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Di-2-butyl trisulphide is an organosulfur compound with the chemical formula C8H18S3. It is a colorless to pale yellow liquid with a strong, pungent odor. di-2-butyl trisulphide is composed of two butyl groups and a trisulfide bridge, which consists of three sulfur atoms. Di-2-butyl trisulphide is primarily used as a synthetic flavoring agent in the food and beverage industry, as well as a fragrance component in the perfumery sector. It is known for its ability to impart a garlic-like or onion-like aroma to various products. Due to its chemical structure, di-2-butyl trisulphide is also of interest in research related to the development of new materials and pharmaceuticals.

5943-32-8

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5943-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5943-32-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,4 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5943-32:
(6*5)+(5*9)+(4*4)+(3*3)+(2*3)+(1*2)=108
108 % 10 = 8
So 5943-32-8 is a valid CAS Registry Number.

5943-32-8Downstream Products

5943-32-8Relevant academic research and scientific papers

Use of a sacriflcial-sulfur electrode in electroorganic chemistry. V. Formation of the sequence CSSSC from S and thiols or thiolates

Do, Quang Tho,Elothmani, Driss,Simonet, Jacques,Guillanton, Georges Le

, p. 273 - 281 (2007/10/03)

At a working potential of about +2.0 V (vs SCE) the carbon-sulfur electrode is a source of the electrogenerated cation S2+. In organic media, this electrophile reacts with thiols (or thiolates) to give a mixture of polysulfides of which the trisulfide is the main product. The reaction between electrogenerated Sy2- and alkyl halides is less selective. Elsevier,.

ACTION OF ELEMENTARY SULFUR ONTO CARBANIONS: A NEW ROUTE TO DIALKYLPOLYSULFIDES

Boscato, J. F.,Catala, J. M.,Franta, E.,Brossas, J.

, p. 1519 - 1520 (2007/10/02)

The reaction of sec-Butyllithium with elemental sulfur leads to the formation of dialkylpolysulfides.

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