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2,2,4-trimethyl-1,3-oxathiolan-5-one, also known as trimethyl-oxathiolane or TMO, is a colorless liquid chemical compound with a molecular formula C7H12OS. It is characterized by a strong, garlic-like odor and is flammable. TMO is recognized for its use as a flavoring agent and fragrance ingredient due to its aromatic properties reminiscent of garlic and onions.

60822-65-3

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60822-65-3 Usage

Uses

Used in Food and Beverage Industry:
2,2,4-trimethyl-1,3-oxathiolan-5-one is used as a flavoring agent for its garlic and onion-like aroma, enhancing the taste and aroma of various food and beverage products.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, 2,2,4-trimethyl-1,3-oxathiolan-5-one is used as a fragrance ingredient, adding a pleasant scent to products while also benefiting from its natural aroma profile.
Used in Insect Repellent Development:
2,2,4-trimethyl-1,3-oxathiolan-5-one is studied for its potential use in insect repellents, leveraging its natural properties to deter insects and provide protection against bites.
Used as a Precursor in Organic Synthesis:
TMO also serves as a precursor in organic synthesis, contributing to the creation of various chemical compounds and products in the chemical industry.
It is crucial to handle 2,2,4-trimethyl-1,3-oxathiolan-5-one with care due to its irritating nature to the eyes, skin, and respiratory system, and the potential for adverse health effects from prolonged exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 60822-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,2 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60822-65:
(7*6)+(6*0)+(5*8)+(4*2)+(3*2)+(2*6)+(1*5)=113
113 % 10 = 3
So 60822-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2S/c1-4-5(7)8-6(2,3)9-4/h4H,1-3H3

60822-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4-trimethyl-1,3-oxathiolan-5-one

1.2 Other means of identification

Product number -
Other names 1,3-Oxathiolan-5-one,2,2,4-trimethyl

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:60822-65-3 SDS

60822-65-3Relevant academic research and scientific papers

NOVEL COMPOUNDS, PHARMACEUTICAL COMPOSITIONS CONTAINING SAME, AND METHODS OF USE FOR SAME

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Page/Page column 49, (2009/12/28)

The class compounds of the present invention may be represented by Formula (I), wherein X may be O, S, or N. R1 and R2 are independently either H, C1-C20 alkyl, cycloalkyl, alkenyl, aryl, arylalkyl, or alkylaryl

NOVEL COMPOUNDS, PHARMACEUTICAL COMPOSITIONS CONTAINING SAME, AND METHODS OF USE FOR SAME

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Page/Page column 15, (2008/12/05)

Compounds having the following general formula, pharmaceutical compositions comprising the compounds, and methods of treating cancer, obesity, and microbial infections using such compositions: wherein: R1 = H, C1-C20 alkyl, cycloalkyl, alkenyl, aryl, aryl

2-Mercaptoaldehyde dimers and 2,5-dihydrothiophenes from 1,3-oxathiolan-5-ones

McIntosh, John M.,Siddiqui, Maqbool A.

, p. 1872 - 1875 (2007/10/02)

Representative 1,3-oxathiolan-5-ones (6), prepared from 2-mercaptoacids, have been reduced to 2-mercaptoaldehydes 1 with diisobutylaluminum hydride.The aldehydes 1, which appear to exist in several dimeric forms, react with vinyltriphenylphosphonium bromide to give 2,5-dihydrothiophenes.

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