U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C20H42
Molecular Weight 282.5475
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EICOSANE

SMILES

CCCCCCCCCCCCCCCCCCCC

InChI

InChIKey=CBFCDTFDPHXCNY-UHFFFAOYSA-N
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

HIDE SMILES / InChI

Molecular Formula C20H42
Molecular Weight 282.5475
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Shear alignment of confined hydrocarbon liquid films.
2002 Jul
Effects of crude oil, oil components, and bioremediation on plant growth.
2004
Determination of the carbon deficiency in the flame ionization detector response of long-chain fatty acid methyl esters and dicarboxylic acid dimethyl esters.
2004 Aug 6
Preparation of microencapsulated phase-change materials (MCPCMs) by means of interfacial polycondensation.
2005 Feb
Melt coaxial electrospinning: a versatile method for the encapsulation of solid materials and fabrication of phase change nanofibers.
2006 Dec
Effects of droplet crystallization and melting on the aroma release properties of a model oil-in-water emulsion.
2006 Mar 8
Capillary wave fluctuations and intrinsic widths of coupled fluid-fluid interfaces: an x-ray scattering study of a wetting film on bulk liquid.
2006 Sep
Piptaderol from Piptadenia africana.
2007 Feb 16
Novel molecular precursor of lanthanide complexes with long chain mono cis-butene dicarboxylate to the controlled synthesis of Y2O3:Eu3+ phosphors.
2008 Mar
Aggregation of amphiphilic pyranines in water: facile micelle formation in the presence of methylviologen.
2008 Mar 18
Effects of eicosane, a component of nanoparticles in diesel exhaust, on surface activity of pulmonary surfactant monolayers.
2008 Nov
Chain length affects antioxidant properties of chlorogenate esters in emulsion: the cutoff theory behind the polar paradox.
2009 Dec 9
Control over microemulsions with solvent blends.
2009 Mar 3
Solubility and molecular conformations of n-alkane chains in water.
2009 May 7
The effect of titanium dioxide nanoparticles on pulmonary surfactant function and ultrastructure.
2009 Sep 30
Synthesis and Characterization of a Linear [Mn(3)(O(2)CMe)(4)(py)(8)] Complex.
2010
In Vivo Antimalarial Effects of Iranian Flora Artemisia khorassanica against Plasmodium berghei and Pharmacochemistry of its Natural Components.
2010 Mar
Relationship between hydrophobicity and antioxidant ability of "phenolipids" in emulsion: a parabolic effect of the chain length of rosmarinate esters.
2010 Mar 10
[Determination of volatile organic compounds in lung cancer cell lines and lung cancer tissue].
2010 May
Antimicrobial peptides in gastrointestinal inflammation.
2010 Nov 25
Characterization of a novel long-chain n-alkane-degrading strain, Dietzia sp. E1.
2010 Nov-Dec
Programmed Death-1 antibody blocks therapeutic effects of T-regulatory cells in cockroach antigen-induced allergic asthma.
2010 Oct
Alkylsulfides of Ag(I) and Au(I) as metallosurfactants.
2010 Oct 19
4,4'-Dichloro-2,2'-[(3aR,7aR/3aS,7aS)-2,3,3a,4,5,6,7,7a-octa-hydro-1H-1,3-benzimidazole-1,3-di-yl)bis-(methyl-ene)]diphenol.
2010 Sep 30
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:41:27 UTC 2023
Edited
by admin
on Fri Dec 15 16:41:27 UTC 2023
Record UNII
3AYA9KEC48
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EICOSANE
INCI  
INCI  
Official Name English
C20 ALKANE
Common Name English
EICOSANE [INCI]
Common Name English
NSC-62789
Code English
N-EICOSANE
Common Name English
PARAFOL 20Z
Common Name English
ICOSANE
Systematic Name English
N-ICOSANE
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
204-018-1
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
SMS_ID
300000009284
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
EPA CompTox
DTXSID1025227
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
MESH
C050821
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
PUBCHEM
8222
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
NSC
62789
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
WIKIPEDIA
ICOSANE
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
CAS
112-95-8
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
HSDB
8350
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
CHEBI
43619
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
FDA UNII
3AYA9KEC48
Created by admin on Fri Dec 15 16:41:27 UTC 2023 , Edited by admin on Fri Dec 15 16:41:27 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
1.2% of chemical composition of the leaf essential oil from Moringa oleifera.