Lauryl Glucoside

Base Information

• Chemical Name: Lauryl Glucoside
• CAS No.: 27836-64-2
• Deprecated CAS: 6801-92-9,265312-14-9,265312-14-9
• Molecular Formula: C18H36 O6
• Molecular Weight: 348.48
• European Community (EC) Number: 248-685-7
• DSSTox Substance ID: DTXSID30893048
• Nikkaji Number: J1.040.433I
• Wikipedia: Lauryl_glucoside
• RXCUI: 1364382
• Metabolomics Workbench ID: 155072
• Mol file: 27836-64-2.mol

Synonyms:Dodecyl D-glucoside;lauryl glucoside;110615-47-9;dodecyl d-glucopyranoside;27836-64-2;D-Glucopyranoside, dodecyl;EINECS 248-685-7;UNII-VB00RDE21R;VB00RDE21R;EC 600-975-8;(3R,4S,5S,6R)-2-dodecoxy-6-(hydroxymethyl)oxane-3,4,5-triol;UNII-76LN7P7UCU;GLUCOSIDE, DODECYL, D-;C18-H36-O6;dodecyl--d-glucopyranoside;SCHEMBL57535;DTXSID30893048;beta-D-GLUCOPYRANOSIDE, DODECYL;DB14746;W-110711

Chemical Property of Lauryl Glucoside

Chemical Property:

• Vapor Pressure: 4.72E-12mmHg at 25°C
• Refractive Index: 1.508
• Boiling Point: 499.1°Cat760mmHg
• PKA: 12.95±0.70(Predicted)
• Flash Point: 255.6°C
• PSA: 99.38000
• Density: 1.12g/cm³
• LogP: 1.72380
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 13
• Exact Mass: 348.25118886
• Heavy Atom Count: 24
• Complexity: 301

Purity/Quality:

98% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O
• Isomeric SMILES: CCCCCCCCCCCCOC1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
• Use Description: Dodecyl D-glucoside is a chemical compound with versatile applications across different fields. In the realm of cosmetics and personal care, it serves as a mild and non-irritating surfactant and emulsifier, making it a valuable ingredient in skincare products, shampoos, and body washes. Its gentle cleansing properties help in the formulation of products suitable for sensitive skin. In the field of biotechnology, it can be used in various biochemical and molecular biology experiments as a non-denaturing detergent to solubilize and stabilize membrane proteins and lipid bilayers. Furthermore, in the field of agriculture and agrochemicals, it may be employed in the formulation of agricultural adjuvants and pesticides to enhance their effectiveness and spreadability on plant surfaces. Its multifaceted contributions underscore its significance in cosmetics, biotechnology, and agriculture, offering benefits ranging from skincare to scientific research and agriculture, playing crucial roles in each of these diverse fields.

Technology Process of Lauryl Glucoside

There total 8 articles about Lauryl Glucoside 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: 76.0%

D-Glucose (2280-44-6) + 1-dodecyl alcohol (112-53-8) → dodecyl β-D-glucopyranoside (27836-64-2)

Guidance literature:

With Adipic acid; choline chloride; at 80 - 95 ℃; Reagent/catalyst; Inert atmosphere; Green chemistry;

Reference yield:

1-dodecyl alcohol (112-53-8) + cellulose (9004-34-6) → dodecyl β-D-glucopyranoside (27836-64-2)

Guidance literature:

cellulose; With water; at 99.84 ℃; for 1.5h; Ionic liquid;

1-dodecyl alcohol; at 89.84 ℃; for 24h; under 30.003 Torr; Ionic liquid;

DOI:10.1002/cssc.201000371

Reference yield:

1-dodecyl alcohol (112-53-8) + cellulose (9004-34-6) → 5-hydroxymethyl-2-furfuraldehyde (67-47-0) + dodecyl β-D-glucopyranoside (27836-64-2)

Guidance literature:

cellulose; With 1-butyl-3-methylimidazolium chloride; at 105 - 120 ℃; for 1h; under 7.50075 - 15.0015 Torr;

at 100 ℃; for 0.05h;

1-dodecyl alcohol; Further stages;

DOI:10.1002/cssc.201402722

upstream raw materials:

D-Glucose

1-dodecyl alcohol

cellulose

microcrystalline cellulose

Downstream raw materials:

n-dodecyl 4,6-O-benzylidene-β-D-glucopyranoside