Ethyl linalool

Base Information

• Chemical Name: Ethyl linalool
• CAS No.: 10339-55-6
• Molecular Formula: C11H20O
• Molecular Weight: 168.279
• Hs Code.: 2905290000
• European Community (EC) Number: 233-732-6
• UNII: 5AR9L4D49U
• DSSTox Substance ID: DTXSID9047415
• Nikkaji Number: J42.479J
• Wikidata: Q27261753
• RXCUI: 1376096
• Metabolomics Workbench ID: 130664
• ChEMBL ID: CHEMBL3186789
• Mol file: 10339-55-6.mol

Synonyms:3,7-dimethyl-1,6-nonadien-3-ol

Chemical Property of Ethyl linalool

Chemical Property:

• Appearance/Colour: colorless to light yellow liquid
• Vapor Pressure: 0.0052mmHg at 25°C
• Refractive Index: 1.4603 (589.3 nm 25℃)
• Boiling Point: 244.1 °C at 760 mmHg
• PKA: 14.45±0.29(Predicted)
• Flash Point: 90.9 °C
• PSA: 9.23000
• Density: 0.857 g/cm³
• LogP: 3.71400
• Water Solubility.: 656mg/L at 20℃
• XLogP3: 3.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 168.151415257
• Heavy Atom Count: 12
• Complexity: 170

Purity/Quality:

99% ^*data from raw suppliers

ETHYL LINALOOL 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(=CCCC(C)(C=C)O)C
• Isomeric SMILES: CC/C(=C/CCC(C)(C=C)O)/C
• Uses: Ethyl Linalool is fresh bois de rose herbal wet green lavender bergamot. It has a floral, fresh, bergamot character and is sweeter and less agrestic than Linalool. As with Linalool, it is used in a wide variety of notes for floral bouquets.

Technology Process of Ethyl linalool

There total 2 articles about Ethyl linalool which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

3,7-dimethyl-non-6-en-1-yn-3-ol (24173-47-5) → ethyl linalool (10339-55-6)

Guidance literature:

With palladium on activated charcoal; Lindlar's catalyst; Hydrogenation;

Reference yield:

→ ethyl linalool (10339-55-6)

Guidance literature:

3-Hydroxy-3.7-dimethyl-non-6-en-1-yn, H2 in Petrolether;

Reference yield:

ethyl linalool (10339-55-6) → 3,7-dimethyl-nona-2,6-dien-1-ol (41865-30-9)

Guidance literature:

Multistep reaction; (i) HBr, (ii) KOAc, (iii) aq. NaOH;

upstream raw materials:

3,7-dimethyl-non-6-en-1-yn-3-ol

Downstream raw materials:

3,7-dimethyl-2,6-nonadienal

3,7-dimethyl-nona-2,6-dien-1-ol