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Merck
CN

338338

Sigma-Aldrich

Fmoc-Phe-OH

98%, for peptide synthesis

别名:

N-(9-芴甲氧羰基)-L-苯丙氨酸, Fmoc-L-苯丙氨酸

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About This Item

经验公式(希尔记法):
C24H21NO4
CAS号:
分子量:
387.43
Beilstein:
3597808
EC 号:
MDL编号:
UNSPSC代码:
12352209
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.26

产品名称

Fmoc-Phe-OH, 98%

质量水平

方案

98%

旋光性

[α]20/D −37°, c = 1 in DMF

反应适用性

reaction type: C-H Activation
reaction type: Fmoc solid-phase peptide synthesis
reagent type: ligand
reaction type: Peptide Synthesis

mp

180-187 °C (lit.)

应用

peptide synthesis

官能团

Fmoc
amine
carboxylic acid

储存温度

2-8°C

SMILES字符串

OC(=O)[C@H](Cc1ccccc1)NC(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C24H21NO4/c26-23(27)22(14-16-8-2-1-3-9-16)25-24(28)29-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h1-13,21-22H,14-15H2,(H,25,28)(H,26,27)/t22-/m0/s1

InChI key

SJVFAHZPLIXNDH-QFIPXVFZSA-N

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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Journal of peptide science : an official publication of the European Peptide Society, 23(2), 131-140 (2017-01-10)
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ACS chemical neuroscience, 9(5), 1001-1013 (2017-12-20)
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R Ashton Lavoie et al.
International journal of molecular sciences, 20(7) (2019-04-11)
The growing integration of quality-by-design (QbD) concepts in biomanufacturing calls for a detailed and quantitative knowledge of the profile of impurities and their impact on the product safety and efficacy. Particularly valuable is the determination of the residual level of
R Ashton Lavoie et al.
Biotechnology and bioengineering, 117(2), 438-452 (2019-10-28)
The clearance of host cell proteins (HCPs) is of crucial importance in biomanufacturing, given their diversity in composition, structure, abundance, and occasional structural homology with the product. The current approach to HCP clearance in the manufacturing of monoclonal antibodies (mAbs)

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