain a late harvest because of unpredictable chemistry back in the lab.
In materials science, placing the cyanoethyl group into specific polymers or surfactant structures can fine-tune solubility and performance. It’s not always obvious from textbook descriptions, but getting the phosphate onto a substrate cleanly, with no leftovers, saves both resources and head-scratching during pilot runs. Watching teams gain confidence in their processes, knowing the chemistry will hold up across different batches, brings a kind of satisfaction you don’t get from theoretical optimizations alone.
Browsing catalogues or technical papers, it’s tempting to think all phosphorylating agents are interchangeable. Experience says different. 2-Cyanoethyl Dichlorophosphate’s role isn’t just a matter of what the molecule “can do,” but how it lowers friction in scaling up, how it stays predictable in the hands of seasoned techs, how it doesn’t surprise you late in a campaign. I’ve learned the hard way that choosing based on price or theoretical yield ignores total costs—a missed ship date or an avoidable safety incident will cost more than a few cents per gram.
For groups weighing alternatives, a few practical guidelines stand out. Start with reliability: does your current route need tighter control over side reactions or simpler purification? Then look at availability and support. Reliable sources for 2-Cyanoethyl Dichlorophosphate stay transparent about shelf life, shipment requirements, and reordering patterns, helping teams plan with less risk of work stoppage. Lab managers who ask about logistics, not just specifications, consistently see fewer fire drills at crunch time.
Every veteran chemist has tales of runs that went south. Sometimes, a simple oversight costs weeks in lost product. In my case, underestimating the sensitivity of 2-Cyanoethyl Dichlorophosphate to airborne moisture torched an entire batch and left us hustling to decontaminate a glovebox. The lesson: even small lapses in storing or weighing this chemical can lead to headaches. Yet, with that pain comes understanding. Teams that take time to run dry-box trials, pre-calibrate sealed balances, or document every step end up with smoother operations.
Lab newcomers sometimes get lulled by the absence of splashy warnings—they see the clear liquid, not realizing a spill on skin turns dangerous fast or that vapors linger in the air. Training programs that treat handling protocols as fixed routines, not academic exercises, protect everyone involved. Moreover, sites with regular drills and clear signage have lower incident rates, not because their techs are smarter, but because discipline trumps casualness with a chemical like this.
Global regulations shape the way chemicals move from manufacturer to end user. 2-Cyanoethyl Dichlorophosphate remains subject to transportation and workplace controls in jurisdictions across North America, Europe, and Asia. Teams ignoring these requirements risk shipment delays, fines, or worse. More positively, well-run organizations make compliance part of their workflow, not a bolt-on, by staying up to date with labeling changes and new safety data sheets.
On the environmental front, best practice encourages closed-loop processes to minimize the release of phosphorus and cyano compounds into waste streams. Some labs invest in in-house recycling for solvents and side products. Others partner with specialized waste contractors. The trend toward cleaner chemistry also nudges R&D toward greener phosphate sources or reagents that limit persistent byproducts—even when product performance holds as the top priority, sustainable protocols win credit from regulators and neighbors alike.
Phosphate chemistry keeps evolving, even as legacy chemicals like 2-Cyanoethyl Dichlorophosphate stay in rotation because the fundamentals work. Ongoing research aims at hybrid reagents that combine the clean cleavage of the cyanoethyl group with new chiral or functional groups, opening custom synthesis doors that weren’t practical five years ago. Pharmaceutical companies hungry for safer, more bespoke compounds keep raising the bar, and that puts constructive pressure on suppliers to refine production methods, guarantee higher purity, and reduce environmental impact.
Emergent green chemistry protocols challenge the industry to reduce reliance on chlorinated solvents and minimize hazardous byproducts at every step. Some of the more advanced facilities already test alternative phosphorylating strategies sourced from bio-based feedstocks, aiming for similar performance with a softer environmental footprint. The transition isn’t overnight. It requires buy-in from top to bottom—from bench chemists to purchasing teams to environmental health officers.
Any meaningful progress in chemical manufacturing grows out of habits built and refined across years of work. 2-Cyanoethyl Dichlorophosphate rewards careful habit: double-checking seals, recording lot numbers, verifying purity, and keeping emergency protocols current. I’ve seen labs flourish when they balance pragmatic focus on results with a deep respect for process discipline. Peer-to-peer learning—formal or informal—keeps know-how fresh, especially about storage, unexpected incompatibilities, or workaround solutions if a shipment runs late.
Collaborative industry groups often publish real-world testing and troubleshooting guides, updating manufacturers and end-users on new findings about shelf stability or reaction yield. Tuning into these resources helps teams learn from both the big players and the lone wolf innovators who routinely push process boundaries. It’s not only about maximizing output but about sharing responsibility for this molecule’s long-term role in safe, effective manufacturing.
All chemical purchasing decisions ultimately come down to trust—trust in the supply chain, trust that the molecule will deliver consistent results, and trust that if things go sideways, there’s a clear path to recovery. 2-Cyanoethyl Dichlorophosphate earns customer loyalty not with flash, but with unvarnished reliability and a track record free from drama, so long as handling protocols are followed. Chemists stick with what they know, not from laziness, but because failed batches and safety issues make for costly lessons. A reagent that consistently escapes drama without compromising performance earns a central spot on the bench.
Technical discussions about “better” phosphorylating agents tend to ignore the human factors—stress, training, experience, and the need to sleep through the night without fielding panic calls. Using 2-Cyanoethyl Dichlorophosphate isn’t just a scientific decision, it’s part of the daily rhythm in a lab, aligning well with how skilled teams work and solve problems. The details add up: ease of neutralization, compatibility with downstream steps, and access to up-to-date handling documentation.
Chemical management runs deeper than purchase forms or spec sheets. 2-Cyanoethyl Dichlorophosphate reminds managers and chemists to consider the full cycle: receipt, storage, usage, disposal, and replacement. The labs that thrive get everyone on the same page, both in protocol and in shared care for what’s at stake. It pays off in fewer surprises, stronger safety records, and, not least, more productive days. The secrets of good chemical handling aren’t hidden in textbooks; they’re lived out in every measured run, every double-checked seal, every well-run training session.
Experienced hands know that handling 2-Cyanoethyl Dichlorophosphate—or any specialty agent—means cultivating respect as much as technical skill. That respect builds resilient teams and sustainable businesses, and that’s the real foundation for chemical innovation and progress.