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Merck

1.02711

Copper(II) acetate monohydrate

greener alternative

Alternative plus écologique

for analysis EMSURE® ACS

Synonyme(s) :

Copper(II) acetate monohydrate, Cupric acetate

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A propos de cet article

Formule linéaire :
(CH3COO)2Cu · H2O
Numéro CAS:
Poids moléculaire :
181.63 (anhydrous basis)
UNSPSC Code:
12352103
EC Index Number:
205-553-3
NACRES:
NA.21
MDL number:
Assay:
99.0-102.0% (iodometric)
Grade:
ACS reagent
Form:
solid
Solubility:
72 g/L
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grade

ACS reagent

Quality Segment

product line

EMSURE®

assay

99.0-102.0% (iodometric)

form

solid

potency

501 mg/kg LD50, oral (Rat)

greener alternative product characteristics

Catalysis
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sustainability

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impurities

≤0.01% Insoluble matter

pH

5.2-5.5 (20 °C, 20 g/L in H2O)

mp

115 °C

solubility

72 g/L

density

1.88 g/cm3 at 20 °C

bulk density

1100 kg/m3

anion traces

chloride (Cl-): ≤0.001%, sulfate (SO42-): ≤0.005%

cation traces

Ca: ≤0.005%, Fe: ≤0.002%, K: ≤0.01%, N: ≤0.01%, Na: ≤0.01%, Ni: ≤0.002%, Pb: ≤0.004%, Zn: ≤0.002%

greener alternative category

storage temp.

2-30°C

SMILES string

[Cu+2].[O-]C(=O)C.[O-]C(=O)C.O

InChI

1S/2C2H4O2.Cu.H2O/c2*1-2(3)4;;/h2*1H3,(H,3,4);;1H2/q;;+2;/p-2

InChI key

NWFNSTOSIVLCJA-UHFFFAOYSA-L

General description

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Application


  • 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).

Analysis Note

Assay (iodometric): 99.0 - 102.0 %
Insoluble matter: ≤ 0.01 %
Chloride (Cl): ≤ 0.001 %
Sulfate (SO₄): ≤ 0.005 %
Total nitrogen (N): ≤ 0.01 %
Ca (Calcium): ≤ 0.005 %
Fe (Iron): ≤ 0.002 %
K (Potassium): ≤ 0.01 %
Na (Sodium): ≤ 0.01 %
Ni (Nickel): ≤ 0.002 %
Pb (Lead): ≤ 0.004 %
Zn (Zinc): ≤ 0.002 %
Corresponds to ACS

Legal Information

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


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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Classe de stockage

8B - Non-combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

does not flash

flash_point_c

does not flash



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