Sulfamethazine, 99%, Thermo Scientific Chemicals
Sulfamethazine, 99%, Thermo Scientific Chemicals
Sulfamethazine, 99%, Thermo Scientific Chemicals
Sulfamethazine, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Sulfamethazine, 99%, Thermo Scientific Chemicals

CAS: 57-68-1 | C12H14N4O2S | 278.33 g/mol
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Catalog NumberQuantity
ALFA19276.1425 g
Catalog number ALFA19276.14
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Quantity:
25 g
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Specifications
Chemical Name or MaterialSulfamethazine
CAS57-68-1
Melting Point198°C to 201°C
Recommended StorageAmbient temperatures
EINECS Number200-346-4
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Sulfamethazine blocks the synthesis of dihydrofolic acid by inhibiting dihydropteroate synthase.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Sulfamethazine is an antibacterial. Sulfamethazine blocks the synthesis of dihydrofolic acid by inhibiting dihydropteroate synthase.Sulfamethazine is an antibiotic used to treat bronchitis, prostatitis and urinary tract infections. It is used in disposition and depletion kinetic studies. It is used to develop detection techniques for quantification in fluids such as cows’ milk, honey and swine urine. Sulfamethazine is an antimicrobial sulfur drug that blocks the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. Sulfamethazine is a competitive inhibitor of bacterial para-aminobenzoic acid.

Solubility
Soluble in DMSO (56 mg/mL at 25°C), water (<1mg/mL at 25°C), and ethanol (<1mg/mL at 25°C).

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. S. Kaniou,; K. Pitarakis,; I. Barlagiannic,; I. Pouliosc. Photocatalytic oxidation of sulfamethazine. Chemosphere. 2005, 60 (3) , 372-380.
  2. Craig Knox et. al. DrugBank 3.0: a comprehensive resource for 'omics' research on drugs.. Nucleic Acids Research,. 2011, 39 D1035-D1041.