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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
explosive properties of explosives
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
the study does not need to be conducted because there are no chemical groups present in the molecule which are associated with explosive properties
Justification for type of information:
In accordance with Column 2 adaptation statement of REACH Annex VII, information requirement section 7.11, this study does not need to be conducted based on a structural assessment of the substance. None of the components of the test item does contain chemical groups which are associated with explosive properties.
Cross-referenceopen allclose all
Reason / purpose for cross-reference:
reference to same study
Reference
Endpoint:
melting point/freezing point
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2017-07-10 / 2018-03-26
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Qualifier:
according to guideline
Guideline:
OECD Guideline 102 (Melting point / Melting Range)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method A.1 (Melting / Freezing Temperature)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EPA OPPTS 830.7200 (Melting Point / Melting Range)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Type of method:
differential scanning calorimetry
Key result
Atm. press.:
1 013.25 hPa
Decomposition:
yes
Decomp. temp.:
> 225 °C
Sublimation:
no
Remarks on result:
not determinable

Preliminary Test

Starting at 275°C, the weight of the sample decreased significantly. At 333°C, the sample weight had decreased by 25%. After the experiment, a black molten residue remained in the sample container (original colour: off-white). The change of the colour indicated reaction and/or decomposition of the test item.

Main Study

An endothermic peak was observed between 50°C and 125°C in Experiment 1. Based on the weight loss observed during the preliminary test between 50°C and 125°C the endothermic effect was most likely due to evaporation of volatile components. An endothermic peak was observed between 225°C and 300°C. The endothermic effect was most likely obtained due to melting or reaction and/or decomposition of the test item. After the experiment, a black/brown molten residue remained in the sample container.

To investigate the endothermic peak between 50°C and 125°C, a repeated heating cycle was applied in Experiment 2. With the first heating no changes were observed compared with Experiment 1. During cooling, exothermic peaks between 50°C and 80°C were found (results are archived in the raw data). Based on the results found in the preliminary test, the reason for these effects is unknown. With the second heating, an endothermic peak was observed between 50°C and 100°C. The reason for this effect was unknown. The reason for the exothermic effect observed between 150°C and 175°C is unknown. After the experiment, a dark brown molten residue remained in the sample container.

In order to investigate endothermic peaks between 50°C and 125°C and between 225°C and 300°C, Experiment 3 was stopped directly after the first endothermic peak and Experiment 4 was stopped before the second endothermic peak. After Experiment 3, the sample appeared to have been unchanged, i.e. no melting of the test item was observed. This endothermic peak is most likely due to evaporation of volatile components. After Experiment 4, a brownish coagulated residue remained in the sample container, indicating that the test item reacted and/or decomposed before melting.

Conclusions:
The test item has no measurable melting temperature.
Executive summary:

The melting temperature of the test item was investigated by DSC according to OECD Guideline 102 and EU Method A.1. Reaction and/or decomposition of the test item was observed during DSC experiments at temperatures of > 225°C (> 498K). Melting of the test item was not observed below the temperature at which reaction and/or decomposition started. Based on this, the test item has no measurable melting temperature.

Reason / purpose for cross-reference:
reference to same study
Reference
Endpoint:
boiling point
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2017-07-10 / 2018-03-26
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Qualifier:
according to guideline
Guideline:
OECD Guideline 103 (Boiling Point)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method A.2 (Boiling Temperature)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EPA OPPTS 830.7220 (Boiling Point / Boiling Range)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Type of method:
differential scanning calorimetry
Key result
Atm. press.:
1 013.25 hPa
Decomposition:
yes
Decomp. temp.:
> 225 °C
Remarks on result:
not determinable

Preliminary Test

Starting at 275°C, the weight of the sample decreased significantly. At 333°C, the sample weight had decreased by 25%. After the experiment, a black molten residue remained in the sample container (original colour: off-white). The change of the colour indicated reaction and/or decomposition of the test item.

Main Study

An endothermic peak was observed between 50°C and 125°C in Experiment 1. Based on the weight loss observed during the preliminary test between 50°C and 125°C the endothermic effect was most likely due to evaporation of volatile components. An endothermic peak was observed between 225°C and 300°C. The endothermic effect was most likely obtained due to melting or reaction and/or decomposition of the test item. After the experiment, a black/brown molten residue remained in the sample container.

To investigate the endothermic peak between 50°C and 125°C, a repeated heating cycle was applied in Experiment 2. With the first heating no changes were observed compared with Experiment 1. During cooling, exothermic peaks between 50°C and 80°C were found (results are archived in the raw data). Based on the results found in the preliminary test, the reason for these effects is unknown. With the second heating, an endothermic peak was observed between 50°C and 100°C. The reason for this effect was unknown. The reason for the exothermic effect observed between 150°C and 175°C is unknown. After the experiment, a dark brown molten residue remained in the sample container.

In order to investigate endothermic peaks between 50°C and 125°C and between 225°C and 300°C, Experiment 3 was stopped directly after the first endothermic peak and Experiment 4 was stopped before the second endothermic peak. After Experiment 3, the sample appeared to have been unchanged, i.e. no melting of the test item was observed. This endothermic peak is most likely due to evaporation of volatile components. After Experiment 4, a brownish coagulated residue remained in the sample container, indicating that the test item reacted and/or decomposed before melting.

Conclusions:
The test item has no measurable boiling temperature.
Executive summary:

The boiling temperature of the test item was investigated by DSC according to OECD Guideline 103 and EU Method A.2. Reaction and/or decomposition of the test item was observed during DSC experiments at temperatures of > 225°C (> 498K). Boiling of the test item was not observed below the temperature at which reaction and/or decomposition started. Based on this, the test item has no measurable boiling temperature.

Reason / purpose for cross-reference:
reference to same study
Reference
Endpoint:
relative density
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2017-07-10 / 2018-03-26
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Qualifier:
according to guideline
Guideline:
OECD Guideline 109 (Density of Liquids and Solids)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method A.3 (Relative Density)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EPA OPPTS 830.7300 (Density / Relative Density / Bulk Density)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Type of method:
air comparison pycnometer (for solids)
Key result
Type:
density
Density:
1.24 g/cm³
Temp.:
20 °C
Key result
Type:
relative density
Density:
1.24 other: no units
Temp.:
20 °C

The individual measurements were obtained with an accuracy of < 0.02 g/cm3. According to the guideline, the density of the test item is given as the mean value.

 

Test 1

Test 2

Mean

Density [g/cm3]

1.245

1.238

1.24

Conclusions:
The density of the test item at 20ºC was 1.24 g/cm3 (1.24 × 103 kg/m3). The relative density was 1.24.
Executive summary:

A gas comparison stereopycnometer was used for the determination of the density and relative density of the test item according to OECD Guideline 109 and EU Method A.3. The density of the test item at 20ºC was 1.24 g/cm3 (1.24 × 103 kg/m3). The relative density was 1.24.

Reason / purpose for cross-reference:
reference to same study
Reference
Endpoint:
vapour pressure
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2017-07-10 / 2018-03-26
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Qualifier:
according to guideline
Guideline:
OECD Guideline 104 (Vapour Pressure Curve)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method A.4 (Vapour Pressure)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Type of method:
effusion method: isothermal thermogravimetry
Test no.:
#1
Temp.:
20 °C
Vapour pressure:
0 hPa
Key result
Test no.:
#2
Temp.:
25 °C
Vapour pressure:
0 hPa
Transition / decomposition:
no

The results of the isothermal TGA analysis for the test item and the vapour pressure at 20°C and 25°C are given in the tables below. The vapour pressure regression curve of the log PT of the test item as function of the reciprocal temperatures was: log PT = -3340 × 1/T + 9.01 (r = 0.994, n = 8).

Results of the Vapour pressure Isothermal TGA Analysis

Temperature
[°C]

Weight loss
[µg/min]

νT
[g/cm2/h]

logνT

logPT

PT
[Pa]

100

0.871920

1.04 x 10-4

-3.98

0.04

1.1

 

0.864904

1.03 x 10-4

-3.99

0.03

1.1

110

1.44376

1.72 x 10-4

-3.76

0.32

2.1

 

1.49897

1.79 x 10-4

-3.75

0.34

2.2

120

2.08916

2.49 x 10-4

-3.60

0.52

3.3

 

2.17778

2.60 x 10-4

-3.59

0.55

3.5

130

2.85610

3.41 x 10-4

-3.47

0.70

5.0

 

2.93436

3.50 x 10-4

-3.46

0.71

5.2

Vapour Pressure of the Test Item

Temperature
[°C]

logPT

PT
[Pa]

PT
[mm Hg]

20

-2.38

4.2 x 10-3

3.1 x 10-5

25

-2.19

6.5 x 10-3

4.9 x 10-5

Conclusions:
The vapour pressure of the test item was 0.000042 hPa at 20°C (293K) and 0.000065 hPa at 25°C (298K).
Executive summary:

The isothermal TGA effusion method was applied for the determination of the vapour pressure of the test item according to OECD Guideline 104 and EU Method A.4. The vapour pressure of the test item was 0.000042 hPa at 20°C (293K) and 0.000065 hPa at 25°C (298K).

Reason / purpose for cross-reference:
reference to same study
Reference
Endpoint:
flammable solids
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2017-07-10 / 2018-03-26
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Qualifier:
according to guideline
Guideline:
EU Method A.10 (Flammability (Solids))
Deviations:
no
Qualifier:
according to guideline
Guideline:
UN Manual of Tests and Criteria: Test N.1 (Test method for readily combustible solids)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Test procedure:
burning rate test: preliminary screening test
Burning time:
< 4 min

The flame of the gas burner did ignite the test item pile. The test item burned with an orange flame and turned into a black residue. White smoke was observed. After removal of the ignition source, the flame extinguished after 50 seconds and no propagation of combustion was observed.

Interpretation of results:
not classified based on GHS criteria
Conclusions:
The test item is considered ‘not highly flammable’.
Executive summary:

The preliminary screening test was performed for the determination of the flammability of the test item according to EU Method A.10 and UN Test N.1. No propagation of combustion of the test item along 200 mm length of the pile within 4 minutes was observed. According to the guidelines, performance of the burning rate test is not required. Based on the results obtained, the test item is considered ‘not highly flammable’.

Reason / purpose for cross-reference:
reference to same study
Reference
Endpoint:
oxidising solids
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
the study does not need to be conducted because there are no chemical groups present in the molecule which are associated with oxidising properties and hence, the classification procedure does not need to be applied
Justification for type of information:
In accordance with Column 2 adaptation statement of REACH Annex VII, information requirement section 7.11, this study does not need to be conducted based on a structural assessment of the substance. None of the components of the test item does contain groups that act as an oxidizing agent.
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study

A test item is considered an oxidizing substance when the burning time of a mixture of the substance and cellulose in a 4:1 or 1:1 sample-to-cellulose ratio (by mass) is less than or equal to the mean burning time of a 3:7 reference mixture (by mass) of potassium bromate and cellulose. None of the components of the test item does contain groups that act as an oxidizing agent. The oxygen atoms that are present in the molecular structure of the test item are chemically bonded to carbon or hydrogen. The test item contains a SO3 group. The group is relatively small compared to the molecular structure of the test item. Based on this the test item is considered to pose no function as oxidizing agent. In conclusion, the test item has no oxidizing properties.

Interpretation of results:
GHS criteria not met
Conclusions:
The test item has no oxidizing properties.
Executive summary:

None of the components of the test item does contain groups that act as an oxidizing agent. The oxygen atoms that are present in the molecular structure of the test item are chemically bonded to carbon or hydrogen. The test item contains a SO3 group. The group is relatively small compared to the molecular structure of the test item. Based on this the test item is considered to pose no function as oxidizing agent. In conclusion, the test item has no oxidizing properties.

Reason / purpose for cross-reference:
reference to same study
Reference
Endpoint:
relative self-ignition temperature (solids)
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2017-07-10 / 2018-03-26
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Qualifier:
according to guideline
Guideline:
EU Method A.16 (Relative Self-Ignition Temperature for Solids)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Key result
Relative self-ignition temperature:
> 400 °C
Remarks on result:
no self ignition observed under the test conditions

No endothermic or exothermic effect of the test item was observed between 20°C and 400°C. It demonstrated that the test item is not self-ignitable. After the experiment, the test item had turned into a charred residue. It indicated that the test item had decomposed and/or reacted during the experiment.

Conclusions:
Based on the results obtained the test item is considered ‘not self-ignitable’.
Executive summary:

The self-ignition temperature of the test item was determined according to EU Method A.16. Based on the results obtained the test item is considered ‘not self-ignitable’.

Reason / purpose for cross-reference:
reference to same study
Reference
Endpoint:
surface tension
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2017-07-10 / 2018-03-26
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to same study
Qualifier:
according to guideline
Guideline:
OECD Guideline 115 (Surface Tension of Aqueous Solutions)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method A.5 (Surface Tension)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Type of method:
OECD harmonised ring method
Key result
Surface tension:
62.8 mN/m
Temp.:
20 °C
Conc.:
90 other: vol% of the test item saturation solubility in water
Remarks on result:
other: mean multiplied by Φb and Harkins-Jordan corrected value

The results of the test on the determination of the surface tension of the test solution are given in the table below.

Measurement

Time passed after transfer test solution to test vessel
[minutes]

Surface tension
(mN/m)

individual

mean

mean multiplied by
Φband Harkins-Jordan corrected value

1

15

61.8

61.6

62.8

2

16

61.5

 

 

3

17

61.6

 

 

4

18

61.6

 

 

5

19

61.7

 

 

Conclusions:
The surface tension of a test solution at 90% of the test item saturation solubility in water and at 20°C was 62.8 mN/m. According to this, the test item is considered not to be surface active.
Executive summary:

The OECD harmonized ring method was applied for the determination of the surface tension of the test item according to OECD Guideline 115 and EU Method A.5. The surface tension of a test solution at 90% of the test item saturation solubility in water and at 20°C was 62.8 mN/m. According to this, the test item is considered not to be surface active.

Data source

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

Materials and methods

Test material

1
Reference substance name:
Reaction products of stearic acid with 2-aminoethanol, maleic anhydride and sodium sulphite
EC Number:
942-252-2
IUPAC Name:
Reaction products of stearic acid with 2-aminoethanol, maleic anhydride and sodium sulphite
Test material form:
solid: particulate/powder

Results and discussion

Any other information on results incl. tables

None of the components of the test item does contain chemical groups which are associated with explosive properties. In conclusion, the test item has no explosive properties.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The test item has no explosive properties.
Executive summary:

None of the components of the test item does contain chemical groups which are associated with explosive properties. In conclusion, the test item has no explosive properties.