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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1980
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1980

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 402 (Acute Dermal Toxicity)
GLP compliance:
not specified
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
4-chloro-N-cyclopentylbenzylamine
EC Number:
266-097-9
EC Name:
4-chloro-N-cyclopentylbenzylamine
Cas Number:
66063-15-8
Molecular formula:
C12H16ClN
IUPAC Name:
N-[(4-chlorophenyl)methyl]cyclopentanamine

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Type of coverage:
occlusive
Vehicle:
unchanged (no vehicle)
Duration of exposure:
24 hours
Doses:
male: 100 / 300 / 400 / 500 / 750 μl/kg bw
female: 100 / 350 / 400 / 500 / 600 / 750 μl/kg bw
No. of animals per sex per dose:
10 animals
Control animals:
no

Results and discussion

Effect levelsopen allclose all
Sex:
female
Dose descriptor:
LD50
Effect level:
0.454 mL/kg bw
95% CL:
0.4 - 0.515
Remarks on result:
other: s = 1.2
Sex:
male
Dose descriptor:
LD50
Effect level:
0.391 mL/kg bw
95% CL:
0.334 - 0.457
Remarks on result:
other: s = 1.4

Applicant's summary and conclusion

Interpretation of results:
harmful
Remarks:
Migrated information Criteria used for interpretation of results: EU