QBD10213
Fmoc-N-amido-dPEG®4-acid
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）:
C26H33NO8
化学文摘社编号:
分子量:
487.54
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
51171641
MDL number:
InChI
1S/C26H33NO8/c28-25(29)9-11-31-13-15-33-17-18-34-16-14-32-12-10-27-26(30)35-19-24-22-7-3-1-5-20(22)21-6-2-4-8-23(21)24/h1-8,24H,9-19H2,(H,27,30)(H,28,29)
SMILES string
OC(CCOCCOCCOCCOCCNC(OCC1C(C=CC=C2)=C2C3=C1C=CC=C3)=O)=O
InChI key
NUHRPLKTAAVHCZ-UHFFFAOYSA-N
assay
>90%
form
solid or viscous liquid
reaction suitability
reaction type: Pegylations, reagent type: cross-linking reagent
functional group
amine, carboxylic acid
polymer architecture
shape: linear
functionality: heterobifunctional
shipped in
ambient
storage temp.
−20°C
Features and Benefits
Fmoc-N-amido-dPEG®4-acid is a novel Fmoc-protected amino acid containing a single molecular weight PEG (dPEG®) spacer arm. These reagents are used to introduce a hydrophilic, non-immunogenic spacer into a peptide. Three different lengths of dPEG® allow precise control of spacing and hydrophilicity. The Fmoc group can be removed, exposing the terminal amine, using piperidine as with standard peptide synthesis.Fmoc-N-amido-dPEG®n-acid reagents are novel Fmoc-protected amino acids containing a single molecular weight PEG (dPEG®) spacer arm (18.1 Å). This reagents is used to introduce a hydrophilic, non-immunogenic spacer into a peptide. Fmoc group can be removed, exposing the terminal amine, using piperidine as with standard peptide synthesis.
Legal Information
Products Protected under U.S. Patents # 7,888,536 B2
dPEG is a registered trademark of Quanta BioDesign
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
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