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26733-25-5

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26733-25-5 Usage

Chemical Family

2,2-diethyl-1,3-dithiolane belongs to the family of dithiolanes.

Physical Properties

It is a colorless, oily liquid with a strong, pungent odor.

Uses

It is primarily used as a flavoring agent in the food industry, particularly in meat and savory products, and as a fragrance ingredient in the cosmetic and personal care industry.

Potential Applications

It has potential applications in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical compounds.

Safety Precautions

It is important to handle 2,2-diethyl-1,3-dithiolane with care as it is flammable and can be harmful if inhaled or ingested.

Check Digit Verification of cas no

The CAS Registry Mumber 26733-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,7,3 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26733-25:
(7*2)+(6*6)+(5*7)+(4*3)+(3*3)+(2*2)+(1*5)=115
115 % 10 = 5
So 26733-25-5 is a valid CAS Registry Number.

26733-25-5SDS

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-diethyl-1,3-dithiolane

1.2 Other means of identification

Product number -
Other names 2,2-diethyl-[1,3]dithiolane

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:26733-25-5 SDS

26733-25-5Downstream Products

26733-25-5Relevant articles and documents

Ecofriendly fast batch synthesis of dioxolanes, dithiolanes, and oxathiolanes without solvent under microwave irradiation

Perio, Bertrand,Dozias, Marie-Joelle,Hamelin, Jack

, p. 428 - 430 (2013/09/08)

2,2-Dimethoxypropane and 3,3-dimethoxypentane react with 1,2-ethanediol, thio, and oxathio analogues to give the corresponding protected carbonyls in high yield under mild solvent-free conditions. These environmentally benign conditions under microwave irradiation are applied to a large-scale synthesis.

Ahydrous Cobalt(II) Bromide Dispersed on Silica Gel: A Mild and Efficient Reagent for Thioacetalisation of Carbonyl Compounds

Patney, Harish K.

, p. 5717 - 5718 (2007/10/02)

Anhydrous cobalt(II) bromide dispersed on silica gel has been shown to be a very efficient reagent system for thioacetalisation of a variety of aldehydes and ketones at room temperature.

Comparative radioprotective activity of various pentagonal compounds with two heteroatomes

Robbe,Fernandez,Dubief,et al.

, p. 235 - 243 (2007/10/02)

Various heterocyclic compounds with two heteroatomes were synthesized and their potential radioprotective activity was tested. This study shows the interest of phenylthiazolidines derivatives in chemical radioprotection.

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