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HCID 11040949Erstellt: 4. November 2026

6-azidohexanoic Acid

6-azidovaleric acid · e-Azidocaproic acid · 6-Azido-hexanoic acid · 6-Azidohexanoic acid >=95% · 6-Azidohexanoic acid - A1945 · Click Tag 6-Azidohexanoic acid · 6-Azidohexanoic Acid (CCT-1250)

https://huagongshe.com/de/chemical/11040949

Molekülstruktur von 6-azidohexanoic Acid

Identifikatoren & physikalische Daten

CAS No.79598-53-1
SummenformelC6H11N3O2
Durchschnittliche Molmasse157,17 g/mol
Monoisotopische Masse157,0851266 g/mol
SMILES[N-]=[N+]=NCCCCCC(=O)O
InChIKeyJCORXJUUSVCJEP-UHFFFAOYSA-N
PubChem CID11040949
EC No.633-038-7
DTXSIDDTXSID90452913

Chemische & physikalische Eigenschaften

XLogP1,7
Polarare Oberfläche (TPSA)51,7
H-Brücken-Donoren1
H-Brücken-Akzeptoren4
Frei drehbare Bindungen6
Schwere Atome11
Formalladung0
Komplexität163
Dichte1.074 g/mL
Brechungsindexn/D 1.463
Lagerbedingungen2-8°C
LöslichkeitChloroform (Slightly), Methanol (Slightly)
AggregatzustandOil
FarbeColourless to Pale Yellow
StabilitätLight Sensitive
InChIInChI=1S/C6H11N3O2/c7-9-8-5-3-1-2-4-6(10)11/h1-5H2,(H,10,11)
InChIKeyJCORXJUUSVCJEP-UHFFFAOYSA-N
SMILESC(O)(=O)CCCCCN=[N+]=[N-]

Sicherheit & Vorschriften

GHS-EinstufungWarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesSkin Irrit. 2 (100%)
Wassergefährdungsklasse (WGK)WGK 3
Zollcode29270000
Sicherheitshinweise (S)24/25
Lagerklasse11 - Combustible Solids
GefahrenklasseEye Irrit. 2Skin Irrit. 2STOT SE 3

Anwendungen & Verwendung

Verwenden

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.