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Sulfanilamide

Name: Sulfanilamide
Brand: SIAL

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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Properties

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

SMILES string

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

InChI

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

InChI key

FDDDEECHVMSUSB-UHFFFAOYSA-N

Description

General description

Sulfanilamide is an antibacterial drug.

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.

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This Item	1632004	46874	33626
S2151000 Sulfanilamide	USP 1632004 Sulfanilamide	Supelco 46874 Sulfanilamide	Sigma-Aldrich 33626 Sulfanilamide
grade pharmaceutical primary standard	grade pharmaceutical primary standard	grade analytical standard	grade -
manufacturer/tradename EDQM	manufacturer/tradename USP	manufacturer/tradename -	manufacturer/tradename -
application(s) pharmaceutical (small molecule)	application(s) pharmaceutical (small molecule)	application(s) clinical testing	application(s) -
format neat	format neat	format neat	format -
mp 164-166 °C (lit.)	mp 164-166 °C (lit.)	mp 164-166 °C (lit.)	mp 163-166 °C, 164-166 °C (lit.)
API family sulfanilamide	API family sulfanilamide	API family -	API family -

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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)

Second messengers mediating the proliferation and collagen synthesis of tenocytes induced by low-level laser irradiation.

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

Equine mesenchymal stem cells inhibit T cell proliferation through different mechanisms depending on tissue source.

Danielle D Carrade Holt et al.

Stem cells and development, 23(11), 1258-1265 (2014-01-21)

Mesenchymal stem cells (MSCs) are used in both human clinical trials and veterinary medicine for the treatment of inflammatory and immune-mediated diseases. MSCs modulate inflammation by decreasing the cells and products of the inflammatory response. Stimulated equine MSCs from bone

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Global Trade Item Number

SKU	GTIN
S2151000	04061836917807

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