8.51028
Bis-Boc-amino-oxyacetic acid
Novabiochem®
别名:
Bis-Boc-amino-oxyacetic acid, Boc 2-Aoa-OH
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C12H21NO7 · xH2O
分子量:
291.30 (anhydrous basis)
NACRES:
NA.22
UNSPSC Code:
12352209
产品名称
Bis-Boc-amino-oxyacetic acid, Novabiochem®
product line
Novabiochem®
assay
≥97% (TLC)
form
powder
reaction suitability
reagent type: ligand
manufacturer/tradename
Novabiochem®
application(s)
peptide synthesis
storage temp.
2-8°C
Quality Level
Analysis Note
Colour (visual): white to slight yellow to beige
Appearance of substance (visual): powder
Identity (IR): passes test
Purity (TLC(CMA2)): ≥ 97 %
Water (K. F.): 3.0 - 8.0 %
To see the solvent systems used for TLC of Novabiochem® products please click here.
Appearance of substance (visual): powder
Identity (IR): passes test
Purity (TLC(CMA2)): ≥ 97 %
Water (K. F.): 3.0 - 8.0 %
To see the solvent systems used for TLC of Novabiochem® products please click here.
General description
This reagent can be used to introduce a hydroxylamine functionality to N-terminal or side-chain amino groups. Hydroxylamine-labeled peptides prepared in this manner can be ligated in aqueous solution at pH 3.5 to aldehyde-containing peptides via oxime formation. This bis-protected derivative eliminates oligomer formation which can occur with mono-protected hydroxylamine reagents as a result of double acylation. Coupling of this derivative should be done using an OSu ester.
Literature references
[1] J. C. Spetzler & T. Hoeg-Jensen (2001) J. Peptide Sci., 7, 537.
Literature references
[1] J. C. Spetzler & T. Hoeg-Jensen (2001) J. Peptide Sci., 7, 537.
Other Notes
Replaces: 01-63-0129
Legal Information
Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
11 - Combustible Solids
wgk
WGK 3
法规信息
新产品
此项目有
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持