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Details

Stereochemistry RACEMIC
Molecular Formula C8H18O
Molecular Weight 130.2279
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-OCTANOL

SMILES

CCCCCC(O)CC

InChI

InChIKey=NMRPBPVERJPACX-UHFFFAOYSA-N
InChI=1S/C8H18O/c1-3-5-6-7-8(9)4-2/h8-9H,3-7H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C8H18O
Molecular Weight 130.2279
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Odorant-binding proteins of the malaria mosquito Anopheles funestus sensu stricto.
2010-10-22
Neurotoxicity of fungal volatile organic compounds in Drosophila melanogaster.
2010-10
Adaptive adjustment of the generalization-discrimination balance in larval Drosophila.
2010-09
Integrating heterogeneous odor response data into a common response model: A DoOR to the complete olfactome.
2010-09
Inhibition of predator attraction to kairomones by non-host plant volatiles for herbivores: a bypass-trophic signal.
2010-06-10
Behavioral characterization of individual olfactory memory retrieval in Drosophila melanogaster.
2010
A Neurogenetic Dissociation between Punishment-, Reward-, and Relief-Learning in Drosophila.
2010
Fragile x mental retardation 1 and filamin a interact genetically in Drosophila long-term memory.
2010
Odour intensity learning in fruit flies.
2009-10-07
Characterization of an enantioselective odorant receptor in the yellow fever mosquito Aedes aegypti.
2009-09-15
Specificity and redundancy in the olfactory system of the bark beetle Ips typographus: single-cell responses to ecologically relevant odors.
2009-06
Eight different types of dopaminergic neurons innervate the Drosophila mushroom body neuropil: anatomical and physiological heterogeneity.
2009
Use of headspace SPME-GC-MS for the analysis of the volatiles produced by indoor molds grown on different substrates.
2008-10
Aroma-active components of Lycii fructus (kukija).
2008-08
No evidence for visual context-dependency of olfactory learning in Drosophila.
2008-08
Induction of conidiation by endogenous volatile compounds in Trichoderma spp.
2008-07
Predatory mite attraction to herbivore-induced plant odors is not a consequence of attraction to individual herbivore-induced plant volatiles.
2008-06
A regulatory code for neuron-specific odor receptor expression.
2008-05-27
Multimodal chemosensory integration through the maxillary palp in Drosophila.
2008-05-14
Defense-inducing volatiles: in search of the active motif.
2008-05
Correlation between the pattern volatiles and the overall aroma of wild edible mushrooms.
2008-03-12
Host recognition by the specialist hoverfly Microdon mutabilis, a social parasite of the ant Formica lemani.
2008-02
Thermal disruption of mushroom body development and odor learning in Drosophila.
2007-11-07
Segregation of odor identity and intensity during odor discrimination in Drosophila mushroom body.
2007-10-02
Reverse micellar extraction systems for the purification of pharmaceutical grade plasmid DNA.
2007-08-31
Toxicity of parked motor vehicle indoor air.
2007-04-01
Differentiation of aroma characteristics of pine-mushrooms (Tricholoma matsutake Sing.) of different grades using gas chromatography-olfactometry and sensory analysis.
2007-03-21
Host habitat assessment by a parasitoid using fungal volatiles.
2007-02-06
Characterization of aroma-active compounds in raw and cooked pine-mushrooms (Tricholoma matsutake Sing.).
2006-08-23
Difference in the volatile composition of pine-mushrooms (Tricholoma matsutake Sing.) according to their grades.
2006-06-28
Structural characterization of interfacial n-octanol and 3-octanol using molecular dynamic simulations.
2006-03-02
Volatile constituents of Semnostachya menglaensis Tsui.
2005-11-16
Volatile compounds of Aspergillus strains with different abilities to produce ochratoxin A.
2005-03-09
The role of volatile semiochemicals in mediating host location and selection by nuisance and disease-transmitting cattle flies.
2004-12
[Studies on the chemical constituents of the volatiles of Clerodendron bungei].
2004-02
Subchronic oral toxicity study on the three flavouring substances: octan-3-ol, 2-methylcrotonic acid and oct-3-yl 2-methylcrotonate in Wistar rats.
2003-05
Comparison of volatile compound production in fruit body and in mycelium of Pleurotus ostreatus identified by submerged and solid-state cultures.
2002-10-25
Novel memory mutants in Drosophila: behavioral characteristics of the mutant nemyP153.
2002-07-30
Detection and quantification of ochratoxin A and deoxynivalenol in barley grains by GC-MS and electronic nose.
2002-02-05
Olfactory responses of Ips duplicatus from inner Mongolia, China to nonhost leaf and bark volatiles.
2001-05
Solvent effect on ion-pair extraction of 2-(2-pyridylazo)-1-naphthol-4-sulfonate anion with solvated hydroxonium ion using alcohols and 1-octanol/octane mixed solvents.
2001-02
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:57:29 GMT 2025
Edited
by admin
on Mon Mar 31 18:57:29 GMT 2025
Record UNII
73DZ0U3U1E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-OCTANOL
FCC   FHFI  
Systematic Name English
FEMA NO. 3581
Preferred Name English
(±)-3-OCTANOL
Systematic Name English
ETHYL-N-AMYLCARBINOL
Common Name English
3-OCTANOL [FCC]
Common Name English
OCTAN-3-OL
Systematic Name English
ETHYLAMYLCARBINOL
Systematic Name English
ETHYL AMYL CARBINOL
Systematic Name English
1-ETHYLHEXANOL
Systematic Name English
DL-3-OCTANOL
Common Name English
1-ETHYL-1-HEXANOL
Systematic Name English
N-OCTAN-3-OL
Common Name English
3-OCTANOL, (±)-
Systematic Name English
3-OCTANOL [FHFI]
Common Name English
OCTEN-3-OL-
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
JECFA EVALUATION 3-OCTANOL
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
Code System Code Type Description
SMS_ID
100000161128
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
PRIMARY
CAS
589-98-0
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
PRIMARY
PUBCHEM
11527
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
PRIMARY
CHEBI
80945
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
PRIMARY
EPA CompTox
DTXSID10862252
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
PRIMARY
EVMPD
SUB174625
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
PRIMARY
JECFA MONOGRAPH
397
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-667-4
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
PRIMARY
FDA UNII
73DZ0U3U1E
Created by admin on Mon Mar 31 18:57:29 GMT 2025 , Edited by admin on Mon Mar 31 18:57:29 GMT 2025
PRIMARY