1-ethyl-3-methyl-3H-imidazolium dicyanidoamide(1-)

Phototransformation in air

Link to relevant study record(s)

Reference

Endpoint:

phototransformation in air

Type of information:

(Q)SAR

Adequacy of study:

key study

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

results derived from a valid (Q)SAR model, but not (completely) falling into its applicability domain, with adequate and reliable documentation / justification

Remarks:

The QSAR was performed with the uncharged form of 1-Methyl-3-ethylimidazolium. This difference in charge will not alter the properties of the molecule in such way that it will significantly influence the outcome of this QSAR. This molecule does not fall in the applicability domain as it is a tertiary (heterocyclic) amine.

Justification for type of information:

- QMRF: see 'Overall remarks, attachments'.
- QPRF: see 'Executive summary'.

Qualifier:

no guideline followed

Principles of method if other than guideline:

Calculation using AOPWIN v1.92

GLP compliance:

no

Specific details on test material used for the study:

- CAS No.: 65039-03-4
- SMILES Code: c1cn(C)cn1CC

Estimation method (if used):

PHOTOCHEMICAL REACTION WITH OH RADICALS:
- Computer programme: SRC AopWin v1.92;
- Concentration of OH radicals: 5E+05 molecules/cm³ (northern hemisphere);
- Time frame: 24-hour day;
- Degradation rate constant: 37.2373 E-12 cm³/molecule·s;
- Temperature for which rate constant was calculated: 25 °C.

Key result

DT50:

10.341 h

Test condition:

half-life calculated for the following conditions: sensitizer for indirect photolysis: OH; 0.5E+06 OH/cm³, 24h day; substance presumably within applicability domain

SUMMARY (AOP v1.92):	HYDROXYL RADICALS (25 °C)
Hydrogen Abstraction	1.2373 E-12 cm3/molecule-sec
Reaction with N, S and -OH	0.0000 E-12 cm3/molecule-sec
Addition to Triple Bonds	0.0000 E-12 cm3/molecule-sec
Addition to Olefinic Bonds	0.0000 E-12 cm3/molecule-sec
Addition to Aromatic Rings	36.0000 E-12 cm3/molecule-sec
Addition to Fused Rings	0.0000 E-12 cm3/molecule-sec
OVERALL OH Rate Constant	37.2373 E-12 cm3/molecule-sec
Half-life	0.431 Days (24-hr day; 0.5E6 OH/cm3)
Half-life	10.341 Hrs

Executive summary:

QPRF:AOPWIN

1.	Substance	See “Test material identity”
2.	General information
2.1	Date of QPRF	See “Data Source (Reference)”
2.2	QPRF author and contact details	See “Data Source (Reference)”
3.	Prediction
3.1	Endpoint (OECD Principle 1)	Endpoint	Phototransformation in air
		Dependent variable	Hydroxyl reaction rate constant (cm^3/molecule*sec)
3.2		Model or submodel name	AOPWIN
		Model version	1.92
		Reference to QMRF	QMRF: Estimation of Atmospheric Degradation Using AOPWIN v1.92 (EPI Suite v4.11): Hydroxyl Radical Reaction
		Predicted value (model result)	See “Results and discussion”
		Input for prediction	- Chemical structure via CAS number or SMILES
		Descriptor values	- Structure fragments
3.3	Algorithm (OECD Principle 2)	Domain (On-Line AOPWIN User’s Guide): As the complete training sets for AOPWIN's estimation methodology are not available, describing a precise estimation domain for this methodology is not possible. There is no information on the number of instances of fragments in the training dataset.
		If the substance is a member of one of the following chemical classes, the substance is probably within the applicability domain of the model (based on information by other authors, e.g. Posthumus and Slooff, 2001): alkanes, haloalkanes, alkenes, haloalkenes, polyenes, terpenes, alkynes, aldehydes, ketones, alcohols, glycols, ethers, esters, epoxides, thiols, thioethers, aliphatic amines, hydrazines, nitrites, nitrates, nitriles, P-containing organics, aromatic compounds (alkylbenzenes, halobenzenes, phenols, PAHs, styrene, methoxybenzene, aniline, nitrobenzene, biphenyl, dibenzofurans, dibenzodioxins)		Fulfilled
		The substance is not within the applicability domain of the model if it is a perhalogenated alkane.		Not Fulfilled
		Substance is a secondary, tertiary and heterocyclic amine. Estimated values highly uncertain.		Fulfilled
3.4	The uncertainty of the prediction (OECD principle 4)	- n = 667 - correlation coefficient r^2= 0.963 - standard deviation = 0.218 - absolute mean error = 0.127 - 90% of the estimated rate constants within a factor of two of the experimental data - 95% of the estimated rate constants within a factor of three of the experimental data
3.5	The chemical mechanisms according to the model underpinning the predicted result (OECD principle 5)	Reaction rate constants for hydroxyl radicals are the summation of the following mechanisms: (1) Hydrogen abstraction (2) Reaction with specific nitrogen and sulphur fragments and reaction with hydroxyl (OH) fragments such as alcohols and phenols (3) Addition to triple bonds (4) Addition to olefinic bonds (5) Addition to aromatic rings (6) Addition to fused rings The model works according to the group contribution method which uses fragments and the corresponding reaction values to estimate the reaction rate constant of a given substance.

References

- R Posthumus and W Slooff (2001). Implementation of QSARs in ecotoxicological risk assessments. RIVM report 601516 003. Online: http://rivm.openrepository.com/rivm/bitstream/10029/9559/1/601516003.pdf

- US EPA (2012). On-Line AOPWIN User’s Guide.

Description of key information

For 3-ethyl-1-methyl-1H-Imidazolium salt with N-cyanocyanamide, phototransformation in air was calculated for its organic moiety 1-Methyl-3-ethylimidazolium (CAS 65039-03-4). After evaporation or exposure to the air, the product will be rapidly degraded by photochemical processes. The substance 1-Methyl-3-ethylimidazolium (CAS 65039-03-4) has an estimated half-life in air of ~10.341 hours. As the cut-off time for reaching the stratosphere is 2 days, the substance is considered to have no potential for reaching the stratosphere and/or long-range atmospheric transport.

 

INORGANIC MOIETY

With regard to the inorganic moiety Dicyanamide (CAS 504-66-5) no information on degradation in air is available. Therefore, the assessment is based solely on the data available for 1-Methyl-3-ethylimidazolium (CAS 65039-03-4).

Additional information

QSAR-disclaimer:

In Article 13 of Regulation (EC) No 1907/2006, it is laid down that information on intrinsic properties of substances may be generated by means other than tests, provided that the conditions set out in Annex XI (of the same Regulation) are met. According to Annex XI of Regulation (EC) No 1907/2006 (Q)SAR results can be used if (1) the scientific validity of the (Q)SAR model has been established, (2) the substance falls within the applicability domain of the (Q)SAR model, (3) the results are adequate for the purpose of classification and labeling and/or risk assessment and (4) adequate and reliable documentation of the applied method is provided. For the assessment of 1-Methyl-3-ethylimidazolium, (Q)SAR results were used for phototransformation in air (hydroxyl radical reaction).The criteria listed in Annex XI of Regulation (EC) No 1907/2006 are considered to be adequately fulfilled and therefore the endpoint(s) sufficiently covered and suitable for risk assessment.