Sulfa Drugs by Luna 3µ Phenyl-Hexyl MercuryMS Cartridge 20 x 2.0mm

Sulfa Drugs by Luna 3µ Phenyl-Hexyl MercuryMS Cartridge 20 x 2.0mm
LC Conditions
Column

Luna 3 µm Phenyl-Hexyl 100 Å, LC Column 20 x 2 mm, MercuryMS, Ea

Brand

Luna

Part No

00M-4256-B0-CE

Phase Name

Phenyl-Hexyl

Elution Type

Gradient

Mobile Phase

A: 0.1% Formic acid in Water

B: 0.1% Formic acid in Methanol

Gradient Profile

Step No.

Time(min)

%A

%B

1

0

95

5

2

1

20

80

3

1.2

20

80

4

1.21

95

5

5

2

95

5

Flow Rate

0.60 mL/min

Temperature

22°C

Detection

UV-Vis Abs.-Variable Wave.(UV) @ (25°C)

Detection Info
Sample Notes

SecurityGuard™ Guard Cartridge System extends column lifetime. - SecurityGuard Cartridges, Phenyl 4 x 2.0mm, 10/Pk Part No.: AJ0-4350 - Holder Part No.: KJ0-4282

Order Items Used in This Application

Luna 3 µm Phenyl-Hexyl 100 Å, LC Column 20 x 2 mm, MercuryMS, Ea
00M-4256-B0-CE

Luna 3 µm Phenyl-Hexyl 100 Å, LC Column 20 x 2 mm, MercuryMS, Ea

View Product

  • 1. Sulfanilamide
  • 2. Sulfadiazine
  • 3. Sulfathiazole
  • 4. Sulfamerazine
  • 5. Sulfamethoxazole
  • 6. Sulfaquinoxaline
-OEChem-06211003152D<br><br> 19 19  0     0  0  0  0  0  0999 V2000<br>    3.0000    1.5000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.0000    1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000    1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000    2.5000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000   -2.5000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000    0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8660    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.1340    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8660   -1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.1340   -1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.4030    0.3100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.5970    0.3100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.4030   -1.3100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.5970   -1.3100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.5369    2.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.4631    2.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.4631   -2.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.5369   -2.8100    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  6  1  0  0  0  0<br>  4 16  1  0  0  0  0<br>  4 17  1  0  0  0  0<br>  5  9  1  0  0  0  0<br>  5 18  1  0  0  0  0<br>  5 19  1  0  0  0  0<br>  6  7  2  0  0  0  0<br>  6  8  1  0  0  0  0<br>  7 10  1  0  0  0  0<br>  7 12  1  0  0  0  0<br>  8 11  2  0  0  0  0<br>  8 13  1  0  0  0  0<br>  9 10  2  0  0  0  0<br>  9 11  1  0  0  0  0<br> 10 14  1  0  0  0  0<br> 11 15  1  0  0  0  0<br>M  END
Compound Name

Sulfanilamide

CID

5333

Molecular Formula

C6H8N2O2S

Molecular Weight

172

No. Hydrogen Bond Acceptors

4

No. Hydrogen Bond Donors

2

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