Nonadecanoic acid

Base Information

• Chemical Name: Nonadecanoic acid
• CAS No.: 646-30-0
• Deprecated CAS: 12707-74-3
• Molecular Formula: C19H38 O2
• Molecular Weight: 298.51
• Hs Code.: 2915900090
• European Community (EC) Number: 268-103-5,211-472-4
• NSC Number: 11914
• UNII: H6M3VYC62P
• DSSTox Substance ID: DTXSID3060954
• Nikkaji Number: J535E
• Wikipedia: Nonadecylic_acid
• Wikidata: Q412597
• Metabolomics Workbench ID: 40
• ChEMBL ID: CHEMBL1169674
• Mol file: 646-30-0.mol

Synonyms:nonadecanoic acid

Chemical Property of Nonadecanoic acid

Chemical Property:

• Appearance/Colour: white flakes or powder
• Vapor Pressure: 4.54E-06mmHg at 25°C
• Melting Point: 68-70 °C(lit.)
• Boiling Point: 297 °C (100 mmHg)
• PKA: 4.78±0.10(Predicted)
• Flash Point: 166.1°C
• PSA: 37.30000
• Density: 0.886g/cm³
• LogP: 6.72260
• Storage Temp.: 2-8°C
• Solubility.: Chloroform (Slightly), Methanol (Slightly)
• XLogP3: 8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 17
• Exact Mass: 298.287180451
• Heavy Atom Count: 21
• Complexity: 214

Purity/Quality:

98%, ^*data from raw suppliers

n-NonadecanoicAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Lipids -> Unambiguous Lipids,Other Classes -> Organic Acids
• Canonical SMILES: CCCCCCCCCCCCCCCCCCC(=O)O
• Description: Nonadecyclic acid, or nonadecanoic acid, is a 19-carbon longchain saturated fatty acid with the chemical formula CH3(CH2)17COOH. It forms salts called nonadecylates. Nonadecylic acid can be found in fats and vegetable oils. It is also used by insects as pheromones. Nonadecanoic acid is a 19-carbon saturated fatty acid that is found in fats and vegetable oils. It has been shown to inhibit HL-60 cancer cell proliferation with an IC50 value of 68 μM.
• Uses: n-Nonadecanoic Acid is a saturated fatty acid. It can be found in fats and vegetable oils. It is also used by insects as pheromones. Nonadecanoic acid may be used as an analytical reference standard for the quantification of the analyte in Notopterygium forbesii Boiss using high-performance liquid chromatography technique.

Technology Process of Nonadecanoic acid

There total 31 articles about Nonadecanoic acid 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: 80.0%

1-Eicosene (3452-07-1) → nonadecanoic acid (646-30-0)

Guidance literature:

With potassium permanganate; sulfuric acid; acetic acid; In dichloromethane; water; at 20 ℃; for 21h; Cooling with ice;

DOI:10.15227/orgsyn.060.0011

Reference yield:

p-nitrophenyl stearate → 4-nitro-phenol (100-02-7,78813-13-5,89830-32-0) + nonadecanoic acid (646-30-0)

Guidance literature:

With phosphate buffer; polymer bounded 4-(dialkylamino)pyridine; at 30 ℃; Rate constant; pH 8.0;

DOI:10.1002/anie.199715431

Reference yield:

C38H69NO7 → nonadecanoic acid (646-30-0) + C19H31NO9

Guidance literature:

With potassium permanganate; sodium periodate; potassium carbonate; In acetone; at 37 ℃; for 18h;

DOI:10.1080/10286020.2013.812643

upstream raw materials:

2,4,6-trimethyl-pyridine

rac-octan-2-ol

adipinic acid monoethyl ester

palmitic acid

Downstream raw materials:

nonadecanoic acid methyl ester

ethyl nonadecanoate

nonadecan-1-ol

β-1,2,3-tris(nonadecanoyl)glycerol

Refernces

• 1、 Riaz, Naheed,Tabussum, Asia,Saleem, Muhammad,Ashraf, Muhammad,Nasar, Romana,Jabeen, Bushra,Malik, Abdul,Jabbar, Abdul. "New lipoxygenase inhibitory sphingolipids from Chrozophora plicata". . p. 1080 - 1087. Retrieved 2014/01/06.
• 2、 Wang,Fife. "Ion-induced specificity change in polymer-catalyzed solvolyses of p-nitrophenyl alkanoates". . p. 1543 - 1545. Retrieved 2007/10/03.