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14190

Succinonitrile

Name: Succinonitrile
Brand: SIAL

purum, ≥97.0% (GC)

Synonym(s):

1,2-Dicyanoethane, Butanedinitrile

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About This Item

Linear Formula:

NCCH₂CH₂CN

CAS Number:

110-61-2

Molecular Weight:

80.09

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

329750418

EC Number:

203-783-9

Beilstein/REAXYS Number:

1098380

MDL number:

MFCD00001949

Assay:

≥97.0% (GC)

Form:

solid

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Properties

grade

purum

Quality Level

200

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.)

functional group

nitrile

SMILES string

N#CCCC#N

InChI

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

InChI key

IAHFWCOBPZCAEA-UHFFFAOYSA-N

Description

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.

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Warning

pcodes

P202 - P264 - P273 - P280 - P301 + P312 - P308 + P313

Storage Class

11 - Combustible Solids

ppe

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

pictograms

GHS08,GHS07

hcodes

H302,H361d,H412

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Repr. 2

flash_point_f

269.6 °F

flash_point_c

132 °C

Regulatory Information

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A comparison of the effects of nicotinamide and progesterone on functional recovery of cognitive behavior following cortical contusion injury in the rat.

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

Vibrational spectra of succinonitrile and its [1,4-13C2]-,[2,2,3,3,-2H4]- and 1,4-13C-2,2,3,3-2H4]-isotopomers and a force field of succinonitrile.

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

Interface pattern formation in nonlinear dissipative systems.

Rohit Trivedi et al.

Nature materials, 1(3), 157-159 (2003-03-06)

The problem of interface pattern selection in nonlinear dissipative systems is critical in many fields of science, occurring in physical, chemical and biological systems. One of the simplest pattern formations is the Saffman-Taylor finger pattern that forms when a viscous

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Global Trade Item Number

SKU	GTIN
14190-1KG	04061825770604
14190-250G	04061832098074