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

Details

Stereochemistry ACHIRAL
Molecular Formula C30H62
Molecular Weight 422.8133
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIACONTANE

SMILES

CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC

InChI

InChIKey=JXTPJDDICSTXJX-UHFFFAOYSA-N
InChI=1S/C30H62/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-30H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C30H62
Molecular Weight 422.8133
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Chemical and physical analyses of wax ester properties.
2001
Discovery of novel trimethylalkanes in the internal hydrocarbons of developing pupae of Heliothis virescens and Helicoverpa zea.
2001 Apr
Flavonoids and isoflavonoids with antiplasmodial activities from the root bark of Erythrina abyssinica.
2003 Jul
Degradation of alkanes and highly chlorinated benzenes, and production of biosurfactants, by a psychrophilic Rhodococcus sp. and genetic characterization of its chlorobenzene dioxygenase.
2003 Oct
Molecular structure of crude beeswax studied by solid-state 13C NMR.
2004
STM observation of alkyl-chain-assisted self-assembled monolayers of pyridine-coordinated porphyrin rhodium chlorides.
2004 Jun 22
Tyrosinase-inhibitory long-chain esters from Amberboa ramosa.
2005 Jan
Asymptotic trends in thermodynamic perturbation theory.
2005 Nov 8
Gas chromatography-mass spectrometry analysis of di-n-octyl disulfide in a straight oil metalworking fluid: application of differential permeation and Box-Cox transformation.
2006 Jan 6
Solvents effects on the conformational order of triacontyl modified silica gels as evaluated by Fourier transform infrared spectroscopy.
2006 Nov 17
Solid-phase extraction with C30 bonded silica for analysis of polycyclic aromatic hydrocarbons in airborne particulate matters by gas chromatography-mass spectrometry.
2007 Jun 22
Effects of metal nanoparticles on the secondary ion yields of a model alkane molecule upon atomic and polyatomic projectiles in secondary ion mass spectrometry.
2008 Aug 15
[Studies on the chemical constituents of Lonicera macranthoides].
2008 Jul
Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae).
2009 Jun
Study of triacontyl-functionalized monolithic silica capillary column for reversed-phase capillary liquid chromatography.
2009 Mar 20
Alkane inducible proteins in Geobacillus thermoleovorans B23.
2009 Mar 25
Use of palmae wax hydrocarbon fractions as chemotaxonomical markers in Butia and Syagrus.
2009 May
Regarding "Civilini E, Bertoglio L, Melissano G, Chiesa R. Aortic and esophageal endografting for secondary aortoenteric fistula. Eur J Vasc Endovasc Surg 2008;36(3):297-9".
2009 May
Determination of estrogens and bisphenol A in bovine milk by automated on-line C30 solid-phase extraction coupled with high-performance liquid chromatography-mass spectrometry.
2009 Oct 30
Mangifera indica (mango).
2010 Jan
Silicate-entrapped porous coatings for preparing high-efficiency solid-phase microextraction sorbents.
2010 Jun 11
Substance Class Chemical
Created
by admin
on Fri Dec 15 20:27:19 UTC 2023
Edited
by admin
on Fri Dec 15 20:27:19 UTC 2023
Record UNII
47A73V7096
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIACONTANE
Systematic Name English
NSC-158661
Code English
N-TRIACONTANE
Common Name English
Code System Code Type Description
NSC
158661
Created by admin on Fri Dec 15 20:27:19 UTC 2023 , Edited by admin on Fri Dec 15 20:27:19 UTC 2023
PRIMARY
PUBCHEM
12535
Created by admin on Fri Dec 15 20:27:19 UTC 2023 , Edited by admin on Fri Dec 15 20:27:19 UTC 2023
PRIMARY
HSDB
8360
Created by admin on Fri Dec 15 20:27:19 UTC 2023 , Edited by admin on Fri Dec 15 20:27:19 UTC 2023
PRIMARY
FDA UNII
47A73V7096
Created by admin on Fri Dec 15 20:27:19 UTC 2023 , Edited by admin on Fri Dec 15 20:27:19 UTC 2023
PRIMARY
ECHA (EC/EINECS)
211-349-5
Created by admin on Fri Dec 15 20:27:19 UTC 2023 , Edited by admin on Fri Dec 15 20:27:19 UTC 2023
PRIMARY
CAS
638-68-6
Created by admin on Fri Dec 15 20:27:19 UTC 2023 , Edited by admin on Fri Dec 15 20:27:19 UTC 2023
PRIMARY
CHEBI
31006
Created by admin on Fri Dec 15 20:27:19 UTC 2023 , Edited by admin on Fri Dec 15 20:27:19 UTC 2023
PRIMARY
EPA CompTox
DTXSID0060935
Created by admin on Fri Dec 15 20:27:19 UTC 2023 , Edited by admin on Fri Dec 15 20:27:19 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
1.1% of chemical composition of the leaf essential oil from Moringa oleifera.
PARENT -> CONSTITUENT ALWAYS PRESENT