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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: scientifically acceptable and sufficient documented

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1976
Report date:
1976

Materials and methods

Principles of method if other than guideline:
Five male and five female rats received a single dose (1000 or 5000 mg/kg bw) of KAC 4196 as emulsion in cremophor for 24 hours. The animals were observed for mortality, body weight gain and clinical signs through day 7.
GLP compliance:
not specified
Test type:
standard acute method

Test material

Constituent 1
Chemical structure
Reference substance name:
3,9-dicyclohex-3-enyl-2,4,8,10-tetraoxaspiro[5.5]undecane
EC Number:
229-542-8
EC Name:
3,9-dicyclohex-3-enyl-2,4,8,10-tetraoxaspiro[5.5]undecane
Cas Number:
6600-31-3
Molecular formula:
C19H28O4
IUPAC Name:
3,9-bis(cyclohex-3-en-1-yl)-2,4,8,10-tetraoxaspiro[5.5]undecane
Details on test material:
KAC 4196 = 3,9-dicyclohex-3-enyl-2,4,8,10-tetraoxaspiro[5.5]undecane, chemical pure product

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Type of coverage:
not specified
Vehicle:
other: cremophor
Duration of exposure:
24 hours
Doses:
1000 or 5000 mg/kg bw
No. of animals per sex per dose:
5 male and 5 female rats/dose
Control animals:
not specified

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

None of the animals died. The animals dosed with 1000 mg/kg bw were without findings. Animals which were treated with 5000 mg/kg bw revealed a temporary reduced general condition during an observation period of 7 days.

Applicant's summary and conclusion

Executive summary:

Five male and five female rats received a single dose (1000 or 5000 mg/kg bw) of KAC 4196 as emulsion in cremophor for 24 hours. The animals were observed for mortality, body weight gain and clinical signs through day 7.

None of the animals died. The animals dosed with 1000 mg/kg bw were without findings. Animals which were treated with 5000 mg/kg bw revealed a temporary reduced general condition during an observation period of 7 days. The LD50 dermal is > 5000 mg/kg bw (m + f rats)