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EC number: 232-350-7 | CAS number: 8006-64-2 Any of the volatile predominately terpenic fractions or distillates resulting from the solvent extraction of, gum collection from, or pulping of softwoods. Composed primarily of the C10H16 terpene hydrocarbons: α-pinene, β-pinene, limonene, 3-carene, camphene. May contain other acyclic, monocyclic, or bicyclic terpenes, oxygenated terpenes, and anethole. Exact composition varies with refining methods and the age, location, and species of the softwood source.
- 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
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1967
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- No information on housing conditions of animals, body weight of animals not recorded during the study
Cross-reference
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 967
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- Deviations:
- yes
- Remarks:
- no information on housing conditions of animals, body weight of animals not recorded during the study
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Turpentine, oil
- EC Number:
- 232-350-7
- EC Name:
- Turpentine, oil
- Cas Number:
- 8006-64-2
- Molecular formula:
- UVCB substance molecular formula varied but mainly C10H16, C15H24, C2H6S1, C1H4S1 and C10H18O1
- IUPAC Name:
- Turpentine oil from pulping processes
Constituent 1
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 140-200 g
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Vehicle:
- air
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: Glass cylinder
- Exposure chamber volume: 42 mm * 30 cm
- Pressure in air chamber: 3 mm of water
TEST ATMOSPHERE
- Brief description of analytical method used: 0.4-0.5 mL of sample were withdrawn with a gas-tight syringe and injected into a hydrogen-flame gas chromatograph.
- Samples taken from breathing zone: yes - Analytical verification of test atmosphere concentrations:
- yes
- Duration of exposure:
- >= 1 - 6 h
- Concentrations:
- - 12.6-15.7; 15.8-19.8; 19.9-25.0 and 25.1-31.5 mg/L for 1 hour exposure
- 18-22 mg/L (2 hours exposure); 15-19 mg/L (4 hours exposure) and 7; 8-9; 10-11 and 13-17 mg/L (6 hours exposure) - No. of animals per sex per dose:
- 10-19 animals per concentration
- Control animals:
- yes
- Details on study design:
- - Duration of observation period following administration: 1 week
- Frequency of observations: Turpentine concentration in rat tissue was determined after 15, 30, 60 mins and 2 hours after exposure
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, organ-body weight ratio, distribution and concentration of turpentine in tissues - Statistics:
- All LC50 calculations were done by the Litchfield-Wilcoxon (1949) method.
Results and discussion
- Preliminary study:
- Not applicable
Effect levels
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- 13.7 mg/L air (nominal)
- Based on:
- test mat.
- 95% CL:
- >= 11.1 - <= 14.8
- Exp. duration:
- 4 h
- Mortality:
- - 8.3% (at 12.6-15.7mg/L); 25.0% (at 15.8-19.8mg/L); 92.3% (at 19.9-25.0mg/L) and 90.0% (at 25.1-31.5 mg/L) at 1 hour exposure of turpentine concentration
- Clinical signs:
- other: Convulsions and apnea; increase in respiratory rate and decrease in tidal volume
- Body weight:
- No data
- Gross pathology:
- Organ body-weight and lesions noticed in lungs were similar in type and extent to those found among controls
- Other findings:
- - Lung concentrations were higher 30 minutes after 1 and 2 hours after exposure, than after 15 minutes. All tissues, except lung, followed a typical exponential decay curve
- Brain and spleen had the highest concentrations immediately and 60 minutes after exposure
Any other information on results incl. tables
Table 1: Results of a single 1-hour exposure of rats to different concentrations of turpentine vapor
Range of concentrations (mg/L) |
Logarithm of difference within range |
Mean of range |
Logarithm of difference between means |
mortality (%) |
12.6-15.7 |
0.1 |
14.5 |
8.3 |
|
15.8-19.8 |
0.1 |
17.1 |
0.072 |
25 |
19.9-25.0 |
0.1 |
21.9 |
0.107 |
92.3 |
25.1-31.5 |
0.1 |
27.7 |
0.101 |
90 |
Table 2: Summary of LC50s for rats for various periods of exposure to turpentine vapor
Duration of exposure (hours) |
LC50 (mg/L) |
Fiducial limits (mg/L) |
Slope |
Fiducial limits |
1 |
16.9 |
17.5-22.7 |
1.24 |
1.12-1.36 |
2 |
16.6 |
15.9-17.9 |
1.19 |
1.12-1.26 |
4 |
13.7 |
11.1-14.8 |
1.23 |
1.12-1.35 |
6 |
11.7 |
10.6-12.7 |
1.21 |
1.11-1.32 |
Table 3: Concentration of turpentine in tissues of rats at various intervals after a 1-hour or a 2-hour exposure to vapor of turpentine
Tissue |
Mean recovery (%) |
Concentration after 1 hour exposure (µg/g) |
Concentration after 2 hour exposure (µg/g) |
||||||
Zero time |
15 min |
30 min |
60 min |
Zero time |
15 min |
30 min |
60 min |
||
Brain |
25 |
160 |
63 |
49 |
20 |
127 |
47 |
21 |
15 |
Spleen |
50 |
214 |
127 |
39 |
19 |
94 |
32 |
15 |
17 |
Kidney |
35 |
146 |
58 |
26 |
0 |
97 |
26 |
8 |
12 |
Liver |
15 |
167 |
43 |
33 |
0 |
157 |
34 |
17 |
8 |
Lung |
50 |
101 |
0 |
26 |
0 |
54 |
20 |
25 |
7 |
Blood |
65 |
24 |
16 |
8 |
1 |
4 |
0.4 |
0.7 |
0.9 |
Applicant's summary and conclusion
- Interpretation of results:
- Category 4 based on GHS criteria
- Conclusions:
- Under the test conditions, the inhalation LC50 for turpentine was found to be 13.7 mg/L/4 hours in rats and therefore it is classified as “R20 Harmful by inhalation” according to the annex VI of the Directive 67/548/EEC and category 4 according to the CLP Regulation (EC) N° (1272-2008).
- Executive summary:
In an inhalation acute toxicity study performed following a method similar to OECD guideline 403, groups of male rats (10-19/concentration) were exposed to turpentine vapors at concentrations of 12.6-15.7; 15.8-19.8; 19.9-25.0 and 25.1-31.5 mg/L for 1 hour, 18-22 mg/L for 2 hours, 15-19 mg/L for 4 hours and 7; 8-9; 10-11 and 13-17 mg/L for 6 hours. Surviving animals were then observed for mortality and clinical signs of toxicity for one week and were all macroscopically necropsied which included measurement of organ-bodyweight ratios and distribution and concentration of turpentine in tissues.
8.3, 25, 92.3 and 90% mortalities were observed when animals were exposed to turpentine vapors for 1 hour at various concentrations of 12.6-15.7, 15.8-19.8, 19.9-25.0 and 25.1-31.5 mg/L, respectively. Deaths were always preceded by convulsions and sudden apnea but these were not always followed by death. Increase in respiratory rate and decrease in tidal volume were noticed in exposed animals. Tissue distribution of turpentine in rats showed that brain and spleen had the highest concentrations immediately and 60 minutes after exposure. Organ body-weights and lesions noticed in lungs were similar in type and extent to those found among controls. The 4 hours LC50 for turpentine vapors was calculated to be 13.7 mg/L.
Under the test conditions, the inhalation LC50 for turpentine was found to be 13.7 mg/L/4 hours in rats and therefore it is classified as “R20 Harmful by inhalation” according to the annex VI of the Directive 67/548/EEC and category 4 according to the CLP Regulation (EC) N° (1272-2008).
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