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Potassium lactobionate is a salt derived from the reaction between potassium hydroxide and lactobionic acid. It is known for its ability to regulate electrolytes and osmotic pressure, as well as its chelating properties, which allow it to transport essential elements and medications throughout the body, particularly to areas under oxidative stress.

69313-67-3

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69313-67-3 Usage

Uses

Used in Organ Preservation Solutions:
Potassium lactobionate is used as a key component in organ preservation solutions for its ability to regulate electrolytes and osmotic pressure, which helps in maintaining the integrity of cells and preventing their destruction.
Used in Pharmaceutical Formulations:
Potassium lactobionate is used as a chelating agent in various pharmaceutical formulations, facilitating the delivery of medications and essential elements to targeted areas within the body, especially those experiencing oxidative stress.
Used in Foods:
Potassium lactobionate is used as a food additive for its chelating properties, which can help in the distribution of nutrients and enhance the overall quality of the food products.

Check Digit Verification of cas no

The CAS Registry Mumber 69313-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,1 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69313-67:
(7*6)+(6*9)+(5*3)+(4*1)+(3*3)+(2*6)+(1*7)=143
143 % 10 = 3
So 69313-67-3 is a valid CAS Registry Number.

69313-67-3SDS

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 potassium D-lactobionate

1.2 Other means of identification

Product number -
Other names potassium lactobionate

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:69313-67-3 SDS

69313-67-3Downstream Products

69313-67-3Relevant academic research and scientific papers

LACTOBIONIC ACID PRODUCTION METHODS AND PRODUCTS

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Paragraph 0076; 0077, (2020/08/19)

Systems and methods of making lactobionic acid are described. The systems include two-compartment cation bipolar electrodialysis assemblies having at least one cell that includes a cation ion-exchange membrane and a bipolar membrane. The membranes define the borders of a pair of flow channels for a separate (i) caustic stream and (i) purified lactobionic acid stream. Lactobionate ions in the lactobionic acid stream do not cross a membrane in the electrodialysis assembly, which reduces membrane fouling. The methods include passing a lactobionate salt through a two-compartment cation bipolar electrodialysis assembly. The electrodialysis assembly includes at least one two-compartment cation bipolar membrane cell, and separates the lactobionate salt into a caustic compound and the lactobionic acid. The assembly is designed so the lactobionate ions do not cross an ion exchange membrane in the assembly to form the lactobionic acid, which reduces membrane fouling.

CATALYTIC DEHYDROGENATION OF REDUCING SUGARS IN ALKALINE SOLUTION

Wit, Gert de,Vlieger, Jan J. de,Dalen, Alida C. Kock-van,Heus, Roelf,Laroy, Rob,et al.

, p. 125 - 138 (2007/10/02)

Aldoses in alkaline medium under the catalytic action of platinum of rhodium are converted into aldonic acids with high selectivity and with concomitant evolution of hydrogen gas.The dehydrogenation reaction has been studied for 25 different mono- and di-saccharides, and is generally applicable for reducing sugars.The influence of several reaction variables has been studied, leading to an adsorption model in which both the negatively charged O-1 and the close contact of H-1 with the catalyst surface are considered to be driving forces for the transfer of hydride from C-1 of the sugar to the catalyst.

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