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· · COA & SDS available for every product · Same-day shipping on in-stock items DC 260126 - ≥98%(HPLC) , CAS No.346692-04-4
Synonyms
WNA69204 | C74786 | MFCD00784423 | N-(4-Butylphenyl)-4-fluorobenzene-1-sulfonamide | BDBM50196405 | N-(4-butylphenyl)-4-fluorobenzenesulfonamide | AKOS003265834 | SCHEMBL18058899 | BCP32685 | NCGC00387268-04 | HY-101906 | Oprea1_825888 | STK076838 | A8996
Shipped In
Ice chest + Ice pads
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
WNA69204 | C74786 | MFCD00784423 | N-(4-Butylphenyl)-4-fluorobenzene-1-sulfonamide | BDBM50196405 | N-(4-butylphenyl)-4-fluorobenzenesulfonamide | AKOS003265834 | SCHEMBL18058899 | BCP32685 | NCGC00387268-04 | HY-101906 | Oprea1_825888 | STK076838 | A8996
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
DC260126 is a FFA1 (GPR40) selective antagonist. In FFA1-expressing CHO cells, DC260126 blocks linoleic acid-induced Ca2+ elevation and ERK phosphorylation (IC50 = 6028 μM), as well as palmitic acid potentiated glucose-stimulated insulin secretion. The co
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 504762235 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504762235 Canonical Smiles CCCCC1=CC=C(C=C1)NS(=O)(=O)C2=CC=C(C=C2)F IUPAC Name N-(4-butylphenyl)-4-fluorobenzenesulfonamide InChIKey CNGHPXKWPGIDSK-UHFFFAOYSA-N INCHI 1S/C16H18FNO2S/c1-2-3-4-13-5-9-15(10-6-13)18-21(19,20)16-11-7-14(17)8-12-16/h5-12,18H,2-4H2,1H3 Isomeric SMILES CCCCC1=CC=C(C=C1)NS(=O)(=O)C2=CC=C(C=C2)F Molecular Weight 307.38 Reaxy-Rn 24554546 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24554546&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Class Benzene and substituted derivatives Subclass Sulfanilides Intermediate Tree Nodes Not available Direct Parent Sulfanilides Alternative Parents Benzenesulfonamides Benzenesulfonyl compounds Fluorobenzenes Organosulfonamides Aryl fluorides Aminosulfonyl compounds Organopnictogen compounds Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Organosulfonic acid amide - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Organosulfur compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:DMSO, Max Conc. mg/mL: 30.74, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 30.74, Max Conc. mM: 100 Molecular Weight 307.400 g/mol XLogP3 4.400 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 6 Exact Mass 307.104 Da Monoisotopic Mass 307.104 Da Topological Polar Surface Area 54.600 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 391.000 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 1
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