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Sulfamerazine

VETRANAL®, analytical standard

Synonym(s):

4-Amino-N-(4-methyl-2-pyrimidinyl)benzenesulfonamide, N1-(4-Methylpyrimidin-2-yl)sulfanilamide

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About This Item

Empirical Formula (Hill Notation):
C11H12N4O2S
CAS Number:
Molecular Weight:
264.30
Beilstein:
249133
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Agency

EPA 1694

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

clinical testing

format

neat

SMILES string

Cc1ccnc(NS(=O)(=O)c2ccc(N)cc2)n1

InChI

1S/C11H12N4O2S/c1-8-6-7-13-11(14-8)15-18(16,17)10-4-2-9(12)3-5-10/h2-7H,12H2,1H3,(H,13,14,15)

InChI key

QPPBRPIAZZHUNT-UHFFFAOYSA-N

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General description

Chemical structure: sulfonamide
Sulfamerazine is a sulfonamide antibiotic, used mainly to prevent bacterial infections in both humans and animals.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulfamerazine may be used as a reference standard for the determination of sulfonamide antibiotics in animal muscle, liver and kidney tissues using cation exchange reversed phase sorbent for sample clean-up and analysis by high performance liquid chromatography with diode array detection.

Legal Information

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Solubility and solution thermodynamics of sulfamerazine and sulfamethazine in some ethanol+ water mixtures.
Delgado DR, et al.
Fluid Phase Equilibria, 360, 88-96 (2013)
Determination of sulfonamides in animal tissues using cation exchange reversed phase sorbent for sample cleanup and HPLC-DAD for detection.
Hela W, et al.
Food Chemistry, 83(4), 601-608 (2003)
A practical sulfenylation of 2,5-diketopiperazines.
K C Nicolaou et al.
Angewandte Chemie (International ed. in English), 51(3), 728-732 (2011-12-14)
Yi Li et al.
International journal of pharmaceutics, 415(1-2), 110-118 (2011-06-08)
The ability to detect and quantify polymorphism of pharmaceuticals is critically important in ensuring that the formulated product delivers the desired therapeutic properties because different polymorphic forms of a drug exhibit different solubilities, stabilities and bioavailabilities. The purpose of this
Lionel Billiet et al.
Free radical biology & medicine, 52(8), 1473-1485 (2012-02-14)
Protein sulfenic acids are essential cysteine oxidations in cellular signaling pathways. The thermodynamics that drive protein sulfenylation are not entirely clear. Experimentally, sulfenic acid reduction potentials are hard to measure, because of their highly reactive nature. We designed a calculation

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