Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
other: Expert assessment
Adequacy of study:
key study
Study period:
2018
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: An assessment was performed based on QSAR predictions supported by data on the substance and a suitable analogue

Data source

Reference
Reference Type:
other: expert assessment
Title:
Unnamed
Year:
2018
Report date:
2018

Materials and methods

Test guideline
Qualifier:
no guideline required
Principles of method if other than guideline:
An assessment was performed based on QSAR predictions supported by data on the substance and a suitable analogue
GLP compliance:
no
Test type:
other: An assessment was performed based on QSAR predictions supported by data on the substance and a suitable analogue
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
trans-hex-2-en-1-ol
EC Number:
213-191-2
EC Name:
trans-hex-2-en-1-ol
Cas Number:
928-95-0
Molecular formula:
C6H12O
IUPAC Name:
hex-2-en-1-ol

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Remarks on result:
other: An assessment was performed based on QSAR predictions supported by data on the substance and a suitable analogue

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
Trans-hex-2-en-1-ol substance is not acute toxic via the oral route and does not meet the criteria for classification according to Regulation (EC) No.1272/2008.
Executive summary:

An assessment on the acute oral toxicity of Trans-hex-2-en-1-ol was performed based on QSAR predictions supported by data on the substance and a suitable analogue. It was concluded that the substance is not acute toxic via the oral route and does not meet the criteria for classification according to Regulation (EC) No.1272/2008.