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. 2018 Aug 14;30(1):30. doi: 10.1186/s12302-018-0155-z

Table 1.

Physico-chemical properties of the investigated substances

Compound CAS# Molecular weight (g mol−1) WSsub (mol L−1) log KOW pKa Acid–base reaction
Atrazine 1912-24-9 215.69 5.43 × 10−3 2.61 1.60 Base
Benzotriazole 95-14-7 119.13 1.05 1.44 8.37 Base
Caffeine 58-08-2 194.19 1.65 × 101 0.07 Neutral
Carbamazepine 298-46-4 236.28 3.10 × 10−3 2.45 13.9 Acid
Carbendazim 10605-21-7 191.19 9.27 × 10−2 1.52 4.29 Base
DEET 134-62-3 191.28 Liquid 2.18 Neutral
Diazinon 333-41-5 304.35 1.31 × 10−3 3.81 2.60 Base
Diclofenac 15,307-86-5 296.15 1.87 × 10−4 4.51 3.99 Acid
Ibuprofen 15687-27-1 206.29 3.69 × 10−4 3.97 4.45 Acid
MCPA 94-74-6 200.62 3.13 × 10−2 3.25 3.13 Acid
Mecoprop 7085-19-0 214.65 1.62 × 10−2 3.20 3.78 Acid
4-Nonylphenol 104-40-5 220.36 4.78 × 10−5 5.76 10.7 Acid
Phenanthrene 85-01-8 178.24 3.95 × 10−5 4.46 Neutral
Propiconazole 60207-90-1 342.22 Liquid 3.72 1.09 Base
Tris(2-chloroisopropyl)-phosphate (TCPP) 13674-84-5 327.57 Liquid 2.59 Neutral
Tebuconazole 107534-96-3 307.83 7.78 × 10−4 3.70 1.76 Base
Terbutryn 886-50-0 241.36 7.15 × 10−4 3.74 4.30 Base
Torasemide 56211-40-6 348.42 2.10 × 10−2 3.37 6.68 Acid
Triclosan 3380-34-5 289.55 7.55 × 10−5 4.76 7.90 Acid

Properties are either taken from EPISuite (molecular weight and log KOW of neutral species) or the PubChem database (pKa). Subcooled liquid solubilities (WS) were estimated based on melting points according to Kan and Tomson [18] and Liu et al. [24]