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EC number: 242-060-2 | CAS number: 18172-67-3
- 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
Exposure related observations in humans: other data
Administrative data
- Endpoint:
- exposure-related observations in humans: other data
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Study period:
- No data
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Only 8 volunteers studied. Because of the limited number of subjects, it was not possible to evaluate the relevance of the tendency towards increased airway diameters.
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- publication
- Title:
- Uptake, distribution and elimination of α-pinene in man after exposure by inhalation
- Author:
- Falk AA, Hagberg MT, Löf AE, Wigaeus-Hjelm EM and Zhiping W
- Year:
- 1 990
- Bibliographic source:
- Scand J Work Environ Health 16(5):372-8
Materials and methods
- Type of study / information:
- Subjective perception of irritation of eyes, nose and throat and effects on the central nervous system and pulmonary functions in human volunteers were studied during exposure to (+)-alpha-pinene by inhalation (2 h, 50 W).
- Endpoint addressed:
- other: Subjective perception of irritation of eyes, nose and throat and effects on the central nervous system and pulmonary functions
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The toxicokinetics of (+) and (-)-alpha-pinene was studied in human volunteers exposed by inhalation (2 h, 50 W) in an exposure chamber on four occasions. Subjective perception of irritation of eyes, nose and throat and effects on the central nervous system and pulmonary functions were also studied.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Pin-2(3)-ene
- EC Number:
- 201-291-9
- EC Name:
- Pin-2(3)-ene
- Cas Number:
- 80-56-8
- Molecular formula:
- C10H16
- IUPAC Name:
- 2,6,6-trimethylbicyclo[3.1.1]hept-2-ene
- Test material form:
- not specified
- Details on test material:
- Name of test material (as cited in study report): alpha-pinene
Source: Aldrich, Federal Republic of Germany
Purity: 98 %
Constituent 1
Method
- Ethical approval:
- confirmed, but no further information available
- Remarks:
- study was approved by the Regional Ethical Committee at the Karolinska Institute, Solna, Sweden.
- Details on study design:
- Subjects: Eight healthy men, with a mean (range) age of 31 (24-39) years and weight of 80 (71-96) kg participated in the study. The subjects were not occupationally exposed to solvents and were instructed to refrain from drinking alcoholic beverages for at least 2 days before each exposure. All the participants were given a general medical examination preceding the experiment and were judged to be healthy.
Experimental design: The subjects were exposed to α-pinene for 2 h during light physical exercise (50 W on a bicycle ergometer) in an exposure chamber on four occasions. Two subjects were exposed on each occasion. The concentrations were 10, 225 and 450 mg/m3 for (+)-α-pinene and 450 mg/m3 for (-)-α-pinene. The sequence of the exposure concentrations was based on a Latin square 4 x 4 design. The subjects were informed of the experimental design but were not told the exposure sequence. The volume of the chamber was 12 m3. The air was changed 10 times/h. To prevent the solvent from leaking from the chamber into the surroundings, the inlet flow was 115 m3/h and the outlet flow was 135 m3/h. The solvent was injected into the inflowing air stream by means of a high-performance liquid chromatographic pump (Gilson 302). - Exposure assessment:
- measured
Results and discussion
- Results:
- - Five subjects experienced irritation of their eyes, nose, and throat during the high exposures.
- No statistically significant acute changes in lung function parameters and the tendency of change was towards increased bronchial diameter rather than bronchoconstriction.
Any other information on results incl. tables
Table 7.10.5/1: Preexposure lung function values and the percentage of change 30 min after a 2-h inhalation exposure (50 W) to (+)-α-pinene at concentrations of 10 and 450 mg/m3
|
FEV 1,0 (L) |
VC (L) |
RV (L) |
PEF (L) |
MEF50 (L/s-1) |
sGaw (L/kPa/s) |
Raw (kPaxs/L) |
Preexposure values |
4.8 ± 0.6 |
6.6 ± 0.7 |
2.9 ± 1.1 |
12.7 ± 2.8 |
5.2 ± 1.1 |
2.1 ± 1.0 |
0.14 ± 0.05 |
Percentage of change after 30 min |
|
|
|
|
|
|
|
10 mg/m3 |
0.5 ± 0.1 |
-0.1 ± 13 |
-5.8 ± 24 |
0.4 ± 13 |
1.7 ± 5.6 |
16 ± 55 |
-25 ± 23 |
450 mg/m3 |
3.4 ± 4.7 |
0.8 ± 6.4 |
1.5 ± 26 |
3.2 ± 12 |
5.5 ± 7.6 |
5.4 ± 49 |
-25 ± 26 |
FEV1.0 = forced expiratory volume in 1 s, VC = vital capacity , RV = residual volume, PEF = peak expiratory flow, MEF50 = mean expiratory flow at 50 % of the VC, sGaw = conductance, Raw = resistance
Applicant's summary and conclusion
- Conclusions:
- There was a statistically significant exposure-response relationship among five subjects who experienced a subjective perception of irritation of eyes, noise and throat, especially at high exposures. Short-time exposure to (+)-alpha-pinene did not give rise to acute changes in lung function 30 min after the exposure.
- Executive summary:
In this study, eight male volunteers were exposed to 10, 225 and 450 mg/m3 of (+)-alpha-pinene and 450 mg/m3 of (-)-alpha-pinene
by inhalation (2h with physical exercise workload of 50 W) in a 12 m3 exposure chamber on four occasions. The sequence of exposure concentrations was not the same amongst the volunteers. The subjects were not occupationally exposed to solvents and instructed to refrain from drinking alcoholic beverages for at least 2 days before each exposure. Their general health status was checked prior to the experiment. Continuous monitoring of alpha-pinene concentration in the exposure chamber air during each exposure; alpha-pinene concentrations at selected intervals in exhaled air, in blood and in urine, during and after each exposure were performed. Subjective perception of irritation of eyes, nose and throat and effects on the central nervous system, pulmonary functions before, during and after each exposure were studied.
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