Sulfa Drugs using Gemini 5u C18

Sulfa Drugs using Gemini 5u C18
LC Conditions
Column

Gemini 5 µm C18 110 Å, LC Column 150 x 4.6 mm, Ea

Brand

Gemini

Part No

00F-4435-E0

Phase Name

C18

Elution Type

Isocratic

Mobile Phase

A: 0.1% Formic Acid in Water

B: Methanol

Gradient Profile

Step No.

Time(min)

%A

%B

1

0

70

30

Flow Rate

1.00 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, Gemini C18 4 x 3.0mm, 10/Pk Part No.: AJ0-7597 - Holder Part No.: KJ0-4282

Order Items Used in This Application

Gemini 5 µm C18 110 Å, LC Column 150 x 4.6 mm, Ea
00F-4435-E0

Gemini 5 µm C18 110 Å, LC Column 150 x 4.6 mm, Ea

View Product

  • 1. Sulfathiazole
  • 2. Sulfamerazine
  • 3. Sulfamethoxazole
-OEChem-06211003152D<br><br> 25 26  0     0  0  0  0  0  0999 V2000<br>    3.0000    0.8038    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.7796    1.8970    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.0000    0.8038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000    0.8038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000    1.8038    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000   -3.1962    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.9706    3.2983    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000   -0.1962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8660   -0.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.1340   -0.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000   -2.1962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8660   -1.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.1340   -1.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8660    2.3038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4487    2.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.9487    3.5062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.4030   -0.3862    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.5970   -0.3862    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.4631    2.1138    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.4030   -2.0062    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.5970   -2.0062    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.4631   -3.5062    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.5369   -3.5062    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.0653    2.5754    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.2009    4.0726    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>  1  3  2  0  0  0  0<br>  1  4  2  0  0  0  0<br>  1  5  1  0  0  0  0<br>  1  8  1  0  0  0  0<br>  2 14  1  0  0  0  0<br>  2 15  1  0  0  0  0<br>  5 14  1  0  0  0  0<br>  5 19  1  0  0  0  0<br>  6 11  1  0  0  0  0<br>  6 22  1  0  0  0  0<br>  6 23  1  0  0  0  0<br>  7 14  2  0  0  0  0<br>  7 16  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 17  1  0  0  0  0<br> 10 13  2  0  0  0  0<br> 10 18  1  0  0  0  0<br> 11 12  2  0  0  0  0<br> 11 13  1  0  0  0  0<br> 12 20  1  0  0  0  0<br> 13 21  1  0  0  0  0<br> 15 16  2  0  0  0  0<br> 15 24  1  0  0  0  0<br> 16 25  1  0  0  0  0<br>M  END
Compound Name

Sulfathiazole

CID

5340

Molecular Formula

C9H9N3O2S2

Molecular Weight

255

No. Hydrogen Bond Acceptors

5

No. Hydrogen Bond Donors

2

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