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Decyl glucoside

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
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.055.863 Edit this at Wikidata
UNII
  • 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
  • O(CCCCCCCCCC)[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)CO
Properties
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).

Decyl glucoside is a mild non-ionic surfactant used in cosmetic formularies,[1] 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

References

  1. ^ Fiume MM, Heldreth B, Bergfeld WF, Belsito DV, Hill RA, Klaassen CD, Liebler D, Marks JG Jr, Shank RC, Slaga TJ, Snyder PW, Andersen FA. Safety assessment of decyl glucoside and other alkyl glucosides as used in cosmetics. Int J Toxicol. 2013 Sep-Oct;32(5 Suppl):22S-48S. doi:10.1177/1091581813497764 PMID 24174472
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