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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1982
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data

Data source

Reference
Reference Type:
publication
Title:
Iotroxic acid
Year:
1982
Bibliographic source:
Gekkan Yakuji (Pharmaceuticals Monthly). Vol. 24, Pg. 695, 1982

Materials and methods

Principles of method if other than guideline:
Collection of data, information on materials and methods are not available.
GLP compliance:
not specified
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Iotroxic acid
EC Number:
256-917-3
EC Name:
Iotroxic acid
Cas Number:
51022-74-3
Molecular formula:
C22H18I6N2O9
IUPAC Name:
3-{2-[2-(2-{[(3-carboxy-2,4,6-triiodophenyl)carbamoyl]methoxy}ethoxy)ethoxy]acetamido}-2,4,6-triiodobenzoic acid
Specific details on test material used for the study:
no data

Test animals

Species:
rat
Strain:
not specified
Sex:
male/female
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified
Details on oral exposure:
no data
Doses:
no data
No. of animals per sex per dose:
no data
Control animals:
not specified
Details on study design:
no data
Statistics:
no data

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 9 000 mg/kg bw
Based on:
test mat.
Mortality:
no data
Clinical signs:
no data
Body weight:
no data
Gross pathology:
no data
Other findings:
no data

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
In this acute oral toxicity study, the oral LD50 value in rats after treatment with Iotroxic acid is > 9000 mg/kg.
Executive summary:

In an acute toxicity study, the toxic potential of Iotroxic acid was tested orally on male and female rats. The LD50 of the test substance for rats was found to be greater than 9000 mg/kg bw for both males and females.