Elaidyl alcohol

Base Information

• Chemical Name: Elaidyl alcohol
• CAS No.: 506-42-3
• Molecular Formula: C18H36 O
• Molecular Weight: 268.483
• Hs Code.: 2905290000
• European Community (EC) Number: 209-791-9,208-037-6,247-696-4
• NSC Number: 72786
• UNII: WDY6XJ6RTJ
• DSSTox Substance ID: DTXSID301014859
• Nikkaji Number: J188.472G,J11.819B
• Wikidata: Q20020621
• Metabolomics Workbench ID: 43943
• Mol file: 506-42-3.mol

Synonyms:Elaidyl alcohol;trans-9-Octadecenol;506-42-3;9-Octadecen-1-ol, (E)-;(E)-octadec-9-en-1-ol;Octadecen-1-ol;trans-9-Octadecen-1-ol;9-Octadecen-1-ol, (9E)-;elaidic alcohol;(9e)-octadec-9-en-1-ol;(E)-Octadec-9-enol;WDY6XJ6RTJ;(E)-9-octadecen-1-ol;9-Octadecen-1-ol, trans-;EINECS 208-037-6;NSC-72786;26446-12-8;AI3-15841;9-Octadecenol;EINECS 247-696-4;9-Octadecen-1-ol, (9Z)-;Elaidylalcohol;Oleinalkohol;9(E)-Octadecenol;MFCD00063218;UNII-WDY6XJ6RTJ;trans-octadec-9-en-1-ol;Elaidyl alcohol, >=99%;SCHEMBL5669;SCHEMBL145487;(9E)-9-Octadecen-1-ol #;DTXSID301014859;NSC72786;LMFA05000684;NSC 72786;AKOS015839897;HY-W127491;AS-81757;CS-0185719;O0228;T72539;A828218;A833011;Q20020621

Chemical Property of Elaidyl alcohol

Chemical Property:

• Vapor Pressure: 1E-05mmHg at 25°C
• Melting Point: 37 °C
• Refractive Index: 1.4590
• Boiling Point: 333 °C
• Flash Point: 120.7°C
• PSA: 20.23000
• Density: 0.847g/cm³
• LogP: 6.01620
• Storage Temp.: 2-8°C
• Solubility.: almost transparency in Methanol
• XLogP3: 7.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 15
• Exact Mass: 268.276615768
• Heavy Atom Count: 19
• Complexity: 175

Purity/Quality:

98%,99%, ^*data from raw suppliers

Elaidyl alcohol ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCCCC=CCCCCCCCCO
• Isomeric SMILES: CCCCCCCC/C=C/CCCCCCCCO
• Uses: Elaidyl alcohol is a precursor in the biosynthesis of plasmalogens, a special class of phospholipids that reside in neural membranes.

Technology Process of Elaidyl alcohol

There total 11 articles about Elaidyl alcohol 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: 98.4%

methyl (9E)-octadec-9-enoate (2462-84-2) → (E)-9-octadecen-1-ol (506-42-3,593-47-5,84286-21-5)

Guidance literature:

With hydrogen; In hexane; at 200 ℃; for 8h; under 15001.5 Torr; Solvent;

Reference yield:

cis-Octadecenoic acid (112-80-1,2027-47-6) → 1-octadecanol (112-92-5) + oleoyl alcohol (143-28-2,593-47-5,84286-21-5) + (E)-9-octadecen-1-ol (506-42-3,593-47-5,84286-21-5) + Elaidic acid (112-79-8,2027-47-6) + stearic acid (57-11-4)

Guidance literature:

With hydrogen; aluminum oxide; rhenium; tin; at 250 ℃; for 20h; under 42003.3 Torr; Product distribution; var. temperature and pressure, other catalysts; effect of catalyst composition and preparation on catalytic activity,;

DOI:10.1007/BF02545327

Reference yield:

Elaidic acid (112-79-8,2027-47-6) → (E)-9-octadecen-1-ol (506-42-3,593-47-5,84286-21-5)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; for 4h; Heating;

DOI:10.1002/mrc.1260320503

upstream raw materials:

oleoyl alcohol

elaidic acid ethyl ester

cis-Octadecenoic acid

Elaidic acid

Downstream raw materials:

(9SR,10SR)-octadecane-1,9,10-triol

(9RS,10RS)-9,10-epoxy-octadecan-1-ol

[(E)-octadec-9-enyl] benzoate

4-[((E)-Octadec-9-enyl)oxy]-benzoic acid

Refernces

• 1、 Dyen et al.. "". . p. 431. Retrieved 1966.
• 2、 -. "ALKENYL SUBSTITUTED 2,5-PIPERAZINEDIONES AND THEIR USE IN COMPOSITIONS FOR DELIVERING AN AGENT TO A SUBJECT OR CELL". Paragraph 00291; 00292. . Retrieved 2017/01/02.
• 3、 Pehlivan, Leyla,Metay, Estelle,Laval, Stephane,Dayoub, Wissam,Delbrayelle, Dominique,Mignani, Gerard,Lemaire, Marc. "Reduction of aromatic and aliphatic esters using the reducing systems MoO2(acac)2 or V(O)(OiPr)3 in combination with 1,1,3,3-tetramethyldisiloxane". experimental part. p. 7400 - 7406. Retrieved 2012/01/06.