Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H32O |
| Molecular Weight | 228.414 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCCCCCO
InChI
InChIKey=REIUXOLGHVXAEO-UHFFFAOYSA-N
InChI=1S/C15H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h16H,2-15H2,1H3
| Molecular Formula | C15H32O |
| Molecular Weight | 228.414 |
| 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 |
|---|---|---|
| Three Arabidopsis fatty acyl-coenzyme A reductases, FAR1, FAR4, and FAR5, generate primary fatty alcohols associated with suberin deposition. | 2010-08 |
|
| Contribution of the bees and combs to honey volatiles: blank-trial probe for chemical profiling of honey biodiversity. | 2010-05 |
|
| Binding specificity of locust odorant binding protein and its key binding site for initial recognition of alcohols. | 2009-07 |
|
| Analytical method for determination of allylic isoprenols in rat tissues by liquid chromatography/tandem mass spectrometry following chemical derivatization with 3-nitrophtalic anhydride. | 2008-07-15 |
|
| The effect of various drying techniques on apricot volatiles analysed using direct thermal desorption-GC-TOF/MS. | 2007-09-15 |
|
| Sex pheromone of the pine sawfly, Gilpinia pallida: chemical identification, synthesis, and biological activity. | 2006-11 |
|
| Probing the nucleation mechanism for the binary n-nonane/1-alcohol series with atomistic simulations. | 2006-09-21 |
|
| Suppression of ionization and optimization of assay for 3-hydroxy fatty acids in house dust using ion-trap mass spectrometry. | 2006-04 |
|
| Novel antagonists of alcohol inhibition of l1-mediated cell adhesion: multiple mechanisms of action. | 2002-11 |
|
| Release rates for pine sawfly pheromones from two types of dispensers and phenology of Neodiprion sertifer. | 2001-04 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:59:08 GMT 2025
by
admin
on
Mon Mar 31 18:59:08 GMT 2025
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| Record UNII |
333QVA4G2Q
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Official Name | English | ||
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Common Name | English | ||
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Code | English |
| Code System | Code | Type | Description | ||
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77468
Created by
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12397
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333QVA4G2Q
Created by
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66446
Created by
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629-76-5
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1-Pentadecanol
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211-107-9
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DTXSID0027270
Created by
admin on Mon Mar 31 18:59:08 GMT 2025 , Edited by admin on Mon Mar 31 18:59:08 GMT 2025
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PRIMARY |