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Merck

43720

Sigma-Aldrich

N,N′-Disuccinimidyl carbonate

≥95.0% (NMR), for peptide synthesis

Sinónimos:

N-Succinimidyl carbonate, DSC, Di(N-succinimidyl) carbonate

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About This Item

Fórmula empírica (notación de Hill):
C9H8N2O7
Número de CAS:
Peso molecular:
256.17
Beilstein/REAXYS Number:
1499137
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Nombre del producto

N,N′-Disuccinimidyl carbonate, purum, ≥95.0% (NMR)

grade

purum

Quality Level

assay

≥95.0% (NMR)

form

powder

reaction suitability

reaction type: Carbonylations

impurities

~3% N-hydroxysuccinimide (NMR)

mp

190 °C (dec.) (lit.)

application(s)

peptide synthesis

functional group

imide

storage temp.

−20°C

SMILES string

O=C1CCC(=O)N1OC(=O)ON2C(=O)CCC2=O

InChI

1S/C9H8N2O7/c12-5-1-2-6(13)10(5)17-9(16)18-11-7(14)3-4-8(11)15/h1-4H2

InChI key

PFYXSUNOLOJMDX-UHFFFAOYSA-N

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Application

N,N′-Disuccinimidyl carbonate (DSC) can be used to synthesize:
  • Various carbamate derivatives from primary and sterically hindered secondary alcohols by alkoxycarbonylation.
  • Active carbonate resins from 4-hydroxymethylpolystyrene and 4-hydroxymethyl-3-nitrobenzamido resins via hydroxy functional groups.
  • Aza-glycinyl dipeptides, important intermediates for the preparation of various azapeptides.

It may be also used:
  • In the two-step preparation of 5-(6-(azidomethyl)nicotinamido)pentanoic acid, a copper-chelating picolyl azide derivative.
  • To activate the hydroxyl group of the hapten, γ-hydroxyphenylbutazone (HPBZ) so that HPBZ can effectively bind with human serum albumin(HSA)-immunogen to form a hapten-protein conjugate.

Other Notes

Convenient reagent for preparing N-succinimidyl esters of N-protected amino acids and other acids; activated carbonate, e.g. synthesis of ureas and carbamates; coupling of ligands to proteins (via lysines).

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - STOT RE 2 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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Visite la Librería de documentos

Active carbonate resins for solid-phase synthesis through the anchoring of a hydroxyl function. Synthesis of cyclic and alcohol peptides
Alsina J, et al.
Tetrahedron Letters, 38(5), 883-886 (1997)
A.K. Ghosh et al.
Tetrahedron Letters, 33, 2781-2781 (1992)
Yesica Garcia-Ramos et al.
Journal of peptide science : an official publication of the European Peptide Society, 19(12), 725-729 (2013-11-10)
Aza-glycinyl dipeptides are useful building blocks for the synthesis of a diverse array of azapeptides. The construction of the aza-glycine residue is however challenging, because of the potential for side reactions, such as those leading to formation of oxadiazalone, hydantoin
T. Kokubo et al.
Journal of the American Chemical Society, 109, 606-606 (1987)
N. Nimura et al.
Analytical Chemistry, 58, 2372-2372 (1986)

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