284474-73-3
284474-73-3
Chemical Structure
1-Hexadecanol-d33
- CAS No.: 284474-73-3
- Formula:C16HD33O
- Molecular Weight:275.64
IUPAC Name: hexadecan-d33-1-ol
InChIKey: BXWNKGSJHAJOGX-TUWMXWROSA-N
SMILES: [2H]C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])O
Biological Activity: 1-Hexadecanol-d33 is the deuterium labeled 1-Hexadecanol[1]. 1-Hexadecanol is a fatty alcohol, a lipophilic substrate[2].
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1-Hexadecanol-d33 | 1-Hexadecanol-d33 is the deuterium labeled 1-Hexadecanol. 1-Hexadecanol is a fatty alcohol, a lipophilic substrate. | |||||||||||||||||||||
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1-Hexadecanol (Standard) | 99.06% | 1-Hexadecanol (Standard) is the analytical standard of 1-Hexadecanol. This product is intended for research and analytical applications. 1-Hexadecanol is a fatty alcohol, a lipophilic substrate. 1-Hexadecanol can be used for the research of ferroptosis. | ||||||||||||||||||||
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1-Hexadecanol-d5 | 99.20% | 1-Hexadecanol-d5 is the deuterium labeled 1-Hexadecanol. 1-Hexadecanol is a fatty alcohol, a lipophilic substrate. | ||||||||||||||||||||
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1-Hexadecanol-d4 | 1-Hexadecanol-d4 is the deuterium labeled 1-Hexadecanol. 1-Hexadecanol is a fatty alcohol, a lipophilic substrate. | |||||||||||||||||||||
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1-Hexadecanol-d31 | 1-Hexadecanol-d31 is the deuterium labeled 1-Hexadecanol. 1-Hexadecanol is a fatty alcohol, a lipophilic substrate. | |||||||||||||||||||||
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1-Hexadecanol-d3 | 1-Hexadecanol-d3 is the deuterium labeled 1-Hexadecanol. 1-Hexadecanol is a fatty alcohol, a lipophilic substrate. | |||||||||||||||||||||
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1-Hexadecanol | 99.76% | 1-Hexadecanol is a fatty alcohol, a lipophilic substrate. 1-Hexadecanol can be used for the research of ferroptosis. | ||||||||||||||||||||
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References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief]
- [2]. Nawale L, et al. Anti-proliferative effect of novel primary cetyl alcohol derived sophorolipids against human cervical cancer cells HeLa. PLoS One. 2017 Apr 18;12(4):e0174241. [Content Brief]
