516244
Calcium iodide
AnhydroBeads™, −10 mesh, 99.95% trace metals basis
Synonym(s):
Calcium diiodide
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About This Item
Linear Formula:
CaI2
CAS Number:
Molecular Weight:
293.89
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23
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product line
AnhydroBeads™
Assay
99.95% trace metals basis
impurities
≤550.0 ppm Trace Metal Analysis
particle size
−10 mesh
mp
779 °C (lit.)
SMILES string
I[Ca]I
InChI
1S/Ca.2HI/h;2*1H/q+2;;/p-2
InChI key
UNMYWSMUMWPJLR-UHFFFAOYSA-L
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Application
Calcium iodide can be used:
- As a passivator of CH3NH3PbI3(MAPbI3) perovskite films to achieve high efficiency and long-term stability.
- As a dopant to prepare 3D γ-CsPbI3 perovskite solar cells, to improve their stability and power conversion efficiency.
- As a precursor to synthesize a series of heteroleptic calcium formamidinate derivatives.
- As a catalyst for photooxidative oxylactonization of oxocarboxylic acids.
Legal Information
AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC
accessory
Product No.
Description
Pricing
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Preparation of Tortuous 3D gamma-CsPbI3 Films at Low Temperature by CaI2 as Dopant for Highly Efficient Perovskite Solar Cells
Hang Zhao, et al.
Advanced Functional Materials
, 29, 1808986-1808986 (2019)
Calcium formamidinate derivatives by hydride insertion of carbodiimides
Joshua Dyall, et al.
Dalton Transactions, 48, 4248-4254 (2019)
CaI2:a more effective passivator of perovskite films than PbI2 for high efficiency and long-term stability of perovskite solar cells
Chuanliang Chen, et al.
Journal of Materials Chemistry, 6, 7903-7912 (2018)
Calcium iodide catalyzed photooxidative oxylactonization of oxocarboxylic acids using molecular oxygen as terminal oxidant
Norihiro Tada, et al
Tetrahedron Letters, 54, 256-258 (2013)
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