Decyl glucoside

Decyl glucoside

The structure of decyl glucoside The structure of decyl glucoside
Names
IUPAC name Decyl β-D-glucopyranoside
Systematic IUPAC name (2R,3R,4S,5S,6R)-2-(Decyloxy)-6-(hydroxymethyl)oxane-3,4,5-triol
Identifiers
CAS Number	58846-77-8 checkY
3D model (JSmol)	Interactive image
ChemSpider	55973
ECHA InfoCard
E number
PubChem CID	62142
UNII	Z17H97EA6Y checkY
CompTox Dashboard (EPA)	{{#property:P3117}}
InChI InChI=1/C16H32O6/c1-2-3-4-5-6-7-8-9-10-21-16-15(20)14(19)13(18)12(11-17)22-16/h12-20H,2-11H2,1H3/t12-,13-,14+,15-,16-/m1/s1 Key: JDRSMPFHFNXQRB-IBEHDNSVBI
SMILES O(CCCCCCCCCC)[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)CO
Properties
Chemical formula	C16H32O6
Molar mass	320.426 g·mol−1
Hazards
Safety data sheet (SDS)	MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Decyl glucoside is a mild non-ionic surfactant used in cosmetic formularies, including baby shampoo and in products for individuals with a sensitive skin. Many natural personal care companies use this cleanser because it is plant-derived, biodegradable, and gentle for all hair types.

Decyl glucoside was invented by Robert Prairie in 1934.

Synthesis

Decyl glucoside is produced by the reaction of glucose from corn starch with the fatty alcohol decanol, which is derived from coconut.

See also

• Lauryl glucoside
• Octyl glucoside