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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

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