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经验公式(希尔记法):
C13H26N2O4
化学文摘社编号:
分子量:
274.36
MDL number:
UNSPSC Code:
12352209
NACRES:
NA.22
产品名称
Boc-Lys(Me)2-OH, Novabiochem®
SMILES string
[N+H](CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)[O-])(C)C
InChI
1S/C13H26N2O4/c1-13(2,3)19-12(18)14-10(11(16)17)8-6-7-9-15(4)5/h10H,6-9H2,1-5H3,(H,14,18)(H,16,17)/t10-/m0/s1
InChI key
KPXRFYHPDPDJSY-JTQLQIEISA-N
product line
Novabiochem®
assay
≥98% (TLC)
form
powder
reaction suitability
reaction type: Boc solid-phase peptide synthesis
manufacturer/tradename
Novabiochem®
application(s)
peptide synthesis
functional group
amine
storage temp.
2-30°C
Quality Level
Analysis Note
Colour (visual): white to slight yellow to beige
Appearance of substance (visual): powder
Identity (IR): passes test
Optical rotation α 25/D (c=1 in methanol): +17.0 - +21.0 °
Purity (TLC(CMA1)): ≥ 98 %
Purity (TLC(0110)): ≥ 98 %
To see the solvent systems used for TLC of Novabiochem® products please click here.
Appearance of substance (visual): powder
Identity (IR): passes test
Optical rotation α 25/D (c=1 in methanol): +17.0 - +21.0 °
Purity (TLC(CMA1)): ≥ 98 %
Purity (TLC(0110)): ≥ 98 %
To see the solvent systems used for TLC of Novabiochem® products please click here.
General description
Boc-Lys(Me)2-OH [1] is a building block for the introduction of the naturally occurring proteinogenic amino acid Nε, Nε-dimethyl-L-lysine [2].
Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Boc SPPS
Literature references
[1] F. M. F. Chen & N. L. Benoiton (1978) Can. J. Biochem., 56, 150.
[2] W. K. Paik & S. Kim (1971) Science, 174, 114.
Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Boc SPPS
Literature references
[1] F. M. F. Chen & N. L. Benoiton (1978) Can. J. Biochem., 56, 150.
[2] W. K. Paik & S. Kim (1971) Science, 174, 114.
Other Notes
Replaces: 04-12-0244
Legal Information
Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
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Unnatural amino acids, the non-proteinogenic amino acids that either occur naturally or are chemically synthesized, are becoming more and more important as tools for modern drug discovery research.
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