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1,2,3-Trithiane-4-pentanoic acid, also known as thioctic acid precursor, is an organic compound with the molecular formula C5H8O2S3. It is a colorless to pale yellow crystalline solid that serves as an essential intermediate in the synthesis of thioctic acid, a vital coenzyme in the human body.

1204245-29-3

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1204245-29-3 Usage

Uses

Used in Pharmaceutical Industry:
1,2,3-Trithiane-4-pentanoic acid is used as an intermediate in the synthesis of thioctic acid (α-lipoic acid) for its various pharmaceutical applications. Thioctic acid is a coenzyme involved in the metabolism of carbohydrates, fats, and proteins. It has been widely studied for its potential benefits in treating various health conditions, including diabetes, liver disease, and neurological disorders.
Used in the Process for Preparation of Thioctic Acid with Low Solvent Residue:
1,2,3-Trithiane-4-pentanoic acid is used as a key intermediate in the production of thioctic acid with low solvent residue. This process aims to minimize the environmental impact and improve the safety profile of the final product by reducing the amount of solvents used in the synthesis. The low solvent residue in thioctic acid is particularly important for its use in the pharmaceutical and dietary supplement industries, where purity and safety are paramount.

Check Digit Verification of cas no

The CAS Registry Mumber 1204245-29-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,2,4 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1204245-29:
(9*1)+(8*2)+(7*0)+(6*4)+(5*2)+(4*4)+(3*5)+(2*2)+(1*9)=103
103 % 10 = 3
So 1204245-29-3 is a valid CAS Registry Number.

1204245-29-3SDS

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 5-(trithian-4-yl)pentanoic acid

1.2 Other means of identification

Product number -
Other names UNII-UQ303H498S

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:1204245-29-3 SDS

1204245-29-3Downstream Products

1204245-29-3Relevant academic research and scientific papers

Preparation method of lipoic acid impurity A

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Paragraph 0029-0030; 0035-0036, (2021/08/11)

The invention relates to a preparation method of a lipoic acid impurity A, and belongs to the field of compound synthesis. The invention aims to overcome the defects of complex operation and harsh reaction conditions in the prior art, and provides the preparation method of the lipoic acid impurity A. The preparation method is mild in condition and high in product purity. The preparation method comprises the following steps: (1) dissolving lipoic acid in a reaction solvent, adding an oxidant for reaction, and removing solids and the solvent after the reaction is completed to obtain a compound B; (2) respectively adding the compound B, sodium thiosulfate and a catalyst into water, then adding hydrochloric acid, carrying out hydrolysis ring-opening reaction, and filtering after the reaction is completed to obtain a compound C; and (3) respectively adding the compound C, sodium sulfide and formaldehyde into the reaction solvent for reaction, extracting after the reaction is completed, drying, and purifying to obtain a compound D lipoic acid impurity A. The method is mild in condition, and the prepared lipoic acid impurity A is high in purity.

Preparation method of lipoic acid process impurity

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Paragraph 0006; 0017-0025, (2020/07/12)

The invention relates to a preparation method of a lipoic acid process impurity namely 1,2,3-trithiocyclohexane-4-valeric acid, and belongs to the technical field of preparation of lipoic acid impurities. The preparation method comprises the following steps: carrying out saponification, vulcanization cyclization, acidification, and refining on a lipoic acid intermediate namely 6,8-dichloroethyl caprylate to obtain the product. The preparation method is simple in process, and high in operability and the product is easy to purify.

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