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Merck
CN
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文件

8.55060

Sigma-Aldrich

Rink Acid resin (100-200 mesh)

Novabiochem®

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别名:
4-(2′,4′-Dimethoxyphenyl-hydroxymethyl)-phenoxy resin
UNSPSC代码:
13111023
NACRES:
NA.22

质量水平

产品线

Novabiochem®

形式

beads

反应适用性

reaction type: Fmoc solid-phase peptide synthesis

制造商/商品名称

Novabiochem®

应用

peptide synthesis

官能团

alcohol

储存温度

2-30°C

一般描述

Rink acid resin is a super acid-labile support for the solid phase immobilization of carboxylic acids [1] by Fmoc SPPS. Cleavage can be effected with as little as 10% AcOH in DCM, providing highly acid-sensitive products in high yields and purities. However, care must be taken to prevent product loss during synthetic manipulations [2], owing to the extreme acid sensitivity of this support. Treatment with HCl in THF [3] or Ph2PCl2 [4] has been shown to efficiently convert this resin to the corresponding benzhydryl chloride, to which can be coupled a wide range of functional groups: hydroxylamines [3], alcohols, amines, acids and thiols [4]. Rink acid resin has also been converted to a trifluoroacetate with TFA and used in a similar manner to immobilize amines, thiols, alcohols, and phenols [5]. In a more detailed study, the same authors found 1 M trifluoroacetic anhydride in 2,6-lutidine to give superior results with less degradation of the linker [6, 7]. Rink resin trifluoroacetate has also been used to prepare purines [8, 9].Cleavage of amines and alcohols from this support has been carried out with either 5% TFA in DCM [4] or 20% TFA in DCM [5]; thiols were released with either 5% TFA in DCM [4] or 95% aq. TFA [5].

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

Literature references

[1] H. Rink (1987) Tetrahedron Lett., 28, 3787.
[2] H. U. Immer, et al. in ′Peptides, Chemistry, Structure &Biology, Proc. 11th American Peptide Symposium′, J. E. Rivier & G. R. Marshall (Eds), ESCOM, Leiden, 1990, pp. 1054.
[3] S. L. Mellor & W. C. Chan (1997) J. Chem. Soc., Chem. Commun., 2005.
[4] R. S. Garigipati (1997) Tetrahedron Lett., 38, 6807.
[5] W.K.-D. Brill in ′First Conference on Synthetic Organic Chemistry′, www.mdpi.org/ecsoc, 1997.
[6] W.K.-D. Brill (1998) Syn. Lett., 906.
[7] R. A. Tommesi, et al. (1998) Tetrahedron Lett., 39, 5477.
[8] W.K.-D. Brill (2001) Syn. Lett., 1097.
[9] W.K.-D. Brill & C. Riva-Toniolo (2001) Tetrahedron Lett., 42, 65`5.

联系

Replaces: 01-64-0012

分析说明

Color (visual): white to yellow to beige
Appearance of substance (visual): beads
Loading (determined from the substition of the Fmoc-NH2 loaded resin): 0.35 - 0.80 mmol/g
Swelling Volume (in DMF): lot specific result
The polymer matrix is copoly (styrene - 1% DVB) 100 -200 mesh

法律信息

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

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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商品

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

实验方案

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

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