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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Cs2CO3 is not acutely toxic via the oral route as an LD50 was determined to be above 2000 mg/kg bw based on WoE assessment including the source substance CsCl. An LD50 of 2333 mg/kg bw with the target substance is used as key value.


Cs2CO3 is not acutely toxic via the dermal route as LD50 dermal > 2000 mg/kg bw based on WoE assessment of read-across and target substance data.

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records

Referenceopen allclose all

Endpoint:
acute toxicity: oral
Type of information:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
weight of evidence
Justification for type of information:
HYPOTHESIS FOR THE ANALOGUE APPROACH
Cesium carbonate completely dissociates in water forming cesium cation and the corresponding carbonate anion. Thus, cesium salts with different anion moieties were found to be suitable candidates for read-across. (Eco)toxicological properties were extrapolated to different endpoints by using the lowest effect concentration.
For further information, please refer to the read-across justification in IUCLID section 13.
Reason / purpose for cross-reference:
read-across source
Sex:
female
Dose descriptor:
LD50
Effect level:
1 974 mg/kg bw
Based on:
other: calculated for Cs
Key result
Sex:
female
Dose descriptor:
LD50
Effect level:
2 420 mg/kg bw
Based on:
other: calculated for Cs2CO3
Remarks on result:
other:
Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
no data
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature
Qualifier:
according to guideline
Guideline:
other: no data
GLP compliance:
not specified
Test type:
other: no data
Species:
mouse
Strain:
other: Swiss albino mice (Mus musculus)
Sex:
female
Route of administration:
other: oral
Sex:
female
Dose descriptor:
LD50
Effect level:
2 500 mg/kg bw
Based on:
test mat.
Key result
Sex:
female
Dose descriptor:
LD50
Effect level:
2 420 mg/kg bw
Based on:
other: calculated as cesium carbonate
Interpretation of results:
GHS criteria not met
Conclusions:
The oral LD50 value of cesium chloride in mice was determined to be 2600 mg/kg bw. Calculated as cesium carbonate the LD50 value is 2420 mg/kg bw.
Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
no data
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature
Qualifier:
according to guideline
Guideline:
other: no data
GLP compliance:
not specified
Test type:
other: no data
Species:
rat
Strain:
not specified
Sex:
not specified
Route of administration:
other: oral
Key result
Sex:
not specified
Dose descriptor:
LD50
Effect level:
2 333 mg/kg bw
Based on:
test mat.
Interpretation of results:
Toxicity Category V
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The acute oral LD50 of cesium carbonate in rats was determined to be 2333 mg/kg bw.
Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
2 333 mg/kg bw
Quality of whole database:
Three literature values are used in a weight of evidence approach.

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Link to relevant study records
Reference
Endpoint:
acute toxicity: dermal
Type of information:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Justification for type of information:
HYPOTHESIS FOR THE ANALOGUE APPROACH
Cesium carbonate completely dissociates in water forming cesium cation and the corresponding carbonate anion. Thus, cesium salts with different anion moieties were found to be suitable candidates for read-across. (Eco)toxicological properties were extrapolated to different endpoints by using the lowest effect concentration.
For further information, please refer to the read-across justification in IUCLID section 13.
Reason / purpose for cross-reference:
read-across source
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
other: Cs2CO3
Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
> 2 000 mg/kg bw

Additional information

Acute oral toxicity


According to the review article (Bibra toxicology advice & consulting, 2000) on the toxicity profile of cesium compounds an LD50 value of 2333 mg/kg bw was determined for cesium carbonate when administered to rats orally. Similar LD50 values were determined for mice that were treated with cesium carbonate and cesium chloride. LD50 values were 2420 and 2170 mg/kg bw, respectively.


Acute dermal toxicity


An acute dermal toxicity study with cesium carbonate is not available. Consequently, data from the source substance CsNO3 was used. CsNO3 was tested up to the limit concentration of 2000 mg/kg bw. No test item related toxic effects or other changes were observed. It is assumed that Cs2CO3 has an LD50 above 2000 mg/kg bw.


The assumption of low acute dermal toxicity for the target substance is supported by the fact that bioavailability of the ions formed will be very low via the skin.


Carbonate has further been described in brief profiles published by Eurometaux on systemic toxicological effects of common counterions in metal substances. Carbonates are omnipresent in the environment including human diet and are involved in essential physiological functions. Carbonates pose no toxicological risk for humans and are therefore not contributing to the overall toxicity of the cesium salt.


The low acute oral toxicity of the target substance further concludes the above assumptions.


Further information can be found in the read across justification in IUCLID section 13.

Justification for classification or non-classification

Based on the data for the acute oral toxicity endpoint, the LD50 for the test item was found to be >2000 mg/kg bw. Therefore, the test item is not classified according to Regulation (EC) No 1272/2008 (CLP/GHS) for acute oral toxicity.


 


Baed on the results of an acute dermal toxicity study with the source substance and the intrinsic properties of the test item, it is not classified according to Regulation (EC) No 1272/2008 (CLP/GHS) for acute dermal toxicity.