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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Eye irritation

Currently viewing:

Administrative data

Endpoint:
eye irritation
Remarks:
in vitro
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2008-04-16 - 2008-05-08
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: The study was conducted according to an internationally accepted guideline. All study parameters are based on the specific guideline.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2008
Report date:
2008

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
-
EC Number:
485-280-6
EC Name:
-
Cas Number:
303749-96-4
Molecular formula:
Hill formula: C2H6N10 CAS formula: C2H3N9.H3N
IUPAC Name:
N-(1H-1,2,3,4-tetrazol-5-yl)-1H-1,2,3,4-tetrazol-5-amine amine
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder
Details on test material:
Name 1H-Tetrazol-5-amine-, N-1H4etrazol-5-yl-, monoammonium salt
Appearance white powder
Composition 1H-Tetrazol-5amine-, N-1H-tetrazol-5-yl-, monoammonium salt
CAS-No. 303749-96-4
EINECS-No. not stated
Molecular formula C2H6N10
Molecular weight 170.14 g/mol
Purity > 99 %

Test animals / tissue source

Species:
other: in vitro
Strain:
not specified

Test system

Vehicle:
unchanged (no vehicle)
Controls:
no
Amount / concentration applied:
25 mg
Duration of treatment / exposure:
300 seconds
Number of animals or in vitro replicates:
not applicable

Results and discussion

In vivo

Results
Irritation parameter:
overall irritation score
Basis:
mean
Time point:
other: 300 seconds
Score:
2.42
Max. score:
21
Reversibility:
not specified

Any other information on results incl. tables

Observations

Test Group

Time until Haemor­rhage (s)

Time until Lysis (s)

Time until Coagulation (s)

Irritation Score

Mean Irritation Score

Negative Control

301

301

301

0.00

 

Negative Control

301

301

301

0.00

0.00

Negative Control

301

301

301

0,00

 

Positive Control

14

26

34

19.21

 

0.1 NaOH

 

Positive Control 0.1 NaOH

17

30

37

18.98

19.00

Positive Control

15

28

45

18.82

 

0.1 NaOH

 

Positive Control 1 % SDS

8

59

301

10.53

 

Positive Control 1 % SDS

9

88

301

9.84

10.07

Positive Control

A

91

301

9.85

 

1% SDS

 

 

Test Item

160

301

301

2.35

 

Test Item

134

301

301

2.78

 

Test Item

167

301

301

2.23

2.42

Test Item

149

301

301

2.53

Test Item

169

301

301

2.20

 

Test Item

156

301

301

2.42

 

Applicant's summary and conclusion

Interpretation of results:
Category 2A (irritating to eyes)
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The in vitro skin irritation potential of 1H-Tetrazol-5-amine-, N-1 H-tetrazol-5-yl-, monoammonium salt was determined according to OECD Guideline 405.
The test item 1H-Tetrazol-5-amine-, N-1 H-tetrazol-5-yl-, monoammonium salt showed slight effects on the blood vessels of the CAM, calculated mean irritation score is 2.42.
In conclusion, it can be stated, that in this study and under the experimental conditions reported, the test item 1H-Tetrazol-5-amine-, N-1H-tetrazol-5-yl-, monoammonium salt possesses a slight irritation potential.
Executive summary:

The in vitro skin irritation potential of 1H-Tetrazol-5-amine-, N-1 H-tetrazol-5-yl-, monoammonium salt was determined according to OECD Guideline 405.

One valid experiment was performed.

Hen's eggs with an age of nine days were used. The test item 1 H-Tetrazol-5-amine-, N- 1 H-tetrazol-5-yl-, monoammonium salt was brought onto the surface of the CAM of a hen's egg which had been incubated at 37 °C for nine days. Observation time was five minutes at room temperature.

Physiological sodium chloride solution was used as negative control. The negative control showed no irritating effect on the blood vessels under the membrane.

The positive controls (1% solution of SDS and 0.1 n NaOH) induced a moderate or severe irritation, respectively, on the blood vessels.

The test item 1H-Tetrazol-5-amine-, N-1 H-tetrazol-5-yl-, monoammonium salt showed slight effects on the blood vessels of the CAM, calculated mean irritation score is 2.42.

In conclusion, it can be stated, that in this study and under the experimental conditions reported, the test item 1H-Tetrazol-5-amine-, N-1H-tetrazol-5-yl-, monoammonium salt possesses a slightirritation potential.