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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
12.7.1982-26.7.1982
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Fully documented, non GLP Study.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1982
Report date:
1982

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
Deviations:
yes
Remarks:
No stepwise approach was adopted. Only the average weight of the test animals is given, and not the weight at the beginning and end of the test.
Principles of method if other than guideline:
In addition to the stated guideline, the test substance was applied to damaged skin to investigate systemic effects.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Pent-1-ene
EC Number:
203-694-5
EC Name:
Pent-1-ene
Cas Number:
109-67-1
Molecular formula:
C5H10
IUPAC Name:
pent-1-ene
Details on test material:
- Name of test material (as cited in study report): Pentene-1
- Analytical purity: not reported
- Impurities (identity and concentrations): not reported
- Composition of test material, percentage of components: not reported
- Lot/batch No.: not reported
- Expiration date of the lot/batch: not reported

Test animals

Species:
rabbit
Strain:
other: Russian (Albino)
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Asta-Werke AG, D-4800 Bielefeld 14
- Age at study initiation: 10 - 11 months
- Weight: 2.7 - 2.9 kg
- Housing: single
- Diet (e.g. ad libitum): Standardized feed for test animals ALTROMIN
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 1 days
- gender: female

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +/- 1°C
- Humidity (%): 50 - 60 %
- Air changes (per hr): not reported
- Photoperiod (hrs dark / hrs light): 12h/12h

Test system

Type of coverage:
occlusive
Preparation of test site:
shaved
Vehicle:
unchanged (no vehicle)
Controls:
not required
Amount / concentration applied:
0.5 ml
Duration of treatment / exposure:
4 hours
Observation period:
Observation after 1, 24, 48 and 72 hours
Number of animals:
3 female animals tested
Details on study design:
TEST SITE
- Area of exposure:
- % coverage: 100%
- Type of wrap if used: 6.25cm2 linen piece, covered by a synthetic self-adhesive strip; subsequently the patches were covered by a bandage (acrylastic)

REMOVAL OF TEST SUBSTANCE
- Washing (if done): no
- Time after start of exposure: 4 h

SCORING SYSTEM:
Values for erythema and eschar formation as well as oedema formation were averaged for all animals and summed up. The sum resulted from 16 averages and was divided by 8 to obtain the primary irritation index:
0.0 - 0.5: non irritating
0.6 - 3.0: slightly irritating
3.1 - 5.0: moderately irritating
5.1 - 8.0: strongly irritating

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
animal: # 1-3; intact and scarified skin
Time point:
other: 1, 24, 48 and 72 h
Score:
0
Max. score:
0
Reversibility:
other: not applicable as no effect
Irritation parameter:
edema score
Basis:
animal: # 1-3; intact and scarified skin
Time point:
other: 1, 24, 48 and 72 h
Score:
0
Max. score:
0
Reversibility:
other: not applicable as no effect
Irritant / corrosive response data:
No erythema or oedema formation was observed on any of the test animals. Merely horny skin callus developed on the intact and scarified skin in the second observation period.
Other effects:
No systemic toxicity effects were observed after dermal application of the product.

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
No reaction on intact or scarrified skin was found. The test item 1-Pentene was not skin irritant.
Executive summary:

In the study the test item Pentene-1 was assessed for its possible skin irritation potential.

For this purpose 0.5 ml of the test substance was applied on intact and scarrified skin of three rabbits.

The animals did not show any clinical signs during the course of the study and no cases of mortality were observed.

The skin reaction score was 0, corresponding to no erythema or oedema formation.

The test item Pentene-1 was not skin irritant.