Benzenesulfonamide,4-chloro-N-[(propylamino)carbonyl]- (94-20-2)

Identification
Name:	Benzenesulfonamide,4-chloro-N-[(propylamino)carbonyl]-
Synonyms:	Urea,1-[(p-chlorophenyl)sulfonyl]-3-propyl- (8CI);1-(p-Chlorobenzenesulfonyl)-3-propylurea;1-Propyl-3-(p-chlorobenzenesulfonyl)urea;Adiaben;Asucrol;Catanil;Chloronase;Diabaril;Diabechlor;Diabenal;Diabenese;Diabeneza;Diabet-Pages;Diabetoral;Diabinese;Glisema;Meldian;Melitase;Millinese;N-(p-Chlorobenzenesulfonyl)-N'-propylurea;NSC 44634;NSC 626720;P 607;Stabinol;U 9818;
CAS:	94-20-2
EINECS:	202-314-5
Molecular Formula:	C₁₀H₁₃ClN₂O₃S
Molecular Weight:	276.76
InChI:	InChI=1/C10H13ClN2O3S/c1-2-7-12-10(14)13-17(15,16)9-5-3-8(11)4-6-9/h3-6H,2,7H2,1H3,(H2,12,13,14)
Molecular Structure:
Properties
Melting Point:	128 °C
Density:	1.334 g/cm³
Stability:	Stable. Combustible.
Solubility:	2.2 mg/ml in water @ pH 6; practically insol in water @ pH 7.3; sol in alcohol; moderately sol in chloroform; sparingly sol in ether, benzene In water, 258 mg/l @ 37 deg C
Appearance:	white crystalline powder
Specification:	A halogenated 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 (NO_x).
Report:	NCI Carcinogenesis Bioassay (feed); No Evidence: mouse, rat NCITR* National Cancer Institute Carcinogenesis Technical Report Series. (Bethesda, MD 20014) No. NCI-CG-TR-45 ,1978. . EPA Genetic Toxicology Program.
Color:	Crystals from dil ethanol WHITE, CRYSTALLINE POWDER White, crystalline powder
Safety Data
Hazard Symbols	Xn: Harmful

Benzenesulfonamide,4-chloro-N-[(propylamino)carbonyl]- (94-20-2)

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