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05-6020

Copper(II) nitrate trihydrate

Name: Copper(II) nitrate trihydrate
Brand: SAJ

SAJ special grade, 77.0-80.0% anhydrous basis

Synonym(s):

Cupric nitrate trihydrate

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About This Item

Linear Formula:

Cu(NO₃)₂ · 3H₂O

CAS Number:

10031-43-3

Molecular Weight:

241.60

UNSPSC Code:

12352300

PubChem Substance ID:

329748110

MDL number:

MFCD00149671

Assay:

77.0-80.0% anhydrous basis

Grade:

SAJ special grade

Form:

solid

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Properties

grade

SAJ special grade

assay

77.0-80.0% anhydrous basis

form

solid

availability

available only in Japan

storage temp.

15-25°C

SMILES string

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

InChI

1S/Cu.2NO3.3H2O/c;2*2-1(3)4;;;/h;;;3*1H2/q+2;2*-1;;;

InChI key

SXTLQDJHRPXDSB-UHFFFAOYSA-N

Description

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pictograms

GHS03,GHS05,GHS09

signalword

Danger

hcodes

H272,H314,H410

pcodes

P210 - P260 - P273 - P280 - P303 + P361 + P353 - P305 + P351 + P338

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Ox. Sol. 2 - Skin Corr. 1B

Storage Class

5.1B - Oxidizing hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Mechanistic insights into a novel chromone-appended Cu(II) anticancer drug entity: in vitro binding profile with DNA/RNA substrates and cytotoxic activity against MCF-7 and HepG2 cancer cells.

Imtiyaz Yousuf et al.

Dalton transactions (Cambridge, England : 2003), 44(22), 10330-10342 (2015-05-15)

A new chromone-appended Cu(ii) drug entity () was designed and synthesized as a potential anticancer chemotherapeutic agent. The structural elucidation was carried out thoroughly by elemental analysis, FT-IR, EPR, ESI-MS and single crystal X-ray crystallography. Complex resulted from the in

Gas-phase copper and silver complexes with phosphorothioate and phosphorodithioate pesticides investigated using electrospray ionization mass spectrometry.

Adetayo M Mustapha et al.

Journal of mass spectrometry : JMS, 50(1), 145-152 (2015-01-21)

Efforts to improve agricultural productivity have led to a growing dependency on organophosphorus pesticides. Phosphorothioate and phosphorodithioate pesticides are organophosphorus pesticide subclasses with widespread application for the control of insects feeding on vegetables and fruits. However, even low doses of