Ferrous Bisglycinate - Iron content: 20% , CAS No.20150-34-9

CAS: 20150-34-9 Cat. No.: F302712 Molecular Weight: 203.96 EC Number: 606-444-7 PubChem CID: 9837124

GRADE & PURITY Iron content: 20%

Synonyms

Iron glycinate | BIS(GLYCINATO-.KAPPA.N,.KAPPA.O)IRON | Bisglycine iron(II) salt | lambda2-iron(2+) ion bis(2-aminoacetate) | 2-aminoacetate;iron(2+) | DTXSID30173978 | Iron, bis(glycinato-kappaN,kappaO)- | Ferrous bisglycinate | GIPOFCXYHMWROH-UHFFFAOYSA

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Specifications

Synonyms

Iron glycinate | BIS(GLYCINATO-.KAPPA.N, .KAPPA.O)IRON | Bisglycine iron(II) salt | lambda2-iron(2+) ion bis(2-aminoacetate) | 2-aminoacetate;iron(2+) | DTXSID30173978 | Iron, bis(glycinato-kappaN, kappaO)- | Ferrous bisglycinate | GIPOFCXYHMWROH-UHFFFAOYSA

Specifications & Purity

Iron content: 20%

Storage

Protected from light, Room temperature, Argon charged

Shipped In

Normal

Names and Identifiers

• Pubchem Sid: 504764941
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764941
• Canonical Smiles: C(C(=O)[O-])N.C(C(=O)[O-])N.[Fe+2]
• IUPAC Name: 2-aminoacetate;iron(2+)
• InChIKey: GIPOFCXYHMWROH-UHFFFAOYSA-L
• INCHI: 1S/2C2H5NO2.Fe/c2*3-1-2(4)5;/h2*1,3H2,(H,4,5);/q;;+2/p-2
• Isomeric SMILES: C(C(=O)[O-])N.C(C(=O)[O-])N.[Fe+2]
• PubChem CID: 9837124
• Molecular Weight: 203.96

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Alpha amino acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Alpha amino acids
• Alternative Parents: Carboxylic acid salts Amino acids Organic transition metal salts Monocarboxylic acids and derivatives Carboxylic acids Organic zwitterions Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Alpha-amino acid - Carboxylic acid salt - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic transition metal salt - Organic salt - Organic zwitterion - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Amine - Hydrocarbon derivative - Organic oxide - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Light sensitive；Air sensitive
• Boil Point(°C): 240.9℃ at 760 mmHg
• Molecular Weight: 203.960 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 203.983 Da
• Monoisotopic Mass: 203.983 Da
• Topological Polar Surface Area: 132.000 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 37.400
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 3

XLogP3

References

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2. Hua Wei, Hongli Li, Yutong Zhang, Xin Wang, Zihan Li, Mingyang Zhou, Yongqian Lei, Pengran Guo, Jian Liu, Shenghong Yang.  (2024)  Solid-phase synthesized iron-mediated carbon dots nanozymes with fluorescence and peroxidase-like activity for multi-mode analysis of dopamine.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.112597]

3. Chunjiao Qi, Jintao Chen, Yuhui Shang, Yu Yang, Kangyan Wang, Jinyang Chen.  (2024)  Target-Triggered Ultrafast Chondroitin Gelation Enabled Power-Free and Point-of-Care Bioassays.  ANALYTICAL CHEMISTRY,      [PMID:39436985] [10.1021/acs.analchem.4c04130]

4. Jiayin Li, Wen Wen, Shuzhuo Bai, Jing Zhang, Chenyu Wu, Jintao Wu, QingQing Huang, Yalin Zhang, Chunyi Cai, Liyun Cao, Yijun Liu, Haibo Zhang, Hua Tan, Jianfeng Huang.  (2025)  In situ FeF3 coating on FeNCN to stabilize discharged products Fe0 for enhanced loading and high-rate Na storage performance.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.167961]