219274
Eicosane
99%
Synonyme(s) :
n-Eicosane
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A propos de cet article
Formule linéaire :
CH3(CH2)18CH3
Numéro CAS:
Poids moléculaire :
282.55
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-018-1
Beilstein/REAXYS Number:
1700722
MDL number:
Assay:
99%
Form:
solid
Service technique
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9.8 (vs air)
Quality Level
assay
99%
form
solid
bp
220 °C/30 mmHg (lit.)
mp
35-37 °C (lit.)
solubility
hexane: soluble 100 mg/mL, clear
SMILES string
CCCCCCCCCCCCCCCCCCCC
InChI
1S/C20H42/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3
InChI key
CBFCDTFDPHXCNY-UHFFFAOYSA-N
General description
n-Eicosane encapsulated in the nanosized pores of silica exhibits novel phase change behavior.
Application
Eicosane was used:
- to fabricate a modified carbon paste electrode composed of Cu2+-mediated salbutamol-imprinted polymer nanoparticles
- in formulation of microcapsules of n-eicosane coated with a polysiloxane
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signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1
Classe de stockage
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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Andrew J Brown et al.
Angewandte Chemie (International ed. in English), 54(20), 5864-5868 (2015-03-27)
Given the recent advent of mononuclear single-molecule magnets (SMMs), a rational approach based on lanthanides with axially elongated f-electron charge cloud (prolate) has only recently received attention. We report herein a new SMM, [Li(THF)4[Er{N(SiMe3)2}3Cl]⋅2 THF, which exhibits slow relaxation of the
Sibao Liu et al.
Science advances, 5(2), eaav5487-eaav5487 (2019-02-13)
We present a strategy to synthesize three types of renewable lubricant base oils with up to 90% yield using 2-alkylfurans, derived from nonfood biomass, and aldehydes, produced from natural oils or biomass through three chemistries: hydroxyalkylation/alkylation (HAA), HAA followed by