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Sulfamonomethoxine

VETRANAL®, analytical standard

Sinónimos:

4-Amino-N-(6-methoxy-4-pyrimidinyl)benzenesulfonamide, 4-Methoxy-6-sulfanilamidopyrimidine, N1-(6-Methoxy-4-pyrimidinyl)sulfanilamide, SMM

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About This Item

Fórmula empírica (notación de Hill):
C11H12N4O3S
Número de CAS:
1220-83-3
Peso molecular:
280.30
Beilstein/REAXYS Number:
621128
MDL number:
MFCD00063466
UNSPSC Code:
41116107
PubChem Substance ID:
329753732
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤3.0% water

application(s)

clinical testing

format

neat

SMILES string

COc1cc(NS(=O)(=O)c2ccc(N)cc2)ncn1

InChI

1S/C11H12N4O3S/c1-18-11-6-10(13-7-14-11)15-19(16,17)9-4-2-8(12)3-5-9/h2-7H,12H2,1H3,(H,13,14,15)

InChI key

WMPXPUYPYQKQCX-UHFFFAOYSA-N

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General description

Chemical structure: sulfonamide
Sulfamonomethoxine is classified under the sulfonamide group of compounds.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulfamonomethoxine may be used as an analytical reference standard for the determination of sulfamonomethoxine in:
  • Tissues, milk and eggs of food-producing animals by ultrasound-assisted extraction (UAE) and liquid chromatography combined with tandem mass spectrometry (LC-MS/MS).
  • Food samples of animal origin by QuEChERS (quick, easy, cheap, effective, rugged and safe) extraction procedure, SOSLE (salting-out supported liquid extraction) method and nanoflow liquid chromatography high resolution mass spectrometry (LC-HRMS).
  • Bovine muscles by hydrophilic interaction liquid chromatography (HILIC) combined with LC-MS/MS.
  • Commercial eggs by liquid-liquid extraction (LLE), hybrid solid-phase extraction (SPE) and LC-MS/MS.

Legal Information

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
BCCH7473
BCCF3645
BCCD0481
BCCC2218
BCCB7996

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Multiresidue method for the simultaneous determination of veterinary medicinal products, feed additives and illegal dyes in eggs using liquid chromatography-tandem mass spectrometry.
Piatkowska M, et al.
Food Chemistry, 197, 571-580 (2016)
Analysis of trace levels of sulfonamides in fish tissue using micro-scale pipette tip-matrix solid-phase dispersion and fast liquid chromatography tandem mass spectrometry.
Shen Q, et al.
Food Chemistry, 194, 508-515 (2016)
Matrix-effect free multi-residue analysis of veterinary drugs in food samples of animal origin by nanoflow liquid chromatography high resolution mass spectrometry.
Alcantara-Duran J, et al.
Food Chemistry, 245, 29-38 (2018)
G Zhang et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 25(4), 413-423 (2008-03-19)
A rapid lateral flow immunoassay screening method has been developed for the determination of sulfamonomethoxine (SMM) residues in swine urine. For this purpose, a specific monoclonal antibody (mAb), SMM4B9 for SMM, was generated and characterized. The mAb showed low cross-reactivity
Hiromi Ito et al.
Carbohydrate research, 338(16), 1621-1639 (2003-07-23)
Systematic synthesis and myelin-associated glycoprotein (MAG)-binding activity of novel sulfated GM1b analogues structurally related to Chol-1 (alpha-series) gangliosides, high-affinity ligands for neural siglecs, are described. The suitably protected gangliotriose derivatives, 2-(trimethylsilyl)ethyl 2-acetamido-2-deoxy-6-O-levulinoyl-beta-D-galactopyranosyl-(1-->4)-2,3,6-tri-O-benzyl-beta-D-galactopyranosyl-(1-->4)-2,3,6-tri-O-benzyl-beta-D-glucopyranoside and 2-(trimethylsilyl)ethyl 2-acetamido-2-deoxy-6-O-levulinoyl-beta-D-galactopyranosyl-(1-->4)-2,6-di-O-benzyl-3-O-levulinoyl-beta-D-galactopyranosyl-(1-->4)-2,3,6-tri-O-benzyl-beta-D-glucopyranoside were each glycosylated with alpha-NeuAc-(2-->3)-galactose
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