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EC number: 209-578-0 | CAS number: 586-62-9
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Endpoint summary
Administrative data
Link to relevant study record(s)
Description of key information
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
Additional information
No data on toxicokinetic properties of terpinolene monoconstituent (absorption, distribution, metabolism, elimination) are available in the literature. In accordance with REACH guidance document R.7c., the expected toxicokinetic behaviour of terpinolene monoconstituent is derived from its physicochemical properties and the available toxicological data.
d-limonene and terpinolene monoconstituent are monocyclic monounsaturated terpenes and as shown in the table below, they have very similar physicochemical properties. Therefore information on the structure-related d-limonene is considered to be representative of the toxicokinetic properties of terpinolene monoconstituent.
|
Molecular weight |
Water solubility (mg/L) |
Log Kow |
Vapour pressure (Pa at 25°C) |
d-limonene |
136 |
Column elution method : 3.99 Slow stirring method : 5.69 |
4.38 |
200 |
Terpinolene monoconstituent |
136 |
Column elution method : 4.55 Slow-stirring method : 7.03 |
4.33 |
101 |
Terpinolene monoconstituent is a mono constituent having a relatively low molecular weight of 136. It is a liquid with a low water solubility of about 4.6 mg/L and has high lipophilic properties (log Pow = 4.33). Vapour pressure was determined to be about 101 Pa at 20°C. Detailed information can be found in section 4 of terpinolene monoconstituent IUCLID dossier.
Studies of terpene hydrocarbons indicate that they are rapidly absorbed, distributed, metabolized and excreted. The principal metabolic pathway involves side chain oxidation to yield monocyclic terpene alcohols and carboxylic acids. These metabolites are mainly conjugated with glucuronic acid and excreted in the urine, or to a lesser extent in the feces. A secondary pathway involves epoxidation of either the exocyclic or endocyclic double bond yielding an epoxide that is subsequently detoxicated via formation of the corresponding diol or conjugation with glutathione. Humans are continually exposed to limonene and terpinolene monoconstituent throughout their lifetimes, via consumption of a traditional diet or inhalation of air. Extensive studies on d-limonene show rapid metabolism to polar oxidized metabolites, followed by conjugation and rapid excretion.
Absorption:
Terpinolene monoconstituent being lipophilic (log Kow = 4.33), the rate of uptake into the stratum corneum is expected to be high while the rate of penetration is likely to be limited by the rate of transfer between the stratum corneum and the epidermis. Moreover, it is assumed that the dermal uptake is also limited by its low water solubility. These assumptions are supported by the absence of systemic effects following single-dose dermal application of terpinolene monoconstituent up to 2000 mg/kg bw which would suggest a limited systemic absorption through cutaneous barriers. Moreover, enhanced skin penetration is not expected since terpinolene monoconstituent is not a skin irritant or corrosive. However, it was found to be skin sensitizing therefore some uptake, even limited, must have occurred. Thus, dermal absorption of terpinolene monoconstituent is expected to be limited but not inexistent.
In shaved mice, the dermal absorption of [3H]d/l-limonene from bathing water was rapid, reaching the maximum level in 10 minutes (von Schäfer & Schäfer, 1982). In one study (where one hand exposed to 98% d-limonene for 2 hours), the dermal uptake of d-limonene in humans was reported to be low compared with that by inhalation (Falk et al., 1991); quantitative data were not provided.
Terpinolene monoconstituent has high log Kow (>4) and is a small molecule (molecular weight < 200). Therefore, it could be absorbed orally by passive diffusion. It is of adequate molecular size to participate in endogenous absorption mechanisms within the mammalian gastrointestinal tract. Being lipophilic, it may cross gastrointestinal epithelial barriers even if the absorption may be limited by the inability of the substance to dissolve into gastro-intestinal fluids and hence make contact with the mucosal surface. The acute oral gavage toxicity study identified no evidence of systemic toxicity, i.e. neither mortality nor macroscopic effects although high lethal doses were tested (up to 5 mL/kg bw). Oral bioavailability is confirmed in a combined repeated dose toxicity study with reproduction/developmental toxicity screening test where bodyweight gain was reduced at the highest dose group for females. Macroscopic observations at necropsy showed an increase in liver weight both absolute and relative to terminal body weight in males. Histopathology revealed reversible minimal to slight centrilobular hepatocellular hypertrophy in males treated with 2500 and 5000 ppm. These adaptive changes recorded in liver are compatible with metabolism in this detoxifying organ in response to xenobiotic exposure.
Orally administered, d-limonene is rapidly and almost completely taken up from the gastrointestinal tract in humans as well as in animals (Igimi et al., 1974; Kodama et al., 1976). Infusion of labelled d-limonene into the common bile duct of volunteers revealed that the chemical was very poorly absorbed from the biliary system (Igimi et al., 1991).
Thus, indications of oral uptake of terpinolene monoconstituent at high doses are given while dermal uptake would be more limited.
No study by inhalation was performed. However, considering the low vapour pressure of terpinolene monoconstituent (<500 Pa), exposure by inhalation is likely to be very limited.
d-limonene has a high partition coefficient between blood and air and is easily taken up in the blood at the alveolus (Falk et al., 1990). The net uptake of d-limonene in volunteers exposed to the chemical at concentrations of 450, 225, and 10 mg/m3 for 2 hours during light physical exercise averaged 65% (Falk Filipsson et al., 1993).
Therefore the potential bioavailability of terpinolene monoconstituent can be considered mainly by oral route.
Distribution:
Terpinolene monoconstituent is a small molecule with low water solubility and high lipophilicity which indicates that it could be widely distributed; based on its lipophilic character, the substance would readily cross cellular barriers or would be distributed into fatty tissues with a low potential to accumulate (see Accumulation potential below).
d-Limonene is rapidly distributed to different tissues in the body. A high oil/blood partition coefficient and a long half-life during the slow elimination phase suggest high affinity to adipose tissues (Falk et al., 1990; Falk Filipsson et al., 1993). In rats, the tissue distribution of radioactivity was initially high in the liver, kidneys, and blood after the oral administration of [14C]d-limonene (Igimi et al., 1974); however, negligible amounts of radioactivity were found after 48 hours. Differences between species regarding the renal disposition and protein binding of d-limonene have been observed. For rats, there is also a sex-related variation (Lehman-McKeeman et al., 1989; Webb et al., 1989). The concentration of d-limonene equivalents was about 3 times higher in male rats than in females, and about 40% was reversibly bound to the male rat specific protein, 2µ-globulin (Lehman-McKeeman et al., 1989; Lehman-McKeeman & Caudill, 1992).
Metabolism:
No data are available but, in in vitro genotoxicity studies, differences in cytotoxicity were observed with and without metabolic activation: in Ames test, terpinolene monoconstituent concentrations leading to cytotoxicity were higher in presence of metabolic activation than without metabolic activation. The same effect was observed in chromosome aberration test on human lymphocytes. This indicates that the substance is metabolised by hepatic microsomal fractions.
Also, in a combined repeated dose toxicity study with reproduction/developmental toxicity screening test, adaptive effects such as increased liver weight and minimal to slight diffuse hepatocellular hypertrophy were observed in males at high doses, which is suggestive of metabolism in this organ.
In humans, d-limonene given orally, yields the following major plasma metabolites: perillic acid, limonene-1,2-diol, limonene-8,9-diol, and dihydroperillic acid, probably derived from perillic acid (Poon et al., 1996; Crowell et al., 1994; Vigushin et al., 1998). Peak plasma levels for all metabolites were achieved 4-6 hours after administration, with the exception of limonene-8,9-diol which reached its peak level one hour after administration (Crowell et al., 1994). Phase II glucuronic acid conjugates have been identified in the urine of human volunteers for all metabolites (Poon et al., 1996; Kodama et al., 1974; 1976).
The biotransformation of d-limonene has been studied in many species, with several possible pathways of metabolism. Metabolic differences between species have been observed with respect to the metabolites present in both plasma and urine. About 25-30% of an oral dose of d-limonene in humans was found in urine as d-limonene-8,9-diol and its glucuronide; about 7-11% was eliminated as perillic acid (4-(1- methylethenyl)-1-cyclohexene-1-carboxylic acid) and its metabolites (Smith et al., 1969; Kodama et al., 1976). In another study, perillic acid was reported to be the principal metabolite in plasma in both rats and humans (Crowell et al., 1992). Other reported pathways of d-limonene metabolism involve ring hydroxylation and oxidation of the methyl group (Kodama et al., 1976). Urinary metabolites isolated from male rabbits orally administered [14C]-d-limonene included perillic acid-8,9-diol (major), p-menth-1,8-dien-10-ol, p-menth-1-ene-8,9-diol, perillic acid, p-mentha-1,8-dien-10-yl glucuronic acid and 8-hydroxy-p-menth-1-en-9-ylbeta-glucopyranosiduronic acid [Kodama et al., 1974].
In Phase I metabolism, the biotransformation of d-limonene and terpinolene monoconstituent are catalyzed by NADPH-dependent cytochrome P450 (CYP). d-Limonene (monocyclic hydrocarbon) has been shown to be substrate (upon repeated administration) and competitive inhibitor of the isoenzyme, specifically CYP2B1 and CYP2C11 (Miyazawa et al., 2002). d-limonene has also been shown to induce the members of the CYP2B family in several studies (Maltzman et al., 1991; Hiroi et al., 1995).
Excretion:
Due to its low molecular weight (lower than 300), terpinolene monoconstituent is expected to be mainly excreted in urine and no more than 5-10% may be excreted in bile. Urinary excretion is supported by metabolism data described above but also by the effects identified in the repeated dose toxicity study with reproduction/developmental toxicity screening test. At 3000 and 9000 ppm, partly reversible changes in kidney (tubular degeneration/regeneration, hyaline droplets and granular casts) were observed in main phase and recovery males. Although these effects are specific to male rat, they are suggestive of excretion via urine of the parent molecule or its metabolites.
Clearance from the blood was 1.1 L/kg body weight per hour in males exposed for 2 hours to d-limonene at 450 mg/m3 (Falk Filipsson et al., 1993). About 60% of the radiolabelled d-limonene administered by inhalation was recovered from the urine, with 5% from feces and 2% from expired CO2 in rats (Igimi et al., 1974). Following the inhalation exposure of volunteers to d-limonene at 450 mg/m3 for 2 hours, three phases of elimination were observed in the blood, with half-lives of about 3, 33, and 750 minutes, respectively (Falk Filipsson et al., 1993). About 1% of the amount taken up was eliminated unchanged in exhaled air, whereas about 0.003% was eliminated unchanged in the urine. When male volunteers were administered (per os) 1.6 g [14C]d-limonene, 50-80% of the radioactivity was eliminated in the urine within 2 days with less than 10% appearing in the feces (Kodama et al., 1976). d-limonene has been detected, but not quantified, in breast milk of non-occupationally exposed mothers (Pellizzari et al., 1982).
Accumulative potential:
Terpinolene monoconstituent has a low water solubility (< 100 mg/L) and high log Kow (>4) therefore it has affinity to adipose tissues; however, bioaccumulation is not expected to occur, since it is efficiently metabolized to yield oxygenated metabolites that are subsequently conjugated with glucuronic acid and excreted mainly in the urine.
References:
Belsito, D., Bickers, D., Bruze, M., Calow, P., Greim, H., Hanifin, J.M., Rogers, A.E., Saurat, J.H., Sipes, I.G., Tagami, H., 2008. A toxicologic and dermatologic assessment of cyclic acetates when used as fragrance ingredients. Food Chem. Toxicol. 46 Suppl 12, S1–27.
Ishida, T., Toyota, M., Asakawa, Y., 1989. Terpenoid biotransformation in mammals. V. Metabolism of (+)-citronellal, (+-)-7-hydroxycitronellal, citral, (-)-perillaldehyde, (-)-myrtenal, cuminaldehyde, thujone, and (+-)-carvone in rabbits. Xenobiotica 19, 843–855.
Alicyclic Primary Alcohols, Aldehydes, Acids, and Related Esters,WHO Food Additives Series 50
Falk Filipsson, A., 1998. Concise International Chemical Assessment Document 5 - Limonene, 32 Chapitre 7. Comparative kinetics and metabolism in laboratory animals and humans.
Flavor and Fragrance High Production Volume Chemical Consortia, 2006, HPV Monoterpene Hydrocarbons
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