2-Tridecyloxirane

Base Information

• Chemical Name: 2-Tridecyloxirane
• CAS No.: 18633-25-5
• Molecular Formula: C15H30 O
• Molecular Weight: 226.403
• Hs Code.: 2910900090
• European Community (EC) Number: 242-460-7
• UNII: V2LL9HNF94
• DSSTox Substance ID: DTXSID80885059
• Nikkaji Number: J91.340E
• Mol file: 18633-25-5.mol

Synonyms:2-Tridecyloxirane;Tridecyloxirane;18633-25-5;Oxirane, 2-tridecyl-;Oxirane, tridecyl-;1,2-epoxypentadecane;1-pentadecene oxide;1,2-Pentadecane oxide;V2LL9HNF94;EINECS 242-460-7;2-Tridecyloxirane #;TRIDECYL EPOXYETHANE;UNII-V2LL9HNF94;SCHEMBL284297;DTXSID80885059;PENTADECANE, 1,2-EPOXY-;EN300-269950;F87811;A1-20502;Z1495386305

Chemical Property of 2-Tridecyloxirane

Chemical Property:

• Vapor Pressure: 0.00402mmHg at 25°C
• Boiling Point: 288.6°Cat760mmHg
• Flash Point: 106.7°C
• PSA: 12.53000
• Density: 0.859g/cm³
• LogP: 5.08630
• XLogP3: 6.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 12
• Exact Mass: 226.229665576
• Heavy Atom Count: 16
• Complexity: 144

Purity/Quality:

98%Min ^*data from raw suppliers

1,2-Epoxypentadecane 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCC1CO1

Technology Process of 2-Tridecyloxirane

There total 14 articles about 2-Tridecyloxirane 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: 98.0%

(R)-2-hydroxytetradecyl mesitylenesulfonate → (R)-(+)-1,2-epoxypentadecane (18633-25-5,96938-07-7,96938-06-6)

Guidance literature:

With potassium carbonate; In methanol; at 20 ℃; for 2h;

DOI:10.1016/j.bmc.2012.04.040

Reference yield: 96.0%

1-pentadecene (13360-61-7) → 1,2-epoxypentadecane (18633-25-5)

Guidance literature:

With sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 - 20 ℃;

Reference yield: 92.0%

1-chloropentadecan-2-ol (19446-50-5) → 1,2-epoxypentadecane (18633-25-5)

Guidance literature:

With potassium hydroxide; In diethyl ether; for 6h; Inert atmosphere;

DOI:10.1055/S-0029-1218687

upstream raw materials:

n-pentadecane-1,2-diol

1-chloropentadecan-2-ol

laurylmagnesium bromide

1-pentadecene

Downstream raw materials:

C₁₆H₃₁NO

(R)-(+)-1,2-epoxypentadecane

C₁₅H₃₂O₂

n-pentadecane-1,2-diol