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Documentos

124753

Sigma-Aldrich

Succinamide

98%

Sinónimos:

Succinic diamide

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About This Item

Fórmula lineal:
NH2COCH2CH2CONH2
Número de CAS:
110-14-5
Peso molecular:
116.12
Beilstein/REAXYS Number:
1753983
EC Number:
203-739-9
MDL number:
MFCD00008042
UNSPSC Code:
12352100
PubChem Substance ID:
24847626
NACRES:
NA.22

assay

98%

mp

260-265 °C (dec.) (lit.)

solubility

cold water: soluble 220 part
boiling water: soluble 9 part
alcohol: insoluble
diethyl ether: insoluble

SMILES string

NC(=O)CCC(N)=O

InChI

1S/C4H8N2O2/c5-3(7)1-2-4(6)8/h1-2H2,(H2,5,7)(H2,6,8)

InChI key

SNCZNSNPXMPCGN-UHFFFAOYSA-N

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Categorías relacionadas

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_germany

WGK 3

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

00160

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Sigma-Aldrich

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N-Bromosuccinimide

N-Hydroxysuccinimide 98%

Sigma-Aldrich

130672

N-Hydroxysuccinimide

Chao Xu et al.
Materials science & engineering. C, Materials for biological applications, 84, 32-43 (2018-03-10)
Electroconductive hydrogels with excellent electromechanical properties have become crucial for biomedical applications. In this study, we developed a conductive composite hydrogel via in-situ chemical polymerization based on carboxymethyl chitosan (CMCS), as a biodegradable base macromolecular network, and poly(3,4-ethylenedioxythiophene) (PEDOT), as
T Watanabe et al.
Chemical & pharmaceutical bulletin, 45(9), 1458-1469 (1997-10-23)
A series of succinamide derivatives containing the 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one skeleton (6a-z) was prepared and evaluated for binding affinity to muscarinic receptors in vitro and for antagonism of bradycardia and salivation in vivo in comparison with AF-DX 116 (1a). Structure-activity relationships (SAR)
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
Further studies on the utilization of aspartic acid, succinamide, and asparagine by green algae.
Algeeus S.
Physiologia Plantarum, 3(4), 370-375 (1950)
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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