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Merck
CN

850993

Sigma-Aldrich

2-氨基异丁酸

98%, for peptide synthesis

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别名:
α-氨基异丁酸, 2-甲基丙氨酸, Aib
线性分子式:
(CH3)2C(NH2)COOH
CAS号:
分子量:
103.12
Beilstein:
506496
EC 号:
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

98%

形式

solid

反应适用性

reaction type: solution phase peptide synthesis

mp

≥300 °C

应用

peptide synthesis

SMILES字符串

CC(C)(N)C(O)=O

InChI

1S/C4H9NO2/c1-4(2,5)3(6)7/h5H2,1-2H3,(H,6,7)

InChI key

FUOOLUPWFVMBKG-UHFFFAOYSA-N

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一般描述

2-氨基异丁酸又名α-氨基丁酸,是一种氨基酸,用于液相多肽合成法。强烈促进肽形成螺旋,适合作为肽合成构件。

应用

2-氨基异丁酸可用于合成自组装多肽纳米颗粒。 结构上二-α-取代,对C−H提取呈惰性,因而在肽链中掺入这种化合物可避免发生不需要的反应。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Photochemical methods for peptide macrocyclisation
Chemistry?A European Journal , 27, 69-88 (2021)
Amphiphilic polypeptides with prolonged enzymatic stability for the preparation of self-assembled nanobiomaterials
Royal Society of Chemistry Advances, 8, 34603-34613 (2018)
Yutong Yang et al.
Membranes, 10(11) (2020-11-14)
Amine-containing mixed-matrix membranes incorporated with amino-functionalized multi-walled carbon nanotubes (AF-MWNTs) were synthesized for CO2/H2 separation based on the facilitated transport mechanism. AF-MWNTs were chosen primarily as the mechanical reinforcing filler to enhance the membrane stability. At 107 °C and 0.2-MPa
Evgeniy Salnikov et al.
Journal of biomolecular NMR, 45(4), 373-387 (2009-10-14)
In protein NMR spectroscopy the chemical shift provides important information for the assignment of residues and a first structural evaluation of dihedral angles. Furthermore, angular restraints are obtained from oriented samples by solution and solid-state NMR spectroscopic approaches. Whereas the
Marta De Zotti et al.
Amino acids, 43(4), 1761-1777 (2012-04-10)
The lipopeptaibol trichogin GA IV is a natural, non-ribosomally synthesized, antimicrobial peptide remarkably resistant to the action of hydrolytic enzymes. This feature may be connected to the multiple presence in its sequence of the non-coded residue α-aminoisobutyric acid (Aib), which

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