67776-07-2 Usage
Uses
Used in Pharmaceutical Industry:
2-Keto-D-gulonic Acid Methyl Ester is used as an intermediate in the synthesis of vitamin C for pharmaceutical applications. It serves as a precursor in the production of this essential vitamin, which is vital for maintaining overall health and supporting the immune system.
Used in Cosmetic Industry:
In the cosmetic industry, 2-Keto-D-gulonic Acid Methyl Ester is used as an active ingredient in skincare products. Its role as a precursor to vitamin C allows it to contribute to the promotion of collagen synthesis, which is essential for maintaining skin elasticity and reducing the appearance of wrinkles.
Used in Food and Beverage Industry:
2-Keto-D-gulonic Acid Methyl Ester is utilized as a key ingredient in the fortification of food and beverages with vitamin C. This helps to enhance the nutritional value of these products and ensure that consumers receive adequate amounts of this essential vitamin to support their health and well-being.
Used in Research and Development:
In the field of research and development, 2-Keto-D-gulonic Acid Methyl Ester is employed as a valuable compound for studying the biosynthesis of vitamin C and its role in various biological processes. This helps scientists to better understand the mechanisms of action and potential applications of this important molecule.
Check Digit Verification of cas no
The CAS Registry Mumber 67776-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,7 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67776-07:
(7*6)+(6*7)+(5*7)+(4*7)+(3*6)+(2*0)+(1*7)=172
172 % 10 = 2
So 67776-07-2 is a valid CAS Registry Number.
67776-07-2Relevant academic research and scientific papers
Ascorbic acid synthesis
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, (2008/06/13)
Ascorbic acid is prepared from a 1,4-lactone selected from gulono-1,4-lactone, galactono-1,4-lactone, idono-1,4-lactone and talono-1,4-lactone by a process comprising protection of the hydroxyl groups of the lactone so as to form an intermediate having a free hydroxyl group at either, but not both, the 2- or 3-position, oxidizing this free hydroxyl group to a keto group and hydrolyzing the oxidized intermediate to remove the hydroxyl-protecting groups.
