Lactisole

Lactisole
Names
	IUPAC name Sodium 2-(4-methoxyphenoxy)propanoate
	Other names Lactisole; ORP 178; Propanoic acid, 2-(4-methoxyphenoxy), sodium salt
Identifiers
CAS Number	150436-68-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	4515110 ;
ECHA InfoCard	100.123.510
PubChem CID	5362606;
UNII	ZU3D90W5GZ ;
CompTox Dashboard (EPA)	DTXSID60934059 ;
	InChI InChI=1S/C10H12O4.Na/c1-7(10(11)12)14-9-5-3-8(13-2)4-6-9;/h3-7H,1-2H3,(H,11,12);/q;+1/p-1 Key: SKORRGYRKQDXRS-UHFFFAOYSA-M ; InChI=1/C10H12O4.Na/c1-7(10(11)12)14-9-5-3-8(13-2)4-6-9;/h3-7H,1-2H3,(H,11,12);/q;+1/p-1 Key: SKORRGYRKQDXRS-REWHXWOFAP;
	SMILES [Na+].[O-]C(=O)C(Oc1ccc(OC)cc1)C;
Properties
Chemical formula	C10H11O4Na
Molar mass	218.188 g/mol
Appearance	white to pale cream, crystalline solid
Melting point	190 °C (374 °F; 463 K)
Solubility in water	Soluble in water and propylene glycol, slightly soluble in fat and miscible at room temperature in ethanol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Lactisole is the sodium salt and commonly supplied form of 2-(4-methoxy phenoxy)propionic acid, a natural carboxylic acid found in roasted coffee beans. Like gymnemic acid, it has the property of masking sweet flavors and is used for this purpose in the food industry.^[1]

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Chemically, lactisole is a double ether of hydroquinone. Since it contains an asymmetric carbon atom the molecule is chiral, with the S enantiomer predominating in natural sources and being primarily responsible for the sweetness-masking effect. Commercial lactisole is a racemic mixture of the R and S forms.^[2]

The parent acid of lactisole was discovered in 1989 in roasted Colombian arabica coffee beans in a concentration of 0.5 to 1.2 ppm.^[3]

At concentrations of 100–150 parts per million in food, lactisole largely suppresses the ability to perceive sweet tastes, both from sugar and from artificial sweeteners such as aspartame. A 12% sucrose solution was perceived like a 4% sucrose solution when lactisole was added. However, it is significantly less efficient than gymnemic acid with acesulfame potassium, sucrose, glucose and sodium saccharin. Research found also that it has no effect on the perception of bitterness, sourness and saltiness.^[1] According to a recent study, lactisole acts on a sweet taste receptor heteromer of the TAS1R3 sweet protein receptor in humans, but not on its rodent counterpart.^[4]

The principal use of lactisole is in jellies, jams, and similar preserved fruit products containing large amounts of sugar. In these products, by suppressing sugar's sweetness, it allows fruit flavors to come through. In the United States, lactisole is designated as generally recognized as safe (GRAS) by the Flavor and Extract Manufacturers Association (Fema number: 3773) and approved for use in food as flavoring agent^[5] up to 150 ppm. Currently, lactisole is manufactured and sold by Domino Sugar and its usage levels are between 50 and 150 ppm.^[6] In the European Union lactisole is allowed to be used as a flavouring substance in foods, FL No. 16.041. ^[7]

[1]
Kinghorn, A.D.; Compadre, C.M. (2001). Marcel Dekker (ed.). Alternative Sweeteners (Third Edition, Revised and Expanded ed.). New York. ISBN 0-8247-0437-1.{{cite book}}: CS1 maint: location missing publisher (link)
[2]
T. Nakagita et al "Structural insights into the differences among lactisole derivatives in inhibitory mechanisms against the human sweet taste receptor" PLoS One. 2019; 14(3): e0213552
[3]
Ivon Flament; Yvonne Bessière-Thomas (2002). "The individual constituents". Coffee flavor chemistry. John Wiley and Sons. p. 207. ISBN 0-471-72038-0.
[4]
Jiang, P.; Cui, M; Zhao, B; Liu, Z; Snyder, LA; Benard, LM; Osman, R; Margolskee, RF; Max, M (2005). "Lactisole Interacts with the Transmembrane Domains of Human T1R3 to Inhibit Sweet Taste". Journal of Biological Chemistry. 280 (15): 15238–46. doi:10.1074/jbc.M414287200. PMID 15668251.
[5]
JECFA "Specifications for Flavourings"
[6]
Sugar sans sweetness - lactisole. Prepared Foods, May, 1995 by Fran LaBell Archived 2009-01-22 at the Wayback Machine
[7]
2002/113/EC: Commission Decision of 23 January 2002 amending Commission Decision 1999/217/EC as regards the register of flavouring substances used in or on foodstuffs

[Kinghorn-book3-1] [1]
Kinghorn, A.D.; Compadre, C.M. (2001). Marcel Dekker (ed.). Alternative Sweeteners (Third Edition, Revised and Expanded ed.). New York. ISBN 0-8247-0437-1.{{cite book}}: CS1 maint: location missing publisher (link)

[2] [2]
T. Nakagita et al "Structural insights into the differences among lactisole derivatives in inhibitory mechanisms against the human sweet taste receptor" PLoS One. 2019; 14(3): e0213552

[Flament-2001-3] [3]
Ivon Flament; Yvonne Bessière-Thomas (2002). "The individual constituents". Coffee flavor chemistry. John Wiley and Sons. p. 207. ISBN 0-471-72038-0.

[JBC-15-15238-4] [4]
Jiang, P.; Cui, M; Zhao, B; Liu, Z; Snyder, LA; Benard, LM; Osman, R; Margolskee, RF; Max, M (2005). "Lactisole Interacts with the Transmembrane Domains of Human T1R3 to Inhibit Sweet Taste". Journal of Biological Chemistry. 280 (15): 15238–46. doi:10.1074/jbc.M414287200. PMID 15668251.

[JECFA-5] [5]
JECFA "Specifications for Flavourings"

[Prepared_food-1995-6] [6]
Sugar sans sweetness - lactisole. Prepared Foods, May, 1995 by Fran LaBell Archived 2009-01-22 at the Wayback Machine

[2021/113/EC-7] [7]
2002/113/EC: Commission Decision of 23 January 2002 amending Commission Decision 1999/217/EC as regards the register of flavouring substances used in or on foodstuffs

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Lactisole

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Chemistry

Natural occurrences

Anti-sweet properties

As a food additive

See also

References

External links