trisethyleneiminoquinone химические свойства, назначение, производство
Использование
Alkylating reagent in mutation research.
Определение
ChEBI: A member of the class of 1,4-benzoquinones that is 1,4-benzoquinone in which three of the ring hydrogens are replaced by aziridin-1-yl groups.
Общее описание
Purple needle-like crystals.
Реакции воздуха и воды
Slightly soluble in water.
Профиль реактивности
trisethyleneiminoquinone is an amine. 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.
Пожароопасность
Flash point data is not available for trisethyleneiminoquinone, but trisethyleneiminoquinone is probably combustible.
Профиль безопасности
Poison by
intraperitoneal, intravenous, and parenteral
routes. Experimental teratogenic and
reproductive effects. Questionable
carcinogen with experimental carcinogenic
data. Human mutation data reported. When
heated to decomposition it emits toxic
fumes of NOx. Used as a drug for the
treatment of neoplastic dseases.
trisethyleneiminoquinone препаратная продукция и сырье
сырьё
препарат