AromaDb: A Database of Plant's Aroma Molecules

Amyl Alcohol Details

: IUPAC Name
pentan-1-ol
:Chemical Class
Alcohol
:CAS Registry Number
71-41-0
:Description

:Fragrance Type

Physical and Chemical properties

PUBCHEM ID 6276
Molecular Weight (g/mol) 88.1482
Molecular Formula C5H12O
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 3
IUPAC Name pentan-1-ol
Canonical SMILES CCCCCO
PUBCHEM IUPAC INCHIKEY AMQJEAYHLZJPGS-UHFFFAOYSA-N
Solubility Level 4
Vapour Pressure 0.381

Absorption and Metabolism information

XLOGP3 AA
CACTVS TPSA 20.2
BBB Level 2
Absorption Level 0
EXT PPB#Prediction 0
AlogP98 1.426
EXT CYP2D6#Prediction 0

Toxicological Information

Mouse Female FDA Non-Carcinogen
Mouse Male FDA Multi-Carcinogen
Rat Female FDA Multi-Carcinogen
Rat Male FDA Multi-Carcinogen
Ames Prediction Non-Mutagen
Developmental / Reproductive Toxicity Toxic
Rat Oral LD50 1.84377 g/kg_body_weight
Ocular Irritancy Severe
Hepatotoxic#Prediction 0
Effected Human Genes

Ecological Information

Aerobic Biodegradability Prediction Degradable

Hazard(s) Identification

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

Compound Biological Activity

Serial No.Cas No Gene SymbolOrganismInteractionInteraction Actions PubMed Id
171-41-0CHRNA2Homo sapiensn-pentanol inhibits the reaction [Acetylcholine promotes the reaction [[CHRNA2 protein binds to CHRNB4 protein] which results in increased transport of Barium]] affects^binding|decreases^reaction|increases^reaction|increases^transport 11821649
271-41-0GRIA3n-pentanol results in decreased activity of GRIA3 protein decreases^activity 11429388
Serial No. Activity Name DetailsReferences (PubMed)Other details EPA (U.S) Clinical Trials (U.S. NIH)
1 71-41-0 Amyl Alcohol

Compound Image


2D Structure

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