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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: dermal

Currently viewing:

Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
other: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
weight of evidence
Study period:
2010
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Read across from a well performed GLP study
Justification for type of information:
The justification for the use of the similar substance is detailed in the Read Across document attached in section 13

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2010
Report date:
2010

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 402 (Acute Dermal Toxicity)
GLP compliance:
yes (incl. QA statement)
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Reference substance name:
Oils, fish, oxidized, bisulfited, sodium salts
EC Number:
307-037-4
EC Name:
Oils, fish, oxidized, bisulfited, sodium salts
Cas Number:
97488-98-7
IUPAC Name:
Oils, fish, oxidized, bisulfited, sodium salts

Test animals

Species:
rat
Strain:
other: HsdRccHan(TM)WIST
Sex:
male/female

Administration / exposure

Type of coverage:
semiocclusive
Vehicle:
unchanged (no vehicle)
Duration of exposure:
24 hours
Doses:
2000 mg/Kg
No. of animals per sex per dose:
5 males and 5 females
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Mortality:
males: 0/5
females: 0/5

Applicant's summary and conclusion

Interpretation of results:
other: not classified
Remarks:
According to CLP Criteria used for interpretation of results: EU
Conclusions:
The dermal median lethal dose was > 2000 mg/kg for acute (24-hour) exposure for rat. This does not classify the substance under the CLP regulation.