Merck

47624

Sigma-Aldrich

Fmoc-Lys(Boc)-OH

≥98.0% (HPLC)

登录to View Organizational & Contract Pricing

Select a Size

别名:
Nα-芴甲氧羰基-Nε-叔丁氧羰基-L-赖氨酸
Empirical Formula (Hill Notation):
C26H32N2O6
CAS号:
分子量:
468.54
Beilstein:
4217767
EC 号:
MDL编号:
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.26

检测方案

≥98.0% (HPLC)

形式

solid

旋光性

[α]20/D −12±1°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

官能团

Boc
Fmoc

储存温度

2-8°C

SMILES string

CC(C)(C)OC(=O)NCCCC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C26H32N2O6/c1-26(2,3)34-24(31)27-15-9-8-14-22(23(29)30)28-25(32)33-16-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,21-22H,8-9,14-16H2,1-3H3,(H,27,31)(H,28,32)(H,29,30)/t22-/m0/s1

InChI key

UMRUUWFGLGNQLI-QFIPXVFZSA-N

正在寻找类似产品? Visit 产品对比指南

比较类似商品

查看完整比较结果

显示差异

1 of 4

此商品
3596618.5201247317
Fmoc-Lys(Boc)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47624

Fmoc-Lys(Boc)-OH

H-Lys(Boc)-OH ≥95%

Sigma-Aldrich

359661

H-Lys(Boc)-OH

Fmoc-Lys(Boc)-OH Novabiochem®

Sigma-Aldrich

8.52012

Fmoc-Lys(Boc)-OH

Fmoc-Lys(Fmoc)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47317

Fmoc-Lys(Fmoc)-OH

form

solid

form

powder

form

powder

form

-

optical activity

[α]20/D −12±1°, c = 1% in DMF

optical activity

[α]20/D +18°, c = 1 in acetic acid

optical activity

-

optical activity

-

functional group

Boc, Fmoc

functional group

-

functional group

Boc, amine

functional group

Fmoc

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-30°C

storage temp.

2-8°C

Quality Level

100

Quality Level

200

Quality Level

400

Quality Level

100

一般描述

Fmoc-Lys(Boc)-OH 是一种氨基酸衍生物,用于Fmoc固相合成多肽的试剂。

应用

Fmoc-Lys(Boc)-OH可用于:
  • 通过与甲基苯甲胺(MBHA)树脂偶联固相合成五取代的二氢咪唑基丁基二氢咪唑-3-盐。
  • 基于Fmoc多肽合成线性嵌插剂双萘四酰亚二胺
  • 合成ε-Boc-ε-(3,5-双-三氟甲基-苄基)-α-Fmoc-L-赖氨酸,可用作基于19F NMR的筛选工具。

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)


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Documents related to the products that you have purchased in the past have been gathered in the Document Library for your convenience.

Visit the Document Library

Difficulty Finding Your Product Or Lot/Batch Number?

在网站页面上,产品编号会附带包装尺寸/数量一起显示(例如:T1503-25G)。请确保 在“产品编号”字段中仅输入产品编号 (示例: T1503).

示例

T1503
货号
-
25G
包装规格/数量

其它示例:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

输入内容 1.000309185)

遇到问题?欢迎随时联系我们技术服务 寻求帮助

批号可以在产品标签上"批“ (Lot或Batch)字后面找到。

Aldrich 产品

  • 如果您查询到的批号为 TO09019TO 等,请输入去除前两位字母的批号:09019TO。

  • 如果您查询到的批号含有填充代码(例如05427ES-021),请输入去除填充代码-021的批号:05427ES。

  • 如果您查询到的批号含有填充代码(例如 STBB0728K9),请输入去除填充代码K9的批号:STBB0728。

未找到您寻找的产品?

部分情况下,可能未在线提供COA。如果搜索不到COA,可在线索取。

索取COA

其他客户在看

Slide 1 of 6

1 of 6

Boc-Lys-OH 99%

Sigma-Aldrich

359688

Boc-Lys-OH

Fmoc-Gly-OH ≥98.0% (T)

Sigma-Aldrich

47627

Fmoc-Gly-OH

Fmoc-Tyr(tBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47623

Fmoc-Tyr(tBu)-OH

Fmoc-Trp(Boc)-OH ≥97.0% (HPLC)

Sigma-Aldrich

47561

芴甲氧羰酰-色氨酸

Fmoc-Ile-OH ≥98.0% (T)

Sigma-Aldrich

47628

Fmoc-Ile-OH

Improved synthesis of polyfluorinated l-lysine for 19F NMR-based screening.
Malgesini B, et al.
Molecular Diversity, 13(1), 53-56 (2009)
Solid-phase parallel synthesis of substituted dihydroimidazolylbutyl dihydroimidazol-3-ium salts.
Acharya AN, et al.
Tetrahedron Letters, 43(7), 1157-1160 (2002)
Bis-naphthalene diimide exhibiting an effective bis-threading intercalating ability.
Nojima T, et al.
Nucleic Acids Symposium Series, 3(1), 123-124 (2003)
Marine Bacchi et al.
Protein science : a publication of the Protein Society, 25(12), 2225-2242 (2016-09-28)
Synthetic biology (or chemical biology) is a growing field to which the chemical synthesis of proteins, particularly enzymes, makes a fundamental contribution. However, the chemical synthesis of catalytically active proteins (enzymes) remains poorly documented because it is difficult to obtain
Marta Kulik et al.
Biochimie, 138, 32-42 (2017-04-12)
A fragment of 23S ribosomal RNA (nucleotides 1906-1924 in E. coli), termed Helix 69, forms a hairpin that is essential for ribosome function. Helix 69 forms a conformationally flexible inter-subunit connection with helix 44 of 16S ribosomal RNA, and the nucleotide

相关内容

Natural Amino Acid Building Blocks for Peptide Synthesis

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

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.

联系技术服务部门