Skip to Content
Merck
All Photos(2)

Documents

124753

Sigma-Aldrich

Succinamide

98%

Synonym(s):

Succinic diamide

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
NH2COCH2CH2CONH2
CAS Number:
Molecular Weight:
116.12
Beilstein:
1753983
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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

Looking for similar products? Visit Product Comparison Guide

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 Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

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
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
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
Birgit T Priest et al.
Biochemistry, 43(30), 9866-9876 (2004-07-28)
Sodium channel blockers are used clinically to treat a number of neuropathic pain conditions, but more potent and selective agents should improve on the therapeutic index of currently used drugs. In a high-throughput functional assay, a novel sodium channel (Na(V))

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service