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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

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Diss Factsheets

Administrative data

Endpoint:
vapour pressure
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2009
Report date:
2009

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 104 (Vapour Pressure Curve)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Type of method:
effusion method: Knudsen cell

Test material

Constituent 1
Chemical structure
Reference substance name:
potassium 5-amino-1H-1,2,3,4-tetrazol-1-ide
Cas Number:
136369-04-5
Molecular formula:
CH2KN5
IUPAC Name:
potassium 5-amino-1H-1,2,3,4-tetrazol-1-ide
Test material form:
solid: particulate/powder
Details on test material:
Batch no.: 08KI030

Results and discussion

Vapour pressure
Key result
Temp.:
20 °C
Vapour pressure:
< 0 Pa
Remarks on result:
not measured/tested
Remarks:
No vapour pressure could be determined experimentally; as significance and reproducibility were not sufficient. Vapour pressure was calculated as upper limit from the start and end weights of the Knudsen cell after a time period of nine days. The value at 130°C was 2.2 * 10-04 Pa, indicating, that vapour pressure at 20 or 25°C should lie below 10-05 Pa.

Applicant's summary and conclusion

Conclusions:
No vapour pressure could be determined experimentally; as significance and reproducibility were not sufficient. Vapour pressure was calculated as upper limit from the start and end weights of the Knudsen cell after a time period of nine days. The value at 130°C was 2.2 * 10-04 Pa, indicating, that vapour pressure at 20 or 25°C should lie below 10-05 Pa as is expected for a substance with ionic character. No significant impact on the assessment of the test item’s behaviour in the environment is expected from the remaining uncertainty in vapour pressure. The result of the test is considered valid.
Executive summary:

The vapour pressure of 5-Aminotetrazol Potassium was determined following EU A.4 using the effusion method (weight loss). Two experiments were performed at the nominal temperatures 125 oC and 140 oC. No significant and reproducible weight loss was found. As higher temperatures could not be measured due to the limits of the test system, vapour pressure was calculated as upper limit using the weights at the start and at the end of the experiments. The limit vapour pressure at 130 oC is 2.19 * 10–04 Pa. It can therefore be assumed that vapour pressure at 20 oC and at 25 oC lies below 10-05 Pa.