68398-18-5 Usage
Description
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.
Uses
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.
Check Digit Verification of cas no
The CAS Registry Mumber 68398-18-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,9 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 68398-18:
(7*6)+(6*8)+(5*3)+(4*9)+(3*8)+(2*1)+(1*8)=175
175 % 10 = 5
So 68398-18-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H18S/c1-7-4-5-8-6-9(7)11-10(8,2)3/h7-9H,4-6H2,1-3H3
68398-18-5Relevant articles and documents
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- and 1,4-dimethyl-4-vinyl-1-cyclohexenes with sulfur dichloride gave the corresponding methyl-substituted dichlorothiabicyclononanes.Reductive dechlorination of the latter led to mixtures of isomeric thiabicyclanes, from which dimethyl- and trimethyl-substituted 2-thiabicyclo- and 6-thiabicyclooctanes and 2-thiabicyclo- and 2-thiabicyclononanes were isolated; the effect of the nature of the reducing agent and the conditions on the isomeric composition of the thiabicyclanes was demonstrated.Acetolysis of 4,8-dichloro-5,8-dimethyl-2-thiabicyclononane is accompanied by the formation of two isomeric thiabicyclononadienes in addition to the corresponding hydroxy and acetoxy derivatives.
