N-DODECYL ALPHA-D-MALTOSIDE

Base Information

• Chemical Name: N-DODECYL ALPHA-D-MALTOSIDE
• CAS No.: 116183-64-3
• Molecular Formula: C₂₄H₄₆O₁₁
• Molecular Weight: 510.623
• Hs Code.: 29389090
• Mol file: 116183-64-3.mol

Synonyms:Dodecyla-D-maltoside;Lauryl a-D-maltopyranoside;n-Dodecyl a-D-maltoside;

Chemical Property of N-DODECYL ALPHA-D-MALTOSIDE

Chemical Property:

• Boiling Point: 703.5 °C at 760 mmHg
• Flash Point: 379.3 °C
• PSA: 178.53000
• Density: 1.28g/cm³
• LogP: -0.45200
• Storage Temp.: −20°C

Purity/Quality:

98%, ^*data from raw suppliers

Dodecyl a-D-maltopyranoside ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Dodecyl α-D-Maltoside is used to study behaviour and structure of micelles in water.

Technology Process of N-DODECYL ALPHA-D-MALTOSIDE

There total 6 articles about N-DODECYL ALPHA-D-MALTOSIDE 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%

1-dodecyl-2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranoside (98808-73-2) → lauryl maltoside (74513-18-1,74513-19-2,83212-61-7,104596-59-0,116183-64-3,69227-93-6)

Guidance literature:

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

Reference yield: 54.0%

1-dodecyl alcohol (112-53-8) + 2,3,6,2',3',4',6'-hepta-O-acetyl-α-D-maltosyl bromide (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) → lauryl maltoside (74513-18-1,74513-19-2,83212-61-7,104596-59-0,116183-64-3,69227-93-6)

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:

1-dodecyl alcohol (112-53-8) + α-hepta-O-acetylmaltosyl bromide (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) → lauryl maltoside (74513-18-1,74513-19-2,83212-61-7,104596-59-0,116183-64-3,69227-93-6) + 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

upstream raw materials:

1-dodecyl alcohol

α-hepta-O-acetylmaltosyl bromide

2,3,6,2',3',4',6'-hepta-O-acetyl-α-D-maltosyl bromide

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

Downstream raw materials:

n-dodecyl-b-D-glucopyranoside

C₂₄H₄₆O₁₁*C₄₇H₅₆N₈

C₂₄H₄₆O₁₁*C₅₁H₆₄N₈

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