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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The study is comparable to OECD Guideline 404 with acceptable restrictions (partly limited documentation, e.g. details about the test substance; exposure period 20 h and occlusive coverage conditions [worst case scenario]).

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1972
Report date:
1972

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
no
Principles of method if other than guideline:
Skin irritation was tested using an internal method (BASF test)
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
N-methylformamide
EC Number:
204-624-6
EC Name:
N-methylformamide
Cas Number:
123-39-7
Molecular formula:
C2H5NO
IUPAC Name:
N-methylformamide
Details on test material:
no details

Test animals

Species:
rabbit
Strain:
Vienna White
Details on test animals or test system and environmental conditions:
Body weight: 2.52 - 4.2 kg
no further details

Test system

Type of coverage:
occlusive
Preparation of test site:
not specified
Vehicle:
unchanged (no vehicle)
Controls:
no
Amount / concentration applied:
The application site was covered with an cotton patch of 2.5 X 2.5 cm; patch soaked with the test substance and applied to the skin (appr. 1 ml); no further data
Duration of treatment / exposure:
1, 5, or 15 minutes (washing with Lutrol or 50% aqueous Lutrol) or 20 h (unwashed)
Observation period:
Results were recorded each working day for up to 6 days. 1st scoring 24 h after initiation.
Number of animals:
2 rabbits
Details on study design:
After the reported exposure time the skin was washed (not after 20 h exposure).

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
animal #1
Time point:
other: 24/48/72 h
Score:
1
Max. score:
4
Reversibility:
fully reversible within: 7 days
Irritation parameter:
edema score
Basis:
animal #1
Time point:
other: 24/48/72 h
Score:
0
Max. score:
4
Irritation parameter:
erythema score
Basis:
animal #2
Time point:
other: 24/48/72 h
Score:
1.67
Max. score:
4
Reversibility:
fully reversible within: 7 days
Irritation parameter:
edema score
Basis:
animal #2
Time point:
other: 24/48/72 h
Score:
0
Max. score:
4
Irritant / corrosive response data:
No effects were detected after 1 - 15 minutes exposure; data after 20 h exposure were presented in the Table below.
No edema was detected in any test group.
Other effects:
Body weight was slightly reduced (ca. 10%) in both animals after 20h exposure to ca. 1 ml undiluted test substance.
No further effects reported.

Any other information on results incl. tables

Skin erythema in 2 rabbits after dermal exposure to the undiluted test substance for 20 h

Time after initiation of exposure

20 hours exposure; erythema in

Rabbit 1

Rabbit 2

24 h

2

2

48 h

1

2

72 h

0

1

6 days

0

0

-

Evaluation transformed to OECD-Draize scoring; no edema reported.

Applicant's summary and conclusion

Interpretation of results:
slightly irritating
Remarks:
Migrated information
Conclusions:
The test substance has slight skin irritant properties.
Executive summary:

The study is comparable to OECD Guideline 404 with acceptable restrictions (partly limited documentation, e.g. details about the test substance; exposure period 20 h and occlusive coverage conditions [worst case scenario]).

Two rabbits were dermally exposed to undiluted liquid test substance (ca. 1 ml) for 1, 5, 15 minutes or for 20 h. The coverage was occlusive; the skin was washed after exposure (not after an exposure period of 20 h). Skin reaction was scored 24, 48, and 72 h and day 7 after initiation. No effects were detected after 1 -15 minutes of exposure. Mean erythema score (24/48/72 h) after the 20 h exposure was 1 (animal #1) and 1.67 (animal #2); the effects were reversible. No edema was reported.

Conclusion: The test substance has slight skin irritant properties.