Increased Sensitivity

Increased Sensitivity
LC Conditions
Column

Luna 3 µm C18(2) 100 Å, LC Column 30 x 4.6 mm, Ea

Brand

Luna

Part No

00A-4251-E0

Phase Name

C18(2)

Elution Type

Isocratic

Mobile Phase

A: 10 mM Ammonium formate

B: Methanol

Gradient Profile

Step No.

Time(min)

%A

%B

1

0

80

20

Flow Rate

2.00 mL/min

Temperature

22°C

Detection

UV-Vis Abs.-Variable Wave.(UV) @ (22°C)

Detection Info
Sample Notes

SecurityGuard™ Guard Cartridge System extends column lifetime. - SecurityGuard Cartridges, C18 4 x 3.0mm, 10/Pk Part No.: AJ0-4287 - Holder Part No.: KJ0-4282

Order Items Used in This Application

Luna 3 µm C18(2) 100 Å, LC Column 30 x 4.6 mm, Ea
00A-4251-E0

Luna 3 µm C18(2) 100 Å, LC Column 30 x 4.6 mm, Ea

View Product

  • 1. Cephalexin
-OEChem-05081000422D<br><br> 41 43  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>    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>    9.6562   -2.1416    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>   10.6227   -1.8848    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>   10.8835   -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>    9.4945   -2.7401    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>   11.0602   -2.3241    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>   11.4827   -0.7601    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>  1  9  1  0  0  0  0<br>  1 13  1  0  0  0  0<br>  2 11  2  0  0  0  0<br>  3 15  2  0  0  0  0<br>  4 17  1  0  0  0  0<br>  4 36  1  0  0  0  0<br>  5 17  2  0  0  0  0<br>  6  9  1  0  0  0  0<br>  6 11  1  0  0  0  0<br>  6 12  1  0  0  0  0<br> 10  7  1  1  0  0  0<br>  7 15  1  0  0  0  0<br>  7 27  1  0  0  0  0<br> 18  8  1  1  0  0  0<br>  8 34  1  0  0  0  0<br>  8 35  1  0  0  0  0<br>  9 10  1  0  0  0  0<br>  9 25  1  6  0  0  0<br> 10 11  1  0  0  0  0<br> 10 26  1  0  0  0  0<br> 12 14  2  0  0  0  0<br> 12 17  1  0  0  0  0<br> 13 14  1  0  0  0  0<br> 13 28  1  0  0  0  0<br> 13 29  1  0  0  0  0<br> 14 16  1  0  0  0  0<br> 15 18  1  0  0  0  0<br> 16 30  1  0  0  0  0<br> 16 31  1  0  0  0  0<br> 16 32  1  0  0  0  0<br> 18 19  1  0  0  0  0<br> 18 33  1  0  0  0  0<br> 19 20  2  0  0  0  0<br> 19 21  1  0  0  0  0<br> 20 22  1  0  0  0  0<br> 20 37  1  0  0  0  0<br> 21 23  2  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 24  1  0  0  0  0<br> 23 40  1  0  0  0  0<br> 24 41  1  0  0  0  0<br>M  END
Compound Name

Cephalexin

CID

27447

Molecular Formula

C16H17N3O4S

Molecular Weight

347

No. Hydrogen Bond Acceptors

5

No. Hydrogen Bond Donors

3

Similar Applications

No Similar applications found.