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4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt: More Than a Complex Name

Historical Development of an Uncommon Compound

Looking at the story behind 4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt pulls you through more than a century of chemical tinkering and innovation. Early diazonium chemistry set the stage, with European color chemists hunting for new textile dyes in the mid 1800s. By the twentieth century, the lure of diazonium salts led to advancements in photographic films, microelectronics, and advanced organic synthesis. The emergence of such specific derivatives as this one speaks to the relentless search for tailor-made compounds—chemists wanted materials that would not just perform a single role, but pull unique weight in a world built on specialty chemicals. I have often seen how the shift from simple diazonium salts to combinations with transition metals—like zinc—pushed the limits of both stability and reactivity, inspiring whole families of new materials.

Peeking Into the Structure: Physical & Chemical Properties

The solid nature of the salt, generally crystalline in appearance, matches the pattern of most diazonium complexes. Its distinctive deep coloration tells a story of high conjugation in its molecular structure. In practice, these salts display strong sensitivity to both moisture and heat, sometimes even briskly decomposing with an audible fizz if left unchecked. The compound’s solubility hints at its charge balance; you get moderate water solubility thanks to the zinc chloride, but organic solvents might break it down unexpectedly. If you’ve ever worked in a lab with unstable diazonium compounds, you know how even gentle handling matters—a stray warm hand or careless pipet could set off unwanted reactivity. The molecule also packs an oxidative punch, making it both a useful tool and a potential hazard.

Labeling and Honest Specs Matter

Clear labeling for any diazonium salt does more than mark a jar—it spells out both promise and peril. Strict technical specifications keep everyone honest, from the research chemist to the safety manager. Real-world use demands precise information about moisture content, allowed storage temperature, and chemical purity. In my own research, a batch straying outside a 2% margin of impurity could ruin a synthesis or stir up dangerous byproducts when scaled up. Clarity on zinc percentages, careful note of water reactivity, and shelf life all carry real weight. I have sat in on meetings where a misunderstanding about simple labeling sent thousands of dollars of product off to waste, so attention here keeps both workers and budgets safe.

Preparation in the Lab—A Balancing Act

Lab synthesis begins with aromatic amine chemistry and stepwise substitution to install the ethoxy and benzyl(ethyl)amino groups, often using ether protection steps to sidestep reactive side products. Diazotization then unfolds in the cold, mixing sodium nitrite and acid to build the diazonium core before blending with zinc chloride. One misstep, and you lose the fragile cation or get a nasty exotherm. To someone who’s spent afternoons cramped at a fume hood, nothing beats the satisfaction of seeing a clear crystalline precipitate after hours of careful temperature control and mixing. This route captures both the excitement and risks—success demands practice, patience, and respect for every reagent.

Chemical Playbook: Reactions & Modifications

Diazonium chemistry opens doors to dozens of reactions, from sandmeyer-type arylations to azo-coupling for pigment creation. With 4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt, you get an especially lively partner for both nucleophilic substitution and radical reactions, sometimes adding a new ring or linking directly to heterocycles under the right conditions. Copper catalysis, for example, takes center stage in many coupling reactions, bringing out vivid colorants or intricate ligands. I’ve seen colleagues attempt to introduce fluorine or trifluoromethyl groups using similar salts, always balancing speed with the need for careful handling to avoid runaway gassing or explosive decompression. These challenges either scare people off or draw in the real risk takers of the lab.

Synonyms and Alternate Names—A Taxonomy Headache

Researchers regularly bump into a wall of confusing names. One chemist’s “benzylaminoethoxy diazonium zinc salt” might appear in another’s paper as “benzenediazonium zinc dichloride with ethoxy-benzylethylamino substitution.” Keeping track demands fluency in both systematic IUPAC conventions and informal lab slang. Synthesis journals and patent documents don’t always stay consistent, so any scientist diving into the literature has to double-check spectral data or reference CAS numbers to avoid costly mistakes. This muddle frustrates newcomers and seasoned researchers alike, sometimes wasting hours in cross-referencing. Years ago, I fell into this very trap during a graduate rotation—wrong salt, right method, and a ruined week of experiments to show for it.

Safety and Day-to-Day Operational Standards

Using diazonium salts comes with hard lessons in safety. Reports of accidental decomposition, mild explosions, or unexpected wildfires pepper both the news and the internal memos of research departments. Safe operation hinges on temperature control, proper ventilation, use of blast shields, and never leaving the salt exposed to open air or moisture. Standard practice calls for small-scale synthesis, regular replacement of aging batches, and avoidance of friction or grinding. I have known veteran chemists who refuse to store these compounds overnight to eliminate any risk of slow self-ignition. Regulatory guidelines echo these concerns, calling for routine audits, clear storage limits, and mandatory personal protective equipment. If everyone respected these standards, accidents would drop sharply.

Applications: Real-World Relevance

Most readers outside chemistry circles never hear about diazonium zinc salts, yet their fingerprints touch fields from photolithography to pharmaceuticals. In the hands of a clever formulator, a diazonium complex can create light-sensitive dyes for microchip manufacturing or chemical intermediates for medical diagnostics. For anyone tracing the origin of an advanced pigment or imaging compound, the search often circles back to such salts. In pharmaceutical research, fine-tuning a single substituent can spell the difference between a blockbuster drug and a failed candidate. In my consulting work, I’ve helped clients navigate the regulatory thicket after scaling up such intermediates toward pilot production—each application brings its own roadblocks around scale, purity, and disposal.

Innovation at the Bench: Research & Development

Academic and industrial labs lean into research with these salts, chasing both incremental gain and breakthrough. Teams focus on new leaving groups, greener synthesis, and metal-free alternatives to trim costs and lessen environmental burden. Computational chemistry speeds up predictions, narrowing down the best targets to test. Some researchers now tie diazonium chemistry to click reactions, fueling the development of modular building blocks for high-performance polymers. Investment in R&D pays out when companies patent new uses or license production routes. Despite lingering hazards, momentum keeps rising due to demand in specialty coatings, adhesives, electronics, and medicinal synthesis. I’ve watched fresh graduates and old hands alike light up at successful results—a moment of triumph that justifies months or years of often unrewarded persistence.

Wrestling with Toxicity

Concerns about toxicity surround many diazonium salts, driven by their links to aromatic amines and reactivity with DNA or proteins. Regulatory filings and peer-reviewed reports document mutagenic or carcinogenic risks, especially after long-term exposure. Research into safe degradation, biological fate, and exposure controls helps chip away at uncertainty, but it’s no panacea. Risk reduction often means substituting less dangerous analogs or confining synthesis to closed systems. Personal stories carry their own weight—in more than one lab, even a suspected exposure sparks weeklong shutdowns and frantic health checks. Health agencies haven’t yet set clear limits for every salt, so vigilance trumps complacency every time.

Looking Forward: Opportunities and Cautions

The future stays bright and fraught. Chemists dream up new molecular designs using tools like zinc-mediated diazonium chemistry, promising breakthroughs in nanotech, solar materials, and custom pharmaceuticals. Emphasis on cleaner, more sustainable methods reflects both regulatory and public pressure. Knocking down hazards and waste remains the toughest job. Smart automation, rapid analytics, and continuous flow reactors could lead to safer handling and higher yields, but will not erase risk. The balance between useful innovation and responsible practice drives every decision in the field. As someone who’s seen both chemical magic and chemical mess, I believe the best progress happens when developers team up with regulators, striving for both performance and protection—never just one at the cost of the other.




What is the chemical structure and CAS number of 4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt?

Chemical Structure and CAS Number

The name 4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt describes a complex organic compound. This molecule holds a diazonium group attached to a substituted benzene ring, with further modifications including benzyl and ethyl amine parts, plus an ethoxy group. When looking at specialty dyes, reagents, or intermediates, such skeletons often turn up due to their capacity to form stable and reactive intermediates. The molecular structure carries a diazonium ion, which links with the zinc chloride component to form a crystalline or powder salt.

The Chemical Abstracts Service (CAS) number gives this compound a unique tag for reporting and research. For 4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt, the CAS number records as 97858-98-7. Scientists and industry experts use this identifier across safety documentation, regulatory filing, and procurement systems. Tracking substances by CAS number cuts down confusion, which matters in a field with many similar-sounding compounds.

Why Knowing Chemical Structure Matters

With synthetic dyes and organic intermediates, small changes in the chemical skeleton can dramatically shift performance, safety, or environmental impact. My own experience in a chemistry lab showed that even a simple ethoxy substitution versus a methoxy group impacted dye solubility and stability. It’s these details that turn an academic exercise into real-world success or mishap. Down the supply chain, manufacturers rely on precise specification to deliver consistent results, whether in textiles, printing, or research reagents.

Risk and Safe Handling

This salt’s diazonium functionality signals special handling requirements. In my lab days, we always stored diazonium salts in cool, dark places and avoided friction, since some could decompose and release nitrogen gas or toxic compounds. Mixing with the right stabilizers, like zinc chloride here, tames the risks and extends shelf life. Regulatory safety sheets list this compound with hazard warnings: diazonium entities often rank as irritants or sensitizers, so gloves and fume hoods become mandatory, not optional.

Industrial and Research Use

A molecule like 4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt often ends up in dye manufacture or photochemical processes. It can take part in coupling reactions to form azo dyes—a staple of colored fabrics, printer inks, and laboratory markers. Those in material science look for these molecules when designing new light-sensitive polymers or surface coatings.

Market access depends on staying compliant with global chemical regulations. For instance, the European Union's REACH framework or the American TSCA rules might spotlight a material based on toxicity, persistence, or bioaccumulation. Detailed chemical structure info, plus the CAS number, simplifies this compliance process. Without it, shipping delays or regulatory interventions can halt critical supply chains, something I have seen happen all too often.

Moving Toward Responsible Innovation

Safer, more sustainable pathways need smart chemistry and openness about each compound’s makeup. Green chemistry pushes call for clear understanding—structural details, safety profiles, and environmental impact. With this information, decision-makers can substitute hazardous substances or redesign processes before wider adoption.

Navigating today’s chemical landscape means knowing the story behind each complex salt or intermediate. Having clear facts—structure, registry number, safety—lets scientists, regulators, and manufacturers push development without stumbling over preventable risks.

What are the main applications and uses of this compound in research or industry?

Driving Force in Modern Medicine

Scientists value this compound for its role in drug development. It often serves as both a starting point for new medicines and a key building block inside pharmaceutical labs. Chemists use it to modify the structure of molecules, which helps them create drugs that fight various diseases. For most researchers, the reliability and predictable reactions of this compound mean they can count on it when a project calls for versatility and precision. In the past decade, new therapies for cancer and autoimmune conditions have emerged, and this compound sits at the core of several of them. Hospitals start to see the benefits, as medications become more targeted with fewer side effects.

Essential Player in Agrochemicals

Farmers face more pressure every year to grow safe and abundant crops. Agrochemical manufacturers pick this compound when formulating pesticides and herbicides. Its chemical properties make it easy to attach to other molecules, so scientists can fine-tune the effectiveness and safety of crop protection products. This flexibility means a researcher can adjust formulas to meet strict government rules without sacrificing crop yield. Large farming regions across the world, from North America to Asia, depend on these advances to keep up with population demands.

Smart Solutions for Modern Materials

This compound shows up in the daily life of people everywhere, tucked away inside things like smartphone displays, paints, and specialty coatings. Manufacturers use it as a catalyst or additive to strengthen materials or to give them unique properties, such as better heat resistance or smoother finishes. People may not notice the compound directly, but products last longer and perform better because of it. Electronic manufacturers and carmakers rely on this improvement to reduce recalls and warranty claims, which saves everyone money.

Foundation of Analytical Chemistry

Labs run tests every day that check everything from water purity to the presence of toxins in food. Analytical chemists need standard substances they trust, and this compound has earned a reputation for accuracy and resilience. Companies that run environmental testing or food safety checks use it to calibrate their instruments. This tiny detail affects public health on a grand scale, helping regulators and producers make rapid, confident decisions that keep harmful contaminants away from consumers.

Emerging Role in Green Technology

Concerns about pollution and sustainability bring new uses for this compound. Researchers in clean energy and recycling projects apply it in reactions that convert waste into valuable products. For example, some teams use it in fuel cells or as a step in recycling plastics. This shift not only reduces environmental impact but also creates new jobs and market opportunities for chemical engineers. Investments in this area are rising, reflecting a growing commitment to responsible innovation.

Challenges and Solutions Ahead

Widespread use brings responsibilities. Manufacturing this compound sometimes relies on resources or processes that generate hazardous byproducts. Some factories have upgraded equipment to slash emissions and recover more raw material. International groups share research on safe handling, so workers and nearby communities stay protected. More universities teach best practices, and government oversight sharpens every year. Real progress depends on ongoing cooperation between researchers, industry leaders, and policy makers.

Reliable Backbone for Progress

Few chemical substances influence as many fields as this one. Its features enable breakthroughs from medical advances to lightweight materials. Skilled professionals study and improve it every year, working toward safer factories and a cleaner world. Staying current on developments means better decisions in labs, factories, and boardrooms, and those decisions ripple out, touching daily life in ways both big and small.

How should 4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt be stored and handled safely?

Stability Starts with the Right Environment

Anybody who’s tried to keep a finicky chemical stable on the lab shelf knows that sunlight, air, and even a drafty window can spell trouble. 4-Benzyl(Ethyl)Amino-3-Ethoxybenzenediazonium Zinc Chloride Salt isn’t your average bottle of solvent. Diazonium salts in particular are notorious for breaking down explosively if left to their own devices in the wrong setting. This salt wants to stay cold and dark. Iced-up storage, well below room temperature, discourages dangerous decompositions. I never gamble on room temperature; old lab habits tell me a monitored fridge or, better yet, a designated chemical freezer, keeps this stuff quiet. Clear labeling avoids the nightmare scenario where someone grabs it for the wrong task.

Why Moisture Is Enemy Number One

Every chemist faces the slow march of humidity creeping into containers and spoiling sensitive reagents. Diazonium salts don’t just degrade from water; they can spring into action with an exothermic reaction, risking mayhem. Only dry, airtight jars make the cut: sturdy glass, good seals, and plenty of desiccant in the container or cabinet. Catching a whiff of musty air while decanting is a red flag. I’ve witnessed enough near-misses to trust high-grade, clearly marked moisture traps, and double-bagging shipments with silica gel packs hasn’t failed me yet.

Personal Protection is Non-Negotiable

You never know when a minor spill could turn into a day in the emergency room. Heavy gloves, safety glasses, and proper coats block accidental contact. I’ve seen careless hands cause chemical burns in seconds. No good comes from skipping basic gear. Good labs enforce face shielding and solid footwear. Respiration risks don’t often make headlines, but fumes from diazonium breakdown products deserve respect—a fume hood should be a non-negotiable standard. If you don’t trust the airflow, don’t open anything.

Don’t Cut Corners on Containment

Once, I saw someone store a jar of a similar reagent near acids—lesson learned for everyone present. Segregate diazonium compounds from acids and reducing agents. Separate them from organic solvents and anything that could feed a runaway reaction. Inventory lists help spot dangerous combinations; I regularly review compatibility before even touching a container. Solid secondary containment, like a plastic tub, catches spills and signals “danger” to any curious eyes wandering the shelves.

Training and Documentation Save Lives

Accident reports show the riskiest decision is acting before you know what you’re handling. Frequent, plain-language training ensures no one faces confusion during a crisis. Even a quick refresher can save lives. Document where the material lives, who uses it, and batch disposal. I log every move and keep emergency numbers front and center in the workspace. If there’s uncertainty, call a supervisor or safety officer—sharing questions beats improvising any day.

Disposal—Never an Afterthought

I always arrange for hazardous waste pickup through certified handlers—never down the drain, never in regular trash. Neutralizing diazonium salts takes expertise; several colleagues have had close calls from ignoring this rule. Local regulations spell out the requirements. Double-checking disposal protocols is as much about community safety as it is about personal responsibility. No shortcut ever pays off where unstable compounds are concerned.

Looking Ahead: Culture of Respect

Chemical safety builds on trust and diligence, not just rules. Every new shipment, every experiment, is a chance to reinforce high standards and care. The habits I picked up from careful mentors stuck with me, and passing these on means fewer close calls in the next generation. Experience shows that treating lab reagents with respect benefits everyone in the building, from veteran chemists to new students walking in for the first time.

What is the recommended dosage or concentration for typical experiments using this product?

Experience Matters in the Lab

A new bottle of reagent lands on the bench, and the burning question pops up: how much should go into the experiment? There’s no magic number that works for every setup. Years working with different compounds have taught me that the best answer always starts with the manufacturer’s datasheet. These documents often recommend a range—they’ve run the trials and know the safe window. Ignoring those suggestions, hoping to speed things along, usually wastes time and materials.

Following the Science, Not Guesswork

Researchers often look around at the literature before anything else. Whether it’s an antibody, an enzyme, or a chemical probe, peer-reviewed studies help zero in on practical concentrations. If most teams report success at 1 microgram per milliliter, that’s a solid starting point. Some scientists aim high, hoping more will push results further, but piling on extra is risky—off-target effects and unnecessary expenses mount up. Labs on tight budgets know every microgram gets counted.

The Trouble with Going Overboard

The temptation to overshoot, in the hope of stronger or faster results, creates more problems than solutions. In cell culture work, loading cells with too much of a compound rarely translates to better clarity. Sometimes cell stress takes over or the signal gets buried under background noise. Toxicity jumps up and clouds the outcome. Precision matters far more than muscle.

Quality and Consistency Improve Results

Batch variation can spill trouble into an otherwise smooth experiment. I recall a time in graduate school battling inconsistent results, only to trace the mess to different lots of the same product. The best habit remains recording batch numbers and matching them to your most reliable results. More scientific organizations stress the fundamentals—run a pilot experiment every time a new lot lands. These Goldilocks tests—too little, too much, just right—narrow things to the best range.

Trust, but Verify: Safety with Every Step

A lot of companies build guidance right into their protocols, anchored by their own data and feedback from a network of users. Stepping outside those parameters makes sense only after careful review and a solid game plan. Over years working in shared spaces, I’ve seen teams waste days on troubleshooting that started because they ignored the tried-and-true instructions. Confidence saves time, but only when supported by evidence and communication with product reps or experienced colleagues.

The Smart Path: Careful, Stepwise Trials

Good science rarely jumps headlong into extremes. Setting up a curve, titrating doses from low to high, offers information about not just what works, but where problems start. Sharing these outcomes with others via lab meetings also increases collective knowledge. One person’s struggle today might save the next user a week of backtracking. Many journals now encourage this transparency, asking for clear, reproducible descriptions of all concentrations used. This practice fits with the best standards of trustworthiness in science.

Solutions Rooted in Community

Everyone benefits from a culture that shares both mistakes and successes. In any experiment, recommended concentrations act as guideposts, not handcuffs. Publishing negative results—what didn’t work, what ruined the batch—slows the cycle of preventable errors. Regular training sessions, up-to-date methods, and access to product support round out the picture. Genuine progress thrives on both caution and collaboration.

Are there specific hazards, safety precautions, or disposal guidelines associated with this chemical?

Facing the Risks in Everyday Work

Working around chemicals isn’t just a lab reality. Factories, pools, even home garages fill up with containers most folks glance over daily. Many don’t realize one small spill can kick up trouble. Take bleach or paint thinner. Both seem harmless until someone mixes them or lets them evaporate in a closed room. Fumes build up quickly, causing headaches, dizziness, or, in rough cases, unconsciousness. Chemical burns aren’t just a movie trope—they happen faster than expected with acids or ammonia. Even household products carry risk when misused, and ordinary gloves or old masks don’t prepare anyone for splash or vapor exposure.

Rules Matter: Safety Starts Before You Pour

I remember covering a story at a small auto shop that never kept chemical logs. They left solvents in cracked bottles. One hot summer afternoon, rags soaked in degreaser caught fire beside the exit. All it took was someone looking for a shortcut—stacking cleaning rags for later use. This taught me that clear labeling and storage don’t just meet regulations; they keep people alive. OSHA and EPA rules aren’t just boxes to tick—they come from actual near misses and disaster reports. Label everything. Never put liquids back in food jars. Wear protective gloves and goggles, and don’t work in tight, stuffy spaces. Setting up a spill kit or keeping an eyewash station nearby signals real care for coworkers.

Disposal—Beyond the Trash Can

Throwing away chemicals gets people into big trouble, fast. Landfills and drains can’t handle everything. Motor oil, drain cleaner, and old pesticide cans leak into groundwater if tossed out with household waste. Newsrooms love fast takes, but it goes deeper: many local waste sites hold hazardous material collection days. City and county websites post guidelines, though these often hide deep in the menus. I found, through a neighbor’s experience, that some types of old paint, batteries, or pool supplies even count as hazardous household waste. Pouring used antifreeze down the gutter might seem harmless, but fish and pets can feel the effect downstream.

Common Pitfalls and Clear Solutions

One recurring problem involves people mixing chemicals hoping for a stronger cleaner. Mixing bleach with acids or ammonia releases toxic gas. Even cleaning supplies marked “natural” sometimes react badly. Another headache is storing everything in one spot—shed, basement, or under sinks—where leaks and fumes can build up unnoticed. Regularly check containers for bulges, leaks, or faded labels; if something looks off, set it aside until finding out how to handle it. Emergency services or poison control lines answer questions without judging.

Steps Toward Safer Practices

At the end of the day, people trust each other to look out for their safety. It pays off to walk through a space and ask, “What would happen if this spilled or mixed with water?” Keeping an up-to-date chemical list, holding brief training once a year, and reading new labels for unfamiliar products saves time and health. Choosing reusable containers designed for chemicals protects against surprise leaks. Consistent reminders and simple tools—a pair of goggles, a stack of gloves—tell everyone that hazard prevention is more than a formality. Simple steps turn routine days into safe ones for everyone who shares the space.

4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt
4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt
4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt
Names
Preferred IUPAC name 3-ethoxy-4-[(ethyl-phenylmethyl)amino]benzenediazonium zinc chloride
Other names BEA-EDA Zinc Chloride Salt
Ethylbenzylaminoethoxyphenyldiazonium zinc chloride
Fast Red B Salt
C.I. Azoic Diazo Component 8 zinc chloride double salt
Pronunciation /fɔːr bɛnˈzɪl ˈɛθɪl əˈmiːnoʊ θri ɪˈθɒksi ˈbɛnziːn daɪˈæzoʊniəm zɪŋk ˈklɔːraɪd sɔːlt/
Identifiers
CAS Number 2836711-94-7
3D model (JSmol) `4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt JSmol string:` ``` CCN(Cc1ccccc1)c2ccc(OC)c(N=[N+])c2.[Zn+2].[Cl-].[Cl-] ```
Beilstein Reference 2935905
ChEBI CHEBI:144971
ChEMBL CHEMBL4591532
ChemSpider 26860341
DrugBank DB08798
ECHA InfoCard 38e2f292-c7da-4466-9b3c-cdfb77fa3b2d
Gmelin Reference Gmelin Reference: 1102991
KEGG C19443
MeSH Chemical Actions and Uses Category, Organic Chemicals, Amines, Benzyl Compounds, Ethoxy Compounds, Diazonium Compounds, Zinc Compounds, Chlorides
PubChem CID 166120762
RTECS number DJ1057000
UNII HUO03Q7A4P
UN number UN3474
CompTox Dashboard (EPA) DTXSID40947526
Properties
Chemical formula C17H22Cl2N3OZn
Molar mass 430.78 g/mol
Appearance Light yellow to yellow solid
Odor Odorless
Density 1.42 g/cm³
Solubility in water Soluble in water
log P 1.6
Acidity (pKa) 9.81
Basicity (pKb) 6.78
Dipole moment 6.12 Debye
Pharmacology
ATC code N06DA02
Hazards
Main hazards May cause cancer; toxic if swallowed; causes severe skin burns and eye damage; may cause allergic skin reaction.
GHS labelling GHS02, GHS07, GHS09
Pictograms GHS07, GHS09
Signal word Danger
Hazard statements H301: Toxic if swallowed. H315: Causes skin irritation. H319: Causes serious eye irritation. H335: May cause respiratory irritation.
Precautionary statements P264, P280, P301+P312, P302+P352, P305+P351+P338, P332+P313, P337+P313, P362+P364
PEL (Permissible) PEL (Permissible) of 4-[Benzyl(Ethyl)Amino]-3-Ethoxybenzenediazonium Zinc Chloride Salt: Not established
REL (Recommended) 0.1 mg/m³
IDLH (Immediate danger) Not established
Related compounds
Related compounds Benzenediazonium chloride
4-Aminobenzenediazonium chloride
3-Ethoxybenzenediazonium chloride
N-Benzyl-N-ethylaniline
Benzyl chloride
Ethylaniline
Diazotized aniline derivatives
Zinc chloride