Myristyl glyceryl ether

Base Information

• Chemical Name: Myristyl glyceryl ether
• CAS No.: 1561-06-4
• Molecular Formula: C17H36 O3
• Molecular Weight: 288.471
• Hs Code.: 2909499000
• NSC Number: 40162
• UNII: S4JE3R143V
• DSSTox Substance ID: DTXSID401300970
• Nikkaji Number: J111.054C
• Wikidata: Q27288587
• Metabolomics Workbench ID: 155597
• Mol file: 1561-06-4.mol

Synonyms:Myristyl glyceryl ether;1-o-tetradecylglycerol;3-tetradecoxypropane-1,2-diol;Glycerin 1-tetradecyl ether;1561-06-4;3-Tetradecyloxy-1,2-propanediol;1-O-Tetradecylglycerin;1,2-Propanediol, 3-(tetradecyloxy)-;rac-1-O-Tetradecylglycerol;UNII-S4JE3R143V;S4JE3R143V;NSC 40162;NSC-40162;1, 3-(tetradecyloxy)-;SCHEMBL116830;CHEBI:144328;DTXSID401300970;GLYCEROL 1-TETRADECYL ETHER;3-(tetradecyloxy)-1,2-propanediol;C17H36O3;NSC40162;3-MYRISTYLOXY-1,2-PROPANEDIOL;(+/-)-1-O-TETRADECYLGLYCEROL;1-TETRADECYLOXY-2,3-PROPANEDIOL;J111.054C;T-1962;(+/-)-1-(TETRADECYLOXY)-2,3-PROPANEDIOL;1,2-Propanediol, 3-(tetradecyloxy)- (8CI)(9CI);Q27288587

Chemical Property of Myristyl glyceryl ether

Chemical Property:

• Vapor Pressure: 9.5E-09mmHg at 25°C
• Melting Point: 55 °C
• Boiling Point: 418.3°Cat760mmHg
• PKA: 13.68±0.20(Predicted)
• Flash Point: 206.8°C
• PSA: 49.69000
• Density: 0.927g/cm³
• LogP: 4.05730
• XLogP3: 5.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 16
• Exact Mass: 288.26644501
• Heavy Atom Count: 20
• Complexity: 174

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCOCC(CO)O

Technology Process of Myristyl glyceryl ether

There total 16 articles about Myristyl glyceryl ether 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: 98.0%

4-(n-tetradecyloxymethyl)-2,2-dimethyl-1,3-dioxolane (13879-87-3) → 1-myristyl glycerol (1561-06-4)

Guidance literature:

With hydrogenchloride; In water; for 4h; Reflux;

DOI:10.3390/md16040101

Reference yield: 73.0%

myristyl chloride (2425-54-9) → 1-myristyl glycerol (1561-06-4)

Guidance literature:

With hydrogenchloride; NaH; sodium iodide; In tetrahydrofuran; ethyl acetate; N,N-dimethyl-formamide;

Reference yield: 66.0%

Allyl tetradecyl ether (102364-25-0) → 1-myristyl glycerol (1561-06-4)

Guidance literature:

With cethyltrimethylammonium permanganate; In dichloromethane; at 20 ℃; for 5h;

upstream raw materials:

tetradecyl mesylate

(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol

1-chloro-3-tetradecyloxy-propan-2-ol

3-tetradec-1-en-t-yloxy-propane-1,2-diol

Downstream raw materials:

1-[(4-methoxyphenyl)(diphenyl)methoxy]-3-(tetradecyloxy)propan-2-ol

triphenylmethyl alcohol

1-myristyl-3-trityl glycerol

dibenzyl 3-O-tetradecyl-rac-glycero-1-phosphate

Refernces

• 1、 -. "METHOD FOR PREPARING GLYCEROL ETHER AND GLYCOL ETHER". Paragraph 0079. . Retrieved 2015/03/28.
• 2、 Sutter, Marc,Dayoub, Wissam,Metay, Estelle,Raoul, Yann,Lemaire, Marc. "Selective synthesis of 1-O-Alkyl(poly)glycerol ethers by catalytic reductive alkylation of carboxylic acids with a recyclable catalytic system". . p. 2397 - 2409. Retrieved 2013/02/23.