Setting 
My Cart
Toggle Nav
Close
  • Menu
  • Setting

Phthalylsulfacetamide

Catalog No.
BA1447
A sulfonamide drug that, after oral administration, slowly decomposes in the intestine to release sulfacetamide, thereby producing an antibacterial effect.
Grouped product items
SizePriceStock Qty
Evaluation Sample
$30.00
In stock
1g
$50.00
In stock
5g
$120.00
Ship with 5-10 days
For scientific research use only and should not be used for diagnostic or medical purposes.

Tel: +1-832-696-8203

Email: [email protected]

Worldwide Distributors

Background

Phthalylsulfacetamide (CAS No.: 131-69-1) is a sulfonamide-class antibacterial compound widely utilized as a reference agent in microbiological and pharmacological research, characterized by its ability to inhibit bacterial dihydropteroate synthase and thereby disrupt folate biosynthesis essential for microbial growth and proliferation. As a prodrug-like derivative, it can undergo gradual decomposition under physiological-like conditions to release sulfacetamide, contributing to its antibacterial activity profile. In vitro studies typically demonstrate activity in the low micromolar range, although potency varies depending on the bacterial strain and assay conditions. This compound is commonly employed in cell-based and in vivo experimental systems to investigate antimicrobial efficacy, resistance mechanisms, and pharmacokinetic behavior, as well as to benchmark novel antibacterial candidates during early-stage drug discovery. Experimental concentrations or dosing regimens are determined by specific study designs and endpoints. As with other sulfonamides, careful consideration of potential off-target or adverse biological effects is necessary when interpreting experimental outcomes.

Chemical Properties

Physical AppearanceA solid
Storage -20°C
M.Wt362.36
Cas No.131-69-1
FormulaC16H14N2O6S
SynonymsTamid, Enterosulfon, Enterosulfamid
Solubility≥51.4 mg/mL in DMSO; ≥5.3 mg/mL in EtOH with ultrasonic; insoluble in H2O
Chemical Name2-((4-(N-acetylsulfamoyl)phenyl)carbamoyl)benzoic acid
Canonical SMILESO=C(O)C1=C(C(NC2=CC=C(S(=O)(NC(C)=O)=O)C=C2)=O)C=CC=C1
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

User Guide