Dodecyl beta-lactoside

Base Information

Chemical Name:Dodecyl beta-lactoside
CAS No.:74513-18-1
Molecular Formula:C₂₄H₄₆O₁₁
Molecular Weight:510.623
Hs Code.:
DSSTox Substance ID:DTXSID101217629
Nikkaji Number:J1.269.235H

Synonyms:Dodecyl beta-lactoside;SCHEMBL2921598;DTXSID101217629;Dodecyl 4-O-beta-D-galactopyranosyl-beta-D-glucopyranoside;74513-18-1

Suppliers and Price of Dodecyl beta-lactoside

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
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Total 0 raw suppliers

Chemical Property of Dodecyl beta-lactoside

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:7
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:16
Exact Mass:510.30401228
Heavy Atom Count:35
Complexity:554

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCCCCCCOC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)CO)O)O)O)O)O
Isomeric SMILES:CCCCCCCCCCCCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O[C@H]2[C@@H]([C@H]([C@H]([C@H](O2)CO)O)O)O)O)O

Technology Process of Dodecyl beta-lactoside

There total 6 articles about Dodecyl beta-lactoside 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: 88.7%

: 98808-73-2
1-dodecyl-2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranoside

: 74513-18-1,74513-19-2,83212-61-7,104596-59-0,116183-64-3,69227-93-6
lauryl maltoside

Guidance literature:: With methanol; sodium methylate; for 4h; pH=Ca. 10;

Reference yield: 54.0%

: 112-53-8
1-dodecyl alcohol

: 4753-07-5,5160-10-1,14206-57-6,14227-66-8,14257-35-3,42385-75-1,67650-37-7,68682-05-3,69308-57-2,69349-74-2,70223-96-0,70223-97-1,71276-38-5,85248-99-3,118493-15-5,120575-76-0
2,3,6,2',3',4',6'-hepta-O-acetyl-α-D-maltosyl bromide

: 74513-18-1,74513-19-2,83212-61-7,104596-59-0,116183-64-3,69227-93-6
lauryl maltoside

Guidance literature:: 1-dodecyl alcohol; 2,3,6,2',3',4',6'-hepta-O-acetyl-α-D-maltosyl bromide; With iodine; silver carbonate; In dichloromethane; at 20 ℃; for 12h;

With sulfuric acid; water; In acetone; at 20 ℃; for 0.5h;

With triethylamine; In methanol; water; at 20 ℃;
DOI:10.1002/jlcr.3249

Reference yield:

: 112-53-8
1-dodecyl alcohol

: 4753-07-5,5160-10-1,14206-57-6,14227-66-8,14257-35-3,67650-37-7,68682-05-3,69308-57-2,69349-74-2,70223-96-0,70223-97-1,71276-38-5,85248-99-3,118493-15-5,120575-76-0,42385-75-1
α-hepta-O-acetylmaltosyl bromide

: 74513-18-1,74513-19-2,83212-61-7,104596-59-0,116183-64-3,69227-93-6
lauryl maltoside

: n-dodecyl α-D-glucopyranosyl-(1->4)-α-D-glucopyranoside

Guidance literature:: 1-dodecyl alcohol; α-hepta-O-acetylmaltosyl bromide; With iron(III) chloride; In nitromethane; at 25 ℃; for 1h;

With sodium methylate; In methanol; at 20 ℃;
DOI:10.1016/j.carres.2004.07.016