跳轉至內容
Merck
全部照片(1)

重要文件

41996

Sigma-Aldrich

N-羟基-7-偶氮苯并三氮唑 溶液

~0.6 M in DMF, for peptide synthesis

同義詞:

3H-[1,2,3]-三唑[4,5-b]吡啶-3-醇, HOAt

登入查看組織和合約定價


About This Item

經驗公式(希爾表示法):
C5H4N4O
CAS號碼:
分子量::
136.11
Beilstein:
1211115
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22

product name

N-羟基-7-偶氮苯并三氮唑 溶液, ~0.6 M in DMF

形狀

liquid

品質等級

反應適用性

reaction type: Addition Reactions

濃度

~0.6 M in DMF

雜質

<1.0% water

折射率

n20/D 1.441

密度

0.978 g/mL at 20 °C

應用

peptide synthesis

SMILES 字串

On1nnc2cccnc12

InChI

1S/C5H4N4O/c10-9-5-4(7-8-9)2-1-3-6-5/h1-3,10H

InChI 密鑰

FPIRBHDGWMWJEP-UHFFFAOYSA-N

尋找類似的產品? 前往 產品比較指南

一般說明

1-羟基-7-氮杂苯并三唑溶液,又称3H-[1,2,3]-三唑并[4,5-b]吡啶-3-醇,是一种苯并三唑类添加剂,常用作氨基酸和肽的偶联试剂。它还被用于最小化对映异构体生成。

應用

1-羟基-7-氮杂苯并三唑溶液被用作手性肽核酸的固相合成试剂。

其他說明

偶联添加剂,用于肽合成中的高效无外消旋偶联; 片段偶联。

訊號詞

Danger

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 3 - Repr. 1B

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

136.4 °F - closed cup

閃點(°C)

58 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


從最近期的版本中選擇一個:

分析證明 (COA)

Lot/Batch Number

未看到正確版本?

如果您需要一個特定的版本,您可以透過批號來尋找特定憑證。

已經擁有該產品?

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Simone Di Micco et al.
Frontiers in chemistry, 8, 628609-628609 (2021-02-02)
The most severe outcome of COVID-19 infection is the development of interstitial pneumonia causing acute lung injury (ALI) and/or acute respiratory distress syndrome (ARDS), both responsible for the infected patients' mortality. ALI and ARDS are characterized by a leakage of
L.A. Carpino, A. El-Faham
Tetrahedron, 55, 6813-6813 (1999)
Hsuan-Ni Lin et al.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 34(11), 1883-1893 (2016-02-27)
Fracture healing is regulated by a variety of inflammatory mediators and growth factors which act over time to regenerate the injured tissue. This study used a mouse femur fracture model to quantify the temporal expression pattern of lipid mediators, cytokines
Júlia García-Pindado et al.
Biopolymers, 109(10), e23112-e23112 (2018-03-13)
While revisiting biologically active natural peptides, the importance of the tryptophan residue became clear. In this article, the incorporation of this amino acid, brominated at different positions of the indole ring, into cyclic peptides was successfully achieved. These products demonstrated
Y. Nishiyama et al.
Tetrahedron Letters, 42, 8789-8789 (2001)

我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務