Chlorthalidone
LC Conditions
Column
Chirex (S)-VAL and (R)-NEA, LC Column 250 x 4.6 mm, Ea
Brand
Chirex
Part No
00G-3014-E0
Phase Name
3014 (S)-valine and (R)-1-(alpha-naphthyl)ethylamine
Elution Type
Isocratic
Mobile Phase
A: Hexane/Dichloroethane/Ethanol-TFA (75:20:5) ethanol-TFA 20:1
Gradient Profile
Step No.
Time(min)
%A
%B
1
0
100
0
Flow Rate
7.00 mL/min
Temperature
22°C
Detection
UV-Vis Abs.-Variable Wave.(UV) @ (22°C)
Detection Info
Order Items Used in This Application
- 1. Chlorthalidone
- 2. Chlorthalidone
-OEChem-06211003152D<br><br> 33 35 0 1 0 0 0 0 0999 V2000<br> 7.9184 2.4528 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.1240 0.4634 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.3709 1.0588 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.9889 -2.4528 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.5323 1.3762 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.7157 -0.4495 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.2619 -0.6975 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 9.0369 0.0550 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.6783 0.1072 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0<br> 3.7320 -0.1975 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.4883 0.6936 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.7320 -1.1975 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.6783 -1.5022 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.4011 0.2853 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 0.3025 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.3855 1.6883 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.2112 0.8717 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 -1.6975 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.0000 -0.1975 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.1955 2.2747 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.1084 1.8664 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.0000 -1.1975 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.8819 -0.6975 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.4649 -0.3314 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 0.9225 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.8195 1.9415 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 -2.3175 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.7647 1.1888 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.1318 2.8914 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1.4631 0.1125 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1.4631 -1.5075 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 9.5391 0.4186 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 9.1006 -0.5617 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1 21 1 0 0 0 0<br> 2 5 2 0 0 0 0<br> 2 6 2 0 0 0 0<br> 2 8 1 0 0 0 0<br> 2 17 1 0 0 0 0<br> 3 9 1 0 0 0 0<br> 3 28 1 0 0 0 0<br> 4 13 2 0 0 0 0<br> 7 9 1 0 0 0 0<br> 7 13 1 0 0 0 0<br> 7 23 1 0 0 0 0<br> 8 32 1 0 0 0 0<br> 8 33 1 0 0 0 0<br> 9 10 1 0 0 0 0<br> 9 11 1 0 0 0 0<br> 10 12 1 0 0 0 0<br> 10 15 2 0 0 0 0<br> 11 14 2 0 0 0 0<br> 11 16 1 0 0 0 0<br> 12 13 1 0 0 0 0<br> 12 18 2 0 0 0 0<br> 14 17 1 0 0 0 0<br> 14 24 1 0 0 0 0<br> 15 19 1 0 0 0 0<br> 15 25 1 0 0 0 0<br> 16 20 2 0 0 0 0<br> 16 26 1 0 0 0 0<br> 17 21 2 0 0 0 0<br> 18 22 1 0 0 0 0<br> 18 27 1 0 0 0 0<br> 19 22 2 0 0 0 0<br> 19 30 1 0 0 0 0<br> 20 21 1 0 0 0 0<br> 20 29 1 0 0 0 0<br> 22 31 1 0 0 0 0<br>M END
Compound Name
Chlorthalidone
CID
2732
Molecular Formula
C14H11ClN2O4S
Molecular Weight
338
No. Hydrogen Bond Acceptors
5
No. Hydrogen Bond Donors
3
Similar Applications
Chiral
Chiral Separation of Chlorthalidone on Lux 5µm i-Amylose-1 in NP
Lux 5 µm i-Amylose-1, LC Column 250 x 4.6 mm, Ea
24499