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N-Ethyl-p-toluenesulfonamide

Basic information Safety Supplier Related

N-Ethyl-p-toluenesulfonamide Basic information

Product Name:
N-Ethyl-p-toluenesulfonamide
Synonyms:
  • Benzenesulfonamide, N-ethyl-4-methyl-
  • Ethyl toluenesulfonamide
  • Ethylp-toluenesulfonamide
  • n-ethyl-4-methyl-benzenesulfonamid
  • n-ethyl-4-methylbenzenesulfonamide
  • N-Ethyl-4-methyl-benzenesulfonamide
  • N-Ethyltoluene-4-sulfonamide for synthesis
  • Brinzolamide Impurity 1
CAS:
80-39-7
MF:
C9H13NO2S
MW:
199.27
EINECS:
201-275-1
Product Categories:
  • Nitrogen Compounds
  • Organic Building Blocks
  • Protected Amines
Mol File:
80-39-7.mol
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N-Ethyl-p-toluenesulfonamide Chemical Properties

Melting point:
63-65 °C(lit.)
Boiling point:
208 °C745 mm Hg(lit.)
Density 
1.26 g/cm3
refractive index 
1.5270 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
pka
11.86±0.50(Predicted)
color 
White to Off-White
Stability:
Stable. Incompatible with strong oxidizing agents.
LogP
1.960 (est)
CAS DataBase Reference
80-39-7(CAS DataBase Reference)
NIST Chemistry Reference
4-Toluenesulfonamide, n-ethyl-(80-39-7)
EPA Substance Registry System
N-Ethyl-p-toluenesulfonamide (80-39-7)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37
WGK Germany 
3
TSCA 
Yes
HS Code 
29350090

MSDS

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N-Ethyl-p-toluenesulfonamide Usage And Synthesis

Chemical Properties

off-white crystalline solid

Uses

Plasticizer.

Uses

N-Ethyl-4-toluene sulfonamide is a resin carrier in dental materials used for isolating cavities below restorations; plasticizer in polyvinyl alcohollacquers, polyamides, cellulose acetate, etc.

Uses

N-?Ethyl-?p-?toluenesulfonamide is a reagent used in the sulfonamidation of imidazopyridines.

General Description

Platelets (from dilute alcohol or ligroin) or off-white solid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

An amide. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Fire Hazard

Flash point data for N-Ethyl-p-toluenesulfonamide are not available; however, N-Ethyl-p-toluenesulfonamide is probably combustible.

N-Ethyl-p-toluenesulfonamide Preparation Products And Raw materials

Raw materials

N-Ethyl-p-toluenesulfonamideSupplier

Shouguang Nuomeng Chemical Co Ltd. Gold
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536-5399456 13869682027
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J & K SCIENTIFIC LTD.
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Meryer (Shanghai) Chemical Technology Co., Ltd.
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Alfa Aesar
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TCI (Shanghai) Development Co., Ltd.
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Sales-CN@TCIchemicals.com