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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Skin irritation / corrosion

Currently viewing:

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: basic information given

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1963
Report date:
1963

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Principles of method if other than guideline:
according to BASF-internal standard
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
3-(2-ethylhexyloxy)propylamine
EC Number:
226-420-6
EC Name:
3-(2-ethylhexyloxy)propylamine
Cas Number:
5397-31-9
Molecular formula:
C11H25NO
IUPAC Name:
3-[(2-ethylhexyl)oxy]propan-1-amine

Test animals

Species:
rabbit
Strain:
Vienna White

Test system

Type of coverage:
occlusive
Preparation of test site:
shaved
Vehicle:
unchanged (no vehicle)
Controls:
other: untreated skin of the same animal
Amount / concentration applied:
ca. 1 mL
Duration of treatment / exposure:
1 min, 5 min, 15 min, 20 h
Observation period:
8 days
Number of animals:
2
Details on study design:
TEST SITE
- Area of exposure: 2.5 x 2.5 cm

REMOVAL OF TEST SUBSTANCE
- Washing (if done): 50% Lutrol

SCORING SYSTEM: Draize

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Remarks:
after 1 minute application
Basis:
mean
Time point:
other: 24 h
Score:
3
Max. score:
4
Reversibility:
not reversible
Remarks on result:
other: after 8 days necrosis
Irritation parameter:
edema score
Remarks:
after 1 minute application
Basis:
mean
Time point:
other: 24 h
Score:
2
Max. score:
4
Reversibility:
not reversible
Irritation parameter:
other: necrosis (5 minute application)
Basis:
mean
Time point:
other: 24 hours
Reversibility:
not reversible
Remarks on result:
other: after 24 hours full thickness necrosis
Irritant / corrosive response data:
Skin findings after 1 minute application: severe erythema and edema (skin hemorrhage) (reading after 24 hours).
Other effects:
Urine findings 24 hours after study end: albumin +, Hb spectroscopically +, sediment: hyalineand granular cylinder, after 6 days: nad.
Necropsy (8 days after study end): nothing abnormal detected

Any other information on results incl. tables

Results:

exposure duration

after 24 hours

after 8 days

1 minute

erythema score 3, edema score 3, bleedings

erythema score 2, necrosis

5 and 15 minutes

full thickness necrosis

full thickness necrosis

20 hours

full thickness necrosis

full thickness necrosis

Applicant's summary and conclusion

Interpretation of results:
corrosive
Remarks:
Migrated information