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

35

2

4*

C10E3CCNMe2

F

1

5.19

120

\({{\rm{C}}}_{14}{\rm{G}}{({{\rm{E}}}_{4}{\rm{M}})}_{2}\)

A

35

2

7*

C8N

F

1

10.19

121

\({{\rm{C}}}_{16}{\rm{G}}{({{\rm{E}}}_{4}{\rm{M}})}_{2}\)

A

35

2

ester

122

\({{\rm{C}}}_{14}{\rm{G}}{({{\rm{E}}}_{3}{\rm{M}})}_{2}\)

A

35

2

14

C8C=CC7C (=O) G

B

36

2

123

\({{\rm{C}}}_{14}{\rm{G}}{({{\rm{E}}}_{5}{\rm{M}})}_{2}\)

A

35

2

15

C4C=CC7C (=O) G

B

37

4

miscellaneous

16

C4C=CC8C (=O) G

B

38

2

8*

C11C (=O) NMeC(CO)5

F

1

10.21

31

C11C (=O) E6Me

A

28

2

38

C=CC1OPh2OCC- (=O) E7Me

F

39

3

32

C11C (=O) E5Me

A

28

2

53*

C12P (=O) (CC#N)2

F

1

5.21

33

C11C (=O) E7Me

A

28

2

124

(Me)3SiC6E5Me

 

40

7

34

C11C (=O) E9Me

A

28

2

84*

C8FCOO

F

1

11.13

35

C11C (=O) E13Me

A

28

2

3*

C12S(N)2Me

F

1

5.18

144

C15C (=O) G

AB

41

7

61*

C12S (=O) Me

F

1

10.12

37

C8C=CC11C (=O) G

AB

42

2

75

C12SO3

F

1

10.6

117

C6C=CC9C (=O) G

B

43

2

perfluoroalkyl ethoxylate

141

C5C (=O) G

AB

41

1

17

\({{\rm{C}}}_{6}^{{\rm{F}}}{{\rm{CE}}}_{4}\)

BE

34

10

142

C7C (=O) G

AB

41

3

18

\({{\rm{C}}}_{6}^{{\rm{F}}}{{\rm{CE}}}_{6}\)

BE

34

11

143

C9C (=O) G

AB

41

4

19*

\({{\rm{C}}}_{6}^{{\rm{F}}}{{\rm{CE}}}_{5}\)

BE

34

15

ethoxylate

20

\({{\rm{C}}}_{6}^{{\rm{F}}}{{\rm{CE}}}_{5}{\rm{Me}}\)

BE

34

15

36

C12E13

A

28

4

21

\({{\rm{C}}}_{7}^{{\rm{F}}}{{\rm{CE}}}_{4}{\rm{Me}}\)

BE

34

15

5*

C10E3

F

1

5.22

22

\({{\rm{C}}}_{8}^{{\rm{F}}}{\rm{CC}}\) (=O) \({\rm{N}}{({{\rm{E}}}_{3}{\rm{Me}})}_{2}\)

BE

34

16

9*

C10PhE9

F

1

10.23

23

\({{\rm{C}}}_{10}^{{\rm{F}}}{\rm{CC}}\) (=O) \({\rm{N}}{({{\rm{E}}}_{3}{\rm{Me}})}_{2}\)

BE

34

19

11*

C10E4G

F

1

10.25

phosphate

13*

C10E4

F

1

4.5

64

C12OP (=O) (OMe)2

F

1

10.13

39

C12IsoE3

A

44

4

65

C12P (=O) (OMe)2

F

1

10.13

40

C8E6

A

45

1a

67

C12OP (=O) (Me)OMe

F

1

10.14

41

C10E6

A

45

1b

phosphine oxide

42

C16E8

A

33

10

2*

C14P(Me2) = O

F

46

6

43

C16E12

A

33

11

12*

C10E3CCP(Me2) = O

F

46

10.25

44

C8E4

A

33

3

54

C12P (=O) Me2

F

46

10.2

45

C12E3

A

33

4

62

C12P (=O) Me2

F

46

10.12

46

C12E4

A

33

5

66*

C12P (=O) \({({{\rm{C}}}_{2})}_{2}\)

F

46

10.13

47

C12E5

A

33

6

70*

\({{\rm{C}}}_{9}{\rm{C}}({\rm{CO}})\left({\rm{P}}\right.\) (=O) \(\left.{{\rm{Me}}}_{2}\right)\)

F

46

10.2

48

C12E6

A

33

7

72

C14P(Me2) = O

F

46

10.5

49

C12E8

A

33

8

73*

C12P (=O) \({({{\rm{C}}}_{2})}_{2}\)

F

46

10.5

50

C16E4

A

33

9

74*

C12P (=O) Me2

F

46

10.5

103

C12E3

A

47

20

86*

\({{\rm{C}}}_{10}{\rm{P}}{({{\rm{C}}}_{2})}_{2}\)=O

F

46

11.7

104

C12E4

A

47

20

87*

\({{\rm{C}}}_{8}{\rm{P}}{({{\rm{C}}}_{3})}_{2}\)=O

F

46

11.7

105

C12E5

A

47

20

88*

C6P(Me)(C5)=O

F

46

11.7

112

C10E6

A

48

3

89

\({\rm{P}}{({{\rm{C}}}_{5})}_{3}\)=O

F

46

11.7

113

C10E5

A

48

4

115

C10P (=O) Me2

F

49

2

114

C10E8

A

48

5

116

C12P (=O) Me2

F

49

2

128

C12E9

AB

50

1

saccharide

methyl-ethoxylate

69*

C8-β-D-glucoside

F

1

10.20

10*

C10E6Me

F

1

10.24

90

C8-β-D-glucopyranoside

BC

51

1

24

\({({{\rm{C}}}_{6})}_{2}{{\rm{GE}}}_{8}{\rm{Me}}\)

AB

52

2.3

91

C9-β-D-glucopyranoside

BC

51

f1

25

\({({{\rm{C}}}_{7})}_{2}{{\rm{GE}}}_{8}{\rm{Me}}\)

AB

52

2.3

92*

C10-β-D-glucopyranoside

BC

51

1

26

\({({{\rm{C}}}_{8})}_{2}{{\rm{GE}}}_{8}{\rm{Me}}\)

AB

52

2.3

125*

C8-glucoside

BC

53

3

27

\({({{\rm{C}}}_{7})}_{2}{{\rm{GE}}}_{10}{\rm{Me}}\)

AB

52

2.3

sulfoximine

28

\({({{\rm{C}}}_{7})}_{2}{{\rm{GE}}}_{6}Me\)

AB

52

2.3

1*

C12S (=O) (N)Me

F

46

 

29

\({{\rm{C}}}_{12}{\rm{G}}{({{\rm{E}}}_{4}{\rm{Me}})}_{2}\)

AB

52

7

6

C8S (=O) (N)Me

F

1

 

30*

C12E8Me

F

52

7

     
  1. In the structures, n is the alkyl chain length. Me, Em, G and Ph are methyl (CH3), ethoxy (\({[{{\rm{O}}{\rm{C}}{\rm{H}}}_{2}{{\rm{C}}{\rm{H}}}_{2}]}_{{\rm{m}}}{\rm{O}}\)) where m refers to the number of repeat units, triglyceryl/glycerol unit and phenyl ring groups respectively. Iso is isosorbide ring. Incomplete diagrams are denoted with an asterisk. Where an average ethoxy length was reported E is given to the nearest integer (indicated by a dagger).