Menthoxypropanediol

Menthoxypropanediol
Names
	IUPAC name Menthoxypropanediol
Identifiers
CAS Number	87061-04-9 ;
3D model (JSmol)	Interactive image;
ChemSpider	4515105 ; 13136530 (2S,5R)-5-meth,-2-prop,-yl ; 5254045 (1R,2S,5R)-5-meth,-2-prop,-yl ;
ECHA InfoCard	100.081.149
EC Number	289-296-2;
IUPHAR/BPS	2463;
MeSH	3-Menthoxypropane-1,2-diol
PubChem CID	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;
CompTox Dashboard (EPA)	DTXSID20868962 ;
	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 Key: MDVYIGJINBYKOM-UHFFFAOYSA-N ;
	SMILES CC(C)C1CCC(C)CC1OCC(O)CO;
Properties
Chemical formula	C13H26O3
Molar mass	230.348 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.[1]

References

Leffingwell & Associates. "Cooler Than Menthol". Retrieved 2008-06-14.

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[1] Leffingwell & Associates. "Cooler Than Menthol". Retrieved 2008-06-14.