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Merck
모든 사진(3)

주요 문서

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209201

Sigma-Aldrich

Copper(II) sulfate hydrate

98%

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모든 사진(3)

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 코드:
12352302
PubChem Substance ID:
329752059
NACRES:
NA.55

vapor pressure

7.3 mmHg ( 25 °C)

Quality Level

100

분석

98%

양식

crystalline powder

구성

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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관련 카테고리

픽토그램

CorrosionExclamation markEnvironment
GHS05,GHS07,GHS09

신호어

Danger

유해 및 위험 성명서

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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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

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.
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

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