Sodium acetate trihydrate - UltraBio™, Ultra pure, ≥99% , CAS No.6131-90-4

CAS: 6131-90-4 Cat. No.: S433099 Summenformel: C₂H₃NaO₂·3H₂O Molekulargewicht: 136.08 Beilstein Registry Number: 3732037 EG-Nummer: 612-115-9 PubChem CID: 23665404

GRADE & PURITY UltraBio™, Ultra pure, ≥99%

Synonyms

4550K0SC9B | sodium acetatetrihydrate | Acetic acid sodium salt trihydrate | sodium;acetate;trihydrate | MFCD00071557

Storage

Room temperature

Übersicht

Other Notes

Enzyme substrate for acetate kinase (EC 2.7.2.1)

Sodium acetate trihydrate has been used: As a component of citrate-acetate buffer for hydroxyproline assay. To prepare buffered salt solutions for ultrafiltration experiments. To prepare acetate buffer solution for the electrochemical synthesis of indium tin oxide/gold nanoparticles/nickel oxide/poly(Pyrrole-N-propionic acid) (ITO/GNPs/NiO/poly(PPA)) electrode.

Specifications

Synonyme

4550K0SC9B | sodium acetatetrihydrate | Acetic acid sodium salt trihydrate | sodium;acetate;trihydrate | MFCD00071557

Spezifikationen & Reinheit

UltraBio™, Ultra pure, ≥99%

Biochemische und physiologische Mechanismen

Sodium acetate trihydrate (SAT), an inorganic salt hydrate has been the focus of numerous scientific studies on its potential as a heat energy storage phase transition material (PCM).

Storage

Room temperature

Note

Ultra pure, UltraBio™

Reinheit

≥99%

Namen und Kennungen

Pubchem Sid

528769490

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528769490

Kanonisches Lächeln

CC(=O)[O-].O.O.O.[Na+]

IUPAC Name

sodium;acetate;trihydrate

InChIKey

AYRVGWHSXIMRAB-UHFFFAOYSA-M

INCHI

1S/C2H4O2.Na.3H2O/c1-2(3)4;;;;/h1H3,(H,3,4);;3*1H2/q;+1;;;/p-1

Isomere SMILES

CC(=O)[O-].O.O.O.[Na+]

WGK Deutschland

1

RTECS

AJ4580000

PubChem CID

23665404

Molekulargewicht

136.08

Beilstein

3732037

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Ebene5 Carboxylic acid salts
          • Ebene6 Acetate salts

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid salts
• Direct Parent: Acetate salts
• Alternative Parents: Monocarboxylic acids and derivatives Carboxylic acids Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acetate salt - Organic alkali metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as acetate salts. These are organic compounds containing acetic acid as its acid component.
• External Descriptors: hydrate

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

Chemische und physikalische Eigenschaften

• Löslichkeit: H2O: 1M, clear, colorless
• Schmelzpunkt (°C): 58°C
• Molekulargewicht: 136.080 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 0
• Exact Mass: 136.035 Da
• Monoisotopic Mass: 136.035 Da
• Topological Polar Surface Area: 43.100 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 34.600
• 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: 5

XLogP3