4-Nitrophthalimide(89-40-7) wirh best ada@tuskwei.com Sky;18031153937

4-Nitrophthalimide Basic information

Product Name:	4-Nitrophthalimide
Synonyms:	AKOS B028733;5-NITRO-1,3-DIHYDRO-2H-ISOINDOL-1,3-DIONE;5-NITRO-1H-ISOINDOLE-1,3(2H)-DIONE;5-NITROPHTHALIMIDE;5-NITROISOINDOLINE-1,3-DIONE;5-NITROISOINDOLE-1,3-DIONE;4-NITRO-1,2-BENZENE DICARBOXYLIC ACID, IMIDE;4-NITROPHTHALIMIDE
CAS:	89-40-7
MF:	C8H4N2O4
MW:	192.13
EINECS:	201-905-5
Product Categories:	Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;N;Stains and Dyes;Stains&Dyes, A to
Mol File:	89-40-7.mol

4-Nitrophthalimide Chemical Properties

Melting point	206 °C
Water Solubility	<0.01 g/100 mL at 18 ºC
BRN	180224
Stability:	Stable. Combustible. Incompatible with moisture, water, strong oxidising agents, strong bases.
CAS DataBase Reference	89-40-7(CAS DataBase Reference)
NIST Chemistry Reference	4-Nitro-phthalimide(89-40-7)
EPA Substance Registry System	1H-Isoindole-1,3( 2H)-dione, 5-nitro-(89-40-7)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	37/39-26-36-24/25
RTECS	TI5625000
Hazard Note	Irritant
TSCA	Yes

4-Nitrophthalimide Usage And Synthesis

Chemical Properties	slight yellow powder
General Description	Yellow powder.
Air & Water Reactions	4-Nitrophthalimide can be hydrolyzed. . Insoluble in water.
Reactivity Profile	A nitrated amine. Amines are combustible. The combustion of amines yields noxious NOx. REACTIVITY - 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. Aromatic nitro compounds range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups.
Fire Hazard	Flash point data for 4-Nitrophthalimide are not available, however 4-Nitrophthalimide is probably combustible.

4-Nitrophthalimide Preparation Products And Raw materials

Raw materials	Nitric acid-->O-Phthalimide
Preparation Products	4-Nitrophthalic acid-->4-Nitrophthalic anhydride

The images only for reference.