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Merck

223506

Cloruro de calcio dihydrate

ACS reagent, ≥99%

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Fórmula empírica (notación de Hill):
CaCl2 · 2H2O
Número CAS:
Peso molecular:
147.01
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352300
EC Number:
233-140-8
MDL number:
Assay:
≥99%, 99.0-105.0% (ACS specification)
Grade:
ACS reagent
Form:
powder or crystals
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grade

ACS reagent

Quality Level

vapor pressure

0.01 mmHg ( 20 °C)

assay

≥99%, 99.0-105.0% (ACS specification)

form

powder or crystals

impurities

≤0.003% oxidizers, ≤0.01% NH4OH pptd., ≤0.01% calcium chloride, ≤0.01% insolubles

pH

4.5-8.5 (25 °C, 5%)

mp

176 °C (dec.) (lit.)

anion traces

sulfate (SO42-): ≤0.01%

cation traces

Ba: ≤0.005%, Fe: ≤0.001%, K: ≤0.01%, Mg: ≤0.005%, NH4+: ≤0.005%, Na: ≤0.02%, Sr: ≤0.1%, heavy metals: ≤5 ppm (by ICP)

storage temp.

room temp

SMILES string

O.O.Cl[Ca]Cl

InChI

1S/Ca.2ClH.2H2O/h;2*1H;2*1H2/q+2;;;;/p-2

InChI key

LLSDKQJKOVVTOJ-UHFFFAOYSA-L

General description

Calcium chloride dihydrate is a moisture resistant, cheap and commonly available calcium salt. Its efficacy as a chiral catalyst for various asymmetric organic reactions has been evaluated.

Application

Calcium chloride dihydrate has been used as a calcium supplement for the DMEM (Dulbecco′s modified Eagle′s medium) for use in cell culture studies. It has also been used to prepare the synthetic brine solution.
It may be used in the preparation of calcium-alginate beads.
Calcium chloride dihydrate may be used in combination with sodium borohydride for the asymmetric reduction of 1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-[(1S)-2-hydroxy-1-phenylethylamino]ethanone to form (1R)-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-[(1S)-2-hydroxy-1-phenylethylamino]ethanol.


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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Clase de almacenamiento

13 - Non Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable



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Calcium Chloride (CaCl2) as Catalyst for Asymmetric Organic Reactions.
Tsubogo T, et al.
Topics in Catalysis, 10(13), 935-939 (2014)
A mild, enantioselective synthesis of (R)-salmeterol via sodium borohydride-calcium chloride asymmetric reduction of a phenacyl phenylglycinol derivative
Bream RN, et al.
Journal of the Chemical Society. Perkin Transactions 1, 20, 2237-2242 (2002)
George Pasparakis et al.
International journal of pharmaceutics, 323(1-2), 34-42 (2006-07-11)
The aim of the present work was to investigate the swelling behavior and the in vitro release of the antihypertensive drug verapamil hydrochloride from calcium alginate and chitosan treated calcium alginate beads. Calcium-alginate beads, chitosan-coated alginate beads and alginate-chitosan mixed