| Identification | Back Directory | [Name]
4-hydroxy Nonenal Alkyne | [CAS]
1011268-23-7 | [Synonyms]
4-hydroxy Nonenal Alkyne
(E)-4-hydroxynon-2-en-8-ynal
4-hydroxynon-2(E)-nonen-8-ynal
2-Nonen-8-ynal, 4-hydroxy-, (2E)-
4-hydroxy Nonenal Alkyne Exclusive
4hydroxy Nonenal Alkyne,4 hydroxy Nonenal Alkyne | [Molecular Formula]
C9H12O2 | [MOL File]
1011268-23-7.mol | [Molecular Weight]
152.19 |
| Chemical Properties | Back Directory | [Boiling point ]
292.3±40.0 °C(Predicted) | [density ]
1.016±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -80°C; protect from light | [solubility ]
DMF: 2.5 mg/ml; DMSO: 2 mg/ml; Ethanol: 12.5 mg/ml; PBS (pH 7.2): 5 mg/ml | [pka]
12.98±0.20(Predicted) |
| Hazard Information | Back Directory | [Uses]
4-hydroxy Nonenal (4-HNE) is a major aldehyde produced during the lipid peroxidation of ω-6 polyunsaturated fatty acids, such as arachidonic acid and linoleic acid. It is considered a potential causal agent in numerous diseases, including chronic inflammation, neurodegenerative diseases, atherosclerosis, diabetes, and cancer, in part because it covalently modifies DNA and proteins resulting in genetic mutations and altered cell signaling, respectively. 4-HNE Alkyne is a form of 4-HNE with a terminal alkyne. Such terminal alkyne groups can be used in linking reactions, known as click chemistry, characterized by high dependability and specificity of azide-alkyne bioconjugation reactions. Click chemistry has only recently been applied to the study of oxidized lipids.[Cayman Chemical] | [Definition]
ChEBI:4-hydroxy Nonenal Alkyne is an aliphatic alcohol. | [storage]
Store at -80°C; protect from light |
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