Zinc acetate - 10mM in DMSO , CAS No.557-34-6

CAS: 557-34-6 Cat. No.: Z424741 Summenformel: C₄H₆O₄Zn Molekulargewicht: 183.48 EG-Nummer: 209-170-2 PubChem CID: 11192

GRADE & PURITY 10mM in DMSO

Synonyms

Anhydrous Zinc Acetate | MFCD00012454 | Siltex CL 4 | ZINC ACETATE ANHYDROUS [HSDB] | Rite Aid Cherry Zinc Lozenges | Advanced Jellyfish Sting Kit | DB14487 | zinc (II) acetate | ZINCUM ACETICUM [HPUS] | DIABETIC SKIN CARE FORMULA | Tox21_302016 | Zn(OAc)

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

Zinc acetate is primarily utilized as a precursor or catalyst in various synthetic reactions. In organic chemistry, zinc acetate finds application as a reagent in the formation of carbon-carbon bonds. It can facilitate the synthesis of esters, allylic alcohols, and acetals. For example, it can promote the acylation of alcohols, phenols, and amines to form esters, such as the Fischer esterification reaction. Zinc acetate has also been used in the synthesis of metal-organic frameworks (MOFs). MOFs are porous materials consisting of metal ions or clusters coordinated to organic ligands. Zinc acetate can act as a precursor for the formation of MOFs due to its ability to coordinate with organic linkers and form robust networks.

Application：

Zinc acetate anhydrous is used in the synthesis of layered Zn-arylphosphonates with potential application in sorption, ion exchange or catalysis. It is utilized in the ultrasonic preparation of zinc sulfide nanoparticles coated on silica particles. It is administered orally or parenterally as a nutritional supplement. It finds an application in the field of industries such as wood preservation, manufacturing other zinc salts, polymers, manufacture of ethylene acetate, as a dye mordant, and analytical reagent. It also acts as a plating inhibitor on primary water piping.

Specifications

Synonyme

Anhydrous Zinc Acetate | MFCD00012454 | Siltex CL 4 | ZINC ACETATE ANHYDROUS [HSDB] | Rite Aid Cherry Zinc Lozenges | Advanced Jellyfish Sting Kit | DB14487 | zinc (II) acetate | ZINCUM ACETICUM [HPUS] | DIABETIC SKIN CARE FORMULA | Tox21_302016 | Zn(OAc)

Spezifikationen & Reinheit

10mM in DMSO

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Namen und Kennungen

Pubchem Sid

528771994

Kanonisches Lächeln

CC(=O)[O-].CC(=O)[O-].[Zn+2]

IUPAC Name

zinc;diacetate

InChIKey

DJWUNCQRNNEAKC-UHFFFAOYSA-L

INCHI

1S/2C2H4O2.Zn/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2

Isomere SMILES

CC(=O)[O-].CC(=O)[O-].[Zn+2]

WGK Deutschland

3

RTECS

AK1500000

PubChem CID

11192

Molekulargewicht

183.48

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Carboxylic acids and derivatives
• Subclass: Carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
• External Descriptors: zinc molecular entity - acetate salt

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

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PTPN22 Tchem Hematopoietic cell protein-tyrosine phosphatase 70Z-PEP (1215 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Hygroscopic
• Schmelzpunkt (°C): 200℃
• Molekulargewicht: 183.500 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 181.956 Da
• Monoisotopic Mass: 181.956 Da
• Topological Polar Surface Area: 80.300 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 25.500
• 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

Häufig gestellte Fragen

How should this product be stored?

Store at ?80 °C. Ultra-low temperature storage is required to maintain the specified shelf life.

How is this product shipped?

This product ships frozen with dry ice and cold packs. Unpack on arrival and transfer it to the storage condition stated above; handle dry ice with insulated gloves in a ventilated area.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 557-34-6, the molecular formula is C4H6O4Zn, and the molecular weight is 183.48 g/mol. InChIKey DJWUNCQRNNEAKC-UHFFFAOYSA-L.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.