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Merck
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76177

Supelco

Sulfamethoxazole

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Synonym(s):

4-Amino-N-(5-methyl-3-isoxazolyl)benzenesulfonamide, N1-(5-Methylisoxazol-3-yl)sulfanilamide

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150 UNITS
CN¥3,624.54

CN¥3,624.54

Available to ship onApril 27, 2025Details

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150 UNITS
CN¥3,624.54

About This Item

Empirical Formula (Hill Notation):
C10H11N3O3S
CAS Number:
723-46-6
Molecular Weight:
253.28
Beilstein:
6732984
EC Number:
211-963-3
MDL number:
MFCD00010546
UNSPSC Code:
41116107
PubChem Substance ID:
329766577
NACRES:
NA.24

CN¥3,624.54

Available to ship onApril 27, 2025Details

Request a Bulk Order

grade

certified reference material
TraceCERT®

Quality Level

300

product line

TraceCERT®

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

clinical testing

format

neat

SMILES string

Cc1cc(NS(=O)(=O)c2ccc(N)cc2)no1

InChI

1S/C10H11N3O3S/c1-7-6-10(12-16-7)13-17(14,15)9-4-2-8(11)3-5-9/h2-6H,11H2,1H3,(H,12,13)

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This Item
112077419101109327491011988506001
抗 荧光素-AP、Fab 片段 from sheep

11426338910

抗 荧光素-AP、Fab 片段

抗-地高辛-荧光素，Fab片段 from sheep

11207741910

抗-地高辛-荧光素，Fab片段

抗地高辛-AP，Fab片段 from sheep

11093274910

抗地高辛-AP，Fab片段

抗-HA-荧光素，高亲和力 from rat IgG1

11988506001

抗-HA-荧光素，高亲和力

antibody form

affinity purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

clone

polyclonal

clone

polyclonal

clone

polyclonal

clone

3F10, monoclonal

conjugate

alkaline phosphatase conjugate

conjugate

fluorescein conjugate

conjugate

alkaline phosphatase conjugate

conjugate

fluorescein conjugate

biological source

sheep

biological source

sheep

biological source

sheep

biological source

rat

form

solution

form

lyophilized

form

solution

form

lyophilized

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

General description

Chemical structure: sulfonamide
This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Application

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

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Legal Information

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

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Warning

Hazard Statements

H361fd,H411

Hazard Classifications

Aquatic Chronic 2 - Repr. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

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    Ming Xie et al.
    Water research, 47(13), 4567-4575 (2013-06-15)
    The impact of humic acid fouling on the membrane transport of two pharmaceutically active compounds (PhACs) - namely carbamazepine and sulfamethoxazole - in forward osmosis (FO) was investigated. Deposition of humic acid onto the membrane surface was promoted by the
    Hao Zheng et al.
    Environmental pollution (Barking, Essex : 1987), 181, 60-67 (2013-07-03)
    Sorption of sulfonamides on biochars is poorly understood, thus sulfamethoxazole (SMX) sorption on biochars produced at 300-600 °C was determined as a function of pH and SMX concentration, as well as the inorganic fractions in the biochars. Neutral SMX molecules
    Alexandra G Gonçalves et al.
    Journal of hazardous materials, 239-240, 167-174 (2012-09-27)
    Two carbon materials (multi-walled carbon nanotubes, MWCNTs, and activated carbon) were investigated as ozonation catalysts for the mineralization of the antibiotic sulphamethoxazole (SMX). MWCNTs presented a higher catalytic performance than activated carbons, which was justified by their differences in surface
    Karl J Schreiber et al.
    BMC plant biology, 12, 226-226 (2012-11-28)
    The sulfanilamide family comprises a clinically important group of antimicrobial compounds which also display bioactivity in plants. While there is evidence that sulfanilamides inhibit folate biosynthesis in both bacteria and plants, the complete network of plant responses to these compounds
    Trimethoprim-sulfamethoxazole-associated aseptic meningitis: case reports and review of the literature.
    A M Joffe et al.
    The American journal of medicine, 87(3), 332-338 (1989-09-01)
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