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124753

Succinamide

Name: Succinamide
Brand: ALDRICH

98%

Synonym(s):

Succinic diamide

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About This Item

Linear Formula:

NH₂COCH₂CH₂CONH₂

CAS Number:

110-14-5

Molecular Weight:

116.12

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24847626

EC Number:

203-739-9

Beilstein/REAXYS Number:

1753983

MDL number:

MFCD00008042

Assay:

98%

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Properties

Quality Level

100

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

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

Description

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

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Installation of a ratchet tooth and pawl to restrict rotation in a cyclodextrin rotaxane.

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

A multifunctional single-attachment-point reagent for controlled protein biotinylation.

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

Synthesis of novel succinamide derivatives having a 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one skeleton as potent and selective M2 muscarinic receptor antagonists. II.

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)

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Global Trade Item Number

SKU	GTIN
124753-100G	04061838723116