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Details

Stereochemistry ACHIRAL
Molecular Formula C24H50
Molecular Weight 338.6538
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TETRACOSANE

SMILES

CCCCCCCCCCCCCCCCCCCCCCCC

InChI

InChIKey=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

HIDE SMILES / InChI

Molecular Formula C24H50
Molecular Weight 338.6538
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
128.7 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Confinement-driven weakening of the rotator phase transitions in an alkane through a possible tricritical point.
2010-12-07
Chemical composition of the essential oils of Rhodiola rosea L. of three different origins.
2010-10
Comprehensive compositional analysis of plant cell walls (Lignocellulosic biomass) part I: lignin.
2010-03-11
Treatment of municipal solid waste leachate using a submerged anaerobic membrane bioreactor at mesophilic and psychrophilic temperatures: analysis of recalcitrants in the permeate using GC-MS.
2010-02
[Study on the chemical constituents qf Spongilla Wagner].
2010-01
Cytochrome P450 family member CYP704B2 catalyzes the {omega}-hydroxylation of fatty acids and is required for anther cutin biosynthesis and pollen exine formation in rice.
2010-01
Fruit-surface flavonoid accumulation in tomato is controlled by a SlMYB12-regulated transcriptional network.
2009-12
Chemical Examination of Citrus sinensis Flavedo Variety Pineapple.
2009-11
Spontaneous imbibition dynamics of an n-alkane in nanopores: evidence of meniscus freezing and monolayer sticking.
2009-10-23
Structure and phase transitions of monolayers of intermediate-length n-alkanes on graphite studied by neutron diffraction and molecular dynamics simulation.
2009-08-28
[Study on the chemical constituents of the leaves of Ipomoea batatas].
2009-06
Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae).
2009-06
Conferols A and B, new anti-inflammatory 4-hydroxyisoflavones from Caragana conferta.
2009-04
Silencing of StKCS6 in potato periderm leads to reduced chain lengths of suberin and wax compounds and increased peridermal transpiration.
2009
Structural and phase properties of tetracosane (C24H50) monolayers adsorbed on graphite: an explicit hydrogen molecular dynamics study.
2008-11-04
Gas chromatography-mass spectrometry with supersonic molecular beams.
2008-02
The Arabidopsis cytochrome P450 CYP86A1 encodes a fatty acid omega-hydroxylase involved in suberin monomer biosynthesis.
2008
Raman spectroscopy of natural accumulated paraffins from rocks: evenkite, ozokerite and hatchetine.
2007-12-15
The odor of origin: kinship and geographical distance are reflected in the marking pheromone of male beewolves (Philanthus triangulum F., Hymenoptera, Crabronidae).
2007-10-10
A Staphylococcus aureus ypfP mutant with strongly reduced lipoteichoic acid (LTA) content: LTA governs bacterial surface properties and autolysin activity.
2007-08
Biochemical evaluation of borage (Borago officinalis) rosette leaves through their essential oil and fatty acid composition.
2007-06
Comparative study of normal and branched alkane monolayer films adsorbed on a solid surface. I. Structure.
2007-03-14
Kairomones extracted from rice yellow stem borer and their influence on egg parasitization by Trichogramma japonicum ashmead.
2007-01
Gramicidin A channel in a matrix from a semifluorinated surfactant monolayer.
2006-10-05
[Studies on chemical constituents in flower of Abelmoschus manihot].
2006-10
Late opacification of a silicone intraocular lens caused by ophthalmic ointment.
2006-02
Characterization of waxes used in pictorial artworks according to their relative amount of fatty acids and hydrocarbons by gas chromatography.
2006-01-06
Calculation the surface tension of heptane, eicosane, docosane, tetracosane, and their asymmetric mixtures.
2005-09-01
Medium-chain acyl-CoA dehydrogenase deficiency in gene-targeted mice.
2005-08
A synthetic route to size-controlled fcc and fct FePt nanoparticles.
2005-07-27
Variation of chemical composition of the lipophilic extracts from yellow birch (Betula alleghaniensis) foliage.
2005-06-15
Rheological and structural studies of liquid decane, hexadecane, and tetracosane under planar elongational flow using nonequilibrium molecular-dynamics simulations.
2005-05-08
Emissions of organic compounds and trace metals in fine particulate matter from motor vehicles: a tunnel study in Houston, Texas.
2005-01
Quantitation of hydroxyproline in bone by gas chromatography-mass spectrometry.
2004-05-25
Spectroscopy of the conformational disorder in molecular films: tetracosane and squalane on Pt(111).
2004-02-01
Intramolecular diffusive motion in alkane monolayers studied by high-resolution quasielastic neutron scattering and molecular dynamics simulations.
2004-01-30
[Analysis on mutation of adrenoleukodystrophy gene in exon 1 and exon 5].
2003-02
Fatty acid transport in Saccharomyces cerevisiae. Directed mutagenesis of FAT1 distinguishes the biochemical activities associated with Fat1p.
2002-08-23
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:41:49 GMT 2025
Edited
by admin
on Mon Mar 31 21:41:49 GMT 2025
Record UNII
YQ5H1M1D7I
Record Status Validated (UNII)
Record Version
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Name Type Language
TETRACOSANE
Systematic Name English
NSC-2984
Preferred Name English
N-TETRACOSANE
Common Name English
Code System Code Type Description
WIKIPEDIA
TETRACOSANE
Created by admin on Mon Mar 31 21:41:49 GMT 2025 , Edited by admin on Mon Mar 31 21:41:49 GMT 2025
PRIMARY
PUBCHEM
12592
Created by admin on Mon Mar 31 21:41:49 GMT 2025 , Edited by admin on Mon Mar 31 21:41:49 GMT 2025
PRIMARY
EPA CompTox
DTXSID8060955
Created by admin on Mon Mar 31 21:41:49 GMT 2025 , Edited by admin on Mon Mar 31 21:41:49 GMT 2025
PRIMARY
CHEBI
32936
Created by admin on Mon Mar 31 21:41:49 GMT 2025 , Edited by admin on Mon Mar 31 21:41:49 GMT 2025
PRIMARY
HSDB
8354
Created by admin on Mon Mar 31 21:41:49 GMT 2025 , Edited by admin on Mon Mar 31 21:41:49 GMT 2025
PRIMARY
NSC
2984
Created by admin on Mon Mar 31 21:41:49 GMT 2025 , Edited by admin on Mon Mar 31 21:41:49 GMT 2025
PRIMARY
CAS
646-31-1
Created by admin on Mon Mar 31 21:41:49 GMT 2025 , Edited by admin on Mon Mar 31 21:41:49 GMT 2025
PRIMARY
FDA UNII
YQ5H1M1D7I
Created by admin on Mon Mar 31 21:41:49 GMT 2025 , Edited by admin on Mon Mar 31 21:41:49 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-474-5
Created by admin on Mon Mar 31 21:41:49 GMT 2025 , Edited by admin on Mon Mar 31 21:41:49 GMT 2025
PRIMARY
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