A82605
11-氨基十一酸
97%
别名:
Aminoundecanoic acid
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关于此项目
线性分子式:
NH2(CH2)10CO2H
化学文摘社编号:
分子量:
201.31
Beilstein:
1767291
EC 号:
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
97%
表单
powder
反应适用性
reaction type: solution phase peptide synthesis
颜色
white
mp
188-191 °C (lit.)
应用
peptide synthesis
SMILES字符串
NCCCCCCCCCCC(O)=O
InChI
1S/C11H23NO2/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h1-10,12H2,(H,13,14)
InChI key
GUOSQNAUYHMCRU-UHFFFAOYSA-N
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一般描述
11-氨基十一烷酸，又称为氨基十一酸，常用于液相多肽合成法。还可用作尼龙11的单体前体。
应用
111-氨基十一烷酸可作为linker合成酰胺连接的线性鸟苷二聚体。
储存分类代码
13 - Non Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Development of Minimal Diguanosinyl Motif toward RNA G-Quadruplex-Like Structures in Solution
Chembiochem, 21, 1837-1842 (2020)
Syntheses of 12-aminododecanoic and 11-aminoundecanoic acids from vernolic acid
Journal of the American Oil Chemists' Society, 74, 531-538 (1997)
Liling Zeng et al.
Nano letters, 5(10), 2001-2004 (2005-10-13)
Carboxylic acid-functionalized SWNTs prepared via the reaction of an amino acid, NH2(CH2)nCO2H, with fluoronanotubes show similar levels of sidewall functionalization; however, the solubility in water is controlled by the length of the hydrocarbon side chain (i.e., n). The 6-aminohexanoic acid
P Kyprianou et al.
The Biochemical journal, 207(3), 549-556 (1982-12-01)
1. The theory of Nichol, Ogston, Winzor & Sawyer [(1974) Biochem. J. 143, 435-443] for quantitative affinity chromatography, when adapted for use with a non-specific column from which a multi-site protein can be specifically desorbed by its free ligand, permits
11-Aminoundecanoic acid.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 39, 239-245 (1986-01-01)
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