Skip to Content
Merck

Key Documents

View All Documentation

32091

Sulfamonomethoxine

VETRANAL®, analytical standard

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C11H12N4O3S
CAS Number:
1220-83-3
Molecular Weight:
280.30
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753732
MDL number:
MFCD00063466
Beilstein/REAXYS Number:
621128
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

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

General description

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

Application

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.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

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

Still not finding the right product?

Explore all of our products under Sulfamonomethoxine

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

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCM3578
BCCH7473
BCCF3645
BCCD0481
BCCC2218

Don't see the Right Version?

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

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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
View All Related Papers