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Merck
CN
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主要文件

257583

Sigma-Aldrich

8-溴辛酸

97%

别名:

8-Bromocaprylic acid

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1 G
¥265.40
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1 G
¥265.40
10 G
¥1,017.31
50 G
¥3,621.82

About This Item

线性分子式:
Br(CH2)7CO2H
CAS Number:
分子量:
223.11
Beilstein:
1756103
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.22

¥265.40


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质量水平

方案

97%

反应适用性

reagent type: cross-linking reagent

沸点

147-150 °C/2 mmHg (lit.)

mp

35-37 °C (lit.)

官能团

bromo
carboxylic acid

SMILES字符串

OC(CCCCCCCBr)=O

InChI

1S/C8H15BrO2/c9-7-5-3-1-2-4-6-8(10)11/h1-7H2,(H,10,11)

InChI key

BKJFDZSBZWHRNH-UHFFFAOYSA-N

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一般描述

8-Bromooctanoic acid, also known as 8-bromocaprylic acid, is a cross-linking reagent. It can undergo hydrolysis to form 8-hydroxyoctanoic acid.[1]

应用

8-Bromooctanoic acid can be used as a crosslinking reagent to:
  • prepare 8-mercaptooctanoic acid in the biosynthesis of lipoic acid[2]
  • attach triple helix-forming oligonucleotides (TFOs) to inhibitors in their synthesis[3]

象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Eye Dam. 1 - Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

  • 技术规格说明书

  • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number

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    访问文档库

    Biosynthesis of lipoic acid: characterization of the lipoic acid auxotrophs Escherichia coli W1485-lip2 and JRG33-lip9
    MA Hayden
    Biochemistry, 32, 3778-3782 (1993)
    Triple helix-forming oligonucleotides conjugated to new inhibitors of topoisomerase II: synthesis and binding properties
    M Duca
    Bioconjugate Chemistry, 16, 873-884 (2005)
    Synthesis of heteroatom-substituted analogues of stearic acid.
    RA Pascal
    Journal of Lipid Research, 27, 221-224 (1986)
    Soumen Das et al.
    Journal of labelled compounds & radiopharmaceuticals, 61(14), 1048-1057 (2018-09-02)
    123 I-Iodophenylpentadecanoic acid (IPPA) is a metabolic agent used in nuclear medicine for diagnosis of myocardial defects. Efforts are underway worldwide to develop a 99m Tc substitute of the above radiopharmaceutical for the aforementioned application. Herein, we report synthesis and
    Beibei Hou et al.
    Materials science & engineering. C, Materials for biological applications, 74, 94-102 (2017-03-04)
    How to encapsulate and transport the payload of multiple therapeutic compounds avoiding premature leakage, and simultaneously co-release them rapidly at specific lesions still remains the major concern in clinic. Herein, we designed the UCN@mSiO

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