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W374800

Sigma-Aldrich

L-Menthyl lactate

≥97%, FG

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Synonym(s):
Laevo-menthyl lactate, [(1R,2S,5R)-5-methyl-2-propan-2-ylcyclohexyl] 2-hydroxypropanoate
Empirical Formula (Hill Notation):
C13H24O3
CAS Number:
185915-25-7
Molecular Weight:
228.33
FEMA Number:
3748
MDL number:
MFCD09037384
PubChem Substance ID:
329830650
Flavis number:
9.551

biological source

synthetic

Quality Level

400

grade

FG
Halal

reg. compliance

EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117

Assay

≥97%

optical activity

[α]20/D -81°, c = 5 in ethanol

bp

142 °C/5 mmHg (lit.)

mp

42-47 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

mild; cooling

SMILES string

CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)[C@H](C)O

InChI

1S/C13H24O3/c1-8(2)11-6-5-9(3)7-12(11)16-13(15)10(4)14/h8-12,14H,5-7H2,1-4H3/t9-,10?,11+,12-/m1/s1

InChI key

UJNOLBSYLSYIBM-SGUBAKSOSA-N

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General description

L-Menthyllactate is a flavoring ingredient with a slight minty odor and earthy taste. It provides a long-lasting cooling effect in the mouth. The ingredient has alsobeen proposed as a cosmetic fragrance ingredient .

Application

L-Menthyllactate is used as a cooling ingredient with a pleasant and long-lastingcooling effect in products like toothpaste mints and chewing gum. (2)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Chemistry and technology of flavours and fragrances
David R
Chemistry and Technology of Flavors and Fragrances. (2009)
Peng Bai et al.
Nature medicine, 25(8), 1266-1273 (2019-07-10)
The ability to safely control transgene expression with simple synthetic gene switches is critical for effective gene- and cell-based therapies. In the present study, the signaling pathway controlled by human transient receptor potential (TRP) melastatin 8 (hTRPM8), a TRP channel

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