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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Direct observations: clinical cases, poisoning incidents and other

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Administrative data

Endpoint:
direct observations: clinical cases, poisoning incidents and other
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1991-03-05 to 1991-03-07
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: This study is classified as reliable with restrictions because while there is no statement regarding whether this study was conducted according to GLP or equivalent, the study protocol was provided.

Data source

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

Materials and methods

Study type:
study with volunteers
Endpoint addressed:
skin irritation / corrosion
Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Protocol supplied by testing laboratory. The objective was to evaluate the test material for its potential to cause irritation after a single 24-hour semi-occlusive patch application.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2-methylbutane
EC Number:
201-142-8
EC Name:
2-methylbutane
Cas Number:
78-78-4
Molecular formula:
C5H12
IUPAC Name:
2-methylbutane
Details on test material:
- Name of test material (as cited in study report): 2-methylbutane
- Substance type: C5 aliphatic
- Physical state: unknown
- Test substance characteristics and analysis: responsibility of the sponsor: Exxon Biomedical Sciences, New Jersey

Method

Type of population:
general
Subjects:
- Number of subjects exposed: 30
- Sex: 28 female, 2 male
- Age: 18 - >60
- Known diseases: no skin/dermatological conditions that would interfere with the study results
Ethical approval:
confirmed and informed consent free of coercion received
Route of exposure:
dermal
Reason of exposure:
intentional
Exposure assessment:
not specified
Details on exposure:
Each subject received one application of the test material under semi-occlusive conditions. The sample was applied to the outer surface of the upper arm, to the Webril pad of the Professional Medical, Inc. patch. The test materials remained in contact with the skin for 24 hours, unless irritation was noted. 30 minutes after patch removal, the test sites were scored, and were scored again 24 hours after patch removal. Test subjects remained under observation for a maximum of 4 hours after exposure.
Examinations:
The patches remained on for 24 hours unless irritation was noted, and after removal, the test site was gentrly rinsed with water and gently patted dry with a paper towel. Sites were graded approximately 30 minutes after patch removal, and again 24 hours after the initial patch removal. A scale from 0 to 7 was used to score the reactions to the test material.
Medical treatment:
If the test material elicited severe reactions, the patches were removed and the test site gently rinsed with water and patted dry with paper towel.

Results and discussion

Clinical signs:
No clinical observations were noted, and no adverse reactions were observed during exposure.
Results of examinations:
Overall irritation score: 0.33
This was calculated as the mean of all scores from both time periods (0.5 hours and 24 hours after exposure).
No individual data was provided for this test material.
No data on reversibility was collected.

Any other information on results incl. tables

The results of the study indicate that 2 -methylbutane was clinically non-irritating.

Applicant's summary and conclusion

Conclusions:
The average dermal irritation score for this test material was 0.33 on a scale from 0 to 7. 2 -Methylbutane was considered non-irritating.
Executive summary:

In a dermal irritation study, 30 human volunteers were dermally exposed to n-pentane for 24 hours, via a semi-occlusive patch. Thirty minutes after patch removal, the test sites were scored, and were scored again 24 hours after patch removal. Test subjects remained under observation for a maximum of 4 hours after exposure. If the test material elicited severe reactions, the patches were removed.

The average dermal irritation score for this test material was 0.33 on a scale from 0 to 7. 2 -Methylbutane was considered non-irritating. This study was given a reliability rating of 2, reliable with restrictions, because while there is no statement regarding whether this study was conducted according to GLP or equivalent, the study protocol was provided.