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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
1973-12-18 to 1975-03-06
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Scientifically acceptable, method eqivalent or similar to guideline study.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1975
Report date:
1975

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Version / remarks:
method applied according to BASF-internal standard
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1,4-bis(vinyloxy)butane
EC Number:
223-437-0
EC Name:
1,4-bis(vinyloxy)butane
Cas Number:
3891-33-6
Molecular formula:
C8H14O2
IUPAC Name:
1,4-bis(ethenyloxy)butane

Test animals

Species:
rabbit
Strain:
Vienna White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Gaukler, 6050 Offenbach/Main, Germany
- Age at study initiation: no data
- Weight at study initiation: 2.7 - 3.0 kg
- Housing: no data
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: no data

ENVIRONMENTAL CONDITIONS
- Temperature (°C): no data
- Humidity (%): no data
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): no data

IN-LIFE DATES: From: 1973-12-18 To: 1973-12-27

Test system

Type of coverage:
occlusive
Preparation of test site:
clipped
Vehicle:
unchanged (no vehicle)
Controls:
other: untreated skin of the same animal
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied: ca. 1 mL
Duration of treatment / exposure:
The test substance was applied for 1 min, 5 min, 15 min and 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
- Type of wrap if used:
Application to ear: a cotton ball soaked with test item was fixed to the ear
Application to back: a small piece of cloth was fixed to the back with the help of a gauze patch

REMOVAL OF TEST SUBSTANCE
- Washing: After the short-term applications the test substance was washed off with Lutrol; after the 20-hour application the test substance was not washed off.
- Time after start of exposure: 1 min, 5 min and 15 min

SCORING SYSTEM: observed were the parameters erythema, edema, scaling, and necrosis
Grading system:
"reizlos" Ø: considered as equivalent to Grade 0 (no irritating effect) according to OECD Guideline 404
"fraglich" (+): considered as equivalent to Grade 1 (very slight erythema (barely perceptible)) according to OECD Guideline 404
"leicht" +: considered as equivalent to Grade 2 (well-defined effect) according to OECD Guideline 404
"stark" ++: considered as equivalent to Grade 3 (moderate (to severe)) effect according to OECD Guideline 404
"sehr stark" +++: considered as equivalent to Grade 4 (severe effect) according to OECD Guideline 404

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
mean
Time point:
other: 24 h
Score:
2
Max. score:
4
Reversibility:
other: incipient scaling after 8 days
Remarks on result:
other: 20-hour application to back
Irritation parameter:
erythema score
Basis:
animal #1
Time point:
other: 24 h
Score:
2
Max. score:
4
Reversibility:
other: incipient scaling after 8 days
Remarks on result:
other: 20-hour application to back
Irritation parameter:
erythema score
Basis:
animal #2
Time point:
other: 24 h
Score:
2
Max. score:
4
Reversibility:
other: incipient scaling after 8 days
Remarks on result:
other: 20-hour application to back
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 24 h
Score:
2
Max. score:
4
Reversibility:
other: incipient scaling after 8 days
Remarks on result:
other: 20-hour application to back
Irritation parameter:
edema score
Basis:
animal #1
Time point:
other: 24 h
Score:
2
Max. score:
4
Reversibility:
other: incipient scaling after 8 days
Remarks on result:
other: 20-hour application to back
Irritation parameter:
edema score
Basis:
animal #2
Time point:
other: 24 h
Score:
2
Max. score:
4
Reversibility:
other: incipient scaling after 8 days
Remarks on result:
other: 20-hour application to back
Irritant / corrosive response data:
Application to ear for 20 hours resulted in Grade 3 erythema and edema after 24 hours. Erythema and edema not reported on day 8, however eschar was observed.

Any other information on results incl. tables

Table of results (20 h application of test item) based on grading system as applied in the study report

   

time

animal 1

animal 2

erythema

24 h

+

+

8 d

Ø

Ø

edema

24 h

+

+

8 d

Ø

Ø

scaling

24 h

Ø

Ø

8 d

+

+

 

Table of results (20 h application of test item) translated into the grading system as applied in OECD Guideline 404

  

time

animal 1

animal 2

erythema

24 h

2

2

8 d

0

0

edema

24 h

2

2

8 d

0

0

scaling

24 h

0

0

8 d

2

2

 

Applicant's summary and conclusion

Interpretation of results:
slightly irritating
Remarks:
Migrated information