Tetradecyl acetate

Base Information

• Chemical Name: Tetradecyl acetate
• CAS No.: 638-59-5
• Molecular Formula: C16H32O2
• Molecular Weight: 256.429
• Hs Code.: 2915390090
• European Community (EC) Number: 211-344-8
• UNII: G9O55CT350
• DSSTox Substance ID: DTXSID40862341
• Nikkaji Number: J45.695K
• Wikidata: Q27278976
• Metabolomics Workbench ID: 3976
• ChEMBL ID: CHEMBL2228462
• Mol file: 638-59-5.mol

Synonyms:Tetradecyl acetate;638-59-5;Myristyl acetate;1-Tetradecanol, acetate;Tetradecanol acetate;TETRADECYLACETATE;1-Tetradecanol, 1-acetate;UNII-G9O55CT350;G9O55CT350;EINECS 211-344-8;AI3-11586;n-tetradecyl acetate;tetradecanoyl acetate;1-Tetradecyl acetate;Acetic acid tetradecyl;1-Tetradecanyl acetate;tetradecan-1-yl acetate;SCHEMBL506542;MYRISTYL ACETATE [INCI];CHEMBL2228462;DTXSID40862341;CHEBI:179737;ACETIC ACID, TETRADECYL ESTER;LMFA07010331;MFCD00053737;AKOS016006385;CS-W023024;DS-2512;HY-W042284;Q27278976;B0001-130590

Chemical Property of Tetradecyl acetate

Chemical Property:

• Appearance/Colour: liquid
• Vapor Pressure: 0.00115mmHg at 25°C
• Melting Point: 14°C
• Refractive Index: 1.439
• Boiling Point: 300.051 °C at 760 mmHg
• Flash Point: 133.649 °C
• PSA: 26.30000
• Density: 0.866 g/cm³
• LogP: 5.25060
• Storage Temp.: 2-8°C
• Solubility.: Chloroform (Slightly), Methanol (Slightly)
• XLogP3: 6.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 14
• Exact Mass: 256.240230259
• Heavy Atom Count: 18
• Complexity: 178

Purity/Quality:

99% ^*data from raw suppliers

TetradecylAcetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCOC(=O)C
• Uses: Tetradecyl Acetate is a sex pheromone secreted by various insects.

Technology Process of Tetradecyl acetate

There total 12 articles about Tetradecyl acetate 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: 94.0%

Isopropenyl acetate (108-22-5) + 1-Tetradecanol (112-72-1) → tetradecyl acetate (638-59-5)

Guidance literature:

With 1,3-bis(2,4,6-trimethylphenyl)imidazole hydrochloride; potassium tert-butylate; In benzene; at 80 ℃; for 10h; Inert atmosphere;

DOI:10.1039/b910162d

Reference yield: 72.1%

1-Tetradecanol (112-72-1) + acetic anhydride (108-24-7) → tetradecyl acetate (638-59-5)

Guidance literature:

With pyridine; dmap; In dichloromethane; at 0 - 20 ℃;

DOI:10.1021/jf902575f

Reference yield:

acetic acid (64-19-7,77671-22-8) + 2,6,6-trimethyl-2-tetradecyloxy-[1,3,6]dioxazocan-6-ium; iodide → tetradecyl acetate (638-59-5) + Bis-(2-hydroxy-ethyl)-dimethyl-ammonium; iodide

Guidance literature:

With sodium acetate; In water; at 38 ℃;

DOI:10.1002/anie.200352589

upstream raw materials:

1-Tetradecanol

acetic anhydride

acetic acid

acetyl chloride

Downstream raw materials:

1-tetradecene

1,2-epoxytetradecane

Refernces

• 1、 Rodriguez, Gabriel M,Tashiro, Yohei,Atsumi, Shota. "Expanding ester biosynthesis in Escherichia coli". . p. 259 - 265. Retrieved 2014/04/03.
• 2、 Seo, Seon-M.I.,Junheon, Kim,Eunae, Kim,Park, Hye-M.I.,Kim, Young-Joon,Park, I.L.-Kwon. "Structure-Activity relationship of aliphatic compounds for nematicidal activity against pine wood nematode (Bursaphelenchus xylophilus)". experimental part. p. 1823 - 1827. Retrieved 2010/09/09.