S9381
Succinimide
99.1%
Synonym(s):
2,5-Pyrrolidinedione
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About This Item
Empirical Formula (Hill Notation):
C4H5NO2
CAS Number:
Molecular Weight:
99.09
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
204-635-6
MDL number:
Beilstein/REAXYS Number:
108440
Product Name
Succinimide,
InChI
1S/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)
InChI key
KZNICNPSHKQLFF-UHFFFAOYSA-N
SMILES string
O=C1CCC(=O)N1
assay
99.1%
form
powder or crystals
color
white to off-white
bp
285-290 °C (lit.)
Quality Level
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Storage Class
11 - Combustible Solids
wgk
WGK 1
ppe
Eyeshields, Gloves, type N95 (US)
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David Rennison et al.
Bioorganic & medicinal chemistry, 15(8), 2963-2974 (2007-02-27)
Norbormide [5-(alpha-hydroxy-alpha-2-pyridylbenzyl)-7-(alpha-2-pyridylbenzylidene)-5-norbornene-2,3-dicarboximide] (NRB, 1), an existing but infrequently used rodenticide, is known to be uniquely toxic to rats but relatively harmless to other rodents and mammals. A series of NRB-related analogues were prepared to investigate the structural features responsible for
Nada Perisic-Janjic et al.
Journal of pharmaceutical and biomedical analysis, 72, 65-73 (2012-11-14)
Reversed-phase thin-layer chromatographic (RP TLC) retention coefficients for a newly designed series of N-phenyl-3-methyl succinimide derivatives, of a rationally expected anticonvusant activity, were determined as parameters of their lipophilicity. Basic pharmacokinetic descriptors of the agents were calculated in silico with
Wataru Kamimura et al.
Journal of biomaterials science. Polymer edition, 23(5), 609-628 (2011-02-12)
We have developed a scaffold material consisting of a covalently-bonded structure of alginate and atelocollagen (AtCol). Addition of calcium ions caused the material to form a hydrogel (alginate-modified AtCol gel). The condition of the alginate-modified AtCol gel could be controlled
Srinivasa Reddy Mothe et al.
The Journal of organic chemistry, 76(8), 2521-2531 (2011-03-15)
A one-pot, two-step method to prepare 3-halohydrofurans efficiently by TfOH-catalyzed hydroxylation/halocyclization of cyclopropyl methanols with H(2)O and N-halosuccinimide (NXS, X=1, Br, Cl) or Selectfluor is described. The reactions proceed rapidly under mild and operationally straightforward conditions with a catalyst loading
X Christopher Yu et al.
Analytical chemistry, 83(15), 5912-5919 (2011-06-23)
We report an efficient, high fidelity trypsin digestion method for peptide map analysis. This method minimizes artifacts caused by the sample preparation process, and we show its utility for the accurate determination of succinimide formation in a degraded monoclonal antibody
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