Relevant Data

Food Additives Approved by European Union:


General Information

Synonyms: HEXACYANOFERRATE OF SODIUM, YELLOW PRUSSIATE OF SODA
Chemical Names: SODIUM FERROCYANIDE; SODIUM HEXACYANOFERRATE (II)
CAS number: 13601-19-9
INS:

535

Functional Class: Food Additives
ANTICAKING_AGENT

From apps.who.int


Evaluations

Evaluation year: 1974
ADI: 0-0.025 mg/kg bw
Meeting: 18
Specs Code: S
Report: NMRS 54/TRS 557-JECFA 18/23
Tox Monograph: NMRS 54A/FAS 6-JECFA 18/164
Specification: COMPENDIUM ADDENDUM 9/FNP 52 Add.9/192 (METALS LIMITS) (2001). R; FAO JECFA Monographs 1 vol.2/59

From apps.who.int



GSFA Provisions for SODIUM FERROCYANIDE

Number Food Category Max Level Notes
12.1.1

Salt

14 mg/kg Note 24,Note 107
12.1.2

Salt Substitutes

20 mg/kg Note 24
12.2.2

Seasonings and condiments

20 mg/kg Note 24

From www.fao.org


Computed Descriptors

Download SDF
2D Structure
CID54680695
IUPAC Namesodium;(2R)-2-[(2R)-3,4-dihydroxy-5-oxo-2H-furan-2-yl]-2-hydroxyethanolate
InChIInChI=1S/C6H7O6.Na/c7-1-2(8)5-3(9)4(10)6(11)12-5;/h2,5,8-10H,1H2;/q-1;+1/t2-,5-;/m1./s1
InChI KeyRBWSWDPRDBEWCR-RKJRWTFHSA-N
Canonical SMILESC(C(C1C(=C(C(=O)O1)O)O)O)[O-].[Na+]
Molecular FormulaC6H7O6Na·H2O
WikipediaSodium erythorbate

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight198.106
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count2
Complexity237.0
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 Area110.0
Monoisotopic Mass198.014
Exact Mass198.014
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count13
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count2

From Pubchem


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassDihydrofurans
SubclassFuranones
Intermediate Tree NodesNot available
Direct ParentButenolides
Alternative Parents
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents2-furanone - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Vinylogous acid - Carboxylic acid ester - Enediol - Lactone - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Oxacycle - Organic alkali metal salt - Hydrocarbon derivative - Organic oxide - Organic zwitterion - Alkoxide - Carbonyl group - Organooxygen compound - Organic oxygen compound - Alcohol - Organic salt - Organic sodium salt - Aliphatic heteromonocyclic compound
DescriptionThis 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