| Weight | 108.144 g/mol |
|---|---|
| Formula | C6H8N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
ADIPONITRILE (68411-90-5, 111-69-3)
hexanedinitrile
Score:
#5 in Physical chemistry
,
#472 in Physics
,
#1374 in Chemistry
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- High-Voltage Electrolytes Based on Adiponitrile for Li-Ion Batteries (Journal of The Electrochemical Society, 2009)
- Adiponitrile-based electrochemical double layer capacitor (Journal of Power Sources, 2012)
- Catalytic Isomerization of Cyanoolefins Involved in the Adiponitrile Process. C-CN Bond Cleavage and Structure of the Nickel pi-Allyl Cyanide Complex Ni(eta^3-1-Me-C~3H~4)(CN)(dppb) (Organometallics, 2004)
- Characterization of several -alumina-supported nickel catalysts and activity for selective hydrogenation of hexanedinitrile (Journal of the Chemical Society, Faraday Transactions, 1994)
- Selective hydrogenation of adiponitrile over a skeletal NiP amorphous catalyst (Raney NiP) at 1 atm pressure (Applied Catalysis A-general, 2000)
- Preparation and characterisation of Rh/Al2O3 catalysts and their application in the adiponitrile partial hydrogenation and styrene hydroformylation (Applied Catalysis A-general, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H320: Causes eye irritation
Warning Serious eye damage/eye irritation - Category 2B - H370: Causes damage to organs
Danger Specific target organ toxicity, single exposure - Category 1 - hexanedinitrile
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SMILESC(CCC#N)CC#N
-
InChIKeyBTGRAWJCKBQKAO-UHFFFAOYSA-N
- Pubchem - ADIPONITRILE
- Wikipedia - adiponitrile
Adiponitrile is the organic compound with the formula (CH2)4(CN)2. This dinitrile, a viscous, colourless liquid, is an important precursor to the polymer nylon-6,6. In 2005, about one billion kilograms were produced annually.
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ADIPONITRILE
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