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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
weight of evidence
Study period:
1973
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Only data from review article available.

Data source

Reference
Reference Type:
review article or handbook
Title:
Lithium Carbonate
Author:
Kiso to Rinsho
Year:
1973
Bibliographic source:
Kiso to Rinsho. Clinical Report. (Yubunsha Co., Ltd., 1-5, Kanda Suda-Cho, Chiyoda-ku, KS Bldg., Tokyo 101, Japan) V.1-1960-7,1273,1973 (KSRNAM); via RTECS

Materials and methods

Principles of method if other than guideline:
Only data from review article available. No guideline or method indicated.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Lithium carbonate
EC Number:
209-062-5
EC Name:
Lithium carbonate
Cas Number:
554-13-2
Molecular formula:
CH2O3.2Li
IUPAC Name:
dilithium carbonate

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Control animals:
not specified

Results and discussion

Effect levels
Key result
Sex:
not specified
Dose descriptor:
LD50
Effect level:
525 mg/kg bw

Applicant's summary and conclusion

Interpretation of results:
Category 4 based on GHS criteria
Conclusions:
According to the review article, the LD50 of lithium carbonate is 525 mg/kg bw after oral administration to rats.
Executive summary:

According to the review article, the LD50 of lithium carbonate is 525 mg/kg bw after oral administration to rats. Thus, lithium carbonate has to be classified as cat. 4, H302 (harmful if swallowed) according to Regulation (EC) No 1272/2008 (CLP).