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



Understanding 1-Methyl-4-Propylbenzene: More Than Just a Chemical Compound

Historical Development

Chemistry never stands still. Over decades, chemists have shaped a better understanding of aromatic hydrocarbons like 1-Methyl-4-Propylbenzene. Back in the mid-20th century, labs focused on discovering new organic compounds that could find their way into pharmaceuticals, fuels, and specialty chemicals. The search for branched aromatic molecules had shaped everything from fuel additives to modern surfactant science, and 1-Methyl-4-Propylbenzene emerges from that landscape as both a relic of earlier organic syntheses and a quiet workhorse. I remember reading old organic chemistry books where such molecules would get a single mention, overshadowed by their more reactive cousins. Yet, in recent years, renewed interest in downstream uses and unique reactivities brought it back into the picture, especially when folks started to realize the potential tucked away in its simple-looking structure.

Product Overview

Take a closer look at 1-Methyl-4-Propylbenzene and you see a colorless liquid, clear and seemingly unremarkable. But don’t let that fool you. Companies that handle aromatic compounds value its particular blend of volatility, chemical persistence, and its ability to stick around in organic synthesis, leading to custom intermediates otherwise hard to obtain straight from the big chemical supply houses. Sourcing it isn’t like hunting down some rare earth element, but you’ll notice it’s less common in everyday chemical catalogs. The ones who buy and use it tend to know exactly what it adds to their workflow, whether in specialty surfactants, designer solvents, or even in research where small tweaks in molecular structure matter.

Physical & Chemical Properties

Sitting on the bench, 1-Methyl-4-Propylbenzene tells you a lot about itself with just a quick sniff—sharp and characteristic, a reminder of its aromatic backbone. Lab specs pin it as a liquid at room temperature, boiling somewhere in the region of 200°C, so most standard glassware suffices when handling it. Density runs low, and it doesn’t mix with water, which fits expectations for substituted benzenes. From a reactivity standpoint, the methyl and propyl groups at the ring create interesting steric effects. They can channel reactions to specific positions on the ring, acting as guides or blockers during further modification—something every organic chemist learns to appreciate with practice.

Technical Specifications & Labeling

No one should overlook the importance of careful labeling in the lab. With aromatic hydrocarbons, working safely means clear hazard warnings and handling recommendations. People sometimes lump these substances in together, but 1-Methyl-4-Propylbenzene deserves its own shelf and attention. Most suppliers specify purity close to analytical grade, with tightly constrained limits on isomeric impurities or other alkylated benzenes. During my time in the lab, labels meant more than compliance— they were a quick reminder to handle with gloves, proper ventilation, and a healthy respect for what liquid benzene derivatives can do.

Preparation Method

Traditional routes to 1-Methyl-4-Propylbenzene use Friedel–Crafts alkylation, a go-to reaction in organic chemistry. By reacting toluene with n-propyl chloride and a Lewis acid catalyst, the propyl group finds its way onto the aromatic ring. Temperature and the amount of catalyst steer the selectivity, and the method rewards precision. Solvent-free techniques have started to pop up to reduce waste and improve safety—always a big concern. Green chemistry pushed everyone to be smarter about solvent choices and waste streams, and these days, labs exploring new routes for aromatic hydrocarbons pay special attention to minimizing side products and maximizing yield. That level of care echoes across the field, pressing each generation to outdo the last in terms of safety and environmental footprint.

Chemical Reactions & Modifications

In the world of synthetic chemistry, every extra group on a benzene ring offers both a challenge and an opportunity. The methyl and propyl arms on 1-Methyl-4-Propylbenzene shape electron density and guide further reactions. You may see chemists use it for targeted nitration, sulfonation, or halogenation, keen on accessing unique derivatives for advanced materials or pharmaceuticals. Electrophilic aromatic substitution, a classic move in organic synthesis, plays out a bit differently here. Electrons get tugged to different spots, which makes controlling product distribution easier or trickier, depending on the project. Working in a research-heavy environment, I came to see just how vital that kind of control could be in building complex molecules step-by-step.

Synonyms & Product Names

The world of aromatic chemistry loves its alternate names: 1-Methyl-4-Propylbenzene goes by p-Propyl Toluene and 4-Propyl Toluene in the literature as well as industry reports. These names pop up on bottles and Material Safety Data Sheets, so anyone in a lab or plant has to keep them straight. Mixing up similar names once led to a memorable (and embarrassing) lost morning for me, sorting samples mislabeled from an overseas supplier. It’s a small thing, but in work that involves chemical safety, accuracy in naming keeps disasters at bay.

Safety & Operational Standards

Nobody can ignore safety when dealing with aromatic hydrocarbons. A slack approach courts trouble, especially during bulk handling or transfer. 1-Methyl-4-Propylbenzene doesn’t ignite as easily as gasoline, but it can burn under the right conditions. Fume hoods, flame-resistant lab coats, chemical-resistant gloves, and splash goggles make up the standard gear—non-negotiable. Ventilation and proper storage away from oxidizers or open flames remain the norm in every responsible lab. I recall strict toolbox talks where supervisors hammered home the risk of vapor inhalation and the importance of spill control. Safeguards go hand-in-hand with good habits.

Application Area

The reach of 1-Methyl-4-Propylbenzene extends beyond pure research. Industry sometimes seeks this compound as a building block for specialty resins, performance additives, and as an intermediate for more complex molecules used in surfactant manufacture or custom lubricants. It’s not a headline-grabber, but its subtle influence shows up in sectors that require molecules to behave in reproducible and predictable ways. Specialty solvent blends sometimes feature it for its unique solvency profile. Even fragrance chemistry nibbles at its margins, valuing derivatives with mild, pleasant notes. The fact that it doesn’t draw attention testifies to its effectiveness in roles other chemicals can’t quite match.

Research & Development

Research never stops. Recent years brought deeper dives into the functionalization of alkylbenzenes, with projects looking at catalytic routes, regioselective reactions, and ways to swap out functional groups using milder, safer reagents. R&D labs push for greater sustainability, greener solvents, and steps that cut out hazardous byproducts. Working on related projects, I’ve noticed how this era demands more transparency and safer process designs than the old days. The next wave likely includes advanced catalysis, possibly with reusable supports or enzyme-inspired systems. Scientists scope out each modification to see how it tweaks properties, always with the goal of making something better than before.

Toxicity Research

Safety testing takes no shortcuts. Toxicity profiles for substituted benzenes like 1-Methyl-4-Propylbenzene focus on both acute and chronic risks. Studies probe absorption, breakdown, and long-term effects on living systems. Exposure through inhalation or skin contact makes up the main concern. Regulatory authorities keep a sharp eye on data from workplace incidents and controlled studies. The rule of thumb in the lab always leans conservative—limit exposure, prevent environmental release, and review data regularly. Part of E-E-A-T means staying current on risks and communicating them clearly. Nobody wants to repeat the mistakes of earlier generations who underestimated the resilience of aromatic hydrocarbons in ecosystems and their potential bioaccumulation.

Future Prospects

Chemistry rarely stands still. As new materials and green manufacturing grow in importance, compounds like 1-Methyl-4-Propylbenzene could find fresh relevance. Improved synthetic routes lower environmental impact and make broader applications more practical. Sector shifts toward specialty chemicals, with an emphasis on performance and low toxicity, makes this molecule a likely candidate for further development. My time in the field tells me that tomorrow’s problems will need more versatile, adaptable building blocks, and aromatic hydrocarbons—managed intelligently—belong in that toolbox. Instead of just watching from the sidelines, this molecule may soon enjoy an expanded role, driven by both innovation and a strong push for responsible stewardship.




What is 1-Methyl-4-Propylbenzene used for?

The Chemical’s Role in Industry

Walk through any chemical plant or refinery, and you start to see certain compounds show up on tank labels and datasheets. 1-Methyl-4-propylbenzene, sometimes called p-cymene, is one of those subtle players in industrial chemistry. Its name carries a big, serious ring, but the story rests mainly in its practical applications and the problems it tries to solve.

Production Ties and Real-World Uses

This compound belongs to the alkylbenzene family. It pops up during petroleum refining and sometimes in wood processing, especially from certain essential oils. Producers extract it from turpentine or synthesize it from toluene and propylene, depending on what the plant runs.

The largest share gets locked into making other chemicals. Factories often harness it as a building block for manufacturing specialty resins and synthetic fragrances. In my own experience working on a research project in an academic lab, we saw it used as a solvent for tough organic reactions that regular lab solvents simply couldn’t handle. Its smell reminded me a bit of citrus because p-cymene also shows up in oranges and cumin. That trait draws in companies looking to manufacture food flavorings and perfumes.

Industries also favor p-cymene in producing certain disinfectants and cleaning agents. Some cleaning product manufacturers blend it to give their soaps a stronger degreasing punch, especially where essential oil residues are involved. These practical choices link back to its hydrophobic qualities, which let it break up oily films where water alone fails.

Pharmaceutical and Agricultural Paths

Beyond the obvious industrial side, 1-methyl-4-propylbenzene gets quietly mixed into pharmaceutical processes. Researchers use it as a starting material to prepare drugs and intermediates, especially where bio-derived options hold more appeal than petroleum-only products. In agriculture, it steps in as a constituent for certain pesticides, leveraging its ability to dissolve fats and waxes on pests or plant leaves.

I worked briefly in an agritech internship where p-cymene solutions popped up on our supply lists, made up to strip waxy coatings off fruit for chemical analysis. That job left a strong impression on me—if you forget gloves, your skin absorbs the pungent residual oil in minutes. That sensitivity speaks to the need for good safety training in any lab or production setting dealing with the substance.

Health, Environment, and Future Trends

The world keeps a close eye on health and environmental impacts now, and 1-methyl-4-propylbenzene is no exception. Short exposures don’t seem to cause major harm, but concentrated fumes over time can irritate airways or skin. I remember reading an industrial hygiene report some years ago that stuck with me: refinery workers complained of headaches around storage tanks that leaked fumes from this compound, and air monitors flagged higher readings on warm days. Strong ventilation, careful storage, and spill control lower the risk, but watchdogs want to look deeper.

Places where p-cymene occurs naturally, like forests and citrus groves, rarely face these issues. Problems creep in around processing plants with poor containment or disposal practices. Environmental scientists say good stewardship can keep levels low and protect air and soil. Labs and factories now seek more sustainable ways to extract or recycle the compound, especially as demand holds steady in scents, soaps, and specialty manufacturing.

Finding Solutions and Pushing for Safety

Better worker training, investment in emission controls, and stronger monitoring programs help balance the business benefits and the need for safety. Companies willing to invest in closed-loop processing and alternative solvents cut their waste and protect staff. As regulations tighten and people care more about where their products come from, the industry has to adapt and manage risks, not just chase production figures.

What are the safety precautions when handling 1-Methyl-4-Propylbenzene?

The Hidden Risks in a Bottle

Most folks don’t spend their days thinking about organic chemicals, but if you’ve worked in a lab, a plant, or even managed inventory, you’ve probably crossed paths with an aromatic hydrocarbon or two. One of those — 1-Methyl-4-Propylbenzene — isn’t on every shopping list, but it sits on enough shelves to matter.

This liquid brings a sweet, gasoline-like scent and finds a place in research and specialty processes. That recognizable aroma comes with invisible risks: vapors don’t need much coaxing to fill a small room and challenge the lungs. Eye, skin, and respiratory irritation don’t just happen to the unlucky few; they’re real responses to even quick, careless handling.

Respect the Skin Barrier

Maybe you remember a time you let gloves slide because you were “just measuring a little bit.” I’ve made that mistake with other chemicals and regretted it each time. Contact with skin lets harmful liquids in and doesn’t always bring the stinging pain you’d expect right away. 1-Methyl-4-Propylbenzene can sneak through those cracks, leading not only to irritation but long-term issues that grow with repeated exposure. Always wear nitrile or neoprene gloves. Lab coats, goggles, and, in splash zones, a face shield, cut the risk further.

Vapors Can’t Be Ignored

I’ve worked in labs that smelled of solvents, and those headaches lingered into the night. Aromatics don’t just irritate—they pile on the toxicity with repeated exposure. Standard practice says keep rooms ventilated, but that advice isn’t just for looks. Use chemical fume hoods if you have them; otherwise, push for fans, open windows, and low-vapor procedures.

Keep in mind, it’s easy to slip into routine when pouring or transferring. Even a small spill puts vapor—and risk—right by your face. Pour slowly, avoid open containers, and clear up drips instantly with the right pads, not bare paper towels or rags.

The Power of Labeling and Storage

More than once I’ve seen well-meaning workers set a clear bottle on the wrong shelf, then walk away. Mislabeled chemicals lead to dangerous mix-ups. Every bottle needs a clear label, showing the chemical and hazard information. Store this compound away from oxidizers and heat, out of sunlight, and not above head height—gravity plus glass spells disaster.

Small steps matter. Store only what you need. Don’t let chemicals collect dust or mix with combustible materials. Use grounded, spark-free equipment near volatile liquids. Fires start faster than anyone expects, especially with aromatic vapors hanging around.

Cleanups and Accidents Require a Plan

Spills can send panic running through the most seasoned staff. I keep spill kits where I work, not tucked away in a locked cabinet but right within arm’s reach. If a spill happens, evacuate if the fumes get strong. Ventilate fast and never mop up with bare hands or porous materials.

After an accident, wash any affected skin right away and see a medical professional if irritation sticks around. Workplace safety rules exist for good reason—ignore them, and you can pay a lifetime cost in health.

Building Safe Habits

None of these safety steps take advanced training—just steady habits and clear reminders. Training sessions every few months drive the message home. Posters, quick talks before starting work, or just sharing the story of a close call go further than dry checklists. Chemical hazards feel invisible until they hit, so treat every bottle like it matters.

What is the chemical formula and molecular weight of 1-Methyl-4-Propylbenzene?

1-Methyl-4-Propylbenzene: The Structure and Meaning Behind the Name

1-Methyl-4-propylbenzene sounds like a mouthful, but breaking it down makes sense of its makeup. The name points right at the structure. The core of the molecule, benzene, sets the stage—a familiar six-carbon ring, fragrant in the lab, and a foundational structure for thousands of chemicals. “1-Methyl” marks a single carbon piece (a methyl group, or CH3) stuck on the benzene ring. “4-Propyl” tells about a three-carbon stretch (a propyl group, or C3H7) attached on the opposite side—picture the fourth spot counting around the ring from the methyl’s position. This pattern shapes the molecule’s behavior and gives it a unique chemical identity.

Chemical Formula and Molecular Weight Details

In plain chemistry terms, pile up the elements: there’s one benzene ring (C6H6), a methyl group (+CH3), and a propyl group (+C3H7). Connect them, account for the right atom count, and you get C10H14. This formula shows ten carbon atoms and fourteen hydrogens, built as nature intended from simple hydrocarbon building blocks.

The molecular weight follows right after. Find the atomic weights: carbon comes in at about 12.01 g/mol, and hydrogen weighs in at 1.008 g/mol. Multiply out—ten carbons (10 x 12.01 = 120.10 g/mol), and fourteen hydrogens (14 x 1.008 = 14.112 g/mol). Add the two to hit a total of roughly 134.21 g/mol. That figure—often written as 134.22 g/mol, favoring precision—guides laboratory work and safety sheets.

Importance and Applications in the Real World

My years tinkering with organic chemistry taught me that every part of a molecule like 1-methyl-4-propylbenzene matters, from its balance of carbon and hydrogen to the way it’s built. Industrial chemists spot this compound in the world of petrochemicals, solvents, and even fragrance development. Fewer people talk about how these types of molecules could slide into products as blending agents, precursors in creating resins, or other specialty chemicals. The isomeric relationships—where molecules share formulas but differ in layout—can mean big changes in scent, taste, or reactivity. That’s the case here: switching up a group’s position can make the difference between a sticky byproduct and a valuable intermediate.

Labs track chemical formulas and molecular weights meticulously because mistakes cost money, credibility, and sometimes safety. Shipping labels, hazard warnings, reactor setups—they all depend on knowing the exact chemical identity. Mislabel a drum, and you risk a delayed shipment or, worse, a hazardous spill. Regulatory agencies demand correct chemical info, keeping dangerous missteps in check.

Building Safer and Smarter Practices

Looking at practical steps, I see a few places for improvement. Chemists should use consistent naming and clear structure diagrams, not only in technical papers but everyday logbooks and purchase records. Quality control teams need fast, easy access to molecular weight calculators—manual math leads to slips, no matter how careful you feel. Teams installing software that auto-verifies chemical identities catch errors before they become problems. Training new hires in reading and verifying chemical names, formulas, and applications pays off fast.

Finally, open channels for questions and double-checks create better lab cultures. One mistake in a formula can snowball, but with proper teamwork and up-to-date resources, those errors spot and fix themselves early. 1-Methyl-4-propylbenzene may sound like a tiny piece of the global puzzle, but precision at every step keeps science and safety advancing side by side.

Is 1-Methyl-4-Propylbenzene hazardous or toxic?

Chemicals in Everyday Life

Modern life owes a lot to chemistry. From the paint on our walls to the fuel in our cars, there’s often a mixture of ingredients behind each finished product. One chemical that has popped up in conversations lately is 1-Methyl-4-Propylbenzene, sometimes found in research labs or discussed among professionals working with specialty chemicals. Most people have never heard of it, but curiosity about safety and potential hazards always feels justified.

Putting Toxicity in Context

1-Methyl-4-Propylbenzene falls into the aromatic hydrocarbon family, which includes well-known compounds like toluene and xylene. These substances often appear in solvents, fuels, or industrial processes. Some in this group can irritate the skin, eyes, or respiratory tract with repeated exposure. Poisoning usually comes from inhalation or prolonged contact. For this particular compound, the research stays a bit thin compared to its more famous cousins, but chemical relatives do offer some clues.

Animal studies form the backbone of risk assessment for chemicals like these. Looking at similar compounds, long-term exposure sometimes links to headaches, dizziness, and even nervous system effects. Benzene, a fellow aromatic, ranks as a known human carcinogen. 1-Methyl-4-Propylbenzene does not share benzene’s notorious track record, but it’s wise not to dismiss risk if reliable long-term studies remain limited.

Data and Safe Practices

A wealth of industrial safety sheets treat 1-Methyl-4-Propylbenzene as combustible and potentially irritating. Labels often warn users to avoid inhaling vapors and prevent direct skin contact. Chemical suppliers signal caution, encouraging gloves, goggles, and proper ventilation during handling. Typical poison control advice tells people to move to fresh air, rinse skin, and seek medical advice if symptoms crop up.

National agencies like the U.S. Occupational Safety and Health Administration (OSHA) set exposure standards for many workplace chemicals. This helps shield workers’ health and ensure safe conditions. Unfortunately, 1-Methyl-4-Propylbenzene doesn’t have a dedicated exposure limit, so companies turn to generalized rules covering similar hydrocarbons. This gap means risk management plans lean heavily on experience with the aromatic family.

Addressing the Gaps in Knowledge

Big questions arise when hazard data remains scarce. Knowing how much exposure creates a real risk guides everything from labeling to emergency planning. No single company or research lab carries the whole burden here. Government agencies, universities, and industry groups all play a part in closing knowledge gaps. Calls for expanded research sound especially important for chemicals with growing or changing uses.

If toxicity or environmental concerns show up in future studies, laws can follow. Regulators could consider stricter rules or step up monitoring, especially in industries that use aromatic hydrocarbons day in, day out. Voluntary efforts also matter—a strong culture of safety in the workplace, information campaigns, and routine training sessions all shield people from hidden dangers.

Moving Toward Safer Handling

Aromatic hydrocarbons have been around for generations, but new formulas and applications arrive every year. Having full access to scientific studies, clear guidance from regulators, and honest reporting from industry leaders reduces the chances of surprises. Every lab coat, tanker truck, and toolbox deserves respect and care when handling unfamiliar substances, especially those like 1-Methyl-4-Propylbenzene that ride under the radar.

How should 1-Methyl-4-Propylbenzene be stored and disposed of?

Why Care About This Chemical?

Anyone who spends time in a lab or industrial setting knows that not all chemicals demand the same level of attention, but turning a blind eye to storage and disposal means inviting trouble. 1-Methyl-4-Propylbenzene comes with its own set of challenges, and treating it casually risks health and safety for more than just those using it.

Storage: Make the Right Choices

1-Methyl-4-Propylbenzene carries flammable and health hazards. Tossing it on a crowded shelf with incompatible substances creates a recipe for disaster. Keep it tucked away in a dedicated, flame-proof cabinet, far from oxidizers, acids, and open flames. Ventilation cuts down on build-up of flammable vapors, and a cool, dry spot slows down deterioration. Rusty cans and leaky containers can spell trouble, so opt for tightly sealed, chemical-resistant containers with legible labels.

Personal experience reminds me: in a cluttered storeroom, two careless placements sparked a fire that nearly destroyed valuable material. Proper signage, easy access to fire extinguishers, and an up-to-date chemical inventory provide layers of protection. Treat every drum or bottle like it’s been sitting there for years — always check before handling.

Disposal: Skipping Corners Isn’t Worth the Risk

Pouring chemicals down the sink has ended up destroying local ecosystems and making headlines for all the wrong reasons. 1-Methyl-4-Propylbenzene doesn’t break down cleanly in water and contributes directly to pollution. Old habits need to change. Adhering to local hazardous waste rules isn’t just ticking boxes — it’s about making sure harmful compounds don’t wind their way into rivers or landfills where they threaten wildlife and water supplies.

Working with a certified hazardous waste contractor gives peace of mind. Document the process, from storage to collection and treatment. Avoid mixing this chemical with others, since interactions can create toxic byproducts or explosive reactions. For me, seeing a drum of solvent waste bubble and splatter in a lab sink drove home the lasting harm one careless moment can create. The cost or effort of proper disposal beats decades of cleanup and fighting lawsuits.

Empowering Everyone With Facts

People sometimes treat chemical safety rules like overzealous bureaucracy until they see someone harmed or fined. The U.S. Environmental Protection Agency maintains clear guidelines on storing and transporting flammable organics. The Occupational Safety and Health Administration sets regulations that keep employees from breathing in dangerous vapors or getting exposed through contact. These don't exist to slow progress but to help workplaces and communities thrive without unnecessary risk.

Routine training makes the biggest difference. Businesses can set up regular walkthroughs and drills, reinforcing that handling isn't just a box-ticking exercise. Having eye-wash stations and spill kits plus updated Material Safety Data Sheets within reach cuts down panic during emergencies. Leadership needs to emphasize good habits, not just protocols. I’ve found that taking half a day to walk through procedures, discuss near-misses, and update signage leaves a stronger impression than a hundred unread emails.

Building a Safer Path Forward

Safe handling of chemicals like 1-Methyl-4-Propylbenzene benefits everyone. Smart storage and responsible disposal reflect not only professional standards but real care for people, neighborhoods, and the planet. Sharing clear instructions and reminders based on real-world incidents keeps best practices alive, not just buried in dense documentation.

1-Methyl-4-Propylbenzene
1-Methyl-4-Propylbenzene
1-Methyl-4-Propylbenzene
Names
Preferred IUPAC name 4-Propyl-1-methylbenzene
Other names 1-Isopropyltoluene
p-Cumene
4-Propyl-1-methylbenzene
Pronunciation /waɪ ˈmɛθ.əl fɔː ˈproʊ.pɪl ˈbɛn.ziːn/
Identifiers
CAS Number 1076-19-1
Beilstein Reference 1209228
ChEBI CHEBI:89682
ChEMBL CHEMBL15800
ChemSpider 14389
DrugBank DB13921
ECHA InfoCard 03b3a7e7-cda8-4b55-959d-1b8cbc76798b
EC Number 202-730-6
Gmelin Reference 79251
KEGG C06725
MeSH D000431
PubChem CID 8956
RTECS number CY9100000
UNII UXE1K88G1J
UN number UN2301
CompTox Dashboard (EPA) DTXSID2020324
Properties
Chemical formula C10H14
Molar mass 134.22 g/mol
Appearance Colorless liquid
Odor aromatic
Density 0.862 g/mL at 25 °C
Solubility in water Insoluble
log P 3.7
Vapor pressure 0.27 mmHg (25 °C)
Acidity (pKa) 44.0
Magnetic susceptibility (χ) -81.0·10⁻⁶ cm³/mol
Refractive index (nD) 1.4720
Viscosity 0.753 cP (20°C)
Dipole moment 1.10 D
Thermochemistry
Std molar entropy (S⦵298) 251.6 J/mol·K
Std enthalpy of formation (ΔfH⦵298) -46.1 kJ/mol
Std enthalpy of combustion (ΔcH⦵298) -5356 kJ/mol
Pharmacology
ATC code R02AA20
Hazards
GHS labelling GHS02, GHS07
Pictograms GHS02
Signal word Warning
Hazard statements H226, H315, H319, H335
Precautionary statements P210, P261, P273, P301+P310, P331, P403+P235
NFPA 704 (fire diamond) 1-1-0
Flash point 64 °C (closed cup)
Autoignition temperature 482 °C
Explosive limits 1.0–6.3%
Lethal dose or concentration LD₅₀ oral rat 4300 mg/kg
LD50 (median dose) LD50 (median dose) of 1-Methyl-4-Propylbenzene: "Oral, rat: 6,000 mg/kg
NIOSH RN 622-96-8
PEL (Permissible) Not established
REL (Recommended) NIOSH REL: 5 ppm (25 mg/m3)
IDLH (Immediate danger) The IDLH (Immediate danger) of 1-Methyl-4-Propylbenzene is **900 ppm**.
Related compounds
Related compounds Toluene
Ethylbenzene
Propylbenzene
Cumene
1-Methyl-3-Propylbenzene
1-Methyl-4-Ethylbenzene
Isopropylbenzene
1,2,4-Trimethylbenzene