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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
supporting study
Study period:
1987
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Documentation insufficient for assessment.

Data source

Reference
Reference Type:
secondary source
Title:
Unnamed
Year:
1987

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EPA OPP 81-3 (Acute inhalation toxicity)
Deviations:
not specified
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Lactic acid
EC Number:
200-018-0
EC Name:
Lactic acid
Cas Number:
50-21-5
Molecular formula:
C3H6O3
IUPAC Name:
2-hydroxypropanoic acid
Details on test material:
- Name of test material (as cited in study report): L(+) lactic acid 80%

Test animals

Species:
rat
Strain:
Fischer 344
Sex:
male/female

Administration / exposure

Route of administration:
inhalation: aerosol
Type of inhalation exposure:
nose only
Vehicle:
other: unchanged (no vehicle)
Analytical verification of test atmosphere concentrations:
not specified
Duration of exposure:
4 h
Concentrations:
7.94 mg/L (air)
No. of animals per sex per dose:
5 animals/sex
Control animals:
yes

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 7.94 mg/L air

Any other information on results incl. tables

Animals were observed during exposure for signs of toxicity. Rapid breathing and eye tearing was observed in the treatment group. One and three hours after exposure, the treated and control groups had a hunched posture, red stained fur surrounding the eyes(tearing), ruffled fur, and appeared ungroomed with solid fur. Female rats exposed to the test substance appeared lethargic at one (2/5) and three hours (5/5). The two female rats that were lethargic after 1 hour also had a rapid, shallow breathing and appeared to be gasping after one and three hours. By 24 hours, most animals appeared normal and no unusual behavior or appearance was observed for the remainder of the test period. However, of the treated female rats 4/5 had ruffled, ungroomed fur at 24 hours, and 3/5 had ruffled, ungroomed fur 2, 3 and 4 days after treatment. One female from the treatment group had hunched posture, rapid and shallow breathing, and slight tremors, but these signs were observed on day 5 post-treatment. One female from the treatment group died on day 8 post-treatment. No gross lesions were observed at necropsy.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: other: CLP (EC 1272/2008)