Lauryl glycidyl ether

Base Information

Chemical Name:Lauryl glycidyl ether
CAS No.:2461-18-9
Deprecated CAS:60616-93-5,136959-08-5
Molecular Formula:C15H30 O2
Molecular Weight:242.402
Hs Code.:2910900090
European Community (EC) Number:219-554-1
UNII:84653J97E3
DSSTox Substance ID:DTXSID0025494
Nikkaji Number:J216.101J
Wikidata:Q27269499
ChEMBL ID:CHEMBL1574716
Mol file:2461-18-9.mol

Synonyms:1-dodecyl glycidyl ether;C12Ge cpd

Suppliers and Price of Lauryl glycidyl ether

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
2-[(Dodecyloxy)methyl]oxirane
10mg
$ 45.00

TCI Chemical
Glycidyl Lauryl Ether >98.0%(GC)
5g
$ 217.00

TCI Chemical
Glycidyl Lauryl Ether >98.0%(GC)
1g
$ 65.00

American Custom Chemicals Corporation
2-[(DODECYLOXY)METHYL]OXIRANE 95.00%
10G
$ 1653.51

American Custom Chemicals Corporation
2-[(DODECYLOXY)METHYL]OXIRANE 95.00%
5G
$ 1104.98

American Custom Chemicals Corporation
2-[(DODECYLOXY)METHYL]OXIRANE 95.00%
1G
$ 686.88

AK Scientific
Dodecylglycidylether
5g
$ 355.00

Total 18 raw suppliers

Chemical Property of Lauryl glycidyl ether

Chemical Property:

Vapor Pressure:0.00164mmHg at 25°C
Melting Point:11.8-12.3 °C
Refractive Index:1.452
Boiling Point:303.7°Cat760mmHg
Flash Point:145.3°C
PSA：21.76000
Density:0.898g/cm³
LogP:4.32270
XLogP3:5.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:13
Exact Mass:242.224580195
Heavy Atom Count:17
Complexity:159

Purity/Quality:

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

2-[(Dodecyloxy)methyl]oxirane ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Chemical Classes:Plastics & Rubber -> Glycidyl Ethers
Canonical SMILES:CCCCCCCCCCCCOCC1CO1

Technology Process of Lauryl glycidyl ether

There total 6 articles about Lauryl glycidyl 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: 85.0%

: 112-53-8
1-dodecyl alcohol

: 3132-64-7,82584-73-4
1,2-Epoxy-3-bromopropane

: 2461-18-9
dodecyl glycidyl ether

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 20 ℃; for 16h;
DOI:10.1016/S0968-0896(02)00245-6

Reference yield:

: 112-53-8
1-dodecyl alcohol

: 106-89-8,24969-06-0,13403-37-7
epichlorohydrin

: 2461-18-9
dodecyl glycidyl ether

Guidance literature:: With tetrabutylammomium bromide; sodium hydroxide; In hexane;
DOI:10.1016/j.molstruc.2009.02.013

Reference yield:

: 17677-15-5
1-chloro-3-dodecyloxy-propan-2-ol

: 2461-18-9
dodecyl glycidyl ether

Guidance literature:: With sodium hydride; In hexane; toluene; at 20 ℃; for 0.0833333h;
DOI:10.1002/(SICI)1099-1344(200002)43:2<147::AID-JLCR301>3.0.CO;2-H