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Toxicological information

Skin irritation / corrosion

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Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
Nov 2016
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2017
Report date:
2017

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Version / remarks:
2015
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
1-Ethyl-3-methylimidazolium Diethyl Phosphate
Cas Number:
848641-69-0
Molecular formula:
C6H11N2 C4H10O4P
IUPAC Name:
1-Ethyl-3-methylimidazolium Diethyl Phosphate
Test material form:
liquid
Details on test material:
Batch No 187-9-113-Y
Expiry date: 2021-1-30
Specific details on test material used for the study:
Yellow liquid
Batch no.: Batch 1.3
20% water (Correction factor 1.25)

Test animals

Species:
rabbit
Strain:
New Zealand White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Manfred Bauer Kaninchen, 74632 Neuenstein, Germany
- Age at study initiation: approx. 8.5 months
- Weight at study initiation: 3.5 - 3.9 kg
- Housing: individually in cages measuring 380 mm x 425 mm x 600 mm
- Diet (e.g. ad libitum): ssniff k-H V 2333 (ssniff Spezialdiäten GmbH, 59494 Soest, Germany), ad libitum
- Water (e.g. ad libitum): tap water ad libitum
- Acclimation period: 7 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 +/- 3°C
- Humidity (%): 30 - 70%
- Air changes (per hr):
- Photoperiod (hrs dark / hrs light): 12/12

IN-LIFE DATES:
From: 07.11. To: 29.11.2016

Test system

Type of coverage:
semiocclusive
Preparation of test site:
clipped
Vehicle:
unchanged (no vehicle)
Controls:
not required
other: the surrounding untreated skin served as a control
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.625 mL
- Concentration (if solution): pure

VEHICLE
- Amount(s) applied (volume or weight with unit): n.a.

NEGATIVE CONTROL
- Amount(s) applied (volume or weight): no required

POSITIVE CONTROL
- Amount(s) applied (volume or weight): not required
Duration of treatment / exposure:
4 h
Observation period:
14 days
readings: 60 min, 24, 48, 72 h, 7 and 14 d after patch removal
Number of animals:
3
Details on study design:
TEST SITE
- Area of exposure: approx. 6 cm(2)
- % coverage: 100
- Type of wrap if used: gauze patch

REMOVAL OF TEST SUBSTANCE
- Washing (if done): none
- Time after start of exposure: n.a.

OBSERVATION TIME POINTS
(indicate if minutes, hours or days)
60 min, 24, 48, 72 h, 7 and 14 days after patch removal

SCORING SYSTEM: according to Draize

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Irritation parameter:
edema score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Irritant / corrosive response data:
Under the present test conditions, none of the three rabbits exposed for 4 hours to 0.625 mL of the test item (semi-occlusive conditions) revealed any skin reaction.
Other effects:
There were no systemic intolerance reactions.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
According to GHS and EC regulation 1272/2008 the test item is non-irritating.
Executive summary:

The test substance was tested for its skin irritant properties in 3 New Zealand White rabbits. Due to the water content of 20% 0.625 mL of the substance were applied to the clipped skin. None of the three rabbits exposed for 4 h revealed any skin reaction. There were no systemic intolerance reactions.