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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
other information
Study period:
No data
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Only a very brief report in a secondary source is available on the unspecified isomer. Primary Russian publication (Volkova et al. 1998) could not be obtained

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
[Unknown]
Author:
Volkova NV et al.
Year:
1998
Bibliographic source:
Vrednie chemichescie veshestva. Prirodnie organicheskie soedinenia (Hazardous substances. Nature products), 285
Reference Type:
secondary source
Title:
Unnamed
Year:
2003

Materials and methods

Principles of method if other than guideline:
No data on methodology given in secondary source
GLP compliance:
not specified
Test type:
other: no data

Test material

Constituent 1
Reference substance name:
alpha pinene epoxide (unspecified isomer)
IUPAC Name:
alpha pinene epoxide (unspecified isomer)
Constituent 2
Chemical structure
Reference substance name:
2,7,7-trimethyl-3-oxatricyclo[4.1.1.02,4]octane
EC Number:
216-869-6
EC Name:
2,7,7-trimethyl-3-oxatricyclo[4.1.1.02,4]octane
Cas Number:
1686-14-2
Molecular formula:
C10H16O
IUPAC Name:
2,7,7-trimethyl-3-oxatricyclo[4.1.1.0~2,4~]octane
Test material form:
not specified
Details on test material:
- Name of test material (as cited in study report): pinane, 2,3-epoxy-- Molecular formula (if other than submission substance): C10-H16-O- Molecular weight (if other than submission substance): 152.235- Smiles notation (if other than submission substance): C1([C@@H]2[C@@]3(O[C@@H]3C[C@@H]1C2)C)(C)C- InChl (if other than submission substance): 1S/C10H16O/c1-9(2)6-4-7(9)10(3)8(5-6)11-10/h6-8H,4-5H2,1-3H3 - Structural formula attached as image file (if other than submission substance): see Fig. 1- Substance type: no data in citing source- Physical state: no data in citing source- Analytical purity: no data in citing source- Impurities (identity and concentrations): no data in citing source- Composition of test material, percentage of components: no data in citing source- Isomers composition: no data in citing source- Purity test date: no data in citing source- Lot/batch No.: no data in citing source- Expiration date of the lot/batch: no data in citing source- Stability under test conditions: no data in citing source- Storage condition of test material: no data in citing source

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified
Doses:
No data in citing source
No. of animals per sex per dose:
No data in citing source
Control animals:
not specified

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
ca. 2.4 mL/kg bw
Based on:
not specified
Remarks on result:
other: No exposure duration or confidence intervals given.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated informationCriteria used for interpretation of results: EU
Conclusions:
A secondary source (RTECS) provides limited details of an acute oral [presumably gavage] toxicity study conducted on rats given pinene alpha epoxide (unspecified isomer). The reported oral LD50 was 2.4 ml/kg bw [about 2.4 g/kg bw].
Executive summary:

A secondary source (RTECS) provides limited details of an acute oral toxicity study conducted on rats given pinene alpha epoxide (unspecified isomer) [presumably by gavage]. [The original Russian publication could not be obtained.] The reported oral LD50 was 2.4 ml/kg bw [about 2.4 g/kg bw].

According to the EU CLP and DSD regulations, this would not require classification for acute oral toxicity.