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Merck

276839

Zinc chloride solution

1.0 M in diethyl ether

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About This Item

Linear Formula:
ZnCl2
CAS Number:
Molecular Weight:
136.30
NACRES:
NA.55
PubChem Substance ID:
UNSPSC Code:
12352302
MDL number:
Form:
liquid
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Product Name

Zinc chloride solution, 1.0 M in diethyl ether

InChI

1S/2ClH.Zn/h2*1H;/q;;+2/p-2

SMILES string

Cl[Zn]Cl

InChI key

JIAARYAFYJHUJI-UHFFFAOYSA-L

form

liquid

concentration

0.95-1.10 M (silver nitrate titration)
1.0 M in diethyl ether

density

0.835 g/mL at 25 °C

Quality Level

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General description

Zinc chloride in combination with 1-ethyl-3-methylimidazolium chloride comprises a molten salt, which is employed in the electrodeposition studies of zinc on various substrates (glassy carbon and nickel). ZnCl2 participates as a catalyst in the preparation of carbonyl-methylene condensation products and poly(propylene fumarate).

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

target_organs

Central nervous system, Respiratory system

supp_hazards

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

-40.0 °F - closed cup

flash_point_c

-40 °C - closed cup


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Electrodeposition of zinc from a Lewis acidic zinc chloride-1-ethyl-3-methylimidazolium chloride molten salt.
Lin Y-F and Sun I.
Electrochimica Acta, 44(16), 2771-2777 (1999)
Albert K Shung et al.
Journal of biomaterials science. Polymer edition, 13(1), 95-108 (2002-05-11)
Diethyl fumarate and propylene glycol were reacted in the presence of a zinc chloride catalyst to synthesize poly(propylene fumarate) (PPF) over a period of 12 hours. The kinetics of the transesterification polymerization at 130 degrees C, 150 degrees C, and
Zinc chloride as a new catalyst for Knoevenagel condensation.
Shanthan RP and Venkataratnam RV.
Tetrahedron Letters, 32(41), 5821-5822 (1991)
Jessica Duprez et al.
PloS one, 7(10), e46831-e46831 (2012-10-12)
Rat pancreatic islet cell apoptosis is minimal after prolonged culture in 10 mmol/l glucose (G10), largely increased in 5 mmol/l glucose (G5) and moderately increased in 30 mmol/l glucose (G30). This glucose-dependent asymmetric V-shaped profile is preceded by parallel changes
Masatoshi Ishida et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(45), 14329-14341 (2012-09-26)
The synthesis, characterization, photophysical properties, and theoretical analysis of a series of tetraaza porphyrin analogues (H-Pn: n=1-4) containing a dipyrrin subunit and an embedded 1,10-phenanthroline subunit are described. The meso-phenyl-substituted derivative (H-P1) interacts with a Mg(2+) salt (e.g., MgCl(2), MgBr(2)

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