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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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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)
Solubility and solution thermodynamics of sulfamerazine and sulfamethazine in some ethanol+ water mixtures.
Delgado DR, et al.
Fluid Phase Equilibria, 360, 88-96 (2013)
Xian Zhang et al.
Environmental science and pollution research international, 19(5), 1392-1404 (2012-06-30)
Estrogenic compounds and antibiotic residues in environment are receiving significant attention because of their potential adverse effects on ecosystems and human health. The objectives of this study were to determine the occurrence and seasonal variability of eight kinds of estrogenic
Jia Pan et al.
Chemical communications (Cambridge, England), 47(1), 352-354 (2010-08-24)
A phosphine-mediated one-step disulfide formation from S-nitrosothiols has been developed. This reaction can convert unstable S-nitrosothiols to stable disulfides via sulfenamide intermediates under very mild conditions. It has the potential to be used for the detection of S-nitrosothiols.
Regioselective hydroxysulfenylation of alpha,beta-unsaturated imines: enhanced stability of an intermediate radical.
Masafumi Ueda et al.
Angewandte Chemie (International ed. in English), 47(30), 5600-5604 (2008-06-17)

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