Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

A toxicokinetics statement can be written from the physico-chemical parameters as well as the toxicity data available on the substance.

Key value for chemical safety assessment

Bioaccumulation potential:
low bioaccumulation potential

Additional information

The physico-chemical parameters as well as the toxicity data available on the substance can estimate the absorption data according to the different routes of administration:

- inhalation route:

The low vapor pressure value permit to estimate a weak exposure by inhalation for the workers.

However, the Log Kow value is high (6.39, calculated by EPISUITE) and the water solubility is low. This lipophilic substance may be taken up by micellular solubilisation. The acute oral toxicity test did not show any significative clinical sign (LD50 > 2000 mg/kg). So the inhalation absorption could occur but the exposure by inhalation for the workers is expected to be low.

- dermal absorption:

The molecular weight of 340 triggers a possible dermal uptake. With a water solubility below 1 mg/l, dermal uptake is likely to be low as the substance must be sufficiently soluble in water to partition from the stratum corneum into the epidermis. The high Log Kow value (6.39) favours dermal absorption, but the low water solubility and the fact that Log Kow is above 6 could limit absorption across the skin. Uptake into the stratum corneum itself may be slow.

The surface tension value being below 10 mN/m, the substance will not enhance the potential dermal uptake.

A sensitization test show a dryness and edema and it was noted a potential sensitization to the skin.

The in vitro dermal irritation test do not class the substance as irritating to the skin.

These data show that the substance can penetrate the skin but moderately.

- oral absorption:

This lipophilic substance may be taken up by micellular solubilisation (Molecular weight < 500, Log Kow > 4 and low water solubility). The acute oral toxicity test did not show any significative clinical sign (LD50 > 2000 mg/kg).

So the oral absorption can occur.

No information is available regarding the distribution, metabolization and elimination of the substance.