≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Information
Furosemide (Frusemide) sodium is a potent and orally active inhibitor ofNa-K-Cl cotransporter (NKCC). Furosemide sodium is a subtype-selective antagonist ofgamma-aminobutyric acid type A (GABAA) receptor.
Targets
NKCC ; GABAA receptor
| ALogP | -0.071 |
|---|---|
| Recuento HBD | 2 |
| Enlace rotable | 5 |
| Pubchem Sid | 504769585 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504769585 |
| Sonrisas canónicas | C1=COC(=C1)CNC2=CC(=C(C=C2C(=O)[O-])S(=O)(=O)N)Cl.[Na+] |
| IUPAC Name | sodium;4-chloro-2-(furan-2-ylmethylamino)-5-sulfamoylbenzoate |
| InChIKey | DLFCAVBMDSKMEY-UHFFFAOYSA-M |
| INCHI | 1S/C12H11ClN2O5S.Na/c13-9-5-10(15-6-7-2-1-3-20-7)8(12(16)17)4-11(9)21(14,18)19;/h1-5,15H,6H2,(H,16,17)(H2,14,18,19);/q;+1/p-1 |
| Isómeros SMILES | C1=COC(=C1)CNC2=CC(=C(C=C2C(=O)[O-])S(=O)(=O)N)Cl.[Na+] |
| PubChem CID | 23673593 |
| Peso molecular | 352.73 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Benzenesulfonamides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Aminobenzenesulfonamides |
| Alternative Parents | 4-halobenzoic acids Aminobenzoic acids Halobenzoic acids Benzenesulfonyl compounds Benzoic acids Aniline and substituted anilines Benzoyl derivatives Phenylalkylamines Secondary alkylarylamines Chlorobenzenes Organosulfonamides Aryl chlorides Heteroaromatic compounds Furans Vinylogous amides Aminosulfonyl compounds Carboxylic acid salts Amino acids Carboxylic acids Oxacyclic compounds Organic metal halides Organic oxides Organic sodium salts Organic zwitterions Organochlorides Organooxygen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Aminobenzenesulfonamide - Aminobenzoic acid - Aminobenzoic acid or derivatives - Halobenzoic acid - 4-halobenzoic acid - Halobenzoic acid or derivatives - 4-halobenzoic acid or derivatives - Benzenesulfonyl group - Benzoic acid or derivatives - Benzoic acid - Benzoyl - Phenylalkylamine - Aniline or substituted anilines - Chlorobenzene - Halobenzene - Secondary aliphatic/aromatic amine - Aralkylamine - Organosulfonic acid amide - Aryl chloride - Aryl halide - Heteroaromatic compound - Furan - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Vinylogous amide - Sulfonyl - Aminosulfonyl compound - Amino acid - Carboxylic acid salt - Amino acid or derivatives - Secondary amine - Organoheterocyclic compound - Organic metal halide - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Organic alkali metal salt - Organic oxide - Organic sodium salt - Organohalogen compound - Organochloride - Organonitrogen compound - Amine - Hydrocarbon derivative - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Organosulfur compound - Organic salt - Organic zwitterion - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as aminobenzenesulfonamides. These are organic compounds containing a benzenesulfonamide moiety with an amine group attached to the benzene ring. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 F2307459 | Certificate of Analysis | Mar 11, 2026 | F413242 |
| F2307460 | Certificate of Analysis | Mar 11, 2026 | F413242 |
| F2307461 | Certificate of Analysis | Mar 11, 2026 | F413242 |
| F2307462 | Certificate of Analysis | Mar 11, 2026 | F413242 |
| F2307463 | Certificate of Analysis | Mar 11, 2026 | F413242 |
| F2307465 | Certificate of Analysis | Mar 11, 2026 | F413242 |
| F2308069 | Certificate of Analysis | Mar 11, 2026 | F413242 |
| F2308124 | Certificate of Analysis | Mar 11, 2026 | F413242 |
| Solubilidad | Solubility (25°C) In vitro DMSO: 71 mg/mL (201.28 mM); Water: 71 mg/mL (201.28 mM); Ethanol: Insoluble; |
|---|---|
| Sensibilidad | Moisture sensitive |
| DMSO (mg/ml) Solubilidad máxima | 71 |
| DMSO (mM) Solubilidad máxima | 201.287103450231 |
| Agua (mg/ml) Solubilidad máxima | 71 |
| Agua (mM) Solubilidad máxima | 201.287103450231 |
| Peso molecular | 352.730 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 5 |
| Exact Mass | 351.99 Da |
| Monoisotopic Mass | 351.99 Da |
| Topological Polar Surface Area | 134.000 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 486.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 2 |
