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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
vapour pressure
Type of information:
experimental study
Adequacy of study:
key study
Study period:
31Oct2017 - 09Jan2018
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2018
Report date:
2018

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
EU Method A.4 (Vapour Pressure)
Deviations:
no
Qualifier:
according to guideline
Guideline:
OECD Guideline 104 (Vapour Pressure Curve)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EPA OPPTS 830.7950 (Vapor Pressure)
Deviations:
no
GLP compliance:
yes
Type of method:
effusion method: isothermal thermogravimetry

Test material

Constituent 1
Chemical structure
Reference substance name:
3,7-dihydropurin-6-one;sodium
Cas Number:
45738-97-4
Molecular formula:
C5H3N4NaO
IUPAC Name:
3,7-dihydropurin-6-one;sodium
Test material form:
solid: particulate/powder
Details on test material:
- Appearance: White powder
- Purity / Composition: 98%
- Test item storage: Room temperature
Specific details on test material used for the study:
SOURCE OF TEST MATERIAL
- Batch No.of test material: 16K235305
- Purity: 98.0%

STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: At room temperature

Results and discussion

Vapour pressureopen allclose all
Key result
Temp.:
20 °C
Vapour pressure:
ca. 0 Pa
Key result
Temp.:
20 °C
Vapour pressure:
ca. 0 mm Hg
Key result
Temp.:
25 °C
Vapour pressure:
ca. 0 Pa
Key result
Temp.:
25 °C
Vapour pressure:
ca. 0 mm Hg

Applicant's summary and conclusion

Conclusions:
The isothermal TGA effusion method was applied for the determination of the vapour pressure of Sodium hypoxanthine.
The vapour pressure of the test item at 20°C (293K) was: < 1.3 × 10-8 [Pa] , < 1.0 × 10-10 [mm Hg]
The vapour pressure of the test item at 25°C (298K) was: < 7.2 × 10-8 [Pa] , < 5.4 × 10-10 [mm Hg]
Executive summary:

In the range of 200°C and 230°C a log p versus 1/T curve for the test item could not be determined since the coefficient of correlation (r) was < 0.99 (data is archived in the raw data). This is most likely due to reaction and/or decomposition of the test item.  Since no accurate vapour pressure could be calculated from the obtained results the weight losses of the test item were compared with the results of benzo(ghi)perylene at the same temperatures. Since the weight loss of the test item was lower than the weight loss of the reference compound, the vapour pressure of the test item is considered to be below the vapour pressure of benzo(ghi)perylene.

The vapour pressure of the test item at 20°C (293K) was: < 1.3 × 10-8 [Pa] , < 1.0 × 10-10 [mm Hg]

The vapour pressure of the test item at 25°C (298K) was:  < 7.2 × 10-8 [Pa] , < 5.4 × 10-10 [mm Hg]