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05-5850

Sigma-Aldrich

Copper(II) chloride dihydrate

JIS special grade, ≥99.0%

Sinónimos:

Cupric chloride dihydrate

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About This Item

Fórmula lineal:
CuCl2 · 2H2O
Número de CAS:
10125-13-0
Peso molecular:
170.48
EC Number:
231-210-2
MDL number:
MFCD00149674
UNSPSC Code:
12352302
PubChem Substance ID:
329748103

grade

JIS special grade

vapor density

>1 (vs air)

assay

≥99.0%

form

solid

reaction suitability

reagent type: catalyst
core: copper

availability

available only in Japan

pH

3.0-3.8

mp

100 °C (dec.) (lit.)

SMILES string

Cl[Cu]Cl.[H]O[H].[H]O[H]

InChI

1S/2ClH.Cu.2H2O/h2*1H;;2*1H2/q;;+2;;/p-2

Inchi Key

MPTQRFCYZCXJFQ-UHFFFAOYSA-L

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signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Bin Wu et al.
Carbohydrate research, 351, 68-73 (2012-03-01)
Two new glucoside esters 1 and 2 were produced as stress metabolites in the fresh leaves of Portulaca oleracea, in response to abiotic stress elicitation by CuCl(2). A new sugar ester (3) and two known compounds (4 and 5) were
Iron(II)-catalyzed trifluoromethylation of potassium vinyltrifluoroborates.
Andrew T Parsons et al.
Angewandte Chemie (International ed. in English), 51(12), 2947-2950 (2012-02-14)
Francesca Cima et al.
Chemosphere, 89(1), 19-29 (2012-05-01)
After the widespread ban of TBT, due to its severe impact on coastal biocoenoses, mainly related to its immunosuppressive effects on both invertebrates and vertebrates, alternative biocides such as Cu(I) salts and the triazine Irgarol 1051, the latter previously used
Kenji Funaki et al.
Organic letters, 14(24), 6186-6189 (2012-12-12)
Direct arylation of thiophenes and benzothiophenes with aryltrimethylsilanes was effectively catalyzed by PdCl(2)(MeCN)(2) in the presence of CuCl(2) as an oxidant. The reaction preferentially occurred at the β-position of both thiophenes and benzothiophenes.
Shuxia Zhou et al.
Pharmaceutical research, 30(5), 1311-1327 (2013-02-16)
Metal-catalyzed oxidation (MCO) of proteins is of primary concern in the development of biotherapeutics as it represents a prominent degradation pathway with potential undesired biological and biotherapeutic consequences. We developed a fluorogenic derivatization methodology to study the MCO of IgG1
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