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Details

Stereochemistry ACHIRAL
Molecular Formula C11H22
Molecular Weight 154.2924
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-UNDECENE

SMILES

CCCCCCCCCC=C

InChI

InChIKey=DCTOHCCUXLBQMS-UHFFFAOYSA-N
InChI=1S/C11H22/c1-3-5-7-9-11-10-8-6-4-2/h3H,1,4-11H2,2H3

HIDE SMILES / InChI

Molecular Formula C11H22
Molecular Weight 154.2924
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Biological activity of volatiles from marine and terrestrial bacteria.
2010-12-22
Trichoderma viride cellulase induces resistance to the antibiotic pore-forming peptide alamethicin associated with changes in the plasma membrane lipid composition of tobacco BY-2 cells.
2010-12-14
Variability over 1 week in the urinary concentrations of metabolites of diethyl phthalate and di(2-ethylhexyl) phthalate among eight adults: an observational study.
2010-12
The influence of a 1,1-diarylvinyl moiety on the photochromism of naphthopyrans.
2010-11-07
Robust photocatalytic water reduction with cyclometalated Ir(III) 4-vinyl-2,2'-bipyridine complexes.
2010-10-28
Genome-wide analysis of two-component systems and prediction of stress-responsive two-component system members in soybean.
2010-10
Liquid-crystalline self-organization of isocyanide-containing dendrimers induced by coordination to gold(I) fragments.
2010-02-03
[Study on classification of ethylene treated and non-ethylene treated watermelons by visible/near infrared spectroscopy].
2009-04
Co-ordination of early and late ripening events in apples is regulated through differential sensitivities to ethylene.
2009
Molecular characterization of seven genes encoding ethylene-responsive transcriptional factors during plum fruit development and ripening.
2009
Ethylene production by metabolic engineering of the yeast Saccharomyces cerevisiae.
2008-09
Rate constants for the gas-phase reactions of OH radicals with E-7-tetradecene, 2-methyl-1-tridecene and the C(7)-C(14) 1-alkenes at 295 +/- 1 K.
2008-07-28
Chemical composition and anti-inflammatory effects of essential oil from Farfugium japonicum flower.
2008
Ethylene-induced differential gene expression during abscission of citrus leaves.
2008
Enantioselective gas chromatographic separation of racemic N-alkylated barbiturates: application of C11-Chirasil-Dex as chiral stationary phase in GC.
2007-09-18
Is hydrogen abstraction an important pathway in the reaction of alkenes with the OH radical?
2007-08-21
Defensive secretion components of the host Parastizopus armaticeps as kairomones for the cleptoparasite Eremostibes opacus.
2006-04
A kinetic model of the formation of organic monolayers on hydrogen-terminated silicon by hydrosilation of alkenes.
2005-12-22
Production of volatile compounds in cheese by Pseudomonas fragi strains of dairy origin.
2005-07
Mechanism of the hydrosilylation reaction of alkenes at porous silicon: experimental and computational deuterium labeling studies.
2005-06-23
Ethylene insensitivity conferred by the Green-ripe and Never-ripe 2 ripening mutants of tomato.
2005-05
Monomeric and polymeric anionic gemini surfactants and mixed surfactant systems in micellar electrokinetic chromatography. Part II: characterization of chemical selectivity using two linear solvation energy relationship models.
2005-01
Monomeric and polymeric anionic gemini surfactants and mixed surfactant systems in micellar electrokinetic chromatography. Part I: characterization and application as novel pseudostationary phases.
2005-01
Analytical investigation of the self-desorption of the oligomers of mixtures of a polydisperse ethoxylated surfactant with sodium dodecylsulfate from a silica/water interface.
2003-05-01
Use of genomics tools to isolate key ripening genes and analyse fruit maturation in tomato.
2002-10
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:48:05 GMT 2025
Edited
by admin
on Mon Mar 31 19:48:05 GMT 2025
Record UNII
1446756A8F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-73983
Preferred Name English
1-UNDECENE
HSDB  
Systematic Name English
1-UNDECENE [HSDB]
Common Name English
.ALPHA.-UNDECENE
Systematic Name English
N-1-UNDECENE
Common Name English
.ALPHA.-NONYLETHYLENE
Systematic Name English
.ALPHA.-UNDECYLENE
Common Name English
1-HENDECENE
Systematic Name English
Code System Code Type Description
PUBCHEM
13190
Created by admin on Mon Mar 31 19:48:05 GMT 2025 , Edited by admin on Mon Mar 31 19:48:05 GMT 2025
PRIMARY
CAS
821-95-4
Created by admin on Mon Mar 31 19:48:05 GMT 2025 , Edited by admin on Mon Mar 31 19:48:05 GMT 2025
PRIMARY
ECHA (EC/EINECS)
212-483-7
Created by admin on Mon Mar 31 19:48:05 GMT 2025 , Edited by admin on Mon Mar 31 19:48:05 GMT 2025
PRIMARY
CHEBI
77444
Created by admin on Mon Mar 31 19:48:05 GMT 2025 , Edited by admin on Mon Mar 31 19:48:05 GMT 2025
PRIMARY
EPA CompTox
DTXSID5061168
Created by admin on Mon Mar 31 19:48:05 GMT 2025 , Edited by admin on Mon Mar 31 19:48:05 GMT 2025
PRIMARY
NSC
73983
Created by admin on Mon Mar 31 19:48:05 GMT 2025 , Edited by admin on Mon Mar 31 19:48:05 GMT 2025
PRIMARY
FDA UNII
1446756A8F
Created by admin on Mon Mar 31 19:48:05 GMT 2025 , Edited by admin on Mon Mar 31 19:48:05 GMT 2025
PRIMARY
HSDB
1090
Created by admin on Mon Mar 31 19:48:05 GMT 2025 , Edited by admin on Mon Mar 31 19:48:05 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
Major component of the volatile oil.