nitrate amine salt of N-[3-dimethylaminopropyl]- C14-C20 amides, saturated, reaction products with ethylene oxide

Particle size distribution (Granulometry)

Administrative data

Endpoint:

particle size distribution (granulometry)

Data waiving:

study scientifically not necessary / other information available

Justification for data waiving:

the study does not need to be conducted because the substance is marketed or used in a non solid or granular form

Cross-reference

Cross-reference 1

Reason / purpose for cross-reference:

reference to same study

Reference

Endpoint:

appearance / physical state / colour

Type of information:

experimental study

Adequacy of study:

key study

Study period:

From 2015-07-24 to 2016-06-24

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:

no guideline available

GLP compliance:

not specified

Other quality assurance:

other: ISO 14001

Physical state at 20°C and 1013 hPa:

solid

Form:

other: waxy solid

Colour:

White

Substance type:

organic

Conclusions:

Cyastat SN is an organic solid substance, appearing under the form of white waxy solid at ambient temperature and pressure.

Executive summary:

The substance, Cyastat SN, was tested for several physico-chemical properties. In this context, the appearance of the sample was described, indicating that Cyastat SN is a white waxy solid substance

Cross-reference 2

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:

From 2015-07-24 to January 2017

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

GLP compliance:

not specified

Other quality assurance:

other: ISO 14001

Type of method:

differential scanning calorimetry

Melting / freezing pt.:

39 °C

Decomposition:

no

Melting pojnt / melting range of the test substance determined on 1st heat cycle.

Specimen No.	Onset (Melting Point) (°C)	Peak (°C)	Endset (°C)	Melting Range (°C)	Enthalpy (joules/g)
1	39.00	47.68	53.1	39 - 53	59.870
2	38.89	46.63	52.8	39 - 53	57.709

Specimen weights and appearance during DSC experiments.

Specimen No.	Initial specimen wt (mg)	Appearance
1	4.6870	Both specimens were a sticky white waxy solid before and after experiment with no discoloration observed.
2	7.6100

Conclusions:

The melting temperature of Cyastat SN was 39°C.

Executive summary:

Melting point of Cyastat SN has been determined according to OECD test guideline 102. Using Differential Scanning Calorimetry (DSC), the melting temperature of the test substance was determined to be equal to 39°C

Cross-reference 3

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:

From 2015-07-24 to Januaery 2017

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

GLP compliance:

not specified

Other quality assurance:

other: ISO 14001

Type of method:

differential scanning calorimetry

Decomposition:

yes

Decomp. temp.:

> 196 - < 220 °C

The test substance does not boil, instead it decomposes. Decomposition was confirmed by performing multiple DSC scans at different heating rates. The onset at 2.5°C/min is 195°C. Consequently, increasing the scan speed to 20°C/min delays the onset of decomposition to 220°C. Decomposition is a 2nd order reaction and is dependent upon the heating rate. Boiling point is a 1st order reaction independent of heating rate. Thus the different onset temperatures observed confirms that the thermal event is decomposition. The table below provides the onsets of decomposition at three different scan rates.

Onset of Decomposition for Test Substance.

Specimen No.	Onset (°C)	Heating Rate (°C/minute)
1	196	2.5
2	196	2.5
3	211	10
4	211	10
5	221	20
6	218	20

Specimen weights and appearance during DSC experiments.

Specimen N°	Initial specimen wt (mg)	Post run appearance
1	4.822	All of the specimens experienced a color change of white to brown. There was condensation of all specimens on top of the DSC pan lid through the pinhole confirming decomposition.
2	4.719
3	5.001
4	4.914
5	4.558
6	5.067

Conclusions:

The Cyastat SN decompose before boiling

Executive summary:

Boiling Point has been determined according to OECD guideline 103. Using Differential scanning calorimetry (DSC), it was showed that the Cyastat SN decompose before boiling.

Cross-reference 4

Reason / purpose for cross-reference:

reference to same study

Reference

Endpoint:

density, other

Type of information:

experimental study

Adequacy of study:

key study

Study period:

From 2017-07-24 to january 2017

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

GLP compliance:

not specified

Other quality assurance:

other: ISO14001

Type of method:

pycnometer method

Type:

density

Density:

1.08 g/cm³

Temp.:

23.4 °C

Summary of Density Results, specimen weights, and room temperature during analysis.

Test Substance Specimen No.	Average true volume (n=10) (mL)	Average Density (n=10) (g/mL)	S.D.	Initial specimen weight (g)	Final sample weight (g)	Temperature (°C)
1	5.9307	1.0812	0.0003	6.4123	6.4123	23.4
2	5.8536	1.0810	0.0003	6.3277	6.3276	23.4

Conclusions:

The density of Cyastat SN was 1.09 g/cm3 at 23.4°C

Executive summary:

Density of Cyastat SN has been determined according to OECD test guideline 103. Using a pycnometer method, the density of the test substance was determined to be 1.08 g/cm3 at 23.4 °C.

Cross-reference 5

Reason / purpose for cross-reference:

reference to same study

Reference

Endpoint:

partition coefficient

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

test procedure in accordance with generally accepted scientific standards and described in sufficient detail

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:

no guideline followed

Version / remarks:

See principles of method if other than guideline

Principles of method if other than guideline:

The octanol water partitioning coefficient was estimated using the solubility of the test substance in the pure phases (n-octanol and water). This is because the test substance is a salt and surface active which means neither the shake-flask method (OECD 107) nor the HPLC method (OECD 117) are suitable to determine the log POW of the test substance

GLP compliance:

not specified

Other quality assurance:

other: ISO14001

Type of method:

HPLC method

Partition coefficient type:

octanol-water

Analytical method:

liquid chromatography

Type:

log Pow

Partition coefficient:

> 0.32 - < 1.75

Temp.:

20 °C

pH:

6.8

Details on results:

The test substance is more soluble in octanol than in water and there was no undissolved test substance in concentrations prepared for concentrations less than 40.5 weight %. Concentrations at 10, 20, 30, and 40 weight % were clear solutions. Therefore, only three supernatants were collected on concentrations higher than 40 weight %. The three initial concentrations whereby undissolved test substance was observed were prepared at 45, 50, and 55 weight %. The supernatants were collected after 24, 48, and 72 hours equilibrium and diluted with THF. The LC/CAD results showed 40.5, 40.7, and 40.3 weight % respectively.

Conclusions:

The log Kow was determined to be in the range of 0.32 -1.75 depending on the concentration of the substance.

Executive summary:

Log Kow o the Cyastat SN was determined based on solubility of the test substance in water and in octanol. The solubility in Octanol and water were determinated by LC/CAD method.

Cross-reference 6

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:

From 2015-07-24 to 2016-06-24

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:

yes

Remarks:

a pan was used instead of a plate

GLP compliance:

not specified

Other quality assurance:

other: ISO 14001

Type of method:

effusion method: isothermal thermogravimetry

Test no.:

#1

Temp.:

50 °C

Vapour pressure:

0.163 Pa

Test no.:

#2

Temp.:

60 °C

Vapour pressure:

0.186 Pa

Test no.:

#3

Temp.:

70 °C

Vapour pressure:

0.21 Pa

Test no.:

#4

Temp.:

80 °C

Vapour pressure:

0.21 Pa

The evaporation rate of the test substance was determined at 5 temperatures between 60 and 175°C. The equation in the plot above was used to calculate the vapor pressure. See results in Table 8.2. The calculated vapor pressure based on evaporation rates was plotted against temperature in order to derive the vapor pressure equation. The calculated vapor pressures were done in mm Hg because all calibration tables were done in this unit. After, the calculated vapor pressures for the test substance were converted to Pascal as per OECD Guideline.

Table 8.2. Experimental evaporation rates of test substance with calculated vapor pressure.

Temp. (°C)	Evaporation Rate (µg/min)	log Evaporation Rate (µg/min)	Temp. (1/K)	Log Vapor Pressure (mmHg)	Calculated Vapor Pressure (mm Hg)	Calculated Vapor Pressure (Pascal)
60	0.0684	-1.164943898	0.003002	-2.855596556	0.001394	0.1859
80	0.0875	-1.057991947	0.002832	-2.745346474	0.001797	0.2396
50	0.0601	-1.221125528	0.003095	-2.913510686	0.001220	0.1627
70	0.0770	-1.113509275	0.002914	-2.802575817	0.001576	0.2101

 

Conclusions:

The vapour pressure of Cyastat SN was determined to be equal to 0.16 Pa at 50°C.

Executive summary:

Density of Cyastat SN has been determined according to OECD test guideline 104. Using TGA method, the vapour pressure of the test substance was determined to be 0.16 Pa at 50 °C.

Cross-reference 7

Reason / purpose for cross-reference:

reference to same study

Reference

Endpoint:

water solubility

Type of information:

experimental study

Adequacy of study:

key study

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 105 (Water Solubility)

GLP compliance:

not specified

Other quality assurance:

other: ISO 14001

Type of method:

flask method

Water solubility:

< 0.5 other: w/%

Conc. based on:

test mat.

Incubation duration:

24 h

Temp.:

20 °C

pH:

6.8

Water solubility results done by LC/CAD contingent on initial concentrations at 20 °C

*Initial concentration (Weight %)	Solubility (Weight %)
	24 hours	48 hours	72 hours	Mean	Maximum Difference **(M.D)
1.0	0.73	0.70	0.72	0.717	4.19
4.0	2.57	2.54	2.61	2.57	2.72
16.0	10.54	10.44	10.76	10.6	3.02
22.2	13.78	13.56	13.68	13.7	1.61
39.0	19.69	19.91	18.80	19.5	5.70

*This is the initial concentration of the test substance in water. At all of these concentrations there was undissolved test substance. The pH of all collected supernatants was 6.8. 

**We calculate the M.D. as follows:

                               M.D. = ((highest value - lowest value) / mean value) x 100

where: mean value is the mean of the highest and lowest value

According to OECD 105, the maximum difference should be <15% “If the concentrations measured in at least the two last vessels do not differ by more than 15%, the test is satisfactory.” However, this statement is valid for very pure test substances consisting of single components. This test substance consists of multiple components varying in water solubility. The results are not increasing with additional equilibrium time, thus analysis is satisfactory.

Conclusions:

The water solubility of Caystat SN was estimated to be less than 0.5%/w

Executive summary:

Water solubility of Caystat SN has been determined according to OECD test guideline 105. Using LC/CAD, the water solubility of the test substance was determined to be less than 0.5%/w at 20 °C.

Cross-reference 8

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:

From 2015-07-24 to January 2017

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)

GLP compliance:

not specified

Other quality assurance:

other: ISO 14001

Type of method:

ring method

Specific details on test material used for the study:

A 1 g/L test solution was prepared of the test substance in distilled water. Two aliquots were poured into test vessels immediately after preparation.
A 1 g/L test solution was used after determining that solubility of the test substance in water exceeds 0.3 wt%. The test solution is water clear and less than 200 mPa s (200 centipoise).

Surface tension:

42.7 mN/m

Temp.:

20 °C

Conc.:

1 g/L

Surface Tensions of 1 g/L Test Substance in Water at 20°C.

Surface Tension of test solution #1 (mN/m)	Surface Tension of test solution #2 (mN/m)	Equilibrium Time after pouring into test vessel
42.7	42.7	20 seconds
42.6	42.8	90 seconds
42.7	42.7	180 seconds
42.8	42.7	300 seconds

The surface tension of the above test solution does not have any dependence on time.

Conclusions:

The surface tension of Cyastat SN was 42.7 mN/m at 20°C

Executive summary:

Surface tension of Cyastat SN has been determined according to OECD test guideline 115. Using a Kruss digital Tensiometer K-10 and Dunouy ring method, the surface tension of the test substance was determined to be equal to 42.7 mN/m at 20°C