Sodium ascorbate
Relevant Data
Food Additives Approved in the United States
Food Additives Approved by WHO:
General Information
Chemical name | Sodium ascorbate |
E No. | E 301 |
INS. | 301 |
CAS number | 134-03-2 |
Group | No |
Component of the group |
Group I, Additives (Group I) |
From webgate.ec.europa.eu
Authorisation of the use of this additive in Food Additives
The additive is authorised to be used in the following category(ies):
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From webgate.ec.europa.eu
Computed Descriptors
Download SDF2D Structure | |
CID | 23667548 |
IUPAC Name | sodium;(2R)-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2H-furan-3-olate |
InChI | InChI=1S/C6H8O6.Na/c7-1-2(8)5-3(9)4(10)6(11)12-5;/h2,5,7-10H,1H2;/q;+1/p-1/t2-,5+;/m0./s1 |
InChI Key | PPASLZSBLFJQEF-RXSVEWSESA-M |
Canonical SMILES | C(C(C1C(=C(C(=O)O1)O)[O-])O)O.[Na+] |
Molecular Formula | C6H7O6Na |
Wikipedia | sodium ascorbate |
From Pubchem
Computed Properties
Property Name | Property Value |
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Molecular Weight | 198.106 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 2 |
Complexity | 237.0 |
CACTVS Substructure Key Fingerprint | A A A D c Y B g O C A A A A A A A A A A A A A A A A A A A Q A A A A A A A A A A A A A A A A A A A A A A G g A A C A A A C B S g g A I A C A A A B g C I A A D Q C A I A A A A g I A A A C A B A A E g B F A A A I A A C U A A F w A A L I Q J A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = = |
Topological Polar Surface Area | 110.0 |
Monoisotopic Mass | 198.014 |
Exact Mass | 198.014 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 13 |
Defined Atom Stereocenter Count | 2 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Isotope Atom Count | 0 |
Covalently-Bonded Unit Count | 2 |
From Pubchem
Taxonomic Classification
Kingdom | Organic compounds |
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Superclass | Organoheterocyclic compounds |
Class | Dihydrofurans |
Subclass | Furanones |
Intermediate Tree Nodes | Not available |
Direct Parent | Butenolides |
Alternative Parents | |
Molecular Framework | Aliphatic heteromonocyclic compounds |
Substituents | 2-furanone - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Vinylogous acid - 1,2-diol - Carboxylic acid ester - Lactone - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Oxacycle - Organic alkali metal salt - Hydrocarbon derivative - Organic oxide - Organic zwitterion - Organic oxygen compound - Primary alcohol - Organooxygen compound - Alcohol - Carbonyl group - Organic salt - Organic sodium salt - Aliphatic heteromonocyclic compound |
Description | This compound belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. |
From ClassyFire