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Merck

S2151000

Sulfanilamide

European Pharmacopoeia (EP) Reference Standard

Synonym(s):

p-Aminobenzenesulfonamide

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About This Item

Linear Formula:
H2NC6H4SO2NH2
CAS Number:
63-74-1
Molecular Weight:
172.20
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329824507
MDL number:
MFCD00007939
Beilstein/REAXYS Number:
511852

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InChI

1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)

SMILES string

Nc1ccc(cc1)S(N)(=O)=O

InChI key

FDDDEECHVMSUSB-UHFFFAOYSA-N

grade

pharmaceutical primary standard

API family

sulfanilamide

manufacturer/tradename

EDQM

mp

164-166 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

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1 of 4

This Item
3362616330071632004
Sulfanilamide European Pharmacopoeia (EP) Reference Standard

S2151000

Sulfanilamide

Sulfanilamide puriss. p.a., ≥98% (calc. to the dried substance)

Sigma-Aldrich

33626

Sulfanilamide

Sulfanilamide Melting Point Standard United States Pharmacopeia (USP) Reference Standard

USP

1633007

Sulfanilamide Melting Point Standard

Sulfanilamide United States Pharmacopeia (USP) Reference Standard

USP

1632004

Sulfanilamide

grade

pharmaceutical primary standard

grade

-

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

manufacturer/tradename

EDQM

manufacturer/tradename

-

manufacturer/tradename

USP

manufacturer/tradename

USP

application(s)

pharmaceutical (small molecule)

application(s)

-

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

format

neat

format

-

format

neat

format

neat

API family

sulfanilamide

API family

-

API family

sulfanilamide

API family

sulfanilamide

mp

164-166 °C (lit.)

mp

163-166 °C, 164-166 °C (lit.)

mp

164-166 °C (lit.)

mp

164-166 °C (lit.)

General description

Sulfanilamide is an antibacterial drug.[1]
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Application

This European Pharmacopoeia reference standard is intended for use only as specifically prescribed in the European Pharmacopoeia.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

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SPECTROSCOPIC STUDIES OF CUTANEOUS PHOTOSENSITIZING AGENTS?II. SPIN TRAPPING OF PHOTOLYSIS PRODUCTS FROM SULFANILAMIDE AND 4-AMINOBENZOIC ACID USING 5, 5-DIMETHYL-1-PYRROLINE-1-OXIDE.
Chignell, Colin F., et al.
Photochemistry and Photobiology, 34.2 , 147-156 (1981)
Danielle D Carrade Holt et al.
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Guilherme B Bubols et al.
Prenatal diagnosis, 34(13), 1268-1276 (2014-07-22)
Because we have previously demonstrated the relation between polyphenol-rich foods (PRF) consumption and ductus arteriosus constriction, in this work, pregnant sheep were submitted to oral PRF intake for 14 days to understand how this process occurs. Fetal Doppler echocardiography, oxidative and
Mei-Hsiu Chen et al.
Lasers in medical science, 30(1), 263-272 (2014-09-19)
For decades, low-level laser therapy (LLLT) has widespread applications in tendon-related injuries. Although the therapeutic effect of LLLT could be explained by photostimulation of target tissue and cells, how tenocytes sense photonic energy and convert them into cascades of cellular
Mohammad Islamuddin et al.
PLoS neglected tropical diseases, 9(1), e3321-e3321 (2015-01-09)
In the absence of vaccines and limitations of currently available chemotherapy, development of safe and efficacious drugs is urgently needed for visceral leishmaniasis (VL) that is fatal, if left untreated. Earlier we reported in vitro apoptotic antileishmanial activity of n-hexane
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