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2-(3-CARBOXYPROPYL)-4,4-DIMETHYL-2-TRIDECYL-3-OXAZOLIDINYLOXY is a complex organic compound with a unique structure that features a carboxypropyl group, a dimethyl group, a tridecyl group, and an oxazolidinyloxy group. 2-(3-CARBOXYPROPYL)-4,4-DIMETHYL-2-TRIDECYL-3-OXAZOLIDINYLOXY is characterized by its ability to interact with lipid membranes and is commonly used as a lipid spin label in various scientific studies.

29545-48-0

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29545-48-0 Usage

Uses

Used in Electron Paramagnetic Resonance (EPR) Studies:
2-(3-CARBOXYPROPYL)-4,4-DIMETHYL-2-TRIDECYL-3-OXAZOLIDINYLOXY is used as a lipid spin label for a wide range of EPR studies, which are essential for understanding the behavior and interactions of molecules within lipid membranes.
Used in Studies to Elucidate Molecular Interactions with Membrane Surfaces:
In this application, 2-(3-CARBOXYPROPYL)-4,4-DIMETHYL-2-TRIDECYL-3-OXAZOLIDINYLOXY is used to investigate the interactions of various molecules with the surface of lipid membranes. This helps researchers gain insights into the molecular mechanisms underlying membrane-associated processes.
Used in Kinetics of Lipid Transfer Between Lipid Bilayers:
2-(3-CARBOXYPROPYL)-4,4-DIMETHYL-2-TRIDECYL-3-OXAZOLIDINYLOXY is employed to study the kinetics of lipid transfer between different lipid bilayers. Understanding these processes is crucial for elucidating the mechanisms of lipid exchange and transport in cellular systems.
Used in Behavior of Molecules Within a Lipid Bilayer:
2-(3-CARBOXYPROPYL)-4,4-DIMETHYL-2-TRIDECYL-3-OXAZOLIDINYLOXY is used to analyze the behavior of molecules within the lipid bilayer, providing valuable information on their mobility, orientation, and interactions with other molecules.
Used in Probing the Fluid Dynamics of the Plasma Membrane:
As a lipid spin label, 2-(3-CARBOXYPROPYL)-4,4-DIMETHYL-2-TRIDECYL-3-OXAZOLIDINYLOXY is utilized to probe the fluid dynamics of the plasma membrane, which is essential for understanding the biophysical properties of cell membranes and their role in cellular processes.

Check Digit Verification of cas no

The CAS Registry Mumber 29545-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,4 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29545-48:
(7*2)+(6*9)+(5*5)+(4*4)+(3*5)+(2*4)+(1*8)=140
140 % 10 = 0
So 29545-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H42NO4/c1-4-5-6-7-8-9-10-11-12-13-14-17-22(18-15-16-20(24)25)23(26)21(2,3)19-27-22/h4-19H2,1-3H3,(H,24,25)

29545-48-0 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Aldrich

  • (253634)  5-DOXYL-stearicacid,freeradical  

  • 29545-48-0

  • 253634-10MG

  • 397.80CNY

  • Detail
  • Aldrich

  • (253634)  5-DOXYL-stearicacid,freeradical  

  • 29545-48-0

  • 253634-25MG

  • 999.18CNY

  • Detail

29545-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-doxylstearic acid

1.2 Other means of identification

Product number -
Other names 5-DOXYL-STEARIC ACID FREE RADICAL

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:29545-48-0 SDS

29545-48-0Downstream Products

29545-48-0Relevant 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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