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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: well documented guideline study with deviations, no GLP

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1984
Report date:
1984

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
yes
Principles of method if other than guideline:
Method: other: BASF-test
GLP compliance:
no
Test type:
other: BASF-test
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
1,1-dimethoxytrimethylamine
EC Number:
225-063-3
EC Name:
1,1-dimethoxytrimethylamine
Cas Number:
4637-24-5
Molecular formula:
C5H13NO2
IUPAC Name:
1,1-dimethoxy-N,N-dimethylmethanamine
Details on test material:
IUCLID4 Test substance: other TS

TS-Freetext:
Dimethylformamid-dimethylacetal, no further data

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
olive oil
Doses:
2150 and 5000 mg/kg bw
No. of animals per sex per dose:
5
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Mortality:
in both treatment groups
2150 mg/kg bw: 1 male rat
5000 mg/kg bw: 2 female rats
Gross pathology:
One female animal:
Stomach: atonic.
One female animal:
Organs: na abnormalities detected.
One male animal:
cadaverous, diagnosis not possible.

Applicant's summary and conclusion

Interpretation of results:
practically nontoxic
Remarks:
Migrated information Criteria used for interpretation of results: OECD GHS
Conclusions:
The oral LD50 of the test item was found to be greater than 5000 mg/kg bw.
Executive summary:

After oral application of the test substance to 5 male and 5 female Wistar rats per dosage group via gavage, the oral LD50 was found to be greater than 5000mg/kg bw.