15395
Boc-6-Ahx-OH
≥99.0% (T)
别名:
6-(Boc-氨基)羊油酸, Boc-6-氨基己酸, 叔丁氧羰酰基 6-氨基己酸
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选择尺寸
关于此项目
线性分子式:
(CH3)3CO2CNH(CH2)5CO2H
化学文摘社编号:
分子量:
231.29
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2049561
InChI
1S/C11H21NO4/c1-11(2,3)16-10(15)12-8-6-4-5-7-9(13)14/h4-8H2,1-3H3,(H,12,15)(H,13,14)
SMILES string
CC(C)(C)OC(=O)NCCCCCC(O)=O
InChI key
RUFDYIJGNPVTAY-UHFFFAOYSA-N
assay
≥99.0% (T)
form
solid
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
35-40 °C
application(s)
peptide synthesis
storage temp.
2-8°C
Quality Level
Other Notes
引入 ε 的保护衍生物各种化合物中的 -氨基己基部分。 在亲和层析中引入氨基己酸间隔臂。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
A J Schroit et al.
Biochemistry, 22(15), 3617-3623 (1983-07-19)
An efficient method for the synthesis and purification of a variety of iodinated phospholipid analogues is described. 1-Acyl-2-[[[3-(3-[125I]iodo-4-hydroxyphenyl)- propionyl]amino]caproyl]phosphatidylcholine (125I-PC) was prepared by alkylation of 1-acyl-2-(aminocaproyl)phosphatidylcholine with monoiodinated Bolton-Hunter reagent. 125I-Labeled phosphatidic acid, phosphatidylethanolamine, and phosphatidylserine were produced from 125I-PC
Affinity chromatography of carboxypeptidase B.
M Sokolovsky
Methods in enzymology, 34, 411-414 (1974-01-01)
The literature on affinity chromatography.
M Wilchek et al.
Methods in enzymology, 34, 3-10 (1974-01-01)
J. Frank et al.
Helvetica Chimica Acta, 60, 2550-2550 (1977)
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