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209201

Sigma-Aldrich

Copper(II) sulfate hydrate

98%

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About This Item

Linear Formula:
CuSO4 · xH2O
CAS Number:
23254-43-5
Molecular Weight:
159.61 (anhydrous basis)
EC Number:
231-847-6
MDL number:
MFCD00149682
UNSPSC Code:
12352302
PubChem Substance ID:
329752059
NACRES:
NA.55

vapor pressure

7.3 mmHg ( 25 °C)

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

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Related Categories

Signal Word

Danger

Hazard Statements

H302,H318,H410

Hazard Classifications

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

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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
Wei Zhao et al.
Dalton transactions (Cambridge, England : 2003), (8)(8), 1509-1517 (2005-04-13)
Three novel metal-organic frameworks (MOFs), [Cu(1)SO4].H2O (4), [Cu2(2)2(SO4)2].4H2O (5) and [Cu(3)(H2O)]SO4.5.5H2O (6), were obtained by hydrothermal reactions of CuSO4.5H2O with the corresponding ligands, which have different flexibility. The structures of the synthesized complexes were determined by single-crystal X-ray diffraction analyses.
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
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

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