1841512-95-5
1841512-95-5
Chemical Structure
17-Azidoheptadecanoic acid
- CAS No.: 1841512-95-5
- Formula:C17H33N3O2
- Molecular Weight:311.46
InChIKey: SFAZATFDYDNQPI-UHFFFAOYSA-N
SMILES: O=C(O)CCCCCCCCCCCCCCCCN=[N+]=[N-]
Biological Activity: 17-Azidoheptadecanoic acid is a fatty acid azide with an azide linker. 17-Azidoheptadecanoic acid can undergo copper-catalyzed click chemistry reactions with alkynes, DBCO, and BCN for protein modification[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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17-Azidoheptadecanoic acid | 99.88% | 17-Azidoheptadecanoic acid is a fatty acid azide with an azide linker. 17-Azidoheptadecanoic acid can undergo copper-catalyzed click chemistry reactions with alkynes, DBCO, and BCN for protein modification. | ||||||||||||||||||||
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17-Hydroxyheptadecanoic acid | 99.70% | 17-Hydroxyheptadecanoic acid (ω-Hydroxyheptadecanoic acid) is an ester product. | ||||||||||||||||||||
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16-Azidohexadecanoic acid | 98.0% | 16-Azidohexadecanoic acid is a fatty acid metabolism probe and a substrate of fatty acid transport protein (FATP). 16-Azidohexadecanoic acid serves as a metabolic probe for fatty acid analysis via click chemistry and HPLC/MS detection. | ||||||||||||||||||||
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15-Azido-pentadecanoic acid | 99.88% | 15-Azido-pentadecanoic acid is a click chemistry reagent containing an azide group. Azido Palmitic Acid can be used to identify and characterize post-translationally palmitylated proteins with using a simple and robust two-step labeling and detection technique. 15-Azido-pentadecanoic acid is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. | ||||||||||||||||||||
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18-Azido-stearic acid | ≥95.0% | 18-Azido-stearic acid is a click chemistry reagent containing an azide group. 18-Azido-stearic acid can be used as a hydrophobic bioconjugation linker (using N-Myristoyltransferase) that can be further modified at the azido-position using Click-chemistry. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. | ||||||||||||||||||||
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Azido Myristic Acid | 99.89% | Azido Myristic Acid is a click chemistry reagent containing an azide group. Azido Myristic Acid can be used to identify and characterize post-translationally myristylated proteins with using a simple and robust two-step labeling and detection technique. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. | ||||||||||||||||||||
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NH2-C16-azide | NH2-C16-azide is a 16-azidohexadecylamine derivative and synthetic intermediate, which can serve as a PROTAC Linker. NH2-C16-azide is applicable to research related to PROTAC synthesis, such as acting as the linker for PROTAC CDK9 degrader-13 (HY-184693). | |||||||||||||||||||||
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Stearic acid-1-13C | 99.90% | Stearic acid-1-13C is the 13C labeled Stearic acid. Stearic acid is a long chain dietary saturated fatty acid which exists in many animal and vegetable fats and oils. | ||||||||||||||||||||
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Stearic acid-13C18 | 99.2% | Stearic acid-13C18is the 13C-labeled Stearic acid. Stearic acid is a long chain dietary saturated fatty acid which exists in many animal and vegetable fats and oils. | ||||||||||||||||||||
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Oleic acid (18-azido) | Oleic acid (18-azido) is a clickable fatty acid that can be used in click chemistry reactions. | |||||||||||||||||||||
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