124753
Succinamide
98%
Synonym(s):
Succinic diamide
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About This Item
Linear Formula:
NH2COCH2CH2CONH2
CAS Number:
Molecular Weight:
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
Related Categories
Application
Succinamide has been used in the characterization of a novel biuret hydrolase from the cysteine hydrolase superfamily. It was used as nitrogen supplement in the culture medium of Scenedesmus obliquus and green algae.
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Regulatory Information
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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
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
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
Adaptable synthesis of C-glycosidic multivalent carbohydrates and succinamide-linked derivatization.
Gavin J Miller et al.
Organic letters, 12(22), 5262-5265 (2010-10-22)
A modular approach to the synthesis of trivalent C-glycosidic carbohydrates is described. The approach is illustrated employing carboxylate-terminated C-glycosidic d-mannose, d-glucose, and d-galactose derivatives with different length C1-linked spacer units and also core units with different length linker units attached.
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