Skip to Content
Merck
All Photos(3)

Key Documents

More Documents

225193

Sigma-Aldrich

Sodium 3-nitrobenzenesulfonate

98%

Synonym(s):

3-Nitrobenzenesulfonic acid sodium salt

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
O2NC6H4SO3Na
CAS Number:
127-68-4
Molecular Weight:
225.15
Beilstein:
3639982
EC Number:
204-857-3
MDL number:
MFCD00007490
UNSPSC Code:
12352100
PubChem Substance ID:
24853484
NACRES:
NA.22

Quality Level

100

Assay

98%

solubility

water: 50 mg/mL, clear to slightly hazy, faintly yellow to yellow

SMILES string

[Na+].[O-][N+](=O)c1cccc(c1)S([O-])(=O)=O

InChI

1S/C6H5NO5S.Na/c8-7(9)5-2-1-3-6(4-5)13(10,11)12;/h1-4H,(H,10,11,12);/q;+1/p-1

InChI key

LJRGBERXYNQPJI-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Sodium 3-nitrobenzenesulfonate (3-Nitrobenzenesulfonic acid sodium salt) was used in the synthesis of quinoline.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H317 - H319

Hazard Classifications

Eye Irrit. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Trifluoroacetic acid ReagentPlus®, 99%

Sigma-Aldrich

T6508

Trifluoroacetic acid

Jay P Kitt et al.
Journal of the American Chemical Society, 139(10), 3851-3860 (2017-02-22)
Permeabilization of the outer mitochondrial membrane is an integral step in apoptosis. The resulting release of pro-apoptotic signaling proteins leads to cell destruction through activation of the cysteine-aspartic protease (caspase) cascade. However, the mechanism of outer mitochondrial membrane (OMM) permeabilization
V Calderara et al.
Water science and technology : a journal of the International Association on Water Pollution Research, 44(5), 7-13 (2001-11-07)
This paper describes the ozone oxidation kinetics of 1-naphthalene (1 NS), 1,5-naphthalene (1,5NDS), and 3-nitrobenzene (3NBS) sulphonic acid. The presence of hydroxyl radicals and their effect on the overall rate of reaction was studied. Second order kinetic constants of direct
Hao Xu et al.
Science (New York, N.Y.), 327(5968), 986-990 (2010-02-20)
Cationic organic intermediates participate in a wide variety of useful synthetic transformations, but their high reactivity can render selectivity in competing pathways difficult to control. Here, we describe a strategy for inducing enantioselectivity in reactions of protio-iminium ions, wherein a
Dwight Macdonald et al.
Bioorganic & medicinal chemistry letters, 15(23), 5241-5246 (2005-09-20)
The discovery and SAR of a new series of substituted 8-arylquinoline PDE4 inhibitors are herein described. This work has led to the identification of several compounds with excellent in vitro and in vivo profiles, including a good therapeutic window of
Nichina Gomi et al.
Biodegradation, 22(6), 1239-1245 (2011-04-29)
We examined the degradation of amaranth, a representative azo dye, by Bjerkandera adusta Dec 1. The degradation products were analyzed by high performance liquid chromatography (HPLC), visible absorbance, and electrospray ionization time-of-flight mass spectroscopy (ESI-TOF-MS). At the primary culture stage
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service