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33626

Sigma-Aldrich

Sulfanilamide

puriss. p.a., ≥98% (calc. to the dried substance)

Synonyme(s) :

p-Aminobenzenesulfonamide

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About This Item

Formule linéaire :
H2NC6H4SO2NH2
Numéro CAS:
63-74-1
Poids moléculaire :
172.20
Numéro Beilstein :
511852
Numéro CE :
200-563-4
Numéro MDL:
MFCD00007939
Code UNSPSC :
12352100
eCl@ss :
39093202
ID de substance PubChem :
57648871
Nomenclature NACRES :
NA.21

Qualité

puriss. p.a.

Niveau de qualité

100

Pureté

≥98% (calc. to the dried substance)

Forme

solid

Impuretés

≤0.002% heavy metals (as Pb)

Résidus de calcination

≤0.1% (as SO4)

Perte

≤0.5% loss on drying, 105 °C

Couleur

white to faint beige

Pf

163-166 °C
164-166 °C (lit.)

Traces d'anions

chloride (Cl-): ≤100 mg/kg
sulfate (SO42-): ≤200 mg/kg

Spectre d'activité de l'antibiotique

Gram-negative bacteria
Gram-positive bacteria

Mode d’action

DNA synthesis | interferes
enzyme | inhibits

Chaîne SMILES 

Nc1ccc(cc1)S(N)(=O)=O

InChI

1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)

Clé InChI

FDDDEECHVMSUSB-UHFFFAOYSA-N

Informations sur le gène

human ... CA1(759) , CA2(760) , CA5A(763) , CA5B(11238) , CA9(768)
mouse ... Car13(71934) , Car5a(12352)

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Catégories apparentées

Description générale

Chemical structure: sulfonamide
Sulfanilamide (p-Aminobenzenesulfonamide) is a para-amino substituted benzenesulfonamide. Its ortho-mono and diiodo derivatives have been synthesized.

Application

  • Study of new azo-azomethine derivatives of sulfanilamide: synthesis, characterization, spectroscopic, antimicrobial, antioxidant and anticancer activity: This study explores new derivatives of sulfanilamide synthesized through diazonium salt reactions and coupling with 2-hydroxy-3-methoxybenzaldehyde, providing insights into their potential antimicrobial, antioxidant, and anticancer activities (HS Al-Atbi, IJ Al-Assadi, et al., 2020).

Conditionnement

33626-100G; 33626-6X100G

Autres remarques

Keep container tightly closed in a dry and well-ventilated place.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Certificats d'analyse (COA)

Lot/Batch Number
BCCG9106
BCCF1962
BCCF0496
BCCC8160
BCCC7803

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Caroline A Dobbin et al.
Journal of immunology (Baltimore, Md. : 1950), 169(2), 958-965 (2002-07-05)
We propose that the 70-kDa heat shock protein (HSP70) protects virulent Toxoplasma gondii from the effects of the host by immunomodulation. This hypothesis was tested using quercetin and antisense oligonucleotides targeting the start codon of the virulent T. gondii HSP70
The Iodination of p-Aminobenzenesulfonamide and Some Symmetrical Azobenzenesulfonamides.
Scudi JV.
Journal of the American Chemical Society, 59(8), 1480-1483 (1937)
Joseph A Hollenbaugh et al.
Journal of immunology (Baltimore, Md. : 1950), 177(5), 3004-3011 (2006-08-22)
We previously reported that IFN-gamma secreted by donor cytotoxic T cell 1 (Tc1) cells was the most important factor in promoting EG7 (an OVA transfection the EL4 thymoma) rejection in mice. In this study, we show that the ability of
Traci L Ness et al.
Journal of immunology (Baltimore, Md. : 1950), 173(11), 6938-6948 (2004-11-24)
CCR1 has previously been shown to play important roles in leukocyte trafficking, pathogen clearance, and the type 1/type 2 cytokine balance, although very little is known about its role in the host response during sepsis. In a cecal ligation and
Edward E Knaus et al.
Bioorganic & medicinal chemistry letters, 21(19), 5892-5896 (2011-08-20)
A series of compounds incorporating regioisomeric phenylethynylbenzenesulfonamide moieties has been investigated for the inhibition of four human carbonic anhydrase (hCA, EC 4.2.1.1) isoforms, hCA I, II, IX and XII. Inhibition between the low nanomolar to the milliomolar range has been
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