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2-Chloroallyl N,N-Diethyldithiocarbamate: The Story, the Impact, and the Road Ahead

Historical Development

Looking at the timeline of chemical discoveries, the story of 2-Chloroallyl N,N-Diethyldithiocarbamate doesn't often find a spotlight outside specialist circles. This compound, a representative of the dithiocarbamate family, emerged out of the growing twentieth-century interest in combating pests and improving yields in agriculture. Chemists exploring sulfur-organic bonds in fungicides and pesticides realized that tinkering with the structural motifs of dithiocarbamates could bring new properties to the table. Years of lab work pulled this molecule out of obscurity, cementing its place in practical agricultural chemistry. The surge in global population, food demand, and the threat of agricultural diseases pressed scientific minds to go deeper, search for agents that could offer more than the classic copper-based formulas or basic carbamates.

Product Overview

Most people outside of crop science or organic synthesis don’t recognize this chemical by name, but its presence underpins crucial protective roles, especially where mold or fungus bites into global food security. Its action doesn’t work by brute force; instead, it leverages subtle chemical pathways to block specific enzymes or disrupt vital cell structures in pests or pathogens. These capabilities created a market for intermediates in rubber vulcanization, pesticide synthesis, and sometimes medicine. Year after year, growers and chemists alike pressed for solutions that wouldn’t just hammer pests into submission but would do the job with fewer knock-on ecological effects and manageable residues.

Physical & Chemical Properties

2-Chloroallyl N,N-Diethyldithiocarbamate shows up as a crystalline solid, sporting a distinctive yellow-green hue. It doesn’t hide its identity; that sulfur-rich aroma is unmistakable if you’ve ever worked with thiol compounds. Solubility behaves as you'd expect from a molecule carrying both non-polar and slightly polar features: moderate compatibility with organic solvents like acetone or chloroform, but not with water. Decades in the lab have shown it to be thermally stable through moderate heat, yet sensitive enough to break down when exposed to strong acids or bases. This balance between stubbornness and reactivity forms the backbone of both its usefulness and its risk profile. Handling this compound without proper extraction hoods or gloves can quickly introduce headaches or skin discomfort, so the tools matter as much as the chemical knowledge.

Technical Specifications & Labeling

Labels on containers holding this substance make no attempt at ambiguity—they deliver clear warnings, hazard symbols, and concentration data. Legal standards in most jurisdictions force suppliers to outline the purity, melting point, and storage temperature in language regulators understand. These guidelines don’t spring from bureaucracy alone; they stem from incidents past, where mishandling or mislabeling left some users jeopardized. Specifications bridge science and safety, dictating conditions such as limits on allowable impurities, moisture content, and shelf-life. Without these milestones, the risk of accidental exposure or degraded performance rises fast, especially in bulk applications.

Preparation Method

The process of making this compound rarely leaves room for improvisation. Synthetic chemists usually combine diethyldithiocarbamate salts with 2-chloropropene or related chlorinated intermediates, using carefully controlled temperatures and stoichiometry. Side products creep in unless the variables are watched with care—too much heat and you’ll break the sulfur bonds; too little and the conversion rate plummets. Purification relies on extraction and crystallization skills honed over years. Cutting corners leads to by-products that could sabotage the entire batch, so every technician I’ve known insists on quality checks at every stage, even if quotas loom large. Experience teaches that investment in robust process controls isn’t optional—it’s survival.

Chemical Reactions & Modifications

Reactivity defines much of the utility for compounds like 2-Chloroallyl N,N-Diethyldithiocarbamate. Modifications at the chloro group offer chemists entry points for further derivatization, be it for agricultural chemistry, pharmaceuticals, or material science. It works as a nucleophile, engaging in substitution reactions that slap on fresh functional groups or ring systems. In industry, tweaking the basic structure lets you aim for improved specificity—perhaps targeting a narrower spectrum of pests or dialing down toxicity against non-target species. Each experiment represents not just academic curiosity but the grounded hope for tools with more function and less fallout. Failures abound, but the odd breakthrough gets woven into best practices downstream.

Synonyms & Product Names

From dusty procurement sheets to reference databases, this compound walks under various names: 2-Chloroallyl N,N-Diethyldithiocarbamate, S-(2-Chloroallyl) Diethyldithiocarbamate, or even specialty trade names depending on the intended use. The patchwork of aliases sometimes confuses newcomers and slows effective communication between regulatory authorities, research labs, and industries. Over time, best practices ask for stricter harmonization—one chemical, one name, wherever possible. This clarity helps avoid safety mishaps, intellectual property disputes, and misapplied research findings.

Safety & Operational Standards

Anyone handling this chemical spends more time studying safety procedures than reading about its synthetic versatility. Skin or inhalation exposure carries real risks, ranging from mild irritation to more stubborn systemic effects. Proper protective equipment, efficient air extraction, and clear emergency procedures form the backbone of any facility using or storing this chemical. Regulatory compliance, from OSHA in the United States to REACH in Europe, cuts through any temptation toward shortcuts. Lessons from old lab accidents or warehouse fires stick with working professionals, reminding them that vigilance beats regret any day. Routine training, not just one-off seminars, reinforces the culture of attention this industry needs.

Application Area

Fields as varied as modern agriculture, polymer science, and experimental pharmacology find a place for this compound. Its roots run deepest in agrochemicals, where growers use it as a pre-plant or seed treatment to check the advance of specific soil-borne pathogens. Rubber production also leans on dithiocarbamates to improve vulcanization and produce more robust, flexible products. Sometimes, researchers use it as a tool in biochemistry or toxicology, employing its reactivity to probe enzyme systems or as a lead structure for developing new analytical standards. The breadth keeps growing—not because of hype, but through demonstrated performance under real-world conditions.

Research & Development

Every institution striving to secure food supplies, battle environmental threats, or deliver new material technologies includes dithiocarbamates somewhere on its R&D map. Whether it’s tweaking substitution patterns to blunt environmental persistence or chasing ever-faster decomposition times, the research agenda doesn’t sit on comfortable laurels. New analytical techniques—spectroscopy, chromatography, high-throughput screening—keep squeezing new insights out of old systems. Funding bodies, once cautious, have started backing multidisciplinary teams focused on sustainable synthesis, green chemistry, and lifecycle management. Field trials last over more than a season, measuring both target efficacy and off-target environmental shifts. Translating lab data into marketplace solutions calls for teamwork bridging synthetic chemists, toxicologists, and regulatory affairs experts.

Toxicity Research

Deep dives into safety profiles don’t aim just to check regulatory boxes, but to protect ecosystems and human health over generations. Toxicologists examine acute and chronic exposure scenarios, from lab rats to environmental runoff in water bodies. Studies chart the metabolic fate of the molecule, seeking to illuminate pathways for high or low toxicity. Sometimes, intermediate metabolites raise red flags, sparking reformulations or new restrictions. Academic collaborations play a role, too, often supported by independent review panels to keep the process transparent. Advances in computational modeling and genomics now allow the field to predict long-term impacts before they play out, shifting the balance toward prevention.

Future Prospects

The unfolding story of 2-Chloroallyl N,N-Diethyldithiocarbamate points in several directions. Pressures from tighter environmental regulations, consumer demand for cleaner production, and rising costs of legacy agrochemicals drive a search for alternatives and refinements. Some stakeholders see the next decade as a pivot point, where biodegradable analogues or enhanced application technologies could make older formulations less attractive. Others push for integrated pest management strategies, treating such compounds no longer as silver bullets but as components within a wider toolbox. Research communities align efforts with the circular economy—designing molecules that perform, degrade, and leave behind minimal trace. My own work, like that of many colleagues, circles back to the maxim that progress gets shaped less by breakthroughs than by careful, honest appraisal of risks, benefits, and real-world tradeoffs.




What is 2-Chloroallyl N,N-Diethyldithiocarbamate used for?

Meet the Chemical with a Lot of Syllables

Most people never say “2-Chloroallyl N,N-Diethyldithiocarbamate” at their kitchen table. This compound works quietly in the background, tucked away in industrial settings and science labs. It doesn’t make headlines, but it plays its part where it matters, especially in agriculture and manufacturing. My first encounter with the stuff didn’t come from a chemistry class—someone talked about it at a farm, flipping through a bag of seeds. Turns out, some seeds get a chemical cloak, breaking them free from diseases that linger in the soil.

The Fungicide on Your Seeds

Corn fields and wheat beds stretch far and wide because farmers beat disease that would wipe out crops. Diseases like smut, bunt, or damping-off could turn a promising harvest into a loss. Seed companies treat seeds with 2-Chloroallyl N,N-Diethyldithiocarbamate and push back against fungi and soil-borne nasties. While many folks spend time arguing about pesticides and their impact, this kind of treatment keeps yield strong and food supplies stable. I saw this play out during a season when untreated seeds produced spotty patches and treated ones grew healthy stands, saving all the work and money poured into that land.

Rubber and the Tire Industry

The chemical doesn't just stick to farms. Rubber factories bring it in because it acts as a vulcanization accelerator. Vulcanization means you harden rubber, getting car tires and even shoe soles tough enough for daily pounding. Factories that skip this invisible helper end up paying for weaker products—tires losing shape and grip, boots splitting at the seams. Economic impact grows from there. Rolling out strong tires at lower cost matters for anyone who needs transportation. It shows how chemicals from the “unseen shelf” shape everyday life, beyond the grocery aisles and medicine cabinets.

Worker Safety and the Need for Guardrails

Safety always rides shotgun with industrial chemicals. The compounds do their jobs, but not without risk if handled carelessly. Skin contact can cause irritation; in some cases, breathing the dust brings bigger concerns. I’ve known friends who spend their days in rubber plants, and rules around chemical handling mean they go home in better health. Gloves, masks, and regular training can keep trouble at bay. Regulators step in by tracking exposure and keeping limits strict—the Environmental Protection Agency lists this compound among those needing close management. Following those standards becomes the balance between progress and protection, a lesson I’ve witnessed after a few close calls in a farm supply warehouse gone wrong.

Alternatives and Looking Forward

People push for greener routes as concerns over the environment grow. Researchers hustle to find fungicides or accelerators that stick closer to nature without losing effectiveness. From what I’ve followed in chemical trade journals, new blends pop up but don’t fully elbow aside older formulas like 2-Chloroallyl N,N-Diethyldithiocarbamate. Switching over takes investment, and farmers and manufacturers watch costs. Some boosters vouch for organic or biological treatments, but backing them with consistent results comes slow. For now, this chemical hangs on, helping to feed people and move them from place to place, waiting for science to hand off the baton.

What are the safety precautions when handling 2-Chloroallyl N,N-Diethyldithiocarbamate?

Why Lab Safety Gets Personal

I’ve worked in labs where strange-smelling powders and murky liquids regularly land on the bench top. 2-Chloroallyl N,N-Diethyldithiocarbamate stands out because of its tricky nature and the questions it brings up about safety. Safety practices often go beyond lab manuals—they keep your skin, lungs, and peace of mind intact. Handling this compound, skipping steps can land you in a hospital bed or, worse, with long-term issues nobody wants to talk about until it’s too late.

Knowing What’s at Stake

Most MSDS sheets highlight the usual: skin, eyes, lungs. This chemical brings together a reactive chloro group and a sulfur-rich dithiocarbamate backbone. One whiff, and your nose tells you it isn’t something to get casual about. Even brief exposure can irritate your skin or eyes, while inhaling dust or vapor runs risks from coughing fits to serious respiratory struggles. Swallowing even a small amount is downright dangerous. If this product gets in your eyes, you risk chemical burns and even vision changes. On bare hands, it can leave more than just redness—prolonged or repeated exposure can trigger allergies after just one bad encounter.

What Works: Gloves, Goggles, and Good Habits

Some people assume any generic glove or goggle does the job. I’ve learned nitrile gloves and tight-sealed face protection go much further than quick fixes like latex or loose glasses. Choose gloves and goggles rated for chemical splash—not just dust. This compound loves to sneak through pinholes and tiny gaps. No glove lasts forever, so change them if splashes land on your hands.

Fume hoods aren’t overkill. I spent my first semester as a grad student believing a cracked window “helped.” Airborne dithiocarbamates don’t play nice. Always weigh and transfer this powder under a properly functioning hood. Wipe down surfaces after any use—even a tiny spill can stick around, waiting to cause a rash on the next shift. Open containers only when tools and trays are clean and dry.

No Substitute for Common Sense

I used to see lab coats thrown over chairs. A real, chemical-resistant coat, buttoned up, keeps your arms protected. Wash it every week if you’re working with these sorts of substances. I always keep a jug of eye wash and a drench shower at arm’s reach. You’ll never regret knowing you can decontaminate in seconds if splashes catch you.

Ditch snacks and drinks in the workspace—nobody wants to ruin lunch over a sloppy transfer. Labeling matters, too. Never trust memory or faded masking tape; write dates, initials, and full chemical names. The last thing you need is confusion while reaching for a bottle during crunch time.

Building a Culture That Lasts

Safety training works best when everyone buys in. Encourage newer students or staff to ask questions and call out risky shortcuts. Open discussion lets experienced hands share stories—sometimes, hearing how a near-miss happened makes the dangers real. If you see someone handling a chemical carelessly, step in. Collective mindfulness wins out over top-down mandates every time. In my years at the bench, the teams that joked, reminded, and watched out for each other rarely sent anyone to the campus clinic.

The goal isn’t just to avoid disaster—it’s to keep science fun and futures open. Treat 2-Chloroallyl N,N-Diethyldithiocarbamate with respect, choose your gear wisely, keep your station clean, and look after your team. Safety isn’t a checklist; it’s a habit that keeps you coming back to the lab ready to work another day.

What is the chemical structure and molecular formula of 2-Chloroallyl N,N-Diethyldithiocarbamate?

The Backbone: Breaking Down the Formula

2-Chloroallyl N,N-Diethyldithiocarbamate brings a hefty name, but its makeup holds no mystery for anyone with some background in organic chemistry. Its molecular formula, C8H14ClNS2, packs in carbon, hydrogen, a chloride, nitrogen, and sulfur. Plenty of agrochemicals and fungicides use this chemistry to disrupt unwanted growth and shield crops. The backbone—an allylic compound—gives the molecule its reactive side, thanks to the double bond and the presence of chlorine at the second carbon atom. Attach that to the N,N-diethyldithiocarbamate group, and it’s clear how the molecule picks up both its stability and its knack for biological activity.

Why Structure Matters for Function

Chemistry and farming went hand in hand for as long as I can remember. The way atoms line up in a chemical like this goes beyond textbook curiosity. Chlorine offers a direct impact: it alters the electron-rich sites, making the molecule far more likely to bind to specific enzymes in pests or fungus. The two ethyl groups on the nitrogen offer bulk and increase the overall molecule’s oil solubility. That’s great for the chemical’s ability to spread across plant surfaces or move through insects’ defenses.

Visualizing the structure, you’ve got an allylic chain—CH2=CH-CH2—with a chlorine dangling off the middle carbon. Hooked onto this is the dithiocarbamate fragment (N(C2H5)2-CS2), where the nitrogen ties to two ethyl groups and side by side sulfur atoms finish the tail. Together, these features make a powerful agent for disruption, especially in agricultural sprays and soil treatments aiming to keep crops safe from blight or root rot.

Potential Hazards and Considerations

Any compound containing both chlorine and a dithiocarbamate backbone waves a few red flags in the lab. I’ve read reports showing that these molecules, while potent, can break down under sunlight or in moist soils, sometimes turning into compounds that might harm fish or useful insects. Regulatory agencies like the EPA keep their eyes open and suppliers on their toes for these reasons. Limiting runoff and managing application methods become just as important as the original chemistry lesson.

Improving Use and Reducing Risk

Having handled dithiocarbamate products, I found basic steps like careful mixing, shielding sprays from waterways, and sticking to labeled rates do a lot to limit risk. Research into less persistent breakdown products promises to make these tools safer over time. Developing coatings and slow-release formulas also helps by delivering the right dose instead of flooding the soil or plants. University outreach programs in farming communities point out these chemical structures, show people what they’re really handling, and bring up questions that matter: How long before it breaks down, and who or what might it affect in the meantime?

Why All This Detail Matters

On any given day, organic chemists, agronomists, and environmental scientists come together over molecules like 2-Chloroallyl N,N-Diethyldithiocarbamate. They draw out the structures, review data on uptake and toxicity, and keep one eye on tomorrow’s solutions. Without getting lost in jargon, it’s clear that understanding both the formula and the layout of atoms helps everyone—from the person spraying a field to the researcher charting the future of crop protection. The closer we look, the more informed our choices become, putting chemical knowledge to work for healthier crops and a safer world.

How should 2-Chloroallyl N,N-Diethyldithiocarbamate be stored?

Understanding the Substance Beyond the Label

2-Chloroallyl N,N-Diethyldithiocarbamate comes with a name that’s mouthful, but the reality is pretty simple: this chemical catches the eye of folks dealing with fungicides, rubber, and agriculture. Years spent around chemical storerooms taught me that a little care and a bit of respect for what you’re handling matter. Overlooking how you store a substance like this doesn’t just eat through your budget—it can put health and safety on the line.

Treat Moisture and Heat as Enemies

Moisture and heat play tricks on chemical stability. Humidity interacts with 2-Chloroallyl N,N-Diethyldithiocarbamate, breaking it down and pulling harsh odors into the air. Even a small spill can start to irritate your throat and eyes. Heat speeds up decomposition, ramping up the chance of dangerous byproducts. I learned to keep these chemicals sealed tightly, using original containers with clear hazard labels, and checking the caps, lids, and locks on bottles every few weeks.

Ventilation Means Protection

Breathing in the fumes isn’t just unpleasant—it’s risky. Anyone who’s spent time in a cramped chemical closet without decent airflow recognizes that dizzy feeling and the sting in the nose. Good ventilation clears the air, literally. Storing the chemical in spaces with vents, fans, or windows cuts down on fumes and keeps accidental exposure on the lower side. Sometimes, a fume hood or exhaust fan made all the difference in a lab I once worked in, especially after a cracked bottle let out its punchy aroma.

Segregation of Chemicals Reduces Hazard

Stacking containers of 2-Chloroallyl N,N-Diethyldithiocarbamate next to strong oxidizers or acids is asking for trouble. It’s like putting matches with gasoline. I remember one warehouse try to squeeze everything in for convenience, and a small leak mixed with the wrong neighbor ended up bringing hazmat in. Keeping chemicals physically separated, with dedicated shelves, color-coded bins, and even secondary containment trays, stops cross-contamination and prevents reactions even when spills happen.

Personal Protection and Clear Information

PPE (personal protective equipment) isn't just for show. Gloves and splash-proof goggles come in handy, especially while opening or transferring small batches. Spills or splashes can harm skin and eyes quickly. Keeping the material safety data sheet (SDS) nearby gives anyone at the storage location the vital info—what to do if there’s a spill, a fire, or accidental contact. That sheet deserves an easy-to-spot place, close to the stock, not locked in an office drawer.

Long-Term Storage: See It as a System, Not a Chore

Over time, containers get worn or the contents react with the packing. Inspect containers every few months for cracks, bulging, or leakage. Rotate old stock to the front and send unopened product to the back. Quick checks save on big headaches like emergency cleanups or environmental fines. If you notice unusual smells, discoloration, or damaged packaging, don’t take a chance: isolate the container and bring in professionals.

Final Thoughts: Building Respect, Not Fear

2-Chloroallyl N,N-Diethyldithiocarbamate demands sensible handling. Every chemical has its quirks and hazards. Safe storage starts with knowing these risks and investing in simple routines—sealed containers, solid labeling, regular checks, clean airflow, and common sense. These steps work whether you’re in a giant facility or a small shop. Safety culture saves money, prevents harm, and earns trust from coworkers and regulators. Build that respect, and you don’t have to worry about which bottle hides the next surprise.

What are the potential health hazards of 2-Chloroallyl N,N-Diethyldithiocarbamate exposure?

Connecting the Dots from Chemistry to Daily Health

Chemicals with long names often stay in textbooks and laboratories, but some make their way into real-world use. 2-Chloroallyl N,N-Diethyldithiocarbamate stands as one of those chemicals that doesn’t get public attention until problems surface. This compound often appears in agriculture and rubber production. Most folks never interact with it at home, but for workers and communities near manufacturing sites, the story changes.

How the Body Reacts to This Compound

After years of working around industrial chemicals, one lesson sticks out: people suffer most when the rules for safety and health fall short. 2-Chloroallyl N,N-Diethyldithiocarbamate can cause trouble for the skin, lungs, and internal organs. Once on the skin, irritation happens fast. Rashes, redness, and blisters sometimes follow just a short exposure. If this chemical turns up in the air, it tends to irritate eyes and throats. Workers might complain about coughing or burning sensations in their nose, especially when ventilation runs poorly or protective gear gets ignored.

Swallowing or inhaling higher concentrations ratchets up the risk. Some research links exposure to damage in the liver and kidneys, organs that filter and process toxins. Odd tastes and upset stomachs hint at mild poisoning, but unchecked contact or spills bring more severe symptoms. Early research and case reports highlight dizziness, headaches, and sometimes nerve problems. These effects don't always show up right away—sometimes the danger comes from repeated or prolonged encounters with just a little every day.

The Bigger Picture: Environmental and Long-term Impacts

Once released into soil or water, this chemical doesn’t vanish. It can linger, migrating through soil and possibly seeping into local drinking water. Environmental persistence means that exposure may reach beyond employees, affecting families and neighbors. This is a pattern seen before: a chemical made for one job seeps out and poisons more than its intended target.

Studies on long-term effects keep trickling in, but one thing stands clear—chronic exposure heightens the risk of organ damage and possibly cancer. The U.S. Environmental Protection Agency and other watchdogs flag this substance for careful handling. Some scientists point out a lack of comprehensive human studies, urging the need for more clarity as technology advances.

A Personal Take on Practical Solutions

Decades in the field taught me no shortcuts beat solid prevention and education. For workers, gloves, masks, and daily hygiene make the biggest difference. Washing up before meals, using protective sleeves, and keeping chemical containers sealed sound simple but save lives. Companies that invest in regular safety training and keep spills contained do more good than any after-the-fact treatment.

Communities can press for greater transparency. Mandatory spill reports and easier access to information empower those living nearby. Policymakers willing to visit worksites and listen to workers—not just managers—end up making safer laws. Agencies should keep pushing for better testing, tracking the compound in soil and water near major users.

In the end, lowering exposure always works out better than treating harm after it’s done. Simple steps—education, protection, and oversight—stand as the foundation for long-term health where chemicals like 2-Chloroallyl N,N-Diethyldithiocarbamate play a role.

2-Chloroallyl N,N-Diethyldithiocarbamate
2-Chloroallyl N,N-Diethyldithiocarbamate
2-Chloroallyl N,N-Diethyldithiocarbamate
Names
Preferred IUPAC name N,N-Diethylcarbamodithioate; 2-chloroprop-2-en-1-yl
Other names Vapam
SDC
Carbam
CDEC
Pronunciation /tuː-klɔːroʊ-ˈæl.i.l naɪˌnaɪ diːˌɛθ.ɪlˈdaɪθaɪ.oʊˌkɑːr.bə.meɪt/
Identifiers
CAS Number 1476-36-4
3D model (JSmol) `/carbon3dmodel/2C1ClH2N(C2H5)2CS2/jsmol`
Beilstein Reference **126668**
ChEBI CHEBI:83437
ChEMBL CHEMBL502661
ChemSpider 23243804
DrugBank DB08439
ECHA InfoCard 03e8e56e-b8fd-41d4-8994-3c2b4fa401bb
EC Number 216-043-3
Gmelin Reference 79589
KEGG C18602
MeSH Dichlormate
PubChem CID 153884
RTECS number KH8925000
UNII W8NN095900
UN number UN3077
CompTox Dashboard (EPA) DTXSID9050605
Properties
Chemical formula C8H14ClNS2
Molar mass 221.80 g/mol
Appearance Light yellow liquid
Odor Unpleasant
Density 1.08 g/cm³
Solubility in water Insoluble in water
log P 2.96
Vapor pressure 1.2 x 10^-3 mmHg (25°C)
Acidity (pKa) 11.21
Basicity (pKb) 6.51
Magnetic susceptibility (χ) -64.5 × 10⁻⁶ cm³/mol
Refractive index (nD) 1.563
Viscosity Viscous liquid
Dipole moment 3.61 D
Thermochemistry
Std molar entropy (S⦵298) 519.6 J·mol⁻¹·K⁻¹
Pharmacology
ATC code S01XA10
Hazards
Main hazards Harmful if swallowed. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation. Toxic to aquatic life.
GHS labelling GHS02,GHS07
Pictograms GHS06,GHS08
Signal word Warning
Hazard statements H302, H315, H319, H335
Precautionary statements P261, P264, P270, P271, P272, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P308+P311, P312, P321, P330, P332+P313, P333+P313, P337+P313, P362+P364, P403+P233, P405, P501
Flash point 80 °C
Autoignition temperature Autoignition temperature: 320°C
Lethal dose or concentration LD50 oral rat 175 mg/kg
LD50 (median dose) LD50 (median dose): Oral rat 510 mg/kg
NIOSH KN5075000
PEL (Permissible) PEL (Permissible Exposure Limit) for 2-Chloroallyl N,N-Diethyldithiocarbamate: "15 mg/m3 (skin)
REL (Recommended) 0.1 mg/m³
IDLH (Immediate danger) Unknown
Related compounds
Related compounds Dazomet
Metham sodium
Thiram
Zineb
Maneb