Quinacrine
LC Conditions
Column
Chirex (S)-LEU and (R)-NEA, LC Column 250 x 4.6 mm, Ea
Brand
Chirex
Part No
00G-3020-E0
Phase Name
3020 (S)-tert-leucine and (R)-1-(alpha-naphthyl)ethylamine
Elution Type
Isocratic
Mobile Phase
A: Hexane/Dichloroethane/Ethanol-TFA (55:35:10) w/ ethanol-TFA (20:1)
Gradient Profile
Step No.
Time(min)
%A
%B
1
0
100
0
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. Quinacrine
- 2. Quinacrine
-OEChem-06211003142D<br><br> 58 60 0 1 0 0 0 0 0999 V2000<br> 2.8000 -4.0068 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0<br> 9.8602 -1.9585 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.7320 2.5173 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.3301 -0.9827 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.3301 -3.9827 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.4641 -0.4827 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0<br> 5.4641 0.5173 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5981 1.0173 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5981 2.0173 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.3301 -1.9827 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5981 -0.9827 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.7320 3.5173 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 2.0173 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.1962 -2.4827 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.4641 -2.4827 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 7.1962 -3.4827 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.4641 -3.4827 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.8660 4.0173 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.0000 2.5173 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.0901 -1.9480 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5702 -1.9480 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.0901 -4.0173 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5702 -4.0173 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.9962 -2.4618 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.9962 -3.5035 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.6641 -2.4618 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.6641 -3.5035 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 10.7282 -2.4552 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.4641 -1.1027 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.0747 0.4097 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.6762 1.0999 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.9875 1.1250 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.3860 0.4347 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.2087 1.9097 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.8101 2.5999 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.8671 -0.6727 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.2881 -0.4457 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.0611 -1.2927 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.9081 -1.5196 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.3426 3.4097 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.9441 4.0999 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.4675 1.5424 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.2646 1.5424 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.1760 4.5543 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.3291 4.3273 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.5560 3.4804 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.3100 3.0543 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1.4631 2.8273 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1.6900 1.9804 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.0829 -1.3280 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5773 -1.3280 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 8.0829 -4.6373 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.5773 -4.6373 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 9.5319 -3.8156 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.1284 -2.1498 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 10.4203 -2.9933 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 11.2663 -2.7631 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 11.0361 -1.9170 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1 27 1 0 0 0 0<br> 2 24 1 0 0 0 0<br> 2 28 1 0 0 0 0<br> 3 9 1 0 0 0 0<br> 3 12 1 0 0 0 0<br> 3 13 1 0 0 0 0<br> 4 6 1 0 0 0 0<br> 4 10 1 0 0 0 0<br> 4 36 1 0 0 0 0<br> 5 16 2 0 0 0 0<br> 5 17 1 0 0 0 0<br> 6 7 1 0 0 0 0<br> 6 11 1 0 0 0 0<br> 6 29 1 0 0 0 0<br> 7 8 1 0 0 0 0<br> 7 30 1 0 0 0 0<br> 7 31 1 0 0 0 0<br> 8 9 1 0 0 0 0<br> 8 32 1 0 0 0 0<br> 8 33 1 0 0 0 0<br> 9 34 1 0 0 0 0<br> 9 35 1 0 0 0 0<br> 10 14 2 0 0 0 0<br> 10 15 1 0 0 0 0<br> 11 37 1 0 0 0 0<br> 11 38 1 0 0 0 0<br> 11 39 1 0 0 0 0<br> 12 18 1 0 0 0 0<br> 12 40 1 0 0 0 0<br> 12 41 1 0 0 0 0<br> 13 19 1 0 0 0 0<br> 13 42 1 0 0 0 0<br> 13 43 1 0 0 0 0<br> 14 16 1 0 0 0 0<br> 14 20 1 0 0 0 0<br> 15 17 2 0 0 0 0<br> 15 21 1 0 0 0 0<br> 16 22 1 0 0 0 0<br> 17 23 1 0 0 0 0<br> 18 44 1 0 0 0 0<br> 18 45 1 0 0 0 0<br> 18 46 1 0 0 0 0<br> 19 47 1 0 0 0 0<br> 19 48 1 0 0 0 0<br> 19 49 1 0 0 0 0<br> 20 24 2 0 0 0 0<br> 20 50 1 0 0 0 0<br> 21 26 2 0 0 0 0<br> 21 51 1 0 0 0 0<br> 22 25 2 0 0 0 0<br> 22 52 1 0 0 0 0<br> 23 27 2 0 0 0 0<br> 23 53 1 0 0 0 0<br> 24 25 1 0 0 0 0<br> 25 54 1 0 0 0 0<br> 26 27 1 0 0 0 0<br> 26 55 1 0 0 0 0<br> 28 56 1 0 0 0 0<br> 28 57 1 0 0 0 0<br> 28 58 1 0 0 0 0<br>M END
Compound Name
Quinacrine
CID
237
Molecular Formula
C23H30ClN3O
Molecular Weight
399
No. Hydrogen Bond Acceptors
4
No. Hydrogen Bond Donors
1
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