1.02711

Kupfer(II)-Acetatmonohydrat

for analysis EMSURE^® ACS

• Synonym(e): Kupfer(II)-Acetatmonohydrat, Kupferacetat
• Lineare Formel: (CH₃COO)₂Cu · H₂O
• CAS-Nummer: 6046-93-1
• Molekulargewicht: 181.63 (anhydrous basis)
• MDL-Nummer: MFCD00149570
• UNSPSC-Code: 12352103
• EG-Index-Nummer: 205-553-3
• NACRES: NA.21

Eigenschaften

• Qualität: ACS reagent
• Qualitätsniveau: 300
• Produktlinie: EMSURE^®
• Assay: 99.0-102.0% (iodometric)
• Form: solid
• Wirksamkeit: 501 mg/kg LD₅₀, oral (Rat)
• Grünere Alternativprodukt-Eigenschaften: Catalysis; Learn more about the Principles of Green Chemistry.
• sustainability: Greener Alternative Product
• Verunreinigungen: ≤0.01% Insoluble matter
• pH-Wert: 5.2-5.5 (20 °C, 20 g/L in H₂O)
• mp (Schmelzpunkt): 115 °C
• Löslichkeit: 72 g/L
• Dichte: 1.88 g/cm³ at 20 °C
• Schüttdichte: 1100 kg/m³
• Anionenspuren: chloride (Cl^-): ≤0.001%; sulfate (SO₄^2-): ≤0.005%
• Kationenspuren: Ca: ≤0.005%; Fe: ≤0.002%; K: ≤0.01%; N: ≤0.01%; Na: ≤0.01%; Ni: ≤0.002%; Pb: ≤0.004%; Zn: ≤0.002%
• Grünere Alternativprodukt-Kategorie: Aligned
• Lagertemp.: 2-30°C
• InChI: 1S/2C2H4O2.Cu.H2O/c2*1-2(3)4;;/h2*1H3,(H,3,4);;1H2/q;;+2;/p-2
• InChIKey: NWFNSTOSIVLCJA-UHFFFAOYSA-L

Beschreibung

Allgemeine Beschreibung

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product has been enhanced for catalysis. Click here for more information.

Anwendung

• Click-chemistry mediated synthesis of OTBN-1,2,3-Triazole derivatives exhibiting STK33 inhibition with diverse anti-cancer activities.: This study utilizes Copper(II) acetate monohydrate in the click-chemistry synthesis of OTBN-1,2,3-triazole derivatives, demonstrating their potential as inhibitors of serine/threonine kinase 33 (STK33), which could be significant for developing new anticancer treatments (Vala DP et al., 2024).


• Synthesis and antifungal activity of slow-release pyridinylcarbonyl chitooligosaccharide copper complexes.: This research describes the synthesis of slow-release antifungal agents using Copper(II) acetate monohydrate to form copper complexes with pyridinylcarbonyl chitooligosaccharides, highlighting their efficacy against various fungal pathogens (Liu W et al., 2022).


• Bis-triazolylchalcogenium-Functionalized Benzothiadiazole Derivatives as Light-up Sensors for DNA and BSA.: The paper reports on the development of bis-triazolylchalcogenium-functionalized benzothiadiazole derivatives synthesized using Copper(II) acetate monohydrate, which are used as fluorescent sensors for detecting DNA and bovine serum albumin (BSA) (Krüger R et al., 2021).


• LED-driven photocatalysis of toluene, trichloroethylene and formaldehyde by cuprous oxide modified titanate nanotube arrays.: This study involves the use of Copper(II) acetate monohydrate in the synthesis of cuprous oxide-modified titanate nanotubes, enhancing the photocatalytic degradation of various organic pollutants under LED illumination (Chen CH et al., 2022).

Hinweis zur Analyse

Gehalt (iodometrisch): 99,0–102,0 %
Unlösliche Anteile: ≤ 0,01 %
Chlorid (Cl): ≤ 0,001 %
Sulfat (SO₄): ≤ 0,005 %
Gesamtstickstoff (N): ≤ 0,01 %
Ca (Calcium): ≤ 0,005 %
Fe (Eisen): ≤ 0,002 %
K (Kalium): ≤ 0,01 %
Na (Natrium): ≤ 0,01 %
Ni (Nickel): ≤ 0,002 %
Pb (Blei): ≤ 0,004 %
Zn (Zink): ≤ 0,002 %
Entspricht ACS

Rechtliche Hinweise

EMSURE is a registered trademark of Merck KGaA, Darmstadt, Germany

Sicherheitshinweise

• Piktogramme: GHS05,GHS07,GHS09
• Signalwort: Danger
• H-Sätze: H302 - H314 - H410
• P-Sätze: P260 - P273 - P280 - P301 + P312 - P303 + P361 + P353 - P305 + P351 + P338
• Gefahreneinstufungen: Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B
• Lagerklassenschlüssel: 8B - Non-combustible, corrosive hazardous materials
• WGK: WGK 3
• Flammpunkt (°F): does not flash
• Flammpunkt (°C): does not flash