Lux i-Amylose-3 Separation for Thalidomide
LC Conditions
Column
Lux 5 µm i-Amylose-3, LC Column 250 x 4.6 mm, Ea
Brand
Lux
Part No
00G-4779-E0
Phase Name
i-Amylose-3
Elution Type
Isocratic
Mobile Phase
A: Acetonitrile
B: Diethylamine
Gradient Profile
Step No.
Time(min)
%A
%B
1
14
100
0.1
Flow Rate
1.00 mL/min
Temperature
25°C
System
Agilent Technologies Agilent Technologies 1100 Series
Detection
LC/UV (DAD, PDA) @ 254 nm (nanometers)
Detection Info
Sample Notes
2 mg/mL in Ethanol
Order Items Used in This Application
- 1. Thalidomide
- 2. Thalidomide
-OEChem-06211003152D<br><br> 29 31 0 1 0 0 0 0 0999 V2000<br> 6.2619 -1.7320 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.9889 1.7552 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.9889 -1.7552 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 9.2619 0.0000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.2619 0.0000 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.7619 -0.8660 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.2619 0.0000 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0<br> 6.7619 0.8660 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.7619 0.8660 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.7619 -0.8660 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.6783 0.8047 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.6783 -0.8047 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.7320 0.5000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.7320 -0.5000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.2619 0.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 1.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 -1.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.0000 0.5000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.0000 -0.5000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.9519 -0.5369 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.8695 1.4766 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.1793 1.0781 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.3445 1.0781 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.6542 1.4766 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.0719 -1.4030 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 1.6200 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 -1.6200 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1.4631 0.8100 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1.4631 -0.8100 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1 10 2 0 0 0 0<br> 2 11 2 0 0 0 0<br> 3 12 2 0 0 0 0<br> 4 15 2 0 0 0 0<br> 5 7 1 0 0 0 0<br> 5 11 1 0 0 0 0<br> 5 12 1 0 0 0 0<br> 6 10 1 0 0 0 0<br> 6 15 1 0 0 0 0<br> 6 25 1 0 0 0 0<br> 7 8 1 0 0 0 0<br> 7 10 1 0 0 0 0<br> 7 20 1 0 0 0 0<br> 8 9 1 0 0 0 0<br> 8 21 1 0 0 0 0<br> 8 22 1 0 0 0 0<br> 9 15 1 0 0 0 0<br> 9 23 1 0 0 0 0<br> 9 24 1 0 0 0 0<br> 11 13 1 0 0 0 0<br> 12 14 1 0 0 0 0<br> 13 14 1 0 0 0 0<br> 13 16 2 0 0 0 0<br> 14 17 2 0 0 0 0<br> 16 18 1 0 0 0 0<br> 16 26 1 0 0 0 0<br> 17 19 1 0 0 0 0<br> 17 27 1 0 0 0 0<br> 18 19 2 0 0 0 0<br> 18 28 1 0 0 0 0<br> 19 29 1 0 0 0 0<br>M END
Compound Name
Thalidomide
CID
5426
Molecular Formula
C13H10N2O4
Molecular Weight
258
No. Hydrogen Bond Acceptors
4
No. Hydrogen Bond Donors
1
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