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About This Item
Linear Formula:
CH3(CH2)22CH3
CAS Number:
Molecular Weight:
338.65
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-474-5
Beilstein/REAXYS Number:
1758462
MDL number:
Assay:
99%
InChI key
POOSGDOYLQNASK-UHFFFAOYSA-N
InChI
1S/C24H50/c1-3-5-7-9-11-13-15-17-19-21-23-24-22-20-18-16-14-12-10-8-6-4-2/h3-24H2,1-2H3
SMILES string
CCCCCCCCCCCCCCCCCCCCCCCC
assay
99%
bp
391 °C (lit.)
Quality Level
solubility
chloroform: soluble 10%, clear, colorless
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General description
Tetracosane is a linear alkane. Structural characteristics of confined squalane and tetracosane under shear flow conditions have been investigated. Solubility of tetracosane in ethane and ethylene have been investigated.
Viscosity, liquid density, and surface tension data of its binary and ternary mixtures with various n-alkanes (n-heptane, n-decane or n-hexadecane) have been evaluated. Its solubility in various hydrocarbon solvents (heptane, dodecane, isomeric mixtures of decahydronapthalene, m- and p-xylene) has been studied.
Application
Tetracosane is the suitable solvent used in the synthesis of ZnS nanoparticle. It may be employed as the wax component to study the reduction in pour point of hydrocarbon solvents containing wax crystals on addition of polymer additives.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Viscosity and liquid density of asymmetric hydrocarbon mixtures.
Queimada AJ, et al.
International Journal of Thermophysics, 24(5), 1221-1239 (2003)
Solubilities of tetracosane in hydrocarbon solvents.
Brecevic L and Garside J.
Journal of Chemical and Engineering Data, 38(4), 598-601 (1993)
Shear behavior of squalane and tetracosane under extreme confinement. I. Model, simulation method, and interfacial slip.
Gupta SA, et al.
J. Chem. Phys. , 107(23), 10316-10326 (1997)
Pan Liao et al.
Nature chemical biology, 17(2), 138-145 (2020-10-21)
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Cyclopropenoid fatty acids (CPEFA), found in oilseeds from Malvaceae and Sterculiaceae, have been shown to interfere with the endogenous synthesis of several bioactive lipids of dairy fat, such as cis-9, trans-11 18:2 and cis-9 18:1, by inhibiting Δ9-desaturase. No previous
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