2058-58-4 Usage
Description
D-(-)-Asparagine monohydrate is an optically active form of asparagine with a D-configuration, which means it is a non-superimposable mirror image of the L-configuration. It is a crystalline powder and is known for its unique properties and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
D-(-)-Asparagine monohydrate is used as an active pharmaceutical ingredient for the development of drugs targeting specific medical conditions. Its unique structure allows it to interact with biological systems in a way that can be beneficial for therapeutic purposes.
Used in Nutritional Supplements:
D-(-)-Asparagine monohydrate is used as a dietary supplement to support protein synthesis and overall health. Its role in the body's metabolic processes makes it a valuable addition to nutritional products aimed at enhancing athletic performance and general well-being.
Used in Research and Development:
D-(-)-Asparagine monohydrate is used as a research compound in the field of biochemistry and molecular biology. Its unique properties make it an important tool for studying the structure and function of proteins and other biomolecules, as well as for developing new drugs and therapies.
Used in Cosmetics Industry:
D-(-)-Asparagine monohydrate is used as an ingredient in the cosmetics industry, where it may be incorporated into skincare and beauty products for its potential benefits to skin health and appearance. Its role in protein synthesis could contribute to the development of anti-aging and skin repair formulations.
Used in Food Industry:
D-(-)-Asparagine monohydrate may be used in the food industry as a flavor enhancer or as a component in the production of certain food additives. Its unique properties could potentially contribute to the development of new flavors or improve the taste and texture of existing products.
Synthesis Reference(s)
Chemical and Pharmaceutical Bulletin, 35, p. 2994, 1987 DOI: 10.1248/cpb.35.2994
Check Digit Verification of cas no
The CAS Registry Mumber 2058-58-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2058-58:
(6*2)+(5*0)+(4*5)+(3*8)+(2*5)+(1*8)=74
74 % 10 = 4
So 2058-58-4 is a valid CAS Registry Number.
InChI:InChI:1S/C4H8N2O3/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H2,6,7)(H,8,9)
2058-58-4Relevant articles and documents
Pasteur-like resolution of quasi-racemates in solid and gas phases
Kostyanovsky, Remir G.,Nikolaev, Eugene N.,Kharybin, Oleg N.,Kadorkina, Gul'Nara K.,Kostyanovsky, Vasilii R.
, p. 97 - 99 (2003)
Isotopomeric quasi-racemates (IQR), i.e., 1:1 mixtures of enantiomers one of which contains an isotopic label, can undergo crystallisation as conglomerates or true quasi-racemates. In the former case, each single crystal contains, predominantly or exclusi
Useful Impurities for Optical Resolutions. 3. An Improved Pasteur-Type Resolution of Conglomerates and a New Empirical Method for Assignment of Absolute Configuration
Addadi, Lia,Gati, Edna,Lahav, Meir
, p. 1251 - 1252 (1981)
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Self-Reporting Inhibitors: A Single Crystallization Process To Obtain Two Optically Pure Enantiomers
Ye, Xichong,Cui, Jiaxi,Li, Bowen,Li, Na,Zhang, Jie,Wan, Xinhua
, p. 8120 - 8124 (2018/06/29)
Collection of two optically pure enantiomers in a single crystallization process can significantly increase the chiral separation efficiency but this is difficult to realize. Now a self-reporting strategy is presented for visualizing the crystallization process by a dyed self-assembled inhibitor made from the copolymers with tri(ethylene glycol)-grafting polymethylsiloxane as the main chain and poly(N6-methacryloyl-l-lysine) as side chains. When applied with seeds together for the fractional crystallization of conglomerates, the inhibitors can label the formation of the secondary crystals and guide the complete separation process of two enantiomers with colorless crystals as the first product and red crystals as the second. This method leads to high optical purity of d/l-Asn?H2O (99.9 % ee for d-crystals and 99.5 % for l-crystals) in a single crystallization process. It requires a small amount of additives and shows excellent recyclability.
SEPARATING AGENT AND MANUFACTURING METHOD THEREOF
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Paragraph 0067; 0068; 0069; 0070; 0071; 0072; 0087; 0088, (2015/01/07)
An embodiment of the present invention is a separating agent wherein a group represented by a chemical formula of: or a group represented by a chemical formula of: is introduced on a surface thereof.