Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
no data
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1956
Report date:
1956

Materials and methods

Principles of method if other than guideline:
Before OECD Guideline 404 was established in 1982, skin irritation was tested using an internal method (BASF test). White Vienna rabbits were used. 2 animals were treated for 1, 5 and 15 minutes and 2 other animals for 20 hours using occlusive conditions. An application site of 2.5 x 2.5 cm was covered with the liquid test substance on a patch. After the application time of 1, 5, and 15 minutes, respectively, the skin was first washed with undiluted Lutrol 9, then with an aqueous Lutrol solution (50 %). The skin of the animals that had been treated with the test substance for 20 hours, remained unwashed.
The short exposure time of 15 minutes is thought not to impair the evaluation of the skin irritation potential significantly. As a 50% aqueous preparation is the limit of solubility, no higher concentrations would have been achieved if neat AH salt had been tested and this deviation from the test guideline is thought not to impair the evaluation of the skin irritation potential significantly.
GLP compliance:
no
Remarks:
pre-GLP study

Test material

Constituent 1
Chemical structure
Reference substance name:
Adipic acid, compound with hexane-1,6-diamine (1:1)
EC Number:
222-037-3
EC Name:
Adipic acid, compound with hexane-1,6-diamine (1:1)
Cas Number:
3323-53-3
Molecular formula:
C6H16N2.C6H10O4
IUPAC Name:
hexanedioic acid - hexane-1,6-diamine (1:1)

Test animals

Species:
rabbit
Strain:
Vienna White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Breeder
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: 1 week

ENVIRONMENTAL CONDITIONS
- Photoperiod (hrs dark / hrs light): 12h/12h

Test system

Type of coverage:
semiocclusive
Preparation of test site:
clipped
Vehicle:
water
Controls:
yes, concurrent no treatment
Amount / concentration applied:
TEST MATERIAL
- Concentration (if solution): 50%; saturated solution; pH = 7.5
Duration of treatment / exposure:
1, 5 and 15 minutes
Observation period:
No data
Number of animals:
2
Details on study design:
TEST SITE
- Area of exposure: back, an application site of 2.5 X 2.5 cm was covered with the liquid (37°C; approx. 1 ml)

REMOVAL OF TEST SUBSTANCE
- Washing: yes, the sites were wiped with a mixture of acetic acid and polyethylene glycol (Lutrol) after the end of the exposure period.

SCORING
Descriptive scores of the raw data have been converted to Draize numerical scores.

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
mean
Remarks:
n = 2
Time point:
other: unspecified
Score:
0
Max. score:
4
Remarks on result:
no indication of irritation
Remarks:
short-time test with 1; 5; 15 min exposure
Irritation parameter:
edema score
Basis:
mean
Remarks:
n = 2
Time point:
other: unspecified
Score:
0
Max. score:
4
Remarks on result:
no indication of irritation
Remarks:
short-time test with 1; 5; 15 min exposure
Irritant / corrosive response data:
None of two animals showed any effects of irritation at any application site.
primary dermal irritation index (PDII), mean of n=2: Score = 0

Any other information on results incl. tables

Limited documentation; no further details.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The substance is not irritating to the skin according to EU GHS classification and according to annex VI-Directive 67/548/EEC.
Executive summary:

Application of a saturated aqueous solution of the test substance (concentration ca. 50%) to the back of two rabbits for up to 15 minutes did not produce any signs of irritation.