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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
1977, other details not available
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:
1977
Report date:
1978

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
no remarks
GLP compliance:
no
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
3,7-dimethyloct-6-en-1-yn-3-ol
EC Number:
249-482-6
EC Name:
3,7-dimethyloct-6-en-1-yn-3-ol
Cas Number:
29171-20-8
Molecular formula:
C10H16O
IUPAC Name:
3,7-dimethyloct-6-en-1-yn-3-ol
Details on test material:
- Name of test material (as cited in study report): Dehydro-linalool
- Physical state: Liquid

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
No indication

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
olive oil
Remarks:
emulsion
Details on oral exposure:
Not indicated
Doses:
no remarks
No. of animals per sex per dose:
Not indicated
Control animals:
not specified
Details on study design:
Not indicated
Statistics:
Not indicated

Results and discussion

Preliminary study:
No remarks
Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
3 100 mg/kg bw
Mortality:
Deaths occurred on day 1
Clinical signs:
Clinical signs consisted of staggering, atony, narcosis with pain and cornea reflex not present, tremors, salivation, lacrimation, spastic movements, exsiccosis.
Body weight:
No indication
Gross pathology:
No remarks
Other findings:
Necropsy of pre-mature deaths consisted of dilated atrium, acute congested hyperaemia of the heart, single edemateous lungs, atonic stomach / intestines. No necropsy findings were seen in animals sacrificed scheduled.

Any other information on results incl. tables

Not relevant

Applicant's summary and conclusion

Conclusions:
The LD50 oral in rats was calculated to be about 3100 mg/kg bw.
Executive summary:

Deaths occurred on day 1. Clinical signs consisted of staggering, atony, narcosis with pain and cornea reflex not present, tremors, salivation, lacrimation, spastic movements, exsiccosis. Necropsy of pre-mature deaths consisted of dilated atrium, acute congested hyperaemia of the heart, single edemateous lungs, atonic stomach / intestines. No necropsy findings were seen in animals sacrificed scheduled. The LD50 oral in rats was calculated to be about 3100 mg/kg bw.