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Merck
CN

46826

磺胺甲基嘧啶

VETRANAL®, analytical standard

别名:

4-氨基-N-(4-甲基-2-嘧啶基)苯磺酰胺, N1-(4-甲基嘧啶-2-基)磺胺

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关于此项目

经验公式(希尔记法):
C11H12N4O2S
化学文摘社编号:
分子量:
264.30
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
204-866-2
Beilstein/REAXYS Number:
249133
MDL number:
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InChI key

QPPBRPIAZZHUNT-UHFFFAOYSA-N

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)

SMILES string

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

grade

analytical standard

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

Quality Level

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General description

化学结构:磺胺
磺胺嘧啶是一种磺胺类抗生素,主要用于预防人和动物中的细菌感染。

Application

有关合适仪器技术的更多信息,请参考产品分析证书。如需进一步支持,请联系技术服务。
磺胺嘧啶可作为参考标准品用于使用阳离子交换反相吸附剂对动物肌肉、肝脏和肾脏组织中的磺胺类抗生素进行测定,以用于样品纯化并通过高效液相色谱和二极管阵列检测进行分析。

Legal Information

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

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

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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)
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
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)
Florian M Koch et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(13), 3679-3692 (2011-03-03)
The first catalytic asymmetric synthesis of β-sultones is reported. This development has enabled a rapid access to a number of highly enantioenriched biologically interesting sulfonyl and sulfinyl compound classes, which makes use of the inherent ring strain of the four-membered

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