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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Link to relevant study record(s)

Reference
Endpoint:
basic toxicokinetics, other
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
other:

Description of key information

After reviewing the available literature, it is believed that there is sufficient information on pidolic acid to support the case for waiving toxicokinetic studies.
It is concluded that after absorption, pidolic acid is likely to be incorporated into normal metabolism either to be terminally oxidized or to produce glutathione (an essential component of detoxification mechanisms from bacteria to humans) and glutamate (an amino acid and an essential part of the normal diet). The absorption, distribution, metabolism and excretion of such compounds is well understood in mammals and therefore further toxicokinetic studies in animals cannot be considered necessary or an appropriate use of animals.

Key value for chemical safety assessment

Bioaccumulation potential:
no bioaccumulation potential
Absorption rate - oral (%):
70
Absorption rate - dermal (%):
20
Absorption rate - inhalation (%):
100

Additional information