Terpineol: Past, Present, and the Road Ahead
Historical Development
People have known terpineol since the late nineteenth century, mostly through its connection to turpentine distillation. Early chemists noticed its fragrant potential and got to work isolating the compound for use in perfumes and flavorings. Over time, the world’s biggest producers, mainly relying on pine tree resin, set up large-scale operations to meet growing demand. By the 1920s, terpineol had firmly entered the toolbox of the cosmetics and cleaning industries, each seeking out the compound’s unique fragrance. In recent decades, expanded synthetic routes launched by advances in organic chemistry allowed for production from cheap turpentine, making terpineol widely available and much more affordable. Today’s supply chain links forestry, green chemistry, and life sciences—innovation pushing this classic molecule into new territory.
Product Overview
Terpineol, a monoterpene alcohol, appears in various isomeric forms—alpha-terpineol taking the lead in commerce. Its sweet, lilac-like scent draws the attention of perfumers and flavorists alike. Besides personal care and cleaning goods, terpineol features in medicine as an expectorant or mild anesthetic. People working in labs find it an effective solvent, with both industrial and specialty applications. Producers now offer both natural and synthetic versions, with purity and traceability driving decisions in the food, fragrance, and pharmaceutical sectors. Regulations often require disclosures about source and production method, placing extra responsibility on suppliers aiming for high-value markets.
Physical & Chemical Properties
At room temperature, terpineol looks like a colorless or pale lilac-scented liquid. Its boiling point hovers near 219°C, with a density around 0.935 g/cm³. Soluble in alcohol but less so in water, terpineol’s polarity makes it easy to formulate into oil-based and water-based products. Key features such as low volatility, stable shelf life, and gentle reactivity allow the compound to offer both safety and performance in demanding conditions. Molecular formula C10H18O and molar mass of 154.25 g/mol round out its basic chemical ID. Spectroscopists and chemists use IR, NMR, and GC-MS tools to verify structure and purity, granting buyers and regulators the proof they need to trust a given batch.
Technical Specifications & Labeling
Manufacturers and distributors label terpineol with grades (technical, fragrance, FCC for food), isomeric content (alpha, beta, gamma), water content, and common contaminants. Documentation must point to any solvents or carrier oils used and state compliance with QC benchmarks such as ISO 9235 for natural aromatics or IFRA for safety in perfume use. Hazard pictograms typically illustrate flammability and irritation risks. Batch number, shelf life, and production date all need to be clear to meet industry traceability and recall standards. Those who need kosher, halal, or allergen-free credentials look for specific label marks and certifications to back up supplier claims. Pharmacopeial standards remain especially stringent, as medical use places terpineol under extra scrutiny for residual solvents and microbiological purity.
Preparation Method
Terpineol comes either by direct extraction from pine oil or through synthetic routes involving turpentine or isoprene chemistry. The industry standard relies on hydrating alpha-pinene (from turpentine) in acidic conditions, producing a mix of isomers that get separated via distillation. Some specialists run extra purification steps, including vacuum distillation or molecular sieves, to boost selectivity and yield. More companies seek greener alternatives, with biocatalysis starting to get attention as an energy-saving, cleaner way to obtain pure terpineol. The pressure to reduce petrochemical input and waste encourages investment in smarter processes, with both cost and supply security pushing innovation forward.
Chemical Reactions & Modifications
Chemists value terpineol’s reactive alcohol group and conjugated double bonds. The molecule takes well to esterification, oxidation, and etherification reactions, generating derivatives useful in perfumery, pharmaceuticals, and polymers. Terpineol esters show improved solubility and altered scent, allowing fragrance formulators to play with texture and volatility profiles. Oxidation products such as terpin hydrate serve as mild pharmaceuticals for cough and cold symptoms. In specialty coatings, terpineol acts as a solubilizer and flow modifier. Research teams continue exploring terpineol’s reactivity for green chemistry, aiming to cut down on harsh reagents and by-products. The abundance of raw pine chemicals ensures a steady pipeline for new synthesis and process development.
Synonyms & Product Names
Terpineol hides behind a handful of names in common commerce, including lilaol, p-menth-1-en-8-ol, and alpha-terpineol. In flavor and fragrance listings, you’ll see it under FEMA No. 3045 or CAS No. 8000-41-7. Perfume and cleaning product manufacturers tend to use label-friendly synonyms such as “lilac alcohol.” Grocery and pharmacy shelves often mention simply “terpineol” in medicinal products, with details in small print for legal compliance. Clear identification matters for buyers searching for botanical or synthetic versions, and for those keeping allergen and IFRA records up to date.
Safety & Operational Standards
Workplace safety around terpineol requires basic chemical hygiene. Prolonged skin exposure can lead to mild irritation, while accidental ingestion causes stomach upset. Flammability and inhalation risks set the tone for safe handling in labs and production plants. Standard operating procedures call for goggles, gloves, and local ventilation where vapors build up. Regulatory agencies call for SDS (Safety Data Sheets) with details about fire-fighting, first aid, and environmental controls. In end-use products, limits on concentration keep household exposure comfortably below established safety thresholds. Companies exporting terpineol face complex labeling and transport rules in different markets, including restrictions on storage temperatures and packaging formats. Regular audits and staff training keep risk in check throughout the value chain.
Application Area
Terpineol’s sweet, floral aroma makes it a favorite in soaps, shampoos, perfumes, and household cleaners. Food technologists use it as a flavoring agent in chewing gum, candies, baked goods, and beverages, appreciating its safety record and complex taste. Pharmaceutical firms rely on terpineol’s mild anesthetic and antiseptic effects for throat lozenges and cough syrups. Agricultural products use it as a green solvent alternative for botanicals in crop protection. Paints, inks, and coatings take advantage of its solvency for resins and dyes. Its use in electronics comes as a processing solvent for ceramics and as a formulation aid in screen printing pastes. Every year, new research papers describe unexpected uses, from pest repellents to fuel additives, building on terpineol’s flexible profile.
Research & Development
Academic groups keep busy probing terpineol’s antimicrobial and anti-inflammatory properties, looking for leads in drug discovery. Green chemistry teams use it as a model system for developing eco-friendly catalysts and enzyme-based transformations. Analytical scientists refine detection methods to spot low-level residues in food, workplace air, or consumer goods. Ingredient companies tap into structure–activity studies to fine-tune terpineol’s olfactory impact for custom fragrance blends. Collaboration between forestry operations and biotech startups looks set to improve yields from renewable feedstocks, turning terpineol into an icon for sustainable chemistry. Regulatory scientists, watching the shift toward “clean” and “natural” labels, keep reviewing safety studies and updating recommendations.
Toxicity Research
Decades of toxicological data lay a foundation for terpineol’s reputation as a safe food and fragrance additive. Acute oral toxicity sits well above common use limits, giving it a wide margin of safety. Patch testing in humans shows only rare reactions. Inhalation studies in rodents highlight possible nose and throat irritation at high vapor concentrations, but everyday use in consumer products falls safely below those levels. Scientists monitor long-term exposure effects, using animal models and cell assays to look for hidden risks such as mutagenicity or reproductive effects, finding little cause for concern so far. Current research focuses on combined effects with other essential oil constituents, supporting better consumer guidance for allergy and sensitivity labeling.
Future Prospects
The next chapter for terpineol looks set to run through green chemistry and innovation in product design. Growing appetite for plant-based and sustainable ingredients keeps demand robust in food, fragrance, and pharma. Researchers hunting for low-toxicity, biodegradable solvents see terpineol as a potential game changer in paints, inks, and specialty coatings. Synthetic biology may soon turn wood and agricultural waste into custom blends, slashing dependency on traditional turpentine harvests. In the regulatory world, stricter scrutiny of supply chain transparency will separate trustworthy producers from the rest, favoring those who embrace traceability and published test results. Lastly, digital platforms and artificial intelligence will make it easier to formulate new applications—linking terpineol’s tried-and-true appeal with tomorrow’s green products.
What Terpineol Really Offers
Terpineol isn’t the flashiest name in the world of chemicals, but take a look in your medicine cabinet or a cleaning supply shelf, and you might be closer to it than you’d guess. At its core, terpineol brings a soft, lilac-like scent that seems to show up everywhere—from fancy soaps to household cleaners and even in some food flavorings. The strength of terpineol lies not just in its aroma, but in the way it fits into different corners of everyday life.
Where People Meet Terpineol
Walk down any personal care aisle. The gentle, floral notes in a bottle of hand wash? Terpineol does much of the heavy lifting there. Perfumers and soap makers have long relied on it to bring a fresh, approachable character to their products. It gives a “clean” sensation without that harsh bite found in synthetic scents. These days, consumers ask about what’s inside the products on their shelves. Knowing that a fragrance ingredient is found in nature—like the pine tree, or even petitgrain oil—seems to matter more with each passing year.
Household Uses Go Beyond Scent
Beyond the first whiff, terpineol proves valuable in cleaning products. Many glass cleaners, surface sprays, and disinfectants tap terpineol’s solvent power. It helps break down grease and sticky residues, thanks to its ability to work well with water and oil, making cleanup less of a hassle. Several studies back up its usefulness against bacteria and fungi, which explains why it shows up in hospital-grade disinfectants just as much as bathroom sprays.
Food and Pharma: Playing Small but Key Roles
Terpineol’s food-grade cousin finds a home as a flavoring in candies, chewing gum, and even some baked goods. It offers a light citrusy lift—think subtle pine mixed with orange. The U.S. Food and Drug Administration regards it as generally safe in small amounts. My experience working on a bakery production line helped highlight how small tweaks in flavoring agents could make a big difference in the final product’s popularity. Terpineol was rarely the star, but it often helped balance the more dominant notes, keeping flavors from turning artificial or overwhelming.
In pharmaceuticals, terpineol’s mild antiseptic activity makes it useful in sore throat sprays and mouthwashes. Pharmaceutical developers often hunt for ingredients that can both preserve a formula and keep things palatable, and terpineol walks that line nicely. This points to a growing challenge in the medicinal world: winning patients’ trust with recognizable ingredients that do their job safely.
The Importance of Responsible Use
Like many ingredients in your home, the benefits of terpineol depend on how it’s used and sourced. Modern consumers and watchdogs look for proof of product safety and environmental responsibility. Reputable manufacturers work to source terpineol through greener ways, and researchers continue to look at potential for skin reactions, mostly at high concentrations.
There’s a clear need for chemists and companies to keep their labels honest and their processes responsible. Reading through scientific reports and watching conversations among formulation chemists, one thing stands out: transparency isn’t just a buzzword. Shoppers want to know not just what’s inside the bottle, but where it comes from and what kind of impact its use might leave behind. Terpineol offers plenty to daily life, especially when the care behind its use matches its usefulness.
The Everyday Use of Terpineol
Terpineol isn't a stranger to daily life—it's in soaps, perfumes, air fresheners, and even in some natural cleaning sprays. People get exposed to it on a regular basis without giving it much thought. Personal care companies lean on terpineol for its pleasant aroma and mild properties. Natural sources like pine oil and cajeput oil supply plenty of it, which adds to that clean, uplifting scent familiar in household products.
Skin Safety: Facts and Realities
Most folks apply products with terpineol directly to their skin. Based on published dermatology studies, the risk of skin irritation or allergic reaction stays quite low in most people. Concentrations used in commercial personal care items typically hover well below levels that raise red flags. The Cosmetic Ingredient Review (CIR) says it's generally safe at trace-to-moderate concentrations found in creams, lotions, or soaps. Dermatologists I’ve spoken with rarely see a case of allergic contact dermatitis caused by terpineol unless concentration climbs way above what’s seen in ordinary shampoos or moisturizers.
Still, not everyone has the same skin. Those with eczema, sensitive skin, or a long history of fragrance allergies could notice reactions. Swelling, itching, or redness sometimes pops up in people with delicate skin barriers when they use products packed with essential oils. Companies ought to label ingredient lists clearly for folks trying to avoid any triggers, even from natural oils.
Inhalation: Breathing Easy?
Essential oils fill my home with their scents on weekends, so I pay attention to what research says about breathing them in. Terpineol’s aroma drifts through many essential oil diffusers and cleaning sprays, and years of workplace safety data give a helpful road map. The National Institute for Occupational Safety and Health (NIOSH) and the EPA haven’t flagged low-level terpineol specifically as an acute inhalation hazard for healthy adults. Testing on volunteers and animal studies suggest that inhaling the trace amounts that float through home or office air brings little risk of lasting harm.
It’s a different story for jobs where people might handle drums of terpineol—chemical workers need good ventilation, gloves, and periodic air checks. Households with children or pets should keep diffusers in well-ventilated areas and take breaks between sessions. Asthma or other chronic lung conditions already create tougher circumstances, so it makes sense for anyone with a respiratory condition to check with a health professional before filling a room with any scented product, even those labeled ‘natural.’
Research Gaps and Safer Choices
Most studies on terpineol’s safety lean toward short-term use, with fewer long-term studies in diverse populations. Groups like infants, pregnant women, and older adults tend not to get represented much in these trials. If science catches up to these everyday gaps, clearer advice on long-term use may follow.
I recommend reading the labels, patch-testing skincare products, and being cautious with heavy use of diffusers. If terpineol causes any irritation, rash, or headache, switching to fragrance-free options could be the better route. Plenty of unscented soaps and lotions get the cleaning done without any fragrance at all.
Building more transparency in ingredient lists, improving labeling laws, and sharing data among researchers, doctors, and companies could improve consumer confidence down the line. Keeping an eye on future research and sharing any new reactions with your doctor helps create a safer landscape for everyone.
Aroma and Scent in Daily Life
Open a bottle of pine oil cleaner or walk past someone wearing a floral perfume, and you might already know terpineol’s signature. This natural compound, found in pine oil and some essential oils, brings a smooth, lilac-like scent that lifts the mood of a room. Studies highlight that manufacturers use terpineol to shape the base of countless fragrances. It’s in soaps, perfumes, and even air fresheners. Many people don't think about the roots of their favorite scents, but terpineol often acts as the engine behind them.
Therapeutic Properties and Everyday Health
Terpineol’s role doesn’t end at smelling pleasant. Over the past decade, scientific papers have dug into its antimicrobial and antioxidant qualities. Research published in journals such as Fitoterapia and the Journal of Applied Microbiology points out its ability to inhibit the growth of certain bacteria and fungi. People who use natural remedies might reach for essential oils rich in terpineol during cold season. One personally memorable winter, a vapor rub with terpineol soothed a relentless cough better than menthol-only brands. The reason: terpineol seems to help open nasal airways, according to small-scale studies. The difference between a restless night and a good sleep can hinge on these subtle effects.
Food Flavoring and Beverage Use
Take a deeper look at processed foods, and terpineol shows up again, this time as a flavoring agent. Regulatory bodies in the US and Europe approve it for human consumption within set limits. A slight sweetness, paired with citrusy or woody notes, lets food scientists build authentic-tasting products. My background in food service showed how much effort goes into achieving just the right “orange” note in a soft drink, where terpineol often provides that finishing touch. Without compounds like this, that nuanced flavor might fall flat.
Solvent Abilities and Industrial Utility
Cleaners that cut through greasy kitchen messes sometimes owe their bite to terpineol. The chemical structure gives it strong solvent properties, letting it dissolve oils and residues easily. Paint and printing ink producers rely on it for its quick evaporation and pleasant scent, which contrasts strongly with older, more pungent solvents. Industrial workers appreciate not having to breathe in the overpowering fumes common with traditional solvents. Terpineol helps modern manufacturing with fewer headaches—literally.
Sustainability Angle
Sustainability is a word thrown around a lot in materials science and consumer goods. Terpineol can claim an edge here: most of what’s found in commercial products comes from renewable sources like pine trees and turpentine oil, instead of petroleum. A move toward bio-based ingredients carries weight as both producers and consumers push for greener products that take less toll on the environment.
Safety Considerations
No compound is risk-free. Some people develop allergic reactions, mostly after direct skin contact with pure, concentrated terpineol. Major safety organizations report that food and fragrance applications present little risk at normal levels. Still, safe handling always matters, especially for those using essential oils undiluted or working with terpineol in industrial settings.
Looking Ahead: Embracing Versatility
From freshening rooms to caring for health, flavoring food, or tackling industrial mess, terpineol weaves through daily life more than most realize. With sound science backing its benefits and more producers focusing on renewable sources, it stands as a useful ingredient worth understanding and respecting.
Notes, Nuance, and Reminiscence
Walk through a pine forest on a cool day: terpineol lives in that sharp, gently floral scent. Whenever I open a bottle of hand soap with “pine” or “lilac” on the label, memory takes me back to the woods. Terpineol shares this connection to both the wild and the familiar. It delivers a scent both clean and a little sweet, like spring’s first breeze through open windows.
Terpineol tends to show up in the world wherever freshness gets bottled, whether it’s in perfumery, soapmaking, or even flavoring. Natural sources include pine oil, lilac blossoms, and eucalyptus leaves. What strikes most people about the smell is a blend of floral, piney, and even slightly citrus-like notes. If you catch the scent of a just-cut Christmas tree or the soft perfume of lilac blooming near a fence, chances are you’re smelling terpineol or something awfully close.
Personal Experience Meets Scientific Fact
The first time someone handed me a laboratory sample of terpineol, I expected medicine or cleaning products. Instead, it reminded me of a walk along a garden path after it rained. I learned pretty quickly that terpineol’s importance goes beyond just pleasant fragrance. Chemists and product developers pick terpineol not just for smell, but for comfort and recall. People trust this scent; they’ve lived with it in laundry, incense, vapor rubs, and even some citrus-flavored candies.
Chemically, terpineol exists in several forms, each carrying its own nuance. The most common, alpha-terpineol, leans toward lilac and hyacinth notes. Beta-terpineol drifts a little more toward balsam and green. These facts come from trustable sources, like GC-MS analysis in published fragrance databases and ingredient disclosures in regulatory filings. Alpha-terpineol specifically enjoys a GRAS (Generally Recognized as Safe) status, so it moves easily from industrial to home use.
Why the Smell Matters
A scent shapes emotion. Marketing studies repeatedly show consumers equate terpineol with a sense of cleanliness or purity. Take air fresheners; add terpineol, and people report a “fresher” home, even if nothing else changes. The psychological link is undeniable, drawing from both tradition and biochemistry. Brands rely on this to stir nostalgic feelings—connecting right to lived experience.
Terpineol does more than just freshen a room, though. It plays a role in the safety and acceptability of products. Ingredient transparency counts, especially for those sensitive to fragrance allergens. A company can support user confidence—and align with global standards—by listing terpineol on ingredient panels. The IFRA (International Fragrance Association) and other governing bodies limit levels for skin-contact products, reflecting a balance between aroma and responsible formulating.
People deserve honesty around what they’re breathing or putting on their skin. For companies: test for sensitivities, offer fragrance-free alternatives, and inform consumers. For the rest of us, recognizing terpineol in everyday life enriches appreciation for the world—one subtle breath at a time.
Possible Steps Forward
Greater public awareness of scents like terpineol opens the door to better choices. Regulators, manufacturers, and users share a stake in clear labeling, robust research, and safety standards. Ongoing studies into natural alternatives and synthetic routes help the industry respond to allergen or environmental concerns without sacrificing the familiar comfort people expect. Crowdsourcing fragrance feedback and making space for sensitive populations keeps product shelves both inclusive and inviting.
Terpineol’s distinctive smell bridges memory, science, and daily life. Understanding it brings us closer to the natural and the made—whether that’s pine needles in fresh air or a splash of lilac in the bath.
What is Terpineol?
Terpineol belongs to a group of related organic compounds. These molecules carry a noticeable lilac or piney scent, which shows up clearly in perfumes, soaps, and cleaning products. Anyone who’s ever walked through a pine forest or sniffed a violet-scented soap has probably encountered terpineol, whether they realized it or not.
Sourcing Terpineol: Nature Gets There First
Terpineol shows up naturally in many plants. Pine oil contains it. Lilacs, eucalyptus, and some citrus fruits also produce terpineol in smaller amounts. Extraction from essential oils like pine oil takes time and raw material, but there’s no doubt about its physical presence in the trees and flowers all over the world. The flavor and fragrance industries both prize natural terpineol for its fresh, pleasant quality.
Synthetic Production Steps Onto the Scene
The world asks for terpineol in much greater quantities than even pine forests can easily provide. Squeezing it out of natural sources only goes so far; forests take decades to grow and essential oil yields run low. Synthetic processes step in and fill this gap. Industrial labs create terpineol mostly by tweaking other terpene chemicals, like turpentine, which comes from pine resin. Those methods allow abundant and reliable supply.
Difference in Effects? Take a Hard Look
From a chemistry perspective, molecules of terpineol look and behave the same whether they come from natural extraction or a factory reactor. The nose won’t pick up a difference, nor will most product users. The final result delivers the same lilac-like scent and similar flavor profile. Still, for anyone focused on “natural” ingredients, synthetic origins may matter. Labels can carry emotional weight, and product manufacturers know that. So “natural terpineol” sometimes fetches a higher price and gets showcased in marketing, even if the scientific difference ends up nil.
Why the Debate Matters in Real Life
Conversation about natural versus synthetic terpineol touches more than the perfume world. People care deeply about transparency, health, and sustainability. If terpineol comes from forests, that raises questions about responsible sourcing and the pressure on wild ecosystems. Industries that rely only on natural extraction sometimes risk depleting plant populations. On the flip side, synthetic production calls for energy, solvents, and industrial infrastructure; that brings its own environmental footprint to the table. People weighing their own values or looking for greener lifestyles need real information, not marketing hype.
Transparency Builds Trust
Clear information about sourcing practices helps buyers make meaningful choices. I’ve walked the aisles of natural food stores, scanned ingredient lists, and talked to small business owners who prize honest labeling. Knowing where terpineol comes from helps everyone in the chain: growers, manufacturers, and end users. The more transparency companies show, the more customers can trust the promises on product labels.
Looking for Solutions
One step forward: more companies base their decisions not simply on price or production yield, but on responsible forestry, green chemistry, and independent testing. Stronger tracing systems and third-party certifications provide extra peace of mind. Governments and industry groups can enforce clear labeling standards. Consumers show their power, too, by supporting companies who lead with integrity and facts.
Final Thoughts
Terpineol’s story highlights a challenge facing many everyday ingredients. Choices about natural versus synthetic reflect bigger questions—of environment, trust, and personal values. In the end, informed choices rely on science, honesty, and thoughtful stewardship of both nature and technology.

| Names | |
| Preferred IUPAC name | 4-(Propan-2-yl)cyclohex-1-en-1-ol |
| Other names |
alpha-Terpineol
Terpenol dl-Terpineol Tebetanol Tetrahydro-4-methyl-2-(1-methylethyl)-2H-pyran-2-ol |
| Pronunciation | /ˈtɜːr.pɪ.ni.ɒl/ |
| Identifiers | |
| CAS Number | 8000-41-7 |
| Beilstein Reference | Beilstein Reference: 1721215 |
| ChEBI | CHEBI:26946 |
| ChEMBL | CHEMBL14804 |
| ChemSpider | 18727 |
| DrugBank | DB14029 |
| ECHA InfoCard | 01-2119453856-25-xxxx |
| EC Number | 232-268-1 |
| Gmelin Reference | **783** |
| KEGG | C06535 |
| MeSH | D013737 |
| PubChem CID | 10215 |
| RTECS number | YO8345000 |
| UNII | 3OWL53L36A |
| UN number | UN2912 |
| Properties | |
| Chemical formula | C10H18O |
| Molar mass | 154.25 g/mol |
| Appearance | Colorless liquid with a lilac odor |
| Odor | Lilac |
| Density | 0.936 g/cm³ |
| Solubility in water | slightly soluble |
| log P | 2.8 |
| Vapor pressure | 0.24 mmHg (25°C) |
| Acidity (pKa) | pKa 19.2 |
| Basicity (pKb) | 5.44 |
| Magnetic susceptibility (χ) | -8.41×10⁻⁶ cm³/mol |
| Refractive index (nD) | 1.474 |
| Viscosity | 185.53 cP (25°C) |
| Dipole moment | 2.74 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 217.8 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -469.1 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -4822.8 kJ/mol |
| Pharmacology | |
| ATC code | R05CB07 |
| Hazards | |
| GHS labelling | GHS07, GHS08 |
| Pictograms | GHS02,GHS07 |
| Signal word | Warning |
| Hazard statements | H226, H315, H319, H411 |
| Precautionary statements | P210, P262, P273, P280, P301+P312, P305+P351+P338, P337+P313 |
| NFPA 704 (fire diamond) | 2-2-0 |
| Flash point | 87°C |
| Autoignition temperature | 220 °C |
| Explosive limits | 0.85–6.7% |
| Lethal dose or concentration | LD50 (oral, rat): 4,300 mg/kg |
| LD50 (median dose) | LD50 (median dose): Oral, rat: 4,300 mg/kg |
| NIOSH | WSH6490000 |
| PEL (Permissible) | 50 ppm |
| REL (Recommended) | 19 mg/m³ |
| IDLH (Immediate danger) | 100 ppm |
| Related compounds | |
| Related compounds |
Menthol
Linalool Pinene Camphor Geraniol |
