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Details

Stereochemistry ABSOLUTE
Molecular Formula 2C6H7O6.Fe
Molecular Weight 406.077
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FERROUS ASCORBATE

SMILES

[Fe++].[H][C@@]1(OC(=O)C(O)=C1[O-])[C@@H](O)CO.[H][C@@]2(OC(=O)C(O)=C2[O-])[C@@H](O)CO

InChI

InChIKey=RFBYLSCVRUTUSB-ZZMNMWMASA-L
InChI=1S/2C6H8O6.Fe/c2*7-1-2(8)5-3(9)4(10)6(11)12-5;/h2*2,5,7-10H,1H2;/q;;+2/p-2/t2*2-,5+;/m00./s1

HIDE SMILES / InChI

Molecular Formula C6H7O6
Molecular Weight 175.1162
Charge -1
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula Fe
Molecular Weight 55.845
Charge 2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Direct reduced iron is an alternative iron source produced by heating an iron ore. In nature, most of the iron has an oxidized form.

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 09:08:56 UTC 2023
Edited
by admin
on Sat Dec 16 09:08:56 UTC 2023
Record UNII
DI3477D0PI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FERROUS ASCORBATE
WHO-DD  
Common Name English
(2R)-2-((1S)-1,2-DIHYDROXYETHYL)-4,5-DIHYDROXYFURAN-3-ONE, IRON(2+)
Systematic Name English
IRON(II) ASCORBATE
Common Name English
FERRATE(2-), BIS(L-ASCORBATO(2-)-O2,O3)-, DIHYDROGEN
Systematic Name English
L-ASCORBIC ACID, IRON(2+) SALT (2:1)
Common Name English
Ferrous ascorbate [WHO-DD]
Common Name English
FERRATE(2-), BIS(L-ASCORBATO(2-)-.KAPPA.O2,.KAPPA.O3)-, HYDROGEN (1:2)
Systematic Name English
ASCOFER
Brand Name English
NEDIFER
Brand Name English
FERRATE(2-), BIS(L-ASCORBATO(2-)-.KAPPA.O2,.KAPPA.O3)-, DIHYDROGEN
Systematic Name English
COMPLEFER
Brand Name English
IRON(2+) DI-L-ASCORBATE
Systematic Name English
L-ASCORBIC ACID, IRON COMPLEX
Common Name English
IRON(2+) BIS((2S)-2-((2R)-3,4-DIHYDROXY-5-OXO-2,5-DIHYDRO-2-FURANYL)-2-HYDROXYETHANOLATE)
Systematic Name English
J290.062I
Code English
Classification Tree Code System Code
WHO-VATC QB03AA10
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
WHO-ATC B03AA10
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
CFR 21 CFR 184.1307A
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
Code System Code Type Description
CAS
24808-52-4
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY
ECHA (EC/EINECS)
246-469-7
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY
DRUG BANK
DB14490
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY
FDA UNII
DI3477D0PI
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY
SMS_ID
100000078447
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY
EVMPD
SUB13859MIG
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY
RXCUI
4356
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY RxNorm
ChEMBL
CHEMBL3707305
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY
EPA CompTox
DTXSID701018439
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY
DRUG CENTRAL
4540
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY
PUBCHEM
86763295
Created by admin on Sat Dec 16 09:08:56 UTC 2023 , Edited by admin on Sat Dec 16 09:08:56 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY