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METHYL 5-DOXYL-STEARATE, also known as a free radical spin label, is a chemical compound derived from stearic acid and doxyl group. It is characterized by its ability to provide information on the local environment and dynamics of molecules in various systems due to its paramagnetic properties.
Used in Pharmaceutical Industry:
METHYL 5-DOXYL-STEARATE is used as a reactant free radical spin label for the synthesis of alkyl phospholipid analogs of perifosine and miltefosine, which are involved in cytotoxicity studies. This application aids in the development of new drugs and understanding their interactions with biological systems.
Used in Material Science:
METHYL 5-DOXYL-STEARATE is used as a probe for studying micellular properties via electron spin (paramagnetic) resonance. This helps in understanding the behavior of micelles and their interactions with other molecules, which is crucial for the development of advanced materials and drug delivery systems.
Used in Dermatology:
METHYL 5-DOXYL-STEARATE is used as a probe for spin-labeled stearates partitioning into the lipid domain of the stratum corneum. This application helps in understanding the skin's barrier properties and the interaction of various substances with the skin, which is essential for the development of effective skincare products and treatments.
Used in Biophysics:
METHYL 5-DOXYL-STEARATE is used as a probe for location determinations in sodium dodecyl sulfate micelles. This application provides insights into the structure and dynamics of micelles, which are important for understanding their function in various biological processes and the development of novel materials.
Used in Biochemistry:
METHYL 5-DOXYL-STEARATE is used as a probe for studying the local mobility and structure of micelles. This helps in understanding the behavior of micelles in different environments and their role in various biological processes.
Used in Medical Research:
METHYL 5-DOXYL-STEARATE is used in ESR (Electron Paramagnetic Resonance) studies of metalloporphyrin intercalation into liposome membranes. This application aids in understanding the interactions between metalloporphyrins and liposome membranes, which is crucial for the development of new drugs and therapies.

38568-24-0

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38568-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38568-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,5,6 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38568-24:
(7*3)+(6*8)+(5*5)+(4*6)+(3*8)+(2*2)+(1*4)=150
150 % 10 = 0
So 38568-24-0 is a valid CAS Registry Number.
InChI:InChI=1/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

38568-24-0 Well-known Company Product Price

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  • Aldrich

  • (253618)  Methyl5-DOXYL-stearate,freeradical  

  • 38568-24-0

  • 253618-10MG

  • 1,377.09CNY

  • Detail

38568-24-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-(3-λ<sup>1</sup>-oxidanyl-4,4-dimethyl-2-tridecyl-1,3-oxazolidin-2-yl)butanoate

1.2 Other means of identification

Product number -
Other names 5-Doxylstearic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:38568-24-0 SDS

38568-24-0Downstream Products

38568-24-0Relevant academic research and scientific papers

Improved yields in the synthesis of spin-labeled fatty acids

Mravljak, Janez,Pecar, Slavko

, p. 3763 - 3771 (2007/10/03)

Paramagnetic amide side products (6a-g) have been isolated from the reaction mixture in the synthesis of spin-labeled fatty acids of the doxyl type. After their hydrolysis to the corresponding acid, 7, the overall yield of spin-labeled fatty acids is significantly increased compared with published procedures.

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