2-Benzothiazolamine

2-Aminobenzothiazole

2-Benzothiazolamine;Benzothiazole,2-amino-;Benzothiazole,1-amino-;Benzothiazoline,2-imino-;2-Aminobenzothiazole;2(3H)-Benzothiazolimine;2-Benzothiazolylamine;2-Iminobenzothiazoline;1,3-Benzothiazol-2-ylamine;NSC 4670;Benzo[d]thiazol-2-amine;2-Aminobenzo[d]thiazole;ABT;SKA 1;1,3-Benzothiazol-2-amine;Cerium ionophore I;120045-46-7;35858-53-8

136-95-8

C7H6N2S

InChIKey=UHGULLIUJBCTEF-UHFFFAOYSA-N

150.2

150.20

116315

205-268-4

08K5TLY3EQ

4670

2811

DTXSID1024467

PLATES FROM WATER|LEAFLETS FROM WATER

2934200090

Analysis Reagents

67.2

1.9

Beige to grayish Powder or Flakes

0.5 (NTP, 1992)

132 °C

190-195 °C @ Press: 0.05 Torr

139.8±23.2 °C

1.5500 (estimate)

H2O: <0.1 g/100 mL at 19 ºC;soluble in alcohol, chloroform, diethyl ether.

-20°C

0.00331mmHg at 25°C

Oral-mouse LD50: 1000 mg/kg; peritoneal-mouse LD50: 200 mg/kg

Flammable; burning produces toxic nitrogen oxides and sulfur oxide fumes

128.6 Ų [M+H]+

DISTILLS WITHOUT DECOMPOSITION

Insoluble in water.

Amines, Phosphines, and Pyridines

An amine, organosulfide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.