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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
eye irritation: in vitro / ex vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
14.01.-15.09.2000
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Well documented in vitro study report which meets basic scientific principles

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2000
Report date:
2000

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
enucleated eye test
GLP compliance:
yes

Test material

Constituent 1
Details on test material:
- Name of test material: (S)1-Phenylpropylamin (CAS 3789-59-1)

Test animals / tissue source

Species:
rabbit

Test system

Vehicle:
unchanged (no vehicle)
Controls:
yes

Results and discussion

In vivo

Results
Irritation parameter:
other: corneal swelling [%]
Basis:
mean
Time point:
other: 240 min
Score:
98.2

Applicant's summary and conclusion

Conclusions:
Following assessment of the data for all endpoints, the test material was considered to have the potential to cause ocular irritancy in vivo.