10-Nonadecanol

Base Information

• Chemical Name: 10-Nonadecanol
• CAS No.: 16840-84-9
• Molecular Formula: C19H40 O
• Molecular Weight: 284.526
• Hs Code.: 2905199090
• European Community (EC) Number: 240-864-8
• NSC Number: 158534
• DSSTox Substance ID: DTXSID90168562
• Nikkaji Number: J236.869B
• Wikidata: Q83038176
• Mol file: 16840-84-9.mol

Synonyms:10-Nonadecanol;Nonadecan-10-ol;16840-84-9;EINECS 240-864-8;AI3-36473;dinonyl carbinol;NSC158534;SCHEMBL1258963;C(CCCCCCCC)C(O)CCCCCCCCC;DTXSID90168562;NSC 158534;NSC-158534;(5-Bromopyrimidin-2-yl)aceticacidethylester;FT-0607194;E84134

Chemical Property of 10-Nonadecanol

Chemical Property:

• Vapor Pressure: 4.07E-06mmHg at 25°C
• Refractive Index: 1.4357 (estimate)
• Boiling Point: 344.8°Cat760mmHg
• Flash Point: 127.5°C
• PSA: 20.23000
• Density: 0.836g/cm³
• LogP: 6.62870
• XLogP3: 8.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 16
• Exact Mass: 284.307915895
• Heavy Atom Count: 20
• Complexity: 149

Purity/Quality:

99% ^*data from raw suppliers

10-NONADECANOL 95.00% ^*data from reagent suppliers

Safty Information:

• Safety Statements: S22:Do not inhale dust.; S24/25:Avoid contact with skin and eyes.

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCC(CCCCCCCCC)O

Technology Process of 10-Nonadecanol

There total 5 articles about 10-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: 95.0%

10-Nonadecanon (504-57-4) → nonadecan-10-ol (16840-84-9)

Guidance literature:

With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 0 - 25 ℃; for 2h;

Reference yield:

1-Bromononane (693-58-3) + formic acid ethyl ester (109-94-4) → nonadecan-10-ol (16840-84-9)

Guidance literature:

1-Bromononane; With iodine; magnesium; In tetrahydrofuran;

formic acid ethyl ester; In tetrahydrofuran; at 65 - 70 ℃; for 72h; Further stages.;

DOI:10.1016/j.bmc.2007.03.017

Reference yield:

1-decanoic acid (334-48-5) → nonadecan-10-ol (16840-84-9)

Guidance literature:

Multi-step reaction with 2 steps

1: thorium oxide / 375 - 400 °C

2: nickel; silica gel / 120 °C / Hydrogenation

With silica gel; thorium dioxide; nickel;

upstream raw materials:

10-Nonadecanon

caprinaldehyde

nonylmagnesium bromide

1-Bromononane

Downstream raw materials:

C₂₇H₄₅BrO₂

nonadecan-10-amine

Refernces

• 1、 Sugandhi, Eko W.,Falkinham III, Joseph O.,Gandour, Richard D.. "Synthesis and antimicrobial activity of symmetrical two-tailed dendritic tricarboxylato amphiphiles". . p. 3842 - 3853. Retrieved 2008/02/09.
• 2、 Dusart, Odile. "Synthese et proprietes superficielles d'alkylsulfonates de sodium secondaires et symetriques a l'interface eau-air et eau-alcanes". . p. 491 - 496. Retrieved 2007/10/02.