Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: other routes
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Citation in a peer reviewed journal.

Data source

Referenceopen allclose all

Reference Type:
secondary source
Title:
Unnamed
Year:
2008
Reference Type:
secondary source
Title:
IUCLID2000
Author:
EU
Year:
2000
Bibliographic source:
IUCLID2000 as it is found in ESIS.

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
Tada 2008 and also ESIS cited in their publications a study on the acute intraperitoneal toxicity with mice and the result of the study.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Aspartic acid
EC Number:
200-291-6
EC Name:
Aspartic acid
Cas Number:
56-84-8
Molecular formula:
C4H7NO4
IUPAC Name:
aspartic acid

Test animals

Species:
mouse

Administration / exposure

Route of administration:
intraperitoneal

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
6 000 mg/kg bw

Applicant's summary and conclusion

Conclusions:
The intraperitoneal LD50 with mice is reported to 6000 mg/kg bw.
Executive summary:

Tada 2008 and also ESIS cited in their publications a study on the acute intraperitoneal toxicity with mice and the result of the study. The intraperitoneal LD50 with mice is reported to 6000 mg/kg bw.