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Toxicological information

Eye irritation

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Administrative data

eye irritation: in vitro / ex vivo
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
2017- 08-17 to 2018-01-16
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference Type:
study report
Report date:

Materials and methods

Test guideline
according to guideline
OECD Guideline 437 (Bovine Corneal Opacity and Permeability Test Method for Identifying i) Chemicals Inducing Serious Eye Damage and ii) Chemicals Not Requiring Classification for Eye Irritation or Serious Eye Damage)
Version / remarks:
adopted July 2013
GLP compliance:

Test material

Constituent 1
Chemical structure
Reference substance name:
EC Number:
EC Name:
Cas Number:
Molecular formula:
Test material form:
Details on test material:
- Name: Vinylcyclohexane
- CAS No.: 695-12-5
- Batch No.: VCH/7/17K1
- Expiry date: 30 March 2019
- Purity: 99.8 %
- Appearance: Clear, colourless liquid
Specific details on test material used for the study:
- Storage conditions: Fridge: (2-8 °C), keep container tightly closed, keep away from ignition sources
- Stability: stable under normal temperature and pressure
- Solubility: H2O: < 0,1 g/L ; EtOH: >1 g/L; acetone: >1 g/L; CH3CN: >1 g/L; DMSO: >1 g/L
- Treatment of test material prior to testing: The test item is a liquid substance. It was tested directly, without dilution or preparation of a solution.

Test animals / tissue source

not specified
Details on test animals or tissues and environmental conditions:
- Source: Müller Fleisch GmbH, Enzstr. 2-4, 75217 Birkenfeld, Germany
- Age: 12 to 60 months

- Temperature (°C): 32 ± 1 °C
- The eyes were transported to the test facility in Hanks' Balanced Salt Solution with 1% Penicillin-Streptomycin solution (Penicillin 100 U/mL, Steptomycin 100 µg/mL) in a suitable cooled container.

Test system

unchanged (no vehicle)
yes, concurrent positive control
yes, concurrent negative control
Amount / concentration applied:
750 µL
Duration of treatment / exposure:
10 minutes
Duration of post- treatment incubation (in vitro):
2 hours
Number of animals or in vitro replicates:
Details on study design:
SELECTION AND PREPARATION OF CORNEAS: The corneas were excised with a scalpel and cut from the globe with a 2-3 mm ring of sclera around the outside. Each cornea was transferred to a cornea holder in which pre-warmed cMEM (32 ± 1 °C) without phenol red was filled. The holders were then incubated for 1 hour in the incubation chamber at 32 ± 1 °C.

QUALITY CHECK OF THE ISOLATED CORNEAS: After arrival of the corneas, they were examined. Only corneas which were free from damages were used.

NUMBER OF REPLICATES: 3 for each treatment group

NEGATIVE CONTROL USED: HBSS (Hank’s Balanced Salt Solution 10-fold concentrated, diluted in demin. water (1:10), batch no.: 20170831)

POSITIVE CONTROL USED: Dimethylformamide (undiluted)

APPLICATION DOSE AND EXPOSURE TIME: 750 µL application dose, 2 hours exposure time

TREATMENT METHOD: closed chamber


- Number of washing steps after exposure period: After 10 min exposure time the corneas were rinsed thoroughly with cMEM without phenol red and afterwards they were finally rinsed also with cMEM without phenol red. Then, the anterior chamber was filled with cMEM without phenol red and the corneas were stored additional 2 hours at 32 ± 1 °C.
- POST-EXPOSURE INCUBATION: 2 hours, afterwards the cMEM was renewed in both chambers (front and anterior chamber). Then, the final opacity value of each cornea was recorded. The cMEM without phenol red was removed from the front chamber, and 1 mL sodium fluorescein solution (concentration: 4 mg/mL) was added to the front chamber. The chambers were then closed again and incubated for 90 minutes at 32 ± 1 °C. After incubation, the content of the posterior chamber was thoroughly mixed. Then, the permeability of the cornea was measured as optical density of the liquid with a microtiter plate photometer at 492 nm.

- Corneal opacity: Corneal opacity is measured quantitatively as the amount of light transmission through the cornea
The change of opacity value of each treated cornea with test item, positive control and negative control was calculated by subtracting the initial basal opacity from the post treatment opacity reading for each cornea. The average change in opacity of the negative control cornea was calculated and this value was subtracted from the change in opacity of each treated cornea with test item and positive control to obtain a corrected opacity.
Opacity = [(I0/1)-b]/a
a = 0.0251 and b = 0.9894 being Opacitometer-specific empirically determined variables
l0 = the empirically determined illuminance through a cornea holder with windows and
Medium, here: I0= 1093.96
I = the measured illuminance (unit: LUX)
- Corneal permeability: Permeability is measured quantitatively as the amount of sodium fluorescein dye that passes across the full thickness of the cornea, as detected in the medium in the posterior chamber.
The corrected OD492 value of each cornea treated with test item and positive control was calculated by subtracting the mean negative control cornea value from the original permeability value for each cornea. The mean OD492 value for each treatment group (test item, positive control and negative control) was determined by averaging the final corrected OD492 values of the treated corneas for one treatment group.

SCORING SYSTEM: In Vitro Irritancy Score (IVIS)
IVIS = mean opacity value + (15 x corrected OD492 value)
The IVIS of each replicate of the positive control and of the test item were calculated from
the following equation:
IVIS = (opacity difference — mean opacity difference of the negative control) + [15 x (OD492-mean OD492 of the negative control)]
The IVIS cut-off values for identifying test substances as inducing serious eye damage (UN GHS Category 1) and test substances not requiring classification for eye irritation or serious eye damage (UN GHS No Category) are given in Table 1 (see "Any other information on materials and methods").
An identification of test substances that should be classified as irritating to eyes (UN GHS Category 2 or Category 2A) or test substances that should be classified as mildly irritating to eyes (UN GHS Category 2B) cannot be made. For this purpose, further testing with another suitable method is required.

Results and discussion

In vitro

Irritation parameter:
in vitro irritation score
Run / experiment:
mean (triplicates)
Vehicle controls validity:
not examined
Negative controls validity:
Positive controls validity:
Remarks on result:
other: no prediction can be made
Other effects / acceptance of results:
- Acceptance criteria met for negative control: Yes
- Acceptance criteria met for positive control: Yes

Applicant's summary and conclusion

Interpretation of results:
other: no prediction can be made
In conclusion, based on the mean in vitro irritation score of 4.48 in the bovine corneal opacity and permeability assay (OECD 437), no prediction can be made on classification, since according to OECD Guideline no. 437 (Jul. 2013), a substance with an IVIS > 3 and ≤ 55 induces effects on the cornea, cannot be classified in an UN GHS Category.
Executive summary:

In a primary eye irritation study,conducted according to OECD Guideline 437, 750 µL of Vinylcyclohexane (Purity 99.8%) was applied to the bovine corneas of slaughtered cattle 12- 60 months old for 10 minutes at at 32 ± 1 °C. After removal of the test item and 2 hours post-incubation, opacity and permeability values were measured.  Irritation was scored by the method of in vitro Irritancy Score. The test substance showed an IVIS of 4.48, which is in the range > 3 and ≤ 55, and therefore, no prediction can be made on classification.