Chiral Separation of Carbinoxamine on Lux 5µm i-Amylose-1 in NP
LC Conditions
Column
Lux 5 µm i-Amylose-1, LC Column 250 x 4.6 mm, Ea
Brand
Lux
Part No
00G-4762-E0
Phase Name
i-Amylose-1
Elution Type
Isocratic
Mobile Phase
A: 0.1% DEA in Hexane
B: 0.1% DEA in THF
Gradient Profile
Step No.
Time(min)
%A
%B
1
0
90
10
Flow Rate
1.00 mL/min
Temperature
22°C
Detection
UV-Vis Abs.-Variable Wave.(UV) @ (22°C)
Detection Info
Order Items Used in This Application
- 1. Carbinoxamine
- 2. Carbinoxamine
-OEChem-06211003142D<br><br> 39 40 0 1 0 0 0 0 0999 V2000<br> 4.5981 -3.7500 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.7320 0.7500 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 3.2500 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.4641 1.7500 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5981 0.2500 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0<br> 3.7320 1.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 2.2500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5981 -0.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.4641 0.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.7320 -1.2500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.4641 -1.2500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.3301 0.2500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.0000 3.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.7320 3.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.7320 -2.2500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.4641 -2.2500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5981 -2.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.1962 0.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.3301 2.2500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.1962 1.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5981 1.1000 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.3426 1.6423 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.9441 2.3326 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.2554 2.3577 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.6540 1.6674 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.1951 -0.9400 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.0010 -0.9400 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.3301 -0.3700 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.3100 4.2869 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1.4631 4.0600 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1.6900 3.2131 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.0420 3.2131 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.2690 4.0600 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.4220 4.2869 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.1951 -2.5600 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.0010 -2.5600 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.7331 0.4400 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.3301 2.8700 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.7331 2.0600 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1 17 1 0 0 0 0<br> 2 5 1 0 0 0 0<br> 2 6 1 0 0 0 0<br> 3 7 1 0 0 0 0<br> 3 13 1 0 0 0 0<br> 3 14 1 0 0 0 0<br> 4 9 1 0 0 0 0<br> 4 19 2 0 0 0 0<br> 5 8 1 0 0 0 0<br> 5 9 1 0 0 0 0<br> 5 21 1 0 0 0 0<br> 6 7 1 0 0 0 0<br> 6 22 1 0 0 0 0<br> 6 23 1 0 0 0 0<br> 7 24 1 0 0 0 0<br> 7 25 1 0 0 0 0<br> 8 10 2 0 0 0 0<br> 8 11 1 0 0 0 0<br> 9 12 2 0 0 0 0<br> 10 15 1 0 0 0 0<br> 10 26 1 0 0 0 0<br> 11 16 2 0 0 0 0<br> 11 27 1 0 0 0 0<br> 12 18 1 0 0 0 0<br> 12 28 1 0 0 0 0<br> 13 29 1 0 0 0 0<br> 13 30 1 0 0 0 0<br> 13 31 1 0 0 0 0<br> 14 32 1 0 0 0 0<br> 14 33 1 0 0 0 0<br> 14 34 1 0 0 0 0<br> 15 17 2 0 0 0 0<br> 15 35 1 0 0 0 0<br> 16 17 1 0 0 0 0<br> 16 36 1 0 0 0 0<br> 18 20 2 0 0 0 0<br> 18 37 1 0 0 0 0<br> 19 20 1 0 0 0 0<br> 19 38 1 0 0 0 0<br> 20 39 1 0 0 0 0<br>M END
Compound Name
Carbinoxamine
CID
2564
Molecular Formula
C16H19ClN2O
Molecular Weight
290
No. Hydrogen Bond Acceptors
3
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