Basic information Safety Supplier Related

2-AMINO-1-PROPENE-1,1,3-TRICARBONITRILE

Basic information Safety Supplier Related

2-AMINO-1-PROPENE-1,1,3-TRICARBONITRILE Basic information

Product Name:
2-AMINO-1-PROPENE-1,1,3-TRICARBONITRILE
Synonyms:
  • 1,1,3-Tricyano-2-aminopropene
  • 2-AMino-1-propene-1,1,3-tricarbonitrile, 97% 5GR
  • 2-Amino-1,1,3-propenetricarbonitrile 97%
  • 2-AMINO-1-PROPENE-1,1,3-TRICARBONITRILE
  • 2-AMINO-1,1,3-TRICYANOPROPENE
  • 2-Amino-1,1,3-trycino-1-propene
  • Aminotrycinopropene
  • 3-aminoprop-1-ene-1,1,3-tricarbonitrile
CAS:
868-54-2
MF:
C6H4N4
MW:
132.12
EINECS:
212-777-5
Mol File:
868-54-2.mol
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2-AMINO-1-PROPENE-1,1,3-TRICARBONITRILE Chemical Properties

Melting point:
171-173 °C (lit.)
Boiling point:
234.02°C (rough estimate)
Density 
1.262
refractive index 
1.7000 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
-2.92±0.70(Predicted)
form 
powder to crystal
color 
White to Gray to Brown
Merck 
14,480
BRN 
1756131
CAS DataBase Reference
868-54-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
22-24/25
RIDADR 
UN 3259 8/PG 3
WGK Germany 
3
RTECS 
UD2340000
HazardClass 
6.1
PackingGroup 
III
HS Code 
29269095

MSDS

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2-AMINO-1-PROPENE-1,1,3-TRICARBONITRILE Usage And Synthesis

Chemical Properties

light pink to beige or light brownish. 2-Amino-1-propene-1,1,3-tricarbonitrile [868-54-2], 2-amino-1,1,3-tricyanopropene, malononitrile dimer, (NC)2C=C (NH2) CH2CN, Mr 132.13, mp 171 – 173℃, is a light brownish powder, insoluble in water.

Uses

2-Amino-1,1,3-propenetricarbonitrile stimulates choline acetyltransferase activity in animals. A neurotrophic agent with potential therapeutic effect on cholinergic disorders.

Biochem/physiol Actions

2-Amino-1,1,3-propenetricarbonitrile is a key intermediate in synthesis of various heterocyclic compounds. 2-Amino-1,1-3-tricyanopropene undergoes condensation reaction with aromatic nitroso compounds to form useful coloring agents. 2-Amino-1,1-3-tricyanopropene reacts with 1,3-dithiole-derived polyenals to form push–pull systems with (Z)-geometry around the newly formed carbon-carbon double bond.

Synthesis

Malononitrile dimer is obtained from the base-catalyzed dimerization of malononitrile. It has been investigated as a potential precursor for new dyes but it has no current industrial significance.

2-AMINO-1-PROPENE-1,1,3-TRICARBONITRILESupplier

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