Decyl ether

Base Information

• Chemical Name: Decyl ether
• CAS No.: 2456-28-2
• Molecular Formula: C20H42 O
• Molecular Weight: 298.553
• Hs Code.: 2909199090
• European Community (EC) Number: 219-533-7
• NSC Number: 83605
• UNII: DA81HI310Z
• DSSTox Substance ID: DTXSID4062430
• Nikkaji Number: J27.109H
• Wikidata: Q27276304
• Mol file: 2456-28-2.mol

Synonyms:Decyl ether;Didecyl ether;2456-28-2;DI-N-DECYL ETHER;Decane, 1,1'-oxybis-;Capric ether;1-decoxydecane;1,1'-Oxybisdecane;1-(Decyloxy)decane;UNII-DA81HI310Z;DA81HI310Z;EINECS 219-533-7;NSC 83605;NSC-83605;n-Decyl ether;decylether;Decane,1'-oxybis-;1-(Decyloxy)decane #;COSMACOL ETHER 10;SCHEMBL93211;DIDECYL ETHER [INCI];1,1'-OXYBIS(DECANE);DTXSID4062430;CAA45628;NSC83605;MFCD00026539;STL453672;AKOS040744773;CS-0336237;D0035;FT-0624752;D89584;Q27276304

Chemical Property of Decyl ether

Chemical Property:

• Vapor Pressure: 8.08E-05mmHg at 25°C
• Melting Point: -16°C
• Refractive Index: 1.4420
• Boiling Point: 351.9°Cat760mmHg
• Flash Point: 143.9°C
• PSA: 9.23000
• Density: 0.817g/cm³
• LogP: 7.28440
• XLogP3: 9.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 18
• Exact Mass: 298.323565959
• Heavy Atom Count: 21
• Complexity: 149

Purity/Quality:

98%,99%, ^*data from raw suppliers

Decyl Ether >95.0%(GC) ^*data from reagent suppliers

Safty Information:

• Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Other Classes -> Ethers, Other
• Canonical SMILES: CCCCCCCCCCOCCCCCCCCCC
• Uses: Electrical insulators, water repellent, lubricant in plastic molding and processing, antistatic agent, intermediate.

Technology Process of Decyl ether

There total 19 articles about Decyl 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: 97.0%

triethylsilane (617-86-7) + caprinaldehyde (112-31-2) → decyl ether (2456-28-2) + hexaethyl disiloxane (994-49-0)

Guidance literature:

With uranyl(VI) triflate; In dichloromethane-d2; at 20 ℃; for 0.1h;

DOI:10.1021/acscatal.9b01408

Reference yield: 92.0%

caprinaldehyde (112-31-2) → decyl ether (2456-28-2)

Guidance literature:

With hydrogen; Pd-C;

Reference yield: 77.0%

1-decanoic acid (334-48-5) → decyl ether (2456-28-2)

Guidance literature:

With 1,1,3,3-Tetramethyldisiloxane; copper(II) bis(trifluoromethanesulfonate); In methyl cyclohexane; at 100 ℃; for 16h; sealed tube;

DOI:10.1016/j.tet.2012.06.080

upstream raw materials:

1-Decanol

1-methyl pyridinium iodide

Iododecane

1-bromo dodecane

Downstream raw materials:

decane

Refernces

Synthesis and bioevaluation of a series of alkyl ethers of p-N-N-bis(2-chloroethyl)aminophenol

10.1002/jps.2600710520

The research involves the synthesis and bioevaluation of a series of alkyl ethers of p-N,N-bis(2-chloroethyl)aminophenol. The study aimed to develop less toxic derivatives of phenol mustard with potential antineoplastic activity. Key chemicals involved in the research include p-N,N-bis(2-chloroethyl)aminophenol, various alkyl bromides (such as ethyl, butyl, hexyl, octyl, decyl, dodecyl, and tetradecyl bromides), thionyl chloride, and propylene glycol. The synthesis process involved reacting p-N,N-bis(2-hydroxyethyl)aminophenol with alkyl bromides to form the alkyl ethers, followed by chlorination with thionyl chloride to produce the final nitrogen mustard derivatives. These compounds were then evaluated for their acute toxicity in mice and their effects on survival in L-1210 leukemic mice. The results showed that the alkyl ethers demonstrated significantly lower acute toxicity than the parent phenol mustard, with the decyl ether producing the greatest increase in mean survival time. The study highlights the potential of these compounds as less toxic alternatives for antitumor therapy.