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(2E)-3,7-Dimethyl-1-(methylthio)-2,6-octadiene, also known as p-Menth-2-ene-1-thiol, is a naturally occurring organic compound found in various plants, including mint. It is a colorless liquid with a strong, characteristic odor. (2E)-3,7-Dimethyl-1-(methylthio)-2,6-octadiene is known for its anti-inflammatory and antimicrobial properties, making it a versatile ingredient for various applications.

72927-81-2

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72927-81-2 Usage

Uses

Used in Flavor and Fragrance Industry:
(2E)-3,7-Dimethyl-1-(methylthio)-2,6-octadiene is used as a flavor and fragrance ingredient for its strong, characteristic odor. It adds a unique scent and taste to food and beverage products, enhancing their overall appeal.
Used in Perfume Production:
(2E)-3,7-Dimethyl-1-(methylthio)-2,6-octadiene is used as a key ingredient in the production of perfumes and other scented products. Its strong and distinctive odor contributes to the creation of various fragrances that are used in personal care and cosmetic products.
Used in Pharmaceutical Applications:
(2E)-3,7-Dimethyl-1-(methylthio)-2,6-octadiene is used as a potential candidate for pharmaceutical applications due to its anti-inflammatory and antimicrobial properties. It can be incorporated into medications and treatments to help alleviate inflammation and fight against microbial infections.
Used in Cosmetic Applications:
(2E)-3,7-Dimethyl-1-(methylthio)-2,6-octadiene is used in cosmetic applications for its anti-inflammatory and antimicrobial properties. It can be incorporated into skincare and beauty products to provide benefits such as soothing irritated skin and promoting a healthy skin microbiome.

Check Digit Verification of cas no

The CAS Registry Mumber 72927-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,2 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72927-81:
(7*7)+(6*2)+(5*9)+(4*2)+(3*7)+(2*8)+(1*1)=152
152 % 10 = 2
So 72927-81-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H20S/c1-10(2)6-5-7-11(3)8-9-12-4/h6,8H,5,7,9H2,1-4H3/b11-8+

72927-81-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-3,7-dimethyl-1-methylsulfanylocta-2,6-diene

1.2 Other means of identification

Product number -
Other names 2,6-Octadiene,3,7-dimethyl-1-(methylthio)-,(E)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:72927-81-2 SDS

72927-81-2Downstream Products

72927-81-2Relevant academic research and scientific papers

The pheromone system of the male danaine butterfly, Idea leuconoe

Schulz,Nishida

, p. 341 - 349 (2007/10/03)

Male Idea leuconoe butterflies release a complex mixture of volatiles from their pheromone glands (hairpencils) during courtship. The pheromone components geranyl methyl thioether (2), viridifloric β-lactone (3) and 6-hydroxy-4-dodecanolide (10) have been synthesized for the first time. Therefore, the structural assignment of these new natural products could be proved. Related 7-hydroxy-5-alkanolides are also present in the extract. The volatiles are embedded in a lipidic matrix with more than 150 components. This matrix consists of alkanes, alkenes, 2,5-dialkyltetrahydrofurans, secondary alkanols and alkenols as well as alkanones and alkenones. Several regioisomers of the oxidized hydrocarbons occur. The elucidation of double bond positions has been performed by MS using DMDS adducts.

C-PRENYLATION OF ISOPENTENYL DERIVATIVES WITH SULFONIUM SALTS

Badet, B.,Julia, M.,Marazano, C.

, p. 2007 - 2010 (2007/10/02)

Reaction of isopentenyl acetate (or n-butyl ether) with oil soluble prenyl sulfonium salts in the presence of a hintered amine leads to prenylation on the terminal carbon atom.

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