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S5632

Supelco

Sulfaméthizol

analytical standard, ≥99% (HPLC)

Synonyme(s) :

4-amino-N-(5-méthyl-1,3,4-thiadiazol-2-yl)benzènesulfonamide

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About This Item

Formule empirique (notation de Hill):
C9H10N4O2S2
Numéro CAS:
144-82-1
Poids moléculaire :
270.33
Numéro Beilstein :
255002
Numéro CE :
205-641-1
Numéro MDL:
MFCD00053363
Code UNSPSC :
41116107
ID de substance PubChem :
329824459
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Agence

EPA 1694

Pureté

≥99% (HPLC)

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

clinical testing

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

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)

Clé InChI

VACCAVUAMIDAGB-UHFFFAOYSA-N

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Description générale

Sulfamethizole is an antibacterial drug used in the treatment of the urinary tract infections.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulfamethizole may be used as a reference standard to examine the antibiotic remnants in honey by multianalyte/multiclass ultra-performance liquid chromatography–tandem mass spectrometry (UPLC–MS/MS) method.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H317

Conseils de prudence

P280

Classification des risques

Skin Sens. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
MKCV0123
MKCV3152
MKCS0622
MKCR4942
MKCN7577

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Coordination chemistry of sulfamethizole: crystal structures of [Cu (sulfamethizolate) 2 (py) 2 (OH 2)]? H 2 O,[M (sulfamethizolate) 2 (py) 2 (OH 2) 2][M= Co and Ni] and {Cu (sulfamethizolate) 2 (dmf) 2}?.
Borras E, et al.
Polyhedron, 19(15), 1859-1866 (2000)
Development of a rapid method for the determination of antibiotic residues in honey using UPLC-ESI-MS/MS.
Kivrak I, et al.
Food Sci. Technol., 36(1), 90-96 (2016)
Tony L Yaksh et al.
Anesthesiology, 108(5), 938-949 (2008-04-24)
Intrathecal N-methyl-d-aspartate antagonists have antihyperalgesic efficacy. The authors examined toxicity in a canine model of chronic lumbar intrathecal infusion. Dogs (10-16 kg) were prepared with lumbar intrathecal catheters connected to vest-mounted pumps (100 microl/h). In phase 1, stepwise incrementations in
Mark R Sannes et al.
The Journal of infectious diseases, 197(3), 430-434 (2008-01-11)
To determine whether poultry contact/consumption predicts colonization with antimicrobial-resistant Escherichia coli, 567 newly hospitalized patients and 100 vegetarians were assessed microbiologically and epidemiologically. Multivariable analysis showed that poultry contact/consumption, other dietary habits, and antimicrobial use did not significantly predict resistance.
Robert R Muder
Seminars in respiratory and critical care medicine, 28(6), 672-677 (2007-12-21)
Stenotrophomonas (Xanthomonas) maltophilia is a nonfermentative, gram-negative bacillus that is widely distributed in natural and human-made environments. In the nonhospital setting it is an uncommon pathogen, typically causing soft tissue infection of contaminated wounds. In the hospital setting, particularly among
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