Nonadecane

Base Information

• Chemical Name: Nonadecane
• CAS No.: 629-92-5
• Molecular Formula: C19H40
• Molecular Weight: 268.527
• European Community (EC) Number: 211-116-8
• NSC Number: 77136
• UN Number: 1325
• UNII: NMY21D3Y5T
• DSSTox Substance ID: DTXSID9047170
• Nikkaji Number: J1.705A
• Wikipedia: Nonadecane
• Wikidata: Q150911
• Metabolomics Workbench ID: 5273
• Mol file: 629-92-5.mol

Synonyms:nonadecane;perdeuterated nonadecance

Chemical Property of Nonadecane

Chemical Property:

• Appearance/Colour: white crystalline solid
• Vapor Pressure: 0.000325mmHg at 25°C
• Melting Point: 32 °C
• Refractive Index: 1.4410
• Boiling Point: 330.145 °C at 760 mmHg
• Flash Point: 168.333 °C
• PSA: 0.00000
• Density: 0.785 g/cm³
• LogP: 7.65790
• XLogP3: 9.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 16
• Exact Mass: 268.313001276
• Heavy Atom Count: 19
• Complexity: 123
• Transport DOT Label: Flammable Solid

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s): Xn;C;F
• Hazard Codes: Xn;C;F

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

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

Technology Process of Nonadecane

There total 31 articles about Nonadecane 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: 93.0%

Arachidic acid (506-30-9) → n-nonadecane (629-92-5) + carbon monoxide (201230-82-2)

Guidance literature:

With hydrogen; at 200 ℃; for 24h; under 7500.75 Torr; Microwave irradiation;

DOI:10.1021/acscatal.9b04784

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;

upstream raw materials:

nonadecan-2-one

heneicosanedioic acid

cis-Octadecenoic acid

oenanthic acid

Downstream raw materials:

2-methylheptane

3-methylheptane

Isobutane

methylbutane

Refernces

• 1、 Huijbers, Mieke M. E.,Zhang, Wuyuan,Tonin, Fabio,Hollmann, Frank. "Light-Driven Enzymatic Decarboxylation of Fatty Acids". supporting information. p. 13648 - 13651. Retrieved 2018/09/21.
• 2、 Mazziotta, Andrea,Madsen, Robert. "Ruthenium-Catalyzed Dehydrogenative Decarbonylation of Primary Alcohols". . p. 5417 - 5420. Retrieved 2017/10/06.