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Henry's Law Constants

www.henrys-law.org

Rolf Sander

Atmospheric Chemistry Division

Max-Planck Institute for Chemistry
Mainz, Germany


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Henry's Law Constants

Notes

References

Errata

Contact, Impressum, Acknowledgements


When referring to the compilation of Henry's Law Constants, please cite this publication:

R. Sander: Compilation of Henry's law constants (version 4.0) for water as solvent, Atmos. Chem. Phys., 15, 4399-4981 (2015), doi:10.5194/acp-15-4399-2015


Henry's Law ConstantsOrganic species with oxygen (O)Alcohols (ROH) → 3,7-dimethyl-1,6-octadien-3-ol

FORMULA:C10H18O
TRIVIAL NAME: linalool
CAS RN:78-70-6
STRUCTURE
(FROM NIST):
InChIKey:CDOSHBSSFJOMGT-UHFFFAOYSA-N

Hcp d ln Hcp / d (1/T) Reference Type Notes
[mol/(m3Pa)] [K]
2.0×10−1 4400 Leng et al. 2013 M
4.6×10−1 Altschuh et al. 1999 M
4.8×10−1 Copolovici and Niinemets 2005 V
4.8×10−1 Niinemets and Reichstein 2002 V
2.1×10−1 14000 Li et al. 1998 V
2.5×10−1 Savary et al. 2014 Q
6.9×10−1 Hilal et al. 2008 Q
1.5×10−2 Hertel and Sommer 2006 Q 166)

References

  • Altschuh, J., Brüggemann, R., Santl, H., Eichinger, G., and 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.
  • Copolovici, L. O. and Niinemets, U.: Temperature dependencies of Henry's law constants and octanol/water partition coefficients for key plant volatile monoterpenoids, Chemosphere, 61, 1390-1400, doi:10.1016/J.CHEMOSPHERE.2005.05.003, 2005.
  • Hertel, M. O. and Sommer, K.: Limiting separation factors and limiting activity coefficients for 2-furfural, γ-nonalactone, benzaldehyde, and linalool in water at 100 ° C, J. Chem. Eng. Data, 51, 1283-1285, doi:10.1021/JE0600404, 2006.
  • Hilal, S. H., Ayyampalayam, S. N., and 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.
  • Leng, C., Kish, J. D., Kelley, J., Mach, M., Hiltner, J., Zhang, Y., and Liu, Y.: Temperature-dependent Henry's law constants of atmospheric organics of biogenic origin, J. Phys. Chem. A, 117, 10 359-10 367, doi:10.1021/JP403603Z, 2013.
  • Li, J., Perdue, E. M., Pavlostathis, S. G., and Araujo, R.: Physicochemical properties of selected monoterpenes, Environ. Int., 24, 353-358, doi:10.1016/S0160-4120(98)00013-0, 1998.
  • Niinemets, U. and Reichstein, M.: A model analysis of the effects of nonspecific monoterpenoid storage in leaf tissues on emission kinetics and composition in Mediterranean sclerophyllous Quercus species, Global Biogeochem. Cycles, 16, 1110, doi:10.1029/2002GB001927, 2002.
  • Savary, G., Hucher, N., Petibon, O., and Grisel, M.: Study of interactions between aroma compounds and acacia gum using headspace measurements, Food Hydrocolloids, 37, 1-6, doi:10.1016/J.FOODHYD.2013.10.026, 2014.

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 (2015) for further details.

Notes

166) Value at T = 373 K.

The numbers of the notes are the same as in Sander (2015). References cited in the notes can be found here.

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