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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Skin irritation / corrosion

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Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP Guideline study (OECD 404)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1985
Report date:
1985

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
no
Qualifier:
according to guideline
Guideline:
other: EPA - Pesticide assessment guidelines
Deviations:
not specified
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Methyl isothiocyanate
EC Number:
209-132-5
EC Name:
Methyl isothiocyanate
Cas Number:
556-61-6
Molecular formula:
C2H3NS
IUPAC Name:
isothiocyanatomethane
Details on test material:
Test article name : METHYLSENFOEL (MITC)
Source: DEGUSSA AG
Purity: technical

Test animals

Species:
rabbit
Strain:
New Zealand White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Kleintierfarm madoerin AG (CH 4414 Fuellinsdorf, Switzerland)
- Age at study initiation: 15-16 week-old
- Weight at study initiation: 2.4/2.6 kg
- Housing: individually in stainless steel cages equipped with an automatic cleaning and drinking system.
- Diet (e.g. ad libitum): pelleted standard kliba 341, ad libitum
- Water (e.g. ad libitum):Tap water, ad libitum
- Acclimation period: 4 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22+/-2
- Humidity (%): 55+/-10%
- Air changes (per hr): 10-15
- Photoperiod (hrs dark / hrs light):12/12 (8h music/light period)

Test system

Type of coverage:
occlusive
Preparation of test site:
shaved
Vehicle:
unchanged (no vehicle)
Controls:
no
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 ml
- Concentration (if solution): no data

no VEHICLE
Duration of treatment / exposure:
4 hours
Observation period:
4 hours
Number of animals:
3 = 1 male + 2 females
Details on study design:
TEST SITE
- Area of exposure: the dorsal
- % coverage: patch = 3x3cm
- Type of wrap if used: Skin was recovered with a patch of surgical gauze. The gauze was covered with aluminium foil and then covered with an occlusive dressing. The dressing was wrapped around the abdomen and anchored with an elastic bandage.

REMOVAL OF TEST SUBSTANCE :
Just after the animals death (approximately 1 hour after treatment), the dressing was removed.

SCORING SYSTEM: idem in guideline of OECD 404

Results and discussion

In vivo

Results
Remarks on result:
other: All animals died within the 4-hour treatment phase, therefore no irritation index could be determined
Irritant / corrosive response data:
All animals died within the 4-hour treatment phase, therefore no irritation index could be determined. The index given below was determined just after removing the occlusive bandage, when the animals were already dead. After 1 hour: for each animal, erythema score = 4 and edema score = 2. After 4 hours: all animals died.
Other effects:
Toxic symptoms/mortality: Between one and four hours after application start all animals showed sedation, crying, spasms, dyspnea and curved body position.

Applicant's summary and conclusion

Interpretation of results:
other: unconclusive
Conclusions:
All animals died within the 4 -hour treatment phase, therefore no irritation index could be determined.
Executive summary:

The purpose of this primary study skin irritation study was to assess possible irritation potential when single doses of MITC are placed on the skin on rabbits. All animals died within the 4 -hour treatment phase, therefore no irritation index could be determined.