Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

Safety Information

124753

Sigma-Aldrich

Succinamide

98%

Synonym(s):

Succinic diamide

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
NH2COCH2CH2CONH2
CAS Number:
110-14-5
Molecular Weight:
116.12
Beilstein:
1753983
EC Number:
203-739-9
MDL number:
MFCD00008042
UNSPSC Code:
12352100
PubChem Substance ID:
24847626
NACRES:
NA.22

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

Looking for similar products? Visit Product Comparison Guide

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 Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

124753-VAR:
124753-100G:
124753-5G:
124753-BULK:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCM6562
MKCM6466
MKCH5636
MKCH5639
MKCB6585

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

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

Slide 1 of 3

1 of 3

Acetamide ≥99.0% (GC)

Sigma-Aldrich

00160

Acetamide

N-Bromosuccinimide ReagentPlus®, 99%

Sigma-Aldrich

B81255

N-Bromosuccinimide

N-Hydroxysuccinimide 98%

Sigma-Aldrich

130672

N-Hydroxysuccinimide

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))
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
T Watanabe et al.
Chemical & pharmaceutical bulletin, 45(6), 996-1007 (1997-06-01)
A series of 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one derivatives containing the succinamide skeleton has been synthesized and evaluated for M1, M2 and M3 muscarinic receptor binding affinities (in vitro) and M2 and M3 muscarinic receptor antagonistic activities (in vivo). Some of them showed higher
Xiaobin Zhang et al.
Drug delivery, 11(5), 301-309 (2005-03-04)
To investigate the effect of RMP-7 and its derivative on drug transport across blood brain barrier (BBB), RMP-7 and DSPE-PEG-NHS [1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-n-[poly(ethyleneglycol)]-hydroxy succinamide, PEG M 3400] were conjugated under mild conditions and the reaction ratio was determined using MALDI-TOF-MS (matrix-assisted laser
Olaf F A Larsen et al.
Proceedings of the National Academy of Sciences of the United States of America, 102(38), 13378-13382 (2005-09-10)
Femtosecond 2D-IR spectroscopy has been used to study the structure of a [2]rotaxane composed of a benzylic amide macrocycle that is mechanically interlocked onto a succinamide-based thread. Both the macrocycle and the thread contain carbonyl groups, and by determining the
View All Related Papers

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