(Z)-3-hexenyl isovalerate Details
:
IUPAC Name
[(Z)-hex-3-enyl] 3-methylbutanoate
:Chemical Class
Sesquiterpene
:CAS Registry Number
:Description
Cis-3-hexenyl isovalerate is a type of isovalerate ester derived from 3-hexenol, characterized by a cis-configured double bond in its structure. It functions as a volatile compound commonly found in essential oils and acts as an attractant for insects.
:Fragrance Type
swet, apple-like odour
Physical and Chemical properties
| PUBCHEM ID | 5367681 |
| Molecular Weight (g/mol) | 184.27 g/mol |
| Molecular Formula | C11H20O2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 7 |
| IUPAC Name | [(Z)-hex-3-enyl] 3-methylbutanoate |
| Canonical SMILES | CC/C=CCCOC(=O)CC(C)C |
| PUBCHEM IUPAC INCHIKEY | AIQLNKITFBJPFO-WAYWQWQTSA-N |
| Solubility Level | 3 |
| Vapour Pressure |
Absorption and Metabolism information
| XLOGP3 AA | 3.2 |
| CACTVS TPSA | 26.3 |
| BBB Level | 1 |
| Absorption Level | 0 |
| EXT PPB#Prediction | TRUE |
| AlogP98 | 3.192 |
| EXT CYP2D6#Prediction | FALSE |
Toxicological Information
| Mouse Female FDA | Non-Carcinogen |
| Mouse Male FDA | Multi-Carcinogen |
| Rat Female FDA | Single-Carcinogen |
| Rat Male FDA | Single-Carcinogen |
| Ames Prediction | Non-Mutagen |
| Developmental / Reproductive Toxicity | Non-Toxic |
| Rat Oral LD50 | 2.80587 g/kg_body_weight |
| Ocular Irritancy | None |
| Hepatotoxic#Prediction | FALSE |
| Effected Human Genes |
Ecological Information
| Aerobic Biodegradability Prediction | Degradable |
Hazard(s) Identification
| Physical hazards | not classified |
| Health hazards | Moderate |
| Environmental hazards | not classified |
Compound Biological Activity
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| Serial No. | Activity Name | Details | References (PubMed) | Other details EPA (U.S) | Clinical Trials (U.S. NIH) |
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Compound Image
2D Structure
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