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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
eye irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
22 February 1985 to 01 May1985
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1985
Report date:
1985

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
5-methyl-s-triazolo[1,5-a]pyrimidin-7-ol
EC Number:
219-706-7
EC Name:
5-methyl-s-triazolo[1,5-a]pyrimidin-7-ol
Cas Number:
2503-56-2
Molecular formula:
C6H6N4O
IUPAC Name:
5-methyl-s-triazolo[1,5-a]pyrimidin-7-ol
Test material form:
solid: particulate/powder

Test animals / tissue source

Species:
rabbit
Strain:
New Zealand White
Details on test animals or tissues and environmental conditions:
TEST ANIMALS
- Source: Cpb/TNO Zeist, The Netherlands
- Weight at study initiation: 2478-2742 g
- Housing: individually in metal cages with perforated floors
- Diet: standard diet ( LK01 Hope Farms Woerden) 100-120 g/d
- Water: tap water ad libitum
- Acclimation period: 3 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20±1 °C
- Humidity (%): 45-55%
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light):12/12

Test system

Vehicle:
unchanged (no vehicle)
Remarks:
grounded before instillation
Controls:
not required
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 58 mg (slightly below 0.1 mL) ground to a fine powder

VEHICLE: none
Duration of treatment / exposure:
NA
Observation period (in vivo):
at 1, 24, 48 and 72 hours after instillation (for one rabbit a 9 day observation was included)
Number of animals or in vitro replicates:
3 females
Details on study design:
REMOVAL OF TEST SUBSTANCE
- Washing (if done): none

SCORING SYSTEM: Draize

TOOL USED TO ASSESS SCORE: at 24 hfluorescein staining was used

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
cornea opacity score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
0
Remarks on result:
no indication of irritation
Remarks:
fluorescein examination did not show any damage
Irritation parameter:
iris score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
0
Irritation parameter:
conjunctivae score
Remarks:
redness
Basis:
mean
Time point:
24/48/72 h
Score:
1.4
Max. score:
2
Reversibility:
fully reversible within: 9 days
Irritation parameter:
chemosis score
Basis:
mean
Time point:
24/48/72 h
Score:
0.1
Max. score:
2
Reversibility:
fully reversible

Any other information on results incl. tables

Animal no

1

2

3

1

24

48

72

1

24

48

72

1

24

48

72

cornea

0

0

0

0

0

0

0

0

0

0

0

0

iris

0

0

0

0

0

0

0

0

0

0

0

0

conjunctivae

 

 

 

 

 

 

 

 

 

 

 

 

redness

1

0

0

0

1

1

1

1

1

1

1

0

chemosis

0

0

0

0

2

1

0

1

2

0

0

0

 

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The substance is considered non-irritant to the eyes
Executive summary:

Three female rabbits received 58 mg (slightly below 0.1 mL) of the substance in the eye. The eyes were observed for signs of irritation after 1, 24, 48 and 72 hours. No effects were found on the cornea and the iris. The effects on the conjunctivae were limited and fully reversible at an additional observation after 9 days. The substance is considered not irritating to the eyes.