253618
甲基5-DOXYL-硬脂酸盐，自由基
别名:
2-(4-甲氧基-4-氧代丁基)-4,4-二甲基-2-十三烷基-3-噁唑烷基氧基, 2-(4-甲氧基-4-氧代丁基)-4,4-二甲基-2-十三烷基-3-噁唑烷基氧基，自由基
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选择尺寸
关于此项目
经验公式（希尔记法）:
C23H45NO4
化学文摘社编号:
分子量:
399.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352000
MDL number:
InChI
1S/C23H44NO4/c1-5-6-7-8-9-10-11-12-13-14-15-18-23(19-16-17-21(25)27-4)24(26)22(2,3)20-28-23/h5-20H2,1-4H3
SMILES string
CCCCCCCCCCCCCC1(CCCC(=O)OC)OCC(C)(C)N1[O]
InChI key
XKWHHWBOJRTEHX-UHFFFAOYSA-N
functional group
ester, ether
storage temp.
2-8°C
Quality Level
General description
自旋标记物
Application
Reactant free radical spin label involved in:
- Synthesis of alkyl phospholipid analogs of perifosine and miltefosine for cytotoxicity studies
- Studies of micellular properties via electron spin (paramagnetic) resonance
- Spin-labeled stearates partitioning into the lipid domain of stratum corneum
- Location determinations in sodium dodecyl sulfate micelles
- Studies of local mobility and structure of micelles via its use as a probe
- ESR (EPR) studies of metalloporphyrin intercalation into liposome membranes
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
141.8 °F - closed cup
flash_point_c
61 °C - closed cup
M L Bianconi et al.
Biochemical and biophysical research communications, 152(1), 344-350 (1988-04-15)
ESR spectra of membrane spin probes are conventionally used to obtain structural information. Here we show, for the first time, that when a membrane-soluble compound undergoes a chemical reaction, time-dependent changes in the ESR spectra of membrane spin probes can
Nataly Lebedeva et al.
The journal of physical chemistry. B, 110(20), 9791-9799 (2006-05-19)
A strategy to locate spectroscopic probes in micelles is presented which involves establishing a "benchmark" probe, i.e., one whose position is well-known and against which other probe positions may be established. Theoretically calculated values of the fraction of the micelle
Catarina Pereira-Leite et al.
Physical chemistry chemical physics : PCCP, 20(21), 14398-14409 (2018-05-18)
Gastrointestinal (GI) toxicity is a major drawback of the chronic use of nonsteroidal anti-inflammatory drugs (NSAIDs). The NSAIDs topical actions on the protective phospholipid layers of the GI mucosa seem to be a central toxicity mechanism of these pharmaceuticals. This
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