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31739

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Sulfisoxazole

VETRANAL®, analytical standard

Synonyme(s) :

4-amino-N-(3,4-diméthyl-5-isoxazolyl)benzènesulfonamide

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About This Item

Formule empirique (notation de Hill):
C11H13N3O3S
Numéro CAS:
127-69-5
Poids moléculaire :
267.30
Numéro Beilstein :
6737262
Numéro CE :
204-858-9
Numéro MDL:
MFCD00003150
Code UNSPSC :
41116107
ID de substance PubChem :
329753912
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

VETRANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

forensics and toxicology
pharmaceutical (small molecule)

Format

neat

Chaîne SMILES 

Cc1noc(NS(=O)(=O)c2ccc(N)cc2)c1C

InChI

1S/C11H13N3O3S/c1-7-8(2)13-17-11(7)14-18(15,16)10-5-3-9(12)4-6-10/h3-6,14H,12H2,1-2H3

Clé InChI

NHUHCSRWZMLRLA-UHFFFAOYSA-N

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Description générale

Sulfisoxazole belongs to the sulfonamide class of antibacterial compounds.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulfisoxazole may be used as a reference standard for the determination of sulfisoxazole in:
  • Honey after acidic hydrolysis by using post-column derivatization and high performance liquid chromatography (HPLC)-fluorescence detection.
  • Hospital, urban wastewater and river water by automated off-line solid phase extraction (SPE) followed by analysis using ultra-high-performance liquid chromatography combined with quadrupole linear ion trap tandem mass spectrometry (UHPLC-QqLIT).
  • Foodstuffs of animal origin by UHPLC coupled to tandem mass spectrometry (MS/MS).
  • Raw milk samples by SPE followed by UPLC equipped with time of flight mass spectrometry (TOF MS).

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Informations légales

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
BCCG6595
BCBW6421
BCBT2201
SZBC109XV
SZB7116XV

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Rapid analysis of multiclass antibiotic residues and some of their metabolites in hospital, urban wastewater and river water by ultra-high-performance liquid chromatography coupled to quadrupole-linear ion trap tandem mass spectrometry
Gros M, et al.
Journal of Chromatography A, 1292(1), 173-188 (2013)
Quantitative analysis of twelve sulfonamides in honey after acidic hydrolysis by high-performance liquid chromatography with post-column derivatization and fluorescence detection
Maudens KE, et al.
Journal of Chromatography A, 1047(1), 85-92 (2004)
Comprehensive fast multiresidue screening of 150 veterinary drugs in milk by ultra-performance liquid chromatography coupled to time of flight mass spectrometry
Ortelli D, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 877(23), 2363-2374 (2009)
Application of ion-exchange cartridge clean-up in food analysis: V. Simultaneous determination of sulphonamide antibacterials in animal liver and kidney using high-performance liquid chromatography with ultraviolet and mass spectrometric detection
Ito Y, et al.
Journal of Chromatography A, 898(1), 95-102 (2000)
Melina Mondelli et al.
Journal of inorganic biochemistry, 102(2), 285-292 (2007-11-03)
The synthesis, structural characterization, voltammetric experiments and antibacterial activity of [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] were studied and compared with similar previously reported copper complexes. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O crystallized in a monoclinic system, space group C2/c where the nickel ion was in a slightly
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