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Taurine sodium, a chemical compound derived from the combination of taurine—an amino acid-like compound—and sodium, a vital mineral for various bodily functions, is recognized for its potential health benefits. It is known for its role in improving athletic performance, reducing muscle fatigue, and enhancing endurance, while also exhibiting antioxidant properties and supporting cardiovascular health. Taurine sodium is integral in the regulation of nerve impulses and muscle contractions, making it a popular ingredient in energy drinks and supplements.

7347-25-3

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7347-25-3 Usage

Uses

Used in Energy Drinks and Supplements:
Taurine sodium is used as a performance enhancer for its potential to improve athletic performance, reduce muscle fatigue, and enhance endurance. It is particularly favored by athletes and individuals seeking to boost their physical capabilities.
Used in Antioxidant Formulations:
Taurine sodium is used as an antioxidant agent due to its properties that may help support cardiovascular health and protect the body from oxidative stress.
Used in Cardiovascular Health Support:
Taurine sodium is used as a cardiovascular health supporter, potentially aiding in the maintenance of heart function and overall cardiovascular system health.
Used in Nerve Impulse and Muscle Contraction Regulation:
Taurine sodium is used as a regulator of nerve impulses and muscle contractions, which is crucial for normal muscle function and neurological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 7347-25-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,4 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7347-25:
(6*7)+(5*3)+(4*4)+(3*7)+(2*2)+(1*5)=103
103 % 10 = 3
So 7347-25-3 is a valid CAS Registry Number.
InChI:InChI=1/C2H7NO3S.Na/c3-1-2-7(4,5)6;/h1-3H2,(H,4,5,6);/q;+1/p-1

7347-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name TAURINE SODIUM

1.2 Other means of identification

Product number -
Other names 2-Aminoethane-1-sulfonic acid sodium salt

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:7347-25-3 SDS

7347-25-3Relevant academic research and scientific papers

A Preparation method of Taurine surfactant derived from natural oil

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Paragraph 0098-0100; 0102, (2021/05/11)

The present invention relates to a process for preparing taurine based surfactants from natural oils. The present invention relates to a method for preparing a taurine surfactant, and more particularly, to a method for preparing a taurine surfactant by direct reaction of taurine with natural oil without further processing. In addition, the taurine-based surfactant produced by the method may be used as an efficient raw material, has excellent physical properties and detergency, and has excellent cleaning power when the detergent composition and detergent are prepared.

Synthetic method and medicinal preparation of sodium taurocholate

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Paragraph 0068-0069; 0072-0073; 0076-0077; 0080-0081, (2021/11/03)

The method comprises the following steps: S10, dissolving taurine and a base in water for salt formation reaction, drying the generated salt after the reaction is ended, and obtaining taurine sodium. S20, the taurine sodium and cholic acid are subjected to condensation reaction under 2 - ethoxy -1 - ethoxycarbonyl -1 and 2 - 80 - 120 °C dihydroquinoline, and a product solution containing sodium taurocholate is obtained. S30, sodium taurocholate in the product solution is separated and purified to obtain the sodium taurocholate product. To the method, taurine and a base are subjected to salt formation reaction to obtain sodium taurocholate, and condensation reaction is carried out, so that an existing 'one-pot' is changed into a two-step method. In addition, the synthetic method provided by the invention is simple to operate and low in cost.

Preparation method of sodium taurate

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Paragraph 0093-0095, (2020/05/30)

The invention provides a preparation method of sodium taurate. The preparation method comprises the following steps: dissolving sodium hydroxyethyl sulfonate and a raw material sodium taurate into a guanidyl-containing ionic liquid, performing a reaction to obtain an ionic liquid solution containing a mixed product of sodium ditaurate and sodium tritaurate, introducing liquid ammonia into the ionic liquid solution of the mixed product, performing a reaction to obtain an ionic liquid solution of the product sodium taurate, adding the ionic liquid solution of the product sodium taurate into an alcohol solvent for solvating out, and separating out the obtained precipitated solid to obtain the product sodium taurate. The sodium taurate preparation method is high in product yield, good in purity, high in raw material utilization rate, simple and convenient in process and mild in reaction condition, the production efficiency of sodium taurate can be greatly improved, and the production costis reduced, so that the sodium taurate preparation method has a very good industrial application prospect.

Method for preparing taurine

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Paragraph 0046; 0048; 0049; 0050; 0052, (2019/04/06)

The invention provides a method for preparing taurine. The method comprises the following steps: carrying out an addition reaction on ethylene oxide and sodium hydrogen sulfite in the presence of a heterogeneous catalyst so as to obtain sodium hydroxyethyl sulfonate at high selectivity; carrying out an ammonolysis reaction on the synthesized sodium hydroxyethyl sulfonate under catalysis of a homogeneous catalyst; and neutralizing, crystallizing, separating and the like, thereby obtaining the finished taurine. Compared with the traditional production process, the process disclosed by the invention has the advantages that by-products in the addition reaction process can be obviously reduced, the temperature and pressure of the ammonolysis reaction are reduced, the reaction time is shortened,and industrial production is easily realized.

A PROCESS FOR PRODUCING TAURINE

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Paragraph 0028, (2018/08/09)

The present application provides a process for preducing taurine, comprising the steps as follows: (a) mixing isethionic acid with taurine salt solution until the system pH reaches a certain value in a range from 5.0 to 9.5; (b) separating liquid phase and solid phase of the system; wherein said solid phase is the crude product of taurine, and said liquid phase is isethionate solution; (c) reacting ammonia solution with said liquid phase obtained from step (b) to obtain taurine salt solution. It uses isethionic acid to adjust the pH of the taurine salt solution, avoiding the problem causing by using sulphate acid to adjust the pH in the traditional process. By the recycling use of the cations in taurine salts, a new raw material or reagent does not need to be added which is benefit to reducing the use of dangerous chemical materials, simplifying the production process greatly, improving the utilization rate of raw materials, increasing the yield of the product and decreasing production cost significantly.

High-yield circular production method of taurine

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Page/Page column 8, (2018/09/30)

The high-yield circular production method of taurine includes the following steps: S1, ethylene oxide reacts with sodium bisulfite solution to generate sodium hydroxyethyl sulfonate; S2, sodium hydroxyethyl sulfonate obtained in S1 is subjected to ammonolysis reaction in ammonia, and ammonia gas is recycled through flash evaporation upon completion of the reaction; S3, a reaction solution obtained after flash evaporation in S2 is sent to pass through an acidic cation exchange resin column, a material liquid containing taurine is collected, the inactivated resin column is subjected to regeneration with sulfur dioxide or carbon dioxide aqueous solution, and an eluent acquired during regeneration can be recycled directly or recycled after treated by sulfur dioxide; S4, the material liquid collected in S3 is subjected to post treatment to acquire taurine.

PEPTIDIC LINKERS AND CRYPTOPHYCIN CONJUGATES, USEFUL IN THERAPY, AND THEIR PREPARATION

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Page/Page column 239; 240, (2018/12/02)

The present disclosure relates to compounds of formula (I): RCG1-L-P (I) wherein RCG1 represents a reactive chemical group being reactive towards a chemical group present on a polypeptide such as an antibody; P represents H, OH or an activated O; and L represents a specific linker. The disclosure also relates to cryptophycin payloads, as well as to cryptophycin conjugates, to compositions containing them and to their therapeutic use, especially as anticancer agents. The disclosure also relates to the process for preparing these conjugates.

Method of fully recycling mother liquid to produce taurine

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Paragraph 0024; 0025, (2016/10/10)

The invention discloses a method of fully recycling mother liquid to produce taurine.The method specifically includes: utilizing ethylene oxide and sodium hydrogen sulfite to prepare 2-hydroxy ethyl sodium sulfonate; preparing sodium taurate through high temperature high pressure and concentration; removing impurities through 2-stage neutralizing to obtain a taurine crude product; subjecting the mother liquid to press filtering and catalysis to further remove sodium sulfate, recycling to a synthesis section, combining with an ammonia solution of hydroxy ethyl sodium sulfonate, enabling a mixture to enter a synthesis tower for reaction, and controlling a proportion of hydroxy ethyl sodium sulfonate to the mother liquid to enable hydroxy ethyl sodium sulfonate which does not react completely in the mother liquid to react completely.Therefore, discharging pollution of the mother liquid is avoided completely, and total reaction yield is increased.

Method for preparing taurine and co-producing bicarbonate

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Paragraph 0043; 0044, (2016/10/08)

The invention discloses a method for preparing taurine and co-producing bicarbonate. The method comprises the step of leading carbon dioxide gas or adding a carbon dioxide water solution to an amino ethyl sulfonate water solution of alkali metal or ammonium to regulate a pH value so as to obtain the taurine and the bicarbonate. The method can replace an existing taurine preparation method of using sulfuric acid or sulfur dioxide to regulate the pH value, meanwhile can treat boiler exhaust gas, turns the carbon dioxide in the exhaust gas into wealth, co-produces the bicarbonate and is a safe, environmentally-friendly and energy-saving method for producing the taurine and co-producing the bicarbonate.

Cyclic process for the production of taurine from alkali isethionate and alkali vinyl sulfonate

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Paragraph 0052; 0053, (2015/11/23)

The present invention discloses a cyclic process for the production of taurine from alkali isethionate and alkali vinyl sulfonate in a high overall yield of greater than 95% by continuously converting the byproducts of the ammonolysis reaction, sodium ditaurinate and sodium tritaurinate, to sodium taurinate. Pure sodium ditaurinate and sodium tritaurinate are prepared from diethanolamine and triethanolamine as starting materials, respectively, and are subjected to the ammonolysis reaction to yield a mixture of sodium taurinate, sodium ditaurinate, and sodium tritaurinate.

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