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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Developmental toxicity / teratogenicity

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Administrative data

Endpoint:
developmental toxicity
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study results were published in a peer reviewed journal.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1976

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
No information was provided to indicate specific guidelines.
GLP compliance:
not specified

Test material

Constituent 1
Reference substance name:
Triethanolamine
IUPAC Name:
Triethanolamine
Constituent 2
Reference substance name:
2,2',2''-nitrilotriethanol
EC Number:
203-049-8
EC Name:
2,2',2''-nitrilotriethanol
Cas Number:
102-71-6
IUPAC Name:
2,2',2''-nitrilotriethanol
Test material form:
not specified
Details on test material:
Test Substance: Triethanolamine

Test animals

Species:
rat
Strain:
other: Charles River CD rats

Administration / exposure

Route of administration:
dermal
Vehicle:
not specified
Details on exposure:
Application of semipermanent hair dye preparations (2 ml/kg) containing 0.1- 1.5% triethanolamine
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
19 days
Frequency of treatment:
Substance was administered on gestation days 1, 4, 7, 10, 13, 16, and 19
Doses / concentrations
Remarks:
Doses / Concentrations:
0.1 - 1.5%
Basis:
no data
No. of animals per sex per dose:
No data

Results and discussion

Results: maternal animals

Maternal developmental toxicity

Details on maternal toxic effects:
Maternal toxic effects:not examined

Effect levels (maternal animals)

Basis for effect level:
other: effect type not specified

Results (fetuses)

Details on embryotoxic / teratogenic effects:
Embryotoxic / teratogenic effects:no effects

Fetal abnormalities

Abnormalities:
not specified

Overall developmental toxicity

Developmental effects observed:
not specified

Any other information on results incl. tables

No embryotoxic or teratogenic effects were produced.

Applicant's summary and conclusion

Conclusions:
No embryotoxic or teratogenic effects were produced.
Executive summary:

The developmental toxicity of the substance was determined via exposure of pregnant Charles River CD rats to preparations containing 0.1 - 1.5% triethanolamine by the dermal route. No embryotoxic or teratogenic effects were produced.