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MilliporeSigma

275247

4-(2-Aminoethyl)benzenesulfonamide

99%

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25 G

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About This Item

Linear Formula:
H2NCH2CH2C6H4SO2NH2
CAS Number:
35303-76-5
Molecular Weight:
200.26
EC Number:
252-501-0
MDL number:
MFCD00010301
UNSPSC Code:
12352100
PubChem Substance ID:
24856636
NACRES:
NA.22

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Quality Level

100

assay

99%

form

powder

mp

150-152 °C (lit.)

functional group

amine

SMILES string

NCCc1ccc(cc1)S(N)(=O)=O

InChI

1S/C8H12N2O2S/c9-6-5-7-1-3-8(4-2-7)13(10,11)12/h1-4H,5-6,9H2,(H2,10,11,12)

InChI key

FXNSVEQMUYPYJS-UHFFFAOYSA-N

Gene Information

human ... CA1(759), CA2(760), CA5A(763), CA5B(11238), CA9(768)
mouse ... Car13(71934), Car5a(12352)

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This Item
479993694967648701
4-(2-Aminoethyl)benzenesulfonamide 99%

Sigma-Aldrich

275247

4-(2-Aminoethyl)benzenesulfonamide

Methyl 4-(aminomethyl)benzoate hydrochloride 97%

Sigma-Aldrich

479993

Methyl 4-(aminomethyl)benzoate hydrochloride

N-(2-Aminoethyl)-4-(trifluoromethyl)benzenesulfonamide 97%

Sigma-Aldrich

694967

N-(2-Aminoethyl)-4-(trifluoromethyl)benzenesulfonamide

4-(2-Aminoethyl)pyridine 96%

Sigma-Aldrich

648701

4-(2-Aminoethyl)pyridine

assay

99%

assay

97%

assay

97%

assay

96%

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

200

mp

150-152 °C (lit.)

mp

243 °C (dec.) (lit.)

mp

111-115 °C

mp

-

form

powder

form

-

form

solid

form

-

functional group

amine

functional group

amine, ester

functional group

amine, fluoro

functional group

amine

Gene Information

human ... CA1(759), CA2(760), CA5A(763), CA5B(11238), CA9(768)
mouse ... Car13(71934), Car5a(12352)

Gene Information

-

Gene Information

-

Gene Information

-

General description

The human hepatocellular carcinoma (HCC) cells were treated with its inhibitor 4-(2-aminoethyl)benzenesulfonamide[1].

Application

4-(2-Aminoethyl)benzenesulfonamide was used to develop a model system to study the implementation of a microfluid chip required for Fourier transform measurements of biochemical interactions[2].

pictograms

Corrosion
GHS05

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Met. Corr. 1 - Skin Irrit. 2

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF7180V
WXBF3180V
WXBD9828V
WXBD6348V
WXBD3491V

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Layne D Williams et al.
Analytical chemistry, 82(14), 6025-6031 (2010-06-24)
Surface plasmon resonance (SPR) is a popular technique for label-free detection of biomolecular interactions at a surface. SPR yields quantitative kinetic association and dissociation constants of surface interactions such as the binding of two molecular species, one present in the
C H Mastrangelo et al.
Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference, 2010, 5318-5321 (2010-11-26)
New developments in microfluidic chip technology enable the construction of chemical spectrum analyzers that can probe the binding interactions between chemical entities. In this paper we report the implementation of a microfluidic chip suitable for Fourier transform measurements of biochemical
Su-jong Yu et al.
Acta pharmacologica Sinica, 32(7), 912-920 (2011-06-15)
The hypoxic condition within large or infiltrative hypovascular tumors produces intracellular acidification, which could activate many signaling pathways and augment cancer cell growth and invasion. Carbonic anhydrase-IX (CA-IX) is an enzyme lowering pH. This study is to examine whether hypoxia
P Megyeri et al.
Immunology, 86(4), 629-635 (1995-12-01)
Monocytes freshly isolated from human blood produced large amounts of superoxide when triggered by phorbol ester. After monocytes were cultured for 18-24 hr in endotoxin-free, non-adherent conditions, they produced low amounts of superoxide. Addition of lipopolysaccharide (LPS), interferon-gamma (IFN-gamma), tumour
Gayan S Jayawickrama et al.
PloS one, 13(4), e0196404-e0196404 (2018-04-25)
The mammalian kynurenine aminotransferase (KAT) enzymes are a family of related isoforms that are pyridoxal 5'-phosphate-dependent, responsible for the irreversible transamination of kynurenine to kynurenic acid. Kynurenic acid is implicated in human diseases such as schizophrenia where it is found
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