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Merck
CN

209201

Copper(II) sulfate hydrate

98%

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About This Item

Linear Formula:
CuSO4 · xH2O
CAS Number:
Molecular Weight:
159.61 (anhydrous basis)
NACRES:
NA.55
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-847-6
MDL number:
Assay:
98%
Form:
crystalline powder
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vapor pressure

7.3 mmHg ( 25 °C)

Quality Level

assay

98%

form

crystalline powder

composition

Degree of hydration, 4-6

SMILES string

O.[Cu++].[O-]S([O-])(=O)=O

InChI

1S/Cu.H2O4S.H2O/c;1-5(2,3)4;/h;(H2,1,2,3,4);1H2/q+2;;/p-2

InChI key

CYKLGTUKGYURDP-UHFFFAOYSA-L



signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Storage Class

13 - Non Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable



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Nicholas A T Irwin et al.
Current biology : CB, 31(1), 66-76 (2020-10-31)
DNA replication is a ubiquitous and conserved cellular process. However, regulation of DNA replication is only understood in a small fraction of organisms that poorly represent the diversity of genetic systems in nature. Here we used computational and experimental approaches
Min Luo et al.
Nature cell biology, 22(12), 1447-1459 (2020-11-18)
The Hippo pathway plays critical roles in cell growth, differentiation, organ development and tissue homeostasis, whereas its dysregulation can lead to tumorigenesis. YAP and TAZ are transcription co-activators and represent the main downstream effectors of the Hippo pathway. Here, we
Damijana Urankar et al.
Journal of combinatorial chemistry, 10(6), 981-985 (2008-10-17)
Azoamides, previously established as bioactive intracellular GSH-depleting agents, were decorated with a terminal alkyne moiety to 4 and then were transformed, by copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC), into different ligand-arm functionalized azoamides 6. Azides 5 having ligand-arms amenable for binding to



Global Trade Item Number

SKUGTIN
209201-1KG04061838770639
209201-25G04061832562643