2-ethoxyethylamine

Phototransformation in air

Administrative data

Endpoint:

phototransformation in air

Type of information:

calculation (if not (Q)SAR)

Remarks:

Migrated phrase: estimated by calculation

Adequacy of study:

key study

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: Accepted calculation method; substance presumably within applicabilty domain of the model

Data source

Reference

Reference 1

Reference Type:

other: EPIWin calculation

Title:

Unnamed

Year:

2014

Report date:

2014

Reference 2

Reference Type:

other: Estimation software

Title:

Estimation Programs Interface Suite for Microsoft Windows, v4.11

Author:

US EPA

Year:

2012

Bibliographic source:

United States Environmental Protection Agency, Washington, DC, USA; November 2012

Materials and methods

Test guideline

Qualifier:

no guideline followed

Principles of method if other than guideline:

Calculation using AOPWIN v1.92

GLP compliance:

no

Test material

Test material information

Constituent 1

Reference substance name:

2-ethoxyethylamine

EC Number:

203-801-5

EC Name:

2-ethoxyethylamine

Cas Number:

110-76-9

Molecular formula:

C4H11NO

IUPAC Name:

2-ethoxyethylamine

Constituent 2

Reference substance name:

O(CCN)CC

IUPAC Name:

O(CCN)CC

Details on test material:

- Name of test material: Ethanamine, 2-ethoxy-

Study design

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: 6.45829 E-11 cm³/molecules·s
- Temperature for which rate constant was calculated: 25°C

Results and discussion

Dissipation half-life of parent compound

DT50:

5.962 h

Test condition:

half-life calculated for the following conditions: sensitizer for indirect photolysis: OH; 0.5 E06 OH/cm³, 24h day; substance presumably within applicability domain

Any other information on results incl. tables

Photodegradation in air: Hydroxyl radicals (25°C)

Hydrogen Abstraction	43.5829 E-12 cm3/molecule-sec
Reaction with N, S and -OH	21.0000 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	0.0000 E-12 cm3/molecule-sec
Addition to Fused Rings	0.0000 E-12 cm3/molecule-sec
Overall OH Rate Constant	64.5829 E-12 cm3/molecule-sec
Half-life	0.248 Days (24-hr day; 0.5E6 OH/cm3)
Half-life	5.962 Hrs

Estimate refers to the uncharged molecule.

Applicant's summary and conclusion

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.		Not 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.