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Merck
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文件

14190

Sigma-Aldrich

丁二腈

purum, ≥97.0% (GC)

同義詞:

1,2-二氰基乙烷, Butanedinitrile

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About This Item

線性公式:
NCCH2CH2CN
CAS號碼:
分子量::
80.09
Beilstein:
1098380
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

等級

purum

品質等級

化驗

≥97.0% (GC)

形狀

solid

bp

265-267 °C (lit.)

mp

50-54 °C (lit.)

溶解度

water: soluble 130 g/L

密度

0.985 g/mL at 25 °C (lit.)

SMILES 字串

N#CCCC#N

InChI

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

InChI 密鑰

IAHFWCOBPZCAEA-UHFFFAOYSA-N

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一般說明

Succinonitrile has plastic crystalline nature. It is the precursor of 1,4-diaminobutane.

應用

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.

訊號詞

Warning

危險聲明

危險分類

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

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
Comparison of the teratogenic potential of two aliphatic nitriles in hamsters: succinonitrile and tetramethylsuccinonitrile.
P A Doherty et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 3(1), 41-48 (1983-01-01)
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

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