9-Octadecen-1-ol, 1-methanesulfonate, (9Z)-

Base Information

• Chemical Name: 9-Octadecen-1-ol, 1-methanesulfonate, (9Z)-
• CAS No.: 35709-09-2
• Deprecated CAS: 1236479-54-1
• Molecular Formula: C19H38 O3 S
• Molecular Weight: 346.575
• Hs Code.: 2905290000
• European Community (EC) Number: 252-686-8
• Mol file: 35709-09-2.mol

Synonyms:EINECS 252-686-8;(E)-Octadec-9-en-1-yl methanesulfonate;9-Octadecen-1-ol, 1-methanesulfonate, (9Z)-;59101-13-2;(Z)-9-Octadecen-1-yl methanesulfonate;C19H38O3S;C19-H38-O3-S;35709-09-2;9-Octadecen-1-ol, methanesulfonate, (Z)-;SCHEMBL1048730;SCHEMBL2999938;Octadec-9-en-1-yl methanesulfonate;72641-08-8

Chemical Property of 9-Octadecen-1-ol, 1-methanesulfonate, (9Z)-

Chemical Property:

• Vapor Pressure: 2.1E-08mmHg at 25°C
• Refractive Index: 1.465
• Boiling Point: 465.7°Cat760mmHg
• Flash Point: 235.4°C
• PSA: 51.75000
• Density: 0.954g/cm³
• LogP: 7.08090
• Storage Temp.: −20°C
• XLogP3: 7.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 17
• Exact Mass: 346.25416624
• Heavy Atom Count: 23
• Complexity: 355

Purity/Quality:

98%Min ^*data from raw suppliers

Oleylmethanesulphonate ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCC=CCCCCCCCCOS(=O)(=O)C
• Isomeric SMILES: CCCCCCCC/C=C/CCCCCCCCOS(=O)(=O)C
• Uses: Oleyl Mesylate, is a derivative of Oleyl Alcohol (O235935), which can be used a nonionic surfactant, emulsifier, emollient and thickener in skin creams, lotions and many other cosmetic products. This compound can also be used in the synthesis of lipidic alcohols and amines.

Technology Process of 9-Octadecen-1-ol, 1-methanesulfonate, (9Z)-

There total 7 articles about 9-Octadecen-1-ol, 1-methanesulfonate, (9Z)- 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: 96.0%

oleoyl alcohol (143-28-2,593-47-5,84286-21-5) + methanesulfonyl chloride (124-63-0) → oleyl methanesulfonate (35709-09-2)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃;

DOI:10.1002/(SICI)1099-0690(200002)2000:4<665::AID-EJOC665>3.0.CO;2-A

Reference yield: 90.0%

diethyl ether (60-29-7,927820-24-4) + oleoyl alcohol (143-28-2,593-47-5,84286-21-5) → oleyl methanesulfonate (35709-09-2)

Guidance literature:

With sodium hydrogencarbonate; In pyridine; ethanol; chloroform; water; methanesulfonyl chloride;

Reference yield: 78.0%

→ oleyl methanesulfonate (35709-09-2)

Guidance literature:

With triethylamine; In dichloromethane; at 0 - 20 ℃; for 4h;

upstream raw materials:

oleoyl alcohol

methanesulfonyl chloride

Methyl oleate

diethyl ether

Downstream raw materials:

rac-1-(Z-9-octadecenyl)glycerol

cholesteryl cis-9'-octadecenyl ether

2,3-bis[(Z)-octadec-9-enyloxy]propanol

N-oleylmorpholine