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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: dermal
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: restriction: short study description; original data not available

Data source

Reference
Reference Type:
secondary source
Title:
Unnamed
Year:
1968

Materials and methods

Principles of method if other than guideline:
no information about test method
GLP compliance:
not specified
Test type:
other: no data

Test material

Constituent 1
Reference substance name:
Trisodium nitrilotriacetate
EC Number:
225-768-6
EC Name:
Trisodium nitrilotriacetate
Cas Number:
5064-31-3
IUPAC Name:
trisodium 2,2',2''-nitrilotriacetate
Details on test material:
NTA monohydrate, 25% aqueous solution

Test animals

Species:
rabbit
Strain:
not specified
Sex:
male/female

Administration / exposure

Type of coverage:
occlusive
Vehicle:
water
Duration of exposure:
up to 24 hours
Doses:
1000, 1580, 2510, 3980, 6310, 10000 mg/kg
No. of animals per sex per dose:
1
Control animals:
not specified

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 10 000 mg/kg bw
Clinical signs:
other: No nervousness or muscular incoordination developed. Activity and appetite reduced for 2-3 days at the higher levels; mild weakness.

Applicant's summary and conclusion

Interpretation of results:
practically nontoxic
Remarks:
Migrated information Criteria used for interpretation of results: EU