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Diss Factsheets

Toxicological information

Basic toxicokinetics

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Administrative data

Endpoint:
basic toxicokinetics in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
4 (not assignable)

Data source

Reference
Reference Type:
publication
Title:
Fragrance material review on b-ionone
Author:
Ide, I., Toki, S.,
Year:
2007
Bibliographic source:
Food and Chemical Toxicology 45 (2007);Ide, I., Toki, S., 1970. Metabolism of b-ionone. Isolation, characterization and identification of the metabolites in the urine of rabbits. Biochemical Journal 119, 281–287.

Materials and methods

Objective of study:
metabolism
Test guideline
Qualifier:
according to guideline
Guideline:
other:
Principles of method if other than guideline:
Data is from J.Food and Chemical Toxicology
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
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
Molecular formula:
C13H20O
IUPAC Name:
4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-3-en-2-one
Test material form:
other: oily liquid
Details on test material:
-Name of test material (as cited in study report): 4-(2,6,6-trimethylcyclohex-1-ene-1-yl)-but-3-ene-2-one
- Substance type: Organic
- Physical state: liquid
Radiolabelling:
not specified

Test animals

Species:
rabbit
Strain:
other: albino
Sex:
male
Details on test animals or test system and environmental conditions:
male albino rabbit weighing about 3.0 kg at a dose of 1 g/kg/day

Administration / exposure

Route of administration:
other: by stomach tube
Vehicle:
other: gum Arabic
Details on exposure:
4-(2,6,6-trimethylcyclohex-1-ene-1-yl)-but-3-ene-2-one (b-Ionone) in aqueous suspension with gum Arabic was administered by stomach tube to a male albino rabbit weighing about 3.0 kg at a dose of 1 g/kg/day for seven days. The total administered dose was 23 g.
Duration and frequency of treatment / exposure:
seven days
Doses / concentrations
Remarks:
Doses / Concentrations:
23 g
Control animals:
not specified

Results and discussion

Main ADME results
Type:
metabolism
Results:
Five free metabolites in urine was identified .These included 3-oxo-b-ionone, 3-oxo-b-ionol, dihydro-3-oxob- ionol, 3-hydroxy-b-ionol and unchanged b-ionone. Additionally, two glucuronides of b-ionol were detected.

Metabolite characterisation studies

Metabolites identified:
yes
Details on metabolites:
The results showed that there were five free metabolites in urine. These included 3-oxo-b-ionone, 3-oxo-b-ionol, dihydro-3-oxob-ionol, 3-hydroxy-b-ionol and unchanged b-ionone.Additionally, two glucuronides of b-ionol were detected.Glucuronides were hydrolyzed with b-glucuronidase and
were identified as the glucuronides of 3-oxo-b-ionol and dihydro-3-oxo-b-ionol.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information): no bioaccumulation potential based on study results
Urine samples were extracted and analyzed for b-ionone and its metabolites. The results showed that there were five free metabolites in urine. These included 3-oxo-b-ionone, 3-oxo-b-ionol, dihydro-3-oxob-ionol, 3-hydroxy-b-ionol and unchangedb-ionone. Additionally, two glucuronides ofb-ionol were detected.Glucuronides were hydrolyzed withb-glucuronidase and were identified as the glucuronides of 3-oxo-b-ionol and dihydro-3-oxo-b-ionol.
Executive summary:

4-(2,6,6-trimethylcyclohex-1-ene-1-yl)-but-3-ene-2-one (b-Ionone) in aqueous suspension with gum Arabic was administered by stomach tube to a male albino rabbit weighing about 3.0 kg at a dose of 1 g/kg/day for seven days. The total administered dose was 23 g. Urine was collected everyday during the dosing period and for 4 days after the last dose. Urine samples were extracted and analyzed forb-ionone and its metabolites. The results showed that there were five free metabolites in urine. These included 3-oxo-b-ionone, 3-oxo-b-ionol, dihydro-3-oxob-ionol, 3-hydroxy-b-ionol and unchangedb-ionone. Additionally, two glucuronides ofb-ionol were detected.Glucuronides were hydrolyzed withb-glucuronidase and were identified as the glucuronides of 3-oxo-b-ionol and dihydro-3-oxo-b-ionol