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Squalane - 95%, high purity , CAS No.111-01-3
Basic Description
Synonyms
squalane-d62 | CAS-111-01-3 | Dodecahydrosqualene | Spinacane | Hexamethyltetracosane | SQUALANE | Robane | Pripure 3759 | Squalane [NF] | Cosbiol | Tetracosane, 2,6,10,15,19,23-hexamethyl- | NSC 6851 | Perhydrosqualene | 2,6,10,15,19,23-Hexamethyltetraco
Specifications & Purity
≥95%
Storage Temp
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
Product Describtion:
Dielectrophoretic deformation of thin liquid fillm of squalane has been investigated.Microfluidized squalenes are efficient adjuvants, eliciting both humoral and cellular immune responses.
Product Application：
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
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
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
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)
Chemical and Physical Properties
Solubility
Soluble in ether, chloroform, benzene, slightly soluble in ethanol, acetone, methanol, insoluble in water
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).
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8 Citations
F2525451
