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Catalog Number:
23166
CAS Number:
165191-88-8
1,2-Dioleoyl -sn- glycéro-3-phosphatidyléthanolamino (+)-biotine
Purity:
≥ 97% (RMN)
Documents
$100.05 /5 mg
Taille
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Product Information

1,2-Dioleoyl-sn-glycero-3-phosphatidylethanolamino (+)-biotin is a specialized phospholipid compound that plays a crucial role in bioconjugation and drug delivery applications. This compound is particularly valued in the fields of biochemistry and molecular biology due to its ability to facilitate the incorporation of biotin into various biomolecules, enhancing their stability and functionality. Its unique structure allows for effective interaction with cell membranes, making it an ideal candidate for use in targeted drug delivery systems and in the development of biotinylated probes for imaging and diagnostics.

Researchers have successfully utilized 1,2-Dioleoyl-sn-glycero-3-phosphatidylethanolamino (+)-biotin in the formulation of liposomes and nanoparticles, which can encapsulate therapeutic agents and improve their bioavailability. This compound's amphiphilic nature ensures optimal solubility in biological environments, thereby enhancing the efficacy of drug formulations. Additionally, its compatibility with various biological systems makes it a versatile tool for scientists exploring new therapeutic strategies and diagnostic methods.

CAS Number
165191-88-8
Purity
≥ 97% (RMN)
Molecular Formula
C 51 H 92 N 3 O 10 PS
Molecular Weight
970.34
MDL Number
MFCD09952676
PubChem ID
73173794
Appearance
Solide blanc
Optical Rotation
[a] D 20 = +26 ± 2º (C=1 dans CHCl 3 )
Conditions
Conserver à 0-8 °C
General Information
CAS Number
165191-88-8
Purity
≥ 97% (RMN)
Molecular Formula
C 51 H 92 N 3 O 10 PS
Molecular Weight
970.34
MDL Number
MFCD09952676
PubChem ID
73173794
Appearance
Solide blanc
Optical Rotation
[a] D 20 = +26 ± 2º (C=1 dans CHCl 3 )
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

1,2-Dioleoyl-sn-glycero-3-phosphatidylethanolamino (+)-biotin is widely utilized in research focused on:

  • Drug Delivery Systems: This compound is often employed in the formulation of liposomes, enhancing the delivery of therapeutic agents directly to target cells, which improves treatment efficacy and reduces side effects.
  • Bioconjugation: It serves as a valuable tool in bioconjugation techniques, allowing researchers to attach biotin to various biomolecules, facilitating the study of protein interactions and cellular processes.
  • Cell Membrane Studies: The compound is used in the creation of model membranes for studying lipid behavior and membrane dynamics, providing insights into cell signaling and membrane protein function.
  • Diagnostics: In diagnostic applications, it aids in the development of biosensors and assays, where biotin's strong affinity for streptavidin is leveraged to detect specific biomolecules with high sensitivity.
  • Vaccine Development: This chemical plays a role in vaccine formulations, particularly in the design of adjuvants that enhance immune responses, contributing to more effective vaccines.

Citations