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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Lab not following OECD guidelines or GLP

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1987
Report date:
1987

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Internal SOP: TA 310, TA 160, TA 120
Deviations:
not specified
Principles of method if other than guideline:
20 ml/kg administrated as received/ Method of calculation: Weil method
GLP compliance:
no
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Diethoxymethane
EC Number:
207-330-6
EC Name:
Diethoxymethane
Cas Number:
462-95-3
Molecular formula:
C5H12O2
IUPAC Name:
diethoxymethane

Test animals

Species:
rat
Strain:
other: CRL: CD (SD) BR
Sex:
male/female

Administration / exposure

Type of coverage:
not specified
Vehicle:
unchanged (no vehicle)
Doses:
20 ml/kg
No. of animals per sex per dose:
5
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 20 mL/kg bw
Based on:
test mat.
Remarks on result:
other: 95% CL: no range calculable
Mortality:
none
Clinical signs:
other: all normal

Any other information on results incl. tables

Skin absorption: Not evident

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Not toxic by dermal route