Uses
ChemicalBook > CAS DataBase List > 4-(2-Aminoethyl)benzenesulfonamide

4-(2-Aminoethyl)benzenesulfonamide

Uses
Product Name
4-(2-Aminoethyl)benzenesulfonamide
CAS No.
35303-76-5
Chemical Name
4-(2-Aminoethyl)benzenesulfonamide
Synonyms
TIMTEC-BB SBB003544;OTAVA-BB BB7020410047;Glipizide Impurity 32;Glipizide Impurity 14;LABOTEST-BB LT00080735;Glimepiride Impurity 26;4-Aminoethylbenzenesulfonamide;P-Aminoethylbenzenesulfonamide;Glimepiride Sulfonamide Impurity;4-(2-Aminoethyl)benzesulfonamide
CBNumber
CB5480434
Molecular Formula
C8H12N2O2S
Formula Weight
200.26
MOL File
35303-76-5.mol
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4-(2-Aminoethyl)benzenesulfonamide Property

Melting point:
150-152 °C (lit.)
Boiling point:
387.4±44.0 °C(Predicted)
Density 
1.2581 (rough estimate)
vapor pressure 
0Pa at 25℃
refractive index 
1.5690 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
pka
10.16±0.10(Predicted)
form 
Solid
color 
White
Water Solubility 
15.5g/L at 20℃
InChI
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)
InChIKey
FXNSVEQMUYPYJS-UHFFFAOYSA-N
SMILES
C1(S(N)(=O)=O)=CC=C(CCN)C=C1
LogP
-3.1 at 19.8℃
CAS DataBase Reference
35303-76-5(CAS DataBase Reference)
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Safety

Hazard Codes 
C,Xi,Xn
Risk Statements 
34-22-36/37/38-20/21/22
Safety Statements 
45-36/37/39-26-36-24/25
RIDADR 
UN3259
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
8
PackingGroup 
III
HS Code 
29350090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H290May be corrosive to metals

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P234Keep only in original container.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
275247
Product name
4-(2-Aminoethyl)benzenesulfonamide
Purity
99%
Packaging
25g
Price
$96.9
Updated
2025/07/31
TCI Chemical
Product number
A1363
Product name
4-(2-Aminoethyl)benzenesulfonamide
Purity
>98.0%(HPLC)(T)
Packaging
25g
Price
$61
Updated
2025/07/31
TRC
Product number
A608790
Product name
4-(2-Aminoethyl)benzenesulfonamide
Packaging
10g
Price
$50
Updated
2021/12/16
AK Scientific
Product number
J91166
Product name
4-(2-Aminoethyl)benzenesulfonamide
Packaging
25g
Price
$25
Updated
2021/12/16
Apolloscientific
Product number
OR9989
Product name
4-(2-Aminoethyl)benzenesulphonamide
Packaging
25g
Price
$28
Updated
2021/12/16
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4-(2-Aminoethyl)benzenesulfonamide Chemical Properties,Usage,Production

Uses

4-(2-Aminoethyl)benzenesulfonamide is used as the starting material in the synthesis of Des(5-methylpyrazinecarbonyl) trans-4-Methyl Glipizide (D292605); a degradation product of Glimepiride (G410150) which is a sulfonylurea hypoglycemic agent and an antidiabetic. 4-(2-Aminoethyl)benzenesulfonamide is also used as a reagent in the synthesis of deorphaning pyrrolopyrazines as potent multi-target antimalarial agents.

Chemical Properties

white to yellowish crystalline powder

Uses

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.

General Description

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

Flammability and Explosibility

Not classified

Synthesis

223253-87-0

35303-76-5

The general procedure for the synthesis of 4-(2-aminoethyl)benzenesulfonamide from the compound (CAS:223253-87-0) was as follows: compound II was dissolved in 80 mL of acetone. Under the condition of ice water bath, 150 mL of concentrated ammonia was added to the reaction mixture and the reaction was stirred at room temperature. After completion of the reaction, the mixture was poured into 500 mL of ice water and the solid was collected by filtration. The filter cake was acidified with 200 mL of 2N hydrochloric acid. Subsequently, the mixture was heated to reflux for 6 hours and filtered. The filtrate was dissolved in hot water and the pH was adjusted to 11-12 with 2N KOH solution. after cooling in an ice bath, the solution was boiled naturally and cooled again to precipitate a pale yellow precipitate. After filtration, it was dried under vacuum to obtain 21.6 g (0.108 mol) of compound III, i.e., 4-(2-aminoethyl)benzenesulfonamide.

References

[1] Patent: CN107879955, 2018, A. Location in patent: Paragraph 0050

4-(2-Aminoethyl)benzenesulfonamide Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 4-(2-Aminoethyl)benzenesulfonamide manufacturers

Guangzhou Tosun Pharmaceutical Ltd
Product
Glipizide Impurity 4 35303-76-5
Price
US $0.00-0.00/mg
Min. Order
5mg
Purity
95%+
Supply Ability
1000mg
Release date
2025-02-10
Zhuozhou Wenxi import and Export Co., Ltd
Product
4-(2-Aminoethyl)benzene sulfonamide 35303-76-5
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-11
Zhuozhou Wenxi import and Export Co., Ltd
Product
4-(2-Aminoethyl)benzene sulfonamide 35303-76-5
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-09

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