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About This Item
Empirical Formula (Hill Notation):
C6H11N3O2
CAS Number:
Molecular Weight:
157.17
UNSPSC Code:
12352106
MDL number:
Assay:
≥95%
Form:
liquid
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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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 900930-250MG | 04061832874883 |
| 900930-1G | 04061826656037 |
