Nickel(II) stearate - Ni：~10% , CAS No.2223-95-2

CAS: 2223-95-2 Cat. No.: N138515 Molecular Weight: 625.67 EC Number: 218-744-1

GRADE & PURITY Ni：~10%

Synonyms

nickel(2+);octadecanoate | nickel(2+) dioctadecanoate | Nickel(II)stearate | Nickel(2+) stearate | EINECS 218-744-1 | Octadecanoic acid, nickel(2+) salt | SCHEMBL136593 | NICKEL STEARATE | Octadecanoic acid, nickel(2+) salt (2:1) | Nickel(II) stearate | D

Storage

Room temperature

Shipped In

Normal

Overview

Application

It is used as animal pharmaceutical.

Specifications

Synonyms

nickel(2+);octadecanoate | nickel(2+) dioctadecanoate | Nickel(II)stearate | Nickel(2+) stearate | EINECS 218-744-1 | Octadecanoic acid, nickel(2+) salt | SCHEMBL136593 | NICKEL STEARATE | Octadecanoic acid, nickel(2+) salt (2:1) | Nickel(II) stearate | D

Specifications & Purity

Ni：~10%

Storage

Room temperature

Shipped In

Normal

Names and Identifiers

• Pubchem Sid: 488188322
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488188322
• Canonical Smiles: CCCCCCCCCCCCCCCCCC(=O)[O-].CCCCCCCCCCCCCCCCCC(=O)[O-].[Ni+2]
• IUPAC Name: nickel(2+);octadecanoate
• InChIKey: JMWUYEFBFUCSAK-UHFFFAOYSA-L
• INCHI: 1S/2C18H36O2.Ni/c2*1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;/h2*2-17H2,1H3,(H,19,20);/q;;+2/p-2
• Isomeric SMILES: CCCCCCCCCCCCCCCCCC(=O)[O-].CCCCCCCCCCCCCCCCCC(=O)[O-].[Ni+2]
• Molecular Weight: 625.67
• Reaxy-Rn: 3919703
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3919703&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Fatty Acyls
• Subclass: Fatty acids and conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Long-chain fatty acids
• Alternative Parents: 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 - 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
• Description: 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

Chemical and Physical Properties

• Solubility: Insoluble in water
• Molecular Weight: 625.600 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 30
• Exact Mass: 624.463 Da
• Monoisotopic Mass: 624.463 Da
• Topological Polar Surface Area: 80.300 Ų
• Heavy Atom Count: 41
• 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: 3

XLogP3

References

1. 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]

2. Zhengquan Jiang, Chenglong Wang, Wenwei Ma, Ming Li, Laigui Yu, Shengmao Zhang, Weihua Li.  (2025)  Eco-Friendly Trinickel Disulfide Nanoparticles Advancing Poly-α-olefin Lubrication.  LANGMUIR,      [PMID:40670900] [10.1021/acs.langmuir.5c01914]