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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1970s-1980s
Reliability:
2 (reliable with restrictions)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1975
Report date:
1975

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 420 (Acute Oral Toxicity - Fixed Dose Method)
GLP compliance:
no
Test type:
fixed dose procedure

Test material

Constituent 1
Reference substance name:
C10-C16-(linear and branched)-alkyl esters of salicylic acid
IUPAC Name:
C10-C16-(linear and branched)-alkyl esters of salicylic acid
Constituent 2
Reference substance name:
Reference substance 001
Cas Number:
8002-03-7
Test material form:
liquid
Specific details on test material used for the study:
the substance is administrated in a peanut oil solution.

Test animals

Species:
rat
Strain:
Wistar
Sex:
male

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
peanut oil
Doses:
4830 mg/kg bw administrated in 0.01ml (solution in peanut oil)/gr bw
No. of animals per sex per dose:
10
Control animals:
not specified

Results and discussion

Effect levels
Key result
Sex:
male
Dose descriptor:
LD50
Effect level:
> 4 830 mg/kg bw
Based on:
act. ingr.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
No oral toxicity
Executive summary:

At the concentration of 0.01ml/gr bw (Wistar male rats), the results obtained support the conclusion that the substance may be considered non-hazardous.