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Sulfanilamide

Name: Sulfanilamide
Brand: USP

United States Pharmacopeia (USP) 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:

329751186

MDL number:

MFCD00007939

Beilstein/REAXYS Number:

511852

eCl@ss:

39093202

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Properties

grade

pharmaceutical primary standard

API family

sulfanilamide

manufacturer/tradename

USP

mp

164-166 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

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.

Application

Sulfanilamide USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia. Also, for use with USP monographs such as:

Silver Sulfadiazine
Sulfacetamide Sodium
Sulfamethoxazole
Sulfamethoxazole and Trimethoprim Injection

Analysis Note

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.

Other Notes

Sales restrictions may apply.

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This Item	S2151000	46874	PHR1184
USP 1632004 Sulfanilamide	S2151000 Sulfanilamide	Supelco 46874 Sulfanilamide	Supelco PHR1184 Sulfanilamide
grade pharmaceutical primary standard	grade pharmaceutical primary standard	grade analytical standard	grade certified reference material, pharmaceutical secondary standard
manufacturer/tradename USP	manufacturer/tradename EDQM	manufacturer/tradename -	manufacturer/tradename -
format neat	format neat	format neat	format neat
application(s) pharmaceutical (small molecule)	application(s) pharmaceutical (small molecule)	application(s) clinical testing	application(s) pharmaceutical (small molecule)
API family sulfanilamide	API family sulfanilamide	API family -	API family sulfanilamide
mp 164-166 °C (lit.)	mp 164-166 °C (lit.)	mp 164-166 °C (lit.)	mp -

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Storage Class

11 - Combustible Solids

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
1632004-5G	04061838747471

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