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化驗
99%
形狀
liquid
折射率
n20/D 1.434 (lit.)
bp
285-287 °C (lit.)
mp
−29 °C (lit.)
溶解度
H2O: soluble
alcohol: soluble
chloroform: soluble
密度
0.995 g/mL at 25 °C (lit.)
SMILES 字串
N#CCCCC#N
InChI
1S/C5H6N2/c6-4-2-1-3-5-7/h1-3H2
InChI 密鑰
ZTOMUSMDRMJOTH-UHFFFAOYSA-N
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應用
Glutaronitrile (1,3-Dicyanopropane) was used in the preparation of dicarbonyl compounds.
Glutaronitrile can be used as:
- An electrolyte additive in high energy/power Li-ion batteries.
- A glutarate ligand source to prepare zinc glutarate (ZnGA) by reacting with zinc perchlorate hexahydrate.
- A reactant to synthesize pentanedithioamide by reacting with Lawesson′s reagent in the presence of boron trifluoride etherate (BF3.OEt2).
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 3 Oral
儲存類別代碼
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
水污染物質分類（WGK）
WGK 3
閃點（°F）
233.6 °F - closed cup
閃點（°C）
112 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Xingyong Wang et al.
The Journal of organic chemistry, 78(11), 5273-5281 (2013-05-15)
A palladium-catalyzed addition of potassium aryltrifluoroborates to aliphatic nitriles has been developed, leading to a wide range of alkyl aryl ketones with moderate to excellent yields. Moreover, several dinitriles (e.g., malononitrile, glutaronitrile, and adiponitrile) were applicable to this process for
γ-butyrolactone and glutaronitrile as 5 V electrolyte additive and its electrochemical performance for LiNi0. 5Mn1. 5O4
Xu Yun, et al.
Journal of alloys and compounds, 698, 207-214 (2017)
C Cabezas et al.
Astronomy and astrophysics, 636 (2020-05-28)
Nitriles constitute almost 15% of the molecules observed in the interstellar medium (ISM), surprisingly only two dinitriles have been detected in the ISM so far. The lack of astronomical detections for dinitriles may be partly explained by the absence of
Hydrothermal synthesis of single-crystalline zinc glutarate and its structural determination
Kim Jong-Seong, et al.
Chemistry of Materials, 16(16), 2981-2983 (2004)
The BF3.OEt2-Assisted Conversion of Nitriles into Thioamides with Lawesson?s Reagent
Nagl Michael, et al.
Synthesis, 2008(24), 4012-4018 (2008)
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