14190
Succinonitrile
purum, ≥97.0% (GC)
Synonym(s):
1,2-Dicyanoethane, Butanedinitrile
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About This Item
Linear Formula:
NCCH2CH2CN
CAS Number:
Molecular Weight:
80.09
Beilstein:
1098380
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
purum
Quality Level
Assay
≥97.0% (GC)
form
solid
bp
265-267 °C (lit.)
mp
50-54 °C (lit.)
solubility
water: soluble 130 g/L
density
0.985 g/mL at 25 °C (lit.)
SMILES string
N#CCCC#N
InChI
1S/C4H4N2/c5-3-1-2-4-6/h1-2H2
InChI key
IAHFWCOBPZCAEA-UHFFFAOYSA-N
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General description
Succinonitrile has plastic crystalline nature. It is the precursor of 1,4-diaminobutane.
Application
Succinonitrile dispersed with ionic liquids entrapped in a host polymer was used to constitute gel polymer electrolytes. It was used as dopant to investigate the ionic conductivity and X-ray absorption spectroscopic results for lithium and copper salt doped succinonitrile.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Repr. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Jared M Campbell et al.
BMC cancer, 19(1), 1242-1242 (2019-12-23)
Cell cycle analysis is important for cancer research. However, available methodologies have drawbacks including limited categorisation and reliance on fixation, staining or transformation. Multispectral analysis of endogenous cell autofluorescence has been shown to be sensitive to changes in cell status
A Combined Conductivity and XAS Study of Plastically Crystalline Electrolytes.
Chadwick AV, et al.
Journal of Physics. Conference Series, 249(1) (2010)
Possible role of hydroxyl radicals in the metabolism of succinonitrile.
E P Hayes et al.
Biochemical pharmacology, 34(22), 4081-4084 (1985-11-15)
B W Mangum
Clinical chemistry, 29(7), 1380-1384 (1983-07-01)
In an investigation of the melting and freezing behavior of succinonitrile, the triple-point temperature was determined to be 58.0805 degrees C, with an estimated uncertainty of +/- 0.0015 degrees C relative to the International Practical Temperature Scale of 1968 (IPTS-68).
Tijs M Lammens et al.
ChemSusChem, 4(6), 785-791 (2011-05-11)
Succinonitrile is the precursor of 1,4-diaminobutane, which is used for the industrial production of polyamides. This paper describes the synthesis of biobased succinonitrile from glutamic acid and glutamine, amino acids that are abundantly present in many plant proteins. Synthesis of
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