Wusu, Tacheng Prefecture, Xinjiang, China admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:



1,1-Diphenylhydrazine: Unpacking the Legacy, Properties, and Prospects

Historical Development

In the changing landscape of chemical research, 1,1-Diphenylhydrazine has carved out a role shaped by utility and intrigue. More than a century ago, organic chemists started isolating a range of hydrazine derivatives, driven partly by the search for new pharmaceuticals and dye intermediates. The ancestry of 1,1-Diphenylhydrazine rides on those efforts, rooted in curiosity about nitrogen-rich organic compounds. As aromatic chemistry matured in the late 19th and early 20th centuries, researchers recognized the potential in diphenyl structures for tailoring molecules that could react in multiple ways, paving the way for a broader understanding of both synthetic routes and reactivity patterns. After its identification, 1,1-Diphenylhydrazine emerged as both a reagent and a subject in its own right, illustrating how organic synthesis can lead to practical and theoretical breakthroughs alike.

Product Overview

Plenty of hydrazine compounds catch a chemist’s eye, but 1,1-Diphenylhydrazine provides a sharp contrast with its simple but bulky structure. Formed by linking two phenyl rings through a hydrazine core, it stands out due to its aromatic features and ability to serve as a building block in both academic and industrial labs. This molecule is not usually found as an end-product on the shelves of drug stores or hardware suppliers. Instead, chemists use it for synthesizing other specialty molecules, exploiting its nitrogen content and reactivity with both electrophilic and nucleophilic agents. Every lab notebook that’s included this molecule bears witness to how versatile organic compounds can change direction depending on the needs and creativity of the experimenter.

Physical & Chemical Properties

From the perspective of someone who has handled a variety of aromatic compounds, the properties of 1,1-Diphenylhydrazine display a familiar pattern. It forms off-white or slightly colored crystalline solids under ambient conditions, with the aromatic rings lending a faintly sweet, chemical odor—nothing like the harshness of aliphatic hydrazines. The melting point falls in a range familiar to those who work with substituted benzenes, usually above room temperature. Insolubility in water gives it clear separation from many inorganic hydrazines, while solubility in organic solvents like ethanol or chloroform allows for a flexible approach in the lab. Chemically, its reactivity traces back to the hydrazine backbone, which can be oxidized or used to form azo, azoxy, or other nitrogen-rich compounds. Anyone who has watched the evolution of color in a test tube after adding an oxidizing agent to this compound understands the promise and caution associated with nitrogen chemistry.

Technical Specifications & Labeling

Researchers demand strictness in labeling, purity, and verification when dealing with intermediates like 1,1-Diphenylhydrazine. Pure forms are expected to reach upwards of 98% purity in reputable catalogs, and documentation includes melting points, batch numbers, and storage requirements. Given the substance's stability under recommended conditions, labs store it away from heat, light, and oxidizers in tightly sealed bottles with universally recognized hazard labels. The need for clear labeling grows from both the toxic potential and regulatory framework that governs hydrazine derivatives, reminders that even familiar substances require respect and diligence.

Preparation Method

Manufacturing 1,1-Diphenylhydrazine often starts with the reduction of azobenzene, a process that can be accomplished with a variety of reducing agents. Instructors remember the thrill of demonstrating sodium dithionite or other reducing agents as they transform bright orange azobenzene into something colorless, a tangible moment as the hydrazine backbone takes shape. Alternatives range from catalytic hydrogenation to metal-acid reductions, with each route offering a tradeoff between yield, scalability, and selectivity. This chemistry underscores a broader truth: modifying reaction conditions, tweaking reagent concentrations, and carefully controlling temperature can make or break yields, and long hours spent optimizing these factors reflect a dedication seen in synthetic chemistry across the globe.

Chemical Reactions & Modifications

The true value of 1,1-Diphenylhydrazine lies in its readiness to undergo further transformation. The –NH–NH– core is primed for N-alkylation, N-acylation, or oxidation, serving as a link in making compounds that appear in modern dyes, pharmaceuticals, and analytical reagents. Oxidation forms azobenzene or azoxybenzene, a lesson in balancing redox chemistry that anyone who’s run thin-layer chromatographies can appreciate. Coupling reactions, often catalyzed by transition metals, extend its utility, taking the molecule far beyond its simple starting form. In each case, its dual phenyl groups offer both steric hindrance and pi-stacking options, factors that both hinder and enable further synthetic creativity. Anybody navigating the challenges of multi-step synthesis sees 1,1-Diphenylhydrazine as a pivot point—a molecule with enough stability to handle but reactive enough to change.

Synonyms & Product Names

Language in chemistry often confuses outsiders, and this compound is no exception. Besides the official IUPAC title, it turns up under names like N,N-Diphenylhydrazine or hydrazinodiphenyl, as well as older identifiers in regional catalogs. Commercial supply houses might abbreviate or rebrand, but most researchers recognize the key structure embedded in every alternative name. Decoding these synonyms is as much a part of chemical training as running the actual reactions.

Safety & Operational Standards

Few things matter more in a lab than managing risks tied to toxicity and reactivity. Although 1,1-Diphenylhydrazine does not carry all the extreme hazards of simple hydrazine, its aromatic core and nitrogen content demand mindfulness. Gloves, goggles, and well-ventilated spaces are not optional. Chronic exposure can carry health impacts, and researchers rely on both institutional protocols and personal discipline to avoid spills, inhalation, or chronic skin exposure. Safe disposal routes, built around minimizing nitrogen compound releases, reflect lessons learned the hard way—through the history of industrial accidents and incremental improvements to safety culture. There’s nothing abstract about exposure limits or ventilation requirements: every chemist remembers incidents, large or small, that reinforce the habit of double-checking the fume hood.

Application Area

Every molecule that finds its way onto a lab shelf carries legacy uses and new potential. For 1,1-Diphenylhydrazine, historical ties to dye production remain relevant, as the chemical world continues to revisit classic aromatic transformations. Analytical chemists use it as an intermediate for color development or as a reagent to identify certain functional groups, particularly because of its interactions with transition metals and electrophilic centers. In pharmaceutical development, derivatives serve as platforms for candidate drugs, never quite becoming mainstay blockbusters but offering new routes to bioactivity. Collections of research articles reveal its use in the specialty chemicals sector, feeding into polymers, advanced materials, and even agrochemical testing. Every course on advanced organic synthesis revisits its story, and with the ongoing expansion of green chemistry, old molecules like this keep returning in fresh approaches and applications.

Research & Development

Progress in organic chemistry never sticks to a fixed path, and 1,1-Diphenylhydrazine stands as proof that even longstanding molecules offer new research possibilities. Scientists continue to apply this compound in exploring new C–N bond formation techniques, understanding mechanisms of electron transfer, and refining synthetic methodology. Material scientists examine its utility in creating specialized organic electronic components or as precursors for novel polymers. For all the advances in technology, every new method still leans on a foundation laid by earlier generations who first worked out its reactivity and stability. Peering into contemporary literature, one finds that even now, researchers evaluate spin-off molecules for use as ligands or catalysts, suggesting that the basic structure has not exhausted its value by any measure.

Toxicity Research

Toxicity profiles for aromatic hydrazines have drawn scrutiny for generations. Research points to concerns about potential carcinogenicity, impacts on liver enzymes, and possible hematological effects. Regulatory agencies use chronic exposure studies, animal models, and structure-activity relationships to predict risks and set exposure guidelines. Responsible researchers stay updated on these findings, prioritizing risk assessments and adequate training for everyone who comes into contact with the compound. Toxicity awareness does not stem only from regulations or paperwork—it grows from collective experience and a hard-won understanding of how mistakes in earlier decades shaped better practices today. Every lab inspection or safety seminar helps to reinforce these lessons, shaping a culture where the drive for discovery does not outpace the commitment to protect colleagues and the environment.

Future Prospects

Organic chemistry keeps cycling through phases of innovation, and classic molecules like 1,1-Diphenylhydrazine stand ready for rediscovery. As modern techniques improve selectivity and sustainability in synthesis, researchers look again at compounds with versatile backbones and multiple reactive sites. There’s genuine intrigue in how this molecule can contribute to future drug discovery, advanced functional materials, or even as a template for new catalysts in green chemistry. Learners and professionals alike benefit from studying past successes and failures involving 1,1-Diphenylhydrazine, shaping better experiments and fostering a deeper understanding of risk and reactivity. By building on a layered history with new technology and ethical rigor, the chemical community keeps expanding what’s possible—reminding everyone that progress often stands on the shoulders of molecules with a proven track record.




What is 1,1-Diphenylhydrazine used for?

Where 1,1-Diphenylhydrazine Shows Up

Factories, research labs, and a handful of chemical plants handle 1,1-diphenylhydrazine for a fairly narrow set of jobs. Its primary use involves making benzidine. Benzidine once sat at the core of dyes for fabrics, coloring leather, and a few plastics, but now folks know benzidine poses real cancer risks. Rules around 1,1-diphenylhydrazine reflect the dangers tied to this process, so strong limits shape what happens around it.

Outside the world of big chemical manufacturing, not a lot of people bump into it. A few researchers dig into it for analytical chemistry or look at its behavior in scientific studies, but these are mostly people in lab coats behind fume hoods. Most people will never find themselves in a situation where they touch, buy, or even see this compound.

Why Handling 1,1-Diphenylhydrazine Raises Red Flags

Concerns over health come first for people working near this chemical. The Environmental Protection Agency and the Centers for Disease Control and Prevention highlight dangers including toxicity and links to cancer. Long-term exposure can harm the liver and kidneys and possibly trigger serious blood disorders. These risks push everyone handling it to use strong gloves, face shields, and heavy-duty ventilation.

Communities living near the factories have a right to ask, “How safe am I?” Small leaks or spills travel through air and water, sometimes showing up in groundwater samples. That opens up questions about long-term effects on people’s health and whether old facilities built before modern rules might have left traces in soil or water.

How to Store and Dispose of It Safely

Companies limit how much they keep around and store every bit in containers designed for strong chemicals. Locks, warnings, and alarms all try to stop accidental contact. If someone tries to dump it down the drain or toss it out with regular trash, the chemical can create more danger, especially for landfill workers and water processing plants. That’s why every gram gets tracked and shipped off to disposal sites that specialize in hazardous waste.

Looking for Alternatives and Reducing Risks

Producing less hazardous waste remains a central goal for chemical companies. Over time, new dyes and plastic materials have stepped up in place of benzidine-based ones, and that means less need for 1,1-diphenylhydrazine. Plants hitting today’s strict environmental standards use better technology for leaks and train staff to spot problems early.

By staying careful and moving toward safer chemicals where possible, workplaces and communities both stand to gain. There will always be a need for certain risky substances in specific fields. Better transparency, new research, and up-to-date safety gear put more control in the hands of workers and local residents. My wish would be to see even greater investment in green chemistry so that substances with these risks become relics of the past, and communities feel secure, no matter what lies behind factory walls.

Is 1,1-Diphenylhydrazine hazardous or toxic?

Understanding the Substance

1,1-Diphenylhydrazine carries a heavy reputation in the world of chemistry. Used in making dyes and certain pharmaceuticals, it grabs attention for all the wrong reasons: its link to health hazards and environmental concerns. The strong, almost chemical-like odor of this pale solid hints at its reactive nature. If anyone has worked in a lab or industrial setting, the warning labels on the drum stand out as loud as sirens.

Health Hazards Cannot Be Ignored

You spend enough years working with chemicals, you learn to respect anything with a track record for toxicity. 1,1-Diphenylhydrazine falls into the group of substances the U.S. Environmental Protection Agency monitors closely. Research points to a risk of cancer and organ damage after long-term exposure. Animal studies show that repeated contact affects the liver, kidneys, and blood system in unsettling ways.

Symptoms hit hard if a person breathes in dust or fumes—think dizziness, headaches, even nosebleeds. Direct contact with skin or eyes can trigger irritation or worse. Not everyone reads safety data sheets, but the ones for this material tell a clear story: handle it with gloves, goggles, and ventilation. People who dismiss these suggestions end up with health problems.

Environmental Impact Spreads Fast

It’s not just personal health on the line. If 1,1-Diphenylhydrazine spills into soil or water, it spreads trouble fast. Local wildlife can absorb toxic chemicals through water, affecting food chains and damaging fragile ecosystems. The U.S. Agency for Toxic Substances and Disease Registry warns about its persistence—meaning, it sticks around in the environment, breaking down slowly and keeping risks alive for months or even longer.

Factories must track and report their emissions by law under the Toxics Release Inventory Program. Disposing of this chemical takes careful planning; dumping it down the drain isn’t just illegal, it’s reckless. Every time regulations catch someone cutting corners, communities nearby deal with contaminated water or sick animals.

The Role of Prevention and Control

Chemicals like 1,1-Diphenylhydrazine prove that caution should never become just a guideline. Strong ventilation systems and proper personal protection make a difference. Regular health checkups for workers in contact with the chemical help catch issues early. Training keeps mistakes down to a minimum—chemistry teachers repeat safety lessons for a reason.

On a bigger scale, stricter policies on chemical release protect both workers and neighbors. Companies have a responsibility to follow the rules. Bringing in new technologies to detect leaks and treat waste before it leaves a facility goes further than just ticking boxes for compliance. Even small improvements in safety can mean the difference between a normal day in the lab and a long-term health problem.

Moving Forward with Caution

Over my time around industrial chemicals, nothing stays more true: hazard labels mean something. Regulations exist because real people got hurt. Communities, scientists, and industry leaders need frank conversations about the risks and clear standards for control. Protecting lives and the planet never deserves shortcuts. If 1,1-Diphenylhydrazine stays in use, oversight and responsibility must always lead the way.

What are the storage and handling precautions for 1,1-Diphenylhydrazine?

Understanding the Chemical

1,1-Diphenylhydrazine turns up in some research labs and certain industrial setups. Its main claim to fame? A pretty versatile role in the synthesis of dyes, pharmaceuticals, and even some pesticides. Once you open a bottle marked with this stuff, things get a little more serious. This compound delivers more than just chemical curiosity—it brings multiple health risks if treated carelessly. Anyone dealing with it experiences the need for clear respect and steady habits.

Storage Precautions

The chemical won’t go up in smoke or dissolve in a puddle if tossed on a shelf, but things can go wrong fast if it’s left under the wrong conditions. High heat breaks it down, giving off noxious or potentially harmful fumes, so you keep it somewhere cool. A standard, well-ventilated chemical storage area away from direct sunlight and heat sources offers safety and longevity. Those tiny differences in temperature sometimes speed up unexpected reactions. Humidity sneaks in and degrades material quality. So, no loose caps—only containers with the tightest seal deserve a spot on the storage rack.

Keeping chemicals apart is not busywork. Anyone who's worked in a crowded chemical cabinet knows: group the acids, bases, oxidizers, and reducers with care. Strong acids and oxidizers don’t get along with 1,1-Diphenylhydrazine. If even a small leak spills into another open container, you could wind up with fires or toxic vapors. Glass containers with solid screw tops usually hold strong against corrosion or leaks—plastic sometimes warps or leaks over time. Labels matter as much as the contents. Faded or misunderstood labels can spark confusion, misplacement, or double dosing, multiplying risks for everyone.

Handling Practices

Most harms come not from dramatic explosions, but from unintentional skin contact, inhalation, or accidental ingestion. My own practice involves long sleeves, nitrile gloves, goggles, and a splash-proof lab apron anytime the bottle leaves storage. Using a fume hood isn’t overkill; with 1,1-Diphenylhydrazine, it’s smart. Anyone who’s underestimated fumes before knows they linger in closed spaces and can take you by surprise with headaches, irritation, or much worse.

Transferring chemical powder or liquid without spills takes patience. Gravity works against quick hands. Pour slow, keep bench tops uncluttered, and clean up the second anything drops. Keeping emergency gear ready—think eyewash bottles, safety showers, spill kits—makes the difference during accidents. Simple habits leave room for fewer regrets.

Disposal deserves its own focus. Dumping leftover material in general waste causes headaches later. Collected hazardous waste gets delivered to certified disposal sites. My workplace logs every transfer, records every disposal, and trusts only trained staff for the chore. These habits comply with state and federal rules, avoiding fines and—more importantly—accidents.

Supporting Safer Standards

Research on 1,1-Diphenylhydrazine and related compounds confirms links to several health risks, from acute poisoning to possible links with cancer. The US Environmental Protection Agency and the Occupational Safety and Health Administration flag strict limits, covering everything from permissible exposure to handling standards. Regular safety audits, proper labeling, and documented safety protocols keep everyone alert and in compliance. Safety culture isn’t abstract; it’s built by the person who never skips a glove or skips the logbook, no matter how rushed the day.

Respect for chemicals like 1,1-Diphenylhydrazine means upholding habits, not shortcuts. From storage to final disposal, attention to detail prevents dangers before they appear.

What is the chemical structure of 1,1-Diphenylhydrazine?

Looking at the Molecule

1,1-Diphenylhydrazine stands out in the world of organic chemistry. Its formula, C12H12N2, signals a structure rooted in two benzene rings and a hydrazine group. The backbone includes a chain of nitrogen atoms, attached to the first position of each. The two phenyl rings do not stack side by side—they anchor themselves to one nitrogen, while the other nitrogen sits with two hydrogens.

If you draw it out, the molecule carries a phenyl group on each side of a single nitrogen atom, then connects to the second nitrogen. The connection looks like this: Ph–N2–Ph (Ph representing a phenyl ring). The real shape bends slightly, a small angle between the rings, which stems from the electron distribution.

Why This Structure Matters

Chemistry teaches you that small changes in structure can shift a compound's reactivity, toxicity, or how it behaves when mixed into other things. With 1,1-Diphenylhydrazine, those phenyl rings add stability. They act like guards, making the core hydrazine group less reactive than it looks on paper. These rings can block other chemicals from reaching the nitrogen atoms. That matters if you plan to use the compound for synthesis, since it changes which reactions work and which ones stall.

I once worked in a lab where we tested dyes and intermediates for pharmaceuticals. 1,1-Diphenylhydrazine's structure allowed us to use it in coupling reactions without too much risk of unwanted explosions or fast decomposition—a problem often seen in simple hydrazine derivatives. Experience taught me early on you cannot ignore the bulky groups on a molecule, since they steer what you can safely do with it.

Risks and Health Considerations

Despite stability, 1,1-Diphenylhydrazine still carries the risks tied to hydrazine. The nitrogen-nitrogen bond can break down, especially under heat. Inhalation can cause harm, and lab protocols treat the compound with care. Regulatory studies list potential links to cancer in some animals, prompting safety gloves, eye protection, and fume hoods for anyone using the chemical in practice.

The Environmental Protection Agency classifies related hydrazines as hazardous, and Europe’s REACH program tracks companies handling it. Documentation demands up-to-date procedures, since researchers and workers need clear details to stay safe. I recall a colleague's minor skin exposure, which led to an immediate review of our safety protocols—it reminded us that even seemingly stable molecules deserve respect.

Better Practices for Safer Use

Labs and factories working with 1,1-Diphenylhydrazine should anchor their processes to clear procedures and reliable chemical training. Storing the chemical in airtight, labeled containers away from heat helps keep things safe. Responding quickly to spills with the right neutralizers and protective equipment gives staff more control over hazardous situations.

Education comes in as the best upfront solution. Teaching trainees how small changes to a molecule’s structure alter handling needs or toxicity can prevent many mistakes. Those phenyl rings give a sense of security, but no chemical in this group should be handled without clear respect for its risks and requirements.

How should spills or exposures to 1,1-Diphenylhydrazine be managed?

Facing Chemical Spills: Taking Responsibility Seriously

Picture a small lab during a late-night research shift. Someone drops a flask. A clearly marked bottle oozes a light yellow substance across the bench. Few folks recognize the name, but the label reads “1,1-Diphenylhydrazine.” In these moments, protocol isn’t just bureaucracy — it means keeping people safe and the work environment healthy. 1,1-Diphenylhydrazine is not just some rare chemical sitting out of sight. It can trigger harmful effects — ranging from eye and skin irritation to more dangerous impacts with longer-term or higher exposures. The National Institute for Occupational Safety and Health (NIOSH) links overexposure to symptoms like headaches, nausea, and in animal studies, even cancer risks. Knowing how to act in that split second saves a lot of trouble down the line.

Clear Steps Save Lives

If something spills, don’t look for a shortcut. Evacuate anyone unnecessary from the area — no heroics. One lesson I learned early on: Always trust the safety goggles and gloves, even if it “looks clean enough.” Ventilation can make a huge difference, so open windows or crank up the fume hood. Never sweep a powder spill with a dry broom. Proper absorbent materials—think commercial spill kits with neutralizers—work best for small releases. For liquid, absorb before collecting any waste. Designate chemical containers for disposal so nothing hazardous gets thrown in regular trash. Place everything in the proper hazardous waste stream. Inhaling vapors by accident or touching bare skin leads to unnecessary trips to health professionals—or worse.

Staying Prepared: Not Just a Checklist

Fresh training keeps everyone sharp. I remember instructors repeating, “If you don’t review your emergency plan, you’ll forget it at the wrong moment.” Regular drills matter more than just ticking a box — they actually helped me remember the spill protocol when my nerves tried to freeze up. Keep spill kits and personal protective equipment stocked. Never store flammables near heat or open flames. Make sure Safety Data Sheets (SDS) sit somewhere easy to grab. SDS notes tell you what to expect and how to treat accidental exposures — they’re written for emergencies, not just compliance officers.

Facing the Human Side of Exposure

Once, a colleague wiped up a small drop without gloves, convinced it “wasn’t much.” His skin flared up minutes later. He washed up, but reporting even tiny exposures meant getting checked out by occupational health. They stressed the real risks do not always depend on the size of the spill. Immediate rinsing eyes or skin under running water, swapping to clean clothing, and seeking medical attention beats underestimating a chemical’s punch. This experience changed the culture around me: nobody jokes about “toughing it out” after that.

Building a Culture of Safety

Genuine care for coworkers helps establish a respectful safety culture. Peer-checking protocols isn’t micromanagement — it keeps people healthy enough to go home at night. For employers, investing in the basics, like updated training and clear signage, pays off. The Occupational Safety and Health Administration (OSHA) outlines these expectations clearly, treating safety violations with fines — or shutting labs entirely. It all starts with the everyday choices: recognize potential hazards, act quickly on spills, report exposures, and protect both yourself and your team. Simple steps, but they prove their value every day.

1,1-Diphenylhydrazine
1,1-Diphenylhydrazine
1,1-Diphenylhydrazine
Names
Preferred IUPAC name N-phenylidenebenzenamine
Other names N,N-Diphenylhydrazine
Hydrazobenzene
Pronunciation /ˌwʌnˌwʌn daɪˈfɛnɪl haɪˈdræziːn/
Identifiers
CAS Number 122-66-7
Beilstein Reference 395679
ChEBI CHEBI:51072
ChEMBL CHEMBL15640
ChemSpider 17252
DrugBank DB06710
ECHA InfoCard 03a4d925-9668-4bad-a968-9c72ef8fa9a4
EC Number 202-218-8
Gmelin Reference 68263
KEGG C02572
MeSH D004190
PubChem CID 7518
RTECS number MV3150000
UNII CEU1V7N70H
UN number UN2582
Properties
Chemical formula C12H12N2
Molar mass 198.26 g/mol
Appearance White to yellow crystalline solid
Odor aromatic
Density 1.16 g/cm³
Solubility in water Slightly soluble
log P 1.96
Vapor pressure 1 mmHg (at 106°C)
Acidity (pKa) 15.68
Basicity (pKb) 6.83
Magnetic susceptibility (χ) -41.5×10⁻⁶ cm³/mol
Refractive index (nD) 1.617
Viscosity 1.34 cP (25°C)
Dipole moment 2.83 D
Thermochemistry
Std molar entropy (S⦵298) 322.5 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) 104.9 kJ mol⁻¹
Std enthalpy of combustion (ΔcH⦵298) -1977 kJ/mol
Hazards
Main hazards May cause cancer. Causes damage to organs through prolonged or repeated exposure. Harmful if swallowed. Causes skin and eye irritation. Suspected of causing genetic defects. Harmful to aquatic life with long lasting effects.
GHS labelling GHS02, GHS07
Pictograms GHS06,GHS08
Signal word Warning
Hazard statements H302 + H332: Harmful if swallowed or if inhaled.
Precautionary statements P260, P264, P270, P301+P312, P330, P501
NFPA 704 (fire diamond) 1,1-Diphenylhydrazine: 2-2-0
Flash point 143°C
Autoignition temperature > 550°C
Lethal dose or concentration Lethal dose or concentration (LD50): "LD50 oral (rat): 369 mg/kg
LD50 (median dose) LD50 (median dose): 210 mg/kg (oral, rat)
NIOSH WY2450000
PEL (Permissible) PEL: 5 mg/m³
REL (Recommended) 0.5 mg/m3
IDLH (Immediate danger) IDLH: 50 mg/m³
Related compounds
Related compounds Hydrazine
Aniline
Azobenzene
Benzidine
1,2-Diphenylhydrazine