253618
Methyl 5-DOXYL-stearate, free radical
동의어(들):
2-(4-Methoxy-4-oxobutyl)-4,4-dimethyl-2-tridecyl-3-oxazolidinyloxy, 2-(4-Methoxy-4-oxobutyl)-4,4-dimethyl-2-tridecyl-3-oxazolidinyloxy, free radical, 5-MeSL
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C23H45NO4
CAS Number:
Molecular Weight:
399.61
MDL number:
UNSPSC 코드:
12352000
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
작용기
ester
ether
저장 온도
2-8°C
SMILES string
CCCCCCCCCCCCCC1(CCCC(=O)OC)OCC(C)(C)N1[O]
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
InChI key
XKWHHWBOJRTEHX-UHFFFAOYSA-N
관련 카테고리
일반 설명
Spin label
애플리케이션
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
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
141.8 °F - closed cup
Flash Point (°C)
61 °C - closed cup
가장 최신 버전 중 하나를 선택하세요:
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
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
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