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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
eye irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Meets generally accepted scientific standards. No data on purity of test substance. No GLP.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1976
Report date:
1976

Materials and methods

Principles of method if other than guideline:
The test substance was applied to the conjunctival sac of white Vienna rabbits. The non-treated adjacent eye served as control, to which talcum powder was applied. The animals were observed several times on the treatment day and 8 days afterwards, and findings were recorded on working days. The test substance was not washed out 24 hours after instillation. Findings were graded using a scheme convertable into the Draize scheme.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Anilinoacetonitrile
EC Number:
221-129-0
EC Name:
Anilinoacetonitrile
Cas Number:
3009-97-0
Molecular formula:
C8H8N2
IUPAC Name:
2-(phenylamino)acetonitrile
Details on test material:
- Name of test material (as cited in study report): Phenylglycinnitril
- Physical state: solid
- Analytical purity: no data

Test animals / tissue source

Species:
rabbit
Strain:
Vienna White

Test system

Vehicle:
unchanged (no vehicle)
Controls:
not required
Amount / concentration applied:
50 mm3
Duration of treatment / exposure:
continuous
Observation period (in vivo):
8 days
Number of animals or in vitro replicates:
2

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
cornea opacity score
Basis:
mean
Time point:
other: 24, 48 h
Score:
1
Reversibility:
not reversible
Remarks on result:
other: Individual Scores of the BASF Test have been converted into the OECD Draize Scheme.
Irritation parameter:
iris score
Basis:
mean
Time point:
other: 24, 48 h
Score:
0
Remarks on result:
other: Individual Scores of the BASF Test have been converted into the OECD Draize Scheme.
Irritation parameter:
conjunctivae score
Basis:
mean
Time point:
other: 24, 48 h
Score:
1
Reversibility:
fully reversible within: 8 days
Remarks on result:
other: Individual Scores of the BASF Test have been converted into the OECD Draize Scheme.
Irritation parameter:
chemosis score
Basis:
mean
Time point:
other: 24, 48 h
Score:
0
Remarks on result:
other: Individual Scores of the BASF Test have been converted into the OECD Draize Scheme.

Any other information on results incl. tables

Table1: Individual Scores of cornea, iris and conjunctivae that have been converted from BASF test into the OECD Draize Scheme.

time

animal 1

animal 2

corneal opacity

24 h

1

1

48 h

1

1

72 h

no data

no data

8 d

1

1

iris

24 h

0

0

48 h

0

0

72 h

no data

no data

8 d

0

0

conjunctiva

erythema/edema

24 h

1/0

1/0

48 h

1/0

1/0

72 h

no data

no data

8 d

0/0

0/0

Applicant's summary and conclusion