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2-Naphthylamine Hydrochloride: A Commentary on Progress, Challenges, and Future

Historical Development

Looking back more than a century, 2-naphthylamine hydrochloride came into chemistry labs thanks to relentless curiosity about dyes and organic chemicals. Chemists in late nineteenth-century Europe, pushed by demand from textile and pigment industries, worked out how to pull naphthylamines from coal tar, and soon the hydrochloride salt form landed in research journals. Scientists realized early on this substance packed significant punch in synthetic dye production, yet safety warnings didn’t echo across factories until decades later. The price of industrial progress sometimes comes much heavier than anyone bargains for—those early years lacked both transparency and regulation, and workers paid with their health.

Product Overview

2-Naphthylamine hydrochloride stands out in the world of aromatic amines. Chemically, it’s the hydrochloride salt form of 2-naphthylamine, created to stabilize the notoriously volatile base. This salt improves shelf life and handling, key in both laboratory and pilot-scale settings, where purity and predictability matter. It’s a white to pale tan powder, often sold in tightly sealed drums to block out humidity and light, since even minor moisture triggers degradation. Chemists and suppliers mark this product as non-hygroscopic compared to the base, though real-world storage conditions vary enough to require diligence and regular monitoring.

Physical and Chemical Properties

Anyone handling 2-naphthylamine hydrochloride quickly notices its distinctive, persistent odor—a hallmark of many aromatic amines. Its melting point typically falls just above 200°C, lending stability for shipping but demanding heat control during processing. The salt dissolves easily in water and ethanol, a trait essential for both chemical testing and downstream manufacturing. Under ultraviolet light, solutions show mild fluorescence, tipping off users to possible contamination with other naphthyl derivatives. The compound’s chemical backbone—a naphthalene ring fused to an amine—gives it strong reactivity, especially in electrophilic aromatic substitution and diazotization reactions that form the bedrock of certain dye syntheses and organic intermediates.

Technical Specifications & Labeling

Quality control specialists look for a minimum purity of 98%, which helps reduce risk in experimental runs and commercial production. Labels must list the batch or lot number, manufacture and expiration dates, purity, and suppliers’ contact details—miss one, and regulatory headaches soon follow. Transport regulations classify it under UN2811 (toxic substances), and anyone selling, buying, or using it in regulated economies expects to see hazard pictograms warning of carcinogenicity. Beyond legal compliance, real safety in the workplace comes from visible, durable labeling matched by up-to-date safety data sheets (SDS) at every storage site.

Preparation Method

To make 2-naphthylamine hydrochloride, manufacturers start with beta-naphthol. Through amination with ammonium chloride and iron filings, they convert the naphthol via a reduction process to 2-naphthylamine. After purification, they dissolve the powdered amine in hydrochloric acid, then concentrate the solution and allow crystals to form out as the hydrochloride salt. This method stirs up toxic vapors and both the amine and its salt need careful containment, especially since process residues carry health hazards. Purification steps include solvent washes, vacuum drying, and sieving to reach the purity expected for laboratory and industry uses.

Chemical Reactions and Modifications

Chemists explore 2-naphthylamine hydrochloride for its versatility in forming azo dyes, coupling reactions, and as an intermediate for other nitrogen-containing compounds. Its amine group makes it highly reactive with nitrous acid to form diazonium salts, a necessary step for dye coupling on textile fibers that demand bright, enduring colors. Nitration leads to more complex aromatic structures, while acylation produces stable amide derivatives for specialized dye and pigment lines. The naphthalene backbone helps anchor new substituents, making the molecule a favorite in constructing more elaborate synthetic schemes for pharmaceutical research, despite its declining use due to long-term health risks.

Synonyms and Product Names

The chemical trades under several names: "Beta-Naphthylamine Hydrochloride," "2-Naphthalenamine hydrochloride," "Naphthylamine-2 hydrochloride," or just "2-NA·HCl" in shorthand. Some suppliers use proprietary product numbers or catalog identifiers to stand out in a field crowded with look-alike organic salts. Workers encounter dozens of synonyms in publications and shipping manifests—clear labeling and harmonized documentation remain essential for avoiding dangerous mix-ups.

Safety and Operational Standards

Working with 2-naphthylamine hydrochloride means accepting its well-documented health risks. Direct exposure raises the probability of bladder cancer, a fact proven by occupational medicine and reinforced by decades of epidemiological data. Safety measures start with closed-loop ventilation, high-grade chemical gloves, and lab coats washed separately from home laundry. Eye washers and spill kits belong within arm’s reach in every workspace, because one misstep can cost dearly. Many labs restrict its use to trained personnel only, demanding respirators or fume hoods during opening, transfer, and experimental steps. Disposal follows strict protocols—no short-cuts, no improvisation, since regulatory fines pale next to the human toll of exposure. Reviewing the safety data sheet before every project pays off more than any shortcut.

Application Area

Historically, producers leveraged 2-naphthylamine hydrochloride to make azo dyes for textiles, leather, and paper. Its ability to form strong, colorful bonds once powered fortunes in Germany’s dye industry, making it a staple export for decades. Even as the world grew wary of toxic chemical legacies, chemists kept relying on it for certain specialized dyes and as an intermediate for agricultural chemicals, rubber antioxidants, and experimental drugs. Over time, more environmentally friendly and less hazardous amines pushed it into niche laboratory use, limited mainly to research on aromatic amine chemistry or in the occasional synthesis of reference materials for regulatory labs. The burden of its cancer risk limits its appeal, but the compound still finds mention in older patents or specialty chemical catalogs.

Research and Development

Recent research rarely promotes new uses for 2-naphthylamine hydrochloride, but studies keep investigating its behavior in environmental and biological systems. Analytical chemists map its breakdown products in wastewater, tying chemical persistence to past industrial footprints. Toxicologists simulate its metabolism in human cells, chasing elusive biomarkers of early bladder changes. A handful of synthetic chemists modify the naphthalene ring to test new routes that bypass carcinogenicity, attempting to marry old-school reactivity with new safety profiles. Until the risks subside, most innovation aims not to expand use, but to monitor residues and find safer replacements. Investment in alternate synthetic routes for dyes and specialty chemicals draws on the same principles, yet leans harder toward greener, less persistent molecules.

Toxicity Research

Toxicity defines the modern reality of 2-naphthylamine hydrochloride more than any other property. Decades of investigation show a direct link between workplace exposure and urothelial cancer, a lesson written in the statistics of factory workers from prewar dye plants. Animal studies confirm findings—metabolites of the chemical damage DNA in bladder tissues, and no dose seems truly safe. This legacy shaped occupational health policy worldwide, forcing companies to limit exposures, switch chemicals, or close down production lines. In modern labs, any research involving this carcinogen runs under strict controls, with heavy documentation, disposable gear, double-containment, and real-time air monitoring. Its toxicology profile continues to inform safety standards across the chemical sector, pushing researchers to adopt automation, sealed process flows, and molecular design strategies that avoid similar molecular pitfalls.

Future Prospects

The legacy of 2-naphthylamine hydrochloride underscores how knowledge changes practice in chemical industries. As legacy uses fade, new research focuses on remediation and safer analogs, neither of which bring headlines but both matter for public health. Regulatory agencies around the globe phase out its large-scale use, while still allowing narrowly defined research or testing. Safer, biodegradable aromatic amines rise to fill the vacuum, spurred by stricter laws and far more demanding supply chains. Future prospects depend less on using this compound, and more on learning from its impact—acting before chemicals become widespread threats, choosing molecular frameworks less likely to harm, and investing in technologies that monitor and prevent contamination long before people or nature bear the cost. The enduring example of 2-naphthylamine hydrochloride drives home how full transparency, rigorous oversight, and human-centered chemistry project the most important changes into tomorrow’s laboratories and factories.




What is 2-Naphthylamine Hydrochloride used for?

Roots in the Dye Industry

2-Naphthylamine hydrochloride plays a role in the dye industry. During my chemistry studies, the complexity behind dye production caught my attention. Companies turn to this compound because it helps build certain vivid shades found in textiles and inks. It forms an essential building block for azo dyes, which are known for their strength and brightness. Factories valued these properties back in the 1900s when the textile industry boomed, and many still lean on time-tested formulations that center around 2-naphthylamine-derived dyes.

Historical Workforce Risks

Factory floors didn’t always run on safety-conscious routines. A few decades ago, many who worked hands-on with 2-naphthylamine hydrochloride weren’t told much about what they handled. Cancer risk is the centerpiece in this story. There’s no skirting around it: 2-naphthylamine’s link to bladder cancer is documented in numerous epidemiological studies. Textile and rubber workers from the past bore the brunt of these risks until modern regulations stepped in. These days, Europe and the United States both classify the chemical as a human carcinogen, restricting or outright banning its process use except in highly controlled research settings.

Lessons in Regulation

History shaped public health policies on industrial chemicals. Regulatory bodies like OSHA and the EU’s REACH didn’t appear spontaneously; they exist because people got sick. The shift away from 2-naphthylamine hydrochloride in dye manufacturing didn’t just protect workers, it forced a move toward safer alternatives. Today, research labs still work with the chemical, but strict controls — full PPE, fume hoods, specialized disposal — keep direct exposure nearly zero. If there’s something to learn here, it’s that safety guidelines rarely come before tragedy. There’s a sense of responsibility now woven into every lab and plant handling this stuff.

Legacy in Chemical Research

Chemists use 2-naphthylamine hydrochloride as a reagent for certain organic reactions and analytical methods. In drug development, researchers sometimes reach for old compounds as reference points, benchmarks, or to help shape new synthesis pathways. I remember preparing a lab demo with aromatic amines, watching students’ faces as they learned what these chemicals used to mean for a city’s economy — and for the health of its people. The compound’s use in scientific work still pops up, but no one takes that lightly any longer.

What Safer Chemistry Looks Like

Replacing hazards keeps pushing the industry forward. Stronger employee training, better waste treatment, equipment upgrades, and thorough record-keeping turn risky substances into reminders of what not to repeat. Alternatives to 2-naphthylamine hydrochloride include safer dye precursors, and research keeps moving the line further from carcinogenic risk. For businesses today, the cost of cutting corners is often higher than the price of doing things right. Safer chemical choices and routine audits show that lessons from the past still carry real weight.

Building Trust Through Transparency

Industries face a responsibility to share knowledge about risks attached to legacy chemicals. Clear labeling, open dialogue with local communities, and swift reporting of unsafe practices help rebuild trust after periods of harm. Chemists, teachers, and regulators can offer that clarity. Looking at the journey of 2-naphthylamine hydrochloride — where it led and what it left behind — means understanding much more than color on fabric: it’s a case study in progress, shaped by science, advocacy, and an insistence that common sense and safety always matter.

What are the safety precautions when handling 2-Naphthylamine Hydrochloride?

Understanding the Risks

People working with chemicals like 2-Naphthylamine Hydrochloride know these aren’t just lines in a safety manual—they’re real risks with real consequences. Even on days when the warehouse feels routine, facing a substance flagged as a carcinogen changes the atmosphere. The International Agency for Research on Cancer (IARC) points out the close link between 2-Naphthylamine and bladder cancer. You feel a little more awake after reading something like that. Long-term contact, even when nothing seems wrong in the short term, stacks up in the body. So safety isn’t just about ticking boxes; it’s about protecting years of life ahead.

Protective Equipment: More Than Just Gear

There’s nothing theoretical about a chemical splash. Standard-issue goggles and nitrile gloves turn into lifelines with compounds like this. Skin contact can bring on rashes or, in the worst case, set the stage for much more dangerous outcomes. I’ve seen co-workers swap out gloves for cheaper options, thinking “close enough,” but medical-grade, chemical-resistant gloves make a difference. Splash-proof goggles, not just normal safety glasses, keep the dust or droplets at bay.

Air Quality and Ventilation

Air in the lab changes fast, especially with powders or dusts. Inhaling tiny particles rarely makes a splashy scene, but over time, those particles confuse the lungs. Lab regulations push for fume hoods, not just open windows. Speaking from my own hours on the floor, the smell and taste in the air tell you when extraction is working. Spot checks and filter changes take a few minutes and prevent problems from months of buildup. Respirators offer an extra layer if airborne concentration pushes past those safe thresholds.

Hygiene Practices: Going Beyond Routine

Each lunch break or bathroom trip risks cross-contamination. It’s tempting to carry on working after brushing off your hands, but full hand-washing with soap—no shortcuts—blocks absorption and spreading. Chemicals hide in grime under fingernails. Clean lab coats and, for bigger spills, disposable coveralls keep clothes and skin safe. Shared equipment needs actual cleaning, not just a wipe with a tissue.

Emergency Response and Training

Accidents happen even on careful shifts. Knowing the shower location or how to use an eyewash station gets more real after seeing a splash caught just in time. Spill kits need clear labels and up-to-date materials. From the start, training shouldn’t sign off after a slideshow; it should include practice runs and real questions. I’ve watched rehearsals shave crucial seconds off real emergencies. Quick action lowers risk, especially with substances known to harm health long-term.

Disposal and Environmental Responsibility

Pouring chemicals down a drain isn't just bad form—it risks the water supply. 2-Naphthylamine hydrochloride should always go through a specialist hazardous waste program. That route keeps carcinogens out of places where nobody chose the risk. It feels like extra work in the moment, but beats finding out months later that shortcuts created a bigger mess.

Solutions and Safer Practices

Safer substitutes make sense when they exist, but regulatory limits or scientific needs sometimes lock in the compound. Administrative controls—tighter shift limits, regular health checks, stricter supervision—cut exposure time. Sharing the real human risks behind chemical names in every staff meeting makes the safety manual more than a binded list of rules. In the end, the aim is simple: keep a clean sheet for those who come into contact with hazardous chemicals, so work never costs someone their health.

What is the chemical formula and molecular weight of 2-Naphthylamine Hydrochloride?

The Basics: Chemical Formula and Structure

2-Naphthylamine Hydrochloride lands in the category of aromatic amines, a group of chemicals that hold importance in dye production and scientific research. Its chemical formula is C10H8N·HCl. This means there are ten carbon atoms, eight hydrogen atoms, and one nitrogen atom connected in the core naphthalene structure. The hydrochloride part adds one chlorine atom and another hydrogen, combining with the amine group to turn it into a salt. This alteration bumps up water solubility and makes the substance easier to handle in the lab. 

Calculating the Molecular Weight

Looking at the numbers tells you a lot about how this molecule behaves. The molecular weight, which reflects the mass of each unit, comes out as 193.65 g/mol. Breaking that down, it’s the sum of the naphthylamine group (C10H8N, weighing 156.18 g/mol) and the hydrochloride addition (HCl, 36.46 g/mol). Chemists use this value to measure out precise quantities. The weight shows up in every reaction, every experiment, and plays a real role in making dyes, testing toxicology, and figuring out how certain molecules interact in biological systems.

Why Chemistry Details Matter in Everyday Science

That formula isn’t just trivia. In practice, the formula and molecular weight drive safety, storage, and usage. For example, 2-Naphthylamine itself drew heavy concern in the twentieth century as toxicologists uncovered its links to bladder cancer among dye workers. Handling protocols, like how much to use, how to store, and cleanup steps, depend on the compound’s chemical details. All these precautions come down to knowing what’s in the bottle and exactly how much mass each measure holds. Even a small error in weighing can affect exposure levels, testing results, or product purity.

The Real Impact Behind the Math

Through years of reading chemical safety sheets and prepping labs, I’ve seen the difference rigorous formula knowledge makes. One day, measuring out compounds by mass instead of guessing saves time and prevents health risks. Simple, careful math keeps users from overexposure. With substances like 2-Naphthylamine Hydrochloride, that attention to detail means protecting people in the workspace and making sure results hold up. The formula acts like a roadmap—one that steers clear of shortcuts.

Moving Forward: Solutions for Safer Handling

Science loves accuracy, but in the real world, human mistakes happen. Training workers on chemical formulas and molecular weights protects everyone from overexposure or costly mistakes. Digital scales now deliver readings to a precision the old triple beams never matched. Barcode inventory and automated batch tracking flag when substances are low, out of date, or handled by the wrong person. Industry pushes for dye alternatives that skip over hazardous reagents entirely, but for now, knowledge remains the quickest safety tool on hand.

Keeping up with formula specifics—like those for 2-Naphthylamine Hydrochloride—is not about memorizing for its own sake. It’s about connecting facts to action, putting research into context, and giving lab workers the information to make smarter decisions.

How should 2-Naphthylamine Hydrochloride be stored?

Taking Chemical Storage Seriously

Handling 2-naphthylamine hydrochloride brings a weight of responsibility. Anyone who’s worked in a chemical lab knows the feeling—safety protocols aren’t just red tape, but essential for wellbeing. This substance once found regular use in dye production, and its risks have put it under strict regulatory oversight. Scientific evidence links it to severe health hazards, especially bladder cancer. That reality alone should steer storage practices, not convenience or routine.

Protecting Personal Health: Gloves, Masks, Barriers

Personal experience in an academic lab highlighted just how easily spills or airborne powders can turn into long-term health troubles. Direct contact or inhaling dust from 2-naphthylamine hydrochloride spells danger—nitrile gloves and good eye protection offer a solid first step, and those working with open containers benefit from NIOSH-approved respirators. No one should handle these containers without proper lab coats and barrier protection clothing. One misstep with a material known for its carcinogenic properties lingers for decades.

Choosing the Best Storage Spot

Keep the container in a cool, dry place, far from direct sunlight and moisture. Humidity can cause clumping or degradation, and sunlight may drive unwanted reactions. A shelf in a dedicated poison cabinet, which locks and bears clear hazard labels, signals its risk to every passerby. That label isn't just bureaucracy—it tells visiting staff, cleaning personnel, and everyone in the facility there’s no room for mistakes with this compound around.

Keeping Substances Apart for Safety

There’s a lesson learned from tight, chaotic stockrooms: strong acids, oxidizers, and active metals shouldn’t share space with 2-naphthylamine hydrochloride. Chemical compatibility charts make their way into veteran lab managers’ minds over years on the job. Good practice keeps hazardous chemicals on separate shelves and makes rare accidents less costly for people and property. Spill trays under the containers can help contain small leaks, making cleanup safer and faster.

Thinking Beyond the Container

It’s not all about the jar in the corner. Inventory tracking and dated labels pull their weight during audits and inspections, but they also help prevent accidental use of expired or degraded chemicals. Secure lids, tightly fastened, stop vapors from entering the room—nobody wants to breathe even a little of what could cause cancer years later. These days, clear signage detailing the exact risks and emergency contacts sits within arm’s reach. Colleagues work safer when everyone knows what each container holds.

Ventilation Lowers the Chance of Trouble

Chemical storage rooms need reliable ventilation. I’ve seen what happens when old air stagnates in a poorly designed storehouse: the smell, the headaches, the worry of unseen exposure. Fume hoods and air-exchange systems matter because they dilute and safely remove stray vapors. Frequent checks on airflow help everyone inside breathe easier. It’s much better to catch a ventilation problem early than to clean up after a long-term exposure.

Clear Disposal Pathways Reduce Chance of Harm

Sooner or later, storage isn’t enough. Disposal must follow hazardous waste regulations. Experience tells me that working with local environmental and safety offices makes this process clear. Designated waste streams, regular pickups, and strict tracking mean nobody just pours remnants away or tosses them in regular trash. Safe disposal closes the loop—protecting people, neighborhoods, and the wider world from a notorious chemical hazard.

Is 2-Naphthylamine Hydrochloride considered hazardous or carcinogenic?

Looking at What Science Says

2-Naphthylamine Hydrochloride pops up in conversations about industrial chemicals, especially those tied to dye and pigment manufacturing. Studies dating back decades have drawn clear links between this chemical and cancer, especially in people who spent long hours working with it. Bladder cancer shows up frequently in the research. Data from several occupational studies make it hard to ignore that strong connection—it’s not just one research group saying this.

The International Agency for Research on Cancer (IARC) puts 2-Naphthylamine and its salts, including this hydrochloride form, in Group 1, meaning there’s strong evidence it causes cancer in humans. Over time, researchers in the US, Europe, and Asia backed these findings up. Looking at this chemical in a lab setting, scientists noticed genetic mutations and damage to DNA, which give away its carcinogenic punch.

Personal background working in research safety taught me to treat every Group 1 agent with the utmost seriousness. I saw stories where workers got sick because factory management delayed pulling the plug on chemical use that posed a clear risk. Policies grew tighter over my career. In the 1970s and 80s, authorities started banning or severely controlling the use of 2-Naphthylamine worldwide. In the US, the Occupational Safety and Health Administration (OSHA) now includes this chemical on its list of substances requiring strict control wherever it’s still present—essentially, it sits on shelves only in tightly supervised labs. Most folks today have never come across it, and that’s a good thing.

Health Risks Beyond Cancer

The biggest headline is bladder cancer, but exposure may trigger other health effects too. People report skin irritation or respiratory issues if they work with it without protection. Chronic, long-term exposure always ups the health risk. My colleagues, many of whom focused their careers on industrial hygiene, often shared stories where just a few years of lax safety led to lifelong health problems for workers. Regulatory agencies flag even small exposures as dangerous, with guidelines shaped to avoid anything above trace levels.

Environmental and Social Costs

This chemical doesn’t just disappear. Factory leaks or poor disposal practices can contaminate soil and groundwater, leading to unexpected exposure for local communities—not just factory staff. There’s a history here: older manufacturing sites left toxic legacies in many industrial towns. Local governments and safety groups have fought long battles to clean up these sites and warn the next generation not to repeat the same mistakes. Post-war Europe holds many examples, and similar stories are easy to find in North America and Asia. The consequences affect public health funding, property values, and community trust.

What Do We Do With Past Mistakes?

Stopping all use was a tough pill for some industries, but science and lived experience made it clear. Substituting safer chemicals became a huge focus. Now, the process starts with thorough risk assessment before bringing anything new into production. Engineers, chemists, and safety officers work together, weighing not just short-term profits but long-term harm. Regular testing, personal protective equipment, and waste management plans form the backbone of modern chemical safety.

Looking at what happened with 2-Naphthylamine Hydrochloride shapes how labs and factories operate today. The chemical serves as a clear example of what happens when we ignore early warning signs. By listening to scientific consensus and learning from real-world harm, industries lower risks and put safety above shortcuts.

2-Naphthylamine Hydrochloride
2-Naphthylamine Hydrochloride
Names
Preferred IUPAC name 2-naphthalenamin-1-ium chloride
Other names 2-Naphthalenamine hydrochloride
beta-Naphthylamine hydrochloride
2-Aminonaphthalene hydrochloride
Naphthalen-2-amine hydrochloride
Pronunciation /tuː-ˈnæfθɪl.əˌmiːn haɪˌdrɒˈklɔːraɪd/
Identifiers
CAS Number 612-89-7
Beilstein Reference **136611**
ChEBI CHEBI:38749
ChEMBL CHEMBL502958
ChemSpider 18635277
DrugBank DB11578
ECHA InfoCard 100.005.219
EC Number 214-009-5
Gmelin Reference 14773
KEGG C14482
MeSH D009287
PubChem CID 7066
RTECS number SL8225000
UNII S35T77QRZY
UN number 1652
CompTox Dashboard (EPA) DTXSID8050229
Properties
Chemical formula C10H10ClN
Molar mass 189.66 g/mol
Appearance White to light tan crystalline powder
Odor Odorless
Density 1.246 g/cm³
Solubility in water Soluble
log P -0.14
Vapor pressure 0.000246 mmHg at 25°C
Acidity (pKa) 2.7
Basicity (pKb) -4.2
Magnetic susceptibility (χ) -47.0e-6 cm³/mol
Refractive index (nD) 1.693
Dipole moment 2.77 D
Thermochemistry
Std molar entropy (S⦵298) 122 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -5.0 kJ/mol
Pharmacology
ATC code D01AE53
Hazards
Main hazards Carcinogenic, toxic if swallowed, harmful if inhaled, causes skin and eye irritation
GHS labelling GHS labelling of 2-Naphthylamine Hydrochloride: `"Danger; H301, H317, H350, H373; P201, P261, P280, P301+P310, P308+P313, P405, P501"`
Pictograms GHS06,GHS08
Signal word Danger
Hazard statements H301: Toxic if swallowed. H311: Toxic in contact with skin. H331: Toxic if inhaled. H350: May cause cancer.
Precautionary statements P201, P202, P260, P264, P270, P273, P280, P308+P313, P301+P310, P302+P352, P305+P351+P338, P308+P311, P321, P330, P405, P501
NFPA 704 (fire diamond) 2-Naphthylamine Hydrochloride: 2-2-2- (Red: 2, Blue: 2, Yellow: 2, White: - )
Flash point 170 °C (338 °F; 443 K)
Lethal dose or concentration LD50 (oral, rat): 450 mg/kg
LD50 (median dose) LD50 (median dose): Oral rat LD50: 800 mg/kg
PEL (Permissible) PEL: 0.1 mg/m³
REL (Recommended) 0.1 mg/m³
IDLH (Immediate danger) Unknown
Related compounds
Related compounds 2-Naphthylamine
1-Naphthylamine
2-Naphthol
1-Naphthol
Naphthalene
Benzidine