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Triallylamine CAS#102-70-5
CAS Number: 102-70-5
Chemical Formula: C3H6N6
Synonyms:
TRIALLYLAMINE: 97.5%
Tris(2-propenyl)amine
N,N-Diallyl-2-propen-1-amine
MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)
Appearance: Transperant Liquid
Triallylamine CAS#102-70-5
A colorless liquid with a fishlike odor. Density 0.800 g / cm3 and insoluble in water. Hence floats on water. Flash point 103°F. Vapors heavier than air. May irritate skin and eyes. Used to make other chemicals.
Triallylamine Chemical Properties |
Melting point | -70°C |
Boiling point | 150-151 °C (lit.) |
density | 0.79 g/mL at 25 °C (lit.) |
vapor density | 4.73 (vs air) |
vapor pressure | 90 mm Hg ( 80 °C) |
refractive index | n |
Fp | 87 °F |
storage temp. | 2-8°C |
form | clear liquid |
pka | pK1:8.31(+1) (25°C) |
color | Colorless to Yellow to Orange |
Water Solubility | 250 g/100 mL |
Stability: | Stable. Flammable. Incompatible with strong oxidizing agents. |
InChI | 1S/C9H15N/c1-4-7-10(8-5-2)9-6-3/h4-6H,1-3,7-9H2 |
InChIKey | VPYJNCGUESNPMV-UHFFFAOYSA-N |
SMILES | C=CCN(CC=C)CC=C |
CAS DataBase Reference | 102-70-5(CAS DataBase Reference) |
NIST Chemistry Reference | 2-Propen-1-amine, N,N-di-2-propenyl-(102-70-5) |
EPA Substance Registry System | Triallylamine (102-70-5) |
Safety Information |
Hazard Codes | C |
Risk Statements | 10-20/21/22-34 |
Safety Statements | 16-26-36/37/39-45 |
RIDADR | UN 2610 3/PG 3 |
WGK Germany | 3 |
RTECS | XX5950000 |
TSCA | TSCA listed |
HazardClass | 3 |
PackingGroup | III |
HS Code | 29211990 |
Storage Class | 3 - Flammable liquids |
Hazard Classifications | Acute Tox. 3 Inhalation |
Hazardous Substances Data | 102-70-5(Hazardous Substances Data) |
Product Application of Triallylamine CAS#102-70-5
Triallylamine (TAA) reacts with primary aromatic amines in the presence of a ruthenium catalyst to form 2-ethyl-3-methylquinolines.
TAA undergoes hydrozirconation followed by transmetalation with germanium tetrachloride to form 1-aza-5-germa-5-chlorobicyclo[3.3.3]undecane. This compound can react with Grignard or lithium reagents to form the corresponding 5-organo compounds.
The cycloaddition of TAA to fluorinated 1,3,4-oxadiazoles affords octahydro-2,7-methanofuro[3,2-c]pyridines.
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