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4-Trifluoromethylbenzyl mercaptan, with the molecular formula C8H7F3S, is a chemical compound characterized by its strong, pungent odor. It is recognized for its use as a fragrance and flavoring agent, particularly in the food and beverage industry, where it imparts a garlic-like aroma to products such as baked goods, candies, and beverages including sodas and energy drinks. Beyond its culinary applications, 4-TRIFLUOROMETHYLBENZYL MERCAPTAN also finds potential uses in the pharmaceutical and agricultural sectors, while being classified as a hazardous material due to its irritating properties.

108499-24-7

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108499-24-7 Usage

Uses

Used in Food and Beverage Industry:
4-Trifluoromethylbenzyl mercaptan is used as a fragrance and flavoring agent for imparting a garlic-like aroma to various food products, enhancing the sensory experience of baked goods, candies, and beverages such as sodas and energy drinks.
Used in Natural Gas Odorants:
4-TRIFLUOROMETHYLBENZYL MERCAPTAN is utilized as a component in natural gas odorants, where its strong odor serves as a warning signal for gas leaks, ensuring safety by making the presence of gas detectable to humans.
Used in Pharmaceutical Industry:
4-Trifluoromethylbenzyl mercaptan has potential applications in the pharmaceutical sector, although specific uses are not detailed in the provided materials. Its role may involve the development of new drugs or as a component in existing formulations.
Used in Agricultural Industry:
Similarly, in agriculture, 4-Trifluoromethylbenzyl mercaptan may have potential uses, which are not specified in the provided materials. It could be employed in the development of pesticides, herbicides, or other agricultural chemicals to improve crop protection or yield.

Check Digit Verification of cas no

The CAS Registry Mumber 108499-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,4,9 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108499-24:
(8*1)+(7*0)+(6*8)+(5*4)+(4*9)+(3*9)+(2*2)+(1*4)=147
147 % 10 = 7
So 108499-24-7 is a valid CAS Registry Number.

108499-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(Trifluoromethyl)phenyl]methanethiol

1.2 Other means of identification

Product number -
Other names 4-Trifluoromethylbenzylthiol

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:108499-24-7 SDS

108499-24-7Upstream product

108499-24-7Relevant academic research and scientific papers

Preparation and in-vitro evaluation of 4-benzylsulfanylpyridine-2- carbohydrazides as potential antituberculosis agents

Herzigova, Petra,Klimesova, Vera,Palat, Karel,Kaustova, Jarmila,Dahse, Hans-Martin,Moellmann, Ute

body text, p. 394 - 404 (2009/11/30)

A set of 4-benzylsulfanylpyridine-2-carbohydrazides was synthesized and evaluated for in vitro antimycobacterial activity against Mycobacterium tuberculosis, non-tuberculous mycobacteria, and multidrug-resistant M. tuberculosis. The activities expressed as the minimum inhibitory concentration (MIC) fall into a range of 2 to 125 μmol/L, most often 4 to 32 μmol/L. The results revealed that the substituents on the benzyl moiety do not influence the antimycobacterial efficacy. The substances exhibited similar activities against sensitive and resistant strains of M. tuberculosis. Furthermore, compounds show low antiproliferative effect and cytotoxicity.

ALKYLAMIDE DERIVATIVES WITH H2-RECEPTOR ANTAGONISTIC AND CYTOPROTECTIVE ACTION

-

, (2008/06/13)

Alkylamide derivatives having the formula, These compounds have a strong antiulcer action depend on histamine H 2-receptor antagonistic action and a cytoprotective action upon gastric mucous membrance.

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