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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1959
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Scientifically valid study without detailed documentation

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1959
Report date:
1959

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Study predates OECD guidelines. However, it follows the principles of a OECD guideline 403 limit test.
GLP compliance:
no
Remarks:
Study performed prior to implementation of GLP
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Sodium dimethyl 5-sulphonatoisophthalate
EC Number:
223-578-8
EC Name:
Sodium dimethyl 5-sulphonatoisophthalate
Cas Number:
3965-55-7
Molecular formula:
C10H10O7S.Na
IUPAC Name:
sodium 3,5-bis(methoxycarbonyl)benzenesulfonate
Test material form:
other: solid

Test animals

Species:
rat
Strain:
other: ChR-CD

Administration / exposure

Route of administration:
inhalation: dust
Type of inhalation exposure:
not specified
Details on inhalation exposure:
> 75 % of particles were < 3µm in diam.
Analytical verification of test atmosphere concentrations:
yes
Duration of exposure:
4 h
Concentrations:
32 mg/lit +/- 20 %
No. of animals per sex per dose:
2 animals per dose
Details on study design:
- Observation period: at least 9 days
- Necropsy of survivors performed: yes

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LC0
Effect level:
>= 32 mg/L air
Based on:
test mat.
Exp. duration:
4 h
Mortality:
no mortality
Clinical signs:
other: Discomfort during exposure
Body weight:
no data
Gross pathology:
None of the pathological changes attributable to treatment found 9 days after exposure

Applicant's summary and conclusion

Conclusions:
Under the conditions of the present study the approximate lethal concentration is > 32 mg/L.
Executive summary:

In an acute inhalation toxicity study ( Haskell Laboratory for Toxicology and Industrial Medicine, 1959, non-GLP) two rats were treated with Sodium Sulfo Dimethylisophtalate dust in concentrations of 32 mg/L +/- 20 % for 4 hours by inhalation. More than 75 % of the dusts particles had a size < 3µm in diameter. As clinical signs discomfort during exposure were noted. Mortality did not occur within the 9 -day observation period. At nercopsy none of the pathological changes were attributable to treatment. The results of the study indicate a LC0 of > 32 mg/L.