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Merck
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8.52106

Sigma-Aldrich

Fmoc-Lys(Me,Boc)-OH

≥98% (TLC), for peptide synthesis, Novabiochem®

别名:

Fmoc-Lys(Me,Boc)-OH, N-α-Fmoc-N-ε-methyl-N-ε-t.-Boc-L-lysine

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About This Item

经验公式(希尔记法):
C27H34N2O6
分子量:
482.57
分類程式碼代碼:
12352209
NACRES:
NA.22

product name

Fmoc-Lys(Me,Boc)-OH, Novabiochem®

品質等級

產品線

Novabiochem®

化驗

≥97.0% (HPLC)
≥98% (TLC)

形狀

powder

反應適用性

reaction type: Fmoc solid-phase peptide synthesis

製造商/商標名

Novabiochem®

應用

peptide synthesis

官能基

amine

儲存溫度

2-8°C

InChI

1S/C27H34N2O6/c1-27(2,3)35-26(33)29(4)16-10-9-15-23(24(30)31)28-25(32)34-17-22-20-13-7-5-11-18(20)19-12-6-8-14-21(19)22/h5-8,11-14,22-23H,9-10,15-17H2,1-4H3,(H,28,32)(H,30,31)/t23-/m0/s1

InChI 密鑰

JHMSFOFHTAYQLS-QHCPKHFHSA-N

一般說明

A novel derivative for the introduction of monomethyl-lysine during Fmoc SPPS [1,2]. Coupling can be carried out using any standard activation method. Removal of the Boc protecting group occurs during the course of the TFA-mediated cleavage reaction. Ref [3] contains methods and protocols for the synthesis of arrays of histone-related peptides containing methylated arginine and lysine-residues.

Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Fmoc SPPS
Overcoming Aggregation in Fmoc SPPS

Literature references

[1] A.J. Bannister (2002) Cell, 109, 801.
[2] A.E. McBride & P.A. Silver (2001) Cell, 106, 5.
[3] S. Rothbart, et al. (2012) Methods Enzymol., 512, 107.

聯結

Replaces: 04-12-1263

分析報告

Color (visual): white to light yellow to beige
Appearance of substance (visual): powder
Identity (IR): passes test
Optical rotation α 25/D (c=1 in DMF): -13.0 - -8.5 °
Purity (TLC(CMA2)): ≥ 98 %
Assay (HPLC, area%): ≥ 97.0 % (a/a)
Solubility (1 mmole in 2 ml DMF): clearly soluble

To see the solvent systems used for TLC of Novabiochem® products please click here.

法律資訊

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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