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86359

Sigma-Aldrich

TentaGel S-NH2

extent of labeling: 0.20-0.35 mmol/g N loading

Synonym(s):

O-(2-Aminoethyl)polyethylene glycol polymer-bound

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About This Item

MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22

product line

TentaGel

Quality Level

form

solid

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

extent of labeling

0.20-0.35 mmol/g N loading

particle size

110-150 μm

application(s)

peptide synthesis

functional group

amine

storage temp.

2-8°C

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Application

TentaGel S-NH2 can be used:
  • As a support in the synthesis of L-Leu based peptides and oligomers, which are used as catalysts in Julia-Colonna epoxidation of chalcones.
  • In the synthesis of 1,3-dialkyl quinazoline-2,4-diones.
  • To synthesize N-substituted amidinoaryloxypyridine analogs as potent factor Xa inhibitors.

Legal Information

TentaGel is a trademark of Rapp Polymere GmbH

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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’.

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Highly enantioselective enone epoxidation catalyzed by short solid phase-bound peptides: dominant role of peptide helicity
Berkessel A, et al.
Organic Letters, 3(24), 3839-3842 (2001)
Solid-phase synthesis of 1, 3-dialkyl quinazoline-2, 4-diones
Buckman BO and Mohan R
Tetrahedron Letters, 37(26), 4439-4442 (1996)
Solid-phase synthesis of N-substituted amidinophenoxy pyridines as factor Xa inhibitors
Mohan R, et al.
Bioorganic & Medicinal Chemistry Letters, 8(14), 1877-1882 (1998)

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