Menthoxypropanediol

Menthoxypropanediol

Stereo skeletal formula of menthoxypropanediol ((1R,2S,5R)-5-meth,-2-prop,-yl)
Names
IUPAC name Menthoxypropanediol
Identifiers
CAS Number	87061-04-9 Y
ChemSpider	4515105 Y 13136530 (2S,5R)-5-meth,-2-prop,-yl Y 5254045 (1R,2S,5R)-5-meth,-2-prop,-yl Y
EC Number	289-296-2
IUPHAR/BPS	2463
Jmol 3D model	Interactive image
MeSH	3-Menthoxypropane-1,2-diol
PubChem	5362595 16006278 (2S,5R)-5-meth,-2-prop,-yl 6850757 (1R,2S,5R)-5-meth,-2-prop,-yl 44467722 (1S,2R,5S)-5-meth,-2-prop,-yl 15195782 (2S)-2-ol, (1R,2S,5R)-5-meth,-2-prop,-yl
InChI InChI=1S/C13H26O3/c1-9(2)12-5-4-10(3)6-13(12)16-8-11(15)7-14/h9-15H,4-8H2,1-3H3 Y Key: MDVYIGJINBYKOM-UHFFFAOYSA-N Y
SMILES CC(C)C1CCC(C)CC1OCC(O)CO
Properties
Chemical formula	C13H26O3
Molar mass	230.35 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Menthoxypropanediol is a synthetic derivative of menthol. While the cooling strength of 3-(l-menthoxy)propane-1,2-diol ( also known as Cooling agent 10 [tradename of Takasago]) is accepted as being about 20-25% that of menthol, it is also noted that "in a Vaseline ointment, 3-(l-menthoxy)propane-1,2-diol shows a cool feeling 2.0 to 2.5 times stronger than that of l-menthol". It is used in various cosmetic chemical concoctions.