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lauryl glucoside, APG0814, LAURYL GLUCOSIDE, ALKYL D-GLUCOPYRANOSIDE,  110615-47-9

lauryl glucoside, APG0814LAURYL GLUCOSIDEALKYL D-GLUCOPYRANOSIDE,  110615-47-9

lauryl glucoside

CAS: 110615-47-9

Molecular Formula: C18H36O6

Names and Identifiers

Name lauryl glucoside
Synonyms APG0814
lauryl glucoside
LAURYL GLUCOSIDE
Lauryl polyglucose
ALKYL D-GLUCOPYRANOSIDE
Alkyl D-Glucopyranoside
(C10-16)alkyl D-glycopyranoside
(C10-16)Alkyl D-Glycopyranoside
D-Glucopyranoside, C10-16-alkyl, oligomeric
D-Glucopyranose,Oligomeric,C10-C16-Alkylglycosides
D-GLUCOPYRANOSE,OLIGOMERIC,C10-C16-ALKYLGLYCOSIDES
Glucopyranose, oligometric, C10-16-alkyl glycosides
D-Glucopyranose, oligomeric, C10-16-alkyl glycosides
D-Glucopyranose, Oligomeric, C10-16-Alkyl Glycosides
CAS 110615-47-9
EINECS 600-975-8

Physico-chemical Properties

Molecular Formula C18H36O6
Molar Mass 348.47484
Density 1.16 at 20℃
Boling Point 301℃ at 101.3kPa
Vapor Presure 0.008Pa at 20℃
Appearance Solid
Storage Condition Room Temprature

Introduction

This product has good thickening, high temperature resistance, high concentration of strong acid, strong alkali and electrolyte. HLB value 10-12. PH value (10% aqueous solution):11.5-12.5; Viscosity (20 ℃ mPa.s):2000-4000(40 ℃) is widely used in personal care and household washing: shampoo, hand sanitizer, facial cleanser, shower gel and other cosmetics and transparent soap, laundry detergent, detergent and other daily chemical detergents, especially in the field of pregnant and infant cosmetics. It is easy to rinse and is especially suitable for tableware detergent and hard surface cleaning.

Reference Information

LogP -0.07 at 20℃
surface tension 29.5mN/m at 1g/L and 23 ℃
introduction dodecyl glucoside belongs to alkyl glucoside and is a new type of nonionic surfactant. it can be used in many aspects such as main active substances of detergents, various detergents, cosmetic surfactants, pharmaceutical additives, industrial emulsifiers, etc.
features dodecyl glucoside has the advantages of non-irritation to skin, good compatibility, mild to eye irritation, non-toxic, good biodegradability, etc.
preparation in a four-port reaction bottle equipped with electric stirrer, thermometer, water separator and feeding device
, add quantitative glucose monohydrate, lauryl alcohol and catalyst, control a certain reaction temperature and pressure, take samples regularly during the reaction process and analyze with self-made Fehling reagent to determine the reaction end point. After the reaction, the product is neutralized with sodium hydroxide, and then the excess alcohol is evaporated under reduced pressure. The product is bleached with 30%
H2O2, and finally made into a 50% aqueous solution.

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