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Merck
CN

900930

6-Azidohexanoic acid

≥95%

别名:

6-Azidocaproic acid

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关于此项目

经验公式(希尔记法):
C6H11N3O2
化学文摘社编号:
分子量:
157.17
UNSPSC Code:
12352106
MDL number:
Assay:
≥95%
Form:
liquid
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assay

≥95%

form

liquid

reaction suitability

reagent type: cross-linking reagent

availability

available only in USA

refractive index

n/D 1.463

solubility

DMF: soluble, DMSO: soluble, THF: soluble, chloroform: soluble, dichloromethane: soluble

density

1.074 g/mL

storage temp.

2-8°C

InChI

1S/C6H11N3O2/c7-9-8-5-3-1-2-4-6(10)11/h1-5H2,(H,10,11)

InChI key

JCORXJUUSVCJEP-UHFFFAOYSA-N

Application

6-Azidohexanoic acid is a six-carbon saturated fatty acid with an ω-terminal azide group. This building block can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC), forming a stable amide bond. The terminal azide group allows conjugation with compounds containing alkyne groups through a copper(I)-catalyzed cycloaddition reaction, also known as click chemistry. 6-Azidohexanoic acid is useful for crosslinking, synthesis of chemical probes, and other bioconjugation strategies.


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Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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分析证书(COA)

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Activated Microglia Targeting Dendrimer?Minocycline Conjugate as Therapeutics for Neuroinflammation.
Sharma R, et al.
Bioconjugate Chemistry, 28(11), 2874-2886 (2017)
Efficient Access to New Chemical Space Through Flow?Construction of Druglike Macrocycles Through Copper?Surface?Catalyzed Azide?Alkyne Cycloaddition Reactions.
Bogdan A R and James K
Chemistry?A European Journal , 16(48), 14506-14512 (2010)
Conception of Stretchable Resistive Memory Devices Based on Nanostructure?Controlled Carbohydrate?block?Polyisoprene Block Copolymers.
Hung C C, et al.
Advances in Functional Materials, 27(13) (2017)



全球贸易项目编号

货号GTIN
900930-250MG04061832874883
900930-1G04061826656037