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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

Currently viewing:

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
Not specified
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: pre-GLP study
Cross-reference
Reason / purpose for cross-reference:
reference to same study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1967
Report date:
1967

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
No remarks
GLP compliance:
no
Remarks:
pre-GLP
Test type:
other: not specified
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
3,7-dimethylnona-1,6-dien-3-ol
EC Number:
233-732-6
EC Name:
3,7-dimethylnona-1,6-dien-3-ol
Cas Number:
10339-55-6
Molecular formula:
C11H20O
IUPAC Name:
3,7-dimethylnona-1,6-dien-3-ol
Details on test material:
Ethyllinalool, no further information

Test animals

Species:
mouse
Strain:
other: CFW
Sex:
male
Details on test animals or test system and environmental conditions:
Weight: 17-22 g

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
unchanged (no vehicle)
Details on oral exposure:
72 hours observation for mortality
Doses:
Not indicated
No. of animals per sex per dose:
5
Control animals:
not specified
Details on study design:
No remarks
Statistics:
Not indicated

Results and discussion

Preliminary study:
Not indicated
Effect levels
Key result
Sex:
male
Dose descriptor:
LD50
Effect level:
5 283 mg/kg bw
Mortality:
The oral LD50 in mice was determined to be 5283 +/- 383 mg/kg bw.
LD50's were calculated by the method of Miller and Tainter (Proc. Soc. Exptl. Biol. Med. 57:261, 1944).
Clinical signs:
other: Not indicated
Gross pathology:
Not indicated
Other findings:
Not indicated

Any other information on results incl. tables

Not relevant

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The substance does not have to be classified according to the classification criteria outlined in 67/548/EEC and 1272/2008/EC.
Executive summary:

The oral LD50 in mice was determined to be 5283 +/- 383 mg/kg bw.