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Diss Factsheets
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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
Direct observations: clinical cases, poisoning incidents and other
Administrative data
- Endpoint:
- direct observations: clinical cases, poisoning incidents and other
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1981
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Results from publication with well described details
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:
- Acute poisoning with pine oil - metabolism of monoterpenes
- Author:
- Köppel C, Tenczer J, Tönnesmann U, Schirop T and Ibe K
- Year:
- 1 981
- Bibliographic source:
- Archives of Toxicology 49(1):73-8
Materials and methods
- Study type:
- poisoning incident
- Endpoint addressed:
- basic toxicokinetics
- Principles of method if other than guideline:
- The blood and urine monoterpene concentrations were continuously monitored from a patient attempting suicide by ingestion of 400-500 mL pine oil.
- GLP compliance:
- no
Test material
- Reference substance name:
- Turpentine, oil
- EC Number:
- 232-350-7
- EC Name:
- Turpentine, oil
- Cas Number:
- 8006-64-2
- IUPAC Name:
- 8006-64-2
- Reference substance name:
- Turpentine, oil (gum)
- IUPAC Name:
- Turpentine, oil (gum)
- Test material form:
- other: liquid
- Details on test material:
- Name of test material (as cited in study report): pine oil
Composition of test material, percentage of components: 57% alpha-pinene, 8% beta-pinene, 26% carene, 6% limonene and 3% other hydrocarbons
Constituent 1
Constituent 2
Method
- Type of population:
- general
- Subjects:
- A 49 year old male (height 185 cm, body weight 85 kg)
- Ethical approval:
- not specified
- Route of exposure:
- oral
- Reason of exposure:
- intentional
- Exposure assessment:
- estimated
- Details on exposure:
- 400-500 mL of pine oil
- Examinations:
- - blood and urine analyses for α-pinene concentration
- detection of metabolites in urine
- circulatory functions, temperature, pulse
- electro encephalogram (EEG) - Medical treatment:
- After continuous stomach lavage 250 mL paraffine oil and saline laxatives were given. Hemoperfusions with activated charcoal and amberlite and a hemodialysis were performed.
Results and discussion
- Clinical signs:
- Psychomotric excitation, headache, erythem of mouth and larynx, a flush of the face, ataxia, and a spontaneous hyperventilation. With a latence of 10 h after ingestion the consciousness of the patient was impaired and the circulatory parameters became instable although a hypovolemy could be excluded.
- Results of examinations:
- The circulatory parameters and the laboratory data were in the normal range. The EEG recorded the second day revealed a decelerated activity. No epileptogenic activities could be detected. The patient had a retrograde amnesia for the period of somnolence and sopor. At this time a leukocytosis (21000/mm3), a slight raise of the transaminases, and a reduction of the pseudocholinesterase (1446 U/L) were observed. The renal functions were not affected except a transient oliguria which was due to the drop of the blood pressure.
- Effectivity of medical treatment:
- After infusion of dopamine and dobutamine, the circulatory functions stabilized. Hemoperfusion eliminates monoterpenes quite effectively from the blood compartment thereby protecting the renal functions.
- Outcome of incidence:
- Three weeks later the patient left the clinic without any bodily complaints.
Applicant's summary and conclusion
- Conclusions:
- Psychomotric excitation, headache, erythem of mouth and larynx, a flush of the face, ataxia, and a spontaneous hyperventilation can be observed after ingestion of a letal dose of pine oil (400-500 mL). Impaired conciousness and instable circulatory parameters can happen several hours after ingestion. After infusion of dopamine and dobutamine, the circulatory functions stabilized. Hemoperfusion eliminated monoterpenes thereby protecting the renal functions.
- Executive summary:
A patient attempting suicide ingested 400-500 mL pine oil and was admitted to the clinic. Since more than the potentially lethal dose had been ingested hemoperfusions with activated charcoal and amberlite and a hemodialysis were performed. Clinical signs observed were: psychomotric excitation, head ache, erythem of mouth and larynx, a flush of the face, ataxia, and a spontaneous hyperventilation. With a latence of 10 h after ingestion the consciousness of the patient was impaired and the circulatory parameters became instable although a hypovolemy could be excluded. Three weeks later the patient left the clinic without any bodily complaints.
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