AromaDb: A Database of Plant's Aroma Molecules

2-Octanol Details

: IUPAC Name
octan-2-ol
:Chemical Class
Alcohol
:CAS Registry Number
123-96-6
:Description

:Fragrance Type
oily

Physical and Chemical properties

PUBCHEM ID 20083
Molecular Weight (g/mol) 130.228
Molecular Formula C8H18O
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 5
IUPAC Name octan-2-ol
Canonical SMILES CCCCCCC(C)O
PUBCHEM IUPAC INCHIKEY SJWFXCIHNDVPSH-UHFFFAOYSA-N
Solubility Level 4
Vapour Pressure

Absorption and Metabolism information

XLOGP3 AA
CACTVS TPSA 20.2
BBB Level 1
Absorption Level 0
EXT PPB#Prediction 1
AlogP98 2.716
EXT CYP2D6#Prediction 0

Toxicological Information

Mouse Female FDA Non-Carcinogen
Mouse Male FDA Multi-Carcinogen
Rat Female FDA Non-Carcinogen
Rat Male FDA Non-Carcinogen
Ames Prediction Non-Mutagen
Developmental / Reproductive Toxicity Toxic
Rat Oral LD50 2.33285 g/kg_body_weight
Ocular Irritancy None
Hepatotoxic#Prediction 0
Effected Human Genes

Ecological Information

Aerobic Biodegradability Prediction Degradable

Hazard(s) Identification

Physical hazards not classified
Health hazards Moderate
Environmental hazards not classified
About Table Headings

Compound Biological Activity

Serial No.Cas No Gene SymbolOrganismInteractionInteraction Actions PubMed Id
1123-96-6CFTRHomo sapiens2-octanol results in increased activity of CFTR protein increases^activity 14967738
Serial No. Activity Name DetailsReferences (PubMed)Other details EPA (U.S) Clinical Trials (U.S. NIH)
1 123-96-6 2-Octanol

Plant Variety and Essential oils

Serial No. Plant NameVariety NameEssential OilCompound Percentage
1 Chamomile, German chamomile, Gule-babuna Vallary Chamomilla recutita Vallary essential oil
2 Horsechestnut Aesculus hippocastanum essential oil

Compound Image


2D Structure

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