Ferric citrate pentahydrate - AR , CAS No.6043-74-9

CAS: 6043-74-9 Cat. No.: F110791 Peso molecular: 335.02 PubChem CID: 61300

GRADE & PURITY AR

Synonyms

A832727 | iron(3+) citrate | 2-hydroxypropane-1,2,3-tricarboxylate;iron(3+) | FERRIC CITRATE [INCI] | FT-0627304 | Auryxia | 2-hydroxy-1,2,3-propanetricarboxylic acid iron salt | Iron 2-hydroxy-1,2,3-propanetricarboxylate | Citric acid, iron(3+) salt (1:1

Storage

Protected from light,Room temperature

Shipped In

Normal

Specifications

Sinónimos

A832727 | iron(3+) citrate | 2-hydroxypropane-1, 2, 3-tricarboxylate;iron(3+) | FERRIC CITRATE [INCI] | FT-0627304 | Auryxia | 2-hydroxy-1, 2, 3-propanetricarboxylic acid iron salt | Iron 2-hydroxy-1, 2, 3-propanetricarboxylate | Citric acid, iron(3+) salt (1:1

Especificaciones y pureza

AR

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature

Enviado en

Normal

Grado

AR

Nombres e identificadores

• Pubchem Sid: 488183477
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183477
• Sonrisas canónicas: C(C(=O)[O-])C(CC(=O)[O-])(C(=O)[O-])O.[Fe+3]
• IUPAC Name: 2-hydroxypropane-1,2,3-tricarboxylate;iron(3+)
• InChIKey: NPFOYSMITVOQOS-UHFFFAOYSA-K
• INCHI: 1S/C6H8O7.Fe/c7-3(8)1-6(13,5(11)12)2-4(9)10;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);/q;+3/p-3
• Isómeros SMILES: C(C(=O)[O-])C(CC(=O)[O-])(C(=O)[O-])O.[Fe+3]
• PubChem CID: 61300
• Peso molecular: 335.02

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Tricarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Tricarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Tricarboxylic acids and derivatives
• Alternative Parents: Tertiary alcohols Carboxylic acid salts Organic transition metal salts Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tricarboxylic acid or derivatives - Tertiary alcohol - Carboxylic acid salt - Organic transition metal salt - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.
• 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

Propiedades químicas y físicas

• Sensibilidad: Light sensitive.
• Peso molecular: 244.940 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 2
• Exact Mass: 244.938 Da
• Monoisotopic Mass: 244.938 Da
• Topological Polar Surface Area: 141.000 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 211.000
• 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: 2

XLogP3

Referencias

1. Jia-Qi Liu, Xin Ma, Dong-Feng Liu, Chuan-Wang Yang, Dao-Bo Li, Di Min, Han-Qing Yu.  (2023)  Multiple roles of released c-type cytochromes in tuning electron transport and physiological status of Geobacter sulfurreducens.  BIOTECHNOLOGY AND BIOENGINEERING,  120  (5): (1346-1356).  [PMID:36779277] [10.1002/bit.28351]

2. Zhixing Xiao, Lizhuang Yang, Chuang Chen, Dan Chen, Xue Zhou.  (2022)  Redox reaction between solid-phase humins and Fe(III) compounds: Toward a further understanding of the redox properties of humin and its possible environmental effects.  JOURNAL OF ENVIRONMENTAL MANAGEMENT,      [PMID:35220098] [10.1016/j.jenvman.2022.114793]

3. Baoyu Liu, Jiajin Huang, Zhantu Liao, Chongzhi Zhu, Qiaoli Chen, Guan Sheng, Yihan Zhu, Yi Huang, Jinxiang Dong.  (2021)  Integrating pore interconnectivity and adaptability in a single crystal hierarchical zeolite for liquid alkylation.  AICHE JOURNAL,  67  (6): (e17177).  [PMID:] [10.1002/aic.17177]

4. Guodong Du, Yakun Xi, Xiaohui Tian, Yanbin Zhu, Yingke Zhou, Chengji Deng, Hongxi Zhu, Angulakshmi Natarajan.  (2019)  One-step hydrothermal synthesis of 3D porous microspherical LiFePO4/graphene aerogel composite for lithium-ion batteries.  CERAMICS INTERNATIONAL,      [PMID:] [10.1016/j.ceramint.2019.06.035]

5. Guodong Du, Yingke Zhou, Xiaohui Tian, Guan Wu, Yakun Xi, Shengyu Zhao.  (2018)  High-performance 3D directional porous LiFePO4/C materials synthesized by freeze casting.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2018.05.142]

6. Xiaofeng Tu, Yingke Zhou, Yijie Song.  (2016)  Freeze-drying synthesis of three-dimensional porous LiFePO4 modified with well-dispersed nitrogen-doped carbon nanotubes for high-performance lithium-ion batteries.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2016.12.220]

7. Jing Zhang, Yujun Wei, Penghui Chen, Zhijian Huang, Qixu Yu, Jing Tan, Hongzhen Zeng, Shudong Yu.  (2025)  Iron-catalyzed Laser-Induced Graphene on Cellulose Paper for Solar-driven Interfacial Evaporation.  Materials Horizons,      [PMID:40814273] [10.1039/D5MH01166C]