| Weight | 80.09 g/mol |
|---|---|
| Formula | C4H4N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
SUCCINONITRILE (110-61-2)
Score:
#73 in Materials science
,
#720 in Physics
,
#2108 in Chemistry
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- The plastic-crystalline phase of succinonitrile as a universal matrix for solid-state ionic conductors (Nature Materials, 2004)
- In-situ Observation of Hot tearing Formation in Succinonitrile-Acetone (Acta Materialia, 2001)
- Composite effects in poly(ethylene oxide ) -succinonitrile based all-solid electrolytes (Electrochemistry Communications, 2006)
- Succinonitrile as a Versatile Additive for Polymer Electrolytes (Advanced Functional Materials, 2007)
- Surface-tension-anisotropy measurements of succinonitrile and pivalic acid: Comparison with microscopic solvability theory (Physical Review A, 1992)
- Positron Annihilation Study of Defects in Succinonitrile (Physical Review Letters, 1979)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(CC#N)C#N
-
InChIKeyIAHFWCOBPZCAEA-UHFFFAOYSA-N
- Pubchem - SUCCINONITRILE
- Wikipedia - succinonitrile
Succinonitrile, also butanedinitrile, is a nitrile, with the formula of C2H4(CN)2. It is a colorless solid that melts at 57C, hence its waxy consistency. Succinonitrile is produced by the addition of hydrogen cyanide to acrylonitrile: CH2=CHCN + HCN NCCH2CH2CN Hydrogenation of succinonitrile yields putrescine (1,4-diaminobutane).
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SUCCINONITRILE
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