Registration Dossier

Diss Factsheets

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
supporting study
Study period:
1986
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: see 'Remark'
Remarks:
The data obtained from a source of secondary literature are related to a substance which shows the same functional groups . The data derived from read-across is considered reliable because the molecules have the same functional groups due to the action irritating.

Data source

Referenceopen allclose all

Reference Type:
secondary source
Title:
3-Cyclohexene-1-carboxylic acid
Year:
2013
Bibliographic source:
CHEMIDplus
Reference Type:
secondary source
Title:
3-Cyclohexene-1-carboxylic acid
Year:
2013
Bibliographic source:
RTECS
Reference Type:
publication
Title:
No information
Year:
1986
Bibliographic source:
Prehled Prumyslove Toxikologie; Organicke Latky,' Marhold, J., Prague, Czechoslovakia, Avicenum, 1986 (-,315,1986)

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
no data
GLP compliance:
no

Test material

Constituent 1
Reference substance name:
3-Cyclohexene-1-carboxylic acid
IUPAC Name:
3-Cyclohexene-1-carboxylic acid
Constituent 2
Chemical structure
Reference substance name:
Cyclohex-3-ene-1-carboxylic acid
EC Number:
225-314-7
EC Name:
Cyclohex-3-ene-1-carboxylic acid
Cas Number:
4771-80-6
Molecular formula:
C7H10O2
IUPAC Name:
cyclohex-3-ene-1-carboxylic acid
Test material form:
not specified

Test animals

Species:
rabbit
Strain:
not specified

Test system

Type of coverage:
not specified
Controls:
not specified

Results and discussion

In vivo

Results
Irritation parameter:
other: REACTION: Severe
Irritant / corrosive response data:
REACTION: Severe

Applicant's summary and conclusion

Interpretation of results:
irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
According to Directive 67/548/EEC and to Regulation (EC) n. 1272/2008, the substance is classified for this property.