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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Basic toxicokinetics

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Administrative data

Endpoint:
basic toxicokinetics in vivo
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable publication which meets basic scientific principles

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Metabolism of Geraniol and Linalool in the Rat and effects on liver and Lung Microsomal Enzymes.
Author:
Chadha A, Madyastha M
Year:
1984
Bibliographic source:
Xenobiotica 14: 365-374
Reference Type:
secondary source
Title:
No information
Author:
Chadha A, Madyastha M
Year:
2008
Bibliographic source:
RIFM database

Materials and methods

Objective of study:
metabolism
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Geraniol
EC Number:
203-377-1
EC Name:
Geraniol
Cas Number:
106-24-1
Molecular formula:
C10H18O
IUPAC Name:
3,7-dimethylocta-(E)-2,6-dien-1-ol
Constituent 2
Reference substance name:
trans-3,7-Dimethyl-2,6-octadien-1-ol
IUPAC Name:
trans-3,7-Dimethyl-2,6-octadien-1-ol
Details on test material:
- Name of test material (as cited in study report): Geraniol
- Analytical purity: >99.5% pure,

Test animals

Species:
rat
Strain:
other: IISc strain
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 160 - 200 g
- Housing: after dosing individually
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
CMC (carboxymethyl cellulose)
Details on exposure:
VEHICLE
- Concentration: 1%
Duration and frequency of treatment / exposure:
6 days
Doses / concentrations
Remarks:
Doses / Concentrations:
600 mg/kg bw/d
Control animals:
yes, concurrent vehicle
Details on dosing and sampling:
PHARMACOKINETIC STUDY (Absorption, distribution, excretion)
- Tissues and body fluids sampled . liver, lung
- Time and frequency of sampling:24 h after 1, 3 or 6 doses.

Results and discussion

Any other information on results incl. tables

Results:

- Significant increase in liver cytochrome P-450 after 3 days.

- steady increase in liver geraniol hydroxylase activity (36% at 6 days).

- No change in cytochrome b5, NADPH- or NADH-cytochrome c reductases.

- No effect on any parameter using lung microsome.

Applicant's summary and conclusion