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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: see 'Remark'
Remarks:
Data from secondary source which meets basic scientific principles. Due to structural similarities of the registered substance trans-ß-ionone (CAS 79-77-6) and the used test substance ß-ionone (CAS 14901-07-6) the study data could be taken into account for assessment.
Cross-reference
Reason / purpose for cross-reference:
reference to same study

Data source

Referenceopen allclose all

Reference Type:
secondary source
Title:
Short term toxicity study on alpha-ionone, beta-ionone and citral
Author:
Givaudan
Year:
1980
Bibliographic source:
cited in the RIFM/FEMA database, location 43485
Report date:
1980
Reference Type:
secondary source
Title:
Fragrance material review on alpha-ionone
Author:
Lalko J et al.
Year:
2007
Bibliographic source:
Food and Chemical Toxicology 45 (2007) S235–S240
Reference Type:
secondary source
Title:
A toxicologic and dermatologic assessment of ionones when used as fragrance ingredients
Author:
Belsito D et al.
Year:
2007
Bibliographic source:
Food and Chemical Toxicology 45 (2007) S130–S167

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Administration: daily, 5 times
GLP compliance:
not specified
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Reference substance name:
4-(2,6,6-trimethylcyclohex-1-ene-1-yl)-but-3-ene-2-one
EC Number:
238-969-9
EC Name:
4-(2,6,6-trimethylcyclohex-1-ene-1-yl)-but-3-ene-2-one
Cas Number:
14901-07-6
IUPAC Name:
4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-3-en-2-one

Test animals

Species:
rat
Strain:
not specified

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
not specified
Details on oral exposure:
- Administration: daily, 5 times
Doses:
no data
No. of animals per sex per dose:
10 animals/dose
Control animals:
not specified

Results and discussion

Effect levelsopen allclose all
Sex:
not specified
Dose descriptor:
LD50
Effect level:
7 120 mg/kg bw
Remarks on result:
other: +/- 1000 mg/kg bw for deaths occuring within 24 h
Sex:
not specified
Dose descriptor:
other: LD10
Effect level:
4 120 mg/kg bw
Remarks on result:
other: for deaths occuring within 24 h
Sex:
not specified
Dose descriptor:
other: LD90
Effect level:
12 300 mg/kg bw
Remarks on result:
other: for deaths occuring within 24 h
Sex:
not specified
Dose descriptor:
LD50
Effect level:
3 290 mg/kg bw
Remarks on result:
other: +/- 500 mg/kg bw for deaths occuring within 10 days
Sex:
not specified
Dose descriptor:
other: LD10
Effect level:
2 150 mg/kg bw
Remarks on result:
other: for deaths occuring within 10 days
Sex:
not specified
Dose descriptor:
other: LD90
Effect level:
5 040 mg/kg bw
Remarks on result:
other: for deaths occuring within 10 days
Mortality:
All deaths had occurred by 24 hours

Applicant's summary and conclusion