Table 1 Nonionic surfactants in PhDat detailing database key, surfactant structure, experimental method (assigned an index to save space - see Table 3), reference and figure number.
From: A dataset for aqueous surfactant phase behavior as a function of temperature and composition
No. | Structure | Ex. | Rf. | Fg. | No. | Structure | Ex. | Rf. | Fg. |
|---|---|---|---|---|---|---|---|---|---|
amine | 119 | \({{\rm{C}}}_{12}{\rm{G}}{({{\rm{E}}}_{4}{\rm{Me}})}_{2}\) | A | 2 | |||||
4* | C10E3CCNMe2 | F | 5.19 | 120 | \({{\rm{C}}}_{14}{\rm{G}}{({{\rm{E}}}_{4}{\rm{M}})}_{2}\) | A | 2 | ||
7* | C8N | F | 10.19 | 121 | \({{\rm{C}}}_{16}{\rm{G}}{({{\rm{E}}}_{4}{\rm{M}})}_{2}\) | A | 2 | ||
ester | 122 | \({{\rm{C}}}_{14}{\rm{G}}{({{\rm{E}}}_{3}{\rm{M}})}_{2}\) | A | 2 | |||||
14 | C8C=CC7C (=O) G | B | 2 | 123 | \({{\rm{C}}}_{14}{\rm{G}}{({{\rm{E}}}_{5}{\rm{M}})}_{2}\) | A | 2 | ||
15 | C4C=CC7C (=O) G | B | 4 | miscellaneous | |||||
16 | C4C=CC8C (=O) G | B | 2 | 8* | C11C (=O) NMeC(CO)5 | F | 10.21 | ||
31† | C11C (=O) E6Me | A | 2 | 38 | C=CC1OPh2OCC- (=O) E7Me | F | 3 | ||
32† | C11C (=O) E5Me | A | 2 | 53* | C12P (=O) (CC#N)2 | F | 5.21 | ||
33† | C11C (=O) E7Me | A | 2 | 124 | (Me)3SiC6E5Me | 7 | |||
34† | C11C (=O) E9Me | A | 2 | 84* | C8FCOO | F | 11.13 | ||
35† | C11C (=O) E13Me | A | 2 | 3* | C12S(N)2Me | F | 5.18 | ||
144 | C15C (=O) G | AB | 7 | 61* | C12S (=O) Me | F | 10.12 | ||
37 | C8C=CC11C (=O) G | AB | 2 | 75 | C12SO3 | F | 10.6 | ||
117 | C6C=CC9C (=O) G | B | 2 | perfluoroalkyl ethoxylate | |||||
141 | C5C (=O) G | AB | 1 | 17 | \({{\rm{C}}}_{6}^{{\rm{F}}}{{\rm{CE}}}_{4}\) | BE | 10 | ||
142 | C7C (=O) G | AB | 3 | 18 | \({{\rm{C}}}_{6}^{{\rm{F}}}{{\rm{CE}}}_{6}\) | BE | 11 | ||
143 | C9C (=O) G | AB | 4 | 19* | \({{\rm{C}}}_{6}^{{\rm{F}}}{{\rm{CE}}}_{5}\) | BE | 15 | ||
ethoxylate | 20 | \({{\rm{C}}}_{6}^{{\rm{F}}}{{\rm{CE}}}_{5}{\rm{Me}}\) | BE | 15 | |||||
36† | C12E13 | A | 4 | 21 | \({{\rm{C}}}_{7}^{{\rm{F}}}{{\rm{CE}}}_{4}{\rm{Me}}\) | BE | 15 | ||
5* | C10E3 | F | 5.22 | 22 | \({{\rm{C}}}_{8}^{{\rm{F}}}{\rm{CC}}\) (=O) \({\rm{N}}{({{\rm{E}}}_{3}{\rm{Me}})}_{2}\) | BE | 16 | ||
9* | C10PhE9 | F | 10.23 | 23 | \({{\rm{C}}}_{10}^{{\rm{F}}}{\rm{CC}}\) (=O) \({\rm{N}}{({{\rm{E}}}_{3}{\rm{Me}})}_{2}\) | BE | 19 | ||
11* | C10E4G | F | 10.25 | phosphate | |||||
13* | C10E4 | F | 4.5 | 64 | C12OP (=O) (OMe)2 | F | 10.13 | ||
39 | C12IsoE3 | A | 4 | 65 | C12P (=O) (OMe)2 | F | 10.13 | ||
40 | C8E6 | A | 1a | 67 | C12OP (=O) (Me)OMe | F | 10.14 | ||
41 | C10E6 | A | 1b | phosphine oxide | |||||
42 | C16E8 | A | 10 | 2* | C14P(Me2) = O | F | 6 | ||
43 | C16E12 | A | 11 | 12* | C10E3CCP(Me2) = O | F | 10.25 | ||
44 | C8E4 | A | 3 | 54 | C12P (=O) Me2 | F | 10.2 | ||
45 | C12E3 | A | 4 | 62 | C12P (=O) Me2 | F | 10.12 | ||
46 | C12E4 | A | 5 | 66* | C12P (=O) \({({{\rm{C}}}_{2})}_{2}\) | F | 10.13 | ||
47 | C12E5 | A | 6 | 70* | \({{\rm{C}}}_{9}{\rm{C}}({\rm{CO}})\left({\rm{P}}\right.\) (=O) \(\left.{{\rm{Me}}}_{2}\right)\) | F | 10.2 | ||
48 | C12E6 | A | 7 | 72 | C14P(Me2) = O | F | 10.5 | ||
49 | C12E8 | A | 8 | 73* | C12P (=O) \({({{\rm{C}}}_{2})}_{2}\) | F | 10.5 | ||
50 | C16E4 | A | 9 | 74* | C12P (=O) Me2 | F | 10.5 | ||
103 | C12E3 | A | 20 | 86* | \({{\rm{C}}}_{10}{\rm{P}}{({{\rm{C}}}_{2})}_{2}\)=O | F | 11.7 | ||
104 | C12E4 | A | 20 | 87* | \({{\rm{C}}}_{8}{\rm{P}}{({{\rm{C}}}_{3})}_{2}\)=O | F | 11.7 | ||
105 | C12E5 | A | 20 | 88* | C6P(Me)(C5)=O | F | 11.7 | ||
112 | C10E6 | A | 3 | 89 | \({\rm{P}}{({{\rm{C}}}_{5})}_{3}\)=O | F | 11.7 | ||
113 | C10E5 | A | 4 | 115 | C10P (=O) Me2 | F | 2 | ||
114 | C10E8 | A | 5 | 116 | C12P (=O) Me2 | F | 2 | ||
128 | C12E9 | AB | 1 | saccharide | |||||
methyl-ethoxylate | 69* | C8-β-D-glucoside | F | 10.20 | |||||
10* | C10E6Me | F | 10.24 | 90 | C8-β-D-glucopyranoside | BC | 1 | ||
24 | \({({{\rm{C}}}_{6})}_{2}{{\rm{GE}}}_{8}{\rm{Me}}\) | AB | 2.3 | 91 | C9-β-D-glucopyranoside | BC | f1 | ||
25 | \({({{\rm{C}}}_{7})}_{2}{{\rm{GE}}}_{8}{\rm{Me}}\) | AB | 2.3 | 92* | C10-β-D-glucopyranoside | BC | 1 | ||
26 | \({({{\rm{C}}}_{8})}_{2}{{\rm{GE}}}_{8}{\rm{Me}}\) | AB | 2.3 | 125* | C8-glucoside | BC | 3 | ||
27 | \({({{\rm{C}}}_{7})}_{2}{{\rm{GE}}}_{10}{\rm{Me}}\) | AB | 2.3 | sulfoximine | |||||
28 | \({({{\rm{C}}}_{7})}_{2}{{\rm{GE}}}_{6}Me\) | AB | 2.3 | 1* | C12S (=O) (N)Me | F | |||
29 | \({{\rm{C}}}_{12}{\rm{G}}{({{\rm{E}}}_{4}{\rm{Me}})}_{2}\) | AB | 7 | 6 | C8S (=O) (N)Me | F | |||
30* | C12E8Me | F | 7 | ||||||