What is the 2,8-EPITHIO-P-MENTHANE?

2,8-EPITHIO-P-MENTHANE is , while it's Molecular Formula is C 10 H 18 S. Used in Flavor and Fragrance Industry: 2,8-EPITHIO-P-MENTHANE is used as a flavoring agent for its sulfureous taste with juicy fruity notes and tropical nuances of passion fruit, pineapple, and mango. It is also used as a fragrance ingredient for its earthy, citrus aroma with menthol-like undertones. Used in Aromatherapy: 2,8-EPITHIO-P-MENTHANE can be used in aromatherapy for its high strength odor and its ability to impart a refreshing and uplifting scent. It can be used in diffusers or blended with other essential oils for various therapeutic benefits.

What is the CAS number for 2,8-EPITHIO-P-MENTHANE?

The CAS number of 2,8-EPITHIO-P-MENTHANE is 68398-18-5.

What is 2,8-EPITHIO-P-MENTHANE (68398-18-5) used for?

2,8-EPITHIO-P-MENTHANE is a colorless to pale yellow clear liquid with an earthy, citrus aroma and menthol-like undertones. It has a high strength odor and is recommended to be smelled in a 0.10% solution or less. At 1 ppm level, it tastes sulfureous with juicy fruity notes and imparts tropical nuances of passion fruit, pineapple, and mango, along with a grapefruit citrus note.InChI:InChI=1/C10H18S/c1-7-4-5-8-6-9(7)11-10(8,2)3/h7-9H,4-6H2,1-3H3

What is the 2,8-EPITHIO-P-MENTHANE?

2,8-EPITHIO-P-MENTHANE is , while it's Molecular Formula is C 10 H 18 S. Used in Flavor and Fragrance Industry: 2,8-EPITHIO-P-MENTHANE is used as a flavoring agent for its sulfureous taste with juicy fruity notes and tropical nuances of passion fruit, pineapple, and mango. It is also used as a fragrance ingredient for its earthy, citrus aroma with menthol-like undertones. Used in Aromatherapy: 2,8-EPITHIO-P-MENTHANE can be used in aromatherapy for its high strength odor and its ability to impart a refreshing and uplifting scent. It can be used in diffusers or blended with other essential oils for various therapeutic benefits.

What is the CAS number for 2,8-EPITHIO-P-MENTHANE?

The CAS number of 2,8-EPITHIO-P-MENTHANE is 68398-18-5.

What is 2,8-EPITHIO-P-MENTHANE (68398-18-5) used for?

2,8-EPITHIO-P-MENTHANE is a colorless to pale yellow clear liquid with an earthy, citrus aroma and menthol-like undertones. It has a high strength odor and is recommended to be smelled in a 0.10% solution or less. At 1 ppm level, it tastes sulfureous with juicy fruity notes and imparts tropical nuances of passion fruit, pineapple, and mango, along with a grapefruit citrus note.InChI:InChI=1/C10H18S/c1-7-4-5-8-6-9(7)11-10(8,2)3/h7-9H,4-6H2,1-3H3

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Quality manufacturer supply 2,8-EPITHIO-P-MENTHANE 68398-18-5 in stock with high standard

Molecular Formula: C₁₀H₁₈S
Molecular Weight: 170.319
Boiling Point: 222.7 °C at 760 mmHg
Flash Point: 79 °C
PSA： 25.30000
Density: 0.941 g/cm³
LogP: 3.31660

2,8-EPITHIO-P-MENTHANE(Cas 68398-18-5) Usage

Aroma threshold values	High strength odor; recommend smelling in a 0.10% solution or less.
Taste threshold values	At 1 ppm level, it tastes sulfureous with juicy fruity notes. It has tropical nuances of passion fruit, pineapple and mango. It imparts a grapefruit citrus note.

InChI:InChI=1/C10H18S/c1-7-4-5-8-6-9(7)11-10(8,2)3/h7-9H,4-6H2,1-3H3

68398-18-5 Relevant articles

REACTION OF SULFUR HALIDES WITH UNSATURATED COMPOUNDS. XX. REACTION OF SULFUR DICHLORIDE WITH 1-METHYL-4-ISOPROPENYL- AND 1,4-DIMETHYL-4-VINYL-1-CYCLOHEXENES. SYNTHESIS OF THIABICYCLOOCTANES AND THIABICYCLONONANES

Tolstikov, G. A.,Lerman, B. M.,Komissarova, N. G.,Zelenova, L. M.

, p. 283 - 291 (2007/10/02)

The reaction of 1-methyl-4-isopropenyl- ...

68398-18-5 Process route

: 1208985-44-7
(1R,5R)-4,7,7-trimethyl-6-thiabicyclo[3.2.1]oct-3-ene

: 5718-75-2
(1R,4R,5R)-4,7,7-trimethyl-6-thiabicyclo[3.2.1]octane

: 5718-75-2,68398-18-5,84415-79-2
(1S ,2R ,4R )-2,8-epithio-p -menthane

Conditions

Conditions	Yield
With methanol; palladium on activated charcoal; under 88260.9 Torr; Hydrogenation;

: 138-86-3,555-08-8,8022-90-0,9003-73-0,95327-98-3
limonene.

: 5718-74-1
1,3,3-trimethyl-2-thia-bicyclo[2.2.2]octane

: 6784-08-3,65675-80-1
4,7,7-trimethyl-6-thiabicyclo <3.2.1> oct-3-ene

: 86759-87-7
4,8-dimethyl-2-thiabicyclo <3.3.1> non-7-ene

: 5718-75-2,68398-18-5,84415-79-2
endo-4-methyl-7,7-dimethyl-6-thiabicyclo <3.2.1> octane

Conditions

Conditions	Yield
With bis(acetylacetonate)nickel(II); sulfur dichloride; diisobutylaluminium hydride; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given; 1) hexane, 5 deg C, 20 h, 2) toluene, r.t., 2 h;