The product was great and in the R&D for evaluation
209201
Copper(II) sulfate hydrate
Copper(II) sulfate hydrate
98%
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25 G
R$ 268,00
1 KG
R$ 523,00
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25 G
R$ 268,00
1 KG
R$ 523,00
About This Item
Fórmula linear:
CuSO4 · xH2O
Número CAS:
Peso molecular:
159.61 (anhydrous basis)
Número CE:
Número MDL:
Código UNSPSC:
12352302
ID de substância PubChem:
NACRES:
NA.55
Produtos recomendados
pressão de vapor
7.3 mmHg ( 25 °C)
Nível de qualidade
Ensaio
98%
Formulário
crystalline powder
composição
Degree of hydration, 4-6
cadeia de caracteres SMILES
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
chave InChI
CYKLGTUKGYURDP-UHFFFAOYSA-L
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Categorias relacionadas
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1
Código de classe de armazenamento
13 - Non Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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Nicholas A T Irwin et al.
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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.
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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