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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

After uptake (orally, intravenously) of N-Glycyl-L-tyrosine the concentration in blood is assumed to reach steady state levels. For risk assessment purposes oral absorption of N-Glycyl-L-tyrosine is set at 100%.


N-Glycyl-L-tyrosine is of low volatility due to a very low vapour pressure (0.0015 Pa). From this and from the particle size it is not expected that N-Glycyl-L-tyrosine reaches the nasopharyncheal region or subsequently the tracheobronchial or pulmonary region in significant amounts.


However, being a very hydrophilic substance with a molecular mass of only 238.24 g/mol, any N-Glycyl-L-tyrosine reaching the lungs might be absorbed through aqueous pores (ECHA, 2008). For risk assessment purposes, although it is unlikely that N-Glycyl-L-tyrosine will be available to a high extent after inhalation via the lungs due to the low vapour pressure and high MMAD, the inhalation absorption of N-Glycyl-L-tyrosine is set at 100%.


N-Glycyl-L-tyrosine with high water solubility (44.1 g/L at 20°C) and the log P value below 0 (-0.45) may be too hydrophilic to cross the lipid rich environment of the stratum corneum. Therefore, 10% dermal absorption of N-Glycyl-L-tyrosine is proposed for risk assessment purposes.

Key value for chemical safety assessment

Bioaccumulation potential:
no bioaccumulation potential
Absorption rate - oral (%):
100
Absorption rate - dermal (%):
10
Absorption rate - inhalation (%):
100

Additional information