124753
琥珀酰胺
98%
别名:
丁二酰胺
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关于此项目
线性分子式:
NH2COCH2CH2CONH2
化学文摘社编号:
分子量:
116.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-739-9
Beilstein/REAXYS Number:
1753983
MDL number:
Assay:
98%
InChI key
SNCZNSNPXMPCGN-UHFFFAOYSA-N
InChI
1S/C4H8N2O2/c5-3(7)1-2-4(6)8/h1-2H2,(H2,5,7)(H2,6,8)
SMILES string
NC(=O)CCC(N)=O
assay
98%
mp
260-265 °C (dec.) (lit.)
solubility
cold water: soluble 220 part, boiling water: soluble 9 part, alcohol: insoluble, diethyl ether: insoluble
functional group
amide
Quality Level
Application
琥珀酰胺已被用于表征来自半胱氨酸水解酶超家族的一种新型双缩脲水解酶 。在斜生栅藻和绿藻的培养基中作为氮源补充。
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
Yuhui Lin et al.
Bioconjugate chemistry, 13(3), 605-610 (2002-05-16)
Recently, near-infrared (NIR) fluorescence light has been applied to image various biological events in vivo, because it penetrates tissue more efficiently than light in the visible spectrum. Compounds exhibiting fluorescent properties in the NIR range are key elements for this
Anouk M Rijs et al.
The journal of physical chemistry. A, 115(34), 9669-9675 (2011-04-29)
High-resolution IR spectroscopy has been employed to study isolated, switchable [2]rotaxanes. IR absorption spectra of two-station rotaxanes, their separate thread, and macrocycle components, as well as those of the individual stations incorporated into the thread, have been measured in the
Hideki Onagi et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 9(24), 5978-5988 (2003-12-18)
Eight new [2]rotaxanes have been prepared, incorporating an alpha-cyclodextrin as the rotor, a stilbene as the axle, and trinitrophenyl substituents as capping groups. Strategies have been devised to elaborate these by linking the rotor to the axle, to produce two
Elisabeth Garanger et al.
Bioconjugate chemistry, 20(1), 170-173 (2008-12-17)
The biotin/avidin system is one of the most widely used affinity detection and affinity capture systems in biology. However, the determination of the exact number of biotin tags attached onto a substrate is complicated by the fact that biotin does
Petras P Dzeja et al.
American journal of physiology. Heart and circulatory physiology, 284(4), H1048-H1056 (2003-04-02)
Modulation of mitochondrial respiratory chain, dehydrogenase, and nucleotide-metabolizing enzyme activities is fundamental to cellular protection. Here, we demonstrate that the potassium channel opener diazoxide, within its cardioprotective concentration range, modulated the activity of flavin adenine dinucleotide-dependent succinate dehydrogenase with an
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