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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

oral
rat (OECD 407) NOEL (m/f): >15 mg/kg bw/day (SafePharm Laboratories, 2004)
dermal
Actually, there is no information available.
inhalation
Actually, there is no information available.

Key value for chemical safety assessment

Repeated dose toxicity: via oral route - systemic effects

Endpoint conclusion
Dose descriptor:
NOAEL
15 mg/kg bw/day

Additional information

oral

Currently, there is one key study available:

A 28-day subacute study was conducted with rats which received 1.5, 5 or 15 mg/kg/d (S)-1-phenyl-propylamine (CAS 3789-59-1) by gavage. Based on the results, the NOEL of the test substance was defined at the highest dose level tested. [SafePharm Laboratories, 2004]

 

dermal

Currently, there is no information available.

 

inhalation

Currently, there is no information available.

Justification for classification or non-classification

Regarding the results of these studies in rats, the subacute NOEL of 1-phenylpropylamine is > 15 mg/kg bw/day due to the overall no effects observed. Based on the GHS and the EU criteria for classification and labeling there is currently no need for classification of effects due to repeated oral exposure to the test substance.

 

There are no data available given to classify 1-phenylpropylamine for repeated dermal or inhalative toxicity.