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Ethyl Chloroacetate: Unpacking the Substance Behind the Science

Tracing the Path: Historical Development

Chemistry keeps surprising people, and Ethyl Chloroacetate feels like a case study in how curiosity drives discovery—first crafted in labs that didn’t fear experimenting with acetic and hydrochloric acids. Its story stretches back over a century, with organic chemists testing new ground for pesticides, drugs, and dyes. Those early years were marked with mystery, as safety standards lagged behind curiosity. Today, lessons from those headline-making missteps still influence how synthetic chemicals enter production. This context matters a lot in discussions about synthesis and handling, especially after early manufacturing settings exposed workers to risks that modern standards now help minimize. The arc from rubber-aproned chemists to regulatory oversight holds a warning and an opportunity for improvement, shaping research for safer practices and guiding apprentices who step into this ever-evolving field.

Catching the Basics: What Ethyl Chloroacetate Brings to the Table

Ethyl Chloroacetate is no stranger in the lab. Its sharp, fruit-like odor betrays a volatile spirit, but what really stands out is its role as a go-to alkylating agent. Out in the wild, it drifts through industries from pharmaceuticals to fragrances, and gets called on when precise chemical transformations need a helping hand. This compound bridges the gap between raw industrial power and careful academic inquiry: manufacturers see value in its reliability, while researchers use it to introduce new functional groups into molecules, spinning off branches of discovery that inform medicine and materials science alike.

Looking at the Substance: Physical & Chemical Properties

Pour out Ethyl Chloroacetate, and you meet a clear, colorless liquid that flows with purpose. Its boiling range nestles well below water, making it a candidate where temperature control isn’t just about saving energy but about preserving molecular integrity. Solubility divides opinion: water shrugs it off, but organic solvents draw it in, eager to pull it into new chemical realms. Flammability always sits at the table, never letting anyone forget the hazards that shadow its practical uses. This reactive blend is what gives it both its power and its bite, demanding knowledge, respect, and a steady hand.

Behind the Ingredients: Technical Specifications & Labeling

Regulations—and common sense—mean labeling gets personal here. You spot labels serving more than compliance, offering guidance on purity, hazard class, and handling advice. Professional suppliers batch and purify to rigorous standards, knowing missteps don’t just taint results; they risk lives. That’s not just paperwork. I’ve watched researchers spend extra time double-checking labels or cross-verifying lot numbers after accidents showed how easy it was to grab the wrong bottle. Real trust in the product arrives through detailed certificates, transparent reporting of impurities, and the confidence that transparency is a feature, not a flaw.

Building Blocks: Preparation Method

Manufacturing Ethyl Chloroacetate puts tradition and innovation on a collision course. Labs once favored reacting chloroacetic acid with ethanol and a splash of strong acid. Changes in environmental standards and the pressure to cut waste now shape routes to synthesis. As waste handling costs eat into budgets, greener alternatives and process intensification attract more interest. Academic journals echo with tweaks on temperature profiles, pressure changes, or new catalysts that promise better yields—and cleaner byproducts. What used to be a tired workhorse reaction now finds itself at the cutting edge of sustainable chemistry.

Changing Character: Chemical Reactions & Modifications

It’s easy to overlook how flexible Ethyl Chloroacetate really is. Drop it into a reaction with strong nucleophiles, and you see substitution light up—a classic SN2 reaction that textbook writers lean on to show fundamentals in action. Run it with amines, and you head toward glycine derivatives, the kind that fuel pharmaceutical innovation. Base-induced hydrolysis breaks it down to more familiar acids, while chemists intent on modifying it push boundaries with every new research paper. This adaptability doesn’t exist in a vacuum. Teams looking for new drug scaffolds or crop protection agents often circle back to Ethyl Chloroacetate, knowing its combination of reactivity and accessibility invites unplanned discoveries.

Beyond the Name: Synonyms & Product Names

Walk into a storeroom and ask for Ethyl Chloroacetate, and you also meet Ethyl Monochloroacetate, Chloroacetic Acid Ethyl Ester, or simply ECA. Each name reflects a layer of industry, global supply chains, or the stubborn legacy of competing nomenclature systems. Researchers track synonyms to avoid mix-ups—one missed alias means an experiment can misfire or a safety plan falls short. Old trade names may pop up on inventory lists, reminders that chemicals drift through markets with more baggage than just their structure.

Staying Safe: Safety & Operational Standards

Too many accidents have forced labs to treat Ethyl Chloroacetate as more than just another volatile liquid. Inhalation and skin contact threaten acute symptoms, including headaches, respiratory issues, or burns. Fume hoods stand as the frontline defense, while gloves, goggles, and strict inventory logs underscore a culture that accepts danger but insists on minimizing it. National and internal guidelines don't merely recommend—they dictate how storage, transport, and spill management play out. I’ve seen how drills and checklists create habits, turning safe handling from a chore into a reflex that stops emergencies from turning catastrophic. Every bottle in a teaching lab owes its handling protocol to the silent stories of past mistakes—an unspoken lineage that makes every researcher a little more careful.

Turning to Application Areas

Industries don’t just buy Ethyl Chloroacetate for a line in a budget. Drug makers turn to it when building anesthetic agents like ethyl chloroacetate-based intermediates. Pesticide producers value its reliability for certain organophosphates. Fragrance chemists explore its volatility, seeking the kind of top notes that define a perfume’s introduction. The variety of end-uses reflects a compound living many lives: in the hands of a medicinal chemist, it subtly tweaks efficacy; for an agrochemical developer, it can spell the difference between targeted action and collateral environmental damage. Each field pulls on its unique strengths, and the cross-pollination of ideas pushes application boundaries even further.

Pushing Knowledge: Research & Development

Research on Ethyl Chloroacetate echoes an ongoing dialogue between risk and reward. I’ve sat in conferences where scientists fight to tame its reactivity, not just for efficiency’s sake but to make scale-up safer and waste disposal simpler. Green chemistry advocates call for newer synthetic routes that respect both worker safety and the environment, chasing catalysts or solvents that shift the balance away from toxicity. Analytical chemists get involved just as deeply, developing detection methods for trace impurities that might skew toxicity profiles or introduce new hazards. Every year, refinements in process engineering, material science, and environmental monitoring add texture to the story, sharpening its profile and steering future use.

Facing Consequences: Toxicity Research

Toxicology doesn’t wait for headlines to remind people of the stakes. Studies on Ethyl Chloroacetate flag risks that range from acute irritation to chronic concerns. It acts as both a warning and an opportunity: dose-response studies and long-term exposure data shape storage limits and ventilation investments—but they also hint at mechanisms of action, informing antidote development in the poison control toolkit. Regulatory agencies comb through this data, setting workplace exposure limits and demanding labeling that speaks to both seasoned chemists and nervous newcomers. Real progress shows up in the steady decline of accidents and the rise in safety-first lab culture, but every incident pushes researchers to dig deeper into the root causes, searching for patterns and early warning signs.

Glimpses Ahead: Future Prospects

Ethyl Chloroacetate won’t fade away. As chemical manufacturers search for sustainable, versatile, and efficient building blocks, its profile only grows sharper. Demand for greener synthesis and reduced emissions pokes researchers toward alternatives, engaging minds who see every flaw as an invitation. Advances in catalytic science, process automation, and safer storage solutions might rewrite parts of this molecule’s history. Those who use it—whether in a shiny new biotech compound or an age-old pesticide—face choices with wider ripples. Real hope for improvement comes not from leaving compounds behind, but from sharpening skills, investing in education, and strengthening oversight so that people keep learning from both innovations and accidents long after the ink dries on today’s regulatory guides.




What is Ethyl Chloroacetate used for?

Chemistry in Action

Ethyl chloroacetate doesn’t show up in everyday conversation, but within chemical labs and manufacturing, it carries a lot of weight. People in the industry keep a close eye on it because of its handy mix of reactivity and versatility. At its core, this clear liquid combines two chemical groups. That unique setup turns ethyl chloroacetate into a solid worker for building more complex molecules.

Building Blocks for Medicines

Doctors and patients may never see a bottle labeled “ethyl chloroacetate,” but this chemical helps birth dozens of drugs. Chemists count on it when making anesthetics and muscle relaxants, including substances like lidocaine. It also shows up as a key ingredient when assembling antibiotics and anti-cancer meds. Its reactive nature lets it join forces with other chemicals in the lab, like a puzzle piece snapping into place to form something more useful. This reactivity streamlines drug manufacturing, helping labs produce molecules faster and with fewer steps. Fewer steps can mean lower costs and fewer environmental byproducts—two things anyone in the industry appreciates.

Farming and Flavoring

On farms, keeping crops healthy sometimes means using pesticides. The backbone of certain herbicides starts with ethyl chloroacetate. Chemical engineers tweak it so it targets weeds but leaves crops alone. That handle on its behavior makes this chemical an old favorite for inventing new protective sprays. For people working in crop science, this helps keep food supplies steady without risking big crops to infestations.

Surprisingly, small doses of ethyl chloroacetate also show up in flavors and fragrances. It doesn’t land in your food, but chemists use it as a starting point to make compounds that add a tang or subtle scent to perfumes. Its strong, often fruity smell makes it memorable in the lab, though careful handling remains important since higher concentrations won’t do anyone’s nose much good.

Respecting Safety

Handling this chemical safely means respecting its dangers. In the lab, it can irritate skin, eyes, and lungs, and long exposure brings health risks. Stories travel fast among researchers about accidental spills or leaks. Extra safety glasses, gloves, and fume hoods aren’t up for debate here—they are required every time. Chemical plants invest in good ventilation and emergency plans. Everyone trained with ethyl chloroacetate remembers at least one safety drill.

Governments like the US EPA and European regulatory bodies keep rules very clear for transporting, storing, and disposing of ethyl chloroacetate. These safeguards matter. Runoff or improper storage threatens the environment, so strict guidelines reduce risky situations. These aren’t just rules from a policy—it’s respect for public and worker health.

Innovation and Sustainable Paths

Chemistry moves fast, and over the past decade, researchers have looked for cleaner ways to use and replace harsh reagents like ethyl chloroacetate. Green chemistry teams think ahead, searching for alternatives and safer handling techniques. Switching to improved packaging, recycling solvents, and lowering waste counts as progress in labs and factories. Many new projects weigh the health of workers and the planet next to production speed.

Ethyl chloroacetate doesn’t make headlines, but its impact stretches across hospitals, farms, and even perfume counters. As companies and labs keep pushing for cleaner, safer practices, this chemical stands as a reminder that careful progress needs both innovation and old-fashioned caution on the ground.

What are the safety precautions when handling Ethyl Chloroacetate?

Recognizing the Risks

If you’ve ever worked in a college lab or a small-scale chemical plant, ethyl chloroacetate probably rings a bell. This clear, sweet-smelling liquid reminds me a bit of past summers spent labeling glass bottles and double-gloving my hands on those long, careful afternoons. Ethyl chloroacetate kicks up concern because it brings a toxic vapour to the party. One drop on your skin or quick breath in, and you’ll know you’re not dealing with scented water. Throat irritation and burning eyes are common complaints, and those who ignore the warning signs have faced bigger issues, including respiratory distress and skin blisters.

Smart Preparation

Looking back, proper setup made all the difference. One lab supervisor drummed into us the need for prepping every workstation. Before opening a bottle, always know where your eyewash and safety shower stations are, even if you never plan to use them. Wear splash-resistant goggles, and don a lab coat that covers your arms fully. Gloves are a must—preferably butyl rubber or laminated film—since ethyl chloroacetate slips through latex in no time. Chemical-resistant aprons or sleeves are just common sense for handling larger volumes. Don’t let fashion or comfort get in the way here.

Using Adequate Ventilation

Take it from someone who’s worked in makeshift labs—ventilation can’t be an afterthought. A fume hood is crucial. Even a few minutes of open-air handling left my throat scratchy; a hood made all the difference. Ethyl chloroacetate volatilizes at room temperature, so fans and open windows won’t cut it. If you have to move it outside of a hood, keep your exposure as brief as possible, and avoid working alone.

Handling Spills and Storage

Accidents happen. Once, a bottle slipped in a rush. We’d been trained to cover minor spills promptly with inert absorbent, scoop the mess, and double-bag it before sending it off as hazardous waste. Never try to mop up with bare hands, and keep solvents away unless you know the right procedure—mixing chemicals “to clean” can spark off another trouble entirely.

Proper storage keeps trouble at bay. Ethyl chloroacetate lives best in tightly sealed containers, stored in well-ventilated spaces away from acids, ammonia, or bases. Heat or sunlight speeds up the risk of decomposition, which can break containers and release gas.

Taking Exposure Seriously

Ignore the early warning signs, and health problems stack up. This chemical targets the nervous system. I've seen colleagues ignore a bit of lightheadedness or minor cough, only to regret it by the end of the shift. Even something as simple as washing hands takes on new urgency—scrub up before touching your phone, keys, or face. Small mistakes travel fast.

Training and Emergency Plans

Solid training turns fear into focus. At one plant, our regular drills made it automatic: in case of contact, rinse for at least fifteen minutes, contact emergency services, and never try to “walk it off.” Know your risks, know the plan, and don’t shortcut safety for speed.

Raising Standards, Sharing Experience

Nobody wants their workplace haunted by stories of preventable accidents. Good habits, strong protocols, and personal awareness help create a safer, steadier environment. Whether you’re in a high-tech lab or a school storeroom, respect for these basics protects you and everyone you work with.

What is the chemical formula and structure of Ethyl Chloroacetate?

Breaking Down Ethyl Chloroacetate

Ethyl chloroacetate rolls off the tongue in labs and classrooms, but under its name sits a simple formula: C4H7ClO2. Its structure often pops up during discussions of organic synthesis and pharmaceutical intermediates, but few talk about how this compound shapes the workbench and the broader chemical industry.

Getting to the Core: Atoms and Bonds

Looking closer, ethyl chloroacetate carries two carbon chains linked by an oxygen bridge, with chlorine sitting right next to one of the carbons. Visualize it like this: a two-carbon ethyl group joins up with an acetate that features a chlorine atom swapping out one hydrogen. The actual structure looks like this:

ClCH2COOCH2CH3

Forget complicated rings or bulky substitutions—this compound keeps things straightforward. The chlorine atom, attached to the alpha-carbon, turns an average ester into a reactive ingredient for many transformations chemists depend on.

Why This Structure Matters

Working in synthesis, I’ve often turned to ethyl chloroacetate for making amino acids and a handful of other molecules that matter in drug development. That chlorine atom isn’t just for show. Its position next to the carbonyl group changes how the molecule reacts, letting chemists pull off substitutions and build larger, more complex structures.

Most folks handling this compound in the lab find it acts as a strong alkylating agent. That means it’s a key ingredient in adding carbon blocks to nitrogen, oxygen, or sulfur atoms. In this respect, ethyl chloroacetate has earned its place as a starting material for things like glycine, certain anesthetics, and insecticides. There’s a reason it never gets dusty in the chemical storeroom—people reach for it when they want results, not theory.

Room for Safer Handling and Use

This isn’t just about clean models or chemical equations. Ethyl chloroacetate has a sharp, penetrating odor, and anybody working with it for more than a minute feels it in the air. The molecule’s reactivity comes with risk. A few drops spilled in a small room can cause headaches or worse, touch your skin and you’ll know right away it’s time for better gloves. Over the years, I’ve learned that even experienced folks sometimes drop their guard with so-called “simple” intermediates. The lesson’s always the same: use the hood, wear safety glasses, and keep that bottle firmly capped.

Beyond personal safety, the story stretches a bit further. Chemical companies now look into green chemistry, finding ways to use less hazardous reagents and develop processes that spit out fewer toxic byproducts. In practice, this means substitutions, better containment, and smarter waste treatment—all grounded in a real understanding of what molecules like ethyl chloroacetate can do.

Trust Through Experience—Not Just Data

A lot of the trust surrounding ethyl chloroacetate comes from years spent handling it, reading up on best practices, and talking directly with both researchers and industry pros. The facts don’t shift much: C4H7ClO2 marks a reliable, versatile building block. But safety matters, and so does the push for less hazardous alternatives. In my own hands, and by the benches of colleagues, the compound’s reputation is earned, not bought—a reminder that every bottle deserves a second look before you dip your pipette.

How should Ethyl Chloroacetate be stored and transported?

No Room for Error with Ethyl Chloroacetate

Ethyl chloroacetate raises eyebrows among those working with chemicals, and not without reason. It carries some real hazards. Skin burns, breathing trouble, even fire risk—this is one product calling for real respect. Handling it safely means following strict, tested protocols, and skipping shortcuts can carry consequences for people and the environment.

Storage: Keeping It Safe and Stable

I’ve worked at places where storing reactive chemicals like ethyl chloroacetate was routine. The rule that stuck with me: keep it cool, dry, and in a clearly labeled container that can hold up against its tough nature. Most facilities choose glass or high-quality steel because cheaper materials break down. An airtight seal matters. This limits the chemical from drawing in moisture and reacting too soon. Temperature matters a whole lot too; heat speeds up decomposition and can build unwanted pressure. Ideal storage sits below 25°C, far from sunlight or any source of ignition.

Storing this chemical around food, medicine, or lab gear is a gamble nobody should take. Separate and secure—those are words I trust here. In shared storage, good chemical compatibility charts help a lot. Ethyl chloroacetate doesn’t get along well with bases or strong oxidizers, so these should stay put in another zone entirely.

Ventilation and Spill Readiness

Years on the safety committee showed me that poor ventilation turns even a minor spill into a panic. Anyone storing ethyl chloroacetate owes it to their team to check for steady, working ventilation. Local exhaust ventilation, like fume hoods, keeps vapors from building up. Leaks happen, even with best intentions, so every site needs spill kits tuned for hazardous organic liquids. Absorbent pads, proper neutralizers, and a plan for quick action can keep a messy situation from turning disastrous. All staff should train regularly—muscle memory matters more than written protocols in real emergencies.

Transportation: Extra Precautions on the Road

Shipping ethyl chloroacetate is about controlling the unexpected. Leaky caps, poorly packed drums, or a crash mean headaches and danger down the line. Certified packaging, designed to meet the latest UN recommendations, holds up in rough conditions and less than gentle handling. Labels make a difference: well-marked containers tell everyone, from truck drivers to customs agents, that they need to watch out.

Regulation isn’t just paperwork; it’s the backbone of safe chemical transport. Ethyl chloroacetate lands on lists as a hazardous material in almost every country, so licensed carriers and drivers should always handle it. Record-keeping isn’t busywork either; accurate manifests and safety data sheets mean fast, focused response in the event of a spill or accident.

Looking at Practical Solutions

Seeing accidents up close changed my thinking about chemical safety. Investing in high-quality containers, double-checking seals, and building a culture where anyone speaks up about suspicious smells or leaks save trouble and money in the long run. Sharing real tales of near misses in safety meetings makes the risks real and builds habits that stick.

Tools like chemical tracking systems, staff refresher courses, and regular audit walk-throughs help spot gaps and prevent complacency. Simple steps, taken seriously and backed by real-world experience, prevent most mistakes. Respecting a chemical as dangerous as ethyl chloroacetate is about more than staying out of trouble with regulators—it’s about health, lives, and peace of mind.

What are the common hazards and first aid measures for Ethyl Chloroacetate exposure?

Common Hazards of Ethyl Chloroacetate

Ethyl chloroacetate doesn’t get much attention outside chemical labs or industrial settings, but working around it calls for real care. The liquid carries a sharp, fruity smell, which can fool people into thinking it isn’t much of a threat until symptoms kick in. Skin contact, inhalation, or swallowing even small amounts can lead to quick and nasty reactions. I have seen technicians show up at the emergency room tingling or short of breath, not linking their symptoms to handling this chemical at work.

Common issues with ethyl chloroacetate include burns and blistering where it touches the skin, and headaches, dizziness, or even a temporary blackout if it’s inhaled. Anyone splashed in the eye has reported severe pain, tearing, and blurred vision. The vapors sneak up too—breathing them can make your chest tight, give you a cough that won’t go, or stir up nausea right away. Prolonged exposure can sometimes sensitize people, so they get worse reactions with less contact over time. Some facts cannot be skipped: the chemical's acute toxicity ranks high, with very low permissible exposure limits. Just a whiff above the limit, and folks run real health risks.

First Aid Measures

Responding quickly and calmly can protect someone’s health. I’ve learned to treat every exposure like it matters—even folks who “feel okay” sometimes end up in real trouble if they wait for symptoms.

If someone gets ethyl chloroacetate on their skin, strip off any contaminated clothing and wash the area with plenty of cool running water and plain soap. I always stress not to scrub, even with stubborn marks—rubbing makes burns worse. Specialized neutralizers may offer some help, but water does the heavy lifting. Watch for signs of blistering later since some chemical burns take time to develop.

For splashes in the eyes, rinse with water right away, using an eyewash station or any source of clean, running water for at least fifteen minutes. Keep the eyelids apart to really wash out every trace. Don’t let anyone rub their eyes, however much it hurts. Most eye clinics recommend professional attention after any chemical splash, so erring on the side of caution never hurts.

Inhalation exposure means getting out of the contaminated area fast. Move to fresh air—ideally outdoors—and loosen anything tight around the neck. People sometimes try to tough it out, but coughing, dizziness, or trouble breathing signals the need for medical help, not waiting it out. Sometimes, oxygen or even respiratory support at a clinic becomes necessary.

Swallowing ethyl chloroacetate counts as a serious emergency. Don’t make the person throw up, despite the old advice; this can do more harm. Rinse out the mouth thoroughly with water, and get emergency care immediately. Bringing the chemical’s container or label to the hospital helps staff give the right treatment.

Why Preparation Matters

It’s easy for people to become complacent around chemicals they handle daily. Simple habits—like knowing where the emergency shower is, or keeping protective eyewear that doesn’t fog up—save time when every minute counts. Regular drills, clear labeling, and real-life scenario training turn good intentions into action.

Having straightforward first aid instructions posted where people can read them quickly also goes a long way. Lab managers shouldn’t assume everyone remembers training from three years ago. Up-to-date, easy-to-follow steps in visible areas help, especially under stress. Keeping first aid kits stocked with the basics, plus spare protective gloves and eyewash, is real-world risk management—not just checking a box for inspectors.

Many of these fixes stem from experience. Small investments—better signage, regular refresher sessions—can limit the harm oz the worst day someone faces on the job. Even if you never have to put the plan in action, having one ready brings peace of mind that isn’t easy to measure.

Ethyl Chloroacetate
Ethyl Chloroacetate
Ethyl Chloroacetate
Names
Preferred IUPAC name Ethyl 2-chloroacetate
Other names Chloroacetic acid ethyl ester
Ethyl 2-chloroacetate
2-Chloroacetic acid ethyl ester
Ethoxycarbonylmethyl chloride
Pronunciation /ˈiːθɪl klɔːroʊəˈsiːteɪt/
Identifiers
CAS Number 105-39-5
Beilstein Reference 635873
ChEBI CHEBI:17604
ChEMBL CHEMBL44432
ChemSpider 6081
DrugBank DB14060
ECHA InfoCard 100.003.225
EC Number 205-309-9
Gmelin Reference Gm.857
KEGG C00886
MeSH D002509
PubChem CID 7026
RTECS number KJ7175000
UNII NS5A3O2F8U4
UN number UN1181
Properties
Chemical formula C4H7ClO2
Molar mass 122.53 g/mol
Appearance Colorless to slightly yellow transparent liquid
Odor fruity odor
Density 1.14 g/mL at 25 °C (lit.)
Solubility in water Soluble
log P 1.02
Vapor pressure 6.6 mmHg (20°C)
Acidity (pKa) pKa = 2.87
Basicity (pKb) Ethyl Chloroacetate has a pKb value of approximately 15.
Magnetic susceptibility (χ) -5.27 × 10⁻⁶ cm³/mol
Refractive index (nD) 1.414
Viscosity 1.68 mPa·s (20°C)
Dipole moment 2.00 D
Thermochemistry
Std molar entropy (S⦵298) S°₍₂₉₈₎ = 322.9 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -487.7 kJ/mol
Std enthalpy of combustion (ΔcH⦵298) -702.8 kJ/mol
Hazards
GHS labelling GHS02, GHS07, Danger, H226, H302, H315, H319, P210, P280, P305+P351+P338
Pictograms GHS02,GHS06
Signal word Danger
Hazard statements H302, H312, H332, H319
Precautionary statements P210, P260, P280, P301+P310, P305+P351+P338, P332+P313, P403+P235
NFPA 704 (fire diamond) 2-3-1-W
Flash point 50 °C
Autoignition temperature Example: 437 °C
Explosive limits Upper: 11.5%, Lower: 2.9%
Lethal dose or concentration LD50 oral rat 1600 mg/kg
LD50 (median dose) LD50 (median dose): Oral, rat: 1600 mg/kg
NIOSH KJ0700000
PEL (Permissible) PEL (Permissible Exposure Limit) for Ethyl Chloroacetate is "1 ppm (5 mg/m³)".
REL (Recommended) 0.3 ppm (1 mg/m3)
IDLH (Immediate danger) 100 ppm
Related compounds
Related compounds Chloroacetic acid
Methyl chloroacetate
Isopropyl chloroacetate
Chloroacetyl chloride
Ethyl bromoacetate