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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:
15 Oct 1991 - 29 Oct 1991
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP - Guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1991
Report date:
1991

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
no
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Hexadecyl 2-ethylhexanoate
EC Number:
261-619-1
EC Name:
Hexadecyl 2-ethylhexanoate
Cas Number:
59130-69-7
Molecular formula:
C24H48O2
IUPAC Name:
hexadecyl 2-ethylhexanoate
Details on test material:
- Name of test material (as cited in study report): cetyl-2-ethylhexanoate
- Physical state: colourless liquid
- Analytical purity: not given
- Lot/batch No.: 120300
- Expiration date: December 31st, 1991
- Storage: at room temperature

Test animals

Species:
rabbit
Strain:
other: Kleinrussen, Chbb: HM
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Thomae, Biberach, Germany.
- Age at study initiation: approx. 9 months
- Weight at study initiation: approx. 2540 g
- Housing: individual
- Diet: Ssniff rabbit diet K4, Ssniff GmbH, Soest, Germany; ad libitum
- Water: tap water, ad libitum
- Acclimation period: at least 1 week

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 - 25
- Humidity (%): 45 - 75
- Photoperiod (hrs dark / hrs light): 12/12

Test system

Type of coverage:
semiocclusive
Preparation of test site:
shaved
Vehicle:
unchanged (no vehicle)
Controls:
other: not required, untreated sites of the same animal served as control
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 mL
Duration of treatment / exposure:
4 h
Observation period:
14 days
Reading time points: 1, 24, 48, 72 h and 7 and 14 days after exposure
Number of animals:
3
Details on study design:
TEST SITE
- Area of exposure: 6 cm² on the left or right flank
- Type of wrap if used: gauze patch covered with an adhesive air- and vapor-permeable patch and fixed by using a hypoallergenic adhesive gauze-bandage.

SCORING SYSTEM: Draize scoring system

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
animal #1
Time point:
24/48/72 h
Score:
1.3
Max. score:
4
Reversibility:
fully reversible within: 14 days
Irritation parameter:
erythema score
Basis:
animal #2
Time point:
24/48/72 h
Score:
1.7
Max. score:
4
Reversibility:
fully reversible within: 14 days
Irritation parameter:
erythema score
Basis:
animal #3
Time point:
24/48/72 h
Score:
2
Max. score:
4
Reversibility:
fully reversible within: 14 days
Irritation parameter:
edema score
Basis:
animal #1
Time point:
24/48/72 h
Score:
1.3
Max. score:
4
Reversibility:
fully reversible within: 14 days
Irritation parameter:
edema score
Basis:
animal #2
Time point:
24/48/72 h
Score:
1.3
Max. score:
4
Reversibility:
not fully reversible within: 14 days
Irritation parameter:
edema score
Basis:
animal #3
Time point:
24/48/72 h
Score:
1.3
Max. score:
4
Reversibility:
not fully reversible within: 14 days

Any other information on results incl. tables

Table 1: Evaluation of the dermal reaction

Skin effect

Erythema

Edema

 

1h

24h

48h

72h

Meana

1h

24h

48h

72h

Meana

Animal No.

#1

 

1

 

1

 

1

 

2

 

1.3

 

1

 

1

 

1

 

2

 

1.3

#2

1

1

2

2

1.7

1

1

1

2

1.3

#3

1

1

2

3

2.0

1

1

1

2

1.3

amean of readings at 24, 48 and 72 hours

 

Skin effect

days after exposure

 

7

14

Animal No.

#1

 

i b S

 

+

#2

i b S

+

#3

i b S

+

i = irreversible

b = brownish

S = eschar

+ = reversible

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
CLP: not classified
DSD: not classified