D-erythro-Hex-2-enonic acid, g-lactone, monosodium salt, monohydrate


Chemical Name: D-erythro-Hex-2-enonic acid, g-lactone, monosodium salt, monohydrate
CAS Number: 63524-04-9
Product Number: AG003UCG(AGN-PC-0T8UUC)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties


Properties
MP:
165 °C (dec.)(lit.)
Form:
Solid
Computed Properties
Molecular Weight:
216.121g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
2
Exact Mass:
216.025g/mol
Monoisotopic Mass:
216.025g/mol
Topological Polar Surface Area:
111A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
237
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



Sodium erythorbate monohydrate is a versatile compound used in chemical synthesis for its antioxidant properties and ability to act as a reducing agent. In the field of organic chemistry, it is commonly utilized as a catalyst in various reactions due to its ability to facilitate electron transfer processes. Sodium erythorbate monohydrate can also be employed in the synthesis of pharmaceuticals, polymers, and other complex organic compounds. Its role as a reducing agent makes it particularly valuable in the production of fine chemicals and specialty materials. Additionally, its antioxidant properties make it a useful additive in food and cosmetic industries, where it can help prevent oxidation and enhance product stability.