2-Methylpentadecane

Base Information

• Chemical Name: 2-Methylpentadecane
• CAS No.: 1560-93-6
• Molecular Formula: C16H34
• Molecular Weight: 226.446
• Hs Code.: 2901100000
• European Community (EC) Number: 845-314-6
• NSC Number: 109495
• UNII: 04R9AW5KWV
• DSSTox Substance ID: DTXSID70166026
• Nikkaji Number: J133.570G
• Wikidata: Q81977178
• Mol file: 1560-93-6.mol

Synonyms:2,2,4,4,6,8,8-heptamethylnonane;isocetane;isohexadecane

Chemical Property of 2-Methylpentadecane

Chemical Property:

• Appearance/Colour: colourless liquid
• Vapor Pressure: 0.00785mmHg at 25°C
• Melting Point: -7 C
• Refractive Index: 1.4312
• Boiling Point: 282 C
• Flash Point: 95.3°C
• PSA: 0.00000
• Density: 0.772g/cm³
• LogP: 6.34350
• Water Solubility.: 0.106ug/L(23 oC)
• XLogP3: 8.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 12
• Exact Mass: 226.266051085
• Heavy Atom Count: 16
• Complexity: 115

Purity/Quality:

99%min ^*data from raw suppliers

2-METHYL PENTADECANE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Classes -> Aliphatics, Saturated (>C11)
• Canonical SMILES: CCCCCCCCCCCCCC(C)C

Technology Process of 2-Methylpentadecane

There total 10 articles about 2-Methylpentadecane 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:

tallow oil + decalin (91-17-8) → cis-decahydronaphthalene + trans-decalin + naphthalene (91-20-3,71998-51-1,72931-45-4) + tetralin (119-64-2) + octane (111-65-9) + nonane (111-84-2) + dodecane (112-40-3) + pentadecane (629-62-9) + icosane (112-95-8) + n-docosane (629-97-0) + methane (34557-54-5,27936-85-2) + n-heptane (142-82-5) + Tridecane (629-50-5) + isotridecane (1560-97-0) + tetradecane (629-59-4) + 3-methyl-tridecane (6418-41-3) + 2-methyltridecane (1560-96-9) + 3-methyltetradecane (18435-22-8) + isopentadecane (1560-95-8) + 3-methylpentadecane (2882-96-4) + 2-methylpentadecane (1560-93-6) + Hexadecane (544-76-3) + hepatdecane (629-78-7) + 3-methylhexadecane (6418-43-5) + 2-methyl-hexadecane (1560-92-5) + octadecane (593-45-3) + 3-methyl-heptadecane (6418-44-6) + 2-methylheptadecane (1560-89-0) + n-nonadecane (629-92-5) + phytane (638-36-8) + 2-methyl-eicosane (1560-84-5) + n-tricosane (638-67-5) + octadec-1-ene (112-88-9) + n-undecylcyclohexane (54105-66-7) + 1,3,5-trimethylcyclohexane (1839-63-0) + bicyclopentyl (1636-39-1) + decahydro-2-methyl naphthalene (2958-76-1)

Guidance literature:

With Dimethyldisulphide; hydrogen; cobalt-molybdenum on alumina; at 363 ℃; for 120h; under 75757.6 Torr; Product distribution / selectivity;

Reference yield:

1-hexadecylcarboxylic acid (57-10-3) → pentadecane (629-62-9) + 2-methylpentadecane (1560-93-6) + Hexadecane (544-76-3)

Guidance literature:

With hydrogen; In dodecane; at 20 - 260 ℃; under 9000.9 Torr; Reagent/catalyst; Kinetics; Autoclave;

DOI:10.1002/chem.201203110

Reference yield:

Hexadecane (544-76-3) → 5-methylpentadecane (25117-33-3) + 6-methylpentadecane (10105-38-1) + 3-methylpentadecane (2882-96-4) + 4-methylpentadecane (2801-87-8) + 2-methylpentadecane (1560-93-6)

Guidance literature:

With 0.30 wt % Pd loading SAPO-41 molecular sieve; at 320 ℃; under 15001.5 Torr; Reagent/catalyst; Temperature;

DOI:10.1134/S1070427220040047

upstream raw materials:

Dodecanal

isobutylmagnesium bromide

tridecylmagnesium bromide

acetone

Refernces

• 1、 Bai, Xuefeng,Guo, Chunmu,Jia, Guozhi,Li, Tong,Maximov, A. L.,Su, Xiaofang,Wang, Wei,Wei, Xiaomeng,Wu, Wei. "Pd/SAPO-41 Bifunctional Catalysts with Enhanced Pd Dispersion Prepared by Ultrasonic-Assisted Impregnation: High Selectivity for n-Hexadecane Hydroisomerization". . p. 502 - 511. Retrieved 2020/05/29.
• 2、 Peng, Baoxiang,Zhao, Chen,Kasakov, Stanislav,Foraita, Sebastian,Lercher, Johannes A.. "Manipulating catalytic pathways: Deoxygenation of palmitic acid on multifunctional catalysts". . p. 4732 - 4741. Retrieved 2013/05/22.