Cephalosporins on Kinetex 5µm F5

Cephalosporins on Kinetex 5µm F5
LC Conditions
Column

Kinetex 5 µm F5 100 Å, LC Column 150 x 4.6 mm, Ea

Brand

Kinetex

Part No

00F-4724-E0

Phase Name

F5

Elution Type

Isocratic

Gradient Profile

Step No.

Time(min)

%A

%B

2

0

85

15

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

Kinetex 5 µm F5 100 Å, LC Column 150 x 4.6 mm, Ea
00F-4724-E0

Kinetex 5 µm F5 100 Å, LC Column 150 x 4.6 mm, Ea

View Product

  • 1. Cefadroxil
  • 2. Cefaclor
  • 3. Cefalexin
  • 4. Cephradine
-OEChem-05081000432D<br><br> 42 44  0     1  0  0  0  0  0999 V2000<br>    3.7320   -1.0254    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3120    1.1873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.5393   -0.0159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.8660    2.4746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981    2.4746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>   11.8499   -0.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981    0.4746    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3120   -1.2381    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.7233   -2.6553    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981   -0.5254    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0<br>    5.6064   -0.5296    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0<br>    5.6064    0.4787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7320    0.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.8660   -0.5254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.8660    0.4746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.2785   -0.9813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000    0.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7320    1.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.9841   -1.6899    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0<br>    8.9506   -1.4330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    9.2114   -0.4676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    9.6562   -2.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>   10.1778   -0.2108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>   10.6227   -1.8848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>   10.8835   -0.9194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.8164   -1.3469    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.3673   -1.1016    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.1503   -1.8367    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.2554   -0.4178    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.6540   -1.1080    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.3100    1.5115    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.4631    1.2846    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.6900    0.4376    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.3849   -1.8491    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    8.1608   -3.0946    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.1241   -2.8145    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.8660    3.0946    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    8.7739   -0.0283    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    9.4945   -2.7401    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>   10.3395    0.3877    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>   11.0602   -2.3241    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>   12.2874   -1.1018    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>  1 10  1  0  0  0  0<br>  1 14  1  0  0  0  0<br>  2 12  2  0  0  0  0<br>  3 16  2  0  0  0  0<br>  4 18  1  0  0  0  0<br>  4 37  1  0  0  0  0<br>  5 18  2  0  0  0  0<br>  6 25  1  0  0  0  0<br>  6 42  1  0  0  0  0<br>  7 10  1  0  0  0  0<br>  7 12  1  0  0  0  0<br>  7 13  1  0  0  0  0<br> 11  8  1  1  0  0  0<br>  8 16  1  0  0  0  0<br>  8 28  1  0  0  0  0<br> 19  9  1  1  0  0  0<br>  9 35  1  0  0  0  0<br>  9 36  1  0  0  0  0<br> 10 11  1  0  0  0  0<br> 10 26  1  6  0  0  0<br> 11 12  1  0  0  0  0<br> 11 27  1  0  0  0  0<br> 13 15  2  0  0  0  0<br> 13 18  1  0  0  0  0<br> 14 15  1  0  0  0  0<br> 14 29  1  0  0  0  0<br> 14 30  1  0  0  0  0<br> 15 17  1  0  0  0  0<br> 16 19  1  0  0  0  0<br> 17 31  1  0  0  0  0<br> 17 32  1  0  0  0  0<br> 17 33  1  0  0  0  0<br> 19 20  1  0  0  0  0<br> 19 34  1  0  0  0  0<br> 20 21  2  0  0  0  0<br> 20 22  1  0  0  0  0<br> 21 23  1  0  0  0  0<br> 21 38  1  0  0  0  0<br> 22 24  2  0  0  0  0<br> 22 39  1  0  0  0  0<br> 23 25  2  0  0  0  0<br> 23 40  1  0  0  0  0<br> 24 25  1  0  0  0  0<br> 24 41  1  0  0  0  0<br>M  END
Compound Name

Cefadroxil

CID

47965

Molecular Formula

C16H17N3O5S

Molecular Weight

363

No. Hydrogen Bond Acceptors

6

No. Hydrogen Bond Donors

4

Similar Applications

No Similar applications found.