Tetracylines on Kinetex 5u EVO C18 150x4.6mm
LC Conditions
Column
Kinetex 5 µm EVO C18 100 Å, LC Column 150 x 4.6 mm, Ea
Brand
Kinetex
Part No
00F-4633-E0
Phase Name
EVO C18
Elution Type
Gradient
Mobile Phase
A: 20mM Sodium Phosphate pH 2.0
B: Acetonitrile
Gradient Profile
Step No.
Time(min)
%A
%B
1
0
95
5
2
10
5
95
3
12
5
95
4
12.5
95
5
5
15
95
5
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. Sulfamerazine
- 2. Oxytetracycline
- 3. Ciprofloxacin
- 4. Enrofloxacin
- 5. Sulfamethazine
- 6. Oxacillin
-OEChem-06211003152D<br><br> 30 31 0 0 0 0 0 0 0999 V2000<br> 3.0000 0.1550 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.0000 0.1550 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.0000 0.1550 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.0000 1.1550 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.8660 2.6550 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.7320 1.1550 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.0000 -3.8450 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.0000 -0.8450 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.1340 -1.3450 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.8660 -1.3450 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.0000 -2.8450 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.1340 -2.3450 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.8660 -2.3450 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.8660 1.6550 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.7320 3.1550 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.5981 2.6550 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.5981 1.6550 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.7320 4.1550 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.4631 1.4650 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1.5970 -1.0350 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.4030 -1.0350 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1.5970 -2.6550 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.4030 -2.6550 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.1350 2.9650 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 6.1350 1.3450 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 5.3520 4.1550 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.7320 4.7750 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 4.1120 4.1550 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 2.4631 -4.1550 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 3.5369 -4.1550 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0<br> 1 2 2 0 0 0 0<br> 1 3 2 0 0 0 0<br> 1 4 1 0 0 0 0<br> 1 8 1 0 0 0 0<br> 4 14 1 0 0 0 0<br> 4 19 1 0 0 0 0<br> 5 14 1 0 0 0 0<br> 5 15 2 0 0 0 0<br> 6 14 2 0 0 0 0<br> 6 17 1 0 0 0 0<br> 7 11 1 0 0 0 0<br> 7 29 1 0 0 0 0<br> 7 30 1 0 0 0 0<br> 8 9 2 0 0 0 0<br> 8 10 1 0 0 0 0<br> 9 12 1 0 0 0 0<br> 9 20 1 0 0 0 0<br> 10 13 2 0 0 0 0<br> 10 21 1 0 0 0 0<br> 11 12 2 0 0 0 0<br> 11 13 1 0 0 0 0<br> 12 22 1 0 0 0 0<br> 13 23 1 0 0 0 0<br> 15 16 1 0 0 0 0<br> 15 18 1 0 0 0 0<br> 16 17 2 0 0 0 0<br> 16 24 1 0 0 0 0<br> 17 25 1 0 0 0 0<br> 18 26 1 0 0 0 0<br> 18 27 1 0 0 0 0<br> 18 28 1 0 0 0 0<br>M END
Compound Name
Sulfamerazine
CID
5325
Molecular Formula
C11H12N4O2S
Molecular Weight
264
No. Hydrogen Bond Acceptors
6
No. Hydrogen Bond Donors
2
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