![Table 3 from Determination of octanol‐water partitioning coefficients (KOW) of 61 organophosphorus and carbamate insecticides and their relationship to respective water solubility (S) values | Semantic Scholar Table 3 from Determination of octanol‐water partitioning coefficients (KOW) of 61 organophosphorus and carbamate insecticides and their relationship to respective water solubility (S) values | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/9781be1046b33d17f3208b34d284ab5f04b2878a/12-Table3-1.png)
Table 3 from Determination of octanol‐water partitioning coefficients (KOW) of 61 organophosphorus and carbamate insecticides and their relationship to respective water solubility (S) values | Semantic Scholar
Modeling and prediction of octanol/water partition coefficient of pesticides using QSPR methods | Emerald Insight
![Modeling the octanol–water partition coefficient of substituted phenols by the use of structure information - Jäntschi - 2007 - International Journal of Quantum Chemistry - Wiley Online Library Modeling the octanol–water partition coefficient of substituted phenols by the use of structure information - Jäntschi - 2007 - International Journal of Quantum Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/b43a50ba-8042-472d-92a5-9736850d296f/ntbl001.jpg)
Modeling the octanol–water partition coefficient of substituted phenols by the use of structure information - Jäntschi - 2007 - International Journal of Quantum Chemistry - Wiley Online Library
![Calculation of Molecular Lipophilicity and Drug Likeness for Few Heterocycles : Oriental Journal of Chemistry Calculation of Molecular Lipophilicity and Drug Likeness for Few Heterocycles : Oriental Journal of Chemistry](http://www.orientjchem.org/wp-content/uploads/2010/03/Vol26_No1_cal_lal_table_2.jpg)
Calculation of Molecular Lipophilicity and Drug Likeness for Few Heterocycles : Oriental Journal of Chemistry
![Exploring the octanol–water partition coefficient dataset using deep learning techniques and data augmentation | Communications Chemistry Exploring the octanol–water partition coefficient dataset using deep learning techniques and data augmentation | Communications Chemistry](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs42004-021-00528-9/MediaObjects/42004_2021_528_Fig1_HTML.png)
Exploring the octanol–water partition coefficient dataset using deep learning techniques and data augmentation | Communications Chemistry
![SOLVED: Using the table below to answer the following questions: Molecular Weight (g/mol) Water Solubility Log Kow (Likg) (ug/L) Nonylphenol (NP) 220 5.43 4.48 Nonylphenol monoethoxylate 264 3.02 4.017 Octylphenol (OP) 178 SOLVED: Using the table below to answer the following questions: Molecular Weight (g/mol) Water Solubility Log Kow (Likg) (ug/L) Nonylphenol (NP) 220 5.43 4.48 Nonylphenol monoethoxylate 264 3.02 4.017 Octylphenol (OP) 178](https://cdn.numerade.com/ask_images/18979b0f3a744a9cadb6e1ff74bfda9b.jpg)
SOLVED: Using the table below to answer the following questions: Molecular Weight (g/mol) Water Solubility Log Kow (Likg) (ug/L) Nonylphenol (NP) 220 5.43 4.48 Nonylphenol monoethoxylate 264 3.02 4.017 Octylphenol (OP) 178
![Evaluation of QSAR models for predicting the partition coefficient (log P) of chemicals under the REACH regulation - ScienceDirect Evaluation of QSAR models for predicting the partition coefficient (log P) of chemicals under the REACH regulation - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0013935115300931-gr1.jpg)
Evaluation of QSAR models for predicting the partition coefficient (log P) of chemicals under the REACH regulation - ScienceDirect
![Table 2 from Determination of octanol‐water partitioning coefficients (KOW) of 61 organophosphorus and carbamate insecticides and their relationship to respective water solubility (S) values | Semantic Scholar Table 2 from Determination of octanol‐water partitioning coefficients (KOW) of 61 organophosphorus and carbamate insecticides and their relationship to respective water solubility (S) values | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/9781be1046b33d17f3208b34d284ab5f04b2878a/11-Table2-1.png)
Table 2 from Determination of octanol‐water partitioning coefficients (KOW) of 61 organophosphorus and carbamate insecticides and their relationship to respective water solubility (S) values | Semantic Scholar
![Table 1 from Acute toxicity and n-octanol/water partition coefficients of substituted thiophenols: determination and QSAR analysis. | Semantic Scholar Table 1 from Acute toxicity and n-octanol/water partition coefficients of substituted thiophenols: determination and QSAR analysis. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/7cfa97631a35f1c597e343104c31ed46f85e8abf/2-Table1-1.png)
Table 1 from Acute toxicity and n-octanol/water partition coefficients of substituted thiophenols: determination and QSAR analysis. | Semantic Scholar
![A comparison of log Kow (n-octanol–water partition coefficient) values for non-ionic, anionic, cationic and amphoteric surfactants determined using predictions and experimental methods | Environmental Sciences Europe | Full Text A comparison of log Kow (n-octanol–water partition coefficient) values for non-ionic, anionic, cationic and amphoteric surfactants determined using predictions and experimental methods | Environmental Sciences Europe | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs12302-018-0176-7/MediaObjects/12302_2018_176_Fig1_HTML.png)
A comparison of log Kow (n-octanol–water partition coefficient) values for non-ionic, anionic, cationic and amphoteric surfactants determined using predictions and experimental methods | Environmental Sciences Europe | Full Text
![Calculation of Molecular Lipophilicity and Drug Likeness for Few Heterocycles : Oriental Journal of Chemistry Calculation of Molecular Lipophilicity and Drug Likeness for Few Heterocycles : Oriental Journal of Chemistry](http://www.orientjchem.org/wp-content/uploads/2010/03/Vol26_No1_cal_lal_table_1.jpg)
Calculation of Molecular Lipophilicity and Drug Likeness for Few Heterocycles : Oriental Journal of Chemistry
![Table 1 from Determination of octanol‐water partitioning coefficients (KOW) of 61 organophosphorus and carbamate insecticides and their relationship to respective water solubility (S) values | Semantic Scholar Table 1 from Determination of octanol‐water partitioning coefficients (KOW) of 61 organophosphorus and carbamate insecticides and their relationship to respective water solubility (S) values | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/9781be1046b33d17f3208b34d284ab5f04b2878a/8-Table1-1.png)
Table 1 from Determination of octanol‐water partitioning coefficients (KOW) of 61 organophosphorus and carbamate insecticides and their relationship to respective water solubility (S) values | Semantic Scholar
![Table 5 from The search for reliable aqueous solubility (Sw) and octanol-water partition coefficient (Kow) data for hydrophobic organic compounds; DDT and DDE as a case study | Semantic Scholar Table 5 from The search for reliable aqueous solubility (Sw) and octanol-water partition coefficient (Kow) data for hydrophobic organic compounds; DDT and DDE as a case study | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/17348d3ea0f1786979715b95ce294a19c2671a1d/19-Table5-1.png)
Table 5 from The search for reliable aqueous solubility (Sw) and octanol-water partition coefficient (Kow) data for hydrophobic organic compounds; DDT and DDE as a case study | Semantic Scholar
![Measuring log Kow coefficients of neutral species of perfluoroalkyl carboxylic acids using reversed-phase high-performance liquid chromatography - ScienceDirect Measuring log Kow coefficients of neutral species of perfluoroalkyl carboxylic acids using reversed-phase high-performance liquid chromatography - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0269749118310583-fx1.jpg)