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8.55013

NovaSyn®TG Sieber resin

Novabiochem®

Synonym(s):

9-Fmoc-amino-xanthen-3-yloxy TG resin

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$204.00

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$811.00

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About This Item

NACRES:
NA.22
UNSPSC Code:
13111023

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product line

NovaSyn® TG, Novabiochem®

form

beads

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename

Novabiochem®

application(s)

peptide synthesis

functional group

amine

storage temp.

2-8°C

Quality Level

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This Item
8.551578.550098.55008
reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

functional group

amine

functional group

amine

functional group

amine

functional group

amine

product line

NovaSyn® TG, Novabiochem®

product line

NovaSyn® TG, Novabiochem®

product line

NovaSyn® TG, Novabiochem®

product line

Novabiochem®

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

400

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

General description

NovaSyn TG Sieber resin consists of 130 μm NovaSyn TG bromo resin derivatized with Sieber′s xanhydrylamine linker [1,2]. This resin is ideal for the Fmoc SPPS of partially protected peptide amide fragments. Cleavage from this support is effected by treatment with 1% TFA in DCM, conditions that leave most standard side-chain protecting groups intact. This resin can be reductively alkylated and used to prepare secondary carboxamides [3]. It can also be employed to produce protected peptide fragments in which the C-terminal carboxylic acid group is blocked as a hydroxymethylphenoxy-β-alaninamide ester [4].

Associated Protocols and Technical Articles
Protocols for Loading of Peptide Synthesis Resins

Literature references

[1] P. Sieber (1987) Tetrahedron Lett., 28, 2107.
[2] C. Somlai, et al. in ′Peptides 1992, Proc.22nd European Peptide Symposium′, C. H. Schneider & A. N. Eberle (Eds), ESCOM, Leiden, 1993, pp. 198.
[3] W. C. Chan, et al. (1995) J. Chem. Soc., Chem. Commun., 1475.
[4] W. C. Chan, et al. (1995) J. Chem. Soc., Chem. Commun., 589.

Analysis Note

Color (visual): light yellow to yellow to beige
Appearance of substance (visual): beads
Loading (Photometric determination of the Fmoc-chromophore liberated upon treatment with DBU/DMF): 0.10 - 0.25 mmol/g
Swelling Volume (in DMF): lot specific result
The polymer matrix is NovaSyn TG resin (130µm)

Other Notes

Replaces: 01-64-0092

Legal Information

NOVASYN is a registered trademark of Merck KGaA, Darmstadt, Germany
Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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Articles

Novabiochem® offers a wide range of linkers and derivatized resins for Fmoc solid-phase peptide synthesis with specialized protocols.

Protocols

Review various resins like Merrifield, trityl-based, and hydroxymethyl-functionalized for peptide immobilization for diverse applications.

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