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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1976
Report date:
1976

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:
Before OECD Guideline 404 was first adopted in 1981, skin irritation was tested using a BASF test.
The methods were based on Draize (Federal Register 38, No. 187, § 1500.41, p. 27019 (1973-09-27)).
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Morpholinium toluene-4-sulphonate
EC Number:
237-301-3
EC Name:
Morpholinium toluene-4-sulphonate
Cas Number:
13732-62-2
Molecular formula:
C7H8O3S.C4H9NO
IUPAC Name:
morpholin-4-ium 4-methylbenzenesulfonate
Details on test material:
Name of the test substance used in the study report: Haerter 527 fluessig (approx. 75% aqueous solution)
- Physical state:liquid

Test animals

Species:
rabbit
Strain:
Vienna White
Details on test animals or test system and environmental conditions:
A standardized animal laboratory diet was used.

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:
1 ml of undiluted test substance
Duration of treatment / exposure:
1 min, 5 min, 15 min, 20 h
Observation period:
8 d
Number of animals:
2
Details on study design:
After application, the test substance was washed off with Lutrol.

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
mean
Time point:
other: 1 min
Score:
0.5
Max. score:
4
Reversibility:
fully reversible within: 8 d
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 1 min
Score:
0
Max. score:
4
Irritation parameter:
erythema score
Basis:
mean
Time point:
other: 5 min
Score:
0.5
Max. score:
4
Reversibility:
fully reversible within: 8 d
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 5 min
Score:
0
Max. score:
4
Irritation parameter:
erythema score
Basis:
mean
Time point:
other: 15 min
Score:
0.5
Max. score:
4
Reversibility:
fully reversible within: 8 d
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 15 min
Score:
0
Max. score:
4
Irritation parameter:
erythema score
Basis:
mean
Time point:
other: 20 hours
Score:
2
Max. score:
4
Reversibility:
fully reversible within: 8 d
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 20 hours
Score:
2
Max. score:
4
Reversibility:
fully reversible within: 8 d

Any other information on results incl. tables

Single animal data

 

Treatment

Animal

Measured time point: 24 hours

Erythema

Edema

Additional findings

1 min

1

1

0

Reversible within 8 days

2

0

0

  Reversible within 8 days

5 min

1

1

0

Reversible within 8 days

2

0

0

  Reversible within 8 days

15 min

1

1

0

Reversible within 8 days

2

0

0

  Reversible within 8 days

20 h

1

2

2

Reversible within 8 days

2

2

2

Reversible within 8 days 

 

1 = no clear findings

2 = slight findings

3 = strong findings

4 = very strong findings

Applicant's summary and conclusion