Tridecane

Base Information

• Chemical Name: Tridecane
• CAS No.: 629-50-5
• Molecular Formula: C13H28
• Molecular Weight: 184.365
• Hs Code.: 29011090
• European Community (EC) Number: 211-093-4
• NSC Number: 66205
• UN Number: 1993
• UNII: A3LZF0L939
• DSSTox Substance ID: DTXSID6027266
• Nikkaji Number: J525H
• Wikipedia: Tridecane
• Wikidata: Q150788
• RXCUI: 1811766
• Metabolomics Workbench ID: 4706
• ChEMBL ID: CHEMBL135694
• Mol file: 629-50-5.mol

Synonyms:n-tridecane;tridecane

Chemical Property of Tridecane

Chemical Property:

• Appearance/Colour: colourless liquid
• Vapor Pressure: 1 mm Hg ( 59.4 °C)
• Melting Point: -5.5 °C
• Refractive Index: n20/D 1.425(lit.)
• Boiling Point: 234.5 °C at 760 mmHg
• Flash Point: 101.7 °C
• PSA: 0.00000
• Density: 0.758 g/cm³
• LogP: 5.31730
• Storage Temp.: Store below +30°C.
• Water Solubility.: PRACTICALLY INSOLUBLE
• XLogP3: 6.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 10
• Exact Mass: 184.219100893
• Heavy Atom Count: 13
• Complexity: 66.1
• Transport DOT Label: Combustible Liquid

Purity/Quality:

98%min ^*data from raw suppliers

Tridecane >99.0%(GC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi,Xn
• Statements: 36/37/38-66-65
• Safety Statements: 26-36-24/25-62

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Other Classes -> Aliphatics, Saturated (>C11)
• Canonical SMILES: CCCCCCCCCCCCC
• Uses: Organic synthesis, distillation chaser. n-Tridecane is used as a distillation chaser. It is a component of various fuels and solvents used in industry.

Technology Process of Tridecane

There total 100 articles about Tridecane 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) → 2-methyl-8-propyl-dodecane (55045-07-3) + 2,6-dimethyl-hexadecane + 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) + decane (124-18-5) + dodecane (112-40-3) + pentadecane (629-62-9) + icosane (112-95-8) + n-docosane (629-97-0) + n-hexacosane (630-01-3) + 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) + Hexadecane (544-76-3) + hepatdecane (629-78-7) + 3-methylhexadecane (6418-43-5) + 2-methyl-hexadecane (1560-92-5) + octadecane (593-45-3) + n-nonadecane (629-92-5) + 2-methyl-eicosane (1560-84-5) + n-tricosane (638-67-5) + tetracosane (646-31-1) + n-pentacosane (629-99-2) + norpristane (3892-00-0)

Guidance literature:

With Dimethyldisulphide; hydrogen; cobalt-molybdenum on alumina; at 363 ℃; for 120h; under 23252.3 Torr; Product distribution / selectivity;

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:

cis-Octadecenoic acid (112-80-1,2027-47-6) → nonane (111-84-2) + decane (124-18-5) + n-Undecane (1120-21-4) + dodecane (112-40-3) + Tridecane (629-50-5) + Hexadecane (544-76-3) + hepatdecane (629-78-7) + 1-Methyl-3-ethylbenzene (620-14-4) + n-undecylcyclohexane (54105-66-7) + ethylbenzene (100-41-4,27536-89-6) + 1-Methyl-3-propylbenzene (1074-43-7) + 1,2,3-trimethylcyclopentene (473-91-6)

Guidance literature:

With carbon dioxide; at 360 ℃; for 5h; Reagent/catalyst; Autoclave; High pressure; Green chemistry;

DOI:10.1039/c7gc01853c

upstream raw materials:

1-Tetradecanol

1-tridecene

tridecan-2-one

tridecan-7-one

Downstream raw materials:

1-tridecene

(Z)-tridec-2-ene

(E)-tridec-2-ene

4,4'-bis-[9-(3,6-diphenylcarbazolyl)]-1,1'-biphenyl