N-Phenylmaleimide Chemical Properties

Melting point:

85-87 °C (lit.)

Boiling point:

162-163 °C/12 mmHg (lit.)

Density 

1.2427 (rough estimate)

vapor pressure 

0.021Pa at 25℃

refractive index 

1.5200 (estimate)

Flash point:

162-163°C/12mm

storage temp. 

Sealed in dry,Room Temperature

solubility 

815g/l insoluble

pka

-0.81±0.20(Predicted)

form 

Crystalline Powder or Flakes

color 

Yellow

Water Solubility 

Soluble in water (slightly ), methanol, ethanol, and benzene.

Merck 

14,7299

BRN 

125098

InChIKey

HIDBROSJWZYGSZ-UHFFFAOYSA-N

LogP

1.16 at 25℃

CAS DataBase Reference

941-69-5(CAS DataBase Reference)

NIST Chemistry Reference

N-Phenylmaleimide(941-69-5)

EPA Substance Registry System

N-Phenylmaleimide (941-69-5)

Safety Information

Hazard Codes 

T,Xi,N

Risk Statements 

25-36/37/38-23/24/25-50-43-41-38

Safety Statements 

45-24/25-36/37/39-26-61-39-36/37

RIDADR 

UN 2811 6.1/PG 3

WGK Germany 

3

RTECS 

ON5950000

F 

10-21

Hazard Note 

Irritant

TSCA 

Yes

HazardClass 

6.1

PackingGroup 

III

HS Code 

29251995

MSDS

• Language:English Provider:1-Phenyl-1H-pyrrole-2,5-dione
• Language:English Provider:ACROS
• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

N-Phenylmaleimide Usage And Synthesis

Chemical Properties

yellow crystalline powder or needles

Uses

N-phenylmaleimide can be used as cross-linking agent in rubber vulcanization, can improve the heat resistance, impact resistance, hot melt processability. Also be used to produce heat-resistant polymers.

Uses

N-Phenylmaleimide is used as a dipolarophile in 1,3-cycloaddition reaction with a nitrone, useful for the preparation of crystalline adducts of dienes. It is used as a plastic modifier.

Uses

Dienophile in the Diels-Alder reaction. Usually gives cryst adducts.

General Description

Yellow needles.

Air & Water Reactions

Sparingly water soluble .

Reactivity Profile

N-Phenylmaleimide is an imide. 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-Phenylmaleimide are not available. N-Phenylmaleimide is probably combustible.

Flammability and Explosibility

Non flammable

N-Phenylmaleimide(941-69-5)Related Product Information

• Succinimide
• O-Phthalimide
• Maleimide
• PHENYL VALERATE
• N,N'-1,3-Phenylene bismaleimide
• Phenylhydrazine
• Pyrrole
• N-Benzyl-N-methylethanolamine
• 4-(DICHLOROMETHYL)PYRIDINE HCL
• N-Benzylmaleimide
• N-PHENYLETHYLENEDIAMINE
• N-PHENYLMETHACRYLAMIDE
• N-Phenylanthranilic acid
• N-Phenyl-1-naphthylamine
• N-PHENYLCARBAZOLE HYDROCHLORIDE
• N-PENTYLBORONIC ACID
• N-Phenylglycine potassium salt
• N-Phenyl-bis(trifluoromethanesulfonimide)