When referring to the compilation of Henry's Law Constants, please cite
this publication:
R. Sander: Compilation of Henry's law constants (version 5.0.0) for
water as solvent, Atmos. Chem. Phys., 23, 10901-12440 (2023),
doi:10.5194/acp-23-10901-2023
The publication from 2023 replaces that from 2015,
which is now obsolete. Please do not cite the old paper anymore.
|
FORMULA: | C6H4(NO2)CH3 |
CAS RN: | 99-99-0 |
STRUCTURE
(FROM
NIST):
|
|
InChIKey: | ZPTVNYMJQHSSEA-UHFFFAOYSA-N |
|
|
References |
Type |
Notes |
[mol/(m3Pa)] |
[K] |
|
|
|
8.9×10−1 |
7100 |
Brockbank (2013) |
L |
|
1.8 |
|
Altschuh et al. (1999) |
M |
|
2.8 |
|
Mackay et al. (2006d) |
V |
|
2.0×10−1 |
|
Lide and Frederikse (1995) |
V |
|
2.8 |
|
Mackay et al. (1995) |
V |
|
1.6×10−1 |
3100 |
Goldstein (1982) |
X |
299)
|
1.5 |
|
Keshavarz et al. (2022) |
Q |
|
1.2 |
|
Duchowicz et al. (2020) |
Q |
185)
|
1.4×10−1 |
|
Li et al. (2014) |
Q |
242)
|
4.2×10−1 |
|
Zhang et al. (2010) |
Q |
288)
289)
|
2.8×10−1 |
|
Zhang et al. (2010) |
Q |
288)
290)
|
9.0×10−1 |
|
Zhang et al. (2010) |
Q |
288)
291)
|
1.8×10−1 |
|
Zhang et al. (2010) |
Q |
288)
292)
|
2.0×10−1 |
|
Hilal et al. (2008) |
Q |
|
2.4×10−1 |
|
Modarresi et al. (2007) |
Q |
68)
|
|
4900 |
Kühne et al. (2005) |
Q |
|
1.8 |
|
Duchowicz et al. (2020) |
? |
21)
186)
|
|
3800 |
Kühne et al. (2005) |
? |
|
Data
The first column contains Henry's law solubility constant
at the reference temperature of 298.15 K.
The second column contains the temperature dependence
, also at the
reference temperature.
References
-
Altschuh, J., Brüggemann, R., Santl, H., Eichinger, G., & Piringer, O. G.: Henry’s law constants for a diverse set of organic chemicals: Experimental determination and comparison of estimation methods, Chemosphere, 39, 1871–1887, doi:10.1016/S0045-6535(99)00082-X (1999).
-
Brockbank, S. A.: Aqueous Henry’s law constants, infinite dilution activity coefficients, and water solubility: critically evaluated database, experimental analysis, and prediction methods, Ph.D. thesis, Brigham Young University, USA, URL https://scholarsarchive.byu.edu/etd/3691/ (2013).
-
Duchowicz, P. R., Aranda, J. F., Bacelo, D. E., & Fioressi, S. E.: QSPR study of the Henry’s law constant for heterogeneous compounds, Chem. Eng. Res. Des., 154, 115–121, doi:10.1016/J.CHERD.2019.12.009 (2020).
-
Goldstein, D. J.: Air and steam stripping of toxic pollutants, Appendix 3: Henry’s law constants, Tech. Rep. EPA-68-03-002, Industrial Environmental Research Laboratory, Cincinnati, OH, USA (1982).
-
Hilal, S. H., Ayyampalayam, S. N., & Carreira, L. A.: Air-liquid partition coefficient for a diverse set of organic compounds: Henry’s law constant in water and hexadecane, Environ. Sci. Technol., 42, 9231–9236, doi:10.1021/ES8005783 (2008).
-
Keshavarz, M. H., Rezaei, M., & Hosseini, S. H.: A simple approach for prediction of Henry’s law constant of pesticides, solvents, aromatic hydrocarbons, and persistent pollutants without using complex computer codes and descriptors, Process Saf. Environ. Prot., 162, 867–877, doi:10.1016/J.PSEP.2022.04.045 (2022).
-
Kühne, R., Ebert, R.-U., & Schüürmann, G.: Prediction of the temperature dependency of Henry’s law constant from chemical structure, Environ. Sci. Technol., 39, 6705–6711, doi:10.1021/ES050527H (2005).
-
Lide, D. R. & Frederikse, H. P. R.: CRC Handbook of Chemistry and Physics, 76th Edition, CRC Press, Inc., Boca Raton, FL, ISBN 0849304768 (1995).
-
Li, H., Wang, X., Yi, T., Xu, Z., & Liu, X.: Prediction of Henry’s law constants for organic compounds using multilayer feedforward neural networks based on linear salvation energy relationship, J. Chem. Pharm. Res., 6, 1557–1564 (2014).
-
Mackay, D., Shiu, W. Y., & Ma, K. C.: Illustrated Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals, vol. IV of Oxygen, Nitrogen, and Sulfur Containing Compounds, Lewis Publishers, Boca Raton, ISBN 1566700353 (1995).
-
Mackay, D., Shiu, W. Y., Ma, K. C., & Lee, S. C.: Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals, vol. IV of Nitrogen and Sulfur Containing Compounds and Pesticides, CRC/Taylor & Francis Group, doi:10.1201/9781420044393 (2006d).
-
Modarresi, H., Modarress, H., & Dearden, J. C.: QSPR model of Henry’s law constant for a diverse set of organic chemicals based on genetic algorithm-radial basis function network approach, Chemosphere, 66, 2067–2076, doi:10.1016/J.CHEMOSPHERE.2006.09.049 (2007).
-
Zhang, X., Brown, T. N., Wania, F., Heimstad, E. S., & Goss, K.-U.: Assessment of chemical screening outcomes based on different partitioning property estimation methods, Environ. Int., 36, 514–520, doi:10.1016/J.ENVINT.2010.03.010 (2010).
Type
Table entries are sorted according to reliability of the data, listing
the most reliable type first: L) literature review, M) measured, V)
VP/AS = vapor pressure/aqueous solubility, R) recalculation, T)
thermodynamical calculation, X) original paper not available, C)
citation, Q) QSPR, E) estimate, ?) unknown, W) wrong. See Section 3.1
of Sander (2023) for further details.
Notes
21) |
Several references are given in the list of Henry's law constants but not assigned to specific species. |
68) |
Modarresi et al. (2007) use different descriptors for their calculations. They conclude that a genetic algorithm/radial basis function network (GA/RBFN) is the best QSPR model. Only these results are shown here. |
185) |
Value from the validation set for checking whether the model is satisfactory for compounds that are absent from the training set. |
186) |
Experimental value, extracted from HENRYWIN. |
242) |
Temperature is not specified. |
288) |
Data taken from the supplement. |
289) |
Calculated using the EPI Suite (v4.0) method. |
290) |
Calculated using the SPARC (v4.2) method. |
291) |
Calculated using the COSMOtherm (v2.1) method. |
292) |
Calculated using the ABSOLV (ADMEBoxes v4.1) method. |
299) |
Value given here as quoted by Staudinger and Roberts (1996). |
The numbers of the notes are the same as
in Sander (2023). References cited in the notes can be
found here.
|
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