Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H44 |
| Molecular Weight | 296.5741 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCCCCCCCCCCC
InChI
InChIKey=FNAZRRHPUDJQCJ-UHFFFAOYSA-N
InChI=1S/C21H44/c1-3-5-7-9-11-13-15-17-19-21-20-18-16-14-12-10-8-6-4-2/h3-21H2,1-2H3
| Molecular Formula | C21H44 |
| Molecular Weight | 296.5741 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Chemical composition of the essential oils of Rhodiola rosea L. of three different origins. | 2010-10 |
|
| Predator-released hydrocarbons repel oviposition by a mosquito. | 2010-09 |
|
| Acute and sub-acute toxicity of an insect pheromone, N-heneicosane and combination with insect growth regulator, diflubenzuron, for establishing no observed adverse effect level (NOAEL). | 2010-07 |
|
| Bioremediation of acidic oily sludge-contaminated soil by the novel yeast strain Candida digboiensis TERI ASN6. | 2010-03 |
|
| 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 |
|
| Antibacterial activities of essential oils and extracts of Turkish Achillea, Satureja and Thymus species against plant pathogenic bacteria. | 2010-01-15 |
|
| Mangifera indica (mango). | 2010-01 |
|
| Interfacial structure and melting temperature of alcohol and alkane molecules in contact with polystyrene films. | 2009-03-05 |
|
| Fatty acid derived compounds--the dominant volatile class of the essential oil poor Sonchus arvensis subsp. uliginosus (Bieb.) Nyman. | 2009-03 |
|
| Electroantennogram, flight orientation, and oviposition responses of Aedes aegypti to the oviposition pheromone n-heneicosane. | 2009-03 |
|
| [Characterization of chemical components of essential oil from cupitulum of Chrysanthemum morifolium cultivated in Tongxiang city]. | 2008-03 |
|
| Top note compounds of Chinese traditional bacteria-fermented soybean. | 2008 |
|
| 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 |
|
| Vapor-liquid and critical behavior of binary systems of hydrogen chloride and n-alkanes: experimental data and soft-SAFT modeling. | 2007-08-30 |
|
| Characterization of waxes used in pictorial artworks according to their relative amount of fatty acids and hydrocarbons by gas chromatography. | 2006-01-06 |
|
| Sexual isolation and cuticular hydrocarbon differences between Drosophila santomea and Drosophila yakuba. | 2005-11 |
|
| Effects of pure n-alkanes and crude oil on bacterial phospholipid classes and molecular species determined by electrospray ionization mass spectrometry. | 2005-08-05 |
|
| Emissions of organic compounds and trace metals in fine particulate matter from motor vehicles: a tunnel study in Houston, Texas. | 2005-01 |
|
| Selectivity and efficiency of pyrene attachment to alkanes induced by broadband X-rays. | 2003-03 |
|
| Effect of dispersing oil phase on the biodegradability of a solid alkane dissolved in non-biodegradable oil. | 2002-08 |
|
| Mating alters the cuticular hydrocarbons of female Anopheles gambiae sensu stricto and aedes Aegypti (Diptera: Culicidae). | 2002-05 |
|
| Nestmate recognition in social wasps: manipulation of hydrocarbon profiles induces aggression in the European hornet. | 2002-03 |
|
| Chemical and physical analyses of wax ester properties. | 2001 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:19:54 GMT 2025
by
admin
on
Mon Mar 31 19:19:54 GMT 2025
|
| Record UNII |
I93S5U5DMP
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
8351
Created by
admin on Mon Mar 31 19:19:54 GMT 2025 , Edited by admin on Mon Mar 31 19:19:54 GMT 2025
|
PRIMARY | |||
|
211-118-9
Created by
admin on Mon Mar 31 19:19:54 GMT 2025 , Edited by admin on Mon Mar 31 19:19:54 GMT 2025
|
PRIMARY | |||
|
Heneicosane
Created by
admin on Mon Mar 31 19:19:54 GMT 2025 , Edited by admin on Mon Mar 31 19:19:54 GMT 2025
|
PRIMARY | |||
|
DTXSID9047097
Created by
admin on Mon Mar 31 19:19:54 GMT 2025 , Edited by admin on Mon Mar 31 19:19:54 GMT 2025
|
PRIMARY | |||
|
I93S5U5DMP
Created by
admin on Mon Mar 31 19:19:54 GMT 2025 , Edited by admin on Mon Mar 31 19:19:54 GMT 2025
|
PRIMARY | |||
|
32931
Created by
admin on Mon Mar 31 19:19:54 GMT 2025 , Edited by admin on Mon Mar 31 19:19:54 GMT 2025
|
PRIMARY | |||
|
629-94-7
Created by
admin on Mon Mar 31 19:19:54 GMT 2025 , Edited by admin on Mon Mar 31 19:19:54 GMT 2025
|
PRIMARY | |||
|
12403
Created by
admin on Mon Mar 31 19:19:54 GMT 2025 , Edited by admin on Mon Mar 31 19:19:54 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> CONSTITUENT ALWAYS PRESENT |
1.9% of chemical composition of the leaf essential oil from Moringa oleifera.
|
