Lauryl methyl gluceth-10 hydroxypropyl dimonium chloride

Lauryl methyl gluceth-10 hydroxypropyl dimonium chloride

Names
IUPAC name D-Glucopyranose, methyl ether, ethoxylated, 3-(N-dodecyl-N,N-dimethylammonio)-2-hydroxypropyl ethers (10 mol EO average molar ratio)
Other names Lauryl methyl gluceth-10-hydroxypropyldimonium chloride, Glucquat 125
Identifiers
CAS Number	123005-57-2^N
ChemSpider	none
ECHA InfoCard	100.121.832
EC Number	602-914-0
Properties
Appearance	Pale, yellow liquid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is ^YN ?) Infobox references

Lauryl methyl gluceth-10 hydroxypropyl dimonium chloride is an ingredient in some types of soaps and personal care products. It is used as a substantive conditioning humectant.^[1][2] This chemical is a type of methyl glucoside derivative,^[3] which has been modified by ethoxylation and quaternization.^[4] A synthetic pathway for lauryl methyl gluceth-10 hydroxypropyldimonium chloride and other methyl glucoside humectants has been outlined in trade literature.^[5]

Lauryl methyl gluceth-10 hydroxypropyldimonium chloride is listed as a trade-named raw material, Glucquat 125, in cosmetic and toiletry products.^[6]

References

1. R. Schueller and P. Romanowski, ed. (1999). Conditioning Agents for Hair and Skin, Cosmetic Science and Technology Series. Vol. 21. Marcel Dekker, New York. p. 272. ISBN 9780824719210.
2. A. O. Barel and H. I. Maibach, ed. (Jul 13, 2001). Handbook of Cosmetic Science and Technology. Taylor & Francis. ISBN 9780824702922.
3. "Methyl Glucoside Derivatives". Lubrizol. October 15, 2012. Archived from the original on April 14, 2014. Retrieved April 13, 2014.
4. "Glucquat™ 125 Humectant, Technical Data Sheet TDS-546" (PDF). Lubrizol. February 7, 2007.
5. "Glucam™ and Glucquat™ Humectants and Emollients" (PDF). Lubrizol. 2009. Archived from the original (PDF) on 2013-03-09. Retrieved 2020-02-24.
6. E. W. Flick (1999). Cosmetic and Toiletry Formulations, Second Edition. Vol. 7. Noyes Publications/William Andrew Publishing. p. 370. ISBN 9780815516750.