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S2050000

Sulfamethizol

European Pharmacopoeia (EP) Reference Standard

Synonym(e):

4-Amino-N-(5-methyl-1,3,4-thiadiazol-2-yl)-benzolsulfonamid, N1-(5-Methyl-1,3,4-thiadiazol-2-yl)-sulfanilamid, Sulfamethylthiadiazol

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About This Item

Empirische Formel (Hill-System):
C9H10N4O2S2
CAS-Nummer:
144-82-1
Molekulargewicht:
270.33
Beilstein:
255002
MDL-Nummer:
MFCD00053363
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329824503
NACRES:
NA.24

Qualität

pharmaceutical primary standard

API-Familie

sulfamethizole

Hersteller/Markenname

EDQM

Anwendung(en)

pharmaceutical (small molecule)

Format

neat

Lagertemp.

2-8°C

SMILES String

Cc1nnc(NS(=O)(=O)c2ccc(N)cc2)s1

InChI

1S/C9H10N4O2S2/c1-6-11-12-9(16-6)13-17(14,15)8-4-2-7(10)3-5-8/h2-5H,10H2,1H3,(H,12,13)

InChIKey

VACCAVUAMIDAGB-UHFFFAOYSA-N

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Allgemeine Beschreibung

Sulfamethizole is a sulfonamide derivative used as an antimicrobial drug for the prevention and cure of bacterial infections in both humans and animals.
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Anwendung

This European Pharmacopoeia reference standard is intended for use only as specifically prescribed in the European Pharmacopoeia.

Verpackung

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Sonstige Hinweise

Sales restrictions may apply.

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Preisangaben

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H317

P-Sätze

P280

Gefahreneinstufungen

Skin Sens. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

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Analysenzertifikate (COA)

Lot/Batch Number

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Susceptibility of Danish Escherichia coli strains isolated from urinary tract infections and bacteraemia, and distribution of sul genes conferring sulphonamide resistance.
Kerrn M B, et al.
The Journal of Antimicrobial Chemotherapy, 50(4), 513-516 (2002)
Solubility of sulfamethizole in some propylene glycol+ water mixtures at several temperatures.
Delgado D R, et al.
Fluid Phase Equilibria, 322, 113-119 (2012)
Adrian I Campos et al.
Molecular cell, 74(6), 1291-1303 (2019-05-03)
Alternative to the conventional search for single-target, single-compound treatments, combination therapies can open entirely new opportunities to fight antibiotic resistance. However, combinatorial complexity prohibits experimental testing of drug combinations on a large scale, and methods to rationally design combination therapies
Images in clinical medicine. Actinomycetoma.
Manuelle Viguier et al.
The New England journal of medicine, 372(3), 264-264 (2015-01-15)
Yong-Gang Zhao et al.
Journal of chromatography. A, 1345, 17-28 (2014-05-02)
A novel, simple and sensitive method was developed for the simultaneous determination of 22 sulfonamides (SAs) in chicken breast muscle by using the dispersive micro-solid-phase extraction (d-μ-SPE) procedure combined with ultra-fast liquid chromatography-tandem quadrupole mass spectrometry (UFLC-MS/MS). The excellent core-shell
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