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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Key value for chemical safety assessment

Additional information

No specific toxicokinetic studies are available on Star anise, Illicium verum, ext. A toxicokinetic assessment was made based on the physico-chemical properties of the test substance and the results of toxicity studies (acute oral toxicity, repeated oral dose toxicity study, skin irritation, eye irritation, skin sensitization and in vitro genotoxicity).

 

Physico-chemical properties:

Water solubility: slightly solve in water

Partition coefficient in octanol/water: The necessary info, such as the constituents, molecular structures of main components could not be obtained. So the study cannot be performed.

Melting point/freezing point: 21.35°C (at 101.325 kPa)

Boiling point: 232.9°C (at 101.325 kPa)

Density: 0.918 (at 20°C)

Auto Flammability: Self-ignition temperature is 426(at 101.325 kPa)

Flash point: 97.6(at 101.325 kPa)

Vapour pressure: 8.5kPa (at 20)

 

Absorption:

Oral route:

This is UVCB organic substance with uncertain structure, molecular weight and particle size and so on. The results obtained in the acute toxicity: oral study and therepeated oral dose toxicity studyconfirmed the oral absorption of Star anise, Illicium verum, ext. as no adverse effect observed in both studies. Therefore, it can be considered that the absorption resulting from potential exposure by the oral route is limited.

 

Inhalation:

No data are available for inhalation route of exposure. However, the test substance is a liquid and exposure via inhalation is not likely taking into account. Therefore, it can be considered that the absorption resulting from potential exposure by the inhalation route is limited.

 

Dermal route:

No data are available for dermal route of exposure. However, the test substance is a liquid and skin contact in production and use is not likely. Also there is no adverse effect observed in the studies of skin irritation, skin sensitization and eye irritation. Therefore, it can be considered that the absorption resulting from potential exposure by the dermal route is limited.

 

Distribution:

In the acute oral toxicity study, no mortality and no overt signs of toxicity were noted as well as no abnormalities were noted at necropsy of animals killed at the end of the study. In the repeated dose oral toxicity study, no toxicologically relevant changes were noted. These results indicate no specific systemic distribution of the test substance and/or its metabolites or degradation products.

 

Metabolism:

In the acute oral toxicity study and the repeated dose oral toxicity study, no adverse effect is observed. Also in the study of in vitro cytogenicity/chromosome aberration in mammalian cells, no genotoxicity and no cytotoxicity are observed. In the absence of specific metabolism studies, it is not possible to conclude on the metabolisation potential of the substance, but according to the studies above, there seems no adverse effect of the substance and/or its metabolites or degradation products.

 

Excretion:

There is no indication of a preferred route of excretion for Star anise, Illicium verum, ext. but no adverse effect in oral toxicity studies indicates that excretion of unchanged parent substance and/or metabolites could occur by renal or biliary routes and that bioaccumulation is unlikely.