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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: Comparable to guideline study with acceptable restrictions.
Cross-reference
Reason / purpose for cross-reference:
reference to same study

Data source

Referenceopen allclose all

Reference Type:
other company data
Title:
Unnamed
Year:
1974
Report date:
1974
Reference Type:
secondary source
Title:
No information
Author:
BASF AG
Year:
2008
Bibliographic source:
RIFM database

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:
Study was performed acc. internal BASF method, which was in large part similiar to OECD 404
GLP compliance:
no

Test material

Constituent 1
Reference substance name:
6-methylhept-5-en-2-one
EC Number:
203-816-7
EC Name:
6-methylhept-5-en-2-one
Cas Number:
110-93-0
IUPAC Name:
6-methylhept-5-en-2-one
Details on test material:
- Name of test material (as cited in study report): 6-Methyl-5-hepten-2-one,
- Analytical purity: 98 %
- pH = 5.6

Test animals

Species:
rabbit
Strain:
Vienna White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: M. Gaukler, Offenbach, Germany)
- Weight at study initiation: 2.98 and 2.93 (male), 2.47 and 2.92 kg (female)

Test system

Type of coverage:
occlusive
Vehicle:
unchanged (no vehicle)
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): ca. 0.5 ml
- Concentration (if solution): 100%
Duration of treatment / exposure:
1 min, 5 min, 15 min, 20 h
Observation period:
After exposure (only 1, 5, 15 min.), 24 hrs, 48 h, 5 days, 6 days and 8 days
Number of animals:
toal 4; 2 male, 2 female
Details on study design:
TEST SITE
- Area of exposure: 2.5 cm x 2.5 cm of back skin
- Type of wrap if used: cotton pad (seize: 2.5 cm x 2.5 cm) saturated with the undiluted test substance (ca. 0.5 ml)


REMOVAL OF TEST SUBSTANCE
- Washing (if done): 50% Lutrol (polyethylenglycol) dilution in water
- Time after start of exposure: 1, 5, 15 min and 20 h


SCORING SYSTEM:
Erythema and edema were scored according the below described system:
Although the results in the report were originally not given as Draize scores the data can be transferred into the Draize scoring system (in brackets). (+) = none - negligible effect (0)
+ = slight effect (1)
++ = moderate effect (2)
+++ = severe effect (>= 3)
N = necrosis

Results and discussion

Any other information on results incl. tables

LOCAL EFFECTS
Application of test substance for 1 min - 15 min did not lead to any skin findings. Application for 20 hrs led to questionable to slight redness (score = (+) ) after 24 hrs which was fully reversible in all animals within 48
h, signs of edema were not observed, a slight scaling occurred in 1 animal.

SYSTEMIC TOXICITY There were no signs of clinical toxicity from the dermal exposure.
No mortality occurred.

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Occlusive application of 6-methyl-hept-5-en-2-one for 20 h to rabbit skin lead to slight signs of irritation which were almost reversible within 48 hrs. Although a slight scaling remains after 8 days in only one animal, this finding is not sufficient for classification.