92266-90-5 Usage
Description
10,12-Pentacosadiyn-1-ol is a long-chain unsaturated alcohol with a carbon-carbon triple bond at the 12th and 13th position. It is a member of the pentacosadiyne family and is commonly used in chemical and biological research for its unique properties.
Used in Chemical Research:
10,12-Pentacosadiyn-1-ol is used as a research compound for studying its unique chemical properties and potential applications in various fields.
Used in Biological Research:
10,12-Pentacosadiyn-1-ol is used as a research tool for studying biological membrane structure and function due to its ability to incorporate into lipid bilayers and form stable monolayers.
Used in Organic Electronics:
10,12-Pentacosadiyn-1-ol is used as a component in the development of organic electronic devices, such as sensors and transistors, due to its unique electronic properties.
Used in Surface Chemistry:
10,12-Pentacosadiyn-1-ol is used as a surface-active agent in surface chemistry research, where it can be used to study the interactions between molecules and surfaces.
Used in Biosensor Development:
10,12-Pentacosadiyn-1-ol is used as a component in the development of biosensors, where its unique properties can be utilized for detecting specific biological molecules or processes.
Used in Drug Delivery Systems:
10,12-Pentacosadiyn-1-ol has potential applications in the development of drug delivery systems, where it can be used to improve the delivery and efficacy of therapeutic agents.
Used in Membrane Studies:
10,12-Pentacosadiyn-1-ol is used as a model compound for studying the structure and function of biological membranes, as it can form stable monolayers and incorporate into lipid bilayers.
Used in Chemical Synthesis:
10,12-Pentacosadiyn-1-ol can be used as a starting material or intermediate in the synthesis of other organic compounds, taking advantage of its unique chemical properties.
Note: Due to its chemical reactivity and potential toxicity, proper handling and safety precautions are necessary when working with 10,12-Pentacosadiyn-1-ol.
Check Digit Verification of cas no
The CAS Registry Mumber 92266-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,6 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92266-90:
(7*9)+(6*2)+(5*2)+(4*6)+(3*6)+(2*9)+(1*0)=145
145 % 10 = 5
So 92266-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C25H44O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26/h26H,2-12,17-25H2,1H3
92266-90-5Relevant articles and documents
Impact of the surface charge of polydiacetylene micelles on their interaction with human innate immune protein C1q and the complement system
Thielens, Nicole M.,Belime, Agathe,Gravel, Edmond,Ancelet, Sarah,Caneiro, Charlotte,Doris, Eric,Ling, Wai Li
, p. 434 - 439 (2018)
Polydiacetylene (pDA) micelles have been demonstrated to be effective drug carriers for cancer therapy in mouse model. However, little is known about their interaction with the human complement system, which constitutes an important part of the innate immune system and can cause severe hypersensitivity reactions. Herein, we investigate the influence of micelle surface charge on the binding of complement protein C1q, the target recognition unit that activates the classical complement pathway and performs a range of other important physiological functions. Besides the classical pathway, we also investigate the surface charge effect on complement activities through the other activation pathways, namely, the MBL-dependent lectin pathway and the alternative pathway. We synthesized three samples of pDA micelles bearing neutral, anionic, and cationic surface charge motifs, respectively. Surface plasmon resonance showed that none of these micelles interacted with C1q. Results from serum complement activation assays indicated that all micelles were inert to complement, except for the anionic pDA micelles, which activated the alternative pathway.
Fine-tuning the morphology of self-assembled nanostructures of propargyl ammonium-based amphiphiles
Morin, Emmanuelle,Guenet, Jean-Michel,Díaz, David D.,Remy, Jean-Serge,Wagner, Alain
experimental part, p. 12495 - 12500 (2011/02/27)
N-Methyl-N-(pentacosa-10,12-diyn)-propargylamine organizes itself into an unusual supramolecular pH- and thermo-responsive system. Studies have showed that submillimetric length hollow laths form this unique structure in the presence of hydrochloric acid. Specific chemical modifications on the initial molecule and small-angle neutron scattering experiments were performed to understand the structure of this system. Our results allow us to suggest a possible structure of the laths.
