1-Nonadecanol

Base Information

• Chemical Name: 1-Nonadecanol
• CAS No.: 1454-84-8
• Molecular Formula: C19H40O
• Molecular Weight: 284.526
• Hs Code.: 2905199090
• European Community (EC) Number: 215-930-4
• UNII: A465X576KO
• DSSTox Substance ID: DTXSID90870875
• Nikkaji Number: J45.980A
• Wikipedia: 1-Nonadecanol
• Wikidata: Q27273608
• Mol file: 1454-84-8.mol

Synonyms:1-NONADECANOL;1454-84-8;NONADECANOL;Nonadecan-1-ol;Nonadecyl alcohol;UNII-A465X576KO;C19H40O;A465X576KO;EINECS 215-930-4;AI3-36471;n-Nonadecanol-1;n-nonadecyl alcohol;MFCD00002824;1-Nonadecanol, 99%;SCHEMBL103937;AMY5925;DTXSID90870875;AKOS015839822;CS-W004297;HY-W004297;AS-10300;FT-0608161;N0284;H10890;J-008118;Q27273608;1-Nonadecanol, European Pharmacopoeia (EP) Reference Standard

Chemical Property of 1-Nonadecanol

Chemical Property:

• Appearance/Colour: white crystalline powder
• Vapor Pressure: 3.92E-06mmHg at 25°C
• Melting Point: 60-61 °C (lit.)
• Refractive Index: 1.4328
• Boiling Point: 345.3 °C at 760 mmHg
• PKA: 15.20±0.10(Predicted)
• Flash Point: 140.4 °C
• PSA: 20.23000
• Density: 0.837 g/cm³
• LogP: 6.63030
• XLogP3: 8.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 17
• Exact Mass: 284.307915895
• Heavy Atom Count: 20
• Complexity: 156

Purity/Quality:

98%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Other Classes -> Alcohols and Polyols, Other
• Canonical SMILES: CCCCCCCCCCCCCCCCCCCO

Technology Process of 1-Nonadecanol

There total 15 articles about 1-Nonadecanol 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: 91.0%

1-Bromoheptane (629-04-9) + 12-bromododecanol (3344-77-2) → nonadecan-1-ol (1454-84-8)

Guidance literature:

1-Bromoheptane; With magnesium; In tetrahydrofuran; for 1h; Heating;

12-bromododecanol; With dilithium tetrachlorocuprate; In tetrahydrofuran; at -40 - 20 ℃; for 14h;

DOI:10.1016/j.tet.2005.09.056

Reference yield: 83.0%

nonadecanoic acid (646-30-0) → nonadecan-1-ol (1454-84-8)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; for 1h; Heating;

DOI:10.1016/j.tet.2005.09.056

Reference yield:

diethyl ether (60-29-7,927820-24-4) + 1-chlorooctadecane (3386-33-2) → formaldehyde dinonanedecylacetal (854751-26-1) + octadecane (593-45-3) + nonadecan-1-ol (1454-84-8) + octadec-1-ene (112-88-9)

Guidance literature:

und Kochen des Reaktionsgemisches mit Paraformaldehyd;

upstream raw materials:

nonadecanoic acid

ethyl nonadecanoate

trans-9-octadecene

carbon monoxide

Downstream raw materials:

nonadecanal

nonadecyl acetate

melissyl alcohol

(5S,8RS)-5-methyl-8-phenylsulfonylheptacosane

Refernces

• 1、 Al Dulayymi, Juma'a R.,Baird, Mark S.,Roberts, Evan. "The synthesis of a single enantiomer of a major α-mycolic acid of M. tuberculosis". . p. 11939 - 11951. Retrieved 2007/10/03.
• 2、 Duclos, Richard I.,Makriyannis, Alexandros. "Syntheses of All Four Stereoisomers Which Are Conformationally Constrained 1,4-Dioxanyl Analogs of the Antineoplastic Ether Lipid ET-18-OCH3". . p. 6156 - 6163. Retrieved 2007/10/02.