Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
1980
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1980
Report date:
1980

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:
Method: other: BASF-test.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
3,4-dimethoxyphenethylamine
EC Number:
204-376-9
EC Name:
3,4-dimethoxyphenethylamine
Cas Number:
120-20-7
Molecular formula:
C10H15NO2
IUPAC Name:
2-(3,4-dimethoxyphenyl)ethanamine
Details on test material:
- name of substance: homoveratrylamin
- Purity: 98 %
- substance number: 78/836
- appearance: clear, yellowish, slightly viscous liquid

Test animals

Species:
rabbit
Strain:
Vienna White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Gaukler
- Diet (e.g. ad libitum): Ssniff
- Weight at study initiation: mean 2.91 kg (4h); mean 2.8 kg (1h)

Test system

Type of coverage:
occlusive
Preparation of test site:
other: clipped
Vehicle:
unchanged (no vehicle)
Controls:
other: untreated skin
Amount / concentration applied:
- about 1 g of the undiluted test substance was applied to an area of 2.5 x 2.5 cm.
- occlusive dressing
- no washing of the exposed area
Duration of treatment / exposure:
4 hour(s), 1 hour
Observation period:
8 days
Number of animals:
2 (4 h); 4 (1h)

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
animal #1
Time point:
other: 24 and 48 h
Score:
2
Max. score:
4
Reversibility:
other: observation period only 8 days
Irritation parameter:
erythema score
Basis:
animal #2
Time point:
other: 24 and 48 h
Score:
2.5
Max. score:
4
Reversibility:
other: observation period only 8 days
Irritation parameter:
edema score
Basis:
other: animal #1 and #2
Time point:
other: 24 - 48 h
Score:
2
Max. score:
4
Reversibility:
other: observation period only 8 days
Remarks on result:
other: overall edema
Other effects:
- superficial necrosis observed on day 8 (animal #1).
- loose incrustation on day 8 (animal #2).

Any other information on results incl. tables

Animal No.

4 hour

1 day

2 days

8 days

Erythema

Edema

Erythema

Edema

Erythema

Edema

Erythema

Edema

1

2

2

2 e

2 e

2 e

2 e

Nds

0

2

2

2

2 e

2 e

3 e

2 e

Cr

0

 

e: extending beyound the area of exposure

Nds: dot-like superficially necrosis

Cr: crust removable, intakt skin under

Animal No.

1 hour

1 day

2 days

8 days

Erythema

Edema

Erythema

Edema

Erythema

Edema

Erythema

Edema

1

0

0

2

1

1

0

0 S

0

2

1

0

2 e sn

2 e

3 e sn

2

4 Np

2

3

1

1

2 e

3 e

2 e sn

2 e

0 S

0

4

1

1

2 e

3 e

2 e

2 e

0 S

0

 

e: extending beyound the area of exposure

sn: spotted necrotic-like skin areas

np: necrosis, parchment-like

S: scaling

Applicant's summary and conclusion

Interpretation of results:
Category 2 (irritant) based on GHS criteria
Conclusions:
Based on the results of this study, the test substance homoveratrylamin is highly irritating to skin.