8 Citations
Determine the necessary mass, volume, or concentration for preparing a solution.
This is a demo store. No orders will be fulfilled.
Basic Description
| Synonyms | SQUALANE | 111-01-3 | 2,6,10,15,19,23-Hexamethyltetracosane | Perhydrosqualene | Dodecahydrosqualene | Cosbiol | Hexamethyltetracosane | Vitabiosol | Spinacane | Robane | Tetracosane, 2,6,10,15,19,23-hexamethyl- | Squalan | NSC 6851 | Squalane [NF] | squalane-d62 | Pripure 3759 | NSC-68 |
|---|---|
| Specifications & Purity | 10mM in DMSO |
| Storage Temp | Store at -80°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
product description： Dielectrophoretic deformation of thin liquid fillm of squalane has been investigated. Microfluidized squalenes are efficient adjuvants, eliciting both humoral and cellular immune responses. Squalane influence on the vital pathway that transforms glucose into cholesterol may be pivotal. It regulates or controls the rate of synthesis of the enzyme HMG Co-A reductase, and may contribute to effective treatments for cancer and heart disease. It plays an important role as a terminator in the biomembrane. |
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
- Subclass Triterpenoids
-
Class
Prenol lipids
-
Superclass
Lipids and lipid-like molecules
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Prenol lipids |
| Subclass | Triterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Triterpenoids |
| Alternative Parents | Branched alkanes |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Triterpenoid - Branched alkane - Acyclic alkane - Saturated hydrocarbon - Alkane - Hydrocarbon - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. |
| External Descriptors | Not available |
|
|
|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Names and Identifiers
| IUPAC Name | 2,6,10,15,19,23-hexamethyltetracosane |
|---|---|
| INCHI | InChI=1S/C30H62/c1-25(2)15-11-19-29(7)23-13-21-27(5)17-9-10-18-28(6)22-14-24-30(8)20-12-16-26(3)4/h25-30H,9-24H2,1-8H3 |
| InChIKey | PRAKJMSDJKAYCZ-UHFFFAOYSA-N |
| Smiles | CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C |
| Isomeric SMILES | CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C |
| WGK Germany | 3 |
| RTECS | XB6070000 |
| PubChem CID | 8089 |
| Molecular Weight | 422.81 |
| Beilstein | 776019 |
| Reaxy-Rn | 776019 |
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
| Refractive Index | 1.45-1.452 |
|---|---|
| Flash Point(°F) | 424.4 °F |
| Flash Point(°C) | 218 °C |
| Boil Point(°C) | 350 °C |
| Melt Point(°C) | -38 °C |
| Molecular Weight | 422.800 g/mol |
| XLogP3 | 14.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 21 |
| Exact Mass | 422.485 Da |
| Monoisotopic Mass | 422.485 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 308.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 4 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
Citations of This Product
| 1. Zhong yuan You, Xin Wang, Fuqi Lu, Shuting Wang, Bingxi Hu, Lian Li, Weihai Fang, Ying Liu. (2023) An organic semiconductor/metal Schottky heterojunction based direct current triboelectric nanogenerator windmill for wind energy harvesting. Nano Energy, 109 (108302). |
| 2. Yue Zhang, Wenxiu Pan, Dequan Wang, Han Wang, Yanting Hou, Meijuan Zou, Hongyu Piao. (2023) Solid-in-oil nanodispersion as a novel topical transdermal delivery to enhance stability and skin permeation and retention of hydrophilic drugs l-ascorbic acid. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 185 (82). |
| 3. Bowen Du, Xiao Chen, Yu Ling, Tiantian Niu, Weixiang Guan, Jipeng Meng, Haoquan Hu, Chi-Wing Tsang, Changhai Liang. (2023) Hydrogenolysis-Isomerization of Waste Polyolefin Plastics to Multibranched Liquid Alkanes. ChemSusChem, 16 (3): (e202202035). |
| 4. Anning Liu, Huijuan Jing, Xiaojing Du, Chaoyang Ma, Hongxin Wang. (2022) Efficient Ultrasonic-assisted Aqueous Enzymatic Method for Pecan Nut Kernel Oil Extraction with Quality Analysis. Journal of Oleo Science, |
| 5. Shuai Kong, Chong Shen, Yulu Luo, Qin Meng. (2020) Synthesis and Characterization of Fluorescent Surfactants for Studying the Penetration of Cosmetic Surfactants on the Skin. JOURNAL OF SURFACTANTS AND DETERGENTS, 23 (5): (937-943). |
| 6. Junjin Duan, Yanqin Huang, Fuqing Wei, Jiachun Feng. (2025) A Fluorescent Polyethylene With Good Processability and Mechanical Flexibility Prepared by a One-Step Melt Mixing Strategy. Advanced Materials Technologies, (2402203). |
| 7. Mengjiao Liu, Xin Zhang, Yue Xin, Dongxu Guo, Guangkai Hu, Yifei Ma, Bin Yu, Tao Huang, Chengchang Ji, Meifang Zhu, Hao Yu. (2024) Earthworm-Inspired Ultra-Durable Sliding Triboelectric Nanogenerator with Bionic Self-Replenishing Lubricating Property for Wind Energy Harvesting and Self-Powered Intelligent Sports Monitoring. Advanced Science, 11 (28): (2401636). |
| 8. Wanling Chen, Nanxi Xiang, Jiahong Huang, Huixian Xu, Zhenyuan Wang, Bo Ruan, Jichuan Zhang, Chengyu Wu, Jiaheng Zhang, YanZhen Liang. (2024) Supramolecular collagen nanoparticles for anti-wrinkle, skin whitening, and moisturizing effects. COLLOIDS AND SURFACES B-BIOINTERFACES, (114275). |
Solution Calculators
Reviews
Customer Reviews
Remind me later