FERRIC STEARATE - Fe：5.8-8.0% , CAS No.555-36-2

CAS: 555-36-2 Cat. No.: F189160 Peso molecular: 906.27 Número EC: 209-095-5 PubChem CID: 68388

GRADE & PURITY Fe：5.8-8.0%

Synonyms

FERRIC STEARATE | Iron Tristearate | Iron(III) Stearate | Stearic Acid Iron(III) Salt | iron(iii)stearate | Iron stearate | Iron tristearate, pure | AKOS015839873 | E8Q7454COW | iron(3+);octadecanoate | Q27277011 | EINECS 225-889-4 | iron(3+) trioctadecan

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

FERRIC STEARATE | Iron Tristearate | Iron(III) Stearate | Stearic Acid Iron(III) Salt | iron(iii)stearate | Iron stearate | Iron tristearate, pure | AKOS015839873 | E8Q7454COW | iron(3+);octadecanoate | Q27277011 | EINECS 225-889-4 | iron(3+) trioctadecan

Especificaciones y pureza

Fe：5.8-8.0%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Nombres e identificadores

• Pubchem Sid: 504754286
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754286
• Sonrisas canónicas: CCCCCCCCCCCCCCCCCC(=O)[O-].CCCCCCCCCCCCCCCCCC(=O)[O-].CCCCCCCCCCCCCCCCCC(=O)[O-].[Fe+3]
• IUPAC Name: iron(3+);octadecanoate
• InChIKey: XHQSLVIGPHXVAK-UHFFFAOYSA-K
• INCHI: 1S/3C18H36O2.Fe/c3*1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;/h3*2-17H2,1H3,(H,19,20);/q;;;+3/p-3
• Isómeros SMILES: CCCCCCCCCCCCCCCCCC(=O)[O-].CCCCCCCCCCCCCCCCCC(=O)[O-].CCCCCCCCCCCCCCCCCC(=O)[O-].[Fe+3]
• PubChem CID: 68388
• Peso molecular: 906.27

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Fatty Acyls
      • Subclass Fatty acids and conjugates

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Fatty Acyls
• Subclass: Fatty acids and conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Long-chain fatty acids
• Alternative Parents: Straight chain fatty acids Carboxylic acid salts Organic transition metal salts Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Long-chain fatty acid - Straight chain fatty acid - Carboxylic acid salt - Organic transition metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
• 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

• Peso molecular: 906.300 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 45
• Exact Mass: 905.726 Da
• Monoisotopic Mass: 905.726 Da
• Topological Polar Surface Area: 120.000 Ų
• Heavy Atom Count: 61
• Formal Charge: 0
• Complexity: 196.000
• 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: 4

XLogP3

Referencias

1. Ruoshui Li, Yinsheng Liao, Yanfei Dou, Deng Wang, Guodong Li, Weihai Sun, Jihuai Wu, Zhang Lan.  (2021)  CoFe2O4 nanocrystals for interface engineering to enhance performance of perovskite solar cells.  SOLAR ENERGY,      [PMID:] [10.1016/j.solener.2021.03.073]

2. Qin Zhu, Jiaorong Yan, Qiguang Dai, Qingqing Wu, Yuanpu Cai, Jinyan Wu, Xingyi Wang, Wangcheng Zhan.  (2019)  Ethylene glycol assisted synthesis of hierarchical Fe-ZSM-5 nanorods assembled microsphere for adsorption Fenton degradation of chlorobenzene.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:31732347] [10.1016/j.jhazmat.2019.121581]

3. Bochu Du, Chenghao Lee, Ying Ji.  (2024)  Study of Factors Affecting UV-Induced Photo-Degradation in Different Types of Polyethylene Sheets.  Polymers,  16  (19): (2709).  [PMID:39408419] [10.3390/polym16192709]

4. Xiao-Dong Zhou, Xue-Long Yin, Lang Liu, Xue-Li Huang, Jing-Mei Liu, Ting Liu, He Lin, Feng-Yun Ma.  (2024)  Using isotope-tracer method with deuterium for quantitative study of hydrogen activation mechanism in direct coal liquefaction.  FUEL,      [PMID:] [10.1016/j.fuel.2024.133646]