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14190

Sigma-Aldrich

Succinonitrile

purum, ≥97.0% (GC)

Synonyme(s) :

1,2-Dicyanoethane, Butanedinitrile

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About This Item

Formule linéaire :
NCCH2CH2CN
Numéro CAS:
Poids moléculaire :
80.09
Numéro Beilstein :
1098380
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Qualité

purum

Niveau de qualité

Pureté

≥97.0% (GC)

Forme

solid

Point d'ébullition

265-267 °C (lit.)

Pf

50-54 °C (lit.)

Solubilité

water: soluble 130 g/L

Densité

0.985 g/mL at 25 °C (lit.)

Chaîne SMILES 

N#CCCC#N

InChI

1S/C4H4N2/c5-3-1-2-4-6/h1-2H2

Clé InChI

IAHFWCOBPZCAEA-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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.

Pictogrammes

Health hazardExclamation markEnvironment

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Aquatic Chronic 2 - Repr. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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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)
Todd C Peterson et al.
Journal of neurotrauma, 29(18), 2823-2830 (2012-09-29)
The primary goal of this study was to compare clinically relevant doses of progesterone and nicotinamide within the same injury model. Progesterone has been shown to reduce edema and inflammation and improve functional outcomes following brain injury. Nicotinamide has also
O I Fengler et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(1), 105-117 (2001-02-24)
[1,4-13C2]-succinonitrile, [2,2,3,3-2H4]-succinonitrile, [1,4-13C2-2,2,3,3-2H4]-succinonitrile have been synthesized and, for the first time, the infrared and Raman spectra of these succinonitrile isotopomers have been discussed in detail. The spectra were recorded at ambient temperature and at the temperature of liquid nitrogen and
R C Pedroso et al.
The Analyst, 119(12), 2697-2699 (1994-12-01)
A chromatographic method was developed to detect and confirm the presence of succinonitrile (SDN) in horse urine samples, for antidoping control. The urine samples (5 ml) were extracted with diethyl ether and screened by gas chromatography-nitrogen-phosphorus detector and the confirmation

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